| 1 |
35137040 | Serum N-glycomics of a novel CDG-IIb patient reveals aberrant IgG glycosylation. | 2022 Apr 21 |
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| 2 |
33644825 | Mass spectrometry glycophenotype characterization of ALG2-CDG in Argentinean patients with a new genetic variant in homozygosis. | 2021 Apr |
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| 3 |
31056268 | Development of a filter-aided extraction method coupled with glycosylamine labeling to simplify and enhance high performance liquid chromatography-based N-glycan analysis. | 2019 Aug 30 |
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| 4 |
27137515 | N-Glycan profile analysis of transferrin using a microfluidic compact disc and MALDI-MS. | 2016 Jul |
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| 5 |
24508628 | Asymptomatic phosphomannose isomerase deficiency (MPI-CDG) initially mistaken for excessive alcohol consumption. | 2014 Apr 20 |
1 |
| 6 |
24780636 | Structural change of N-glycan exposes hydrophobic surface of human transferrin. | 2014 Aug |
2 |
| 7 |
23970553 | The epithelial calcium channel TRPV5 is regulated differentially by klotho and sialidase. | 2013 Oct 11 |
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| 8 |
21459485 | A unique N-glycan on human transferrin in CSF: a possible biomarker for iNPH. | 2012 Aug |
3 |
| 9 |
22930475 | Terminal galactose residues on transferrin are increased in midlife adults compared to young adults. | 2012 Nov |
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| 10 |
21431619 | Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type I. | 2011 Aug |
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| 11 |
20080937 | A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip. | 2010 Apr 15 |
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| 12 |
21137062 | Glycosylation of liver acute-phase proteins in pancreatic cancer and chronic pancreatitis. | 2010 Apr |
1 |
| 13 |
16037488 | Hypoglycosylation with increased fucosylation and branching of serum transferrin N-glycans in untreated galactosemia. | 2005 Dec |
1 |
| 14 |
16037491 | Patients with unsolved congenital disorders of glycosylation type II can be subdivided in six distinct biochemical groups. | 2005 Dec |
1 |
| 15 |
12626389 | Increased fucosylation and reduced branching of serum glycoprotein N-glycans in all known subtypes of congenital disorder of glycosylation I. | 2003 May |
1 |
| 16 |
12672704 | N-glycan structures of human transferrin produced by Lymantria dispar (gypsy moth) cells using the LdMNPV expression system. | 2003 Jul |
2 |
| 17 |
11859268 | A prolonged time interval between blood sample collection and centrifugation causes an increase in serum carbohydrate-deficient transferrin. | 2002 Feb |
1 |
| 18 |
12093361 | Deficiency of dolichyl-P-Man:Man7GlcNAc2-PP-dolichyl mannosyltransferase causes congenital disorder of glycosylation type Ig. | 2002 Oct 1 |
1 |
| 19 |
11382750 | Identification of core alpha 1,3-fucosylated glycans and cloning of the requisite fucosyltransferase cDNA from Drosophila melanogaster. Potential basis of the neural anti-horseadish peroxidase epitope. | 2001 Jul 27 |
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| 20 |
10929010 | N-glycan patterns of human transferrin produced in Trichoplusia ni insect cells: effects of mammalian galactosyltransferase. | 2000 Aug |
2 |
| 21 |
10471642 | Microheterogeneity of serum glycoproteins in patients with chronic alcohol abuse compared with carbohydrate-deficient glycoprotein syndrome type I. | 1999 Sep |
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| 22 |
9545549 | Identification of carbohydrate deficient transferrin forms by MALDI-TOF mass spectrometry and lectin ELISABiochim Biophys Acta 1998 Aug 24;1381(3):356. | 1998 Mar 12 |
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