PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
2477227-6	1989	The amounts of sugar that were found relative to peptide indicated the presence of two N-linked oligosaccharides per molecule on both beta-core and hCG beta.	n-linked oligosaccharides	87-112	chorionic gonadotropin subunit beta 3	Homo sapiens	148-156
2482796-1	1989	An N-acetylglucosaminyltransferase III which catalyzes the addition of N-acetylglucosamine through a beta 1-4 linkage (bisecting N-acetylglucosamine) to the beta-linked mannose of the trimannosyl core structure of N-linked oligosaccharides of glycoproteins was measured in human serum, and liver and hepatoma tissues.	n-linked oligosaccharides	214-239	beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase	Homo sapiens	3-38
2556477-7	1989	However, after complete cleavage of N-linked oligosaccharides with endoglycosidase F, the core peptide of cytochrome b558 large subunit from these different cell types had the same Mr (58,000).	n-linked oligosaccharides	36-61	mitochondrially encoded cytochrome b	Homo sapiens	106-118
2477227-11	1989	We propose that the N-linked oligosaccharides on beta-core closely resemble the underlying N-linked structures of hCG beta with the antennary sialic acid, galactose, and N-acetylglucosamine removed.	n-linked oligosaccharides	20-45	chorionic gonadotropin subunit beta 3	Homo sapiens	114-122
2514791-3	1989	In an effort to elucidate the factors controlling the expression of N-linked oligosaccharides on this polypeptide, we have used a combination of sequential exoglycosidase digestion, methylation analysis, and controlled acetolysis to determine the oligosaccharide structures at each of the N-glycosylation sites of type I and type II t-PA when isolated from a human colon fibroblast cell strain and from a Bowes melanoma cell line.	n-linked oligosaccharides	68-93	plasminogen activator, tissue type	Homo sapiens	333-337
2554567-6	1989	Enzymatic deglycosylation experiments demonstrated that in addition to the predicted four N-linked oligosaccharides, gp65 contains O-linked carbohydrates which are resistant to the action of peptide N-Glycanase F, but sensitive to neuraminidase and O-Glycanase.	n-linked oligosaccharides	90-115	neuroplastin	Homo sapiens	117-121
2472431-3	1989	[35S]Cysteine-labeled human umbilical vein endothelial cells synthesized a GMP-140 molecule containing complex N-linked oligosaccharides similar to those previously demonstrated in platelets and the megakaryocytic HEL cell line.	n-linked oligosaccharides	111-136	selectin P	Homo sapiens	75-82
2674947-5	1989	Cytolysin bears N-linked oligosaccharides that are converted to the complex type, while the major trypsin-like protease, granzyme A, bears only high-mannose-type oligosaccharides.	n-linked oligosaccharides	16-41	perforin 1	Rattus norvegicus	0-9
2668269-0	1989	Structure of the phosphorylated N-linked oligosaccharides from the mnn9 and mnn10 mutants of Saccharomyces cerevisiae.	n-linked oligosaccharides	32-57	mannosyltransferase complex subunit MNN9	Saccharomyces cerevisiae S288C	67-71
2668269-0	1989	Structure of the phosphorylated N-linked oligosaccharides from the mnn9 and mnn10 mutants of Saccharomyces cerevisiae.	n-linked oligosaccharides	32-57	alpha-1,6-mannosyltransferase	Saccharomyces cerevisiae S288C	76-81
2668269-1	1989	The N-linked oligosaccharides, from Saccharomyces cerevisiae mnn1 mnn9 mutant mannoprotein extracted from the cells in hot citrate buffer, were separated by ion exchange into a monophosphate diester, a monophosphate monoester, a diphosphate diester, and a diphosphate monoester diester.	n-linked oligosaccharides	4-29	alpha-1,3-mannosyltransferase MNN1	Saccharomyces cerevisiae S288C	61-65
2668269-1	1989	The N-linked oligosaccharides, from Saccharomyces cerevisiae mnn1 mnn9 mutant mannoprotein extracted from the cells in hot citrate buffer, were separated by ion exchange into a monophosphate diester, a monophosphate monoester, a diphosphate diester, and a diphosphate monoester diester.	n-linked oligosaccharides	4-29	mannosyltransferase complex subunit MNN9	Saccharomyces cerevisiae S288C	66-70
2480355-1	1989	The role of trimming and processing of N-linked oligosaccharides on the cell surface expression of the melanoma vitronectin receptor, a member of the integrin family of cell adhesion receptors, was examined by using specific glucosidase and mannosidase inhibitors.	n-linked oligosaccharides	39-64	vitronectin	Homo sapiens	112-123
2480355-3	1989	Conversely, the vitronectin receptor synthesized in the presence of the mannosidase I and II inhibitors, 1-deoxymannojirimycin and swainsonine, was transported normally to the cell surface with its alpha chain N-linked oligosaccharides in an endoglycosidase H-sensitive form.	n-linked oligosaccharides	210-235	vitronectin	Homo sapiens	16-27
2511543-9	1989	Removal of N-linked oligosaccharides from jejunum and colonic forms of L-Ph produced bands on SDS-PAGE with identical mobility, suggesting that the proteins were the same.	n-linked oligosaccharides	11-36	lactase	Rattus norvegicus	71-75
2550193-5	1989	The two major N-linked oligosaccharides of Namalwa EPO were fucose-containing tetraantennary and fucose-containing triantennary structures.	n-linked oligosaccharides	14-39	erythropoietin	Homo sapiens	51-54
2536708-1	1989	The role of the human chorionic gonadotropin (hCG) N-linked oligosaccharides in receptor binding and signal transduction was analyzed using site-directed mutagenesis and transfection studies.	n-linked oligosaccharides	51-76	chorionic gonadotropin subunit beta 5	Homo sapiens	46-49
2731537-8	1989	These results indicate that mammalian-cell-derived recombinant human interferon-beta 1s have identical polypeptides to those of natural human interferon-beta 1 but their carbohydrate moieties, including unusual N-linked oligosaccharides, are individually different from natural ones and depend on the host cell.	n-linked oligosaccharides	211-236	interferon beta 1	Homo sapiens	69-86
2495719-2	1989	In pulse-chase studies with normal fibroblasts, remodeling of N-linked oligosaccharides resulted in the temporal appearance of three molecular-weight forms of acid beta-glucosidase.	n-linked oligosaccharides	62-87	glucosylceramidase beta	Homo sapiens	159-180
2536708-9	1989	The use of site-directed mutagenesis was critical in uncovering site-specific functions of the hCG N-linked oligosaccharides in signal transduction and reveals the importance of the Asn-52 oligosaccharide in this process.	n-linked oligosaccharides	99-124	chorionic gonadotropin subunit beta 5	Homo sapiens	95-98
3264877-5	1988	Digestion with glycosidic enzymes indicated that soluble CSF-1 encoded by the 4-kb cDNA contained both asparagine(N)-linked and O-linked carbohydrate chains, whereas the product of the 1.6-kb clone had only N-linked oligosaccharides.	n-linked oligosaccharides	207-232	colony stimulating factor 1	Homo sapiens	57-62
2535484-0	1989	Structural assessment of the N-linked oligosaccharides of cell-CAM 105 by lectin-agarose affinity chromatography.	n-linked oligosaccharides	29-54	CEA cell adhesion molecule 1	Rattus norvegicus	58-70
2535484-1	1989	The N-linked oligosaccharides of cell-CAM 105, a glycoprotein involved in the intercellular adhesion between rat hepatocytes, were studied by sequential lectin-agarose affinity chromatography of desialylated, [14C]-labelled glycopeptides.	n-linked oligosaccharides	4-29	CEA cell adhesion molecule 1	Rattus norvegicus	33-45
2487679-6	1989	It was concluded that two types of N-linked oligosaccharides as well as sialic acids mediate at least in part the tissue type-specific membrane activity for Thy-1 alloantibody response.	n-linked oligosaccharides	35-60	Thy-1 cell surface antigen	Homo sapiens	157-162
2649653-5	1989	The effects of galactosylation on the structure of the envelope proteins suggest that cleavage of the gp160 precursor into gp120 and gp41 occurs intracellularly, apparently concurrent with the addition of galactose to N-linked oligosaccharides of the envelope proteins.	n-linked oligosaccharides	218-243	glutamyl aminopeptidase	Homo sapiens	102-107
2977291-4	1988	Lec1 cells form only high mannose-type N-linked oligosaccharides because they lack GlcNAc transferase I activity.	n-linked oligosaccharides	39-64	adhesion G protein-coupled receptor L2	Homo sapiens	0-4
2610054-0	1989	Characterization of N-linked oligosaccharides of human urinary kallikrein molecules.	n-linked oligosaccharides	20-45	kallikrein related peptidase 4	Homo sapiens	63-73
2610054-1	1989	The micro-heterogeneity due to varied N-linked oligosaccharides of both active- and pro-types of human urinary kallikrein (HUK) in normal subjects and some patients were investigated by the methods of serial lectin affinity chromatography and crossed affino-immunoelectrophoresis.	n-linked oligosaccharides	38-63	kallikrein related peptidase 4	Homo sapiens	111-121
2647161-2	1989	Using site-directed mutagenesis and gene-transfer, we analyzed the role of the N-linked oligosaccharides of alpha and chorionic gonadotropin (CG)beta in the secretion, assembly, and biologic activity of hCG.	n-linked oligosaccharides	79-104	chorionic gonadotropin subunit beta 5	Homo sapiens	203-206
2647161-7	1989	Analysis of the receptor binding of the hCG glycosylation mutants showed that absence of any or all of the hCG N-linked oligosaccharides had only a minor effect on receptor affinity of the derivatives.	n-linked oligosaccharides	111-136	chorionic gonadotropin subunit beta 5	Homo sapiens	40-43
2647161-7	1989	Analysis of the receptor binding of the hCG glycosylation mutants showed that absence of any or all of the hCG N-linked oligosaccharides had only a minor effect on receptor affinity of the derivatives.	n-linked oligosaccharides	111-136	chorionic gonadotropin subunit beta 5	Homo sapiens	107-110
2551606-1	1989	The mouse sperm receptor, called ZP3, is a glycoprotein (83,000 Mr) that consists of a 44,000 Mr polypeptide chain (402 amino acids), three or four N-linked oligosaccharides, and an undetermined number of O-linked oligosaccharides.	n-linked oligosaccharides	148-173	zona pellucida glycoprotein 3	Mus musculus	33-36
2535725-4	1989	Both the molecular weight disparity and monoclonal antibody discrimination of the two gp80s were abolished by inhibition of envelope protein glycosylation with tunicamycin, whereas the apparent gp70 size differences were resolved by enzymatic removal of N-linked oligosaccharides.	n-linked oligosaccharides	254-279	embigin	Homo sapiens	194-198
2494430-4	1989	At least a subset of the N-linked oligosaccharides in extracellular t-PA was resistant to endo-beta-N-acetyl-D-glucosaminidase H, which removes immature, high-mannose-type oligosaccharides.	n-linked oligosaccharides	25-50	chromosome 20 open reading frame 181	Homo sapiens	68-72
2460458-7	1988	Thus, in vivo the two N-linked oligosaccharides of CG beta are critical for efficient secretion and assembly with the alpha subunit and are likely important for proper folding of the CG beta subunit.	n-linked oligosaccharides	22-47	chorionic gonadotropin subunit beta 3	Homo sapiens	51-58
2460458-7	1988	Thus, in vivo the two N-linked oligosaccharides of CG beta are critical for efficient secretion and assembly with the alpha subunit and are likely important for proper folding of the CG beta subunit.	n-linked oligosaccharides	22-47	chorionic gonadotropin subunit beta 3	Homo sapiens	183-190
3142362-9	1988	Studies on the transferase activity toward fetuin, human chorionic gonadotropin, and glycophorin A indicated that the enzyme preferentially adds the sugar to the sialylated terminal end of N-linked oligosaccharides.	n-linked oligosaccharides	189-214	glycophorin A (MNS blood group)	Homo sapiens	85-98
3264883-14	1988	All results are consistent with the conclusion that the gp39 molecule is an integral membrane glycoprotein composed of heterogeneous N-linked oligosaccharides of both the complex and high mannose types.	n-linked oligosaccharides	133-158	chitinase 3 like 1	Homo sapiens	56-60
2905169-6	1988	Tunicamycin treatment blocks the conversion of the precursor to the mature form, and removal of N-linked oligosaccharides with Endo F reduces the relative molecular weight of P-glycoprotein to 140K.	n-linked oligosaccharides	96-121	ATP binding cassette subfamily B member 1	Homo sapiens	175-189
3174652-7	1988	The N-linked oligosaccharides on lgp120, tetraantennary structures with two lactosamine repeats on one of the branches, were not different from those of glycoproteins on the plasma membrane.	n-linked oligosaccharides	4-29	lysosomal-associated membrane protein 1	Rattus norvegicus	33-39
3264885-8	1988	At least three N-linked oligosaccharides and no significant O-linked sugars were found associated with R-Ta.	n-linked oligosaccharides	15-40	RNA binding fox-1 homolog 2	Homo sapiens	103-107
2840447-1	1988	Recent studies have demonstrated that Rous sarcoma virus-transformed baby hamster kidney (RS-BHK) cells express twofold higher levels of those N-linked oligosaccharides that contain the sequence [GlcNAc-beta(1,6)Man (1,6)] compared to nontransformed parental BHK cells (Pierce and Arango, J. Biol.Chem.	n-linked oligosaccharides	143-168	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	Homo sapiens	203-211
3042455-4	1988	Inhibition of co-translational transfer of N-linked oligosaccharides by tunicamycin produced EN1 and EN3 as intracellular species, and EN3 was sulfated and secreted.	n-linked oligosaccharides	43-68	engrailed homeobox 1	Homo sapiens	93-96
3066525-0	1988	Characterization of N-linked oligosaccharides attached to human renin expressed in COS cells.	n-linked oligosaccharides	20-45	renin	Homo sapiens	64-69
3288503-0	1988	Role of N-linked oligosaccharides attached to human renin expressed in COS cells.	n-linked oligosaccharides	8-33	renin	Homo sapiens	52-57
3288503-4	1988	An Asn-5 and -75 mutant which did not contain any glycosylation sites was unstable in the medium, suggesting that the N-linked oligosaccharides play an important role in stabilization of human renin.	n-linked oligosaccharides	118-143	renin	Homo sapiens	193-198
3346233-11	1988	The results of our study suggest that the Golgi endomannosidase takes part in a processing route for N-linked oligosaccharides which have retained glucose beyond the rough endoplasmic reticulum; the distinctive nature of this pathway may influence the ultimate structure of the resulting carbohydrate units.	n-linked oligosaccharides	101-126	mannosidase endo-alpha	Homo sapiens	48-63
3179269-1	1988	The structures of the N-linked oligosaccharides of the urinary erythropoietin (u-EPO) purified from urine of aplastic anemic patients were analyzed and compared with those for recombinant erythropoietin (r-EPO) prepared with baby hamster kidney (BHK) cells.	n-linked oligosaccharides	22-47	erythropoietin	Homo sapiens	63-77
3179269-1	1988	The structures of the N-linked oligosaccharides of the urinary erythropoietin (u-EPO) purified from urine of aplastic anemic patients were analyzed and compared with those for recombinant erythropoietin (r-EPO) prepared with baby hamster kidney (BHK) cells.	n-linked oligosaccharides	22-47	erythropoietin	Homo sapiens	81-84
3066525-5	1988	Our results suggest that the N-linked oligosaccharides have no effect on the enzymatic activity, but play an important role in stable secretion of human renin.	n-linked oligosaccharides	29-54	renin	Homo sapiens	153-158
3278222-9	1988	N-linked oligosaccharides of gp63 appear to be important for the stability of this molecule, possibly by preventing its autodegradation.	n-linked oligosaccharides	0-25	leishmanolysin like peptidase	Homo sapiens	29-33
2960381-8	1987	Further removal of N-linked oligosaccharides from this Mr 23,000 hormone using N-Glycanase yielded an apo-erythropoietin (Mr 18,000) which possessed substantially reduced biological activity.	n-linked oligosaccharides	19-44	erythropoietin	Homo sapiens	106-120
2827003-6	1988	Although cell-specific variability in posttranslational processing of EGF receptor N-linked oligosaccharides in the hepatoma cell lines was found, no difference between the receptors in PLC/PRF/5 and NPLC/PRF/5 was observed and no aberrant receptor-related species were detected.	n-linked oligosaccharides	83-108	epidermal growth factor receptor	Homo sapiens	70-82
2849025-7	1987	These results suggest that N-linked oligosaccharides are involved in binding of C3b to gC-2, but not gC-1.	n-linked oligosaccharides	27-52	complement C3	Homo sapiens	80-83
2849025-7	1987	These results suggest that N-linked oligosaccharides are involved in binding of C3b to gC-2, but not gC-1.	n-linked oligosaccharides	27-52	solute carrier family 25 member 18	Homo sapiens	87-91
2849025-8	1987	Alternatively, removal of N-linked oligosaccharides from gC-2 might adversely affect polypeptide conformation.	n-linked oligosaccharides	26-51	solute carrier family 25 member 18	Homo sapiens	57-61
3108883-7	1987	Although normal CD3-gamma, CD3-delta, and CD3-epsilon chains were present in this clone, the association with the TCR-gamma homodimer may be the cause of a complete processing of the N-linked oligosaccharides attached to the CD3-delta chain.	n-linked oligosaccharides	183-208	CD3 delta subunit of T-cell receptor complex	Homo sapiens	225-234
2444289-8	1987	Erythrocyte p80 is a glycoprotein with N-linked oligosaccharides, as demonstrated by its binding to concanavalin A (Con A) and Len culinaris lectins.	n-linked oligosaccharides	39-64	coilin	Homo sapiens	12-15
3321055-1	1987	The yeast Saccharomyces cerevisiae X2180 strain with the mnn1 mnn2 mnn9 mutations, all of which affect mannoprotein glycosylation, synthesizes N-linked oligosaccharides having the following structure: (Formula: see text) whereas the mnn1 mnn2 mutant extends the alpha 1----6-linked backbone of some of the core oligosaccharides by adding 20-30 mannose units.	n-linked oligosaccharides	143-168	alpha-1,3-mannosyltransferase MNN1	Saccharomyces cerevisiae S288C	57-66
3321055-1	1987	The yeast Saccharomyces cerevisiae X2180 strain with the mnn1 mnn2 mnn9 mutations, all of which affect mannoprotein glycosylation, synthesizes N-linked oligosaccharides having the following structure: (Formula: see text) whereas the mnn1 mnn2 mutant extends the alpha 1----6-linked backbone of some of the core oligosaccharides by adding 20-30 mannose units.	n-linked oligosaccharides	143-168	alpha-1,3-mannosyltransferase MNN1	Saccharomyces cerevisiae S288C	57-61
3321055-1	1987	The yeast Saccharomyces cerevisiae X2180 strain with the mnn1 mnn2 mnn9 mutations, all of which affect mannoprotein glycosylation, synthesizes N-linked oligosaccharides having the following structure: (Formula: see text) whereas the mnn1 mnn2 mutant extends the alpha 1----6-linked backbone of some of the core oligosaccharides by adding 20-30 mannose units.	n-linked oligosaccharides	143-168	alpha-1,2-mannosyltransferase MNN2	Saccharomyces cerevisiae S288C	62-66
3427025-1	1987	Distance constraints derived from two-dimensional nuclear Overhauser effect measurements have been used to define the orientation of the Man alpha 1-3Man beta linkage in seven different N-linked oligosaccharides, all containing the common pentasaccharide core Man alpha 1-6(Man alpha 1-3)Man beta 1-4GlcNAc beta 1-4GlcNAc.	n-linked oligosaccharides	186-211	adrenoceptor alpha 1D	Homo sapiens	141-148
3298434-5	1987	The p150,95 alpha subunit is synthesized as a precursor of 146,000 Mr, has five to six N-linked oligosaccharides, and has a polypeptide chain backbone of 132,000 Mr. Over 50% of the carbohydrate on the mature alpha subunit of 150,000 Mr was sensitive to Endo H digestion.	n-linked oligosaccharides	87-112	chromatin assembly factor 1 subunit A	Homo sapiens	4-8
3036083-9	1987	The major and the minor VIP-binding proteins were converted respectively into Mr 47,000 and 100,000 species, indicating removal of 20 kDa of N-linked oligosaccharides.	n-linked oligosaccharides	141-166	vasoactive intestinal peptide	Homo sapiens	24-27
3814625-6	1987	From a time course of endo-beta-N-acetylglucosaminidase H digestion, it was determined that hepatic lipase contains a minimum of two N-linked oligosaccharides.	n-linked oligosaccharides	133-158	lipase C, hepatic type	Rattus norvegicus	92-106
3814625-8	1987	Therefore, processing of N-linked oligosaccharides is probably the only post-translational modification responsible for the observed change in the apparent molecular weight of hepatic lipase.	n-linked oligosaccharides	25-50	lipase C, hepatic type	Rattus norvegicus	176-190
3494075-0	1987	Evidence that recombinant IL 1 alpha exhibits lectin-like specificity and binds to homogeneous uromodulin via N-linked oligosaccharides.	n-linked oligosaccharides	110-135	interleukin 1 alpha	Homo sapiens	26-36
3494075-0	1987	Evidence that recombinant IL 1 alpha exhibits lectin-like specificity and binds to homogeneous uromodulin via N-linked oligosaccharides.	n-linked oligosaccharides	110-135	uromodulin	Homo sapiens	95-105
2432113-6	1987	This indicates that endogenous gal and gal transferred by GT to terminal GlcNAc residues are present N-linked oligosaccharides.	n-linked oligosaccharides	101-126	glycoprotein alpha-galactosyltransferase 1	Rattus norvegicus	58-60
3027103-4	1987	Most alpha 1-antitrypsin in this fraction (P1) bears N-linked oligosaccharides of composition similar to that of alpha 1-antitrypsin within the RER; mainly Man8GlcNac2 with lesser amounts of Man7GlcNac2 and Man9GlcNac2; this suggests that the protein has not yet reacted with alpha-mannosidase-I on the cis face of the Golgi complex.	n-linked oligosaccharides	53-78	serpin family A member 1	Homo sapiens	5-24
3768962-4	1986	The smaller one was exposed on the cell surface and showed a trypsin sensitivity characteristic to E-cadherin, suggesting that this is the peptide moiety of E-cadherin whose glycosylation with N-linked oligosaccharides was blocked by tunicamycin.	n-linked oligosaccharides	193-218	cadherin 1	Homo sapiens	99-109
3102228-8	1986	The 125I-labeled complex obtained displayed N-linked oligosaccharides and had an Mr consistent with one molecule of IL-2 cross-linked to the smaller proteolytic fragment of the receptor.	n-linked oligosaccharides	44-69	interleukin 2	Homo sapiens	116-120
3790542-7	1986	In contrast, human hemopexin has five N-linked oligosaccharides and an additional O-linked glycan blocking the N-terminal threonine residue [Takahashi, N., Takahashi, Y., & Putnam, F. W. (1984) Proc.	n-linked oligosaccharides	38-63	hemopexin	Homo sapiens	19-28
3768962-4	1986	The smaller one was exposed on the cell surface and showed a trypsin sensitivity characteristic to E-cadherin, suggesting that this is the peptide moiety of E-cadherin whose glycosylation with N-linked oligosaccharides was blocked by tunicamycin.	n-linked oligosaccharides	193-218	cadherin 1	Homo sapiens	157-167
3017304-1	1986	Sulphation of N-linked oligosaccharides on alpha 2HS-glycoprotein.	n-linked oligosaccharides	14-39	alpha 2-HS glycoprotein	Homo sapiens	43-65
3099750-7	1986	The 100,000 Mr secreted C1 Inh is sensitive to endoglycosidase F but resistant to endoglycosidase H, and it incorporates [3H]galactose, [3H]glucosamine and [3H]galactosamine, indicating the presence of both N-linked oligosaccharides of the complex type and O-linked oligosaccharides.	n-linked oligosaccharides	207-232	serpin family G member 1	Homo sapiens	24-30
3873494-5	1985	Ii-c is resistant to deglycosylation by Endo H, which is specific for high-mannose N-linkages, but can be digested with Endo F, a glycosidase capable of cleaving both complex and high-mannose N-linked oligosaccharides.	n-linked oligosaccharides	192-217	myosin, heavy polypeptide 14	Mus musculus	0-4
3487029-3	1986	The differences in charge heterogeneity of class I molecules between activated T-cells and the other cell subpopulations were abolished by treatment with: (1) endoglycosidase F which removes N-linked oligosaccharides from glycoproteins, and (2) neuraminidase which removes sialic acids from carbohydrate side chains.	n-linked oligosaccharides	191-216	neuraminidase 1	Homo sapiens	245-258
2870429-1	1986	Developmental changes in murine lymphocyte Thy-1 include both quantitative and qualitative alterations involving N-linked oligosaccharides.	n-linked oligosaccharides	113-138	thymus cell antigen 1, theta	Mus musculus	43-48
3937276-5	1985	The possible role of N-linked oligosaccharides for the biological activity of t-PA was studied using t-PA secreted by melanoma cells in the presence of tunicamycin, an inhibitor of N-glycosylation.	n-linked oligosaccharides	21-46	plasminogen activator, tissue type	Homo sapiens	78-82
4052781-6	1985	Degradative experiments using neuraminidase to remove sialic acid residues and endoglycosidase F to remove all N-linked oligosaccharides indicate that the polymorphism of the NILE-related glycoproteins may be due to differences both at the polypeptide level and at the level of glycosylation.	n-linked oligosaccharides	111-136	L1 cell adhesion molecule	Rattus norvegicus	175-179
4044605-7	1985	These polysialosyl units cap N-linked oligosaccharides of the complex-type on neural cell adhesion molecules (N-CAM).	n-linked oligosaccharides	29-54	neural cell adhesion molecule 1	Rattus norvegicus	110-115
3872909-4	1985	In the presence of glycosylation-enhancing factor (GEF) or bradykinin, however, the same cells produce IgE-binding factors with N-linked oligosaccharides (glycosylated form).	n-linked oligosaccharides	128-153	SLC2A4 regulator	Homo sapiens	51-54
3886793-0	1985	Lymphocyte function-associated antigen 1 (LFA-1) contains sulfated N-linked oligosaccharides.	n-linked oligosaccharides	67-92	integrin beta 2	Mus musculus	0-40
3886793-0	1985	Lymphocyte function-associated antigen 1 (LFA-1) contains sulfated N-linked oligosaccharides.	n-linked oligosaccharides	67-92	integrin beta 2	Mus musculus	42-47
3872909-4	1985	In the presence of glycosylation-enhancing factor (GEF) or bradykinin, however, the same cells produce IgE-binding factors with N-linked oligosaccharides (glycosylated form).	n-linked oligosaccharides	128-153	kininogen 1	Homo sapiens	59-69
6333483-6	1984	Treatment of the immunoprecipitated Qa-2 with endoglycosidase F (Endo F) resulted in a decrease in Mr of approximately 5,000-6,000, corresponding to the expected loss of N-linked oligosaccharides, but the decrease did not eliminate structural variability among the clones.	n-linked oligosaccharides	170-195	Qa lymphocyte antigen 2 region	Mus musculus	36-40
3856097-0	1985	Structural characterization of murine Ia antigen N-linked oligosaccharides and localization of specific structures to two unique alpha-chain glycosylation sites.	n-linked oligosaccharides	49-74	Fc gamma receptor and transporter	Homo sapiens	129-140
6208275-8	1984	The role of GIF is to inhibit the assembly of N-linked oligosaccharides on IgE-binding factors during their biosynthesis, and thereby provide them with a biologic activity: suppression of the IgE response.	n-linked oligosaccharides	46-71	macrophage migration inhibitory factor (glycosylation-inhibiting factor)	Mus musculus	12-15
2998004-3	1985	Use of the enzyme endo-beta-N-acetylglucosaminidase H revealed that the fully processed form of gp 3 had high-mannose type and that of gp 5 had only complex type of N-linked oligosaccharides.	n-linked oligosaccharides	165-190	glycoprotein V platelet	Homo sapiens	135-139
6386828-4	1984	Upon treatment with neuraminidase, it was converted to a single component of Mr 42,000, and subsequent, limited treatment with endoglycosidase F gave four evenly spaced components of Mr 35,000-42,000, suggesting that it contained three attachment sites for N-linked oligosaccharides.	n-linked oligosaccharides	257-282	neuraminidase 1	Homo sapiens	20-33
6088499-0	1984	Influence of the N-linked oligosaccharides on the biosynthesis, intracellular routing, and function of the human asialoglycoprotein receptor.	n-linked oligosaccharides	17-42	asialoglycoprotein receptor 1	Homo sapiens	113-140
6386828-9	1984	A similar CNBr sialopeptide was obtained from adult N-CAM; it contained sialic acid, had three N-linked oligosaccharides and reacted with anti-(N-CAM) No.	n-linked oligosaccharides	95-120	neural cell adhesion molecule 1	Homo sapiens	52-57
6437807-3	1984	Within the heavy chain the sulphate was not linked to tyrosine, threonine or serine residues, but appeared to be bound to N-linked oligosaccharides located in the Fab-portion.	n-linked oligosaccharides	122-147	FA complementation group B	Homo sapiens	163-166
6381483-5	1984	When transport from the endoplasmic reticulum is blocked in sec18, N-linked oligosaccharides accumulate with a size corresponding to Man8GlcNAc2 when the normal GLS1 allele is present, and Glc3Man8GlcNAc2 in the gls1 mutant.	n-linked oligosaccharides	67-92	mannosyl-oligosaccharide glucosidase	Saccharomyces cerevisiae S288C	161-165
6381483-5	1984	When transport from the endoplasmic reticulum is blocked in sec18, N-linked oligosaccharides accumulate with a size corresponding to Man8GlcNAc2 when the normal GLS1 allele is present, and Glc3Man8GlcNAc2 in the gls1 mutant.	n-linked oligosaccharides	67-92	mannosyl-oligosaccharide glucosidase	Saccharomyces cerevisiae S288C	212-216
6088499-4	1984	In order to examine the role of N-linked oligosaccharides in the biosynthesis, intracellular routing, and function of the ASGP-R, we have used Hep G2 cells, which have a large number of ASGP-R, and two inhibitors of glycosylation, swainsonine and tunicamycin.	n-linked oligosaccharides	32-57	asialoglycoprotein receptor 1	Homo sapiens	122-128
6208762-5	1984	There is a Fuc attached to the N-linked oligosaccharides of standard hCG beta (Fig.	n-linked oligosaccharides	31-56	chorionic gonadotropin subunit beta 3	Homo sapiens	69-77
6630229-1	1983	Tunicamycin, an inhibitor of asparagine-linked glycosylation of glycoprotein, has been used here to examine the role of N-linked oligosaccharides in secretion of ZP2 and ZP3, two of the three glycoproteins that constitute the mouse egg"s extracellular coat (zona pellucida).	n-linked oligosaccharides	120-145	zona pellucida glycoprotein 2	Mus musculus	162-165
6630229-14	1983	Results of pulse-chase experiments indicate that the low degree of incorporation of ZP2 lacking N-linked oligosaccharides into the zona pellucida is due to a greatly decreased rate of secretion as compared to the core-glycosylated precursor.	n-linked oligosaccharides	96-121	zona pellucida glycoprotein 2	Mus musculus	84-87
6630229-16	1983	These results suggest that N-linked oligosaccharides are necessary for normal secretion of ZP2, but are probably not necessary for ZP3 secretion.	n-linked oligosaccharides	27-52	zona pellucida glycoprotein 2	Mus musculus	91-94
31188144-5	2019	The platelet surface terminal sialic acid was removed by neuraminidase A, and N-linked oligosaccharides was removed by PNGase F. The function of the enzyme-treated platelet was measured.	n-linked oligosaccharides	78-103	N-glycanase 1	Homo sapiens	119-125
11892795-3	1983	We have now used rabbit antisera that recognize ZP3 to immunoprecipitate [35S]methionine-labeled, intracellular precursors of this glycoprotein from growing oocytes cultured in vitro in the presence or absence of tunicamycin, a drug that prevents addition of N-linked oligosaccharides to nascent polypeptide chains.	n-linked oligosaccharides	259-284	zona pellucida glycoprotein 3	Mus musculus	48-51
6793421-9	1981	They suggest that, in rat adipocytes, a glycosidic moiety participates in the insulin-receptor interaction through N-linked oligosaccharides of the "complex type".	n-linked oligosaccharides	115-140	insulin receptor	Rattus norvegicus	78-94
33608773-2	2021	Core fucosylation catalyzed by FUT8 refers to adding the fucosyl moiety to the innermost GlcNAc residue of N-linked oligosaccharides and is involved in many biological processes such as cell differentiation, migration, and signaling transduction.	n-linked oligosaccharides	107-132	fucosyltransferase 8	Mus musculus	31-35
20301289-0	1993	PMM2-CDG (CDG-Ia) CLINICAL CHARACTERISTICS: PMM2-CDG (CDG-Ia) (previously known as congenital disorder of glycosylation type 1a), the most common of a group of disorders of abnormal glycosylation of N-linked oligosaccharides, is divided into three types: infantile multisystem, late-infantile and childhood ataxia-intellectual disability, and adult stable disability.	n-linked oligosaccharides	199-224	phosphomannomutase 2	Homo sapiens	0-4
20301289-0	1993	PMM2-CDG (CDG-Ia) CLINICAL CHARACTERISTICS: PMM2-CDG (CDG-Ia) (previously known as congenital disorder of glycosylation type 1a), the most common of a group of disorders of abnormal glycosylation of N-linked oligosaccharides, is divided into three types: infantile multisystem, late-infantile and childhood ataxia-intellectual disability, and adult stable disability.	n-linked oligosaccharides	199-224	phosphomannomutase 2	Homo sapiens	44-48
32592613-8	2020	Removing N-linked oligosaccharides from CD44, increased its ability to compete with IGFBP-3 for binding HA while reduction of CD44 rendered the protein relatively ineffective at blocking IGFBP-3-HA interactions.	n-linked oligosaccharides	9-34	CD44 molecule (Indian blood group)	Homo sapiens	40-44
32592613-8	2020	Removing N-linked oligosaccharides from CD44, increased its ability to compete with IGFBP-3 for binding HA while reduction of CD44 rendered the protein relatively ineffective at blocking IGFBP-3-HA interactions.	n-linked oligosaccharides	9-34	insulin like growth factor binding protein 3	Homo sapiens	84-91
31443222-4	2019	Secretion of irisin is regulated by N-linked oligosaccharides attached to the protein molecule.	n-linked oligosaccharides	36-61	fibronectin type III domain containing 5	Homo sapiens	13-19
27253379-6	2016	rGal-9 signals through N-linked oligosaccharides and O-linked hexasaccharides on the T cell surface, modulating the gene expression levels of key transcription initiation, promoter proximal-pausing, and chromatin remodeling factors that regulate HIV latency.	n-linked oligosaccharides	23-48	galectin 9	Rattus norvegicus	0-6
28334446-3	2017	PNGase F mediated release of the N-linked oligosaccharides was followed by labeling with aminopyrene trisulfonate.	n-linked oligosaccharides	33-58	N-glycanase 1	Mus musculus	0-6
26821880-1	2016	The enzyme UDP-N-acetylglucosamine: alpha-d-mannoside beta-1-6 N-acetylglucosaminyltransferase V (GnT-V) catalyzes the transfer of GlcNAc from the UDP-GlcNAc donor to the alpha-1-6-linked mannose of the trimannosyl core structure of glycoproteins to produce the beta-1-6-linked branching of N-linked oligosaccharides.	n-linked oligosaccharides	291-316	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B	Homo sapiens	54-96
26821880-1	2016	The enzyme UDP-N-acetylglucosamine: alpha-d-mannoside beta-1-6 N-acetylglucosaminyltransferase V (GnT-V) catalyzes the transfer of GlcNAc from the UDP-GlcNAc donor to the alpha-1-6-linked mannose of the trimannosyl core structure of glycoproteins to produce the beta-1-6-linked branching of N-linked oligosaccharides.	n-linked oligosaccharides	291-316	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	Homo sapiens	98-103
27114034-0	2016	Trimeric HIV-1-Env Structures Define Glycan Shields from Clades A, B, and G. The HIV-1-envelope (Env) trimer is covered by a glycan shield of ~90 N-linked oligosaccharides, which comprises roughly half its mass and is a key component of HIV evasion from humoral immunity.	n-linked oligosaccharides	146-171	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	15-18
27114034-0	2016	Trimeric HIV-1-Env Structures Define Glycan Shields from Clades A, B, and G. The HIV-1-envelope (Env) trimer is covered by a glycan shield of ~90 N-linked oligosaccharides, which comprises roughly half its mass and is a key component of HIV evasion from humoral immunity.	n-linked oligosaccharides	146-171	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	81-95
27114034-0	2016	Trimeric HIV-1-Env Structures Define Glycan Shields from Clades A, B, and G. The HIV-1-envelope (Env) trimer is covered by a glycan shield of ~90 N-linked oligosaccharides, which comprises roughly half its mass and is a key component of HIV evasion from humoral immunity.	n-linked oligosaccharides	146-171	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	97-100
24585773-2	2014	It functions as an adaptor protein that facilitates the ER exit of Ktr3, a mannosyltransferase required for biosynthesis of O-linked oligosaccharides, and the ER exit of Mnn2 and Mnn5, mannosyltransferases, which participate in the biosynthesis of N-linked oligosaccharides.	n-linked oligosaccharides	248-273	mannosyltransferase KTR3	Saccharomyces cerevisiae S288C	67-71
26747427-1	2016	The structure of the N-linked oligosaccharides attached to antithrombin (AT) has been shown to affect its anticoagulant activity and pharmacokinetics.	n-linked oligosaccharides	21-46	serpin family C member 1	Homo sapiens	59-71
26582205-7	2016	We determined the structures of N-linked oligosaccharides of H-Lys13-Try1.	n-linked oligosaccharides	32-57	serine protease 1	Homo sapiens	69-73
26240146-5	2015	Hyperglycosylated hCG was purified from the urine of invasive mole patients, and the structure of its N-linked oligosaccharides was confirmed to be more branched by MS.	n-linked oligosaccharides	102-127	chorionic gonadotropin subunit beta 5	Homo sapiens	18-21
26240146-7	2015	The binding affinity of MCA1024 changed significantly in response to the alteration of hCG N-linked oligosaccharides.	n-linked oligosaccharides	91-116	chorionic gonadotropin subunit beta 5	Homo sapiens	87-90
25810266-6	2015	We show that the mutation altered the conformation of the extracellular beta-propeller domain of the integrin alpha3 subunit preventing correct processing of N-linked oligosaccharides, heterodimerization with beta1 integrin and maturation through cleavage into heavy and light chains in the Golgi.	n-linked oligosaccharides	158-183	integrin subunit alpha 3	Homo sapiens	101-124
25615530-0	2015	Disease-Associated Mutations of TREM2 Alter the Processing of N-Linked Oligosaccharides in the Golgi Apparatus.	n-linked oligosaccharides	62-87	triggering receptor expressed on myeloid cells 2	Homo sapiens	32-37
25665441-6	2015	The present model protein cathepsin Z is synthesized as a larger proenzyme that contains two N-linked oligosaccharides and matures to a shorter single chain enzyme retaining the processed oligosaccharides.	n-linked oligosaccharides	93-118	cathepsin Z	Homo sapiens	26-37
24585773-2	2014	It functions as an adaptor protein that facilitates the ER exit of Ktr3, a mannosyltransferase required for biosynthesis of O-linked oligosaccharides, and the ER exit of Mnn2 and Mnn5, mannosyltransferases, which participate in the biosynthesis of N-linked oligosaccharides.	n-linked oligosaccharides	248-273	alpha-1,2-mannosyltransferase MNN2	Saccharomyces cerevisiae S288C	170-174
24585773-2	2014	It functions as an adaptor protein that facilitates the ER exit of Ktr3, a mannosyltransferase required for biosynthesis of O-linked oligosaccharides, and the ER exit of Mnn2 and Mnn5, mannosyltransferases, which participate in the biosynthesis of N-linked oligosaccharides.	n-linked oligosaccharides	248-273	alpha-1,2-mannosyltransferase MNN5	Saccharomyces cerevisiae S288C	179-183
24649404-6	2014	Surprisingly, we found that ursolic acid decreased the apparent molecular weight of ICAM-1 and altered the structures of N-linked oligosaccharides bound to ICAM-1.	n-linked oligosaccharides	121-146	intercellular adhesion molecule 1	Homo sapiens	156-162
24361341-5	2014	Based on differential sensitivity to glycosidases, the doublet was identified as two high-mannose-type glycoforms of NOX1, whereas the broad band represented NOX1 with complex-type N-linked oligosaccharides.	n-linked oligosaccharides	181-206	NADPH oxidase 1	Mus musculus	158-162
24818024-8	2014	The native TEX101 polypeptide contains ~17 kDa N-linked oligosaccharides and the polypeptide is anchored to sperm membrane via a glycosylphosphatidylinositol lipid linkage.	n-linked oligosaccharides	47-72	testis expressed 101	Bos taurus	11-17
23609441-5	2013	FUT8 catalyzes the transfer of a fucose residue to N-linked oligosaccharides on glycoproteins via an alpha-1,6 linkage, leading to core fucosylation in mammals.	n-linked oligosaccharides	51-76	fucosyltransferase 8	Homo sapiens	0-4
24296889-5	2013	Removal of alpha2,6 sialic acids either by enzymatic desialylation or by stably down-regulating the ST6Gal-I (enzyme that catalyses the addition of alpha2,6-linked sialic acids on N-linked oligosaccharides) by lentiviral driven shRNA decreased the adhesion on both ECM and BM components and invasion through reconstituted BM matrigel.	n-linked oligosaccharides	180-205	beta galactoside alpha 2,6 sialyltransferase 1	Mus musculus	100-108
23632316-6	2013	However, in the IgG-Fc-ZP3E7 protein, we concluded that only one out of three NXS/T glycosylation sites is occupied by N-linked oligosaccharides.	n-linked oligosaccharides	119-144	zona pellucida glycoprotein 3	Homo sapiens	16-36
23200831-4	2013	Deletion of the C-terminal PDZ domain-binding motif caused an increase in EGFP-GLAST with immature endoglycosidase H-sensitive N-linked oligosaccharides, suggesting impaired exit of EGFP-GLAST from the endoplasmic reticulum (ER).	n-linked oligosaccharides	127-152	solute carrier family 1 member 3	Homo sapiens	187-192
22449099-1	2012	BACKGROUND: Previously, we found that beta-galactoside alpha2,6-sialyltransferase (ST6Gal I), an enzyme that adds sialic acids to N-linked oligosaccharides of glycoproteins and is frequently overexpressed in cancer cells, is up-regulated by ionizing radiation (IR) and cleaved to a form possessing catalytic activity comparable to that of the Golgi-localized enzyme.	n-linked oligosaccharides	130-155	ST6 beta-galactoside alpha-2,6-sialyltransferase 1	Homo sapiens	83-91
22390135-6	2012	Accessible glyco-motifs of GI mucins varied according to species and localization of mucin origin, with terminal fucose, the sialyl T-antigen, and N-linked oligosaccharides identified as potentially important.	n-linked oligosaccharides	147-172	mucin 1, cell surface associated	Bos taurus	30-35
22373601-5	2012	Unlike the widely-used bacterial ENGases, Endo H and Endo F1, Endo Tv released exclusively high mannose N-linked oligosaccharides from RNase B, ovalbumin, and yeast invertase.	n-linked oligosaccharides	104-129	ovalbumin	Bos taurus	144-153
22902807-12	2012	Transferrin contained a higher extent of triantennary and often fucosylated N-linked oligosaccharides.	n-linked oligosaccharides	76-101	transferrin	Homo sapiens	0-11
21147166-6	2011	Polymeric IgA was far better ligand than monomeric IgA for both anti-IgA antibody and the most widely expressed human tissue lectin galectin-1 which recognizes O-linked oligosaccharides characteristic of IgA, in contrast to N-linked oligosaccharides present in all immunoglobulins.	n-linked oligosaccharides	224-249	galectin 1	Homo sapiens	132-142
21803400-4	2011	In addition, our results shown that retaining the 6 N-linked oligosaccharides within a short B-domain spacer associated with 2A and furin cleavage site is expressed more efficiently both in vitro in traditional heterologous expression systems as well as in vivo in a mouse model of hemophilia A.	n-linked oligosaccharides	52-77	furin (paired basic amino acid cleaving enzyme)	Mus musculus	132-137
21798344-5	2011	Secreted VPO1 is a monomer with complex N-linked oligosaccharides and exhibits peroxidase activity.	n-linked oligosaccharides	40-65	peroxidasin	Homo sapiens	9-13
20005867-5	2010	Pre-treatment with tunicamycin, which inhibits the biosynthesis of N-linked oligosaccharides, decreased the accumulation of Pt in sensitive cells exposed to oxaliplatin or cisplatin and increased the electrophoretic mobility of MRP1 and MRP4, reproducing the association between decreased glycosylation of MRP1 and MRP4 and decreased Pt accumulation observed in the resistant IGROV-1/OHP cells.	n-linked oligosaccharides	67-92	ATP binding cassette subfamily C member 1	Homo sapiens	228-232
20405899-4	2010	beta-N-Acetylglucosaminidase (endo-beta-GlcNAc-ases, Endo-M) is an endoglycosidase capable of hydrolyzing N,N"-diacetylchitobiose moiety in N-linked oligosaccharides bound to the asparagine amino acid residue in various glycoproteins.	n-linked oligosaccharides	140-165	O-GlcNAcase	Homo sapiens	0-28
20619452-3	2010	hCG-H has triantennary N-linked oligosaccharides and double molecular size O-linked oligosaccharides (hexasaccharide compared with predominantly trisaccharide structures).	n-linked oligosaccharides	23-48	hypertrichosis 2 (generalised, congenital)	Homo sapiens	0-5
19864504-0	2010	Site-specific analysis of N-linked oligosaccharides of recombinant lysosomal arylsulfatase A produced in different cell lines.	n-linked oligosaccharides	26-51	arylsulfatase A	Homo sapiens	77-92
20008117-9	2010	On examination of intrinsic properties of CFTR that may affect its apical stability, we found that N-linked oligosaccharides were not necessary for transport to the apical membrane but were required for efficient apical recycling and, therefore, influenced the turnover of surface CFTR.	n-linked oligosaccharides	99-124	CF transmembrane conductance regulator	Homo sapiens	42-46
20008117-9	2010	On examination of intrinsic properties of CFTR that may affect its apical stability, we found that N-linked oligosaccharides were not necessary for transport to the apical membrane but were required for efficient apical recycling and, therefore, influenced the turnover of surface CFTR.	n-linked oligosaccharides	99-124	CF transmembrane conductance regulator	Homo sapiens	281-285
19759276-1	2010	Glucose residues from N-linked oligosaccharides are removed by glucosidases I and II in the endoplasmic reticulum (ER) or by the alternate endomannosidase pathway in the Golgi apparatus.	n-linked oligosaccharides	22-47	mannosidase, endo-alpha	Rattus norvegicus	139-154
19261995-7	2009	Also, removal of the N-linked oligosaccharides on thyroglobulin reduced the proliferative activity of porcine thyroglobulin, suggesting that the proliferative effect of thyroglobulin is in part exerted by its carbohydrate moiety.	n-linked oligosaccharides	21-46	thyroglobulin	Bos taurus	50-63
19559061-6	2009	The N-linked oligosaccharides assembled on a secretory glycoprotein, HSA/GM-CSF in Kloch1 mutant, contained oligosaccharide Man(13-14)GlcNAc(2), and in Kloch1 mnn1 mutant, contained oligosaccharide Man(9-11)GlcNAc(2), whereas those in the wild-type strain, consisted of oligosaccharides with heterogeneous sizes, Man(>30)GlcNAc(2).	n-linked oligosaccharides	4-29	colony stimulating factor 2	Homo sapiens	73-79
19559061-6	2009	The N-linked oligosaccharides assembled on a secretory glycoprotein, HSA/GM-CSF in Kloch1 mutant, contained oligosaccharide Man(13-14)GlcNAc(2), and in Kloch1 mnn1 mutant, contained oligosaccharide Man(9-11)GlcNAc(2), whereas those in the wild-type strain, consisted of oligosaccharides with heterogeneous sizes, Man(>30)GlcNAc(2).	n-linked oligosaccharides	4-29	alpha-1,3-mannosyltransferase MNN1	Saccharomyces cerevisiae S288C	159-163
19958498-1	2009	BACKGROUND: Lysosomal alpha-mannosidase is an enzyme that acts to degrade N-linked oligosaccharides and hence plays an important role in mannose metabolism in humans and other mammalian species, especially livestock.	n-linked oligosaccharides	74-99	mannosidase alpha class 2B member 1	Homo sapiens	12-39
19538730-9	2009	The presence of N-linked oligosaccharides on murine Muc16 was determined by ConA chromatography.	n-linked oligosaccharides	16-41	mucin 16	Mus musculus	52-57
19538730-10	2009	RESULTS: We demonstrate that murine Muc16 is expressed by mouse ovarian cancer cells as an ~250 kDa glycoprotein that carries both O-linked and N-linked oligosaccharides.	n-linked oligosaccharides	144-169	mucin 16	Mus musculus	36-41
19071032-0	2009	Removal of O-linked and N-linked oligosaccharides is required for optimum detection of NITEGE neoepitope on ADAMTS4-digested fetal aggrecans: implications for specific N-linked glycan-dependent aggrecanolysis at Glu373-Ala374.	n-linked oligosaccharides	24-49	ADAM metallopeptidase with thrombospondin type 1 motif 4	Homo sapiens	108-115
19261995-7	2009	Also, removal of the N-linked oligosaccharides on thyroglobulin reduced the proliferative activity of porcine thyroglobulin, suggesting that the proliferative effect of thyroglobulin is in part exerted by its carbohydrate moiety.	n-linked oligosaccharides	21-46	thyroglobulin	Bos taurus	110-123
19261995-7	2009	Also, removal of the N-linked oligosaccharides on thyroglobulin reduced the proliferative activity of porcine thyroglobulin, suggesting that the proliferative effect of thyroglobulin is in part exerted by its carbohydrate moiety.	n-linked oligosaccharides	21-46	thyroglobulin	Bos taurus	110-123
18682497-7	2008	However, the absence of N-linked oligosaccharides did reduce the stability of wild-type CFTR, causing significantly more-rapid turnover in post-ER compartments.	n-linked oligosaccharides	24-49	CF transmembrane conductance regulator	Homo sapiens	88-92
18288410-4	2008	A morphological examination and annexin V assays revealed that galectin-3-induced cell death is consistent with apoptosis and swainsonine, a potent inhibitor of alpha-mannosidase II, which catalyzes the synthesis of complex type N-linked oligosaccharides, inhibited galectin-3-induced apoptosis in HBL-2 cells.	n-linked oligosaccharides	229-254	galectin 3	Homo sapiens	63-73
18682497-1	2008	The epithelial chloride channel CFTR is a glycoprotein that is modified by two N-linked oligosaccharides.	n-linked oligosaccharides	79-104	CF transmembrane conductance regulator	Homo sapiens	32-36
18754874-2	2008	alpha1,6-Fucosyltransferase (FUT8) transfers a fucose residue to n-linked oligosaccharides on glycoproteins.	n-linked oligosaccharides	65-90	fucosyltransferase 8	Homo sapiens	0-27
18754874-2	2008	alpha1,6-Fucosyltransferase (FUT8) transfers a fucose residue to n-linked oligosaccharides on glycoproteins.	n-linked oligosaccharides	65-90	fucosyltransferase 8	Homo sapiens	29-33
18234732-4	2008	Complete and partial digestions of the expressed protein with PNGase F showed three N-linked oligosaccharides accounted for all forms of Hyal3 detected in expression lysates.	n-linked oligosaccharides	84-109	hyaluronoglucosaminidase 3	Mus musculus	137-142
18288410-5	2008	These results suggest that galectin-3 induces apoptosis in HBL-2 cells by interacting with cell surface N-linked oligosaccharides.	n-linked oligosaccharides	104-129	galectin 3	Homo sapiens	27-37
18048353-1	2008	A limited number of glycoproteins including luteinizing hormone and carbonic anhydrase-VI (CA6) bear N-linked oligosaccharides that are modified with beta1,4-linked N-acetylgalactosamine (GalNAc).	n-linked oligosaccharides	101-126	carbonic anhydrase 6	Bos taurus	91-94
18048353-5	2008	A single peptide recognition determinant encoded in the carboxyl-terminal 19-amino acid sequence of bovine CA6 mediates transfer of GalNAc to each of its two N-linked oligosaccharides.	n-linked oligosaccharides	158-183	carbonic anhydrase 6	Bos taurus	107-110
18264945-9	2008	CONCLUSIONS: We found an abnormality in the N-linked oligosaccharides of the aberrant IgA1.	n-linked oligosaccharides	44-69	immunoglobulin heavy constant alpha 1	Homo sapiens	86-90
17699513-8	2007	We found that the recombinant TM14 protein was glycosylated with N-linked oligosaccharides and interacted with heparin, fibronectin, fibulin-1, and dentin sialophosphoprotein.	n-linked oligosaccharides	65-90	fibulin 7	Mus musculus	30-34
17636254-0	2007	Biosynthesis of truncated N-linked oligosaccharides results from non-orthologous hexosaminidase-mediated mechanisms in nematodes, plants, and insects.	n-linked oligosaccharides	26-51	Beta-N-acetylhexosaminidase	Caenorhabditis elegans	81-95
17565118-6	2007	Gal3/AP recognition depended at least in part on the N-linked oligosaccharides of different glycoproteins.	n-linked oligosaccharides	53-78	galectin 3	Homo sapiens	0-4
17660514-11	2007	Our results indicate that N-linked oligosaccharides play an important role in corin activation.	n-linked oligosaccharides	26-51	corin, serine peptidase	Homo sapiens	78-83
17121844-0	2007	N-linked oligosaccharides on the low density lipoprotein receptor homolog SorLA/LR11 are modified with terminal GalNAc-4-SO4 in kidney and brain.	n-linked oligosaccharides	0-25	low density lipoprotein receptor	Homo sapiens	33-65
17456790-0	2007	N-linked oligosaccharides direct the differential assembly and secretion of inhibin alpha- and betaA-subunit dimers.	n-linked oligosaccharides	0-25	inhibin alpha chain	Cricetulus griseus	76-89
17553346-1	2007	AIM: To find if human soluble tumor necrosis factor receptor II (p75) fused IgG Fc protein (sTNFR II-IgG Fc) could be expressed in Pichia pastoris with an active dimmer form and characterize its N-linked oligosaccharides.	n-linked oligosaccharides	195-220	TNF receptor superfamily member 1B	Homo sapiens	65-68
17197096-6	2007	These results indicate that both sites are highly available and occupied by N-linked oligosaccharides for Kv3.1, 3.3, and 3.4 in rat brain, and furthermore that at least one oligosaccharide is of complex type.	n-linked oligosaccharides	76-101	potassium voltage-gated channel subfamily C member 1	Rattus norvegicus	106-111
17185748-5	2007	Here, we show that luminal DTX expression dramatically increased both the level of cell surface Kv1.1 immunofluorescence staining and the proportion of Kv1.1 with processed N-linked oligosaccharides.	n-linked oligosaccharides	173-198	potassium voltage-gated channel subfamily A member 1	Homo sapiens	152-157
17121844-0	2007	N-linked oligosaccharides on the low density lipoprotein receptor homolog SorLA/LR11 are modified with terminal GalNAc-4-SO4 in kidney and brain.	n-linked oligosaccharides	0-25	sortilin related receptor 1	Homo sapiens	74-79
17121844-0	2007	N-linked oligosaccharides on the low density lipoprotein receptor homolog SorLA/LR11 are modified with terminal GalNAc-4-SO4 in kidney and brain.	n-linked oligosaccharides	0-25	sortilin related receptor 1	Homo sapiens	80-84
17121844-3	2007	We have found that a fraction of SorLA/LR11 that is synthesized in the kidney and the brain bears N-linked oligosaccharides that are modified with terminal beta1,4-linked GalNAc-4-SO(4).	n-linked oligosaccharides	98-123	sortilin related receptor 1	Homo sapiens	33-38
17121844-3	2007	We have found that a fraction of SorLA/LR11 that is synthesized in the kidney and the brain bears N-linked oligosaccharides that are modified with terminal beta1,4-linked GalNAc-4-SO(4).	n-linked oligosaccharides	98-123	sortilin related receptor 1	Homo sapiens	39-43
16925668-5	2006	This was confirmed by high level binding of cells expressing NKRP1A to mouse laminin, which contains a large number of N-linked oligosaccharides with the Galalpha(1,3)Gal structure.	n-linked oligosaccharides	119-144	killer cell lectin-like receptor subfamily B member 1A	Mus musculus	61-67
17055788-0	2006	Human complement factor I glycosylation: structural and functional characterisation of the N-linked oligosaccharides.	n-linked oligosaccharides	91-116	complement factor I	Homo sapiens	6-25
16938437-5	2006	Here, we have observed that NCT N-linked oligosaccharides mediated specific interactions with the secretory pathway lectins calnexin and ERGIC-53.	n-linked oligosaccharides	32-57	nicastrin	Homo sapiens	28-31
16938437-5	2006	Here, we have observed that NCT N-linked oligosaccharides mediated specific interactions with the secretory pathway lectins calnexin and ERGIC-53.	n-linked oligosaccharides	32-57	calnexin	Homo sapiens	124-132
16938437-5	2006	Here, we have observed that NCT N-linked oligosaccharides mediated specific interactions with the secretory pathway lectins calnexin and ERGIC-53.	n-linked oligosaccharides	32-57	lectin, mannose binding 1	Homo sapiens	137-145
16880608-0	2006	Contribution of N-linked oligosaccharides to the expression and functions of beta-glucan receptor, Dectin-1.	n-linked oligosaccharides	16-41	C-type lectin domain family 7, member a	Mus musculus	77-97
16880608-0	2006	Contribution of N-linked oligosaccharides to the expression and functions of beta-glucan receptor, Dectin-1.	n-linked oligosaccharides	16-41	C-type lectin domain family 7, member a	Mus musculus	99-107
16622789-1	2006	The MNN2 gene of S. cerevisiae encodes an alpha (1,2) mannosyl transferase required for branching the outer chain of N-linked oligosaccharides (Rayner J.C. and Munro S. 1998.	n-linked oligosaccharides	117-142	alpha-1,2-mannosyltransferase MNN2	Saccharomyces cerevisiae S288C	4-8
16500903-1	2006	Peptide N-glycanase removes N-linked oligosaccharides from misfolded glycoproteins as part of the endoplasmic reticulum-associated degradation pathway.	n-linked oligosaccharides	28-53	N-glycanase 1	Mus musculus	0-19
16822331-5	2006	Deglycosylation studies using endoglycohydrolases that delete N-linked oligosaccharides (OS) from the molecule show that TEX101 is highly (approximately 47%) N-glycosylated.	n-linked oligosaccharides	62-87	testis expressed gene 101	Mus musculus	121-127
16546121-0	2006	HPLC analysis of discrete haptoglobin isoform N-linked oligosaccharides following 2D-PAGE isolation.	n-linked oligosaccharides	46-71	haptoglobin	Homo sapiens	26-37
16638859-0	2006	N-acetylglucosaminyltransferase V and beta1-6 branching N-linked oligosaccharides are associated with good prognosis of patients with bladder cancer.	n-linked oligosaccharides	56-81	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	Homo sapiens	38-45
16476971-2	2006	Digestion of the 49 and 51 kDa proteins with endoglycosidase H and peptide N-glycosidase F indicated that the U47-encoded proteins were modified with N-linked oligosaccharides.	n-linked oligosaccharides	150-175	envelope glycoprotein O	Human betaherpesvirus 7	110-113
16407250-1	2006	The alpha-1,6-mannosyltransferase encoded by Saccharomyces cerevisiae OCH1 (ScOCH1) is responsible for the outer chain initiation of N-linked oligosaccharides.	n-linked oligosaccharides	133-158	alpha-1,6-mannosyltransferase	Saccharomyces cerevisiae S288C	4-33
16407250-1	2006	The alpha-1,6-mannosyltransferase encoded by Saccharomyces cerevisiae OCH1 (ScOCH1) is responsible for the outer chain initiation of N-linked oligosaccharides.	n-linked oligosaccharides	133-158	initiation-specific alpha-1,6-mannosyltransferase	Saccharomyces cerevisiae S288C	70-74
16237199-6	2006	Comparison of gene expression profiles with matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) profiling of N-linked oligosaccharides suggested that the alpha1-3 fucosyltransferase 9, Fut9, is the enzyme responsible for terminal fucosylation in KID and BRN, a finding validated by analysis of Fut9 knockout mice.	n-linked oligosaccharides	128-153	fucosyltransferase 9	Mus musculus	173-202
16316986-1	2006	alpha1,6-Fucosyltransferase (Fut8) catalyzes the transfer of a fucose residue to N-linked oligosaccharides on glycoproteins via an alpha1,6-linkage to form core fucosylation in mammals.	n-linked oligosaccharides	81-106	fucosyltransferase 8	Mus musculus	0-27
16316986-1	2006	alpha1,6-Fucosyltransferase (Fut8) catalyzes the transfer of a fucose residue to N-linked oligosaccharides on glycoproteins via an alpha1,6-linkage to form core fucosylation in mammals.	n-linked oligosaccharides	81-106	fucosyltransferase 8	Mus musculus	29-33
16377659-1	2006	Beta-mannosidase, a lysosomal enzyme which acts exclusively at the last step of oligosaccharide catabolism in glycoprotein degradation, functions to cleave the unique beta-linked mannose sugar found in all N-linked oligosaccharides of glycoproteins.	n-linked oligosaccharides	206-231	mannosidase, beta A, lysosomal	Mus musculus	0-16
16237199-6	2006	Comparison of gene expression profiles with matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) profiling of N-linked oligosaccharides suggested that the alpha1-3 fucosyltransferase 9, Fut9, is the enzyme responsible for terminal fucosylation in KID and BRN, a finding validated by analysis of Fut9 knockout mice.	n-linked oligosaccharides	128-153	fucosyltransferase 9	Mus musculus	204-208
16237199-6	2006	Comparison of gene expression profiles with matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) profiling of N-linked oligosaccharides suggested that the alpha1-3 fucosyltransferase 9, Fut9, is the enzyme responsible for terminal fucosylation in KID and BRN, a finding validated by analysis of Fut9 knockout mice.	n-linked oligosaccharides	128-153	fucosyltransferase 9	Mus musculus	313-317
15686448-4	2005	Characterization of the N-glycosylation status of recombinant XylT revealed that all three potential N-glycosylation sites of the protein are occupied by N-linked oligosaccharides.	n-linked oligosaccharides	154-179	beta-1,2-xylosyltransferase	Arabidopsis thaliana	62-66
16239475-6	2005	Thus, klotho activates a cell surface channel by hydrolysis of its extracellular N-linked oligosaccharides.	n-linked oligosaccharides	81-106	klotho	Homo sapiens	6-12
16113295-11	2005	N-Glycanase treatment to remove N-linked oligosaccharides shifted the subunit molecular mass of MBP from 130 kDa to 110 kDa.	n-linked oligosaccharides	32-57	myelin basic protein	Homo sapiens	96-99
15843379-9	2005	We also confirmed the presence of the non-sulfated HNK-1 carbohydrate on N-linked oligosaccharides by multistage tandem mass spectrometry.	n-linked oligosaccharides	73-98	beta-1,3-glucuronyltransferase 1 (glucuronosyltransferase P)	Mus musculus	51-56
16364349-5	2006	The improved oligosaccharide profiling was applied to elucidation of N-linked oligosaccharides from Thy-1 isolated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis.	n-linked oligosaccharides	69-94	Thy-1 cell surface antigen	Rattus norvegicus	100-105
16364349-6	2006	It was demonstrated that Thy-1 possesses a significant variety of N-linked oligosaccharides, including Lewis a/x, Lewis b/y, and disialylated structure as a partial structure.	n-linked oligosaccharides	66-91	Thy-1 cell surface antigen	Rattus norvegicus	25-30
17132494-1	2006	Alpha1,6-fucosyltransferase (Fut8) catalyzes the transfer of a fucose residue to N-linked oligosaccharides on glycoproteins by means of an alpha1,6-linkage to form core fucosylation in mammals.	n-linked oligosaccharides	81-106	fucosyltransferase 8	Mus musculus	0-27
17132494-1	2006	Alpha1,6-fucosyltransferase (Fut8) catalyzes the transfer of a fucose residue to N-linked oligosaccharides on glycoproteins by means of an alpha1,6-linkage to form core fucosylation in mammals.	n-linked oligosaccharides	81-106	fucosyltransferase 8	Mus musculus	29-33
16281179-4	2005	As a model of aberrant cells, we used Chinese hamster ovary cells transfected with N-acetylglucosaminyltransferase III (GnT-III), which catalyzes the addition of a bisecting N-acetylglucosamine (GlcNAc) to beta-mannose of the mannosyl core of N-linked oligosaccharides.	n-linked oligosaccharides	243-268	beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase	Cricetulus griseus	83-118
16131661-10	2005	The structures of N-linked oligosaccharides were elucidated from the MS/MS spectra of glycopeptides and exoglycosidase sequencing of PNGase A-released oligosaccharides.	n-linked oligosaccharides	18-43	N-glycanase 1	Homo sapiens	133-139
15628971-0	2005	N-linked oligosaccharides are required to produce and stabilize the active form of chondroitin 4-sulphotransferase-1.	n-linked oligosaccharides	0-25	carbohydrate sulfotransferase 11	Rattus norvegicus	83-116
15862866-3	2005	In enzyme linked lectin assay and hemagglutination inhibition assay, human IgA1, bovine fetuin and other O-glycosylated T antigen-bearing glycoproteins bound to the lectin efficiently in contrast to single N-acetyl lactosamine (LacNAc)-bearing N-linked oligosaccharides released from them and to IgG which is not O-glycosylated.	n-linked oligosaccharides	244-269	immunoglobulin heavy constant alpha 1	Homo sapiens	75-79
15911217-4	2005	In accordance with this, the gene expression of the N-acetylglucosaminyltransferase V, which synthesizes the GlcNAcbeta1-->6 branch of highly branched N-linked oligosaccharides decreased by 30-40% in the drug-treated cells.	n-linked oligosaccharides	154-179	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	Homo sapiens	52-85
15628971-4	2005	In the present paper, we investigated the functional role of the N-linked oligosaccharides attached to C4ST-1.	n-linked oligosaccharides	65-90	carbohydrate sulfotransferase 11	Rattus norvegicus	103-109
15470230-8	2005	In contrast, GlcAT-S recognized not only the terminal Galbeta1-4GlcNAc structure but also the Galbeta1-3GlcNAc structure and showed the highest activity toward triantennary N-linked oligosaccharides.	n-linked oligosaccharides	173-198	beta-1,3-glucuronyltransferase 2	Homo sapiens	13-20
15628971-6	2005	These observations strongly suggest that N-linked oligosaccharides attached to C4ST-1 contribute to the production and stability of the active form of C4ST-1.	n-linked oligosaccharides	41-66	carbohydrate sulfotransferase 11	Rattus norvegicus	79-85
15628971-6	2005	These observations strongly suggest that N-linked oligosaccharides attached to C4ST-1 contribute to the production and stability of the active form of C4ST-1.	n-linked oligosaccharides	41-66	carbohydrate sulfotransferase 11	Rattus norvegicus	151-157
15628971-7	2005	In addition, the N-linked oligosaccharide at the C-terminal region appears to affect the glycosylation pattern of recombinant C4ST; a broad protein band of the wildtype protein resulting from microheterogeneity of N-linked oligosaccharides disappeared and four discrete protein bands with different numbers of N-linked oligosaccharides appeared when the N-linked oligosaccharide at the C-terminal region was deleted.	n-linked oligosaccharides	214-239	carbohydrate sulfotransferase 11	Rattus norvegicus	126-130
15628971-7	2005	In addition, the N-linked oligosaccharide at the C-terminal region appears to affect the glycosylation pattern of recombinant C4ST; a broad protein band of the wildtype protein resulting from microheterogeneity of N-linked oligosaccharides disappeared and four discrete protein bands with different numbers of N-linked oligosaccharides appeared when the N-linked oligosaccharide at the C-terminal region was deleted.	n-linked oligosaccharides	310-335	carbohydrate sulfotransferase 11	Rattus norvegicus	126-130
15604090-1	2005	Core alpha1,6-fucosylation is a conserved feature of animal N-linked oligosaccharides being present in both invertebrates and vertebrates.	n-linked oligosaccharides	60-85	alpha-Tubulin at 84B	Drosophila melanogaster	5-13
15576633-1	2005	We used a novel approach to evaluate how the addition/acquisition and processing/modification of N-linked oligosaccharides play a role in the functional maturation of human organic anion transporter hOAT4.	n-linked oligosaccharides	97-122	solute carrier family 22 member 11	Homo sapiens	199-204
15820978-4	2005	Fc-Epo was secreted from NS/0 myeloma cells as about 35% high molecular weight aggregates, was unstable upon removal of N-linked oligosaccharides and showed poor pharmacokinetics and little efficacy in mice.	n-linked oligosaccharides	120-145	erythropoietin	Homo sapiens	3-6
15820978-5	2005	In contrast, a corresponding Fc-Epo(NDS) was secreted almost exclusively as a unit dimer, was relatively stable to removal of N-linked oligosaccharides, had much improved pharmacokinetic properties and had a significantly improved effect on RBC production.	n-linked oligosaccharides	126-151	erythropoietin	Homo sapiens	32-35
15820978-5	2005	In contrast, a corresponding Fc-Epo(NDS) was secreted almost exclusively as a unit dimer, was relatively stable to removal of N-linked oligosaccharides, had much improved pharmacokinetic properties and had a significantly improved effect on RBC production.	n-linked oligosaccharides	126-151	erythropoietin	Homo sapiens	36-39
15767043-1	2005	The N-linked oligosaccharides on human choriogonadotropin (hCG) and follitropin (hFSH) alpha-subunit loop 2 (alpha2) have a dominant influence on hormone efficacy.	n-linked oligosaccharides	4-29	glycoprotein hormones, alpha polypeptide	Homo sapiens	59-62
14693378-0	2004	Cloning and characterization in Pichia pastoris of PNO1 gene required for phosphomannosylation of N-linked oligosaccharides.	n-linked oligosaccharides	98-123	Pno1p	Saccharomyces cerevisiae S288C	51-55
16260863-6	2005	When ZPC lacking N-linked oligosaccharides was transfected into the cells, the 31-kDa immunoreactive band was detected in both the apical and the basolateral medium.	n-linked oligosaccharides	17-42	zona pellucida sperm-binding protein 3	Canis lupus familiaris	5-8
15145052-10	2004	N-glycosidase F treatment resulted in a reduction of the apparent molecular weight to 107 kDa, showing that LRIG2 was a glycoprotein carrying N-linked oligosaccharides.	n-linked oligosaccharides	142-167	leucine rich repeats and immunoglobulin like domains 2	Homo sapiens	108-113
15176893-1	2004	Using capillary electrophoresis coupled to laser-induced fluorescence (HPCE-LIF), it was possible to profile N-linked oligosaccharides from EPO, including species containing sialic acid, during the course of batch cultures performed either in serum-free or serum-containing medium.	n-linked oligosaccharides	109-134	leukemia inhibitory factor	Mus musculus	76-79
15069543-4	2004	Reduction in the expression of N-linked oligosaccharides, including L-PHA reactive oligosaccharides, on the cell surface by SW treatment resulted in enhancement of HBL-2 cell survival by CD40L stimulation.	n-linked oligosaccharides	31-56	CD40 ligand	Homo sapiens	187-192
15583810-10	2005	Reduction in expression of N-linked oligosaccharides, including L-PHA reactive oligosaccharides, on the cell surface by SW treatment prevented the growth inhibition of HBL-2 cells by galectin-1.	n-linked oligosaccharides	27-52	galectin 1	Homo sapiens	183-193
15208308-5	2004	Like the native protein, recombinant hHARE contains approximately 25 kDa of N-linked oligosaccharides, binds HA in a ligand blot assay, cross-reacts with three anti-rat HARE monoclonal antibodies, and is inactivated by reduction.	n-linked oligosaccharides	76-101	stabilin 2	Homo sapiens	37-42
15208308-5	2004	Like the native protein, recombinant hHARE contains approximately 25 kDa of N-linked oligosaccharides, binds HA in a ligand blot assay, cross-reacts with three anti-rat HARE monoclonal antibodies, and is inactivated by reduction.	n-linked oligosaccharides	76-101	stabilin 2	Homo sapiens	38-42
15085180-1	2004	The 300 kDa cation-independent mannose 6-phosphate receptor (CI-MPR) mediates the intracellular transport of newly synthesized lysosomal enzymes containing mannose 6-phosphate on their N-linked oligosaccharides.	n-linked oligosaccharides	185-210	insulin like growth factor 2 receptor	Homo sapiens	12-59
15085180-1	2004	The 300 kDa cation-independent mannose 6-phosphate receptor (CI-MPR) mediates the intracellular transport of newly synthesized lysosomal enzymes containing mannose 6-phosphate on their N-linked oligosaccharides.	n-linked oligosaccharides	185-210	insulin like growth factor 2 receptor	Homo sapiens	61-67
14693378-1	2004	The yeast Pichia pastoris PNO1 (Phosphomannosylation of N-linked Oligosaccharides) gene, which is involved in phosphomannosylation of N-linked oligosaccharides, was cloned using the Saccharomyces cerevisiae MNN4 gene [Glycobiology 6 (1996) 805] as a probe.	n-linked oligosaccharides	56-81	Pno1p	Saccharomyces cerevisiae S288C	26-30
14693378-1	2004	The yeast Pichia pastoris PNO1 (Phosphomannosylation of N-linked Oligosaccharides) gene, which is involved in phosphomannosylation of N-linked oligosaccharides, was cloned using the Saccharomyces cerevisiae MNN4 gene [Glycobiology 6 (1996) 805] as a probe.	n-linked oligosaccharides	56-81	Mnn4p	Saccharomyces cerevisiae S288C	207-211
14693378-1	2004	The yeast Pichia pastoris PNO1 (Phosphomannosylation of N-linked Oligosaccharides) gene, which is involved in phosphomannosylation of N-linked oligosaccharides, was cloned using the Saccharomyces cerevisiae MNN4 gene [Glycobiology 6 (1996) 805] as a probe.	n-linked oligosaccharides	134-159	Pno1p	Saccharomyces cerevisiae S288C	26-30
14693378-1	2004	The yeast Pichia pastoris PNO1 (Phosphomannosylation of N-linked Oligosaccharides) gene, which is involved in phosphomannosylation of N-linked oligosaccharides, was cloned using the Saccharomyces cerevisiae MNN4 gene [Glycobiology 6 (1996) 805] as a probe.	n-linked oligosaccharides	134-159	Mnn4p	Saccharomyces cerevisiae S288C	207-211
14693378-8	2004	However, the phosphomannosylation ratio of N-linked oligosaccharides on recombinant human antithrombin decreased dramatically from 20% in wild-type strains to less than 1% in the PNO1 disruptant.	n-linked oligosaccharides	43-68	Pno1p	Saccharomyces cerevisiae S288C	179-183
12933790-6	2003	The recombinant rHARE contained approximately 25 kDa of N-linked oligosaccharides and, like the native protein, was able to bind HA in a ligand blot assay, even after de-N-glycosylation.	n-linked oligosaccharides	56-81	stabilin 2	Rattus norvegicus	16-21
12744721-0	2003	N-linked oligosaccharides play a role in disulphide-dependent dimerization of intestinal mucin Muc2.	n-linked oligosaccharides	0-25	solute carrier family 13 member 2	Rattus norvegicus	89-94
12744721-0	2003	N-linked oligosaccharides play a role in disulphide-dependent dimerization of intestinal mucin Muc2.	n-linked oligosaccharides	0-25	mucin 2, oligomeric mucus/gel-forming	Rattus norvegicus	95-99
12551983-2	2003	Glycosidase digestion analysis showed that the U100 gene products are glycoproteins consisting of an 80-kDa protein with complex N-linked oligosaccharides and a 74-kDa protein with immature, high-mannose N-linked oligosaccharides.	n-linked oligosaccharides	129-154	small Cajal body-specific RNA 14	Homo sapiens	47-51
12605599-7	2003	Our studies thus indicate that (a) cleavage within the SEA module of rat Muc3 requires participation of peptide sequences located C-terminal of and distant from the cleavage site, (b) re-association of the fragments requires the SEA module, but is independent of N-linked oligosaccharides, and (c) membrane targeting of the mucin is independent of the SEA-module-cleavage reaction.	n-linked oligosaccharides	263-288	mucin 3	Rattus norvegicus	73-77
12623072-7	2003	These results indicate that, besides proteasome inhibitors, inhibitors of ER mannosidase I and protein synthesis suppress ERAD of the antithrombin deltaGlu mutant at different stages, and processing of N-linked oligosaccharides highly correlated with the efficiency of ERAD.	n-linked oligosaccharides	202-227	serpin family C member 1	Homo sapiens	134-146
12584318-5	2003	Because the only two N-linked oligosaccharides in mASCT1 occur in the carboxyl-terminal region of extracellular loop 2 (ECL2), it was inferred that this region contributes in an inhibitory manner to infections by RD114 and type D primate viruses.	n-linked oligosaccharides	21-46	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	Mus musculus	50-56
12584318-11	2003	These results strongly suggest that combinations of amino acid sequence changes and N-linked oligosaccharides in a critical carboxyl-terminal region of ECL2 control retroviral utilization of both the ASCT1 and ASCT2 receptors.	n-linked oligosaccharides	84-109	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	Mus musculus	200-205
12584318-11	2003	These results strongly suggest that combinations of amino acid sequence changes and N-linked oligosaccharides in a critical carboxyl-terminal region of ECL2 control retroviral utilization of both the ASCT1 and ASCT2 receptors.	n-linked oligosaccharides	84-109	solute carrier family 1 (neutral amino acid transporter), member 5	Mus musculus	210-215
12488460-7	2003	Mature TPP I was found to be partially resistant to endo H treatment; thus, some of its N-linked oligosaccharides are of the complex/hybrid type.	n-linked oligosaccharides	88-113	tripeptidyl peptidase 1	Homo sapiens	7-12
12626411-1	2003	alpha2,6-Sialyltransferase (ST6Gal I) functions in the Golgi to terminally sialylate the N-linked oligosaccharides of glycoproteins.	n-linked oligosaccharides	89-114	ST6 beta-galactoside alpha-2,6-sialyltransferase 1	Rattus norvegicus	28-36
12324456-9	2002	We isolated GP-2 from porcine pancreas extract and determined the structure of its N-linked oligosaccharides by two-dimensional mapping.	n-linked oligosaccharides	83-108	glycoprotein 2	Bos taurus	12-16
12393878-4	2002	We have determined that tenascin-R associated with Purkinje cell bodies and their dendrites in the molecular layer of the cerebellum bears N-linked oligosaccharides terminating with beta1,4-linked GalNAc-4-SO(4), whereas tenascin-R in other regions of the cerebellum does not bear this modification.	n-linked oligosaccharides	139-164	tenascin R	Homo sapiens	24-34
12460896-2	2002	One of the most common forms of glycosylation in transformed cells and human tumors is the highly elevated beta1,6 branching of N-linked oligosaccharides caused by increased transcription of N-acetylglucosaminyltransferase V (GnT-V).	n-linked oligosaccharides	128-153	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	Homo sapiens	107-114
12498206-4	2002	The method was used to demonstrate that the difference between human alpha-2HS-glycoprotein isoforms separated by 2D-gel electrophoresis was partially due to sialylation of both O-linked and N-linked oligosaccharides.	n-linked oligosaccharides	191-216	alpha 2-HS glycoprotein	Homo sapiens	69-91
12460896-2	2002	One of the most common forms of glycosylation in transformed cells and human tumors is the highly elevated beta1,6 branching of N-linked oligosaccharides caused by increased transcription of N-acetylglucosaminyltransferase V (GnT-V).	n-linked oligosaccharides	128-153	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	Homo sapiens	191-224
12460896-2	2002	One of the most common forms of glycosylation in transformed cells and human tumors is the highly elevated beta1,6 branching of N-linked oligosaccharides caused by increased transcription of N-acetylglucosaminyltransferase V (GnT-V).	n-linked oligosaccharides	128-153	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	Homo sapiens	226-231
12382235-0	2002	Terminal alpha-linked galactose rather than N-acetyl lactosamine is ligand for bovine heart galectin-1 in N-linked oligosaccharides of glycoproteins.	n-linked oligosaccharides	106-131	galectin 1	Bos taurus	92-102
12235182-0	2002	The N-linked oligosaccharides at the amino terminus of human apoB are important for the assembly and secretion of VLDL.	n-linked oligosaccharides	4-29	apolipoprotein B	Homo sapiens	61-65
11467948-6	2001	The heterogeneous N-linked oligosaccharides of TNFR-IgG contain sialic acid (Sia), Gal, and GlcNAc as terminal sugar residues.	n-linked oligosaccharides	18-43	TNF receptor superfamily member 1A	Homo sapiens	47-51
12039072-1	2002	Human sex hormone-binding globulin (SHBG) is a homodimeric plasma glycoprotein, and each SHBG monomer may have an O-linked oligosaccharide at Thr(7) and up to two N-linked oligosaccharides at Asn(351) and Asn(367).	n-linked oligosaccharides	163-188	sex hormone binding globulin	Homo sapiens	6-34
12039072-1	2002	Human sex hormone-binding globulin (SHBG) is a homodimeric plasma glycoprotein, and each SHBG monomer may have an O-linked oligosaccharide at Thr(7) and up to two N-linked oligosaccharides at Asn(351) and Asn(367).	n-linked oligosaccharides	163-188	sex hormone binding globulin	Homo sapiens	36-40
12039072-9	2002	Estradiol-induced proliferation of parental MCF-7 cells was also inhibited by treatment with conditioned medium containing wild type SHBG or SHBG mutants lacking N-linked oligosaccharides, or containing an additional N-linked oligosaccharide at residue 327.	n-linked oligosaccharides	162-187	sex hormone binding globulin	Homo sapiens	141-145
11588157-4	2001	Introduction of the antisense beta-1,4-GalT II and V cDNAs separately into human colorectal adenocarcinoma SW480 cells, in which beta-1,4-GalT I, II, and V genes were expressed, resulted in the reduction of RCA-I binding toward N-linked oligosaccharides of the membrane glycoproteins.	n-linked oligosaccharides	228-253	beta-1,4-galactosyltransferase 5	Homo sapiens	30-46
11552737-6	2001	A approximately 35 kDa SP-A immunoreactive protein was detected in the tracheal tissues by immunoblot analysis and was shown to be modified by the addition of N-linked oligosaccharides.	n-linked oligosaccharides	159-184	surfactant protein A1	Homo sapiens	23-27
11443114-5	2001	The structural analyses revealed that the amount of N-linked oligosaccharides bearing the alpha-Gal epitopes in the GnT-III-transfected cells was less than 10% that in parental cells, due to the alteration of the terminal structures as well as a decrease in branch formation.	n-linked oligosaccharides	52-77	GLA	Sus scrofa	90-99
12152683-5	2002	The N-linked oligosaccharides of urinary u-PA do not terminate with the common Gal-GlcNAc element, but with a GalNAc-GlcNAc element which is partially sulfated.	n-linked oligosaccharides	4-29	plasminogen activator, urokinase	Rattus norvegicus	41-45
12023893-5	2002	Biosynthetic studies using this antiserum revealed that hCTR1 was synthesized as a precursor protein of 28 kDa containing N-linked oligosaccharides, and is then converted to a mature protein of approx.	n-linked oligosaccharides	122-147	solute carrier family 31 member 1	Homo sapiens	56-61
12162998-0	2002	Identification of N-linked oligosaccharides of rat insulin-like growth factor binding protein-4.	n-linked oligosaccharides	18-43	insulin-like growth factor binding protein 4	Rattus norvegicus	51-95
12815230-1	2002	UDP-GlcNAc:alpha6-D-mannoside beta1,2-N-acetylglucosaminyltransferase II (GnT II; EC 2.4.1.143) is a medial-Golgi resident enzyme that catalyses an essential step in the biosynthetic pathway leading from high mannose to complex N-linked oligosaccharides.	n-linked oligosaccharides	228-253	alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	Homo sapiens	74-80
11824812-1	2002	The N-linked oligosaccharides were released from the phospholipase A2 (PLA) with glycopeptidases and reductively aminated with the chromophore, p-aminobenzoic acid ethyl ester (ABEE).	n-linked oligosaccharides	4-29	phospholipase A2	Apis mellifera	53-69
11824812-1	2002	The N-linked oligosaccharides were released from the phospholipase A2 (PLA) with glycopeptidases and reductively aminated with the chromophore, p-aminobenzoic acid ethyl ester (ABEE).	n-linked oligosaccharides	4-29	phospholipase A2	Apis mellifera	71-74
11397085-6	2001	The extracellular leucine-rich repeats, and in particular the N-linked oligosaccharides that are present on them appear to be essential for correct localization of the AtSERK1-YFP protein.	n-linked oligosaccharides	62-87	somatic embryogenesis receptor-like kinase 1	Arabidopsis thaliana	168-175
11313366-3	2001	The mature hIntL was a secretory glycoprotein consisting of 295 amino acids and N-linked oligosaccharides, and its basic structural unit was a 120-kDa homotrimer in which 40-kDa polypeptides were bridged by disulfide bonds.	n-linked oligosaccharides	80-105	intelectin 1	Homo sapiens	11-16
11145959-8	2001	It is shown additionally that biglycan expressed in 293 cells may still contain the propeptide sequence and may carry heparan sulfate chains as well as sulfated N-linked oligosaccharides.	n-linked oligosaccharides	161-186	biglycan	Homo sapiens	30-38
11892998-1	2001	Beta-mannosidase is an exoglycosidase involved in the degradation of N-linked oligosaccharides moieties of glycoproteins.	n-linked oligosaccharides	69-94	mannosidase, beta A, lysosomal	Mus musculus	0-16
16233148-5	2001	The relative activity of MBP-fused GnT-I toward high-mannose-type N-linked oligosaccharides was 100% for Man5GlcNAc2, 52% for Man3GlcNAc2, 17% for Man6GlcNAc2.	n-linked oligosaccharides	66-91	myelin basic protein	Homo sapiens	25-28
11179968-0	2001	Structural study of N-linked oligosaccharides of human intercellular adhesion molecule-3 (CD50).	n-linked oligosaccharides	20-45	intercellular adhesion molecule 3	Homo sapiens	55-88
11179968-1	2001	The N-linked oligosaccharides were released from purified human intercellular adhesion molecule (ICAM)-3 by hydrazinolysis.	n-linked oligosaccharides	4-29	intercellular adhesion molecule 3	Homo sapiens	64-104
11179968-6	2001	Structural studies of each oligosaccharide by sequential exo- and endo-glycosidase digestion and by methylation analysis revealed that N-linked oligosaccharides of ICAM-3 are mainly of tri- and tetra-antennary complex-type, about 60% of which contain two to three poly N-acetyllactosamine chains terminated with the type 1 structure and those without the type 1 structure per oligosaccharide.	n-linked oligosaccharides	135-160	intercellular adhesion molecule 3	Homo sapiens	164-170
11139592-4	2001	GalNAc-4-ST2 transfers sulfate to the C-4 hydroxyl of terminal beta1,4-linked GalNAc in the sequence GalNAc-beta1,4GlcNAcbeta-R found on N-linked oligosaccharides and nonterminal beta1,4-linked GalNAc in chondroitin and dermatan.	n-linked oligosaccharides	137-162	carbohydrate sulfotransferase 9	Homo sapiens	0-12
11231017-0	2001	Schizosaccharomyces pombe och1(+) encodes alpha-1,6-mannosyltransferase that is involved in outer chain elongation of N-linked oligosaccharides.	n-linked oligosaccharides	118-143	initiation-specific alpha-1,6-mannosyltransferase	Saccharomyces cerevisiae S288C	26-30
16233148-5	2001	The relative activity of MBP-fused GnT-I toward high-mannose-type N-linked oligosaccharides was 100% for Man5GlcNAc2, 52% for Man3GlcNAc2, 17% for Man6GlcNAc2.	n-linked oligosaccharides	66-91	alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	Homo sapiens	35-40
11204595-3	2001	r-VIII SQ retains six potential glycosylation sites for N-linked oligosaccharides at asparagine residues 41, 239, 582, 1685, 1810 and 2118.	n-linked oligosaccharides	56-81	cytochrome c oxidase subunit 8A	Homo sapiens	2-6
11001942-6	2000	Sulfation of carbonic anhydrase VI by the recombinant GalNAc4ST occurred at position 4 of the GalNAc residue of N-linked oligosaccharides.	n-linked oligosaccharides	112-137	carbohydrate sulfotransferase 8	Homo sapiens	54-63
10995765-1	2000	Endoplasmic reticulum (ER) class I alpha1,2-mannosidase (also known as ER alpha-mannosidase I) is a critical enzyme in the maturation of N-linked oligosaccharides and ER-associated degradation.	n-linked oligosaccharides	137-162	mannosidase alpha class 1A member 2	Homo sapiens	35-55
11001942-8	2000	Dot blot analysis showed that the message of GalNAc4ST was expressed strongly in the human pituitary, suggesting that the cloned GalNAc4ST may be involved in the synthesis of the nonreducing terminal GalNAc 4-sulfate residues found in the N-linked oligosaccharides of pituitary glycoprotein hormones.	n-linked oligosaccharides	239-264	carbohydrate sulfotransferase 8	Homo sapiens	45-54
11001942-8	2000	Dot blot analysis showed that the message of GalNAc4ST was expressed strongly in the human pituitary, suggesting that the cloned GalNAc4ST may be involved in the synthesis of the nonreducing terminal GalNAc 4-sulfate residues found in the N-linked oligosaccharides of pituitary glycoprotein hormones.	n-linked oligosaccharides	239-264	carbohydrate sulfotransferase 8	Homo sapiens	129-138
11093807-4	2000	SDS-PAGE of OVCAR5 cell lysates has revealed that the CA6 epitope is expressed on an 80 kDa non-disulfide-linked glycoprotein containing N-linked oligosaccharides.	n-linked oligosaccharides	137-162	carbonic anhydrase 6	Homo sapiens	54-57
11511812-2	2000	Structural analysis of N-linked oligosaccharides, to which glucuronic acid was transferred by GlcAT-P, by means of two-dimensional mapping of pyridylamino-oligosaccharides and MS spectrometry, demonstrated that the enzyme transferred glucuronic acid to bi-, tri-, and tetra-antennary complex type sugar chains, with almost equal efficiency, indicating that the enzyme has no preference as to the number of acceptor sugar branches.	n-linked oligosaccharides	23-48	beta-1,3-glucuronyltransferase 1	Rattus norvegicus	94-101
10988300-1	2000	N-Linked oligosaccharides terminating with the sequence SO(4)-4-GalNAcbeta1,4GlcNAcbeta1,2Manalpha are present on the pituitary hormones lutropin (LH), thyrotropin, and pro-opiomelanocortin.	n-linked oligosaccharides	0-25	proopiomelanocortin	Homo sapiens	169-189
10988300-3	2000	We have cloned the N-acetylgalactosamine-4-sulfotransferase (GalNAc-4-ST1, GenBank(TM) accession number ), which mediates sulfate addition to the N-linked oligosaccharides on LH and other pituitary glycoproteins with terminal (beta1,4-linked GalNAc based on its homology to HNK-1 sulfotransferase (HNK-1 ST).	n-linked oligosaccharides	146-171	carbohydrate sulfotransferase 8	Homo sapiens	61-73
10988300-3	2000	We have cloned the N-acetylgalactosamine-4-sulfotransferase (GalNAc-4-ST1, GenBank(TM) accession number ), which mediates sulfate addition to the N-linked oligosaccharides on LH and other pituitary glycoproteins with terminal (beta1,4-linked GalNAc based on its homology to HNK-1 sulfotransferase (HNK-1 ST).	n-linked oligosaccharides	146-171	carbohydrate sulfotransferase 10	Homo sapiens	274-296
10988300-3	2000	We have cloned the N-acetylgalactosamine-4-sulfotransferase (GalNAc-4-ST1, GenBank(TM) accession number ), which mediates sulfate addition to the N-linked oligosaccharides on LH and other pituitary glycoproteins with terminal (beta1,4-linked GalNAc based on its homology to HNK-1 sulfotransferase (HNK-1 ST).	n-linked oligosaccharides	146-171	carbohydrate sulfotransferase 10	Homo sapiens	298-306
10988300-10	2000	GalNAc-4-ST1 also efficiently transfers sulfate to N-linked oligosaccharides on native LH and other glycoproteins terminating with beta1,4-linked GalNAc.	n-linked oligosaccharides	51-76	carbohydrate sulfotransferase 8	Homo sapiens	0-12
10998266-2	2000	N-linked oligosaccharides were released from recombinant human EPO expressed in Chinese hamster ovary cells enzymatically and reduced with NaBH(4).	n-linked oligosaccharides	0-25	erythropoietin	Homo sapiens	63-66
11372444-0	2000	[HPLC/ESI MS and MALDI/TOF MS analysis of microheterogeneity of the N-linked oligosaccharides of recombinant human erythropoietin].	n-linked oligosaccharides	68-93	erythropoietin	Homo sapiens	115-129
11027166-3	2000	In the work presented here, the effects of ammonia on EPO N-linked oligosaccharides were analyzed.	n-linked oligosaccharides	58-83	erythropoietin	Homo sapiens	54-57
10842180-4	2000	Using recombinant Dpl expressed in Escherichia coli and mouse neuroblastoma cells we demonstrate that wild type (wt) Dpl, like PrP(C), adopts a predominantly alpha-helical conformation, forms intramolecular disulfide bonds, has two N-linked oligosaccharides, and is presented on the cell surface via a glycosylphosphatidylinositol anchor.	n-linked oligosaccharides	232-257	prion like protein doppel	Mus musculus	117-120
10898315-2	2000	On the other hand, alpha1-6 fucosyl-transferase (alphaFT) catalyzes the addition of fucose from GDP-fucose through an alpha1-6 linkage to the reducing end of N-acetylglucosamine residue of N-linked oligosaccharides of glycoproteins.	n-linked oligosaccharides	189-214	fucosyltransferase 8	Homo sapiens	19-47
10858499-0	2000	The mnn2 mutant of Saccharomyces cerevisiae is affected in phosphorylation of N-linked oligosaccharides.	n-linked oligosaccharides	78-103	alpha-1,2-mannosyltransferase MNN2	Saccharomyces cerevisiae S288C	4-8
10858499-1	2000	We studied the phosphorylation of the inner core region of N-linked oligosaccharides in the mannan defective mutant Saccharomyces cerevisiae mnn2 which was described as unable to synthesize branches on the outer chain.	n-linked oligosaccharides	59-84	alpha-1,2-mannosyltransferase MNN2	Saccharomyces cerevisiae S288C	141-145
10933718-6	2000	In addition, elimination of the two N-linked oligosaccharides from mASCT2 by mutagenesis, as substantiated by protein N-glycosidase F digestions and Western immunoblotting, did not enable it to function as a receptor for RD114 or type D retroviruses.	n-linked oligosaccharides	36-61	solute carrier family 1 (neutral amino acid transporter), member 5	Mus musculus	67-73
10933718-8	2000	Furthermore, elimination of the two N-linked oligosaccharides from extracellular loop 2 of mASCT1 by mutagenesis enabled it to function as an efficient receptor for RD114 and type D retroviruses.	n-linked oligosaccharides	36-61	solute carrier family 1 (glutamate/neutral amino acid transporter), member 4	Mus musculus	91-97
10898315-2	2000	On the other hand, alpha1-6 fucosyl-transferase (alphaFT) catalyzes the addition of fucose from GDP-fucose through an alpha1-6 linkage to the reducing end of N-acetylglucosamine residue of N-linked oligosaccharides of glycoproteins.	n-linked oligosaccharides	189-214	adrenoceptor alpha 1D	Homo sapiens	19-27
10788525-8	2000	Taken together, these data suggest that the formation of the gp65-p22(phox) heterodimer is relatively inefficient and that acquisition of heme by gp65 precedes and is required for its association with p22(phox), a process that requires neither the addition of N-linked oligosaccharides nor modification in the Golgi complex.	n-linked oligosaccharides	260-285	neuroplastin	Homo sapiens	146-150
10845701-8	2000	BSSL from the first lactation month also showed a different composition of sialylated O-linked glycans and the N-linked oligosaccharides consisted of lower amounts of fucosylated structures compared to later in lactation.	n-linked oligosaccharides	111-136	carboxyl ester lipase	Homo sapiens	0-4
10788525-8	2000	Taken together, these data suggest that the formation of the gp65-p22(phox) heterodimer is relatively inefficient and that acquisition of heme by gp65 precedes and is required for its association with p22(phox), a process that requires neither the addition of N-linked oligosaccharides nor modification in the Golgi complex.	n-linked oligosaccharides	260-285	calcineurin like EF-hand protein 1	Homo sapiens	201-204
10764841-0	2000	Use of recombinant endomannosidase for evaluation of the processing of N-linked oligosaccharides of glycoproteins and their oligosaccharide-lipid precursors.	n-linked oligosaccharides	71-96	mannosidase endo-alpha	Homo sapiens	19-34
10779781-6	2000	Deglycosylation experiments with neuraminidase and Endo-F combined with two-dimensional PAGE of single bands of the intracellular vs extracellular IL-12 heterodimer revealed that the alpha-chain was extensively modified with sialic acid adducts to N-linked oligosaccharides before secretion.	n-linked oligosaccharides	248-273	Fc gamma receptor and transporter	Homo sapiens	183-194
10911720-3	2000	We observed a greater variety of N-linked oligosaccharides derived from plasma vWf than from platelet vWf.	n-linked oligosaccharides	33-58	von Willebrand factor	Homo sapiens	79-82
10781814-1	2000	The transfer of xylose from UDP-xylose to the core beta-linked mannose of N-linked oligosaccharides by beta1,2-xylosyltransferase (XylT) is a widespread feature of plant glycoproteins which renders them immunogenic and allergenic in man.	n-linked oligosaccharides	74-99	beta-1,2-xylosyltransferase	Arabidopsis thaliana	103-110
10781814-1	2000	The transfer of xylose from UDP-xylose to the core beta-linked mannose of N-linked oligosaccharides by beta1,2-xylosyltransferase (XylT) is a widespread feature of plant glycoproteins which renders them immunogenic and allergenic in man.	n-linked oligosaccharides	74-99	beta-1,2-xylosyltransferase	Arabidopsis thaliana	131-135
10704524-0	2000	Human alpha-N-acetylgalactosaminidase: site occupancy and structure of N-linked oligosaccharides.	n-linked oligosaccharides	71-96	alpha-N-acetylgalactosaminidase	Homo sapiens	6-37
10704528-0	2000	Characterization of the N-linked oligosaccharides of megalin (gp330) from rat kidney.	n-linked oligosaccharides	24-49	LDL receptor related protein 2	Rattus norvegicus	53-60
10704528-0	2000	Characterization of the N-linked oligosaccharides of megalin (gp330) from rat kidney.	n-linked oligosaccharides	24-49	LDL receptor related protein 2	Rattus norvegicus	62-67
10805531-2	2000	N-Linked oligosaccharides carrying beta1-6GlcNAc branches are associated with tumor invasion and metastasis.	n-linked oligosaccharides	0-25	hemoglobin, beta adult major chain	Mus musculus	35-42
10572095-4	1999	Enzymatic removal of all the N-linked oligosaccharides from fibrinogen Niigata accelerated fibrin monomer polymerization that reached the level of untreated normal fibrin monomers, but the thrombin time was prolonged from 18.2 seconds to 113 seconds (normal: 11.2 seconds to 8.9 seconds).	n-linked oligosaccharides	29-54	fibrinogen beta chain	Homo sapiens	60-70
10601243-2	1999	The two MPRs, the cation-dependent MPR (CD-MPR) and the insulin-like growth factor II/cation-independent MPR, carry out this process by binding with high affinity to mannose 6-phosphate residues found on the N-linked oligosaccharides of their ligands.	n-linked oligosaccharides	208-233	mannose-6-phosphate receptor, cation dependent	Bos taurus	18-38
10601243-2	1999	The two MPRs, the cation-dependent MPR (CD-MPR) and the insulin-like growth factor II/cation-independent MPR, carry out this process by binding with high affinity to mannose 6-phosphate residues found on the N-linked oligosaccharides of their ligands.	n-linked oligosaccharides	208-233	mannose-6-phosphate receptor, cation dependent	Bos taurus	40-46
10736100-9	2000	Oversialylation of N-linked oligosaccharides of IgA1 from patients with pSS might prevent the recognition of IgA by receptors that are responsible for their clearance, resulting in an excess of serum IgA and related immune complexes.	n-linked oligosaccharides	19-44	immunoglobulin heavy constant alpha 1	Homo sapiens	48-52
10736100-9	2000	Oversialylation of N-linked oligosaccharides of IgA1 from patients with pSS might prevent the recognition of IgA by receptors that are responsible for their clearance, resulting in an excess of serum IgA and related immune complexes.	n-linked oligosaccharides	19-44	CD79a molecule	Homo sapiens	48-51
10736100-9	2000	Oversialylation of N-linked oligosaccharides of IgA1 from patients with pSS might prevent the recognition of IgA by receptors that are responsible for their clearance, resulting in an excess of serum IgA and related immune complexes.	n-linked oligosaccharides	19-44	CD79a molecule	Homo sapiens	109-112
10715549-4	2000	No aggregation was seen when N-linked oligosaccharides were attached to the Asn(13) of LHbeta.	n-linked oligosaccharides	29-54	luteinizing hormone subunit beta	Homo sapiens	87-93
16232900-7	2000	The molecular mass of synthesized gp120 decreased from 100 kDa to 61 kDa after endoglycosidase H treatment, indicating that synthesized gp120 had been glycosylated with N-linked oligosaccharides.	n-linked oligosaccharides	169-194	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	34-39
16232900-7	2000	The molecular mass of synthesized gp120 decreased from 100 kDa to 61 kDa after endoglycosidase H treatment, indicating that synthesized gp120 had been glycosylated with N-linked oligosaccharides.	n-linked oligosaccharides	169-194	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	136-141
11229321-1	1999	N-acetylglucosaminyltransferase II (GnTII, EC 2.4.1.143) is a Golgi enzyme involved in the biosynthesis of glycoprotein-bound N-linked oligosaccharides, catalysing an essential step in the conversion of oligomannose-type to complex N-glycans.	n-linked oligosaccharides	126-151	alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	Homo sapiens	36-41
10559782-1	1999	Differences in the N-linked oligosaccharides on isoforms of the neural cell adhesion molecule (N-CAM) on astrocytes were found using a lectin, namely, Datura stramonium agglutinin (DSA).	n-linked oligosaccharides	19-44	neural cell adhesion molecule 1	Rattus norvegicus	95-100
10561465-1	1999	The ST6Gal I is a sialyltransferase that modifies N-linked oligosaccharides of glycoproteins.	n-linked oligosaccharides	50-75	ST6 beta-galactoside alpha-2,6-sialyltransferase 1	Homo sapiens	4-12
10561578-1	1999	A comparative study of cathepsin E with distinct N-linked oligosaccharides and its nonglycosylated mutant.	n-linked oligosaccharides	49-74	cathepsin E	Rattus norvegicus	23-34
10502677-7	1999	However, upon digestion with peptide: N-glycosidase F, the 80-kDa TNSALP of human origin and the soluble enzyme of insect origin migrated to the same position on SDS-polyacrylamide gel, indicating that the size difference between the two enzymes is ascribed to N-linked oligosaccharides.	n-linked oligosaccharides	261-286	alkaline phosphatase, biomineralization associated	Homo sapiens	66-72
10514470-2	1999	These acid hydrolases carry mannose 6-phosphate recognition markers on their N-linked oligosaccharides that are recognized by two distinct MPRs: the cation-dependent mannose 6-phosphate receptor and the insulin-like growth factor II/cation-independent mannose 6-phosphate receptor.	n-linked oligosaccharides	77-102	mannose-6-phosphate receptor, cation dependent	Bos taurus	149-194
10438459-1	1999	Although the precise role of oligosaccharides in metastasis is presently unknown, numerous studies suggest that the beta1-6 branching structure of N-linked oligosaccharides plays a role in tumor metastasis.	n-linked oligosaccharides	147-172	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	Homo sapiens	116-123
10622399-10	1999	plasma half-lives of recombinant hSHBG (t 1/2alpha 0.11+/-0.03 h and t 1/2beta 18.94+/-1.65 h) are shorter than previously measured for natural hSHBG (t 1/2alpha 3.43+/-0.72 h and t 1/2beta 38.18+/-7.22 h) and this is likely due to differences in the composition of their N-linked oligosaccharides.	n-linked oligosaccharides	272-297	sex hormone binding globulin	Homo sapiens	33-38
10622399-14	1999	Thus, the metabolic clearance of hSHBG appears to be determined by the number of N-linked oligosaccharides rather than their location.	n-linked oligosaccharides	81-106	sex hormone binding globulin	Homo sapiens	33-38
10406843-1	1999	In plants as well as in animals beta1, 2N-acetylglucosaminyltransferase I (GlcNAc-TI) is a Golgi resident enzyme that catalyzes an essential step in the biosynthetic pathway leading from oligomannosidic N-glycans to complex or hybrid type N-linked oligosaccharides.	n-linked oligosaccharides	239-264	alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	Homo sapiens	75-84
10328551-0	1999	Establishment of a method for mapping of N-linked oligosaccharides and its use to analyze industrially produced recombinant erythropoietin.	n-linked oligosaccharides	41-66	erythropoietin	Homo sapiens	124-138
10224097-8	1999	Matrilin-2 is substituted with N-linked oligosaccharides but not with glycosaminoglycans.	n-linked oligosaccharides	31-56	matrilin 2	Homo sapiens	0-10
10593514-7	1999	Thy-1/CD3-mediated activation enhanced mostly tyrosine phosphorylation of a 40 kDa protein which was identified as a transmembrane protein lacking N-linked oligosaccharides.	n-linked oligosaccharides	147-172	thymus cell antigen 1, theta	Mus musculus	0-5
10593514-7	1999	Thy-1/CD3-mediated activation enhanced mostly tyrosine phosphorylation of a 40 kDa protein which was identified as a transmembrane protein lacking N-linked oligosaccharides.	n-linked oligosaccharides	147-172	CD3 antigen, epsilon polypeptide	Mus musculus	6-9
10488737-0	1999	N-linked oligosaccharides can protect target cells from the lysis mediated by NK cells but not by cytotoxic T lymphocytes: role of NKG2-A.	n-linked oligosaccharides	0-25	killer cell lectin like receptor C1	Homo sapiens	131-137
10383404-0	1999	In vivo ligand specificity of E-selectin binding to multivalent sialyl Lewisx N-linked oligosaccharides.	n-linked oligosaccharides	78-103	selectin, endothelial cell	Mus musculus	30-40
10383404-1	1999	The in vivo specificity for E-selectin binding to a panel of N-linked oligosaccharides containing a clustered array of one to four sialyl Lewisx (SLex; NeuAcalpha2-3Gal[Fucalpha1-3]beta1-4GlcNAc) determinants was studied in mice.	n-linked oligosaccharides	61-86	selectin, endothelial cell	Mus musculus	28-38
10366763-0	1999	Development of recombinant, immobilised beta-1,4-mannosyltransferase for use as an efficient tool in the chemoenzymatic synthesis of N-linked oligosaccharides.	n-linked oligosaccharides	133-158	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase	Homo sapiens	40-68
10191200-7	1999	Western blots and enzymatic digestions confirmed that the 284R protein is a glycoprotein, which contains only N-linked oligosaccharides, both high mannose (48 kDa) and complex types (67 kDa).	n-linked oligosaccharides	110-135	284R	Bovine adenovirus 3	58-62
10328551-7	1999	Further, the N-linked oligosaccharides of rEPO manufactured by our company almost coincided with those of the erythropoietin European Pharmacopoeia Biological Reference Preparation (Eur.Ph.BRP), a standard product.	n-linked oligosaccharides	13-38	erythropoietin	Rattus norvegicus	42-46
9990141-3	1999	The core protein was shown to contain complex type N-linked oligosaccharides by digestion with N-glycanase and endoglycosidase H. Pulse-chase experiments showed that the mature form of HSPG was formed in the cells in 30 min and released into the medium thereafter.	n-linked oligosaccharides	51-76	CD44 molecule (Indian blood group)	Homo sapiens	185-189
10049729-0	1999	N-linked oligosaccharides of vomeromodulin, a putative pheromone transporter in rat.	n-linked oligosaccharides	0-25	similar to Vomeromodulin	Rattus norvegicus	29-42
10024660-0	1999	Structural characterization of the N-linked oligosaccharides in bile salt-stimulated lipase originated from human breast milk.	n-linked oligosaccharides	35-60	carboxyl ester lipase	Homo sapiens	64-91
10395247-10	1998	In conclusion, the study suggested that PL-Im has two N-linked oligosaccharides which are involved in its biological activity.	n-linked oligosaccharides	54-79	prolactin family 3, subfamily D, member 1	Rattus norvegicus	40-45
9837919-9	1998	These data demonstrate that acquisition and processing of N-linked oligosaccharides of TSHR appear to be essential for correct folding in the endoplasmic reticulum and for cell surface targeting in the Golgi apparatus.	n-linked oligosaccharides	58-83	thyrotropin receptor	Cricetulus griseus	87-91
9838222-2	1998	Recombinant mouse gelatinase B was expressed in the yeast Pichia pastoris and the N-linked oligosaccharides of the truncated glycoprotein variants were analysed by in gel enzymatic release followed by mass spectrometry and normal phase HPLC.	n-linked oligosaccharides	82-107	matrix metallopeptidase 9	Mus musculus	18-30
9890751-0	1999	Biochemical maturation of Spam1 (PH-20) during epididymal transit of mouse sperm involves modifications of N-linked oligosaccharides.	n-linked oligosaccharides	107-132	sperm adhesion molecule 1	Mus musculus	26-31
9890751-0	1999	Biochemical maturation of Spam1 (PH-20) during epididymal transit of mouse sperm involves modifications of N-linked oligosaccharides.	n-linked oligosaccharides	107-132	sperm adhesion molecule 1	Mus musculus	33-38
10052119-0	1999	Structures of N-linked oligosaccharides of glycoproteins from tobacco BY2 suspension cultured cells.	n-linked oligosaccharides	14-39	F-box protein PP2-B11-like	Nicotiana tabacum	70-73
9837919-2	1998	The present studies were designed to evaluate how acquisition and processing of N-linked oligosaccharides play a role in the functional maturation of human TSHR.	n-linked oligosaccharides	80-105	thyroid stimulating hormone receptor	Homo sapiens	156-160
9837919-4	1998	Inhibition of acquisition of N-linked oligosaccharides by tunicamycin treatment in CHO cells stably expressing TSHR produced nonglycosylated TSHR, which was totally nonfunctional.	n-linked oligosaccharides	29-54	thyrotropin receptor	Cricetulus griseus	111-115
9837919-4	1998	Inhibition of acquisition of N-linked oligosaccharides by tunicamycin treatment in CHO cells stably expressing TSHR produced nonglycosylated TSHR, which was totally nonfunctional.	n-linked oligosaccharides	29-54	thyrotropin receptor	Cricetulus griseus	141-145
9848672-6	1998	The profiles of heavily sialylated N-linked oligosaccharides derived from fetuin, recombinant human erythropoietin and kallikrein are reported and the data show that the present method produces a high resolution of the N-linked oligosaccharide profile for fingerprinting glycans derived from glycoproteins.	n-linked oligosaccharides	35-60	erythropoietin	Homo sapiens	100-114
9789065-6	1998	This finding is reflected in the presence of transferrin forms in serum that lack one or both of the two N-linked oligosaccharides and the reduction of mannose incorporation to about one-third of control in glycoproteins of fibroblasts.	n-linked oligosaccharides	105-130	transferrin	Homo sapiens	45-56
9798679-2	1998	For example, the N-linked oligosaccharides containing the [GlcNAc beta(1,6)Man] branch are increased after transformation of many cell types by a number of tumor viruses and oncogenes which induce the expression of N-acetylglucosaminyl-transferase V (GlcNAc-T V), the enzyme that adds this branch.	n-linked oligosaccharides	17-42	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	Homo sapiens	215-249
9798679-2	1998	For example, the N-linked oligosaccharides containing the [GlcNAc beta(1,6)Man] branch are increased after transformation of many cell types by a number of tumor viruses and oncogenes which induce the expression of N-acetylglucosaminyl-transferase V (GlcNAc-T V), the enzyme that adds this branch.	n-linked oligosaccharides	17-42	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	Homo sapiens	251-261
9798679-4	1998	We tested the hypothesis that expression of her-2/neu stimulates GlcNAc-T V gene expression and increases the beta(1,6) branching of N-linked oligosaccharides.	n-linked oligosaccharides	133-158	erb-b2 receptor tyrosine kinase 2	Homo sapiens	44-49
9798679-4	1998	We tested the hypothesis that expression of her-2/neu stimulates GlcNAc-T V gene expression and increases the beta(1,6) branching of N-linked oligosaccharides.	n-linked oligosaccharides	133-158	erb-b2 receptor tyrosine kinase 2	Homo sapiens	50-53
9684342-5	1998	The FACE profiles and corresponding HPAEC-PAD chromatograms of N-linked oligosaccharides obtained by PNGase F digestion and hydrazinolysis provided complementary and corroborating information.	n-linked oligosaccharides	63-88	N-glycanase 1	Mus musculus	101-107
10211704-2	1998	Glycosylated mutant human lysozyme has been used as a model in studies on the biosynthesis of N-acetyllactosamine repeats in N-linked oligosaccharides.	n-linked oligosaccharides	125-150	lysozyme	Homo sapiens	26-34
9766755-7	1998	To demonstrate this possibility, we sought the presence of beta(1-6)-GlcNAc-branched N-linked oligosaccharides on beta1 integrins expressed by T lymphocytes from Sz patients.	n-linked oligosaccharides	85-110	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	Homo sapiens	59-67
9766755-7	1998	To demonstrate this possibility, we sought the presence of beta(1-6)-GlcNAc-branched N-linked oligosaccharides on beta1 integrins expressed by T lymphocytes from Sz patients.	n-linked oligosaccharides	85-110	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	Homo sapiens	114-119
9790067-5	1998	Moreover, anti-CD18 and LRTC1 immunoprecipitates also showed identical mobilities on 1-D gels after enzymatic cleavage of N-linked oligosaccharides and thereby had the same patterns of differential glycosylation.	n-linked oligosaccharides	122-147	integrin subunit beta 2	Rattus norvegicus	15-19
9442118-7	1998	Four distinct oligosaccharide structures were found to effect CD44-mediated HA binding: (a) the terminal alpha2,3-linked sialic acid on N-linked oligosaccharides inhibited binding; (b) the first N-linked N-acetylglucosamine residue enhanced binding; (c) O-linked glycans on N-deglycosylated CD44 enhanced binding; and (d) N-acetylgalactosamine incorporation into non-N-linked glycans augmented HA binding by cell surface CD44.	n-linked oligosaccharides	136-161	CD44 antigen	Cricetulus griseus	62-66
9603429-6	1998	The SH2-immunoprecipitated protein exhibited a molecular weight band shift after removal of N-linked oligosaccharides.	n-linked oligosaccharides	92-117	sperm hammerhead 2	Mus musculus	4-7
9566981-10	1998	Digesting the immunoprecipitated osteoadherin with N-glycosidase reduced its apparent size to 47 kD, thus showing the presence of several N-linked oligosaccharides.	n-linked oligosaccharides	138-163	osteomodulin	Bos taurus	33-45
9525969-4	1998	Protein chaperones calnexin (CNX) and calreticulin (CRT) preferentially interact with glycoproteins containing monoglucosylated N-linked oligosaccharides and are proposed to traffic proteins through degradative and/or secretory pathways.	n-linked oligosaccharides	128-153	calnexin	Homo sapiens	19-27
9525969-4	1998	Protein chaperones calnexin (CNX) and calreticulin (CRT) preferentially interact with glycoproteins containing monoglucosylated N-linked oligosaccharides and are proposed to traffic proteins through degradative and/or secretory pathways.	n-linked oligosaccharides	128-153	calnexin	Homo sapiens	29-32
9525969-4	1998	Protein chaperones calnexin (CNX) and calreticulin (CRT) preferentially interact with glycoproteins containing monoglucosylated N-linked oligosaccharides and are proposed to traffic proteins through degradative and/or secretory pathways.	n-linked oligosaccharides	128-153	calreticulin	Homo sapiens	38-50
9525969-4	1998	Protein chaperones calnexin (CNX) and calreticulin (CRT) preferentially interact with glycoproteins containing monoglucosylated N-linked oligosaccharides and are proposed to traffic proteins through degradative and/or secretory pathways.	n-linked oligosaccharides	128-153	calreticulin	Homo sapiens	52-55
9499380-0	1998	Human alpha-galactosidase A: characterization of the N-linked oligosaccharides on the intracellular and secreted glycoforms overexpressed by Chinese hamster ovary cells.	n-linked oligosaccharides	53-78	alpha-galactosidase A	Cricetulus griseus	6-27
9414612-1	1997	2-Aminoacridone (2-AMAC) has been used to derivatize mixtures of N-linked oligosaccharides released from alpha(1)-acid glycoprotein and immunoglobulin G. In each case, the HPLC profile obtained for the derivatized glycans was compared to that obtained after digestion with sialidase and a two-enzyme array system made up of sialidase and alpha-fucosidase, prior to derivatization by 2-AMAC.	n-linked oligosaccharides	65-90	solute carrier family 35 member G5	Homo sapiens	19-23
9543009-5	1997	The recombinant PrP migrated as a diffuse band of 19-40 kDa but removal of the N-linked oligosaccharides with peptide N-glycosidase F (PNGase F) revealed three protein species of 19, 17 and 15 kDa.	n-linked oligosaccharides	79-104	major prion protein	Cricetulus griseus	16-19
9363442-8	1997	Following 1 h labeling of cells with [3H]mannose, analysis by high pressure liquid chromatography of the labeled N-linked oligosaccharides, combined with treatment with jack bean alpha mannosidase and yeast glucosidase I, shows that the oligosaccharides isolated form a cwh41 delta null mutant are fully glucosylated, retaining the three terminal glucose residues, whereas the oligosaccharides from CWH41 cells do not have any glucose residues.	n-linked oligosaccharides	113-138	mannosyl-oligosaccharide glucosidase	Saccharomyces cerevisiae S288C	270-275
9363442-8	1997	Following 1 h labeling of cells with [3H]mannose, analysis by high pressure liquid chromatography of the labeled N-linked oligosaccharides, combined with treatment with jack bean alpha mannosidase and yeast glucosidase I, shows that the oligosaccharides isolated form a cwh41 delta null mutant are fully glucosylated, retaining the three terminal glucose residues, whereas the oligosaccharides from CWH41 cells do not have any glucose residues.	n-linked oligosaccharides	113-138	mannosyl-oligosaccharide glucosidase	Saccharomyces cerevisiae S288C	399-404
9373934-1	1997	N-Acetylglucosaminyltransferase-V is an important enzyme controlling the branching pattern of N-linked oligosaccharides.	n-linked oligosaccharides	94-119	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	Homo sapiens	0-33
9287314-2	1997	Mannose in N-linked oligosaccharides is assumed to be derived primarily from glucose through phosphomannose isomerase (PMI).	n-linked oligosaccharides	11-36	mannose phosphate isomerase	Homo sapiens	93-117
9295302-8	1997	Subsequent site-directed mutagenesis studies established that Asn19 and Asn23 in the NH2-terminal MSD and Asn1006 in the COOH-terminal MSD are the only sites in MRP that are modified with N-linked oligosaccharides.	n-linked oligosaccharides	188-213	ATP binding cassette subfamily C member 1	Homo sapiens	161-164
9287314-2	1997	Mannose in N-linked oligosaccharides is assumed to be derived primarily from glucose through phosphomannose isomerase (PMI).	n-linked oligosaccharides	11-36	mannose phosphate isomerase	Homo sapiens	119-122
9252404-4	1997	Either acute or chronic treatment of TCRalpha-transfected cells with proteasome inhibitors cause the core-glycosylated TCRalpha chains to progressively shift to an approximately 28-kDa form that lacks N-linked oligosaccharides and the N-terminal signal peptide.	n-linked oligosaccharides	201-226	T cell receptor alpha constant	Homo sapiens	37-45
9299469-2	1997	We identify here the elements involved in the reactivity of the major receptor of rat, NKR-P1A, with N-linked oligosaccharides of glycoproteins.	n-linked oligosaccharides	101-126	killer cell lectin-like receptor subfamily B, member 1A	Rattus norvegicus	87-94
9376679-1	1997	UDP-N-acetylglucosamine: beta-D-mannoside beta-1,4N-acetylglucosaminyltransferase III (GnT-III, EC 2.4.1.144) is a glycoprotein involved in the biosynthesis of N-linked oligosaccharides.	n-linked oligosaccharides	160-185	beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase	Homo sapiens	87-94
9376682-0	1997	Structure determination of N-linked oligosaccharides engineered at the CH1 domain of humanized LL2.	n-linked oligosaccharides	27-52	SUN domain containing ossification factor	Homo sapiens	71-74
9290152-3	1997	It is hypothesized that TfR isolated from diabetic placentae has altered N-glycosylation since proper glycosylation of N-linked oligosaccharides is important for normal TfR binding kinetics to diferric transferrin.	n-linked oligosaccharides	119-144	transferrin receptor	Homo sapiens	24-27
9290152-8	1997	Increased glycosylation of the N-linked oligosaccharides of TfR isolated from diabetic placentae may alter the three-dimensional structure or charge of the receptor, thus reducing its binding affinity for transferrin.	n-linked oligosaccharides	31-56	transferrin receptor	Homo sapiens	60-63
9290152-8	1997	Increased glycosylation of the N-linked oligosaccharides of TfR isolated from diabetic placentae may alter the three-dimensional structure or charge of the receptor, thus reducing its binding affinity for transferrin.	n-linked oligosaccharides	31-56	transferrin	Homo sapiens	205-216
9184840-8	1997	The late appearance of endomannosidase during evolution suggests a need for an alternate deglucosylation route in higher animals which parallels the development of elaborate complex N-linked oligosaccharides.	n-linked oligosaccharides	182-207	mannosidase endo-alpha	Homo sapiens	23-38
9276464-1	1997	Yeast Saccharomyces cerevisiae OCH1 gene encodes the mannosyltransferase that is essential for the outer chain elongation of N-linked oligosaccharides.	n-linked oligosaccharides	125-150	initiation-specific alpha-1,6-mannosyltransferase	Saccharomyces cerevisiae S288C	31-35
9254046-2	1997	A combination of 1H-NMR and mass spectrometry techniques (MALD-MS, ES-MS, and CID-MS-MS) allowed us to elucidate the N-linked oligosaccharides microheterogeneity on three different N-glycosylation sites, Asn233, Asn476, and Asn545, of a baculovirus-expressed recombinant bovine lactoferrin produced in Mamestra brassicae.	n-linked oligosaccharides	117-142	lactotransferrin	Bos taurus	278-289
9201957-7	1997	Deletion of the N-linked oligosaccharides from SP-A by mutagenesis of the consensus sequences for glycosylation had no effect on binding.	n-linked oligosaccharides	16-41	surfactant protein A1	Rattus norvegicus	47-51
9192839-1	1997	Lysosomal alpha-mannosidase (LAMAN) (EC 3.2.1.24) is an exoglycosidase involved in the ordered degradation of N-linked oligosaccharides.	n-linked oligosaccharides	110-135	mannosidase alpha class 2B member 1	Homo sapiens	0-27
9192839-1	1997	Lysosomal alpha-mannosidase (LAMAN) (EC 3.2.1.24) is an exoglycosidase involved in the ordered degradation of N-linked oligosaccharides.	n-linked oligosaccharides	110-135	mannosidase alpha class 2B member 1	Homo sapiens	29-34
9083062-1	1997	N-linked oligosaccharides appear to be important for the function of the epidermal growth factor (EGF) receptor.	n-linked oligosaccharides	0-25	epidermal growth factor receptor	Homo sapiens	73-111
9136890-1	1997	The human transferrin receptor (TfR) has three N-linked oligosaccharides.	n-linked oligosaccharides	47-72	transferrin receptor	Homo sapiens	10-30
9136890-1	1997	The human transferrin receptor (TfR) has three N-linked oligosaccharides.	n-linked oligosaccharides	47-72	transferrin receptor	Homo sapiens	32-35
9084450-2	1997	The importance of the N-linked oligosaccharides on MAG were determined by removal of the eight predicted carbohydrate addition sites by site-directed mutagenesis.	n-linked oligosaccharides	22-47	myelin associated glycoprotein	Homo sapiens	51-54
9003768-0	1996	N-linked oligosaccharides are necessary and sufficient for association of glycosylated forms of bovine RNase with calnexin and calreticulin.	n-linked oligosaccharides	0-25	calnexin	Bos taurus	114-122
9020859-12	1997	Both the recombinant enzyme and rat bone TRAP were shown to be substituted with N-linked oligosaccharides.	n-linked oligosaccharides	80-105	acid phosphatase 5, tartrate resistant	Rattus norvegicus	41-45
9020137-1	1997	beta-1,6-N-Acetylglucosaminyltransferase V (EC 2.4.1.155) catalyzes the transfer of N-acetylglucosamine (GlcNAc) from UDP-GlcNAc in beta(1,6)-linkage to the alpha(1,6)-linked mannose of N-linked oligosaccharides.	n-linked oligosaccharides	186-211	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B	Homo sapiens	0-42
9061364-8	1997	Following homologous recombination in embryonic stem cells and Cre mediated gene deletion, Mgat3-deficient mice were produced that lacked GlcNAc-TIII activity and were deficient in E4-PHA visualized GlcNAc-bisected N-linked oligosaccharides.	n-linked oligosaccharides	215-240	mannoside acetylglucosaminyltransferase 3	Mus musculus	91-96
9239703-9	1997	Structural analysis of their N-linked oligosaccharides combined with other functional studies suggest that GdA and GdS employ their very unusual carbohydrate sequences as functional groups that enable them to manifest their immunosuppressive activities.	n-linked oligosaccharides	29-54	progestagen associated endometrial protein	Homo sapiens	107-110
9239703-9	1997	Structural analysis of their N-linked oligosaccharides combined with other functional studies suggest that GdA and GdS employ their very unusual carbohydrate sequences as functional groups that enable them to manifest their immunosuppressive activities.	n-linked oligosaccharides	29-54	progestagen associated endometrial protein	Homo sapiens	115-118
9003768-0	1996	N-linked oligosaccharides are necessary and sufficient for association of glycosylated forms of bovine RNase with calnexin and calreticulin.	n-linked oligosaccharides	0-25	calreticulin	Bos taurus	127-139
8918549-7	1996	Complete inhibition of the binding of these glycoprotein precursors to calnexin by tunicamycin or castanospermine indicates the importance of partially trimmed N-linked oligosaccharides for their association.	n-linked oligosaccharides	160-185	calnexin	Homo sapiens	71-79
9023541-0	1996	Cloning and analysis of the MNN4 gene required for phosphorylation of N-linked oligosaccharides in Saccharomyces cerevisiae.	n-linked oligosaccharides	70-95	Mnn4p	Saccharomyces cerevisiae S288C	28-32
9023541-6	1996	The results from genetic and biochemical experiments combine to suggest that Mnn4p is required to mediate mannosylphosphate transfer in both the core and outer chain portions of N-linked oligosaccharides.	n-linked oligosaccharides	178-203	Mnn4p	Saccharomyces cerevisiae S288C	77-82
9023549-0	1996	Evaluation of the early processing routes of N-linked oligosaccharides of glycoproteins through the characterization of Man8GlcNAc2 isomers: evidence that endomannosidase functions in vivo in the absence of a glucosidase blockade.	n-linked oligosaccharides	45-70	mannosidase endo-alpha	Homo sapiens	155-170
9023549-5	1996	The observation that isomer A of Man8GlcNAc2 is a specific product of endomannosidase action made it possible to demonstrate the action of this enzyme in vivo without employing a glucosidase blockade and to show that a substantial amount of the deglucosylation of N-linked oligosaccharides is carried out by this enzyme.	n-linked oligosaccharides	264-289	mannosidase endo-alpha	Homo sapiens	70-85
8895216-8	1996	In the mature adult the fibromodulin does not possess either keratan sulfate or non-sulfated polylactosamine chains, though it appears to possess the same number of N-linked oligosaccharides as its counterparts from the younger tissue, but they are not modified further.	n-linked oligosaccharides	165-190	fibromodulin	Homo sapiens	24-36
8872105-6	1996	Defective galactosylation was also observed for patient IgA1 when it was probed with ECL, a lectin that has a specificity for Gal 1,4 N-acetylglucosamine groupings on N-linked oligosaccharides.	n-linked oligosaccharides	167-192	immunoglobulin heavy constant alpha 1	Homo sapiens	56-60
8702502-6	1996	However, beta-chaperone complexes containing the ER chaperones BiP, ERp72, and ERp94 have been detected in slow folding mutants of hCG-beta subunit that lack both of the N-linked oligosaccharides (Feng, W., Matzuk, M. M., Mountjoy, K., Bedows, E., Ruddon, R. W., and Boime, I.	n-linked oligosaccharides	170-195	heat shock protein family A (Hsp70) member 5	Homo sapiens	63-66
8702502-6	1996	However, beta-chaperone complexes containing the ER chaperones BiP, ERp72, and ERp94 have been detected in slow folding mutants of hCG-beta subunit that lack both of the N-linked oligosaccharides (Feng, W., Matzuk, M. M., Mountjoy, K., Bedows, E., Ruddon, R. W., and Boime, I.	n-linked oligosaccharides	170-195	chorionic gonadotropin subunit beta 3	Homo sapiens	131-139
8702538-2	1996	Recent work has shown that CD22 specifically recognizes sialic acid linked alpha2,6 to terminal N-linked oligosaccharides on selected cell surface glycoproteins.	n-linked oligosaccharides	96-121	CD22 molecule	Homo sapiens	27-31
8882733-6	1996	By Western blot analyses developed with biotin-labeled lectins, N-linked oligosaccharides were detected in the 17- and 16-kDa protein subunits of ETL1 and ETL2, and in the 12-kDa protein subunit of ETL2.	n-linked oligosaccharides	64-89	SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1	Homo sapiens	146-150
8663515-5	1996	Moreover, whereas phosphacan interactions with certain proteins are mediated at least in part by N-linked oligosaccharides on the proteoglycan, N-deglycosylation of phosphacan had no effect on its binding to TAG-1/axonin-1.	n-linked oligosaccharides	97-122	protein tyrosine phosphatase receptor type Z1	Homo sapiens	18-28
8617714-7	1996	Deglycosylation experiments with N-glycanase and endoglycosidase H indicated that the S-MBP ligands on thymic CD45 are high mannose type or hybrid type N-linked oligosaccharides.	n-linked oligosaccharides	152-177	mannose-binding lectin (protein A) 1	Mus musculus	86-91
8617714-7	1996	Deglycosylation experiments with N-glycanase and endoglycosidase H indicated that the S-MBP ligands on thymic CD45 are high mannose type or hybrid type N-linked oligosaccharides.	n-linked oligosaccharides	152-177	protein tyrosine phosphatase, receptor type, C	Mus musculus	110-114
8764591-0	1996	N-linked oligosaccharides are required for cell surface expression of the norepinephrine transporter but do not influence substrate or inhibitor recognition.	n-linked oligosaccharides	0-25	solute carrier family 6 member 2	Homo sapiens	74-100
8764057-8	1996	gC2(426t) contains N-linked oligosaccharides, but no O-linked oligosaccharides were detected.	n-linked oligosaccharides	19-44	solute carrier family 25 member 18	Homo sapiens	0-3
8617950-0	1996	Unusual uniformity of the N-linked oligosaccharides of HLA-A, -B, and -C glycoproteins.	n-linked oligosaccharides	26-51	major histocompatibility complex, class I, A	Homo sapiens	55-64
8639667-0	1996	Cell line and site specific comparative analysis of the N-linked oligosaccharides on human ICAM-1des454-532 by electrospray ionization mass spectrometry.	n-linked oligosaccharides	56-81	intercellular adhesion molecule 1	Homo sapiens	91-97
8882733-6	1996	By Western blot analyses developed with biotin-labeled lectins, N-linked oligosaccharides were detected in the 17- and 16-kDa protein subunits of ETL1 and ETL2, and in the 12-kDa protein subunit of ETL2.	n-linked oligosaccharides	64-89	ETL2	Homo sapiens	155-159
8882733-6	1996	By Western blot analyses developed with biotin-labeled lectins, N-linked oligosaccharides were detected in the 17- and 16-kDa protein subunits of ETL1 and ETL2, and in the 12-kDa protein subunit of ETL2.	n-linked oligosaccharides	64-89	ETL2	Homo sapiens	198-202
7588744-1	1995	UDP-N-acetylglucosamine: alpha-6-D-mannoside beta-1,6-N-acetylglucosaminyltransferase V (GlcNAc transferase V), which catalyzes the transfer of N-acetylglucosamine from UDP-N-acetylglucosamine to alpha-6-D-mannoside, is an important enzyme regulating the branch formation in complex-type, N-linked oligosaccharides.	n-linked oligosaccharides	289-314	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	Homo sapiens	54-87
9117260-8	1996	The proteoglycans and their ligands have overlapping localizations in the CNS, and binding of phosphocan to Ng-CAM/L1, NCAM, and tenascin-C is mediated by complex-type N-linked oligosaccharides on the proteoglycan.	n-linked oligosaccharides	168-193	L1 cell adhesion molecule	Rattus norvegicus	108-114
9117260-8	1996	The proteoglycans and their ligands have overlapping localizations in the CNS, and binding of phosphocan to Ng-CAM/L1, NCAM, and tenascin-C is mediated by complex-type N-linked oligosaccharides on the proteoglycan.	n-linked oligosaccharides	168-193	tenascin C	Rattus norvegicus	129-139
7592677-6	1995	These studies indicate that N-linked oligosaccharides are essential for alpha subunit ligand binding and signaling by the human GM-CSF receptor.	n-linked oligosaccharides	28-53	colony stimulating factor 2	Homo sapiens	128-134
8542600-1	1996	beta 1-4 N-acetylglucosaminyltransferase (GnT-III) catalyzes the formation of bisecting N-acetylglucosamine (GlcNAc) in the biosynthesis of N-linked oligosaccharides.	n-linked oligosaccharides	140-165	beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase	Homo sapiens	42-49
8973529-0	1996	Conserved N-linked oligosaccharides of the C-terminal portion of human immunodeficiency virus type 1 gp120 and viral susceptibility to neutralizing antibodies.	n-linked oligosaccharides	10-35	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	101-106
8991513-1	1996	The Saccharomyces cerevisiae mnn10 mutant is defective in the synthesis of N-linked oligosaccharides (Ballou et al., 1989).	n-linked oligosaccharides	75-100	alpha-1,6-mannosyltransferase	Saccharomyces cerevisiae S288C	29-34
8719880-5	1995	Further investigations using glycosidases, glycosylation inhibitors and lectin-affinity chromatography demonstrated that the tumor-associated glycosylation change in GLUT1 was mainly due to the increase in N-acetyl-lactosamine repeats in the N-linked oligosaccharides.	n-linked oligosaccharides	242-267	solute carrier family 2 member 1	Homo sapiens	166-171
7499330-1	1995	beta-D-mannoside beta-1,4-N-acetylglucosaminyltransferase III (GnT-III) catalyzes the addition of N-acetylglucosamine in beta 1-4 linkage to the beta-linked mannose of the trimannosyl core of N-linked oligosaccharides and forms a bisecting GlcNAc structure.	n-linked oligosaccharides	192-217	beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase	Homo sapiens	63-70
7592804-1	1995	Increasing evidence shows that calnexin, a membrane-bound chaperone in the endoplasmic reticulum, is a lectin that binds to newly synthesized glycoproteins that have partially trimmed N-linked oligosaccharides.	n-linked oligosaccharides	184-209	calnexin	Homo sapiens	31-39
8750891-0	1995	Identification of rat serotonin 5-HT2C receptors as glycoproteins containing N-linked oligosaccharides.	n-linked oligosaccharides	77-102	5-hydroxytryptamine receptor 2C	Rattus norvegicus	32-38
7589448-7	1995	These results indicated that a part of N-linked oligosaccharides of fetuin were polysialylated with ST8Sia II.	n-linked oligosaccharides	39-64	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	Mus musculus	100-109
7589448-9	1995	Thus, ST8Sia II can directly synthesize polysialic acid chains on alpha 2,3-sialylated N-linked oligosaccharides of glycoproteins without any initiator sialytransferase.	n-linked oligosaccharides	87-112	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	Mus musculus	6-15
7589110-10	1995	In conclusion, these studies show that E-selectin is heavily glycosylated with complex type N-linked oligosaccharides and that N-glycosylation is important for expression of E-selectin on human endothelial cells.	n-linked oligosaccharides	92-117	selectin E	Homo sapiens	39-49
7588709-3	1995	The beta-trace protein was purified by immunoaffinity chromatography and N-linked oligosaccharides were subjected to carbohydrate structural analysis.	n-linked oligosaccharides	73-98	prostaglandin D2 synthase	Homo sapiens	4-22
7568011-1	1995	The beta 1-6 structure of N-linked oligosaccharides, formed by beta-1,6-N-acetylglucosaminyltransferase (GnT-V), is associated with metastatic potential.	n-linked oligosaccharides	26-51	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 9	Mus musculus	4-12
7568011-1	1995	The beta 1-6 structure of N-linked oligosaccharides, formed by beta-1,6-N-acetylglucosaminyltransferase (GnT-V), is associated with metastatic potential.	n-linked oligosaccharides	26-51	glucosaminyl (N-acetyl) transferase 2, I-branching enzyme	Mus musculus	63-103
7568011-1	1995	The beta 1-6 structure of N-linked oligosaccharides, formed by beta-1,6-N-acetylglucosaminyltransferase (GnT-V), is associated with metastatic potential.	n-linked oligosaccharides	26-51	mannoside acetylglucosaminyltransferase 5	Mus musculus	105-110
7618283-11	1995	We propose that N-linked oligosaccharides are required to maintain a conformation-dependent receptor determinant of MCP.	n-linked oligosaccharides	16-41	CD46 molecule	Homo sapiens	116-119
8690732-1	1995	AcDNA encoding a new alpha2,8-sialyltransferase (ST8Sia IV), which exhibits activity toward the alpha,2,3-linked sialic acids of N-linked oligosaccharides, was cloned from a mouse lung cDNA library by means of the PCR-based approach.	n-linked oligosaccharides	129-154	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1	Mus musculus	21-47
8690732-1	1995	AcDNA encoding a new alpha2,8-sialyltransferase (ST8Sia IV), which exhibits activity toward the alpha,2,3-linked sialic acids of N-linked oligosaccharides, was cloned from a mouse lung cDNA library by means of the PCR-based approach.	n-linked oligosaccharides	129-154	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	Mus musculus	49-58
8690732-7	1995	The linage-specific sialidase treatment of glycoproteins as well as N-linked oligosaccharides from the glycoproteins revealed that ST8Sia IV exhibits an alpha2,8-sialytransferase activity toward alpha2,3-linked sialic acids of N-linked oligosaccharides.	n-linked oligosaccharides	68-93	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	Mus musculus	131-140
8690732-7	1995	The linage-specific sialidase treatment of glycoproteins as well as N-linked oligosaccharides from the glycoproteins revealed that ST8Sia IV exhibits an alpha2,8-sialytransferase activity toward alpha2,3-linked sialic acids of N-linked oligosaccharides.	n-linked oligosaccharides	227-252	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	Mus musculus	131-140
7599134-2	1995	The alpha-ATIII isoform has four N-linked oligosaccharides attached to asparagines 96, 135, 155, and 192.	n-linked oligosaccharides	33-58	serpin family C member 1	Homo sapiens	10-15
8563136-3	1995	Carbohydrate structural analyses were performed on the N-linked oligosaccharides of serum alpha 1-antitrypsin (alpha-1AT) from two Danish children with classical type I CDGS.	n-linked oligosaccharides	55-80	serpin family A member 1	Homo sapiens	90-109
8563136-3	1995	Carbohydrate structural analyses were performed on the N-linked oligosaccharides of serum alpha 1-antitrypsin (alpha-1AT) from two Danish children with classical type I CDGS.	n-linked oligosaccharides	55-80	serpin family A member 1	Homo sapiens	111-120
8563140-1	1995	To investigate the developmental role of complex N-linked oligosaccharides, we previously inactivated the mouse Mgat1 gene which encodes UDP-N-acetylglucosamine: alpha-3-D-mannoside beta-1,2-N-acetylglucosaminyltransferase I (GlcNAc-TI).	n-linked oligosaccharides	49-74	mannoside acetylglucosaminyltransferase 1	Mus musculus	112-117
7782326-1	1995	A cDNA encoding a new alpha 2,8-sialyltransferase (ST8Sia III), which exhibits activity toward the Sia alpha 2,3Gal beta 1, 4GlcNAc sequences of N-linked oligosaccharides, was cloned from mouse brain by means of the polymerase chain reaction-based approach.	n-linked oligosaccharides	145-170	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1	Mus musculus	22-49
7794919-6	1995	In Sf9 cells the glycosylation was entirely biantennary complex, in contrast to the native mGRP-R, where it was entirely tri- and tetraantennary complex N-linked oligosaccharides.	n-linked oligosaccharides	153-178	gastrin releasing peptide receptor	Mus musculus	91-97
7782326-4	1995	However, the kinetic properties of ST8Sia III revealed that it is much more specific to N-linked oligosaccharides of glycoproteins than glycosphingolipids.	n-linked oligosaccharides	88-113	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3	Mus musculus	35-45
7797505-1	1995	UDP-N-acetyl-D-glucosamine:alpha-6-D-mannoside beta-1,2-N-acetylglucosaminyltransferase II (EC 2.4.1.143) (GnT II) is a Golgi resident enzyme that catalyzes an essential step in the biosynthetic pathway leading from high mannose to complex N-linked oligosaccharides.	n-linked oligosaccharides	240-265	alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	Rattus norvegicus	47-90
7797505-1	1995	UDP-N-acetyl-D-glucosamine:alpha-6-D-mannoside beta-1,2-N-acetylglucosaminyltransferase II (EC 2.4.1.143) (GnT II) is a Golgi resident enzyme that catalyzes an essential step in the biosynthetic pathway leading from high mannose to complex N-linked oligosaccharides.	n-linked oligosaccharides	240-265	alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	Rattus norvegicus	107-113
7782326-1	1995	A cDNA encoding a new alpha 2,8-sialyltransferase (ST8Sia III), which exhibits activity toward the Sia alpha 2,3Gal beta 1, 4GlcNAc sequences of N-linked oligosaccharides, was cloned from mouse brain by means of the polymerase chain reaction-based approach.	n-linked oligosaccharides	145-170	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3	Mus musculus	51-61
7663020-8	1995	In contrast, N-linked oligosaccharides from gps2 mutants have much less Gal than wild type, because of reduced levels of the Gal donor, UDP-Gal.	n-linked oligosaccharides	13-38	G protein pathway suppressor 2	Homo sapiens	44-48
7541354-7	1995	The possibility that several binding activities of vitronectin can be ascribed to its glycan moiety was discussed, based on the specific features of the N-linked oligosaccharides on human vitronectin revealed here.	n-linked oligosaccharides	153-178	vitronectin	Homo sapiens	51-62
7541354-7	1995	The possibility that several binding activities of vitronectin can be ascribed to its glycan moiety was discussed, based on the specific features of the N-linked oligosaccharides on human vitronectin revealed here.	n-linked oligosaccharides	153-178	vitronectin	Homo sapiens	188-199
7538125-8	1995	These data indicate that N-linked oligosaccharides assist hCG-beta subunit folding by facilitating disulfide bond formation.	n-linked oligosaccharides	25-50	chorionic gonadotropin subunit beta 3	Homo sapiens	58-66
7541354-0	1995	Structures of the N-linked oligosaccharides on human plasma vitronectin.	n-linked oligosaccharides	18-43	vitronectin	Homo sapiens	60-71
7541354-1	1995	The structures of N-linked oligosaccharides present on human plasma vitronectin were elucidated.	n-linked oligosaccharides	18-43	vitronectin	Homo sapiens	68-79
8717231-4	1995	The N-linked oligosaccharides were released from EPO by the treatment with N-glycosidase F. HPAEC analysis of oligosaccharide standards revealed that elution time of sialylated oligosaccharides were dependent on the number of sialic acid, which contributed to the activity of EPO.	n-linked oligosaccharides	4-29	erythropoietin	Cricetulus griseus	49-52
7706300-7	1995	Tumor necrosis factor-alpha stimulation of HEC causes no change in the profile of endothelial glycoproteins recognized by CD22, but doubles the proportion of total cellular N-linked oligosaccharides capable of binding tightly to CD22.	n-linked oligosaccharides	173-198	tumor necrosis factor	Homo sapiens	0-27
7706300-7	1995	Tumor necrosis factor-alpha stimulation of HEC causes no change in the profile of endothelial glycoproteins recognized by CD22, but doubles the proportion of total cellular N-linked oligosaccharides capable of binding tightly to CD22.	n-linked oligosaccharides	173-198	CD22 molecule	Homo sapiens	229-233
7875291-0	1995	Enzymatic activity of a developmentally regulated member of the sialyltransferase family (STX): evidence for alpha 2,8-sialyltransferase activity toward N-linked oligosaccharides.	n-linked oligosaccharides	153-178	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	Mus musculus	90-93
7875291-0	1995	Enzymatic activity of a developmentally regulated member of the sialyltransferase family (STX): evidence for alpha 2,8-sialyltransferase activity toward N-linked oligosaccharides.	n-linked oligosaccharides	153-178	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 6	Mus musculus	109-136
7875291-5	1995	N-Glycanase treatment and linkage-specific sialidase treatment of glycoproteins revealed that STX transfers sialic acids through alpha 2,8-linkages to only N-linked oligosaccharides of glycoproteins.	n-linked oligosaccharides	156-181	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	Mus musculus	94-97
7539442-3	1995	Previous studies have suggested that cell surface beta 1.4-galactosyltransferase functions as one of these receptors during neurite outgrowth on basal lamina by binding to N-linked oligosaccharides in the E8 domain of laminin.	n-linked oligosaccharides	172-197	glycoprotein alpha-galactosyltransferase 1	Rattus norvegicus	59-80
7537381-1	1995	The B-cell receptor CD22 binds sialic acid linked alpha-2-6 to terminal galactose residues on N-linked oligosaccharides associated with several cell-surface glycoproteins.	n-linked oligosaccharides	94-119	CD22 molecule	Homo sapiens	4-24
7537381-1	1995	The B-cell receptor CD22 binds sialic acid linked alpha-2-6 to terminal galactose residues on N-linked oligosaccharides associated with several cell-surface glycoproteins.	n-linked oligosaccharides	94-119	immunoglobulin binding protein 1	Homo sapiens	50-59
7780197-1	1995	The human transferrin receptor (TfR) contains three N-linked oligosaccharides and glycosylation is required for the proper folding and function of the molecule.	n-linked oligosaccharides	52-77	transferrin receptor	Homo sapiens	10-30
7780197-1	1995	The human transferrin receptor (TfR) contains three N-linked oligosaccharides and glycosylation is required for the proper folding and function of the molecule.	n-linked oligosaccharides	52-77	transferrin receptor	Homo sapiens	32-35
7766897-5	1995	Although Epo produced by tobacco cells was glycosylated with N-linked oligosaccharides, these carbohydrates were smaller than those of the recombinant Epo produced in mammalian cells.	n-linked oligosaccharides	61-86	erythropoietin	Homo sapiens	9-12
7843422-0	1995	Analysis of the N-linked oligosaccharides of human C1s using electrospray ionisation mass spectrometry.	n-linked oligosaccharides	16-41	complement C1s	Homo sapiens	51-54
7826389-7	1995	These observations provide preliminary insights into the role of N-linked oligosaccharides in IL-4 receptor biosynthesis and function at the cell surface.	n-linked oligosaccharides	65-90	interleukin 4	Homo sapiens	94-98
8717231-4	1995	The N-linked oligosaccharides were released from EPO by the treatment with N-glycosidase F. HPAEC analysis of oligosaccharide standards revealed that elution time of sialylated oligosaccharides were dependent on the number of sialic acid, which contributed to the activity of EPO.	n-linked oligosaccharides	4-29	erythropoietin	Cricetulus griseus	276-279
7936661-10	1994	Based on its binding to a variety of lectin columns, Cek8 contains complex N-linked oligosaccharides.	n-linked oligosaccharides	75-100	EPH receptor A4	Gallus gallus	53-57
7876332-6	1994	Treatment of dual-labeled gp300 with PNGase F to cleave N-linked oligosaccharides released approximately 17% of [3H] and little [35S].	n-linked oligosaccharides	56-81	deleted in malignant brain tumors 1	Mus musculus	26-31
7876332-6	1994	Treatment of dual-labeled gp300 with PNGase F to cleave N-linked oligosaccharides released approximately 17% of [3H] and little [35S].	n-linked oligosaccharides	56-81	N-glycanase 1	Mus musculus	37-43
7891293-3	1994	The N-linked oligosaccharides released by PNGase F treatment of the above IgGs were found to consist mainly of neutral, fucosylated, biantennary species.	n-linked oligosaccharides	4-29	N-glycanase 1	Homo sapiens	42-48
7521878-7	1994	Peptide:N-glycosidase F (PNGaseF) treatment removed at least two of the three possible N-linked oligosaccharides from PSGL-1.	n-linked oligosaccharides	87-112	selectin P ligand	Homo sapiens	118-124
8083969-5	1994	The binding of measles virus to MCP was abolished after cleavage of the disulfide bonds by reducing agents as well as after enzymatic release of N-linked oligosaccharides.	n-linked oligosaccharides	145-170	CD46 molecule	Homo sapiens	32-35
7522229-1	1994	The formation of tri- and tetraantennary complex-type N-linked oligosaccharides in animal glycoproteins is partly regulated by UDP-N-acetylglucosamine:beta-6-D-mannoside beta-1,6-N-acetylglucosaminyltransferase (EC 2.4.1.155) (GlcNAc-T V), which generates 2,6-branched mannose.	n-linked oligosaccharides	54-79	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase A	Cricetulus griseus	227-237
7522229-12	1994	In the case of fetuin, each of its three sites for attachment of N-linked oligosaccharides were shown to be utilized equally well by GlcNAc-T V.	n-linked oligosaccharides	65-90	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase A	Cricetulus griseus	133-143
8035198-13	1994	The bulk of the increased radiolabeling was found in N-linked oligosaccharides, including several recognized by the HNK-1 antibody.	n-linked oligosaccharides	53-78	beta-1,3-glucuronyltransferase 1 (glucuronosyltransferase P)	Mus musculus	116-121
8057468-8	1994	Removal of N-linked oligosaccharides on gp120 did not affect binding efficiency.	n-linked oligosaccharides	11-36	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	40-45
8034751-3	1994	The sialylated N-linked oligosaccharides recognized best by CD22 beta are common to many glycoproteins, suggesting that additional regulatory mechanisms may exist.	n-linked oligosaccharides	15-40	CD22 antigen	Mus musculus	60-64
8030209-3	1994	We investigated the contribution of N-linked oligosaccharides (N-CHO) on gD to viral pathogenesis.	n-linked oligosaccharides	36-61	atypical chemokine receptor 1 (Duffy blood group)	Mus musculus	73-75
8054362-8	1994	These results suggest that retention of glucose on N-linked oligosaccharides not only retards the exit of alpha 2-PI and ATIII, but also changes the catabolic rate of alpha 2-PI in the endoplasmic reticulum.	n-linked oligosaccharides	51-76	serpin family F member 2	Homo sapiens	106-116
8054362-8	1994	These results suggest that retention of glucose on N-linked oligosaccharides not only retards the exit of alpha 2-PI and ATIII, but also changes the catabolic rate of alpha 2-PI in the endoplasmic reticulum.	n-linked oligosaccharides	51-76	serpin family C member 1	Homo sapiens	121-126
8054362-8	1994	These results suggest that retention of glucose on N-linked oligosaccharides not only retards the exit of alpha 2-PI and ATIII, but also changes the catabolic rate of alpha 2-PI in the endoplasmic reticulum.	n-linked oligosaccharides	51-76	serpin family F member 2	Homo sapiens	167-177
8034751-5	1994	Semisynthetic N-linked oligosaccharides terminating with 9-O-acetylated, alpha 2-6-linked sialic acids showed markedly reduced binding to CD22 beta relative to their non-O-acetylated counterparts.	n-linked oligosaccharides	14-39	CD22 antigen	Mus musculus	138-142
7515913-0	1994	CD23 interacts with a new functional extracytoplasmic domain involving N-linked oligosaccharides on CD21.	n-linked oligosaccharides	71-96	Fc epsilon receptor II	Homo sapiens	0-4
7515913-0	1994	CD23 interacts with a new functional extracytoplasmic domain involving N-linked oligosaccharides on CD21.	n-linked oligosaccharides	71-96	complement C3d receptor 2	Homo sapiens	100-104
8144652-2	1994	We previously reported that a recombinant soluble form termed CD22 beta Rg is capable of binding alpha 2-6 sialylated complex N-linked oligosaccharides purified from lymphocyte glycoprotein ligands (Powell, L. D., Sgroi, D., Sjoberg, E. R., Stamenkovic, I., and Varki, A.	n-linked oligosaccharides	126-151	CD22 molecule	Homo sapiens	62-66
8187759-5	1994	Inactivation of both Mgat-1 alleles produced deficiencies in GlcNAc-TI activity and complex N-linked oligosaccharides.	n-linked oligosaccharides	92-117	mannoside acetylglucosaminyltransferase 1	Mus musculus	21-27
8187759-8	1994	Complex N-linked oligosaccharides are important for morphogenic processes as neural tube formation, vascularization and the determination of left-right body plan asymmetry were impaired in the absence of a functional Mgat-1 gene.	n-linked oligosaccharides	8-33	mannoside acetylglucosaminyltransferase 1	Mus musculus	217-223
8167156-7	1994	These results suggest that the N-linked oligosaccharides of GLUT1 in Swiss 3T3 cells were altered by TGF-beta 1 to forms with more branched and/or repeated polylactosamines as well as with some substitution in the polylactosamines, resulting in a larger GLUT1 molecule.	n-linked oligosaccharides	31-56	solute carrier family 2 (facilitated glucose transporter), member 1	Mus musculus	60-65
8167156-7	1994	These results suggest that the N-linked oligosaccharides of GLUT1 in Swiss 3T3 cells were altered by TGF-beta 1 to forms with more branched and/or repeated polylactosamines as well as with some substitution in the polylactosamines, resulting in a larger GLUT1 molecule.	n-linked oligosaccharides	31-56	transforming growth factor, beta 1	Mus musculus	101-111
8167156-7	1994	These results suggest that the N-linked oligosaccharides of GLUT1 in Swiss 3T3 cells were altered by TGF-beta 1 to forms with more branched and/or repeated polylactosamines as well as with some substitution in the polylactosamines, resulting in a larger GLUT1 molecule.	n-linked oligosaccharides	31-56	solute carrier family 2 (facilitated glucose transporter), member 1	Mus musculus	254-259
8188697-2	1994	In this study, the sites of N-linked oligosaccharides on GluR6, a member of the kainate class of ionotropic glutamate receptors, were examined.	n-linked oligosaccharides	28-53	glutamate ionotropic receptor kainate type subunit 2	Homo sapiens	57-62
7512967-3	1994	In the N-linked oligosaccharides from all of the IgG2b phenotypes, virtually no sialylation was detected.	n-linked oligosaccharides	7-32	immunoglobulin heavy constant gamma 2B	Mus musculus	49-54
7909499-3	1994	Prevention of post-translational addition of N-linked oligosaccharides by treatment of the resistant cells with tunicamycin resulted in a dramatic enhancement in LAK cell cytotoxicity which was partially inhibited by antibodies against LFA-1 and ICAM-1.	n-linked oligosaccharides	45-70	alpha kinase 1	Homo sapiens	162-165
7909499-3	1994	Prevention of post-translational addition of N-linked oligosaccharides by treatment of the resistant cells with tunicamycin resulted in a dramatic enhancement in LAK cell cytotoxicity which was partially inhibited by antibodies against LFA-1 and ICAM-1.	n-linked oligosaccharides	45-70	integrin subunit alpha L	Homo sapiens	236-241
7909499-3	1994	Prevention of post-translational addition of N-linked oligosaccharides by treatment of the resistant cells with tunicamycin resulted in a dramatic enhancement in LAK cell cytotoxicity which was partially inhibited by antibodies against LFA-1 and ICAM-1.	n-linked oligosaccharides	45-70	intercellular adhesion molecule 1	Homo sapiens	246-252
8144653-5	1994	Analysis of labeled HEC showed both a relative and an absolute increase of alpha 2,6-linked sialic acid on N-linked oligosaccharides after TNF-alpha stimulation.	n-linked oligosaccharides	107-132	tumor necrosis factor	Homo sapiens	139-148
8162991-3	1994	SP-A is an 18-mer of 26 kDa polypeptide chains and contains N-linked oligosaccharides.	n-linked oligosaccharides	60-85	surfactant protein A1	Homo sapiens	0-4
8166649-1	1994	The primary structures of the N-linked oligosaccharides from normal human serum IgA1 were determined by a combination of sequential exoglycosidase digestion, Bio-Gel P-4 chromatography, anion-exchange chromatography and one-dimensional n.m.r.	n-linked oligosaccharides	30-55	immunoglobulin heavy constant alpha 1	Homo sapiens	80-84
8172929-0	1994	Mass spectrometric studies on the N-linked oligosaccharides of baculovirus-expressed mouse interleukin-3.	n-linked oligosaccharides	34-59	interleukin 3	Mus musculus	91-104
8172929-1	1994	A combination of mass spectrometry techniques, high-pH anion-exchange chromatography and enzymatic digestions has been applied to elucidate the structures of the N-linked oligosaccharides on baculovirus-expressed mouse interleukin-3 produced in Bombyx mori larvae.	n-linked oligosaccharides	162-187	interleukin 3	Mus musculus	219-232
7908224-5	1994	Thus, murine plasma contains two forms of HCII that appear to have identical amino acid sequences but differ in the composition of their N-linked oligosaccharides.	n-linked oligosaccharides	137-162	serine (or cysteine) peptidase inhibitor, clade D, member 1	Mus musculus	42-46
8294421-7	1994	The lectin binding properties of phosphodiester alpha-GlcNAcase indicate that it contains sialylated species of both complex type N-linked oligosaccharides and O-linked oligosaccharides.	n-linked oligosaccharides	130-155	N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase	Bos taurus	33-63
8251520-1	1993	N-linked oligosaccharides of mouse zona pellucida glycoproteins ZP2 and ZP3 were prepared as pyridylaminated derivatives.	n-linked oligosaccharides	0-25	zona pellucida glycoprotein 2	Mus musculus	64-67
7506656-0	1993	Structures of the N-linked oligosaccharides on porcine plasma vitronectin.	n-linked oligosaccharides	18-43	vitronectin	Homo sapiens	62-73
7506656-1	1993	The structures of N-linked oligosaccharides, especially the distribution of sialic acid species, present on porcine plasma vitronectin were elucidated.	n-linked oligosaccharides	18-43	vitronectin	Homo sapiens	123-134
7764526-0	1994	Comparison of N-linked oligosaccharides of recombinant human tissue kallikrein produced by Chinese hamster ovary cells on microcarrier beads and in serum-free suspension culture.	n-linked oligosaccharides	14-39	kallikrein 1	Homo sapiens	61-78
8253757-0	1993	Structure of the N-linked oligosaccharides that show the complete loss of alpha-1,6-polymannose outer chain from och1, och1 mnn1, and och1 mnn1 alg3 mutants of Saccharomyces cerevisiae.	n-linked oligosaccharides	17-42	initiation-specific alpha-1,6-mannosyltransferase	Saccharomyces cerevisiae S288C	113-117
8253757-0	1993	Structure of the N-linked oligosaccharides that show the complete loss of alpha-1,6-polymannose outer chain from och1, och1 mnn1, and och1 mnn1 alg3 mutants of Saccharomyces cerevisiae.	n-linked oligosaccharides	17-42	initiation-specific alpha-1,6-mannosyltransferase	Saccharomyces cerevisiae S288C	119-123
8253757-0	1993	Structure of the N-linked oligosaccharides that show the complete loss of alpha-1,6-polymannose outer chain from och1, och1 mnn1, and och1 mnn1 alg3 mutants of Saccharomyces cerevisiae.	n-linked oligosaccharides	17-42	alpha-1,3-mannosyltransferase MNN1	Saccharomyces cerevisiae S288C	124-128
8253757-0	1993	Structure of the N-linked oligosaccharides that show the complete loss of alpha-1,6-polymannose outer chain from och1, och1 mnn1, and och1 mnn1 alg3 mutants of Saccharomyces cerevisiae.	n-linked oligosaccharides	17-42	initiation-specific alpha-1,6-mannosyltransferase	Saccharomyces cerevisiae S288C	134-148
8251520-1	1993	N-linked oligosaccharides of mouse zona pellucida glycoproteins ZP2 and ZP3 were prepared as pyridylaminated derivatives.	n-linked oligosaccharides	0-25	zona pellucida glycoprotein 3	Mus musculus	72-75
8251520-9	1993	The N-linked oligosaccharides of ZP3 were suggested to have essentially the same structures as those of ZP2.	n-linked oligosaccharides	4-29	zona pellucida glycoprotein 3	Mus musculus	33-36
8218172-1	1993	We report the complete structures of the N-linked oligosaccharides and the site-specificity of the N-glycosylation of recombinant gp120 (rgp120) of the HIV-1 BH8 isolate produce by a baculovirus expression system.	n-linked oligosaccharides	41-66	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	130-135
8144855-3	1993	Endoglycosidase treatment and carbohydrate content of PRL was found to be consistent with N-linked oligosaccharides of mannose-rich structure and complex units terminated in sialic acid.	n-linked oligosaccharides	90-115	prolactin	Homo sapiens	54-57
8368484-3	1993	The acceptor substrate in this assay is human transferrin (Tfn) which has been enzymatically modified such that its N-linked oligosaccharides bear the terminal sequence GGnM.	n-linked oligosaccharides	116-141	transferrin	Homo sapiens	46-57
8408060-1	1993	Poly-N-acetyllactosamine (PL) sequences (repeating (3Gal beta 1-4GlcNAc beta 1)n) in complex-type N-linked oligosaccharides often occur in branched tri- and tetraantennary chains containing alpha-linked mannosyl residues disubstituted by N-acetyllactosaminyl units at C-2 and C-6 (2,6-branched mannose).	n-linked oligosaccharides	98-123	complement C2	Cricetulus griseus	268-279
8400551-1	1993	The N-linked oligosaccharides of frog (Rana pipiens) rhodopsin were analysed by sequential exoglycosidase digestion and gel filtration chromatography, following reductive tritiation.	n-linked oligosaccharides	4-29	rhodopsin	Bos taurus	53-62
8368484-3	1993	The acceptor substrate in this assay is human transferrin (Tfn) which has been enzymatically modified such that its N-linked oligosaccharides bear the terminal sequence GGnM.	n-linked oligosaccharides	116-141	transferrin	Homo sapiens	59-62
8407880-0	1993	Structural study of the N-linked oligosaccharides of hepatocyte growth factor by two-dimensional sugar mapping.	n-linked oligosaccharides	24-49	hepatocyte growth factor	Rattus norvegicus	53-77
8407880-1	1993	The structures of the N-linked oligosaccharides on recombinant human hepatocyte growth factor (rh-HGF) expressed by Chinese hamster ovary (CHO) cells were studied by two-dimensional sugar mapping.	n-linked oligosaccharides	22-47	hepatocyte growth factor	Homo sapiens	69-93
8407880-1	1993	The structures of the N-linked oligosaccharides on recombinant human hepatocyte growth factor (rh-HGF) expressed by Chinese hamster ovary (CHO) cells were studied by two-dimensional sugar mapping.	n-linked oligosaccharides	22-47	hepatocyte growth factor	Rattus norvegicus	98-101
8407880-6	1993	The structures of the N-linked oligosaccharides from rat HGF were also studied.	n-linked oligosaccharides	22-47	hepatocyte growth factor	Rattus norvegicus	57-60
8463235-0	1993	Natural ligands of the B cell adhesion molecule CD22 beta carry N-linked oligosaccharides with alpha-2,6-linked sialic acids that are required for recognition.	n-linked oligosaccharides	64-89	basal cell adhesion molecule (Lutheran blood group)	Homo sapiens	23-47
8352935-5	1993	The ESA152 epitope includes the sialic acid termini of N-linked oligosaccharides, as shown by its sensitivity to neuraminidase and endoglycosidase F. The ESA152 antigen is a highly hydrophobic integral membrane protein that resists aqueous extraction, partitions into the detergent phase of Triton-X-114, and solubilizes in chloroform-methanol mixtures.	n-linked oligosaccharides	55-80	neuraminidase 1	Homo sapiens	113-126
7685189-5	1993	Two alpha 1-microglobulin-bikunin precursors (40 and 42 kDa), containing one and two N-linked oligosaccharides, respectively, were detected in the endoplasmic reticulum.	n-linked oligosaccharides	85-110	alpha-1-microglobulin/bikunin precursor	Rattus norvegicus	4-33
8463235-0	1993	Natural ligands of the B cell adhesion molecule CD22 beta carry N-linked oligosaccharides with alpha-2,6-linked sialic acids that are required for recognition.	n-linked oligosaccharides	64-89	CD22 molecule	Homo sapiens	48-52
8381403-3	1993	Using serial lectin affinity chromatography, as well as specific glycosidases, we demonstrate that VIP receptor-linked carbohydrates are predominantly tri- or tetraantennary sialylated N-linked oligosaccharides, 27% of which are fucosylated, and some may have terminal galactose residues.	n-linked oligosaccharides	185-210	vasoactive intestinal peptide	Homo sapiens	99-102
8501138-7	1993	Our results demonstrate that alterations in glycosylation of N-linked oligosaccharides, resulting in the synthesis of high mannose type sugars on molecules that may interact with the beta 2 integrins, leads to an increased adherence of PMA activated neutrophils to endothelial cells.	n-linked oligosaccharides	61-86	potassium calcium-activated channel subfamily M regulatory beta subunit 2	Homo sapiens	183-189
8431454-7	1993	In addition, treating membrane proteins with glycopeptidase F, which removes N-linked oligosaccharides, also generated a glucose transporter of 40 kDa, suggesting that the 55 and 65 kDa GLUT1 proteins have a similar or identical core polypeptide but with different N-linked oligosaccharides.	n-linked oligosaccharides	77-102	solute carrier family 2 (facilitated glucose transporter), member 1	Mus musculus	186-191
8431454-7	1993	In addition, treating membrane proteins with glycopeptidase F, which removes N-linked oligosaccharides, also generated a glucose transporter of 40 kDa, suggesting that the 55 and 65 kDa GLUT1 proteins have a similar or identical core polypeptide but with different N-linked oligosaccharides.	n-linked oligosaccharides	265-290	solute carrier family 2 (facilitated glucose transporter), member 1	Mus musculus	186-191
1443598-1	1992	A rapid quantitative analysis of the sialylated N-linked oligosaccharides of recombinant erythropoietin (EPO) expressed in Chinese hamster ovary (CHO) cells has been developed.	n-linked oligosaccharides	48-73	erythropoietin	Cricetulus griseus	89-103
8348244-0	1993	Microscale sequencing of N-linked oligosaccharides of glycoproteins using hydrazinolysis, Bio-Gel P-4, and sequential exoglycosidase digestion.	n-linked oligosaccharides	25-50	solute carrier family 10 member 4	Homo sapiens	98-101
1482344-5	1992	All nine of the known N-linked oligosaccharides of BuChE are predicted to occur away from the putative active site channel and most are located on one face of the monomer.	n-linked oligosaccharides	22-47	butyrylcholinesterase	Homo sapiens	51-56
1468573-1	1992	Structural analysis of enzymically released N-linked carbohydrate chains of human urokinase (urinary-type plasminogen activator) by 1H NMR spectroscopy and FAB-MS demonstrated that the N-linked oligosaccharides on the only N-glycosylation site contain diantennary structures with the novel GalNAc beta (1-4) [Fuc alpha (1-3)]GlcNAc beta (1-2) element in the upper or the lower branch.	n-linked oligosaccharides	185-210	FA complementation group B	Homo sapiens	156-159
1468573-1	1992	Structural analysis of enzymically released N-linked carbohydrate chains of human urokinase (urinary-type plasminogen activator) by 1H NMR spectroscopy and FAB-MS demonstrated that the N-linked oligosaccharides on the only N-glycosylation site contain diantennary structures with the novel GalNAc beta (1-4) [Fuc alpha (1-3)]GlcNAc beta (1-2) element in the upper or the lower branch.	n-linked oligosaccharides	185-210	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	Homo sapiens	332-341
8419650-0	1993	Complex-type N-linked oligosaccharides of gp120 from human immunodeficiency virus type 1 contain sulfated N-acetylglucosamine.	n-linked oligosaccharides	13-38	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	42-47
8419650-1	1993	The major envelope glycoproteins gp120 and gp41 of human immunodeficiency virus type 1, the causative agent for human AIDS, contain numerous N-linked oligosaccharides.	n-linked oligosaccharides	141-166	Envelope surface glycoprotein gp160, precursor	Human immunodeficiency virus 1	33-38
8419650-2	1993	We report here our discovery that N-acetylglucosamine residues within the complex-type N-linked oligosaccharides of both gp120 and its precursor, gp160, are sulfated.	n-linked oligosaccharides	87-112	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	121-126
8419650-2	1993	We report here our discovery that N-acetylglucosamine residues within the complex-type N-linked oligosaccharides of both gp120 and its precursor, gp160, are sulfated.	n-linked oligosaccharides	87-112	glutamyl aminopeptidase	Homo sapiens	146-151
8419650-8	1993	Charge analysis of the [3H]galactose- and [3H]glucosamine-labeled glycopeptides from gp120 and gp160 indicates that approximately 14% of the complex-type N-linked oligosaccharides are sulfated.	n-linked oligosaccharides	154-179	inter-alpha-trypsin inhibitor heavy chain 4	Homo sapiens	85-90
8419650-8	1993	Charge analysis of the [3H]galactose- and [3H]glucosamine-labeled glycopeptides from gp120 and gp160 indicates that approximately 14% of the complex-type N-linked oligosaccharides are sulfated.	n-linked oligosaccharides	154-179	glutamyl aminopeptidase	Homo sapiens	95-100
1443598-1	1992	A rapid quantitative analysis of the sialylated N-linked oligosaccharides of recombinant erythropoietin (EPO) expressed in Chinese hamster ovary (CHO) cells has been developed.	n-linked oligosaccharides	48-73	erythropoietin	Cricetulus griseus	105-108
1281889-4	1992	Sulfate labeled only the larger of the two MAG components, which contains complex N-linked oligosaccharides, but which appears to be glycosylated to a lesser extent than MAG in vivo.	n-linked oligosaccharides	82-107	myelin associated glycoprotein	Bos taurus	43-46
1317871-6	1992	Although the endomannosidase-mediated deglucosylation pathway appeared to be nonselective, a differential inhibitory effect on the secretion of the various glycoproteins was noted in the presence of CST which was directly related to the number of their N-linked oligosaccharides, ranging from minimal in alpha-fetoprotein to substantial (approximately 65%) in alpha 1-acid glycoprotein.	n-linked oligosaccharides	253-278	mannosidase endo-alpha	Homo sapiens	13-28
1324936-2	1992	The present study focuses for the first time on the potential contribution of N-linked oligosaccharides of the beta subunit in the processing, structure, and function of the insulin receptor.	n-linked oligosaccharides	78-103	insulin receptor	Cricetulus griseus	174-190
1358299-6	1992	Second, the number of N-linked oligosaccharides was estimated in dipeptidylpeptidase IV (DPP IV), a major glycoprotein constituent of the hepatic plasma membrane, comparing the newly synthesized glycoprotein from rough endoplasmic reticulum and the mature form of DPP IV from the plasma membrane.	n-linked oligosaccharides	22-47	dipeptidylpeptidase 4	Rattus norvegicus	65-87
1358299-6	1992	Second, the number of N-linked oligosaccharides was estimated in dipeptidylpeptidase IV (DPP IV), a major glycoprotein constituent of the hepatic plasma membrane, comparing the newly synthesized glycoprotein from rough endoplasmic reticulum and the mature form of DPP IV from the plasma membrane.	n-linked oligosaccharides	22-47	dipeptidylpeptidase 4	Rattus norvegicus	89-95
1533222-0	1992	Characterization of the endomannosidase pathway for the processing of N-linked oligosaccharides in glucosidase II-deficient and parent mouse lymphoma cells.	n-linked oligosaccharides	70-95	mannosidase, endo-alpha	Mus musculus	24-39
1555586-0	1992	Structure of the N-linked oligosaccharides of the human transferrin receptor.	n-linked oligosaccharides	17-42	transferrin receptor	Homo sapiens	56-76
1560005-2	1992	Three N-linked oligosaccharides of hEPO have been partially or fully removed to obtain N-glycan (NG) (2)-, NG(1)-, and NG(0)-hEPO carrying two, one, and no N-linked sugar chains, respectively.	n-linked oligosaccharides	6-31	erythropoietin	Homo sapiens	35-39
1313799-16	1992	177, 751-756), we propose that rat renal IFCR is synthesized as a single polypeptide chain of 220 kDa and is transported slowly to the apical membrane during which four or five N-linked oligosaccharides are processed to the complex type.	n-linked oligosaccharides	177-202	cubilin	Rattus norvegicus	41-45
1552169-5	1992	The demonstration of both the terminal Neu 5Ac (alpha-2,3, or 6) Gal (beta-1,4) GlcNAc sequence in the N-linked oligosaccharides of mucous cells and the terminal disaccharide Gal (beta-1,4) GlcNAc in the N-linked oligosaccharide chains of serous cells suggests the existence of complex type sugar chains N-glycosidically linked to the peptide region of the glycoproteins.	n-linked oligosaccharides	103-128	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	Homo sapiens	48-78
1387363-9	1992	The enhancement was accompanied with an elongation of lactosamine repeats in N-linked oligosaccharides in the 46 kDa mannose 6-phosphate receptor and the homing receptor, the leucocyte antigen CD44.	n-linked oligosaccharides	77-102	mannose-6-phosphate receptor, cation dependent	Homo sapiens	110-145
1387363-9	1992	The enhancement was accompanied with an elongation of lactosamine repeats in N-linked oligosaccharides in the 46 kDa mannose 6-phosphate receptor and the homing receptor, the leucocyte antigen CD44.	n-linked oligosaccharides	77-102	CD44 molecule (Indian blood group)	Homo sapiens	193-197
1518562-5	1992	Endoglycosidase H or F, capable of removing high-mannose and biantennary branched N-linked oligosaccharides, produced a 2-3 kDa decrease in the molecular weight of both NEP 1 and NEP 2.	n-linked oligosaccharides	82-107	membrane metallo-endopeptidase	Rattus norvegicus	169-172
1518562-5	1992	Endoglycosidase H or F, capable of removing high-mannose and biantennary branched N-linked oligosaccharides, produced a 2-3 kDa decrease in the molecular weight of both NEP 1 and NEP 2.	n-linked oligosaccharides	82-107	membrane metallo-endopeptidase-like 1	Rattus norvegicus	179-184
1518562-6	1992	Peptide-N-glycosidase F, capable of removing all classes of N-linked oligosaccharides, produced 8 and 11 kDa decreases in NEP 1 and NEP 2, respectively.	n-linked oligosaccharides	60-85	membrane metallo-endopeptidase	Rattus norvegicus	122-125
1518562-6	1992	Peptide-N-glycosidase F, capable of removing all classes of N-linked oligosaccharides, produced 8 and 11 kDa decreases in NEP 1 and NEP 2, respectively.	n-linked oligosaccharides	60-85	membrane metallo-endopeptidase-like 1	Rattus norvegicus	132-137
1537432-6	1992	We show that the size difference of the polypeptides is instead due to N-linked oligosaccharides attached to the skin N-CAM proteins.	n-linked oligosaccharides	71-96	neural cell adhesion molecule 1	Homo sapiens	118-123
1560031-1	1992	Mesenchymal cell migration and neurite outgrowth are mediated in part by binding of cell surface beta 1,4-galactosyltransferase (GalTase) to N-linked oligosaccharides within the E8 domain of laminin.	n-linked oligosaccharides	141-166	laminin, beta 2 (laminin S)	Gallus gallus	191-198
1372525-4	1992	Application of these methods for the qualitative analysis of the oligosaccharides released from bovine fetuin and bovine asialofetuin by peptide-N-glycosidase F illustrates the usefulness of these techniques as fast, simple, and inexpensive tools for the characterization of N-linked oligosaccharides attached to glycoproteins.	n-linked oligosaccharides	275-300	alpha 2-HS glycoprotein	Bos taurus	121-133
1311366-8	1992	These data suggest that sugar residues of gp106 and gp102 are high-mannose type N-linked oligosaccharides, whereas those of gp65 and gp63 are complex type N-linked oligosaccharides.	n-linked oligosaccharides	80-105	neuroplastin	Homo sapiens	124-128
1311366-8	1992	These data suggest that sugar residues of gp106 and gp102 are high-mannose type N-linked oligosaccharides, whereas those of gp65 and gp63 are complex type N-linked oligosaccharides.	n-linked oligosaccharides	155-180	neuroplastin	Homo sapiens	124-128
1311366-8	1992	These data suggest that sugar residues of gp106 and gp102 are high-mannose type N-linked oligosaccharides, whereas those of gp65 and gp63 are complex type N-linked oligosaccharides.	n-linked oligosaccharides	155-180	leishmanolysin like peptidase	Homo sapiens	133-137
1419071-7	1992	Mature BMP-2 and propeptide contain high mannose and complex N-linked oligosaccharides, respectively.	n-linked oligosaccharides	61-86	bone morphogenetic protein 2	Cricetulus griseus	7-12
1854349-5	1991	The N-linked oligosaccharides seem to be of the complex type rather than the high-mannose or hybrid type and lack terminal sialic acid, as demonstrated by their resistance to endoglycosidases D and H and neuraminidase treatments.	n-linked oligosaccharides	4-29	neuraminidase 1	Homo sapiens	204-217
1660878-1	1991	We have studied the role of N-linked oligosaccharides and proteolytic processing on the targeting of cathepsin D to the lysosomes in the human hepatoma cell line HepG2.	n-linked oligosaccharides	28-53	cathepsin D	Homo sapiens	101-112
1922010-4	1991	In this report we demonstrate that 37k Uf contains two N-linked oligosaccharides which are a mixture of complex and high mannose-type oligosaccharides.	n-linked oligosaccharides	55-80	acid phosphatase 5, tartrate resistant	Sus scrofa	39-41
2043765-8	1991	However, EPO produced with incompletely processed N-linked oligosaccharides exhibits normal in vitro activity but is at least 500-fold less effective in stimulating erythropoiesis in vivo.	n-linked oligosaccharides	50-75	erythropoietin	Cricetulus griseus	9-12
2043765-9	1991	Studies on the survival of bioactive EPO remaining in the circulation demonstrated that EPO with incomplete N-linked oligosaccharides exhibits a sevenfold increased rate of clearance.	n-linked oligosaccharides	108-133	erythropoietin	Cricetulus griseus	88-91
2043765-11	1991	These results suggest a potentially important unique requirement for appropriate complex N-linked oligosaccharides for the intrinsic biologic activity of EPO in vivo.	n-linked oligosaccharides	89-114	erythropoietin	Cricetulus griseus	154-157
2045792-1	1991	Site-directed mutagenesis was used to study the biological significance of a disulphide bridge and two N-linked oligosaccharides in the CD4-binding region of the envelope glycoproteins of human immunodeficiency virus type 1.	n-linked oligosaccharides	103-128	CD4 molecule	Homo sapiens	136-139
1828762-5	1991	Furthermore, the size of the alpha-chain was reduced by 25 kDa by the removal of the N-linked oligosaccharides with peptidase: N-glycosidase F treatment, whereas that of the beta-chain remained unmodified by the enzyme.	n-linked oligosaccharides	85-110	Fc gamma receptor and transporter	Homo sapiens	29-40
2019471-4	1991	The data suggest that c-myc gene has a potential role in the regulation of cellular protein glycosylation and that an elevated expression of c-myc gene in the cells leads to increased branch formation of outer chains in N-linked oligosaccharides concomitant with the acquisition of tumorigenicity.	n-linked oligosaccharides	220-245	MYC proto-oncogene, bHLH transcription factor	Rattus norvegicus	22-27
2019471-4	1991	The data suggest that c-myc gene has a potential role in the regulation of cellular protein glycosylation and that an elevated expression of c-myc gene in the cells leads to increased branch formation of outer chains in N-linked oligosaccharides concomitant with the acquisition of tumorigenicity.	n-linked oligosaccharides	220-245	MYC proto-oncogene, bHLH transcription factor	Rattus norvegicus	141-146
1851001-1	1991	Controversy exists regarding the functional role of N-linked oligosaccharides in the hormone erythropoietin.	n-linked oligosaccharides	52-77	erythropoietin	Homo sapiens	93-107
1712068-10	1991	On the other hand, treatment of Fel d I by N-glycanase under reducing and non-reducing conditions indicated the presence of N-linked oligosaccharides in the beta-chain.	n-linked oligosaccharides	124-149	major allergen I polypeptide chain 2	Felis catus	32-39
2269302-1	1990	Pulse/chase experiments with [35S]methionine demonstrated that in the control cells, ALP synthesized as a 63-kDa precursor form was rapidly converted to a 66-kDa form, by processing of its N-linked oligosaccharides from the high-mannose type to the complex type, which was expressed on the cell surface after 30 min of chase.	n-linked oligosaccharides	189-214	alkaline phosphatase, placental	Homo sapiens	85-88
1645456-14	1991	We conclude that IGF-II can bind to an IGF-II/Man-6-P receptor that lacks N-linked oligosaccharides.	n-linked oligosaccharides	74-99	insulin like growth factor 2	Homo sapiens	17-23
1701438-0	1990	N-linked oligosaccharides on free alpha interfere with its ability to combine with human chorionic gonadotropin-beta subunit.	n-linked oligosaccharides	0-25	chorionic gonadotropin subunit beta 3	Homo sapiens	89-124
1701438-1	1990	The purpose of the study was to examine the role of N-linked oligosaccharides in preventing combination of free alpha molecules with human chorionic gonadotropin (hCG)-beta subunit to form the intact hormone, hCG.	n-linked oligosaccharides	52-77	chorionic gonadotropin subunit beta 5	Homo sapiens	163-166
1701438-1	1990	The purpose of the study was to examine the role of N-linked oligosaccharides in preventing combination of free alpha molecules with human chorionic gonadotropin (hCG)-beta subunit to form the intact hormone, hCG.	n-linked oligosaccharides	52-77	chorionic gonadotropin subunit beta 5	Homo sapiens	209-212
2120048-1	1990	Neurotactin is a 135 kd membrane glycoprotein which consists of a core protein, with an apparent molecular weight of 120 kd, and of N-linked oligosaccharides.	n-linked oligosaccharides	132-157	Neurotactin	Drosophila melanogaster	0-11
2123489-7	1990	Treatment of N-linked oligosaccharides isolated from recultured cells with a variety of glycosidases in conjunction with beta-galactosidase demonstrated the addition of sialic acid N-acetylglucosamine and fucose residues to the galactose residues in recultured cells.	n-linked oligosaccharides	13-38	galactosidase, beta 1	Rattus norvegicus	121-139
2223825-0	1990	N-linked oligosaccharides of the murine transferrin receptor from a plasmacytoma cell line.	n-linked oligosaccharides	0-25	transferrin	Mus musculus	40-51
1699598-5	1990	The removal of N-linked oligosaccharides from PAS IV and CD36 by treatment with endoglycosidase F reduced the apparent Mr of both proteins to approximately 57,000.	n-linked oligosaccharides	15-40	CD36 molecule	Homo sapiens	46-52
2209609-1	1990	Structures of the N-linked oligosaccharides of a recombinant soluble form of human CD4 glycoprotein (sCD4) have been investigated by enzymic microsequencing.	n-linked oligosaccharides	18-43	T-cell surface glycoprotein CD4	Cricetulus griseus	83-86
2209609-1	1990	Structures of the N-linked oligosaccharides of a recombinant soluble form of human CD4 glycoprotein (sCD4) have been investigated by enzymic microsequencing.	n-linked oligosaccharides	18-43	stearoyl-CoA desaturase 5	Homo sapiens	101-105
2117577-0	1990	N-linked oligosaccharides of human transferrin are not required for binding to bacterial transferrin receptors.	n-linked oligosaccharides	0-25	transferrin	Homo sapiens	35-46
2353452-5	1990	Endoglycosidase F treatment or labeling in the presence of tunicamycin suggests that YF prM and NS1 each have two N-linked oligosaccharides.	n-linked oligosaccharides	114-139	influenza virus NS1A binding protein	Homo sapiens	96-99
1693562-4	1990	The amounts of sugar that were found relative to peptide indicated the presence of two N-linked oligosaccharides per molecule on both hCG alpha and free alpha.	n-linked oligosaccharides	87-112	chromogranin A	Homo sapiens	134-143
1969395-3	1990	In hapten inhibition studies, several nonmucin glycoproteins bearing exposed mannosyl residues in N-linked oligosaccharides were effective inhibitors, as was rat mucin.	n-linked oligosaccharides	98-123	solute carrier family 13 member 2	Rattus norvegicus	41-46
2185468-1	1990	The N-linked oligosaccharides from baker"s yeast carboxypeptidase Y were analyzed by 1H NMR and specific mannosidase digestion and found to be identical to those from the Saccharomyces cerevisiae mnn9 mutant bulk mannoprotein.	n-linked oligosaccharides	4-29	mannosyltransferase complex subunit MNN9	Saccharomyces cerevisiae S288C	196-200
1969395-11	1990	In summary, our binding studies revealed, for the first time, that intestinal mucin bears oligomannosyl receptors for type 1 pili and that these receptors are located on N-linked oligosaccharides of the 118-kilodalton link glycopeptide region of the mucin.	n-linked oligosaccharides	170-195	solute carrier family 13 member 2	Rattus norvegicus	78-83
1969395-11	1990	In summary, our binding studies revealed, for the first time, that intestinal mucin bears oligomannosyl receptors for type 1 pili and that these receptors are located on N-linked oligosaccharides of the 118-kilodalton link glycopeptide region of the mucin.	n-linked oligosaccharides	170-195	solute carrier family 13 member 2	Rattus norvegicus	250-255
1691270-5	1990	Altogether the results indicated that the carbohydrate-dependent epitopes of gC-1 from C1300 cells were stabilized by peripheral sugars of N-linked oligosaccharides rather than O-linked ones and that fucose could substitute for terminal galactose in promoting the activity of the carbohydrate-dependent epitopes.	n-linked oligosaccharides	139-164	guanylate cyclase 2e	Mus musculus	77-81
2403553-14	1990	Thus, our results demonstrate that the human transferrin receptor contains O-linked oligosaccharides and that there are differences in the structures of both the O-linked and complex-type N-linked oligosaccharides on the receptors synthesized by different cell types.	n-linked oligosaccharides	188-213	transferrin	Homo sapiens	45-56
2105324-3	1990	GalTase is localized on lamellipodia of migrating cells where it functions as a laminin receptor by binding to specific N-linked oligosaccharides in laminin (Runyan et al., 1988; Eckstein and Shur, 1989).	n-linked oligosaccharides	120-145	glycoprotein alpha-galactosyltransferase 1	Rattus norvegicus	0-7
2324208-8	1990	The applicability of this chromatography for profiling the N-linked oligosaccharides of glycoproteins was demonstrated by generating "oligosaccharide maps" of PNGase F-liberated oligosaccharides from recombinant human tissue plasminogen activator, ribonuclease b, human transferrin, and bovine fetuin.	n-linked oligosaccharides	59-84	transferrin	Homo sapiens	270-281
34489534-4	2021	Both mutation of these asparagines (N2294Q/N2331Q) and treatment with an enzyme that hydrolyses N-linked oligosaccharides (PNGaseF) eliminates the fully glycosylated mature Piezo1 protein.	n-linked oligosaccharides	96-121	piezo type mechanosensitive ion channel component 1	Homo sapiens	173-179
34407556-1	2021	Background The asialoglycoprotein receptor (ASGPR) binds with high affinity factor VIII (FVIII) through its N-linked oligosaccharides.	n-linked oligosaccharides	108-133	asialoglycoprotein receptor 1	Homo sapiens	44-49
34407556-1	2021	Background The asialoglycoprotein receptor (ASGPR) binds with high affinity factor VIII (FVIII) through its N-linked oligosaccharides.	n-linked oligosaccharides	108-133	coagulation factor VIII	Homo sapiens	76-87
34407556-1	2021	Background The asialoglycoprotein receptor (ASGPR) binds with high affinity factor VIII (FVIII) through its N-linked oligosaccharides.	n-linked oligosaccharides	108-133	coagulation factor VIII	Homo sapiens	89-94
2185827-1	1990	Neutral and phosphorylated N-linked oligosaccharides were isolated from Saccharomyces cerevisiae mnn9 and mnn9 gls1 mutant mannoproteins and separated into homologues that differed in the number of terminal alpha 1----3-linked mannoses.	n-linked oligosaccharides	27-52	mannosyltransferase complex subunit MNN9	Saccharomyces cerevisiae S288C	97-101
2185827-1	1990	Neutral and phosphorylated N-linked oligosaccharides were isolated from Saccharomyces cerevisiae mnn9 and mnn9 gls1 mutant mannoproteins and separated into homologues that differed in the number of terminal alpha 1----3-linked mannoses.	n-linked oligosaccharides	27-52	mannosyltransferase complex subunit MNN9	Saccharomyces cerevisiae S288C	106-110
2185827-1	1990	Neutral and phosphorylated N-linked oligosaccharides were isolated from Saccharomyces cerevisiae mnn9 and mnn9 gls1 mutant mannoproteins and separated into homologues that differed in the number of terminal alpha 1----3-linked mannoses.	n-linked oligosaccharides	27-52	mannosyl-oligosaccharide glucosidase	Saccharomyces cerevisiae S288C	111-115
2338162-4	1990	Porcine hemopexin has an apparent Mw of 67,000, binds heme in a 1:1 molar ratio and consists of 24% N-linked oligosaccharides.	n-linked oligosaccharides	100-125	hemopexin	Homo sapiens	8-17