PMID-sentid Pub_year Sent_text comp_official_name comp_offset protein_name organism prot_offset 26194854-1 2015 Natural Killer T (NKT) cells are unique lymphocytes characterized by their expression of a single invariant antigen receptor encoded by Valpha14Jalpha18 in mice and Valpha24Jalpha18 in humans, which recognizes glycolipid antigens in association with the monomorphic CD1d molecule. Glycolipids 210-220 CD1c molecule Homo sapiens 266-269 25587706-9 2015 Thus, TGF-beta-producing CD1c+ DCs are recruited and retained in the renal tubulointerstitium by PTEC-derived fractalkine. ptec-derived fractalkine 97-121 CD1c molecule Homo sapiens 25-29 25977654-0 2015 Facile synthesis of composition-tuned ZnO/Zn x Cd1-x Se nanowires for photovoltaic applications. Zinc Oxide 38-41 CD1c molecule Homo sapiens 47-50 25977654-0 2015 Facile synthesis of composition-tuned ZnO/Zn x Cd1-x Se nanowires for photovoltaic applications. Zinc 38-40 CD1c molecule Homo sapiens 47-50 26052329-5 2015 CD1 and MR1 molecules present lipid and vitamin B metabolite antigens, respectively, and offer a new front of targets for T cell therapies. Niacinamide 40-49 CD1c molecule Homo sapiens 0-3 24833283-0 2015 Preparation and optical properties of alloyed Znx Cd1-x S/alginate core/shell nanoparticles. Alginates 58-66 CD1c molecule Homo sapiens 50-53 24833283-4 2015 The band gap of Znx Cd1-x S/alginate core/shell nanoparticles increases with increasing Zn/Cd molar ratio, and the UV/vis absorption blue-shifts correspondingly. Alginates 28-36 CD1c molecule Homo sapiens 20-23 24833283-4 2015 The band gap of Znx Cd1-x S/alginate core/shell nanoparticles increases with increasing Zn/Cd molar ratio, and the UV/vis absorption blue-shifts correspondingly. Zinc 16-18 CD1c molecule Homo sapiens 20-23 24833283-5 2015 Two emissions related to zinc and sulfide ion vacancies were observed for the Znx Cd1-x S/alginate core/shell nanoparticles due to the surface changes from the alginate coating. Sulfides 34-41 CD1c molecule Homo sapiens 82-85 24833283-5 2015 Two emissions related to zinc and sulfide ion vacancies were observed for the Znx Cd1-x S/alginate core/shell nanoparticles due to the surface changes from the alginate coating. Alginates 90-98 CD1c molecule Homo sapiens 82-85 24833283-5 2015 Two emissions related to zinc and sulfide ion vacancies were observed for the Znx Cd1-x S/alginate core/shell nanoparticles due to the surface changes from the alginate coating. Alginates 160-168 CD1c molecule Homo sapiens 82-85 24833283-6 2015 A cadmium-related emission was observed for both the uncovered Znx Cd1-x S and Znx Cd1-x S/alginate core/shell nanoparticles, which has a significant blue-shift with increasing Zn/Cd molar ratio. Cadmium 2-9 CD1c molecule Homo sapiens 67-70 24833283-6 2015 A cadmium-related emission was observed for both the uncovered Znx Cd1-x S and Znx Cd1-x S/alginate core/shell nanoparticles, which has a significant blue-shift with increasing Zn/Cd molar ratio. Cadmium 2-9 CD1c molecule Homo sapiens 83-86 24833283-6 2015 A cadmium-related emission was observed for both the uncovered Znx Cd1-x S and Znx Cd1-x S/alginate core/shell nanoparticles, which has a significant blue-shift with increasing Zn/Cd molar ratio. znx 63-66 CD1c molecule Homo sapiens 67-70 24833283-6 2015 A cadmium-related emission was observed for both the uncovered Znx Cd1-x S and Znx Cd1-x S/alginate core/shell nanoparticles, which has a significant blue-shift with increasing Zn/Cd molar ratio. Alginates 91-99 CD1c molecule Homo sapiens 83-86 24833283-6 2015 A cadmium-related emission was observed for both the uncovered Znx Cd1-x S and Znx Cd1-x S/alginate core/shell nanoparticles, which has a significant blue-shift with increasing Zn/Cd molar ratio. Zinc 63-65 CD1c molecule Homo sapiens 67-70 25248321-8 2015 Furthermore, RA and/or CD38 ligation increased splenocyte proliferation and differentiation after treatment with the CD1 ligand alpha-galactosylceramide (alphaGalCer), evidenced by an increase in the number of splenic dendritic cells, NKT cells, and germinal center plasmacytes. alpha-galactosylceramide 128-152 CD1c molecule Homo sapiens 117-120 25298532-4 2014 Our structure of CD1c with the mycobacterial phosphomycoketide (PM) shows similarities to that of CD1c-mannosyl-beta1-phosphomycoketide in that the A" pocket accommodates the mycoketide alkyl chain; however, the phosphate head-group of PM is shifted ~6 A in relation to that of mannosyl-beta1-PM. phosphomycoketide 45-62 CD1c molecule Homo sapiens 17-21 25293653-0 2014 Enhanced visible-light photocatalytic H2 production by Znx Cd1-x S modified with earth-abundant nickel-based cocatalysts. Hydrogen 38-40 CD1c molecule Homo sapiens 59-62 25293653-0 2014 Enhanced visible-light photocatalytic H2 production by Znx Cd1-x S modified with earth-abundant nickel-based cocatalysts. Nickel 96-102 CD1c molecule Homo sapiens 59-62 25293653-1 2014 The application of various earth-abundant Ni species, such as NiS, Ni, Ni(OH)2 , and NiO, as a co-catalyst in a Znx Cd1-x S system for visible-light photocatalytic H2 production was investigated for the first time. Nickel 62-65 CD1c molecule Homo sapiens 116-119 25293653-1 2014 The application of various earth-abundant Ni species, such as NiS, Ni, Ni(OH)2 , and NiO, as a co-catalyst in a Znx Cd1-x S system for visible-light photocatalytic H2 production was investigated for the first time. nio 85-88 CD1c molecule Homo sapiens 116-119 25293653-1 2014 The application of various earth-abundant Ni species, such as NiS, Ni, Ni(OH)2 , and NiO, as a co-catalyst in a Znx Cd1-x S system for visible-light photocatalytic H2 production was investigated for the first time. Hydrogen 164-166 CD1c molecule Homo sapiens 116-119 25293653-2 2014 The loading of Ni or NiS enhanced the photocatalytic activity of Znx Cd1-x S because they could promote the electron transfer at the interface with Znx Cd1-x S and catalyze the H2 evolution. Nickel 21-24 CD1c molecule Homo sapiens 69-72 25293653-2 2014 The loading of Ni or NiS enhanced the photocatalytic activity of Znx Cd1-x S because they could promote the electron transfer at the interface with Znx Cd1-x S and catalyze the H2 evolution. Nickel 21-24 CD1c molecule Homo sapiens 152-155 25293653-3 2014 Surprisingly, Ni(OH)2 -loaded Znx Cd1-x S exhibits a very high photocatalytic H2 -production rate of 7160 mumol h(-1) g(-1) with a quantum efficiency of 29.5 % at 420 nm, which represents one of the most efficient metal sulfide photocatalysts without a Pt co-catalyst to date. nickel hydroxide 14-21 CD1c molecule Homo sapiens 34-37 25293653-3 2014 Surprisingly, Ni(OH)2 -loaded Znx Cd1-x S exhibits a very high photocatalytic H2 -production rate of 7160 mumol h(-1) g(-1) with a quantum efficiency of 29.5 % at 420 nm, which represents one of the most efficient metal sulfide photocatalysts without a Pt co-catalyst to date. Hydrogen 78-80 CD1c molecule Homo sapiens 34-37 25293653-3 2014 Surprisingly, Ni(OH)2 -loaded Znx Cd1-x S exhibits a very high photocatalytic H2 -production rate of 7160 mumol h(-1) g(-1) with a quantum efficiency of 29.5 % at 420 nm, which represents one of the most efficient metal sulfide photocatalysts without a Pt co-catalyst to date. metal sulfide 215-228 CD1c molecule Homo sapiens 34-37 25293653-5 2014 However, the loading of NiO deactivated the activity of Znx Cd1-x S because of their unmatched conduction band positions. nio 24-27 CD1c molecule Homo sapiens 60-63 25293653-6 2014 This paper reports the optimization of the Znx Cd1-x S system by selecting an appropriate Ni-based co-catalyst, Ni(OH)2 , from a series of Ni species to achieve the highest photocatalytic H2 -production activity for the first time and also reveals the roles of these Ni species in the photocatalytic activity. nickel hydroxide 112-119 CD1c molecule Homo sapiens 47-50 25293653-6 2014 This paper reports the optimization of the Znx Cd1-x S system by selecting an appropriate Ni-based co-catalyst, Ni(OH)2 , from a series of Ni species to achieve the highest photocatalytic H2 -production activity for the first time and also reveals the roles of these Ni species in the photocatalytic activity. Hydrogen 188-190 CD1c molecule Homo sapiens 47-50 25298532-4 2014 Our structure of CD1c with the mycobacterial phosphomycoketide (PM) shows similarities to that of CD1c-mannosyl-beta1-phosphomycoketide in that the A" pocket accommodates the mycoketide alkyl chain; however, the phosphate head-group of PM is shifted ~6 A in relation to that of mannosyl-beta1-PM. phosphomycoketide 45-62 CD1c molecule Homo sapiens 98-102 25298532-4 2014 Our structure of CD1c with the mycobacterial phosphomycoketide (PM) shows similarities to that of CD1c-mannosyl-beta1-phosphomycoketide in that the A" pocket accommodates the mycoketide alkyl chain; however, the phosphate head-group of PM is shifted ~6 A in relation to that of mannosyl-beta1-PM. pipermethystine 64-66 CD1c molecule Homo sapiens 17-21 25298532-4 2014 Our structure of CD1c with the mycobacterial phosphomycoketide (PM) shows similarities to that of CD1c-mannosyl-beta1-phosphomycoketide in that the A" pocket accommodates the mycoketide alkyl chain; however, the phosphate head-group of PM is shifted ~6 A in relation to that of mannosyl-beta1-PM. pipermethystine 64-66 CD1c molecule Homo sapiens 98-102 25298532-4 2014 Our structure of CD1c with the mycobacterial phosphomycoketide (PM) shows similarities to that of CD1c-mannosyl-beta1-phosphomycoketide in that the A" pocket accommodates the mycoketide alkyl chain; however, the phosphate head-group of PM is shifted ~6 A in relation to that of mannosyl-beta1-PM. mycoketide alkyl 175-191 CD1c molecule Homo sapiens 17-21 25298532-4 2014 Our structure of CD1c with the mycobacterial phosphomycoketide (PM) shows similarities to that of CD1c-mannosyl-beta1-phosphomycoketide in that the A" pocket accommodates the mycoketide alkyl chain; however, the phosphate head-group of PM is shifted ~6 A in relation to that of mannosyl-beta1-PM. mycoketide alkyl 175-191 CD1c molecule Homo sapiens 98-102 25298532-4 2014 Our structure of CD1c with the mycobacterial phosphomycoketide (PM) shows similarities to that of CD1c-mannosyl-beta1-phosphomycoketide in that the A" pocket accommodates the mycoketide alkyl chain; however, the phosphate head-group of PM is shifted ~6 A in relation to that of mannosyl-beta1-PM. Phosphates 212-221 CD1c molecule Homo sapiens 17-21 25298532-4 2014 Our structure of CD1c with the mycobacterial phosphomycoketide (PM) shows similarities to that of CD1c-mannosyl-beta1-phosphomycoketide in that the A" pocket accommodates the mycoketide alkyl chain; however, the phosphate head-group of PM is shifted ~6 A in relation to that of mannosyl-beta1-PM. Phosphates 212-221 CD1c molecule Homo sapiens 98-102 25298532-4 2014 Our structure of CD1c with the mycobacterial phosphomycoketide (PM) shows similarities to that of CD1c-mannosyl-beta1-phosphomycoketide in that the A" pocket accommodates the mycoketide alkyl chain; however, the phosphate head-group of PM is shifted ~6 A in relation to that of mannosyl-beta1-PM. mannosyl-beta1-pm 278-295 CD1c molecule Homo sapiens 17-21 25298532-4 2014 Our structure of CD1c with the mycobacterial phosphomycoketide (PM) shows similarities to that of CD1c-mannosyl-beta1-phosphomycoketide in that the A" pocket accommodates the mycoketide alkyl chain; however, the phosphate head-group of PM is shifted ~6 A in relation to that of mannosyl-beta1-PM. mannosyl-beta1-pm 278-295 CD1c molecule Homo sapiens 98-102 25298532-5 2014 We also demonstrate a bona fide interaction between six human TCRs and CD1c-mycoketide complexes, measuring high to moderate affinities. mycoketide 76-86 CD1c molecule Homo sapiens 71-75 24935257-2 2014 We report that CD1c self-reactive T cells recognize a novel class of self-lipids, identified as methyl-lysophosphatidic acids (mLPAs), which are accumulated in leukemia cells. methyl-lysophosphatidic acids 96-125 CD1c molecule Homo sapiens 15-19 25111504-4 2014 Treatment of CD1c+ mDCs with an ABCG2 inhibitor, Ko143, during LPS stimulation caused increased production of IL-10 and decreased production of pro-inflammatory cytokines and decreased expression of CD83 and CD86. 3-(6-isobutyl-9-methoxy-1,4-dioxo-1,2,3,4,6,7,12,12a-octahydropyrazino(1',2'-1,6)pyrido(3,4-b)indol-3-yl)propionic acid tert-butyl ester 49-54 CD1c molecule Homo sapiens 13-17 25111504-6 2014 Furthermore, CD1c+ mDCs stimulated with LPS plus Ko143 inhibited the proliferation of allogeneic and superantigen-specific syngenic CD4+ T cells and promoted expansion of CD25+FOXP3+ regulatory T (Treg) cells in an IL-10-dependent fashion. 3-(6-isobutyl-9-methoxy-1,4-dioxo-1,2,3,4,6,7,12,12a-octahydropyrazino(1',2'-1,6)pyrido(3,4-b)indol-3-yl)propionic acid tert-butyl ester 49-54 CD1c molecule Homo sapiens 13-17 24515122-6 2014 Biosynthesis of the isobacteriochlorin heme d 1, a cofactor of the dissimilatory nitrite reductase cytochrome cd 1, has also been a subject of much research, although the biosynthetic pathway and its intermediates have evaded discovery for quite some time. isobacteriochlorin heme 20-43 CD1c molecule Homo sapiens 110-114 24398472-1 2014 Three phenothiazine-triphenylamine-based organic dyes (CD-1, CD-2 and CD-3) are designed based on the dye WD-8. phenothiazine-triphenylamine 6-34 CD1c molecule Homo sapiens 55-59 23966631-0 2013 Human CD1c+ myeloid dendritic cells acquire a high level of retinoic acid-producing capacity in response to vitamin D3. Tretinoin 60-73 CD1c molecule Homo sapiens 6-10 24598728-2 2014 Compared to Cd0, Cd1.5 increased fungal abundance but decreased bacterial abundance under both CO2 levels, whilst Cd3.0 and Cd6.0 decreased both fungal and bacterial abundance. N2,N6-bis(4-(2-aminoethoxy)quinolin-2-yl)-4-((4-fluorobenzyl)oxy)pyridine-2,6-dicarboxamide 95-98 CD1c molecule Homo sapiens 17-20 24322372-7 2013 Consistent with in vitro, In CD1c(+) or CD14(+) cells from cirrhotic patients, the gene expression of 2-oxoglutarate-succinate-fumarate transition enzymes were significantly different from the cells of healthy controls. 2-oxoglutarate-succinate-fumarate 102-135 CD1c molecule Homo sapiens 29-33 24106224-1 2013 In this work, two different synthetic pathways were devised to prepare surface and bulk Cu(2+)-modified Znx Cd1-x S photocatalysts through cation-exchange and coprecipitation methods, respectively. cupric ion 88-94 CD1c molecule Homo sapiens 108-111 24106224-3 2013 The optimized Cu(2+)-surface-modified Znx Cd1-x S photocatalyst has a high H2-production rate of 4638.5 mumolh(-1) g(-1) and an apparent quantum efficiency of 20.9% at 420 nm, exceeding that of Cu(2+)-bulk-modified catalyst at the same copper content. cupric ion 14-20 CD1c molecule Homo sapiens 42-45 24106224-3 2013 The optimized Cu(2+)-surface-modified Znx Cd1-x S photocatalyst has a high H2-production rate of 4638.5 mumolh(-1) g(-1) and an apparent quantum efficiency of 20.9% at 420 nm, exceeding that of Cu(2+)-bulk-modified catalyst at the same copper content. Hydrogen 75-77 CD1c molecule Homo sapiens 42-45 24106224-3 2013 The optimized Cu(2+)-surface-modified Znx Cd1-x S photocatalyst has a high H2-production rate of 4638.5 mumolh(-1) g(-1) and an apparent quantum efficiency of 20.9% at 420 nm, exceeding that of Cu(2+)-bulk-modified catalyst at the same copper content. cupric ion 194-200 CD1c molecule Homo sapiens 42-45 24106224-3 2013 The optimized Cu(2+)-surface-modified Znx Cd1-x S photocatalyst has a high H2-production rate of 4638.5 mumolh(-1) g(-1) and an apparent quantum efficiency of 20.9% at 420 nm, exceeding that of Cu(2+)-bulk-modified catalyst at the same copper content. Copper 236-242 CD1c molecule Homo sapiens 42-45 23835090-7 2013 RESULTS: During cladribine treatment the myeloid DCs CD1c(+)/CD19(-) did not change (p=0.73175), and the plasmacytoid DCs CD303(+)/CD123(+) significantly increased (p=0.00034) which resulted in significant changes in the ratio of myeloid DCs to plasmacytoid DCs (p=0.00273). Cladribine 16-26 CD1c molecule Homo sapiens 53-57 24650765-9 2014 In SLE patients treated with corticosteroids, Mer expression on monocytes correlated with prednisone dose, CD1c+ myeloid dendritic cells in patients treated with prednisone had higher levels of Mer expression than those in patients not receiving prednisone. Prednisone 162-172 CD1c molecule Homo sapiens 107-111 24650765-9 2014 In SLE patients treated with corticosteroids, Mer expression on monocytes correlated with prednisone dose, CD1c+ myeloid dendritic cells in patients treated with prednisone had higher levels of Mer expression than those in patients not receiving prednisone. Prednisone 162-172 CD1c molecule Homo sapiens 107-111 24471820-0 2014 Case report: prenatal diagnosis of Hb Hammersmith [beta42(CD1)Phe Ser; HBB: c.128T > C] in a family with an adult male patient. Phenylalanine 62-65 CD1c molecule Homo sapiens 58-61 24471820-0 2014 Case report: prenatal diagnosis of Hb Hammersmith [beta42(CD1)Phe Ser; HBB: c.128T > C] in a family with an adult male patient. Serine 66-69 CD1c molecule Homo sapiens 58-61 24471820-1 2014 Hb Hammersmith [beta42(CD1)Phe Ser; HBB: c.128T > C] is a rare, unstable hemoglobin (Hb) variant. Phenylalanine 27-30 CD1c molecule Homo sapiens 23-26 24471820-1 2014 Hb Hammersmith [beta42(CD1)Phe Ser; HBB: c.128T > C] is a rare, unstable hemoglobin (Hb) variant. Serine 33-36 CD1c molecule Homo sapiens 23-26 24134838-3 2013 GMM-specific, CD1-restricted T cell responses have been detected in the peripheral blood of infected human subjects and monkeys as well as in secondary lymphoid organs of small animals, such as guinea pigs and human CD1-transgenic mice. glucose mycolate 0-3 CD1c molecule Homo sapiens 14-17 24134838-3 2013 GMM-specific, CD1-restricted T cell responses have been detected in the peripheral blood of infected human subjects and monkeys as well as in secondary lymphoid organs of small animals, such as guinea pigs and human CD1-transgenic mice. glucose mycolate 0-3 CD1c molecule Homo sapiens 216-219 23966631-0 2013 Human CD1c+ myeloid dendritic cells acquire a high level of retinoic acid-producing capacity in response to vitamin D3. Cholecalciferol 108-118 CD1c molecule Homo sapiens 6-10 23966631-4 2013 In this study, we show that CD1c+ blood myeloid DCs (mDCs) but not CD141(high) mDCs or plasmacytoid DCs exhibited a high level of RALDH2 mRNA and aldehyde dehydrogenase (ALDH) activity in an RA- and p38-dependent manner when stimulated with 1alpha,25-dihydroxyvitamin D3 (VD3) in the presence of GM-CSF. Tretinoin 130-132 CD1c molecule Homo sapiens 28-32 23966631-9 2013 This study suggests that CD1c+ mDCs are a major human DC subset that produces RA in response to VD3 in the steady state. Tretinoin 78-80 CD1c molecule Homo sapiens 25-29 23885215-4 2013 We demonstrate here that CD1c, which is co-expressed with CD1d on blood dendritic cells and on a fraction of B cells, is able to present alpha-galactosylceramide (alpha-GalCer) as a weak agonist to human iNKT cells, and that the presence of CD1c synergistically enhances alpha-GalCerdependent activation of iNKT cells by CD1d. alpha-galactosylceramide 137-161 CD1c molecule Homo sapiens 25-29 23883429-0 2013 One-step synthesis of highly efficient three-dimensional Cd1-xZnxS photocatalysts for visible light photocatalytic water splitting. Water 115-120 CD1c molecule Homo sapiens 57-60 23883429-2 2013 In this work, highly efficient three-dimensional (3D) Cd1-xZnxS photocatalysts for hydrogen generation under the irradiation of visible light were synthesized via one-step solvothermal pathway. Hydrogen 83-91 CD1c molecule Homo sapiens 54-57 23499788-5 2013 To test this hypothesis, we have synthesized three novel Cd-containing complexes: [Cd2(C12H12O2N)4(H2O)2] 2H2O (Cd1), [Cd2(C11H10O2N)4(H2O)2] 2H2O (Cd2) and [Cd(C7H4N2O2)(C8H6O2)2] 2H2O (Cd3), by using these three ligands. Cadmium 57-59 CD1c molecule Homo sapiens 112-115 23885215-4 2013 We demonstrate here that CD1c, which is co-expressed with CD1d on blood dendritic cells and on a fraction of B cells, is able to present alpha-galactosylceramide (alpha-GalCer) as a weak agonist to human iNKT cells, and that the presence of CD1c synergistically enhances alpha-GalCerdependent activation of iNKT cells by CD1d. alpha-galactosylceramide 137-161 CD1c molecule Homo sapiens 241-245 23885215-6 2013 These results suggest that therapeutic activation of human iNKT cells by alpha-GSLs will be driven preferentially by CD1c+ cell types. alpha-gsls 73-83 CD1c molecule Homo sapiens 117-121 23885215-7 2013 Thus, B cell neoplasias that co-express CD1c and CD1d may be particularly susceptible to alpha-GSL therapy, and cancer vaccines using alpha-GSLs as adjuvants may be most effective when presented by CD1c+ antigen-presenting cells. alpha-gsl 89-98 CD1c molecule Homo sapiens 40-44 23885215-7 2013 Thus, B cell neoplasias that co-express CD1c and CD1d may be particularly susceptible to alpha-GSL therapy, and cancer vaccines using alpha-GSLs as adjuvants may be most effective when presented by CD1c+ antigen-presenting cells. alpha-gsls 134-144 CD1c molecule Homo sapiens 198-202 23569327-7 2013 In addition, BDCA1(+) and BDCA3(+) DCs display similar phagosomal pH and similar production of reactive oxygen species in their phagosomes. Reactive Oxygen Species 95-118 CD1c molecule Homo sapiens 13-18 23905339-1 2013 Cd1-xZnxTe:Cu Thin films were prepared by co-evaporation method. Copper 11-13 CD1c molecule Homo sapiens 0-3 23536373-7 2013 The W/W(V) recipient testes transplanted with F3 offspring germ cells from the DEHP-treated group had a dramatically lower percentage of donor germ cell-derived spermatogenic recovery in seminiferous tubules when compared to the recipient testes transplanted with CD1 control germ cells. Diethylhexyl Phthalate 79-83 CD1c molecule Homo sapiens 264-267 23905339-3 2013 The results show that the resistivity of 10% copper doped Cd1-x ZnxTe films increased several magnitude and the conductive type changed from p-type to n-type after annealing. Copper 45-51 CD1c molecule Homo sapiens 58-61 23905339-5 2013 The transmissivity of 30% cu-doped Cd1-x, ZnxTe films decreased seriously below 10% after annealing, which indicate that they are not suitable to be the top cell materials in tandem structure. Copper 26-28 CD1c molecule Homo sapiens 35-38 23905339-5 2013 The transmissivity of 30% cu-doped Cd1-x, ZnxTe films decreased seriously below 10% after annealing, which indicate that they are not suitable to be the top cell materials in tandem structure. znxte 42-47 CD1c molecule Homo sapiens 35-38 23905339-6 2013 The 20% and 30% cu-doped Cd1-x Zn, Te films were both p-type conductivity. Copper 16-18 CD1c molecule Homo sapiens 25-28 23905339-6 2013 The 20% and 30% cu-doped Cd1-x Zn, Te films were both p-type conductivity. Zinc 31-33 CD1c molecule Homo sapiens 25-28 23359487-4 2013 From a methanol solution containing CNacacH (L) and Cd(OAc)(2) 2 H(2)O (M), a coordination polymer (Cd-1) in which trans-[Cd(CNacac)(2)] units are three-dimensionally linked was obtained. Methanol 7-15 CD1c molecule Homo sapiens 100-104 23530121-0 2013 CD1c tetramers detect ex vivo T cell responses to processed phosphomycoketide antigens. phosphomycoketide 60-77 CD1c molecule Homo sapiens 0-4 23530121-2 2013 Using a CD1c-reactive T cell line (DN6) to complete an organism-wide survey of M. tuberculosis lipids, we identified C32 phosphomycoketide (PM) as a previously unknown molecule and a CD1c-presented antigen. C32 phosphomycoketide 117-138 CD1c molecule Homo sapiens 8-12 23530121-6 2013 These studies identify antigen processing of a natural bacterial antigen in the human CD1c system, indicating that cells act on glycolipids to generate a highly simplified neoepitope composed of a sugar-free phosphate anion. Glycolipids 128-139 CD1c molecule Homo sapiens 86-90 23530121-6 2013 These studies identify antigen processing of a natural bacterial antigen in the human CD1c system, indicating that cells act on glycolipids to generate a highly simplified neoepitope composed of a sugar-free phosphate anion. Sugars 197-202 CD1c molecule Homo sapiens 86-90 23530121-6 2013 These studies identify antigen processing of a natural bacterial antigen in the human CD1c system, indicating that cells act on glycolipids to generate a highly simplified neoepitope composed of a sugar-free phosphate anion. phosphate anion 208-223 CD1c molecule Homo sapiens 86-90 23518712-7 2013 In laquinimod-treated patients with multiple sclerosis we consistently found reduced chemokine and cytokine secretion by conventional CD1c+ dendritic cells upon lipopolysaccharide stimulation. laquinimod 3-13 CD1c molecule Homo sapiens 134-138 23518712-8 2013 Similarly to the animal model of relapsing-remitting multiple sclerosis, dendritic cell subsets were altered in patients upon laquinimod treatment, as the number of conventional CD1c+ and plasmacytoid CD303+ dendritic cells were decreased within peripheral blood mononuclear cells. laquinimod 126-136 CD1c molecule Homo sapiens 178-182 23359487-4 2013 From a methanol solution containing CNacacH (L) and Cd(OAc)(2) 2 H(2)O (M), a coordination polymer (Cd-1) in which trans-[Cd(CNacac)(2)] units are three-dimensionally linked was obtained. cd(oac) 52-59 CD1c molecule Homo sapiens 100-104 23359487-4 2013 From a methanol solution containing CNacacH (L) and Cd(OAc)(2) 2 H(2)O (M), a coordination polymer (Cd-1) in which trans-[Cd(CNacac)(2)] units are three-dimensionally linked was obtained. Cadmium 52-54 CD1c molecule Homo sapiens 100-104 23132493-7 2013 Furthermore, the GMM-specific T cells were able to extravasate and approach the site of infection where CD1c(+) cells accumulated. glucose mycolate 17-20 CD1c molecule Homo sapiens 104-108 22541298-1 2012 Inspired by beta-CD, a macrocyclic oligomers of D-(+)-glucopyranose and a renewable material, which could be obtained from starch, that can promote a lot of organic reactions in water, a green solvent, several amino alcohol-modified beta-CDs CD-1 to CD-7 were synthesized in the yields of 36-61%. betadex 12-19 CD1c molecule Homo sapiens 242-246 22829134-1 2012 alphabeta T-cell lines specific for sulfatide, an abundant myelin glycosphingolipid presented by various CD1 molecules, have been previously derived from PBMCs of patients with demyelinating diseases such as multiple sclerosis (MS) but also from healthy subjects. Sulfoglycosphingolipids 36-45 CD1c molecule Homo sapiens 105-108 22829134-7 2012 Together with previous reports, they support the notion that human Vdelta1 T cells are enriched in CD1-specific T cells and suggest that the Vdelta1 T-cell population that accumulates in MS lesions might be enriched in CD1-sulfatide-specific cells. Sulfoglycosphingolipids 223-232 CD1c molecule Homo sapiens 219-222 22541298-1 2012 Inspired by beta-CD, a macrocyclic oligomers of D-(+)-glucopyranose and a renewable material, which could be obtained from starch, that can promote a lot of organic reactions in water, a green solvent, several amino alcohol-modified beta-CDs CD-1 to CD-7 were synthesized in the yields of 36-61%. d-(+)-glucopyranose 48-67 CD1c molecule Homo sapiens 242-246 22541298-1 2012 Inspired by beta-CD, a macrocyclic oligomers of D-(+)-glucopyranose and a renewable material, which could be obtained from starch, that can promote a lot of organic reactions in water, a green solvent, several amino alcohol-modified beta-CDs CD-1 to CD-7 were synthesized in the yields of 36-61%. Starch 123-129 CD1c molecule Homo sapiens 242-246 22541298-1 2012 Inspired by beta-CD, a macrocyclic oligomers of D-(+)-glucopyranose and a renewable material, which could be obtained from starch, that can promote a lot of organic reactions in water, a green solvent, several amino alcohol-modified beta-CDs CD-1 to CD-7 were synthesized in the yields of 36-61%. Water 178-183 CD1c molecule Homo sapiens 242-246 22541298-1 2012 Inspired by beta-CD, a macrocyclic oligomers of D-(+)-glucopyranose and a renewable material, which could be obtained from starch, that can promote a lot of organic reactions in water, a green solvent, several amino alcohol-modified beta-CDs CD-1 to CD-7 were synthesized in the yields of 36-61%. Amino Alcohols 210-223 CD1c molecule Homo sapiens 242-246 22541298-5 2012 For the optimal one, CD-1, moderate enantioselectivity (56% ee) was achieved in aqueous CH(3)COONa-HCl buffer solution (pH 7.0). (3)coona-hcl 90-102 CD1c molecule Homo sapiens 21-25 22541298-8 2012 The moderate enantioselectivity was attributed to the two different binding models between CD-1 and thioanisole, which could be defined as intramolecular catalysis and intermolecular catalysis, in which intramolecular catalysis gave (S)-methyl phenyl sulfoxide and intermolecular catalysis gave (R,S)-methyl phenyl sulfoxide. methylphenylsulfide 100-111 CD1c molecule Homo sapiens 91-95 22541298-8 2012 The moderate enantioselectivity was attributed to the two different binding models between CD-1 and thioanisole, which could be defined as intramolecular catalysis and intermolecular catalysis, in which intramolecular catalysis gave (S)-methyl phenyl sulfoxide and intermolecular catalysis gave (R,S)-methyl phenyl sulfoxide. methyl phenyl sulfoxide 233-260 CD1c molecule Homo sapiens 91-95 22541298-8 2012 The moderate enantioselectivity was attributed to the two different binding models between CD-1 and thioanisole, which could be defined as intramolecular catalysis and intermolecular catalysis, in which intramolecular catalysis gave (S)-methyl phenyl sulfoxide and intermolecular catalysis gave (R,S)-methyl phenyl sulfoxide. (r,s)-methyl phenyl sulfoxide 295-324 CD1c molecule Homo sapiens 91-95 23057161-6 2012 In contrast, treatment of immature dendritic cells with aspirin, dexamethasone, 1alpha,25-dihydroxyvitamin D3 (VD3) or butyric acid was associated with diminished expression of CD1a, CD1c, CD40, CD80 and CD83. Calcitriol 80-109 CD1c molecule Homo sapiens 183-187 23057161-6 2012 In contrast, treatment of immature dendritic cells with aspirin, dexamethasone, 1alpha,25-dihydroxyvitamin D3 (VD3) or butyric acid was associated with diminished expression of CD1a, CD1c, CD40, CD80 and CD83. Aspirin 56-63 CD1c molecule Homo sapiens 183-187 22296515-1 2012 A chiral coordination nanotube, [Cd(3)(BPT)(2)(H(2)O)(9)] 2H(2)O (Cd-1; BPT = biphenyl-3,4",5-tricarboxylate), has been synthesized from achiral components and structurally characterized. [cd(3)(bpt)( 32-44 CD1c molecule Homo sapiens 66-70 22296515-1 2012 A chiral coordination nanotube, [Cd(3)(BPT)(2)(H(2)O)(9)] 2H(2)O (Cd-1; BPT = biphenyl-3,4",5-tricarboxylate), has been synthesized from achiral components and structurally characterized. )(h(2)o)(9)] 2h(2)o 45-64 CD1c molecule Homo sapiens 66-70 21575695-2 2012 The high-affinity CD1d antigen alpha-galactosylceramide analogue KRN7000 (KRN) activates a cascade of anti-tumor effector cells and clinical studies have already had some initial success. alpha-galactosylceramide 31-55 CD1c molecule Homo sapiens 18-21 23057161-6 2012 In contrast, treatment of immature dendritic cells with aspirin, dexamethasone, 1alpha,25-dihydroxyvitamin D3 (VD3) or butyric acid was associated with diminished expression of CD1a, CD1c, CD40, CD80 and CD83. Butyric Acid 119-131 CD1c molecule Homo sapiens 183-187 23057161-6 2012 In contrast, treatment of immature dendritic cells with aspirin, dexamethasone, 1alpha,25-dihydroxyvitamin D3 (VD3) or butyric acid was associated with diminished expression of CD1a, CD1c, CD40, CD80 and CD83. Dexamethasone 65-78 CD1c molecule Homo sapiens 183-187 19735672-1 2010 The CD1 molecules are cell-surface proteins that bind and present foreign lipids and glycolipids to T cells in a manner similar to the MHC system. Glycolipids 85-96 CD1c molecule Homo sapiens 4-7 22217314-0 2012 A case report of a male patient with Hb Hammersmith [beta42(CD1)Phe Ser, TTT>TCT]. Phenylalanine 64-67 CD1c molecule Homo sapiens 60-63 22217314-0 2012 A case report of a male patient with Hb Hammersmith [beta42(CD1)Phe Ser, TTT>TCT]. Serine 68-71 CD1c molecule Homo sapiens 60-63 22217314-1 2012 All Hb Hammersmith [beta42(CD1)Phe Ser, TTT>TCT] patients reported so far have been female, suggesting that this condition may occur as a negative, fatal intrauterine selection against males. Phenylalanine 31-34 CD1c molecule Homo sapiens 27-30 21893110-0 2011 Ultra-high olfactory sensitivity for the human sperm-attractant aromatic aldehyde bourgeonal in CD-1 mice. benzaldehyde 64-81 CD1c molecule Homo sapiens 96-100 21711522-6 2011 RESULTS: NK cells were conjugated with B-cell targets lacking major histocompatibility complex class I 721.221 cells, and iNKT cells were conjugated with glycolipid-pulsed CD1-bearing targets, then prepared for thin-section electron microscopy. Glycolipids 154-164 CD1c molecule Homo sapiens 172-175 21253820-5 2011 Specifically, CD1 pups, SVZ tissues and isolated NSC and BEC exhibit less GSK-3beta and beta-catenin serine phoslphorylation and greater HIF-1alpha and 2alpha, BDNF, SDF-1 and VEGF, beta-III-tubulin and cleaved notch-1 expression compared to C57BL/6. Serine 101-107 CD1c molecule Homo sapiens 14-17 21253820-7 2011 Further, upon treatment with nanomolar concentrations of a GSK-3beta inhibitor (SB412682), C57 NSC and BEC behaviors could be brought to CD1 levels, consistent with the concept of GSK-3beta functioning as a multifunctional signaling pathway node, modulating several behaviors in these cells. sb412682 80-88 CD1c molecule Homo sapiens 137-140 20652710-12 2011 OxLDL-induced DC differentiation was partially inhibited by quercetin (BDCA-1-29%; BDCA-2-33%; p < 0.05). Quercetin 60-69 CD1c molecule Homo sapiens 71-77 21603161-1 2011 Group I CD1 (CD1a, CD1b, and CD1c) glycoproteins expressed on immature and mature dendritic cells present nonpeptide antigens (i.e., lipid or glycolipid molecules mainly of microbial origin) to T cells. Glycolipids 142-152 CD1c molecule Homo sapiens 29-33 21167756-2 2010 Here we present the crystal structure of CD1c at 2.5 A resolution, in complex with the pathogenic Mycobacterium tuberculosis antigen mannosyl-beta1-phosphomycoketide (MPM). mannosyl-beta1-phosphomycoketide 133-165 CD1c molecule Homo sapiens 41-45 21167756-2 2010 Here we present the crystal structure of CD1c at 2.5 A resolution, in complex with the pathogenic Mycobacterium tuberculosis antigen mannosyl-beta1-phosphomycoketide (MPM). mpm 167-170 CD1c molecule Homo sapiens 41-45 21167756-5 2010 This feature, combined with tryptophan-fluorescence quenching during loading of a dodecameric lipopeptide antigen, provides a compelling model by which both the lipid and peptide moieties of the lipopeptide are involved in CD1c presentation of lipopeptides. Tryptophan 28-38 CD1c molecule Homo sapiens 223-227 20944137-6 2010 CD-1-transfected cells also had higher cell death when treated with CDDP (p<0.05) or PAX, exhibiting 30-60% higher death rates than cells transfected with the wt-p53 gene and 130-160% higher than untransfected cells. Cisplatin 68-72 CD1c molecule Homo sapiens 0-4 20944137-6 2010 CD-1-transfected cells also had higher cell death when treated with CDDP (p<0.05) or PAX, exhibiting 30-60% higher death rates than cells transfected with the wt-p53 gene and 130-160% higher than untransfected cells. Paclitaxel 88-91 CD1c molecule Homo sapiens 0-4 20479116-5 2010 Polyinosine-polycytidylic acid (poly I:C)-activated CD141+ DCs have a superior capacity to cross-present soluble protein antigen (Ag) to CD8+ cytotoxic T lymphocytes than poly I:C-activated CD1c+ DCs. polyinosine-polycytidylic acid 0-30 CD1c molecule Homo sapiens 190-194 20479116-5 2010 Polyinosine-polycytidylic acid (poly I:C)-activated CD141+ DCs have a superior capacity to cross-present soluble protein antigen (Ag) to CD8+ cytotoxic T lymphocytes than poly I:C-activated CD1c+ DCs. Poly I 32-38 CD1c molecule Homo sapiens 190-194 20479116-5 2010 Polyinosine-polycytidylic acid (poly I:C)-activated CD141+ DCs have a superior capacity to cross-present soluble protein antigen (Ag) to CD8+ cytotoxic T lymphocytes than poly I:C-activated CD1c+ DCs. Carbon 39-40 CD1c molecule Homo sapiens 190-194 20479116-5 2010 Polyinosine-polycytidylic acid (poly I:C)-activated CD141+ DCs have a superior capacity to cross-present soluble protein antigen (Ag) to CD8+ cytotoxic T lymphocytes than poly I:C-activated CD1c+ DCs. poly I:C 32-40 CD1c molecule Homo sapiens 190-194 20433173-3 2010 The identified optimal catalyst CD-1 shows interesting characteristics of supramolecular catalysis with selective recognition of aldol acceptors and donors. 3-hydroxybutanal 129-134 CD1c molecule Homo sapiens 32-36 20433173-5 2010 It is revealed that the reaction is initialized first by binding substrates into the cyclodextrin cavity via a synergistic action of hydrophobic interaction and noncovalent interaction with the CD-1 side chain. Cyclodextrins 85-97 CD1c molecule Homo sapiens 194-198 20164370-1 2010 Neonatal exposure to soy isoflavones at levels similar to that of infants fed soy protein formula resulted in higher bone mineral density (BMD), improved bone structure, and greater bone strength at young adulthood in female CD-1 mice (1,2). Isoflavones 25-36 CD1c molecule Homo sapiens 225-229 22536277-5 2012 Nevertheless, recent advances in our understanding of the CD1c structure as well as the biosynthetic pathway of a CD1c-presented antigen, mannose-1, beta-phosphomycoketide, expressed by pathogenic mycobacteria now unravel a new aspect of the group 1 CD1 biology that has not been appreciated in previous studies of CD1a and CD1b molecules. mannose-1 138-147 CD1c molecule Homo sapiens 114-118 22536277-5 2012 Nevertheless, recent advances in our understanding of the CD1c structure as well as the biosynthetic pathway of a CD1c-presented antigen, mannose-1, beta-phosphomycoketide, expressed by pathogenic mycobacteria now unravel a new aspect of the group 1 CD1 biology that has not been appreciated in previous studies of CD1a and CD1b molecules. beta-phosphomycoketide 149-171 CD1c molecule Homo sapiens 58-62 22536277-5 2012 Nevertheless, recent advances in our understanding of the CD1c structure as well as the biosynthetic pathway of a CD1c-presented antigen, mannose-1, beta-phosphomycoketide, expressed by pathogenic mycobacteria now unravel a new aspect of the group 1 CD1 biology that has not been appreciated in previous studies of CD1a and CD1b molecules. beta-phosphomycoketide 149-171 CD1c molecule Homo sapiens 114-118 21461352-7 2011 RESULTS: BDCA-1 expression at baseline was lower in ONE compared to both other groups (ONE 0.15%; LNE 0.27%; LE 0.33%; P < .05), but significantly increased in ONE after training (+50%; P < .05). lne 98-101 CD1c molecule Homo sapiens 9-15 21984904-1 2011 OBJECTIVE: To explore the capacity of human CD1+CD16++ and CD14++CD16- monocytes to phagocyte iron-oxide nanoparticles in vitro. ferric oxide 94-104 CD1c molecule Homo sapiens 44-47 20364866-1 2010 The binding interaction between aggregates of the 5-chloro-2-[[5-chloro-3-(3-sulfopropyl)-3H-benzothiazol-2-ylidene]methyl]-3-(3-sulfopropyl)benzothiazolium hydroxide inner salt ammonium salt (CD-1) and alpha-helix, as well as beta-sheet forming de novo designed peptides, was investigated by absorption spectroscopy, circular dichroism spectroscopy, and cryogenic transmission electron microscopy. 5-chloro-2-[[5-chloro-3-(3-sulfopropyl)-3h-benzothiazol-2-ylidene]methyl 50-122 CD1c molecule Homo sapiens 193-197 20364866-1 2010 The binding interaction between aggregates of the 5-chloro-2-[[5-chloro-3-(3-sulfopropyl)-3H-benzothiazol-2-ylidene]methyl]-3-(3-sulfopropyl)benzothiazolium hydroxide inner salt ammonium salt (CD-1) and alpha-helix, as well as beta-sheet forming de novo designed peptides, was investigated by absorption spectroscopy, circular dichroism spectroscopy, and cryogenic transmission electron microscopy. (3-sulfopropyl)benzothiazolium hydroxide 126-166 CD1c molecule Homo sapiens 193-197 20364866-1 2010 The binding interaction between aggregates of the 5-chloro-2-[[5-chloro-3-(3-sulfopropyl)-3H-benzothiazol-2-ylidene]methyl]-3-(3-sulfopropyl)benzothiazolium hydroxide inner salt ammonium salt (CD-1) and alpha-helix, as well as beta-sheet forming de novo designed peptides, was investigated by absorption spectroscopy, circular dichroism spectroscopy, and cryogenic transmission electron microscopy. salt ammonium salt 173-191 CD1c molecule Homo sapiens 193-197 20100930-7 2010 The long endogenous ligand found inside the binding groove of chCD1-1, together with binding data on various glycolipids and mycolic acid, strongly suggest that the unique avian CD1 family could bind long dual- and possibly triacyl-chain lipids. Glycolipids 109-120 CD1c molecule Homo sapiens 64-67 20100930-7 2010 The long endogenous ligand found inside the binding groove of chCD1-1, together with binding data on various glycolipids and mycolic acid, strongly suggest that the unique avian CD1 family could bind long dual- and possibly triacyl-chain lipids. Mycolic Acids 125-137 CD1c molecule Homo sapiens 64-67 20100930-7 2010 The long endogenous ligand found inside the binding groove of chCD1-1, together with binding data on various glycolipids and mycolic acid, strongly suggest that the unique avian CD1 family could bind long dual- and possibly triacyl-chain lipids. triacyl 224-231 CD1c molecule Homo sapiens 64-67 19948070-0 2009 Human gammadelta T cell recognition of lipid A is predominately presented by CD1b or CD1c on dendritic cells. Lipid A 39-46 CD1c molecule Homo sapiens 85-89 18522857-4 2008 Butyrate treatment throughout the culture period inhibited the expression of CD1 molecules, but not on CD83, CD86, and MHC molecules. Butyrates 0-8 CD1c molecule Homo sapiens 77-80 19594637-6 2009 The hydrophobic alkyl chains are buried in the CD1d groove, with the carbohydrate exposed for TCR recognition, together with the surface of the CD1d molecule. Carbohydrates 69-81 CD1c molecule Homo sapiens 47-50 19269450-2 2009 In this work, two beta-cyclodextrin (beta-CD) bonded stationary phases for reversed-phase HPLC, including 1, 12-dodecyldiol linked beta-CD stationary phase (CD1) and olio (ethylene glycol) (OEG) linked beta-CD stationary phase (CD2), have been synthesized via click chemistry. 1, 12-dodecyldiol 106-123 CD1c molecule Homo sapiens 157-160 18930085-4 2009 GSL-liposomes containing DOPE were clearly broken in late endosomes and this may facilitate effective loading of GSLs onto CD1 molecules. Glycosphingolipids 113-117 CD1c molecule Homo sapiens 123-126 18671950-1 2008 The glycolipid alpha-galactosylceramide (alpha-GalCer), when presented on CD1 molecules by antigen presenting cells (APCs) to invariant NKT (iNKT cells), is a potent immunomodulator. Glycolipids 4-14 CD1c molecule Homo sapiens 74-77 18671950-1 2008 The glycolipid alpha-galactosylceramide (alpha-GalCer), when presented on CD1 molecules by antigen presenting cells (APCs) to invariant NKT (iNKT cells), is a potent immunomodulator. alpha-galactosylceramide 15-39 CD1c molecule Homo sapiens 74-77 18671950-1 2008 The glycolipid alpha-galactosylceramide (alpha-GalCer), when presented on CD1 molecules by antigen presenting cells (APCs) to invariant NKT (iNKT cells), is a potent immunomodulator. alpha-galactosylceramide 41-53 CD1c molecule Homo sapiens 74-77 18794101-0 2008 Sunitinib-induced myeloid lineage redistribution in renal cell cancer patients: CD1c+ dendritic cell frequency predicts progression-free survival. Sunitinib 0-9 CD1c molecule Homo sapiens 80-84 18422659-12 2008 In the field of immunology, the renaissance in mycobacterial polyisoprenoid research has led to the identification of mimetic mannosyl-beta-1-phosphomycoketides of pathogenic mycobacteria as potent lipid antigens presented by CD1c proteins to human T cells. polyisoprenoid 61-75 CD1c molecule Homo sapiens 226-230 18422659-12 2008 In the field of immunology, the renaissance in mycobacterial polyisoprenoid research has led to the identification of mimetic mannosyl-beta-1-phosphomycoketides of pathogenic mycobacteria as potent lipid antigens presented by CD1c proteins to human T cells. mannosyl-beta-1-phosphomycoketides 126-160 CD1c molecule Homo sapiens 226-230 19468063-4 2009 CD1c presented an N-acyl glycine dodecamer peptide (lipo-12) to human T cells, and the response was specific for the acyl linkage as well as the peptide length and sequence. Glycine 25-32 CD1c molecule Homo sapiens 0-4 18522857-6 2008 Butyrate-treated immature DCs also showed decreased expression of CD1 molecules. Butyrates 0-8 CD1c molecule Homo sapiens 66-69 18630620-4 2008 Profiles nearly 400 known leukocyte cell surface molecules are summarized in CD system (CD1-CD350). Cadmium 77-79 CD1c molecule Homo sapiens 88-91 17951048-0 2007 CD1 mediated T cell recognition of glycolipids. Glycolipids 35-46 CD1c molecule Homo sapiens 0-3 18006319-3 2008 Among the several (glyco)lipids identified to cause T-cell stimulation in complex with CD1, alpha-galactosyl ceramide (alpha-GalCer) is one of the most well studied. alpha-galactosylceramide 92-117 CD1c molecule Homo sapiens 87-90 18044879-0 2007 Magnetic circular dichroism evidence for a weakly coupled heme-radical pair at the active site of cytochrome cd1, a nitrite reductase. Heme 58-62 CD1c molecule Homo sapiens 109-112 18044879-1 2007 In nitrite-treated cytochrome cd1 nitrite reductase, heme d1 is electron paramagnetic resonance silent but paramagnetic. Nitrites 3-10 CD1c molecule Homo sapiens 30-33 18022562-1 2007 Human CD1c is a protein that activates alphabeta T cells by presenting self antigens, synthetic mannosyl phosphodolichols, and mycobacterial mannosyl phosphopolyketides. mannosyl phosphodolichols 96-121 CD1c molecule Homo sapiens 6-10 18022562-1 2007 Human CD1c is a protein that activates alphabeta T cells by presenting self antigens, synthetic mannosyl phosphodolichols, and mycobacterial mannosyl phosphopolyketides. mannosyl phosphopolyketides 141-168 CD1c molecule Homo sapiens 6-10 17532287-16 2007 The mechanisms that lead to the inflammatory reaction in cerebral ALD might involve abnormal acylation of gangliosides and phospholipids by VLCFA that would result in immune reaction of brain macrophages and astrocytes bearing CD1 molecules that recognize lipid antigens. Gangliosides 106-118 CD1c molecule Homo sapiens 227-230 17532287-16 2007 The mechanisms that lead to the inflammatory reaction in cerebral ALD might involve abnormal acylation of gangliosides and phospholipids by VLCFA that would result in immune reaction of brain macrophages and astrocytes bearing CD1 molecules that recognize lipid antigens. Phospholipids 123-136 CD1c molecule Homo sapiens 227-230 17951048-1 2007 Specialized subsets of T lymphocytes can distinguish the carbohydrate portions of microbial and self-glycolipids when they are presented by proteins in the CD1 family of antigen presenting molecules. Carbohydrates 57-69 CD1c molecule Homo sapiens 156-159 17951048-2 2007 Recent immunochemical and structural analyses indicate that the chemical composition of the presented carbohydrate, together with its precise orientation above the CD1 binding groove, determines if a particular T cell is activated. Carbohydrates 102-114 CD1c molecule Homo sapiens 164-167 17625898-3 2007 Supported monolayers of amphiphilic cyclodextrins CD1 and CD2 were obtained by adsorption of CD vesicles to hydrophobic substrates, and supported bilayers of amphiphilic cyclodextrins CD1 and CD2 were prepared by adsorption of CD vesicles on cationic substrates. Cyclodextrins 36-49 CD1c molecule Homo sapiens 50-53 17645770-2 2007 We observed a threefold reduction of circulating CD1c(+) MDC immediately after LTX (n = 16; P < 0.01), and normalization between 3 and 12 months after LTX. Leukotriene C4 79-82 CD1c molecule Homo sapiens 49-53 16385629-5 2006 This effect depends on a tyrosine-based motif present in CD1 cytoplasmic tail as well as the actions of four Nef motifs, which are known to be involved in the down-regulation of MHC-I or CD4. Tyrosine 25-33 CD1c molecule Homo sapiens 57-60 17256135-3 2007 Cloretazine significantly inhibited the growth of subcutaneously implanted tumors, including B16F10 murine melanoma in C57BL/6 mice, and H460 human lung carcinoma and WiDr human colon carcinoma in athymic nude CD1 mice. laromustine 0-11 CD1c molecule Homo sapiens 210-213 17243837-7 2007 The reaction coordinates of the ribozyme reaction in TS, RC1-CD1 and RC4-CD2, are 2.35 and 2.33 A, respectively, compared to 2.37 and 2.36 A in water. Water 144-149 CD1c molecule Homo sapiens 61-64 17593659-1 2007 CD1 proteins present self and microbial glycolipids to CD 1-restricted T cells, or in the case of CD1d, to NKT cells. Glycolipids 40-51 CD1c molecule Homo sapiens 0-3 17593659-1 2007 CD1 proteins present self and microbial glycolipids to CD 1-restricted T cells, or in the case of CD1d, to NKT cells. Glycolipids 40-51 CD1c molecule Homo sapiens 55-59 17593661-2 2007 The CD1 molecules have a structure broadly similar to major histocompatibility complex (MHC) class I and class II proteins, but because the antigens CD 1 presents are so different from peptides, it is possible that glycolipid reactive TCRs have properties that distinguish them from TCRs expressed by conventional T cells. Glycolipids 215-225 CD1c molecule Homo sapiens 4-7 17593661-2 2007 The CD1 molecules have a structure broadly similar to major histocompatibility complex (MHC) class I and class II proteins, but because the antigens CD 1 presents are so different from peptides, it is possible that glycolipid reactive TCRs have properties that distinguish them from TCRs expressed by conventional T cells. Glycolipids 215-225 CD1c molecule Homo sapiens 149-153 16078214-0 2006 Hemoglobin Hammersmith [beta 42(CD1) Phe --> Ser] causing severe hemolytic anemia in a Japanese girl. Serine 48-51 CD1c molecule Homo sapiens 32-35 16078214-5 2006 DNA sequence analysis of the polymerase chain reaction-amplified beta-globin gene revealed a point mutation (T --> C) in the second nucleotide of the 42nd codon of the beta-globin chain (beta 42(CD1) Phe --> Ser). Phenylalanine 203-206 CD1c molecule Homo sapiens 190-201 16078214-5 2006 DNA sequence analysis of the polymerase chain reaction-amplified beta-globin gene revealed a point mutation (T --> C) in the second nucleotide of the 42nd codon of the beta-globin chain (beta 42(CD1) Phe --> Ser). Serine 214-217 CD1c molecule Homo sapiens 190-201 16619220-0 2006 Hemoglobin Hammersmith [beta42 (CD1) Phe --> Ser] in a Brazilian girl with congenital Heinz body hemolytic anemia. Phenylalanine 37-40 CD1c molecule Homo sapiens 32-35 16905746-1 2006 Saposin A (Sap-A) is one of five known sphingolipid activator proteins required for the lysosomal degradation of sphingolipids and for the loading of lipid antigens onto antigen-presenting molecules of the CD1 type. Sphingolipids 39-51 CD1c molecule Homo sapiens 206-209 16834351-5 2006 The activation energy for solid-solution formation was determined as approximately 152 kJ/mol, which evidently indicates that the diffusion of Zn2+ ions in the CdSe-ZnSe system is the governing mechanism for the Cd1-xZnxSe solid-solution formation. Zinc 143-147 CD1c molecule Homo sapiens 212-215 16834351-5 2006 The activation energy for solid-solution formation was determined as approximately 152 kJ/mol, which evidently indicates that the diffusion of Zn2+ ions in the CdSe-ZnSe system is the governing mechanism for the Cd1-xZnxSe solid-solution formation. cdse 160-164 CD1c molecule Homo sapiens 212-215 16834351-5 2006 The activation energy for solid-solution formation was determined as approximately 152 kJ/mol, which evidently indicates that the diffusion of Zn2+ ions in the CdSe-ZnSe system is the governing mechanism for the Cd1-xZnxSe solid-solution formation. Selanylidenezinc 165-169 CD1c molecule Homo sapiens 212-215 16547137-9 2006 Damping of the heme response appears to result from a strain exerted by the E-helix via the CD-turn; Phe-43(CD1), in close contact with heme, opposes tilt until the strain is relieved. Heme 15-19 CD1c molecule Homo sapiens 108-111 16547137-9 2006 Damping of the heme response appears to result from a strain exerted by the E-helix via the CD-turn; Phe-43(CD1), in close contact with heme, opposes tilt until the strain is relieved. Phenylalanine 101-104 CD1c molecule Homo sapiens 108-111 16547137-9 2006 Damping of the heme response appears to result from a strain exerted by the E-helix via the CD-turn; Phe-43(CD1), in close contact with heme, opposes tilt until the strain is relieved. Heme 136-140 CD1c molecule Homo sapiens 108-111 17438276-1 2007 Host vesicles composed of amphiphilic beta-cyclodextrin CD1 recognize metal-coordination complexes of the adamantyl-functionalized ethylenediamine ligand L via hydrophobic inclusion in the beta-cyclodextrin cavities at the vesicle surface. betadex 38-55 CD1c molecule Homo sapiens 56-59 17438276-1 2007 Host vesicles composed of amphiphilic beta-cyclodextrin CD1 recognize metal-coordination complexes of the adamantyl-functionalized ethylenediamine ligand L via hydrophobic inclusion in the beta-cyclodextrin cavities at the vesicle surface. Metals 70-75 CD1c molecule Homo sapiens 56-59 17438276-1 2007 Host vesicles composed of amphiphilic beta-cyclodextrin CD1 recognize metal-coordination complexes of the adamantyl-functionalized ethylenediamine ligand L via hydrophobic inclusion in the beta-cyclodextrin cavities at the vesicle surface. adamantyl 106-115 CD1c molecule Homo sapiens 56-59 17438276-1 2007 Host vesicles composed of amphiphilic beta-cyclodextrin CD1 recognize metal-coordination complexes of the adamantyl-functionalized ethylenediamine ligand L via hydrophobic inclusion in the beta-cyclodextrin cavities at the vesicle surface. ethylenediamine 131-146 CD1c molecule Homo sapiens 56-59 17438276-1 2007 Host vesicles composed of amphiphilic beta-cyclodextrin CD1 recognize metal-coordination complexes of the adamantyl-functionalized ethylenediamine ligand L via hydrophobic inclusion in the beta-cyclodextrin cavities at the vesicle surface. betadex 189-206 CD1c molecule Homo sapiens 56-59 17071611-6 2006 Nor were any required for the CD1d molecule to bind and present alpha-galactosyl ceramide after lysosomal processing of a precursor lipid, galactosyl-(alpha1-2)-galactosyl ceramide. alpha-galactosylceramide 64-89 CD1c molecule Homo sapiens 30-33 16078214-0 2006 Hemoglobin Hammersmith [beta 42(CD1) Phe --> Ser] causing severe hemolytic anemia in a Japanese girl. Phenylalanine 37-40 CD1c molecule Homo sapiens 32-35 17073257-4 2006 Rearranged gene-derived receptors like immunoglobulin (Ig) and MHC molecule-restricted alphabeta-type of T-cell receptors (TCR) with high specificities and memories are used to recognize peptide antigens in the acquired immunity, whereas non-rearranged invaliant receptors such as toll-like receptors (TLR), gammasigmaTCR and CD1 molecule-restricted alphabeta TCR are employed to detect lipid/glycolipid or nucleic acid-related antigens in the innate immunity. Glycolipids 393-403 CD1c molecule Homo sapiens 326-329 16597658-2 2006 Recent studies of CD1, an MHC class I homolog encoded outside the MHC, have revealed that it presents diverse glycolipids to T cells. Glycolipids 110-121 CD1c molecule Homo sapiens 18-21 16597658-4 2006 Here, we examine the known antigen structures presented by CD1, the majority of which have sugar moieties that are capable of interacting with TCRs. Sugars 91-96 CD1c molecule Homo sapiens 59-62 16651026-3 2006 Recent studies suggest an association between the cellular machinery that loads CD1 molecules with glycolipids and several key proteins in lipid metabolism. Glycolipids 99-110 CD1c molecule Homo sapiens 80-83 16484319-4 2006 In this study, proliferation of the OSE was quantified in response to superovulation induced by ip injection of pregnant mare serum gonadotropin (PMSG) and human chorionic gonadotropin (hCG) in immature 27-d-old CD1 mice using bromodeoxyuridine (BrdU). serine O-sulfate 36-39 CD1c molecule Homo sapiens 212-215 16210906-1 2006 The recent discovery that T cells recognize endogenous and foreign lipid and glycolipid molecules presented by CD1 proteins has brought a major contribution in the understanding of innate and adaptive immune response to certain harmless antigens and infectious pathogens. Glycolipids 77-87 CD1c molecule Homo sapiens 111-114 16143863-4 2005 Anti-sulfatide antibodies are seen in type 1 diabetes, and immunological presentation of glycosphingolipids by the non-classical CD1 molecules has recently been reported. Glycosphingolipids 89-107 CD1c molecule Homo sapiens 129-132 16198315-0 2005 Temperature-dependent biosynthesis of glucose monomycolate and its recognition by CD1-restricted T cells. glucose mycolate 38-58 CD1c molecule Homo sapiens 82-85 16198315-4 2005 Here, we found that GMM was produced abundantly at 30 degrees C rather than at 37 degrees C and recognized by a GMM-specific, CD1-restricted T cell line that was isolated from mycobacteria-infected human skin. glucose mycolate 20-23 CD1c molecule Homo sapiens 126-129 16198315-4 2005 Here, we found that GMM was produced abundantly at 30 degrees C rather than at 37 degrees C and recognized by a GMM-specific, CD1-restricted T cell line that was isolated from mycobacteria-infected human skin. glucose mycolate 112-115 CD1c molecule Homo sapiens 126-129 16363253-6 2005 Treatment of mice with WX-FX4 (1.5 mg/kg twice daily) led to significant reduction of experimental liver metastasis of a syngeneic T-cell lymphoma in DBA/2 mice (> 90%), and of experimental lung metastasis of a human fibrosarcoma in CD1 nu/nu mice (> 60%). wx-fx4 23-29 CD1c molecule Homo sapiens 236-239 16445682-2 2006 CD1 glycoproteins comprise a family of molecules that are specialized for presenting lipids, glycolipids and lipopeptides to T lymphocytes. Glycolipids 93-104 CD1c molecule Homo sapiens 0-3 16183644-4 2005 In the present study, we report the three-dimensional solution structures of the three CDs (CD1, CD2, and CD3) using a variety of triple resonance NMR experiments. cds 87-90 CD1c molecule Homo sapiens 92-95 16217830-4 2005 For example, in comparison with single CD1, dual CDs can enhance Deltamu and alpha up to the maximum value when enantiomers migrate with the same order in CD1 and CD2, and have the value of rho > 1.0, where rho is the enantioselectivity ratio for CD2 to CD1, while worse Deltamu and alpha are obtained for enantiomers with rho < 1.0. Cadmium 49-52 CD1c molecule Homo sapiens 39-42 15653315-3 2005 These unconventional T cells include glycolipid-specific CD1-restricted T cells and phospholigand-specific gammadelta T cells. Glycolipids 37-47 CD1c molecule Homo sapiens 57-60 16217830-4 2005 For example, in comparison with single CD1, dual CDs can enhance Deltamu and alpha up to the maximum value when enantiomers migrate with the same order in CD1 and CD2, and have the value of rho > 1.0, where rho is the enantioselectivity ratio for CD2 to CD1, while worse Deltamu and alpha are obtained for enantiomers with rho < 1.0. Cadmium 49-52 CD1c molecule Homo sapiens 155-158 16217830-4 2005 For example, in comparison with single CD1, dual CDs can enhance Deltamu and alpha up to the maximum value when enantiomers migrate with the same order in CD1 and CD2, and have the value of rho > 1.0, where rho is the enantioselectivity ratio for CD2 to CD1, while worse Deltamu and alpha are obtained for enantiomers with rho < 1.0. Cadmium 49-52 CD1c molecule Homo sapiens 155-158 15728261-6 2005 Moreover, C22 of TX522 made an additional contact with the CD1 atom of Ile268 because of the rigidity of the triple bond-containing side chain. inecalcitol 17-22 CD1c molecule Homo sapiens 59-62 15886110-1 2005 The discovery of the CD1 antigen-presenting system reveals that T cells survey the lipid content of target cells via T-cell receptor (TCR) contact with CD1 bound to lipids, glycolipids and small molecules. Glycolipids 173-184 CD1c molecule Homo sapiens 21-24 15886110-1 2005 The discovery of the CD1 antigen-presenting system reveals that T cells survey the lipid content of target cells via T-cell receptor (TCR) contact with CD1 bound to lipids, glycolipids and small molecules. Glycolipids 173-184 CD1c molecule Homo sapiens 152-155 15886110-2 2005 Recently, CD1 proteins have been found to present mycobacterial lipopeptides that are involved in scavenging iron from infected cells. Iron 109-113 CD1c molecule Homo sapiens 10-13 15963780-2 2005 (2005) demonstrate in this issue of Immunity that bacterial infection leads to increased synthesis of autologous glycolipids that are recognized by CD1-restricted human T cells, indicating that recognition of inducible self-glycolipids could be a mechanism for microbial detection. Glycolipids 113-124 CD1c molecule Homo sapiens 148-151 15963780-2 2005 (2005) demonstrate in this issue of Immunity that bacterial infection leads to increased synthesis of autologous glycolipids that are recognized by CD1-restricted human T cells, indicating that recognition of inducible self-glycolipids could be a mechanism for microbial detection. Glycolipids 224-235 CD1c molecule Homo sapiens 148-151 15860372-1 2005 Invariant natural killer T (iNKT) cells are a subpopulation of T cells that are reactive with glycolipids that are bound by CD1d antigen-presenting molecules. Glycolipids 94-105 CD1c molecule Homo sapiens 124-127 15721369-4 2005 Using APOBEC3G deletion and point mutants, we mapped the encapsidation determinant to the Zn(2+) coordination residues of the N-terminal catalytic domain (CD1). Zinc 90-92 CD1c molecule Homo sapiens 155-158 15653316-4 2005 The atomic structures of CD1-antigen complexes have defined both the orientation of polar headgroups between the alpha1 and alpha2 helices of CD1 and the manner in which distinct CD1 isoforms bind a range of lipids that have different lengths and numbers of hydrocarbon chains. Hydrocarbons 258-269 CD1c molecule Homo sapiens 25-28 15799073-3 2005 In the present work the in vitro and in vivo concentration ratios of the (+)-(R) to (-)-(S) enantiomers of MK-0767 were determined in plasma from humans (in vitro only) and nonclinical species used in the toxicological evaluation of rac-MK-0767, namely CD-1 mice, Sprague-Dawley rats, beagle dogs, New Zealand white rabbits, and rhesus monkeys. MK0767 107-114 CD1c molecule Homo sapiens 253-257 15601714-8 2005 On the other hand, enzymes devoid of CD1 modified alpha-1,6 linear oligosaccharides and dextran acceptors through the formation of alpha-1,2 linkages. alpha-1,6 linear oligosaccharides 50-83 CD1c molecule Homo sapiens 37-40 15601714-8 2005 On the other hand, enzymes devoid of CD1 modified alpha-1,6 linear oligosaccharides and dextran acceptors through the formation of alpha-1,2 linkages. Dextrans 88-95 CD1c molecule Homo sapiens 37-40 14991603-5 2004 A significant fraction of NKT cells generated in the culture were positive for staining with CD1-alpha-galactosylceramide tetramer, indicating that Valpha14i NKT cells were the major subset among the NKT cells. Galactosylceramides 103-121 CD1c molecule Homo sapiens 93-96 15185366-1 2004 CD1 proteins present mammalian and microbial lipid and glycolipid antigens to different subsets of T cells. Glycolipids 55-65 CD1c molecule Homo sapiens 0-3 15185366-3 2004 In the present study we use four different glycolipids, some of which contain tumor-associated carbohydrate antigens, to develop a procedure to easily detect binding of glycolipids to CD1 proteins on viable cells. Glycolipids 43-54 CD1c molecule Homo sapiens 184-187 15185366-3 2004 In the present study we use four different glycolipids, some of which contain tumor-associated carbohydrate antigens, to develop a procedure to easily detect binding of glycolipids to CD1 proteins on viable cells. Carbohydrates 95-107 CD1c molecule Homo sapiens 184-187 15185366-3 2004 In the present study we use four different glycolipids, some of which contain tumor-associated carbohydrate antigens, to develop a procedure to easily detect binding of glycolipids to CD1 proteins on viable cells. Glycolipids 169-180 CD1c molecule Homo sapiens 184-187 15611286-0 2004 Mycobacterium tuberculosis pks12 produces a novel polyketide presented by CD1c to T cells. Polyketides 50-60 CD1c molecule Homo sapiens 74-78 15611286-1 2004 CD1c-mediated T cells are activated by a mycobacterial phospholipid antigen whose carbohydrate structure precisely corresponds to mammalian mannosyl beta-1-phosphodolichol (MPD), but contains an unusual lipid moiety. Phospholipids 55-67 CD1c molecule Homo sapiens 0-4 15611286-1 2004 CD1c-mediated T cells are activated by a mycobacterial phospholipid antigen whose carbohydrate structure precisely corresponds to mammalian mannosyl beta-1-phosphodolichol (MPD), but contains an unusual lipid moiety. Carbohydrates 82-94 CD1c molecule Homo sapiens 0-4 15611286-1 2004 CD1c-mediated T cells are activated by a mycobacterial phospholipid antigen whose carbohydrate structure precisely corresponds to mammalian mannosyl beta-1-phosphodolichol (MPD), but contains an unusual lipid moiety. mannosyl beta-1-phosphodolichol 140-171 CD1c molecule Homo sapiens 0-4 15611286-1 2004 CD1c-mediated T cells are activated by a mycobacterial phospholipid antigen whose carbohydrate structure precisely corresponds to mammalian mannosyl beta-1-phosphodolichol (MPD), but contains an unusual lipid moiety. mpd 173-176 CD1c molecule Homo sapiens 0-4 15611286-3 2004 The alkane moiety distinguished these mycobacterial lipid antigens from mammalian MPDs and was necessary for activation of CD1c-restricted T cells, but could not be accounted for by any known lipid biosynthetic pathway. Alkanes 4-10 CD1c molecule Homo sapiens 123-127 15165856-8 2004 The position and orientation of the highly conserved residues in the heme pocket (Phe(CD1), Val(E11), distal His(E7) and proximal His(F8)) are similar to those of other globin proteins. Heme 69-73 CD1c molecule Homo sapiens 86-89 14711586-2 2004 To date, much of our understanding of the biology of the CD1/NKT system comes from studies that utilise non-natural glycolipid ligands. Glycolipids 116-126 CD1c molecule Homo sapiens 57-60 12761085-1 2003 CD1-restricted presentation of lipid or glycolipid antigens derived from Mycobacterium tuberculosis has been demonstrated by in vitro experiments using cultured T-cell lines. Glycolipids 40-50 CD1c molecule Homo sapiens 0-3 14702138-4 2003 However, the discovery of CD1-mediated presentation of lipids and glycolipids to a variety of T-cell populations has greatly expanded the repertoire of antigens to which T cells can respond. Glycolipids 66-77 CD1c molecule Homo sapiens 26-29 12818619-5 2003 The former two MHC molecules can present processed peptide antigens, whereas the last CD1 molecule can present glycolipid/lipid antigens. Glycolipids 111-121 CD1c molecule Homo sapiens 86-89 14658918-5 2003 The metal ion (Cd1) sits above the basal plane of three nitrogen atoms, N(1), N(3), and N(4). Metals 4-9 CD1c molecule Homo sapiens 15-18 14658918-5 2003 The metal ion (Cd1) sits above the basal plane of three nitrogen atoms, N(1), N(3), and N(4). Nitrogen 56-64 CD1c molecule Homo sapiens 15-18 12672482-6 2003 The complete amino acid sequence of 157 residues of Theliostyla myoglobin shows that it has a long N-terminal extension of seven residues and contains three functional key residues: CD1-Phe, E7-His, and F8-His. Phenylalanine 186-189 CD1c molecule Homo sapiens 182-185 12644623-1 2003 T cells may recognize glycolipids and lipids of bacterial and self origin associated with the CD1 antigen-presenting molecules. Glycolipids 22-33 CD1c molecule Homo sapiens 94-97 12803931-3 2003 Glycolipids are components of important antigen systems and membrane receptors; they participate in intracellular signalling mechanisms and may be presented to the immune system in the context of the novel CD1 molecules present on T lymphocytes. Glycolipids 0-11 CD1c molecule Homo sapiens 206-209 12644623-2 2003 Understanding the mechanisms governing CD1-self glycolipid interaction will provide information on the molecular rules of glycolipid presentation and suggest new approaches to immunotherapy. Glycolipids 48-58 CD1c molecule Homo sapiens 39-42 12580540-1 2003 In humans, group 1 CD1 glycoproteins present foreign and self lipid and glycolipid antigens to T-cells. Glycolipids 72-82 CD1c molecule Homo sapiens 19-22 12611660-0 2003 Biotransformations of bisphenol A in a mammalian model: answers and new questions raised by low-dose metabolic fate studies in pregnant CD1 mice. bisphenol A 22-33 CD1c molecule Homo sapiens 136-139 12452867-11 2002 In the dermis of PS and TS, equal numbers of mature and immature (CD1a+, CD1c+) DCs are densely interspersed between the lymphocytic infiltrate. ts 24-26 CD1c molecule Homo sapiens 73-77 12360465-3 2002 METHODS: We used a human CD1d (hCD1d) tetramer produced by a baculovirus expressing recombinant CD1d protein complexed with alpha-galactosylceramide (alpha-GalCer) and quantitated hCD1d tetramer reactive cells in blood and liver from controls and patients with primary biliary cirrhosis (PBC). alpha-galactosylceramide 124-148 CD1c molecule Homo sapiens 31-35 12076157-1 2002 Alpha-galactosyl ceramide has been identified to be a potent stimulatory agent for a novel immunological process, mediated by CD1 molecules. alpha-galactosylceramide 0-25 CD1c molecule Homo sapiens 126-129 12077262-7 2002 Using guinea pig cell lines transfected with individual CD1 isoforms as target cells in cytotoxic T cell assays, we found that guinea pig CD1b and CD1c molecules presented M. tuberculosis glycolipid Ags to T cells raised by mycobacterial lipid immunization. Glycolipids 188-198 CD1c molecule Homo sapiens 147-151 11970881-2 2002 Classical NKT cells display TCRs of restricted heterogeneity (Valpha14-Jalpha281) and recognize lipid antigens (e.g., alpha-galactosyl ceramide) presented by nonpolymorphic CD1 molecules. alpha-galactosylceramide 118-143 CD1c molecule Homo sapiens 173-176 11956292-4 2002 CD1a, CD1b, and CD1c molecules similarly load sulfatide on the cell surface without processing, and prime Th1 and Th2 responses. Sulfoglycosphingolipids 46-55 CD1c molecule Homo sapiens 16-20 11722638-0 2001 Glycolipid targets of CD1-mediated T-cell responses. Glycolipids 0-10 CD1c molecule Homo sapiens 22-25 11880205-2 2002 These novel T lymphocytes produce both Th1 and Th2 cytokines, recognize phospholipid and glycolipid antigens presented by CD1 molecules in a similar manner as peptides are recognized by cytotoxic T lymphocytes (CTL), and kill tumor cell targets by a perforin-dependent mechanism like NK cells and CTL. Glycolipids 89-99 CD1c molecule Homo sapiens 122-125 11722638-1 2001 Members of the CD1 family of antigen-presenting molecules bind and present a variety of mammalian and microbial glycolipids for specific recognition by T cells. Glycolipids 112-123 CD1c molecule Homo sapiens 15-18 11722638-3 2001 Most models of CD1-restricted T cells function in infectious, neoplastic, or autoimmune diseases and are based on the premise that CD1-restricted T-cell responses are initiated by alterations in cellular glycolipid content. Glycolipids 204-214 CD1c molecule Homo sapiens 15-18 11722638-3 2001 Most models of CD1-restricted T cells function in infectious, neoplastic, or autoimmune diseases and are based on the premise that CD1-restricted T-cell responses are initiated by alterations in cellular glycolipid content. Glycolipids 204-214 CD1c molecule Homo sapiens 131-134 11693527-0 2001 Polyisoprenyl glycolipids as targets of CD1-mediated T cell responses. polyisoprenyl glycolipids 0-25 CD1c molecule Homo sapiens 40-43 11590193-10 2001 The CD1c exocytosis pathway was sensitive to Brefeldin A, cytochalasin B, and chloroquine. Brefeldin A 45-56 CD1c molecule Homo sapiens 4-8 11590193-10 2001 The CD1c exocytosis pathway was sensitive to Brefeldin A, cytochalasin B, and chloroquine. Cytochalasin B 58-72 CD1c molecule Homo sapiens 4-8 11590193-10 2001 The CD1c exocytosis pathway was sensitive to Brefeldin A, cytochalasin B, and chloroquine. Chloroquine 78-89 CD1c molecule Homo sapiens 4-8 11693527-3 2001 Human CD1c proteins mediate T cell recognition of polyisoprenyl glycolipids, evolutionarily conserved phosphoglycolipids, which function in glycan synthesis pathways. polyisoprenyl glycolipids 50-75 CD1c molecule Homo sapiens 6-10 11693527-3 2001 Human CD1c proteins mediate T cell recognition of polyisoprenyl glycolipids, evolutionarily conserved phosphoglycolipids, which function in glycan synthesis pathways. Polysaccharides 140-146 CD1c molecule Homo sapiens 6-10 11693527-6 2001 This review of the structural diversity and evolutionary relationships of polyisoprenoid glycolipids emphasizes those features of polyisoprenyl glycolipid biosynthesis that are relevant to their functions as targets of CD1-mediated T cell responses. polyisoprenoid glycolipids 74-100 CD1c molecule Homo sapiens 219-222 11693527-6 2001 This review of the structural diversity and evolutionary relationships of polyisoprenoid glycolipids emphasizes those features of polyisoprenyl glycolipid biosynthesis that are relevant to their functions as targets of CD1-mediated T cell responses. polyisoprenyl glycolipid 130-154 CD1c molecule Homo sapiens 219-222 11476900-4 2001 Here we report that DP cells that were treated with PMA and ionomycin up-regulated bcl-2 and down-regulated CD1 expression. Tetradecanoylphorbol Acetate 52-55 CD1c molecule Homo sapiens 108-111 11476900-4 2001 Here we report that DP cells that were treated with PMA and ionomycin up-regulated bcl-2 and down-regulated CD1 expression. Ionomycin 60-69 CD1c molecule Homo sapiens 108-111 11154926-1 2001 Recently, different members of the CD1 family of MHC-like molecules have been shown to sample different intracellular compartments to present lipid and glycolipid antigens to T cells. Glycolipids 152-162 CD1c molecule Homo sapiens 35-38 11448930-8 2001 [3H]thymidine incorporation into COR L23 xenografts grown in CD1 nude mice was reduced by 64% (NU3108), 44% (NU3121), and 65% (DP) 2 h after administration of the nucleoside transport inhibitors. [3h]thymidine 0-13 CD1c molecule Homo sapiens 61-64 11580851-6 2001 The primary function of CD1 molecules is to present lipid and glycolipid antigens to T cells. Glycolipids 62-72 CD1c molecule Homo sapiens 24-27 11693433-4 2001 Glycolipids insert their hydrophobic lipid tails in two pockets below the antigen-binding groove and position their hydrophilic heads on the external part of CD1 molecules. Glycolipids 0-11 CD1c molecule Homo sapiens 158-161 11192257-4 2000 We show that the intravenous injection of TC-71 Ewing"s sarcoma cells into athymic 4-5-week-old Crl/nu/nu (CD1) BR mice reproducibly colonizes specific sites of the skeleton in addition to the lungs and lymph nodes. Technetium 42-44 CD1c molecule Homo sapiens 107-110 11193088-0 2000 Optical biosensing of nitrite ions using cytochrome cd1 nitrite reductase encapsulated in a sol-gel matrix. Nitrites 22-29 CD1c molecule Homo sapiens 52-55 11193088-3 2000 In order to develop an optical biosensing system for the determination of nitrite ions in environmental waters, cytochrome cd1 nitrite reductase has been extracted and purified from the bacterium Paracoccus pantotrophus. Nitrites 74-81 CD1c molecule Homo sapiens 123-126 11193088-4 2000 The protein has been spectroscopically characterised in solution and important kinetic parameters of nitrite reduction of the cytochrome cd1 enzyme, i.e., Km, Vmax and kcat have been determined. Nitrites 101-108 CD1c molecule Homo sapiens 137-140 11193088-5 2000 The influence of pH on the activity of the cytochrome cd1 has been investigated and the results suggest that this enzyme can be used for the determination of nitrite in the pH range 6-9. Nitrites 158-165 CD1c molecule Homo sapiens 54-57 11193088-6 2000 Biosensing experiments with the cytochrome cd1 in solution suggested that the decrease in intensity of the absorption band associated with the d1 haem (which is the nitrite binding site), at 460 nm, with increasing nitrite concentrations would enable the measurement of this analyte with the optimum limit of detection. Nitrites 165-172 CD1c molecule Homo sapiens 43-46 11193088-6 2000 Biosensing experiments with the cytochrome cd1 in solution suggested that the decrease in intensity of the absorption band associated with the d1 haem (which is the nitrite binding site), at 460 nm, with increasing nitrite concentrations would enable the measurement of this analyte with the optimum limit of detection. Nitrites 215-222 CD1c molecule Homo sapiens 43-46 11145856-2 2000 Human group 1 CD1 molecules (CD1a, CD1b, CD1c) are expressed mainly on professional antigen-presenting cells, and mediate presentation of microbial lipid and glycolipid antigens to T cells. Glycolipids 158-168 CD1c molecule Homo sapiens 41-45 11145858-1 2000 The MHC class I-like, non-polymorphic CD1 molecules represent a novel system for the presentation of glycolipid antigens to T lymphocytes. Glycolipids 101-111 CD1c molecule Homo sapiens 38-41 10899914-4 2000 Deletion of the cytoplasmic tail of CD1c, containing a tyrosine-based internalization motif, abolished most of its intracellular localization. Tyrosine 55-63 CD1c molecule Homo sapiens 36-40 10903726-0 2000 Glycosyl-phosphatidylinositol reanchoring unmasks distinct antigen-presenting pathways for CD1b and CD1c. Glycosylphosphatidylinositols 0-29 CD1c molecule Homo sapiens 100-104 10903726-3 2000 To test this hypothesis, glycosyl-phosphatidylinositol (GPI)-modified variants of CD1b and CD1c were engineered by chimerization with a GPI modification signal sequence derived from decay-accelerating factor (DAF). Glycosylphosphatidylinositols 25-54 CD1c molecule Homo sapiens 91-95 10903726-3 2000 To test this hypothesis, glycosyl-phosphatidylinositol (GPI)-modified variants of CD1b and CD1c were engineered by chimerization with a GPI modification signal sequence derived from decay-accelerating factor (DAF). Glycosylphosphatidylinositols 56-59 CD1c molecule Homo sapiens 91-95 10873422-4 2000 The most surprising finding of the CD1 antigen-presenting system is that the antigens presented by CD1 are not peptides, but rather lipid and glycolipid in nature. Peptides 111-119 CD1c molecule Homo sapiens 35-38 10873422-4 2000 The most surprising finding of the CD1 antigen-presenting system is that the antigens presented by CD1 are not peptides, but rather lipid and glycolipid in nature. Peptides 111-119 CD1c molecule Homo sapiens 99-102 10873422-4 2000 The most surprising finding of the CD1 antigen-presenting system is that the antigens presented by CD1 are not peptides, but rather lipid and glycolipid in nature. Glycolipids 142-152 CD1c molecule Homo sapiens 35-38 10873422-4 2000 The most surprising finding of the CD1 antigen-presenting system is that the antigens presented by CD1 are not peptides, but rather lipid and glycolipid in nature. Glycolipids 142-152 CD1c molecule Homo sapiens 99-102 10776535-6 2000 The Cd1 value does not depend on DNA concentration and is determined only by the length of the hydrocarbon chain and the structure of the amphiphile ionic fragment. Hydrocarbons 95-106 CD1c molecule Homo sapiens 4-7 10898493-5 2000 The Ca2+ chelator 1,2-bis(2-aminophenoxy)ethane-N,N,N",N"-tetraacetic acid, BIM-I and wortmannin each had only a small effect on ERK2 activation induced by surface IgM alone but blocked the enhancement of that activation by CD1 9/mIgM coligation. 1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid 18-74 CD1c molecule Homo sapiens 224-227 10779786-1 2000 Both the CD4-CD8- (double negative) and CD4-CD8+ T cell lineages have been shown to contain T cells which recognize microbial lipid and glycolipid Ags in the context of human CD1 molecules. Glycolipids 136-146 CD1c molecule Homo sapiens 175-178 10786796-0 2000 CD1c-mediated T-cell recognition of isoprenoid glycolipids in Mycobacterium tuberculosis infection. isoprenoid glycolipids 36-58 CD1c molecule Homo sapiens 0-4 10786796-2 2000 Here we show that the T-cell antigen receptor and the CD1c protein mediate recognition of an evolutionarily conserved family of isoprenoid glycolipids whose members include essential components of protein glycosylation and cell-wall synthesis pathways. isoprenoid glycolipids 128-150 CD1c molecule Homo sapiens 54-58 10786796-3 2000 A CD1c-restricted, mycobacteria-specific T-cell line recognized two previously unknown mycobacterial hexosyl-1-phosphoisoprenoids and structurally related mannosyl-beta1-phosphodolichols. hexosyl-1-phosphoisoprenoids 101-129 CD1c molecule Homo sapiens 2-6 10786796-3 2000 A CD1c-restricted, mycobacteria-specific T-cell line recognized two previously unknown mycobacterial hexosyl-1-phosphoisoprenoids and structurally related mannosyl-beta1-phosphodolichols. mannosyl-beta1-phosphodolichols 155-186 CD1c molecule Homo sapiens 2-6 10786796-4 2000 Responses to mannosyl-beta1-phosphodolichols were common among CD1c-restricted T-cell lines and peripheral blood T lymphocytes of human subjects recently infected with M. tuberculosis, but were not seen in naive control subjects. mannosyl-beta1-phosphodolichols 13-44 CD1c molecule Homo sapiens 63-67 10727456-5 2000 The CD1c-reactive gamma/delta T cells were cytotoxic and used both perforin- and Fas-mediated cytotoxicity. ammonium ferrous sulfate 81-84 CD1c molecule Homo sapiens 4-8 10776535-7 2000 The Cd1 value increases as the length of the aliphatic chain decreases and upon replacement of mobile hydrogen atoms in the ammonium fragment by methyl groups. Hydrogen 102-110 CD1c molecule Homo sapiens 4-7 10776535-7 2000 The Cd1 value increases as the length of the aliphatic chain decreases and upon replacement of mobile hydrogen atoms in the ammonium fragment by methyl groups. Ammonium Compounds 124-132 CD1c molecule Homo sapiens 4-7 11256748-4 2000 Structural and biochemical analyses demonstrate that antigens presented by CD1 are nonpeptide lipid or glycolipid structures, including examples found in the cell walls of pathogenic mycobacteria. Glycolipids 103-113 CD1c molecule Homo sapiens 75-78 10741415-4 2000 Its specific recognition by alphabeta CD8+ Th2 T cells (1) depends upon an MHC- and CD1-independent presentation mediated by B cells, (2) is determined by the flavonoid carbohydrate and sulfate groups and (3) leads to positive skin prick test in allergic patients. flavonoid carbohydrate 159-181 CD1c molecule Homo sapiens 84-87 10737711-4 2000 HL-60 cells treated with CD1 for 36 h decreased the uptake of [3H]-labeled thymidine, uridine and leucine in a dose dependent manner. Tritium 63-65 CD1c molecule Homo sapiens 25-28 10737711-4 2000 HL-60 cells treated with CD1 for 36 h decreased the uptake of [3H]-labeled thymidine, uridine and leucine in a dose dependent manner. Thymidine 75-84 CD1c molecule Homo sapiens 25-28 10737711-4 2000 HL-60 cells treated with CD1 for 36 h decreased the uptake of [3H]-labeled thymidine, uridine and leucine in a dose dependent manner. Uridine 86-93 CD1c molecule Homo sapiens 25-28 10737711-4 2000 HL-60 cells treated with CD1 for 36 h decreased the uptake of [3H]-labeled thymidine, uridine and leucine in a dose dependent manner. Leucine 98-105 CD1c molecule Homo sapiens 25-28 10375559-0 1999 CD1-mediated immune responses to glycolipids. Glycolipids 33-44 CD1c molecule Homo sapiens 0-3 10631954-2 1999 All four of the known human CD1 proteins (CD1a, CD1b, CD1c and CD1d) as well as murine CD1d have now been shown to mediate T-cell recognition of lipid or glycolipid antigens. Glycolipids 154-164 CD1c molecule Homo sapiens 54-58 10545488-10 1999 Finally, EBV induced a down-regulation of CD21 and an up-regulation of CD1 in CD21(++) thymocytes. (2S)-2-amino-1-[(3aR,6aS)-5-[(5-chloro-1H-indol-3-yl)methyl]hexahydropyrrolo[3,4-c]pyrrol-2(1H)-yl]-3-(1H-indol-3-yl)propan-1-one 9-12 CD1c molecule Homo sapiens 71-74 10448045-2 1999 The first is the well-known "functional" cluster which includes six heme-binding conserved residues (Phe CD1, His F8; aliphatic E11, FG5; hydrophobic F4, G5) and seven other conserved residues (Pro C2; aliphatic H19; hydrophobic B10, B13, B14, CD4, E4) that do not bind the heme but belong to its immediate neighborhood. Heme 68-72 CD1c molecule Homo sapiens 105-108 10448045-2 1999 The first is the well-known "functional" cluster which includes six heme-binding conserved residues (Phe CD1, His F8; aliphatic E11, FG5; hydrophobic F4, G5) and seven other conserved residues (Pro C2; aliphatic H19; hydrophobic B10, B13, B14, CD4, E4) that do not bind the heme but belong to its immediate neighborhood. Phenylalanine 101-104 CD1c molecule Homo sapiens 105-108 10358761-0 1999 The CD1 system: antigen-presenting molecules for T cell recognition of lipids and glycolipids. Glycolipids 82-93 CD1c molecule Homo sapiens 4-7 9880256-3 1999 The CD1-NKT cell pathway regulated immunogobulin G responses to the GPI-anchored surface antigens of Plasmodium and Trypanosoma and may be a general mechanism for rapid, MHC-unrestricted antibody responses to diverse pathogens. Glycosylphosphatidylinositols 68-71 CD1c molecule Homo sapiens 4-7 10358761-4 1999 Identification of naturally occurring antigens presented by CD1 has revealed the surprising finding that these are predominantly a variety of foreign lipids and glycolipids, including several found prominently in the cell walls and membranes of pathogenic mycobacteria. Glycolipids 161-172 CD1c molecule Homo sapiens 60-63 10358761-5 1999 Structural, biochemical, and biophysical studies support the view that CD1 proteins bind the hydrophobic alkyl portions of these antigens directly and position the polar or hydrophilic head groups of bound lipids and glycolipids for highly specific interactions with T cell antigen receptors. Glycolipids 217-228 CD1c molecule Homo sapiens 71-74 9782129-4 1998 Mouse or human CD1 molecules can present the glycolipid alpha-galactosylceramide (alpha-GalCer) to NK T cells from either species. Glycolipids 45-55 CD1c molecule Homo sapiens 15-18 9987600-2 1999 In contrast to MHC-encoded antigen-presenting molecules, CD1 binds and presents lipid and glycolipid antigens for specific recognition by T cell antigen receptors. Glycolipids 90-100 CD1c molecule Homo sapiens 57-60 9856680-0 1998 Hb Hammersmith [beta 42(CD1) Phe-->Ser]: occurrence as a de novo mutation in black monozygotic twins with multiple congenital anomalies. Phenylalanine 29-32 CD1c molecule Homo sapiens 24-27 9856680-7 1998 CONCLUSION: This report describes the occurrence of Hb Hammersmith [B42(CD1)Phe-->Ser] in African-American twins. Phenylalanine 76-79 CD1c molecule Homo sapiens 72-75 9856680-7 1998 CONCLUSION: This report describes the occurrence of Hb Hammersmith [B42(CD1)Phe-->Ser] in African-American twins. Serine 85-88 CD1c molecule Homo sapiens 72-75 9846364-1 1998 Human CD1 molecules bind and display or present lipid and glycolipid antigens from mycobacteria for recognition by T cells. Glycolipids 58-68 CD1c molecule Homo sapiens 6-9 9782129-4 1998 Mouse or human CD1 molecules can present the glycolipid alpha-galactosylceramide (alpha-GalCer) to NK T cells from either species. alpha-galactosylceramide 56-80 CD1c molecule Homo sapiens 15-18 9782129-4 1998 Mouse or human CD1 molecules can present the glycolipid alpha-galactosylceramide (alpha-GalCer) to NK T cells from either species. alpha-galactosylceramide 82-94 CD1c molecule Homo sapiens 15-18 9501468-2 1998 The solubilities of two isomers of those doubly branched beta CDs, 1,2- and 1,3-(G)2-beta CDs, in water were much higher than those of parent non-branched beta CD and mono-branched beta CD, 6-O-alpha-D-glucosyl-beta CD (G-beta CD), while the solubility of another isomer, 1,4-(G)2-beta CD, was significantly lower than these two isomers, though it was higher than that of beta CD. Water 98-103 CD1c molecule Homo sapiens 62-93 9558068-5 1998 We demonstrate that mCD1, like its human CD1 homologues, is found in endosomes, and that it colocalizes extensively with the DM molecule. dm 125-127 CD1c molecule Homo sapiens 21-24 11670523-1 1998 The dimeric dithiolate complex [1,5-bis(mercaptoethyl)-1,5-diazacyclooctanato]zinc(II), [(bme-daco)Zn](2) or Zn-1, and its cadmium analogue, Cd-1, were investigated as models for the active site of zinc-dependent methylation proteins. dithiolate 12-22 CD1c molecule Homo sapiens 141-145 11670523-3 1998 On the basis of (1)H and (13)C NMR spectroscopy and similar reactivity toward alkylating agents, the newly synthesized cadmium complex, Cd-1, is proposed to be isostructural with the previously reported Zn-1 complex, which is known from X-ray crystallography to be dimeric in the solid state (Tuntulani, T.; Reibenspies, J. H.; Farmer, P. J.; Darensbourg, M. Y. Inorg. Cadmium 119-126 CD1c molecule Homo sapiens 136-140 11670523-3 1998 On the basis of (1)H and (13)C NMR spectroscopy and similar reactivity toward alkylating agents, the newly synthesized cadmium complex, Cd-1, is proposed to be isostructural with the previously reported Zn-1 complex, which is known from X-ray crystallography to be dimeric in the solid state (Tuntulani, T.; Reibenspies, J. H.; Farmer, P. J.; Darensbourg, M. Y. Inorg. zn-1 203-207 CD1c molecule Homo sapiens 136-140 11670523-7 1998 An analogous reaction was observed for the cadmium derivative, Cd-1, which displays a (1)H NMR spectrum identical to that of Zn-2. Cadmium 43-50 CD1c molecule Homo sapiens 63-67 11670523-7 1998 An analogous reaction was observed for the cadmium derivative, Cd-1, which displays a (1)H NMR spectrum identical to that of Zn-2. Zinc 125-129 CD1c molecule Homo sapiens 63-67 9726012-7 1998 Compared to the parent line, SJCEM808 had similar cytogenetic abnormalities, lower CD2, CD1, and CD10 expression, and negligible RAG-1 expression. sjcem808 29-37 CD1c molecule Homo sapiens 88-91 9576005-3 1998 Unlike the MHC molecules, which bind short peptides in their antigen-binding groove for presentation to either CD4+ or CD8+ T cells bearing alpha beta T cell receptors, the CD1 molecules appear to accommodate lipid and glycolipid antigens in their hydrophobic cavity for presentation to a wide variety of T cells, including double-negative alpha beta and gamma delta T cells and CD8+ alpha beta T cells. Glycolipids 219-229 CD1c molecule Homo sapiens 173-176 9501468-2 1998 The solubilities of two isomers of those doubly branched beta CDs, 1,2- and 1,3-(G)2-beta CDs, in water were much higher than those of parent non-branched beta CD and mono-branched beta CD, 6-O-alpha-D-glucosyl-beta CD (G-beta CD), while the solubility of another isomer, 1,4-(G)2-beta CD, was significantly lower than these two isomers, though it was higher than that of beta CD. g-beta cd 220-229 CD1c molecule Homo sapiens 62-93 9501468-2 1998 The solubilities of two isomers of those doubly branched beta CDs, 1,2- and 1,3-(G)2-beta CDs, in water were much higher than those of parent non-branched beta CD and mono-branched beta CD, 6-O-alpha-D-glucosyl-beta CD (G-beta CD), while the solubility of another isomer, 1,4-(G)2-beta CD, was significantly lower than these two isomers, though it was higher than that of beta CD. 1,4-(g)2-beta cd 272-288 CD1c molecule Homo sapiens 62-93 9219685-4 1997 The extreme hydrophobicity and shape of the binding site are consistent with observations that human CD1b and CD1c can present mycobacterial cell wall antigens, such as mycolic acid and lipoarabinomannans. Mycolic Acids 169-181 CD1c molecule Homo sapiens 110-114 9219685-4 1997 The extreme hydrophobicity and shape of the binding site are consistent with observations that human CD1b and CD1c can present mycobacterial cell wall antigens, such as mycolic acid and lipoarabinomannans. lipoarabinomannan 186-204 CD1c molecule Homo sapiens 110-114 8902657-1 1996 In a group of nickel sensitized women, we investigated the effects of topical application of testosterone propionate on the epidermic density of CD1 + dendritic cells and on the response to patch tests performed with scaled nickel concentrations. Testosterone Propionate 93-116 CD1c molecule Homo sapiens 145-148 8902657-2 1996 In a significant number of examined subjects, treatment with testosterone propionate induced an increase of the minimum eliciting dose of nickel and an evident reduction of CD1 + dendritic cell epidermic density. Testosterone Propionate 61-84 CD1c molecule Homo sapiens 173-176 8902657-4 1996 This parallelism between the behaviour of the responses to patch tests and the epidermic density of CD1 + dendritic cells induces us to think it possible that testosterone propionate is able to increase the tolerance to contact with allergen by interfering with the activity of Langerhans cells. Testosterone Propionate 159-182 CD1c molecule Homo sapiens 100-103 7915481-4 1994 After 14 days of calcipotriol therapy, there were significantly fewer CD4T cells in the dermis and an increased number of intraepidermal CD1 + Langerhans cells. calcipotriene 17-29 CD1c molecule Homo sapiens 137-140 9984010-0 1996 Recombination and thermal emission of excitons in shallow CdTe/Cd1-xMgxTe quantum wells. cadmium telluride 58-62 CD1c molecule Homo sapiens 63-66 7821106-3 1995 Gastroesophageal reflux episodes were more frequent (P = 0.016) and gastroesophageal reflux indexes were greater (P < 0.010) after isosorbide dinitrate than after placebo in CD-2 group (N = 15) but not in healthy volunteers (N = 14) or CD-1 group (N = 9); six of seven CD-2 patients presenting with gastroesophageal reflux after isosorbide dinitrate had abnormal clearance of refluxate. Isosorbide Dinitrate 134-154 CD1c molecule Homo sapiens 239-243 9974742-0 1994 Interband magneto-optical studies of resonant polaron coupling in CdTe/Cd1-xMnxTe quantum wells. cadmium telluride 66-70 CD1c molecule Homo sapiens 71-74 10008610-0 1993 Transfer hyperfine interaction in Cd1-xMnxTe studied by NMR. hyperfine 9-18 CD1c molecule Homo sapiens 34-37 8182289-0 1993 Reduction in CD1 positive epidermal Langerhans cell numbers in leprosy lesions following epicutaneous application of 2:4 dinitrochlorobenzene. Dinitrochlorobenzene 117-141 CD1c molecule Homo sapiens 13-16 8182289-3 1993 A depletion or reduction in the numbers of CD1+ epidermal LC was observed at both 4 and 24 hours after the application of DNCB in the lesions of both tuberculoid and lepromatous leprosy, compared to untreated lesions. Dinitrochlorobenzene 122-126 CD1c molecule Homo sapiens 43-46 10008035-0 1993 Optical properties of Mg-based II-VI ternaries and quaternaries: Cd1-xMgxTe and Cd1-x-yMgxMnyTe. Magnesium 22-24 CD1c molecule Homo sapiens 65-68 10008035-0 1993 Optical properties of Mg-based II-VI ternaries and quaternaries: Cd1-xMgxTe and Cd1-x-yMgxMnyTe. Magnesium 22-24 CD1c molecule Homo sapiens 80-83 8103687-5 1993 Cyclosporin treatment significantly decreased T cells and normalized the distribution and antigen expression of intraepidermal Langerhans cells, increasing the number of CD1+ dendritic cells. Cyclosporine 0-11 CD1c molecule Homo sapiens 170-173 8446925-5 1993 In order to further examine these issues and to test the applicability of experimentally produced CDDs to human disease, we administered nitrofen (2,4-dichlorophenyl-p-nitrophenyl ether), an herbicide known to produce diaphragmatic defects in rodents, to time-mated CD1 mice by gavage feeding on gestational days 8 and 9. nitrofen 137-145 CD1c molecule Homo sapiens 266-269 10005624-0 1993 Partial valence-band spectra of Fe in Cd1-xFexSe. Iron 32-34 CD1c molecule Homo sapiens 38-41 1469702-8 1992 Certain trends were apparent, such as the fact that compounds with pyrrolidines at the R-7 position were more cytotoxic than those with piperazines, and halogens at R-8 (X-position) were associated with more cytotoxicity relative to hydrogen. Pyrrolidines 67-79 CD1c molecule Homo sapiens 87-90 7505632-5 1993 In contrast, the number of epidermal CD1+ (Langerhans) cells increased in response to FK 506 therapy. Tacrolimus 86-92 CD1c molecule Homo sapiens 37-40 1944366-1 1991 We have previously derived 2 V79 clones resistant to menadione (Md1 cells) and cadmium (Cd1 cells), respectively. Cadmium 79-86 CD1c molecule Homo sapiens 88-91 1375518-2 1992 We found that CD1+CD3- cells proliferate upon stimulation with anti-CD28 monoclonal antibody as well as with a pair of anti-CD2 monoclonal antibodies in the presence of low doses (0.5 ng/ml) of phorbol-13-myristate-12-acetate and/or recombinant interleukin-2. phorbol-13-myristate-12-acetate 194-225 CD1c molecule Homo sapiens 14-17 1375518-3 1992 A minor fraction of CD3+ cells (15%-20%) was also present in the proliferating cell population originating from CD1+CD3- thymocytes stimulated with phorbol-13-myristate-12-acetate and recombinant interleukin-2, either in the presence or in the absence of specific monoclonal antibodies. phorbol-13-myristate-12-acetate 148-179 CD1c molecule Homo sapiens 112-115 1375518-5 1992 Unexpectedly, we noted that highly purified (greater than 99%), CD1+CD3- immature thymocytes could mobilize calcium via CD3, besides CD2 and CD28 surface molecules, suggesting that a minor undetectable fraction (less than 1%) of CD3+ cells was still present in the purified CD3- population. Calcium 108-115 CD1c molecule Homo sapiens 64-67 1723278-3 1991 The combination of concanavalin A (Con A), tetradecanoylphorbol acetate (TPA), and IL-2 was shown to be the most reliable stimulus for the proliferation of CD3-CD1- thymocytes for up to 15 days in a culture system in vitro. Tetradecanoylphorbol Acetate 43-71 CD1c molecule Homo sapiens 160-163 1723278-3 1991 The combination of concanavalin A (Con A), tetradecanoylphorbol acetate (TPA), and IL-2 was shown to be the most reliable stimulus for the proliferation of CD3-CD1- thymocytes for up to 15 days in a culture system in vitro. Tetradecanoylphorbol Acetate 73-76 CD1c molecule Homo sapiens 160-163 10003894-0 1992 Dynamic Jahn-Teller effect on the far-infrared spectrum of Fe2+ in Cd1-xFexTe compounds. ammonium ferrous sulfate 59-63 CD1c molecule Homo sapiens 67-70 10003895-0 1992 Magnetism of Fe2+ ions in Cd1-xFexTe compounds. ammonium ferrous sulfate 13-17 CD1c molecule Homo sapiens 26-29 1634359-0 1992 The unstable Hb Hammersmith or alpha 2 beta 2(42)(CD1)Phe----Ser observed in an Indian child; identification by HPLC and by sequence analysis of amplified DNA. Phenylalanine 54-60 CD1c molecule Homo sapiens 50-53 1634359-0 1992 The unstable Hb Hammersmith or alpha 2 beta 2(42)(CD1)Phe----Ser observed in an Indian child; identification by HPLC and by sequence analysis of amplified DNA. Serine 61-64 CD1c molecule Homo sapiens 50-53 1634359-1 1992 We have identified the unstable hemoglobin variant present in a Chipewayan Indian patient with severe hemolytic anemia as Hb Hammersmith or alpha 2 beta 2(42)(CD1)Phe----Ser. Phenylalanine 163-166 CD1c molecule Homo sapiens 159-162 1634359-1 1992 We have identified the unstable hemoglobin variant present in a Chipewayan Indian patient with severe hemolytic anemia as Hb Hammersmith or alpha 2 beta 2(42)(CD1)Phe----Ser. Serine 170-173 CD1c molecule Homo sapiens 159-162 9999227-0 1991 X-ray near-edge structure of the II-VI compounds containing manganese: Experimental and theoretical studies of Cd1-xMnxTe and Zn1-xMnxTe. Manganese 60-69 CD1c molecule Homo sapiens 111-114 1944366-6 1991 Both Md1 and Cd1 DNAs were more resistant to the peroxide action. Peroxides 49-57 CD1c molecule Homo sapiens 13-16 1701190-4 1990 Statistically significant decreases in the epidermal density of CD1+ cells occurred in the responses to dithranol (p less than 0.05) and nonanoic acid (p less than 0.01). Anthralin 104-113 CD1c molecule Homo sapiens 64-67 1766257-5 1991 With IL-2, 3H-TdR incorporation increased in cells from 5 out of 10 T-ALL patients, including those with CD7+4-8-, CD5+, and CD1+ acute leukemia. Tritium 11-13 CD1c molecule Homo sapiens 125-128 1766257-8 1991 With IL-4, 3H-TdR incorporation was increased in the cells from 2 out of 5 patients with CD7+4-8- acute leukemia and in the cells of 2 of those with CD1+ acute leukemia. Tritium 11-13 CD1c molecule Homo sapiens 149-152 9995427-0 1990 Multiphonon resonant Raman scattering in high-manganese-concentration Cd1-xMnxTe films. Manganese 46-55 CD1c molecule Homo sapiens 70-73 1701190-4 1990 Statistically significant decreases in the epidermal density of CD1+ cells occurred in the responses to dithranol (p less than 0.05) and nonanoic acid (p less than 0.01). pelargonic acid 137-150 CD1c molecule Homo sapiens 64-67 1701190-6 1990 Alterations in the length of the dendritic processes of CD1+ cells were also induced, and semi-quantitative analysis revealed significant decreases in dendrite length in the reactions to sodium lauryl sulphate (p less than 0.05), nonanoic acid (p less than 0.001), croton oil (p less than 0.05), and dithranol (p less than 0.005). Sodium Dodecyl Sulfate 187-209 CD1c molecule Homo sapiens 56-59 1701190-6 1990 Alterations in the length of the dendritic processes of CD1+ cells were also induced, and semi-quantitative analysis revealed significant decreases in dendrite length in the reactions to sodium lauryl sulphate (p less than 0.05), nonanoic acid (p less than 0.001), croton oil (p less than 0.05), and dithranol (p less than 0.005). pelargonic acid 230-243 CD1c molecule Homo sapiens 56-59 1701190-6 1990 Alterations in the length of the dendritic processes of CD1+ cells were also induced, and semi-quantitative analysis revealed significant decreases in dendrite length in the reactions to sodium lauryl sulphate (p less than 0.05), nonanoic acid (p less than 0.001), croton oil (p less than 0.05), and dithranol (p less than 0.005). Anthralin 300-309 CD1c molecule Homo sapiens 56-59 2394762-3 1990 Following this preliminary analysis, lymphocytes were exposed to the metal ions found to inhibit the E-rosette reaction (Fe3+, Ni2+, and Co2+) in order to determine which of the following surface antigens were affected: CD2, CD3, CD4, CD8, CD1, CD22, CD10, and HLA-DR. Our results showed that the in vitro treatment of lymphocytes with Fe3+ or Co2+ caused inhibition of CD2 only, whereas Ni2+ caused inhibition of both CD2 and CD3 antigens. Metals 69-74 CD1c molecule Homo sapiens 240-243 1707770-4 1990 Thirty-two per cent of the samples were positive by IIF but, surprisingly, 72 per cent of the patients were positive by DBA, suggesting the intracellular presence of these molecules, CD1b and CD1c were also detected by DBA at similar percentages. dba 219-222 CD1c molecule Homo sapiens 192-196 1698561-4 1990 CD5 upregulation on TPA-sensitive JM cells appears correlated with inhibition of cell growth, blockage in G1 phase, and phenotypic maturation (downregulation of CD7 and CD1 antigens) and seemed to be related to PKC activation since DiC8 (a PKC activator) mimicked this TPA effect and H7 (a PKC inhibitor) partially reduced it. Tetradecanoylphorbol Acetate 20-23 CD1c molecule Homo sapiens 169-172 1696526-2 1990 We found that CD1+ cells expressed high levels of CD25 antigen upon triggering with specific monoclonal antibodies (mAbs) (anti-CD3, anti-CD2, anti-CD28) in association with low doses of Phorbol-13-myristate-12-acetate (PMA). phorbol-13-myristate-12-acetate 187-218 CD1c molecule Homo sapiens 14-17 1696526-2 1990 We found that CD1+ cells expressed high levels of CD25 antigen upon triggering with specific monoclonal antibodies (mAbs) (anti-CD3, anti-CD2, anti-CD28) in association with low doses of Phorbol-13-myristate-12-acetate (PMA). Tetradecanoylphorbol Acetate 220-223 CD1c molecule Homo sapiens 14-17 9994078-0 1990 Synchrotron-radiation study of Fe 3d states in Cd1-xFexSe (0 <= x <= 0.4). Iron 31-33 CD1c molecule Homo sapiens 47-50 9993142-0 1990 Identification of valence subbands in CdTe-Cd1-xZnxTe strained-layer quantum wells by differential spectroscopy. cadmium telluride 38-42 CD1c molecule Homo sapiens 43-46 34997633-2 2022 Herein, an effective way to fabricate nanostructures- whispering-gallery-mode (WGM) lasers by drop-casting CdSe/CdS@Cd1-x Znx S core/buffer-shell@graded-shell nanoplatelets (NPLs) dispersion onto silica microspheres is presented. cdse 107-111 CD1c molecule Homo sapiens 116-119 2294098-0 1990 Hemoglobin Warsaw (Phe beta 42(CD1)----Val), an unstable variant with decreased oxygen affinity. Phenylalanine 19-22 CD1c molecule Homo sapiens 31-34 2294098-0 1990 Hemoglobin Warsaw (Phe beta 42(CD1)----Val), an unstable variant with decreased oxygen affinity. Valine 39-42 CD1c molecule Homo sapiens 31-34 2294098-0 1990 Hemoglobin Warsaw (Phe beta 42(CD1)----Val), an unstable variant with decreased oxygen affinity. Oxygen 80-86 CD1c molecule Homo sapiens 31-34 2294098-2 1990 In Hb Warsaw Val replaces the Phe normally present at the heme contact position beta 42 (CD1). Valine 13-16 CD1c molecule Homo sapiens 89-92 2294098-2 1990 In Hb Warsaw Val replaces the Phe normally present at the heme contact position beta 42 (CD1). Phenylalanine 30-33 CD1c molecule Homo sapiens 89-92 2294098-2 1990 In Hb Warsaw Val replaces the Phe normally present at the heme contact position beta 42 (CD1). Heme 58-62 CD1c molecule Homo sapiens 89-92 34632633-6 2021 Herein, a gradient alloyed CdSe/Znx Cd1- x S/ZnS and CdSe/CdS/ZnS core/shell/shell QR downconverters showing high efficacy LEDs covering a wide color gamut are reported. znx 32-35 CD1c molecule Homo sapiens 36-39 34611609-4 2021 The module uses polymer donor CD1 and new polymer acceptor PBN-21 with medium optical band gap of 1.9 eV as the active layer. Polymers 16-23 CD1c molecule Homo sapiens 30-33 34095649-7 2021 Elemental mapping showed that the Zn element was mainly distributed in the outermost layer of the hollow spheres; this might be the critical factor that enabled Ni-doped Zn x Cd1-x S to maintain excellent stability. Zinc 34-36 CD1c molecule Homo sapiens 175-178 34095649-7 2021 Elemental mapping showed that the Zn element was mainly distributed in the outermost layer of the hollow spheres; this might be the critical factor that enabled Ni-doped Zn x Cd1-x S to maintain excellent stability. Zinc 170-172 CD1c molecule Homo sapiens 175-178 35481354-1 2022 Synthesis and structural depiction of two new metal-organic frameworks (MOFs), namely, ({Zn(L)(oba)} 4H2O)alpha (Zn-MOF-1) and ({Cd1/2(L)1/2(nipa)1/2(H2O)1/2} (DMF)1/2(H2O))alpha (Cd-MOF-2) (where L = N2,N6-di(pyridin-4-yl)naphthalene-2,6-dicarboxamide, 4,4"-H2oba = 4,4"-oxybisbenzoic acid, and 5-H2nipa = 5-nitroisophthalic acid) are reported. Water 150-153 CD1c molecule Homo sapiens 129-149 31755702-2 2019 Among the metal-dependent HDAC isozymes, HDAC6 is unique in that it contains two catalytic domains, CD1 and CD2. Metals 10-15 CD1c molecule Homo sapiens 100-103 31755702-9 2019 Catalytic activity measurements with HDAC6 CD1 confirm the preference for peptide substrates containing C-terminal acetyllysine residues. N-epsilon-Acetyl-L-lysine 115-127 CD1c molecule Homo sapiens 43-46 31755702-10 2019 However, these measurements also show that CD1 exhibits weak activity for peptide substrates bearing certain small amino acids on the carboxyl side of the scissile acetyllysine residue. N-epsilon-Acetyl-L-lysine 164-176 CD1c molecule Homo sapiens 43-46 34490697-5 2021 Owing to the efficient charge transfer, the Zn x Cd 1-x S-Pt 1 exhibited outstanding photocatalytic performance of CO 2 to CO, with the highest CO generation rate of 75.31 mumol h -1. Zinc 44-46 CD1c molecule Homo sapiens 49-53 34906284-5 2021 After 9 rounds of selection, 4 ssDNA sequences with the highest enrichment were obtained, and the Cd-1 aptamer exhibited the highest affinity to cadmium ions. Cadmium 145-152 CD1c molecule Homo sapiens 98-102 34906284-6 2021 The dissociation constant Kd value of the Cd-1 aptamer was 81.39 muM for cadmium ions. Cadmium 73-80 CD1c molecule Homo sapiens 42-46 34906284-7 2021 Later, we also investigated the binding specificity of Cd-1 aptamer toward other heavy metal ions. Metals 87-92 CD1c molecule Homo sapiens 55-59 34536421-5 2021 Crystallographic studies of CD1c complexes with these three new MPM analogs showed anchoring of the lipid tail and phosphate group that is highly comparable to nature-identical MPM, with considerable conformational flexibility for the mannose head group. Phosphates 115-124 CD1c molecule Homo sapiens 28-32 34536421-5 2021 Crystallographic studies of CD1c complexes with these three new MPM analogs showed anchoring of the lipid tail and phosphate group that is highly comparable to nature-identical MPM, with considerable conformational flexibility for the mannose head group. Mannose 235-242 CD1c molecule Homo sapiens 28-32 34381053-2 2021 Leukemia blasts express CD1c antigen-presenting molecules, which are identical in all individuals and expressed only by mature leukocytes, and are recognized by T cell clones specific for the CD1c-restricted leukemia-associated methyl-lysophosphatidic acid (mLPA) lipid antigen. methyl-lysophosphatidic acid 228-256 CD1c molecule Homo sapiens 24-28 34381053-2 2021 Leukemia blasts express CD1c antigen-presenting molecules, which are identical in all individuals and expressed only by mature leukocytes, and are recognized by T cell clones specific for the CD1c-restricted leukemia-associated methyl-lysophosphatidic acid (mLPA) lipid antigen. methyl-lysophosphatidic acid 228-256 CD1c molecule Homo sapiens 192-196 34381053-2 2021 Leukemia blasts express CD1c antigen-presenting molecules, which are identical in all individuals and expressed only by mature leukocytes, and are recognized by T cell clones specific for the CD1c-restricted leukemia-associated methyl-lysophosphatidic acid (mLPA) lipid antigen. mlpa 258-262 CD1c molecule Homo sapiens 24-28 34381053-2 2021 Leukemia blasts express CD1c antigen-presenting molecules, which are identical in all individuals and expressed only by mature leukocytes, and are recognized by T cell clones specific for the CD1c-restricted leukemia-associated methyl-lysophosphatidic acid (mLPA) lipid antigen. mlpa 258-262 CD1c molecule Homo sapiens 192-196 35510764-4 2022 After being anchored with a photocatalysis center (eosin-5-isothiocyanate, EY), the constructed LHS could sequentially transfer energy between two kinds of chromophores (CD1 and CD2), and further transfer to EY center with a high efficiency of 84%. alpha-glutamyltyrosine 75-77 CD1c molecule Homo sapiens 170-173 35393688-0 2022 Mode of Action and Human Relevance Assessment of Male CD-1 Mouse Renal Adenocarcinoma Associated With Lifetime Exposure to Empagliflozin. empagliflozin 123-136 CD1c molecule Homo sapiens 54-58 34997633-2 2022 Herein, an effective way to fabricate nanostructures- whispering-gallery-mode (WGM) lasers by drop-casting CdSe/CdS@Cd1-x Znx S core/buffer-shell@graded-shell nanoplatelets (NPLs) dispersion onto silica microspheres is presented. Cadmium 112-115 CD1c molecule Homo sapiens 116-119 34997633-2 2022 Herein, an effective way to fabricate nanostructures- whispering-gallery-mode (WGM) lasers by drop-casting CdSe/CdS@Cd1-x Znx S core/buffer-shell@graded-shell nanoplatelets (NPLs) dispersion onto silica microspheres is presented. znx 122-125 CD1c molecule Homo sapiens 116-119 34997633-2 2022 Herein, an effective way to fabricate nanostructures- whispering-gallery-mode (WGM) lasers by drop-casting CdSe/CdS@Cd1-x Znx S core/buffer-shell@graded-shell nanoplatelets (NPLs) dispersion onto silica microspheres is presented. Silicon Dioxide 196-202 CD1c molecule Homo sapiens 116-119 2673064-6 1989 Dermal CD1+DR+ cells (putative Langerhans cells), which are not found in normal skin but are present in lesional psoriasis skin, were virtually cleared from the papillary dermis after CsA therapy. Cyclosporine 184-187 CD1c molecule Homo sapiens 7-10 2807372-10 1989 Nevertheless, the majority of both purified CD1- and CD3- thymocytes expressed AIM antigen after treatment with PMA. Tetradecanoylphorbol Acetate 112-115 CD1c molecule Homo sapiens 44-47 35155954-8 2022 In contrast, with a 15N value between -3.6 and 0%, N2 accounts for over 70% of SG in wells TM1 and CD1, respectively, indicating the atmosphere, the ammonification of OM, and the presence of poor preservation conditions due to a high level of connectivity between the shale bed and the atmosphere acted as the sources of N2. Nitrogen 51-53 CD1c molecule Homo sapiens 99-102 9948012-0 1989 Magnetization steps in dilute magnetic semiconductors to 55 T: Mn2+ pair saturation in Cd1-xMnxTe and steps in Zn1-xMnxSe, Zn1-xMnxTe, and Cd1-xMnxSe. Manganese(2+) 63-67 CD1c molecule Homo sapiens 87-90 9941763-0 1987 Manganese-derived partial density of states in Cd1-xMnxTe. Manganese 0-9 CD1c molecule Homo sapiens 47-50 2517505-3 1989 The present study was to determine what effect sodium valproate at human therapeutic drug plasma levels had on the craniofacial skeletal pattern in the CD-1 mouse embryo relative to oxygen conditions, drug treatment or the interaction of the two. Valproic Acid 47-63 CD1c molecule Homo sapiens 152-156 9946390-0 1988 Magnetic polarons and electronic structure in semimagnetic superlattices: Application to CdTe/Cd1-xMnx cadmium telluride 89-93 CD1c molecule Homo sapiens 94-97 9942541-0 1987 Photoemission study of Cd1-xMnxF2 with fluorite (x <= 0.1) and rutile (x >= 0.925) structures. Calcium Fluoride 39-47 CD1c molecule Homo sapiens 23-26 9940187-0 1986 Magnetoresistance and Hall effect near the metal-insulator transition of Cd1-xMnxSe. Metals 43-48 CD1c molecule Homo sapiens 73-76 3781864-4 1986 Structural analyses revealed that the phenylalanine beta 42 (CD1), one of the critical amino acid residues in the heme pocket, had been replaced by valine. Phenylalanine 38-51 CD1c molecule Homo sapiens 61-64 3008818-0 1986 1H NMR investigation of cytochrome cd1: complexes with electron-donor proteins. Hydrogen 0-2 CD1c molecule Homo sapiens 35-38 3008818-4 1986 The experimental broadening fit a model in which c-551 is in intermediate or fast exchange between free solution and a complex with cd1, with an association constant for the complex in excess of 10(4) M-1. Carbon 46-47 CD1c molecule Homo sapiens 132-135 3781864-4 1986 Structural analyses revealed that the phenylalanine beta 42 (CD1), one of the critical amino acid residues in the heme pocket, had been replaced by valine. Heme 114-118 CD1c molecule Homo sapiens 61-64 3781864-4 1986 Structural analyses revealed that the phenylalanine beta 42 (CD1), one of the critical amino acid residues in the heme pocket, had been replaced by valine. Valine 148-154 CD1c molecule Homo sapiens 61-64 6877904-9 1983 Despite structural and functional similarities between Hb Cheverly and Hb Hammersmith, beta 42 (CD1) Phe-Ser, the clinical manifestations of Hb Cheverly are mild in contrast to the severe disease observed with Hb Hammersmith. Phenylalanine 101-104 CD1c molecule Homo sapiens 96-99 4041267-0 1985 Functional properties of the unstable Hb-Torino: alpha 43 (CD-1) Phe-Val. Phenylalanine 65-68 CD1c molecule Homo sapiens 59-63 6877904-9 1983 Despite structural and functional similarities between Hb Cheverly and Hb Hammersmith, beta 42 (CD1) Phe-Ser, the clinical manifestations of Hb Cheverly are mild in contrast to the severe disease observed with Hb Hammersmith. Serine 105-108 CD1c molecule Homo sapiens 96-99 7198931-1 1982 Methylnitrosourea (MNU), 20 mg/kg, was given IP to CD-1 mic on day 16 of pregnancy and the offspring examined at 3 and 5 weeks of age. Methylnitrosourea 0-17 CD1c molecule Homo sapiens 51-55 6259091-0 1981 Hemoglobin Hammersmith (beta 42 (CD1) Phe replaced by Ser) associated with severe hemolytic anemia. Phenylalanine 38-41 CD1c molecule Homo sapiens 33-36 640848-0 1978 Hemoglobin Louisville (beta 42 (CD1) phenylalanine replaced by leucine) occurring as a fresh mutation in a Canadian woman. Phenylalanine 37-50 CD1c molecule Homo sapiens 32-35 974262-5 1976 Substitution of the next residue, phenylalanine (CD1) beta 42 by serine (Hb Hammersmith), has resulted in chronic severe Heinz body hemolytic anemia. Phenylalanine 34-47 CD1c molecule Homo sapiens 49-52 974262-5 1976 Substitution of the next residue, phenylalanine (CD1) beta 42 by serine (Hb Hammersmith), has resulted in chronic severe Heinz body hemolytic anemia. Serine 65-71 CD1c molecule Homo sapiens 49-52 939244-1 1976 A severely anaemic, but asymptomatic patient, who is a heterozygous carrier of haemoglobin Hammersmith (beta42 (CD1) phenylalanine - Serine), has been studied to elucidate the mechanisms resulting in physiological compensation for the anaemia. Phenylalanine 117-130 CD1c molecule Homo sapiens 112-115 939244-1 1976 A severely anaemic, but asymptomatic patient, who is a heterozygous carrier of haemoglobin Hammersmith (beta42 (CD1) phenylalanine - Serine), has been studied to elucidate the mechanisms resulting in physiological compensation for the anaemia. Serine 133-139 CD1c molecule Homo sapiens 112-115 33548310-2 2021 Here molecular recognition and binding of a drug mimic (CD1) to HSA have been explored in a microfluidic channel when CD1 is encapsulated in beta-cyclodextrin (CD) and heptakis(2,3,6-tri-O-methyl)-beta-cyclodextrin (TRIMEB), respectively, to investigate whether change of the host vehicle modulate the rate of drug binding to the serum protein. betadex 141-158 CD1c molecule Homo sapiens 56-59 5133275-0 1971 Haemoglobin Buccuresti 42(CD1) Phe-Leu, a cause of unstable haemoglobin haemolytic anaemia. Phenylalanine 32-35 CD1c molecule Homo sapiens 27-30 33955216-3 2021 Akin to pristine and CD samples, CD with 1 wt % AlF3 (CD-1.0 wt %) shows excellent electrochemical performance with the capacity and voltage retentions of 93 and 91% after 150 cycles at 0.5C, respectively, and increased ionic conductivity. aluminum fluoride 48-52 CD1c molecule Homo sapiens 54-58 33955216-5 2021 Post-cycling analysis reveals that CD-1.0 wt % can alleviate the formation of rock-salt structure and Mn dissolution. Salts 83-87 CD1c molecule Homo sapiens 35-39 33974566-3 2021 Specifically, SARS-CoV-2 infection after application of low-doses of the acute-lung-injury stimulants bleomycin or ricin caused a severe disease in CD-1 mice, manifested by sustained body weight loss and mortality rates of >50%. Bleomycin 102-111 CD1c molecule Homo sapiens 148-152 33462468-4 2021 We also exploited the atomic-level miscibility of Cd and Zn to synthesize Mn2+:(Cd1-xZnxSe)13 alloy suprastructures with tunable metal synergy: Mn2+:(Cd0.5Zn0.5Se)13 suprastructures demonstrated high catalytic activity (turnover number, 17,964 per cluster in 6 h; turnover frequency, 2,994 per cluster per hour) for converting CO2 to organic cyclic carbonates under mild reaction conditions. cyclic carbonates 342-359 CD1c molecule Homo sapiens 80-83 826080-0 1976 A drug-induced haemolytic anaemia due to Hb Torino (alpha43(CD1)Phe replaced by Val). Phenylalanine 64-67 CD1c molecule Homo sapiens 60-63 826080-2 1976 The unstable haemoglobin, Tb Torino (alpha43(CD1)Phe replaced by Val), has been found for the second time in a family from the Treviso region of Italy. Terbium 26-28 CD1c molecule Homo sapiens 45-48 826080-2 1976 The unstable haemoglobin, Tb Torino (alpha43(CD1)Phe replaced by Val), has been found for the second time in a family from the Treviso region of Italy. Phenylalanine 49-52 CD1c molecule Homo sapiens 45-48 1177282-1 1975 A new case of haemoglobin Bucuresti beta 42 (CD1) Phe yields Leu is described in a Cuban family. Phenylalanine 50-53 CD1c molecule Homo sapiens 45-48 1177282-1 1975 A new case of haemoglobin Bucuresti beta 42 (CD1) Phe yields Leu is described in a Cuban family. Leucine 61-64 CD1c molecule Homo sapiens 45-48 5096522-0 1971 Hemoglobin Louisville (beta-42 (CD1) phe-leu): an unstable variant causing mild hemolytic anemia. Phenylalanine 37-40 CD1c molecule Homo sapiens 32-35 5643522-0 1968 Haemoglobin Torino--alpha-43 (CD1) phenylalanine replaced by valine. Phenylalanine 35-48 CD1c molecule Homo sapiens 30-33 33903869-5 2021 At the concentration of [Cd(NO3)2] = 0.10 M, a two-phase film was formed, where the film consisted of crystallites of cubic CdxPb1-xS with x = 0.071 (lower compared to the film obtained at [Cd(NO3)2] = 0.08 M) and fine-crystalline hexagonal B4-type Cd1-deltaS (space group P63mc). cd(no3) 25-32 CD1c molecule Homo sapiens 249-252 33903869-5 2021 At the concentration of [Cd(NO3)2] = 0.10 M, a two-phase film was formed, where the film consisted of crystallites of cubic CdxPb1-xS with x = 0.071 (lower compared to the film obtained at [Cd(NO3)2] = 0.08 M) and fine-crystalline hexagonal B4-type Cd1-deltaS (space group P63mc). Cadmium 25-27 CD1c molecule Homo sapiens 249-252 33462468-4 2021 We also exploited the atomic-level miscibility of Cd and Zn to synthesize Mn2+:(Cd1-xZnxSe)13 alloy suprastructures with tunable metal synergy: Mn2+:(Cd0.5Zn0.5Se)13 suprastructures demonstrated high catalytic activity (turnover number, 17,964 per cluster in 6 h; turnover frequency, 2,994 per cluster per hour) for converting CO2 to organic cyclic carbonates under mild reaction conditions. Cadmium 50-52 CD1c molecule Homo sapiens 80-83 33462468-4 2021 We also exploited the atomic-level miscibility of Cd and Zn to synthesize Mn2+:(Cd1-xZnxSe)13 alloy suprastructures with tunable metal synergy: Mn2+:(Cd0.5Zn0.5Se)13 suprastructures demonstrated high catalytic activity (turnover number, 17,964 per cluster in 6 h; turnover frequency, 2,994 per cluster per hour) for converting CO2 to organic cyclic carbonates under mild reaction conditions. Zinc 57-59 CD1c molecule Homo sapiens 80-83 33462468-4 2021 We also exploited the atomic-level miscibility of Cd and Zn to synthesize Mn2+:(Cd1-xZnxSe)13 alloy suprastructures with tunable metal synergy: Mn2+:(Cd0.5Zn0.5Se)13 suprastructures demonstrated high catalytic activity (turnover number, 17,964 per cluster in 6 h; turnover frequency, 2,994 per cluster per hour) for converting CO2 to organic cyclic carbonates under mild reaction conditions. Manganese(2+) 74-78 CD1c molecule Homo sapiens 80-83 33462468-4 2021 We also exploited the atomic-level miscibility of Cd and Zn to synthesize Mn2+:(Cd1-xZnxSe)13 alloy suprastructures with tunable metal synergy: Mn2+:(Cd0.5Zn0.5Se)13 suprastructures demonstrated high catalytic activity (turnover number, 17,964 per cluster in 6 h; turnover frequency, 2,994 per cluster per hour) for converting CO2 to organic cyclic carbonates under mild reaction conditions. Metals 129-134 CD1c molecule Homo sapiens 80-83 33462468-4 2021 We also exploited the atomic-level miscibility of Cd and Zn to synthesize Mn2+:(Cd1-xZnxSe)13 alloy suprastructures with tunable metal synergy: Mn2+:(Cd0.5Zn0.5Se)13 suprastructures demonstrated high catalytic activity (turnover number, 17,964 per cluster in 6 h; turnover frequency, 2,994 per cluster per hour) for converting CO2 to organic cyclic carbonates under mild reaction conditions. Manganese(2+) 144-148 CD1c molecule Homo sapiens 80-83 33462468-4 2021 We also exploited the atomic-level miscibility of Cd and Zn to synthesize Mn2+:(Cd1-xZnxSe)13 alloy suprastructures with tunable metal synergy: Mn2+:(Cd0.5Zn0.5Se)13 suprastructures demonstrated high catalytic activity (turnover number, 17,964 per cluster in 6 h; turnover frequency, 2,994 per cluster per hour) for converting CO2 to organic cyclic carbonates under mild reaction conditions. Carbon Dioxide 327-330 CD1c molecule Homo sapiens 80-83 33548310-2 2021 Here molecular recognition and binding of a drug mimic (CD1) to HSA have been explored in a microfluidic channel when CD1 is encapsulated in beta-cyclodextrin (CD) and heptakis(2,3,6-tri-O-methyl)-beta-cyclodextrin (TRIMEB), respectively, to investigate whether change of the host vehicle modulate the rate of drug binding to the serum protein. betadex 141-158 CD1c molecule Homo sapiens 118-121 33548310-2 2021 Here molecular recognition and binding of a drug mimic (CD1) to HSA have been explored in a microfluidic channel when CD1 is encapsulated in beta-cyclodextrin (CD) and heptakis(2,3,6-tri-O-methyl)-beta-cyclodextrin (TRIMEB), respectively, to investigate whether change of the host vehicle modulate the rate of drug binding to the serum protein. Cyclodextrins 56-58 CD1c molecule Homo sapiens 118-121 33548310-2 2021 Here molecular recognition and binding of a drug mimic (CD1) to HSA have been explored in a microfluidic channel when CD1 is encapsulated in beta-cyclodextrin (CD) and heptakis(2,3,6-tri-O-methyl)-beta-cyclodextrin (TRIMEB), respectively, to investigate whether change of the host vehicle modulate the rate of drug binding to the serum protein. heptakis(2,3,6-tri-O-methyl)-beta-cyclodextrin 168-214 CD1c molecule Homo sapiens 56-59 33548310-2 2021 Here molecular recognition and binding of a drug mimic (CD1) to HSA have been explored in a microfluidic channel when CD1 is encapsulated in beta-cyclodextrin (CD) and heptakis(2,3,6-tri-O-methyl)-beta-cyclodextrin (TRIMEB), respectively, to investigate whether change of the host vehicle modulate the rate of drug binding to the serum protein. heptakis(2,3,6-tri-O-methyl)-beta-cyclodextrin 216-222 CD1c molecule Homo sapiens 56-59 33548310-3 2021 Molecular recognition of betaCD encapsulated CD1 by HSA occurs by the conformational selection fit mechanism leading to rapid binding of CD1 to HSA (k1 ~ 700 s-1) when the CD/CD1 complex interacts with HSA. betadex 25-31 CD1c molecule Homo sapiens 45-48 33548310-3 2021 Molecular recognition of betaCD encapsulated CD1 by HSA occurs by the conformational selection fit mechanism leading to rapid binding of CD1 to HSA (k1 ~ 700 s-1) when the CD/CD1 complex interacts with HSA. betadex 25-31 CD1c molecule Homo sapiens 137-140 33548310-3 2021 Molecular recognition of betaCD encapsulated CD1 by HSA occurs by the conformational selection fit mechanism leading to rapid binding of CD1 to HSA (k1 ~ 700 s-1) when the CD/CD1 complex interacts with HSA. betadex 25-31 CD1c molecule Homo sapiens 137-140 33384873-2 2021 The adaptive immune response to Bacillus of Calmette and Guerin (BCG) immunization is responded to by B cells, T Follicular B helper, T regulatory, restriction CD1, CD8+, CD4+, Th1, Th2, and Th17. bacillus of calmette and guerin 32-63 CD1c molecule Homo sapiens 160-163 33535500-0 2021 Comparative Study of the Photocatalytic Hydrogen Evolution over Cd1-xMnxS and CdS-beta-Mn3O4-MnOOH Photocatalysts under Visible Light. Hydrogen 40-48 CD1c molecule Homo sapiens 64-67 33384873-2 2021 The adaptive immune response to Bacillus of Calmette and Guerin (BCG) immunization is responded to by B cells, T Follicular B helper, T regulatory, restriction CD1, CD8+, CD4+, Th1, Th2, and Th17. bcg 65-68 CD1c molecule Homo sapiens 160-163 33201164-0 2020 Synthesis of lead-free Cs4(Cd1-xMnx)Bi2Cl12 (0 <= x <= 1) layered double perovskite nanocrystals with controlled Mn-Mn coupling interaction. bi2cl12 36-43 CD1c molecule Homo sapiens 27-30 33221600-2 2021 In this paper, we report the preparation of two blue light-emitting silver-doped CDs, CD-1 and CD-2, through one- and two-step routes, respectively, by using polyethyleneimine, citric acid, and AgNO3 as raw materials. silver-doped 68-80 CD1c molecule Homo sapiens 86-90 33221600-2 2021 In this paper, we report the preparation of two blue light-emitting silver-doped CDs, CD-1 and CD-2, through one- and two-step routes, respectively, by using polyethyleneimine, citric acid, and AgNO3 as raw materials. cds 81-84 CD1c molecule Homo sapiens 86-90 33221600-2 2021 In this paper, we report the preparation of two blue light-emitting silver-doped CDs, CD-1 and CD-2, through one- and two-step routes, respectively, by using polyethyleneimine, citric acid, and AgNO3 as raw materials. aziridine 158-175 CD1c molecule Homo sapiens 86-90 33221600-2 2021 In this paper, we report the preparation of two blue light-emitting silver-doped CDs, CD-1 and CD-2, through one- and two-step routes, respectively, by using polyethyleneimine, citric acid, and AgNO3 as raw materials. Silver Nitrate 194-199 CD1c molecule Homo sapiens 86-90 33201164-0 2020 Synthesis of lead-free Cs4(Cd1-xMnx)Bi2Cl12 (0 <= x <= 1) layered double perovskite nanocrystals with controlled Mn-Mn coupling interaction. perovskite 73-83 CD1c molecule Homo sapiens 27-30 33201164-6 2020 Diluting the Mn2+ ion concentration through forming Cs4(Cd1-xMnx)Bi2Cl12 (0 < x < 1) alloyed LDP NCs leads to prolonged PL lifetimes and enhanced PL quantum yields. Manganese(2+) 13-17 CD1c molecule Homo sapiens 56-59 33201164-6 2020 Diluting the Mn2+ ion concentration through forming Cs4(Cd1-xMnx)Bi2Cl12 (0 < x < 1) alloyed LDP NCs leads to prolonged PL lifetimes and enhanced PL quantum yields. bi2cl12 65-72 CD1c molecule Homo sapiens 56-59 32916618-3 2020 This was accomplished by translational fusion of Cd-binding peptides to the N- or C-terminus of a PHB synthase that catalyzes PHB synthesis and mediates assembly of Cd2 or Cd1 coated PHB beads, respectively. Cadmium 49-51 CD1c molecule Homo sapiens 172-175 31349605-1 2019 Cadmium zinc telluride selenide (Cd1-xZnxTe1-ySey or CZTS) is one of the emerging CdTe-based semiconductor materials for detecting X- and gamma-ray radiation at or near room temperature (i.e., without cryogenic cooling). cadmium zinc telluride selenide 0-31 CD1c molecule Homo sapiens 33-36 32464336-5 2020 Moreover, the DFT calculation coupled with experiment (Mott-Schottky curves) illustrates the electron transfer behavior of CdS QDs/P-CNT, showing that the Cd-1 site should be the main active center and P doping is beneficial to increase H2 production. Phosphorus 131-132 CD1c molecule Homo sapiens 155-159 31044626-10 2019 Furthermore, the capacity of ILT4+CD1c+ subset producing IFN-gamma was lower than ILT4- CD1c subset in PBMC of HCC patients following Poly I:C stimulation. Poly I-C 134-142 CD1c molecule Homo sapiens 34-38 31299317-0 2019 Capillary electrophoresis and mutational images of hemoglobin sendagi [Beta42 (CD1) PHE VAL; HBB: C.127T G]. Phenylalanine 84-87 CD1c molecule Homo sapiens 79-82 31299317-2 2019 The unstable hemoglobin variant, hemoglobin Sendagi, is characterized by decreased oxygen affinity caused by replacement of one of the critical amino acid residues, phenylalanine beta 42 (CD1) of the beta-chain, with valine in the heme pocket, resulting in methemoglobin formation. Oxygen 83-89 CD1c molecule Homo sapiens 188-191 31299317-2 2019 The unstable hemoglobin variant, hemoglobin Sendagi, is characterized by decreased oxygen affinity caused by replacement of one of the critical amino acid residues, phenylalanine beta 42 (CD1) of the beta-chain, with valine in the heme pocket, resulting in methemoglobin formation. phenylalanine beta 165-183 CD1c molecule Homo sapiens 188-191 31299317-2 2019 The unstable hemoglobin variant, hemoglobin Sendagi, is characterized by decreased oxygen affinity caused by replacement of one of the critical amino acid residues, phenylalanine beta 42 (CD1) of the beta-chain, with valine in the heme pocket, resulting in methemoglobin formation. Valine 217-223 CD1c molecule Homo sapiens 188-191 32343740-7 2020 Immunodominant SA lipid antigens recognized by group 1 CD1-restricted T cells were comprised mainly of cardiolipin and phosphatidyl glycerol, with little contribution from lysyl-phosphatidyl glycerol which is a unique bacterial lipid not present in mammals. Cardiolipins 103-114 CD1c molecule Homo sapiens 55-58 32343740-7 2020 Immunodominant SA lipid antigens recognized by group 1 CD1-restricted T cells were comprised mainly of cardiolipin and phosphatidyl glycerol, with little contribution from lysyl-phosphatidyl glycerol which is a unique bacterial lipid not present in mammals. Phosphatidylglycerols 119-140 CD1c molecule Homo sapiens 55-58 32343740-7 2020 Immunodominant SA lipid antigens recognized by group 1 CD1-restricted T cells were comprised mainly of cardiolipin and phosphatidyl glycerol, with little contribution from lysyl-phosphatidyl glycerol which is a unique bacterial lipid not present in mammals. lysylphosphatidylglycerol 172-199 CD1c molecule Homo sapiens 55-58 32326581-3 2020 In addition, it is possible to tune the CdTe bandgap by introducing, for example, Zn into the composition, forming Cd1-xZnxTe alloys, which can fulfill the Shockley-Queisser limit design criteria for tandem devices. Zinc 82-84 CD1c molecule Homo sapiens 115-118 32244759-7 2020 We also found lipid- and pH-dependent dynamic changes in three exposed tryptophans unique to CD1d among the five human CD1 isotypes. Tryptophan 71-82 CD1c molecule Homo sapiens 93-96 31349605-1 2019 Cadmium zinc telluride selenide (Cd1-xZnxTe1-ySey or CZTS) is one of the emerging CdTe-based semiconductor materials for detecting X- and gamma-ray radiation at or near room temperature (i.e., without cryogenic cooling). cadmium telluride 82-86 CD1c molecule Homo sapiens 33-36 31246396-2 2019 Herein, a new type of CDs (CD1) has been developed that can transform from ACQ to an enhancement of fluorescence by aggregation-induced emission (AIE). cds 22-25 CD1c molecule Homo sapiens 27-30 31246396-2 2019 Herein, a new type of CDs (CD1) has been developed that can transform from ACQ to an enhancement of fluorescence by aggregation-induced emission (AIE). acenaphthenequinone 75-78 CD1c molecule Homo sapiens 27-30 31141702-3 2019 Lenalidomide did not affect the viability or expression of costimulatory molecules, but it potently suppressed the production of the key inflammatory cytokines IL-12 and IL-23, and enhanced the production of the anti-inflammatory cytokine IL-10 by CD1c+ DCs. Lenalidomide 0-12 CD1c molecule Homo sapiens 248-252 31141702-5 2019 Lenalidomide likely targets pathways downstream of the nuclear translocation of the transcription factors nuclear factor kappaB (NF-kappaB) and IFN regulatory 5 (IRF5) in CD1c+ DCs. Lenalidomide 0-12 CD1c molecule Homo sapiens 171-175 31141702-6 2019 Consistent with the direct immunomodulatory effects on DCs, lenalidomide decreased the capacity of CD1c+ DCs to induce differentiation of naive CD4+ T cells into effector cells producing immune activating and myeloma-promoting cytokines. Lenalidomide 60-72 CD1c molecule Homo sapiens 99-103 30387484-0 2019 Synthesis of Cd1-xZnxS photocatalysts for gas-phase CO2 reduction under visible light. N2,N6-bis(4-(2-aminoethoxy)quinolin-2-yl)-4-((4-fluorobenzyl)oxy)pyridine-2,6-dicarboxamide 52-55 CD1c molecule Homo sapiens 13-16 30645027-0 2019 Unique 1D Cd1- x Znx S@O-MoS2 /NiOx Nanohybrids: Highly Efficient Visible-Light-Driven Photocatalytic Hydrogen Evolution via Integrated Structural Regulation. Hydrogen 102-110 CD1c molecule Homo sapiens 10-13 30645027-4 2019 Interestingly, the band alignments, exposure of active sites, and interfacial charge separation of Cd1- x Znx S@O-MoS2 /NiOx are optimized by tuning the Zn-doping content as well as the growth of defect-rich O-MoS2 layer and NiOx nanoparticles, which endow the hybrids with excellent HER performances. Zinc 106-108 CD1c molecule Homo sapiens 99-102 30387484-1 2019 Novel photocatalysts for CO2 reduction, which consist of a cadmium and zinc sulfide solid solution (Cd1-xZnxS), were successfully prepared by a simple two-step technique. N2,N6-bis(4-(2-aminoethoxy)quinolin-2-yl)-4-((4-fluorobenzyl)oxy)pyridine-2,6-dicarboxamide 25-28 CD1c molecule Homo sapiens 100-103 30387484-1 2019 Novel photocatalysts for CO2 reduction, which consist of a cadmium and zinc sulfide solid solution (Cd1-xZnxS), were successfully prepared by a simple two-step technique. zinc sulfide 71-83 CD1c molecule Homo sapiens 100-103 30387484-3 2019 All the synthesized Cd1-xZnxS solid solutions were capable of enabling the chemical transformations of CO2 under the conditions considered. N2,N6-bis(4-(2-aminoethoxy)quinolin-2-yl)-4-((4-fluorobenzyl)oxy)pyridine-2,6-dicarboxamide 103-106 CD1c molecule Homo sapiens 20-23 30387484-4 2019 Carbon monoxide was the major product during the CO2 reduction over Cd1-xZnxS (x = 0-0.87). Carbon Monoxide 0-15 CD1c molecule Homo sapiens 68-71 30387484-4 2019 Carbon monoxide was the major product during the CO2 reduction over Cd1-xZnxS (x = 0-0.87). N2,N6-bis(4-(2-aminoethoxy)quinolin-2-yl)-4-((4-fluorobenzyl)oxy)pyridine-2,6-dicarboxamide 49-52 CD1c molecule Homo sapiens 68-71 30927520-3 2019 Cell culturing in the presence of ghrelin or combination of leptin and ghrelin reduced the percentage of CD86+CD1c+ DCs but did not affect the levels of CD83+CD1c+ and HLA-DR+CD1c+ DCs. Ghrelin 34-41 CD1c molecule Homo sapiens 110-114 30669428-6 2019 Finally, treatment with ascophyllan induced activation of BDCA1 and BDCA3 PBDCs. ascophyllin 24-35 CD1c molecule Homo sapiens 58-63 30260231-8 2018 The use of Cd1- xIn2+2 x/3S4 compounds could be a good alternative to CdIn2S4 and In2S3 to improve CIGS/buffer interfaces with a compromise between photovoltaic conversion efficiency and cadmium content. cdin2s4 70-77 CD1c molecule Homo sapiens 11-14 30534689-0 2018 Ultrahigh-efficiency aqueous flat nanocrystals of CdSe/CdS@Cd1-xZnxS colloidal core/crown@alloyed-shell quantum wells. Cadmium 50-53 CD1c molecule Homo sapiens 59-62 30534689-3 2018 Here, we show high-efficiency water-soluble CdSe/CdS@Cd1-xZnxS core/crown@shell NPLs formed by layer-by-layer grown and composition-tuned gradient Cd1-xZnxS shells on CdSe/CdS core/crown seeds. Water 30-35 CD1c molecule Homo sapiens 53-56 30534689-3 2018 Here, we show high-efficiency water-soluble CdSe/CdS@Cd1-xZnxS core/crown@shell NPLs formed by layer-by-layer grown and composition-tuned gradient Cd1-xZnxS shells on CdSe/CdS core/crown seeds. Water 30-35 CD1c molecule Homo sapiens 147-150 30534689-3 2018 Here, we show high-efficiency water-soluble CdSe/CdS@Cd1-xZnxS core/crown@shell NPLs formed by layer-by-layer grown and composition-tuned gradient Cd1-xZnxS shells on CdSe/CdS core/crown seeds. cdse 44-48 CD1c molecule Homo sapiens 53-56 30534689-3 2018 Here, we show high-efficiency water-soluble CdSe/CdS@Cd1-xZnxS core/crown@shell NPLs formed by layer-by-layer grown and composition-tuned gradient Cd1-xZnxS shells on CdSe/CdS core/crown seeds. cdse 44-48 CD1c molecule Homo sapiens 147-150 30534689-3 2018 Here, we show high-efficiency water-soluble CdSe/CdS@Cd1-xZnxS core/crown@shell NPLs formed by layer-by-layer grown and composition-tuned gradient Cd1-xZnxS shells on CdSe/CdS core/crown seeds. Cadmium 44-47 CD1c molecule Homo sapiens 53-56 30534689-3 2018 Here, we show high-efficiency water-soluble CdSe/CdS@Cd1-xZnxS core/crown@shell NPLs formed by layer-by-layer grown and composition-tuned gradient Cd1-xZnxS shells on CdSe/CdS core/crown seeds. Cadmium 44-47 CD1c molecule Homo sapiens 147-150 30534689-3 2018 Here, we show high-efficiency water-soluble CdSe/CdS@Cd1-xZnxS core/crown@shell NPLs formed by layer-by-layer grown and composition-tuned gradient Cd1-xZnxS shells on CdSe/CdS core/crown seeds. cdse 167-171 CD1c molecule Homo sapiens 53-56 30534689-3 2018 Here, we show high-efficiency water-soluble CdSe/CdS@Cd1-xZnxS core/crown@shell NPLs formed by layer-by-layer grown and composition-tuned gradient Cd1-xZnxS shells on CdSe/CdS core/crown seeds. cdse 167-171 CD1c molecule Homo sapiens 147-150 30534689-3 2018 Here, we show high-efficiency water-soluble CdSe/CdS@Cd1-xZnxS core/crown@shell NPLs formed by layer-by-layer grown and composition-tuned gradient Cd1-xZnxS shells on CdSe/CdS core/crown seeds. Cadmium 49-52 CD1c molecule Homo sapiens 53-56 30534689-3 2018 Here, we show high-efficiency water-soluble CdSe/CdS@Cd1-xZnxS core/crown@shell NPLs formed by layer-by-layer grown and composition-tuned gradient Cd1-xZnxS shells on CdSe/CdS core/crown seeds. Cadmium 49-52 CD1c molecule Homo sapiens 147-150 30514502-2 2018 In this study, we identified a CD1c DC subset with phenotype of CD1c+CD11c+CD19-CD11b+ that was significantly increased in tuberculous pleural effusions and in peripheral blood from patients with TB compared with that from healthy controls (p < 0.0001). Terbium 196-198 CD1c molecule Homo sapiens 31-35 30514502-2 2018 In this study, we identified a CD1c DC subset with phenotype of CD1c+CD11c+CD19-CD11b+ that was significantly increased in tuberculous pleural effusions and in peripheral blood from patients with TB compared with that from healthy controls (p < 0.0001). Terbium 196-198 CD1c molecule Homo sapiens 64-68 30514502-4 2018 After effective anti-TB chemotherapy, the frequency of CD1c+CD11b+ DC subset in peripheral blood and tuberculous pleural effusions was decreased. Terbium 21-23 CD1c molecule Homo sapiens 55-59 30320818-0 2018 Room temperature Fe2+:Cd1-xMnxTe laser generating at 5.4-6 mum. ammonium ferrous sulfate 17-21 CD1c molecule Homo sapiens 22-25 30260231-8 2018 The use of Cd1- xIn2+2 x/3S4 compounds could be a good alternative to CdIn2S4 and In2S3 to improve CIGS/buffer interfaces with a compromise between photovoltaic conversion efficiency and cadmium content. Cadmium 187-194 CD1c molecule Homo sapiens 11-14 29755453-7 2018 The binding of a CLEC10A-specific bivalent ligand (the MUC-1 peptide glycosylated with N-acetylgalactosamine) is limited to CD1c+ DCs and enhances the cytokine secretion (namely TNFalpha, IL-8, and IL-10) induced by TLR 7/8 stimulation. Acetylgalactosamine 87-108 CD1c molecule Homo sapiens 124-128 31950689-0 2018 In Situ Decoration of Znx Cd1-x S with FeP for Efficient Photocatalytic Generation of Hydrogen under Irradiation with Visible Light. Iron 39-42 CD1c molecule Homo sapiens 26-29 31950689-0 2018 In Situ Decoration of Znx Cd1-x S with FeP for Efficient Photocatalytic Generation of Hydrogen under Irradiation with Visible Light. Hydrogen 86-94 CD1c molecule Homo sapiens 26-29 31950689-1 2018 FeP as a noble-metal-free catalyst has been successfully decorated onto the Znx Cd1-x S photocatalyst surface through an in situ phosphating process. Iron 0-3 CD1c molecule Homo sapiens 80-83 29559523-2 2018 A single class of major histocompatibility class-like molecules, called CD1 molecules, can present lipids and glycolipids to the immune system. Glycolipids 110-121 CD1c molecule Homo sapiens 72-75 29888442-3 2018 Herein, a metal-organic framework (MOF)-template strategy was developed to prepare non-noble metal co-catalyst/solid solution heterojunction NiS/Znx Cd1-x S with superior photocatalytic HER activity. Metals 10-15 CD1c molecule Homo sapiens 149-152 29888442-3 2018 Herein, a metal-organic framework (MOF)-template strategy was developed to prepare non-noble metal co-catalyst/solid solution heterojunction NiS/Znx Cd1-x S with superior photocatalytic HER activity. Metals 93-98 CD1c molecule Homo sapiens 149-152 29888442-3 2018 Herein, a metal-organic framework (MOF)-template strategy was developed to prepare non-noble metal co-catalyst/solid solution heterojunction NiS/Znx Cd1-x S with superior photocatalytic HER activity. Nickel 141-144 CD1c molecule Homo sapiens 149-152 29888442-3 2018 Herein, a metal-organic framework (MOF)-template strategy was developed to prepare non-noble metal co-catalyst/solid solution heterojunction NiS/Znx Cd1-x S with superior photocatalytic HER activity. znx 145-148 CD1c molecule Homo sapiens 149-152 29721641-1 2018 In this work, we prepared CdTe quantum dots, and series of Cd1-xMnxTe-alloyed quantum dots with narrow size distribution by an ion-exchange reaction in water solution. Water 152-157 CD1c molecule Homo sapiens 59-62 29721641-4 2018 By means of cyclic voltammetry, we detected features of electrochemical activity of manganese energy levels formed inside the Cd1-xMnxTe-alloyed quantum dot band gap. Manganese 84-93 CD1c molecule Homo sapiens 126-129 30032685-0 2018 Hb Oslo [beta42(CD1)Phe Ile; HBB: c.127T>A]: A Novel Unstable Hemoglobin Variant Found in a Norwegian Patient. Phenylalanine 20-23 CD1c molecule Homo sapiens 16-19 30032685-4 2018 She was found to be carrier of a novel unstable Hb variant, Hb Oslo [beta42(CD1)Phe Ile (TTT>ATT), HBB: c.127T>A] located in the heme pocket of the beta-globin chain. Phenylalanine 80-83 CD1c molecule Homo sapiens 76-79 30032685-4 2018 She was found to be carrier of a novel unstable Hb variant, Hb Oslo [beta42(CD1)Phe Ile (TTT>ATT), HBB: c.127T>A] located in the heme pocket of the beta-globin chain. Isoleucine 84-87 CD1c molecule Homo sapiens 76-79 30032685-4 2018 She was found to be carrier of a novel unstable Hb variant, Hb Oslo [beta42(CD1)Phe Ile (TTT>ATT), HBB: c.127T>A] located in the heme pocket of the beta-globin chain. Heme 135-139 CD1c molecule Homo sapiens 76-79 29237773-10 2018 Finally, alanine scanning of CDR1 and CDR2 sequences of TRBV4-1 revealed two unique residues, Arg30 and Tyr51, as critical in conferring CD1c-restricted autoreactivity, thus elucidating the molecular basis of the observed V gene bias. Alanine 9-16 CD1c molecule Homo sapiens 137-141 29251626-0 2018 Zn x Cd1-x S tunable band structure-directing photocatalytic activity and selectivity of visible-light reduction of CO2 into liquid solar fuels. N2,N6-bis(4-(2-aminoethoxy)quinolin-2-yl)-4-((4-fluorobenzyl)oxy)pyridine-2,6-dicarboxamide 116-119 CD1c molecule Homo sapiens 5-8 29251626-2 2018 As-prepared Zn x Cd1-x S solid solutions show much enhanced photocatalytic efficiency for CO2 photoreduction in aqueous solutions under visible light irradiation, relative to pure CdS analog. N2,N6-bis(4-(2-aminoethoxy)quinolin-2-yl)-4-((4-fluorobenzyl)oxy)pyridine-2,6-dicarboxamide 90-93 CD1c molecule Homo sapiens 17-20 29251626-2 2018 As-prepared Zn x Cd1-x S solid solutions show much enhanced photocatalytic efficiency for CO2 photoreduction in aqueous solutions under visible light irradiation, relative to pure CdS analog. Cadmium 180-183 CD1c molecule Homo sapiens 17-20 31997833-0 2018 The deposition of thin films of cadmium zinc sulfide Cd1-x Zn x S at 250 C from spin-coated xanthato complexes: a potential route to window layers for photovoltaic cells. Zinc 59-61 CD1c molecule Homo sapiens 53-56 31997833-8 2018 This work is the first study to demonstrate Cd1-x Zn x S thin films by a spin coating/melt method from xanthato precursors. Zinc 50-52 CD1c molecule Homo sapiens 44-47 28683540-3 2017 Thus, the main goal of this study was to develop composition-tunable and biocompatible Zn x Cd1 - x S QDs using carboxymethylcellulose polysaccharide as direct capping ligand via green colloidal aqueous route at neutral pH and at room temperature for potential biomedical and environmental applications. Zinc 87-89 CD1c molecule Homo sapiens 92-95 29207574-3 2017 Seven new carbazole derivatives Cd1-Cd7 are incorporated and proposed as high performance near-UV photoinitiators for both the free radical polymerization (FRP) of (meth)acrylates and the cationic polymerization (CP) of epoxides utilizing Light Emitting Diodes LEDs @405 nm. Methacrylates 164-179 CD1c molecule Homo sapiens 32-35 29207574-3 2017 Seven new carbazole derivatives Cd1-Cd7 are incorporated and proposed as high performance near-UV photoinitiators for both the free radical polymerization (FRP) of (meth)acrylates and the cationic polymerization (CP) of epoxides utilizing Light Emitting Diodes LEDs @405 nm. Epoxy Compounds 220-228 CD1c molecule Homo sapiens 32-35 29207574-6 2017 All the more strikingly, in combination with iodonium salt, Cd1-Cd7 are likewise preferred as cationic photoinitiators over the notable photoinitiator bis(2,4,6-trimethylbenzoyl)phenylphosphine oxide (BAPO) for mild irradiation conditions featuring their remarkable reactivity. Phenylbis(2,4,6-trimethylbenzoyl)phosphine oxide 151-199 CD1c molecule Homo sapiens 60-63 29207574-6 2017 All the more strikingly, in combination with iodonium salt, Cd1-Cd7 are likewise preferred as cationic photoinitiators over the notable photoinitiator bis(2,4,6-trimethylbenzoyl)phenylphosphine oxide (BAPO) for mild irradiation conditions featuring their remarkable reactivity. 4-benzylideneamino-2,2,6,6-tetramethylpiperidine-1-oxyl 201-205 CD1c molecule Homo sapiens 60-63 29207574-3 2017 Seven new carbazole derivatives Cd1-Cd7 are incorporated and proposed as high performance near-UV photoinitiators for both the free radical polymerization (FRP) of (meth)acrylates and the cationic polymerization (CP) of epoxides utilizing Light Emitting Diodes LEDs @405 nm. carbazole 10-19 CD1c molecule Homo sapiens 32-35 28988508-5 2017 In this hypothesis generating study, the immunological alterations in circulating immune subsets induced by everolimus included a (non-significant) increase in the frequency of Tregs, a significant increase in monocytic myeloid-derived suppressor cells, a significant decrease in the frequency of immunoregulatory natural killer cells, classical CD141+ (cDC1) and CD1c+ (cDC2) dendritic cell subsets, as well as a decrease in the activation status of plasmacytoid dendritic cells and cDC1. Everolimus 108-118 CD1c molecule Homo sapiens 364-368 28683540-3 2017 Thus, the main goal of this study was to develop composition-tunable and biocompatible Zn x Cd1 - x S QDs using carboxymethylcellulose polysaccharide as direct capping ligand via green colloidal aqueous route at neutral pH and at room temperature for potential biomedical and environmental applications. carboxymethylcellulose polysaccharide 112-149 CD1c molecule Homo sapiens 92-95 28683540-6 2017 The XRD results indicated that monophasic ternary alloyed Zn x Cd1 - x S nanocrystals were produced with homogenous composition of the core as evidenced by EELS and XPS analyses. Zinc 58-60 CD1c molecule Homo sapiens 63-66 28683540-7 2017 In addition, the absorption and emission optical properties of Zn x Cd1 - x S QDs were red shifted with increasing the amount of Cd2+ in the alloyed nanocrystals, which have also increased the quantum yield compared to pure CdS and ZnS nanoparticles. Zinc 63-65 CD1c molecule Homo sapiens 68-71 28683540-7 2017 In addition, the absorption and emission optical properties of Zn x Cd1 - x S QDs were red shifted with increasing the amount of Cd2+ in the alloyed nanocrystals, which have also increased the quantum yield compared to pure CdS and ZnS nanoparticles. Cadmium 224-227 CD1c molecule Homo sapiens 68-71 28683540-7 2017 In addition, the absorption and emission optical properties of Zn x Cd1 - x S QDs were red shifted with increasing the amount of Cd2+ in the alloyed nanocrystals, which have also increased the quantum yield compared to pure CdS and ZnS nanoparticles. Zinc 232-235 CD1c molecule Homo sapiens 68-71 28768549-4 2017 METHODS: Therefore, we have analyzed the central long-term complications in the offspring from CD1 diabetic mothers treated with streptozotozin, as well as the possible reversion of these alterations by insulin administration to neonates. streptozotozin 129-143 CD1c molecule Homo sapiens 95-98 28925020-0 2017 One-Pot Synthesis of Size-Controllable Core-Shell CdS and Derived CdS@Znx Cd1-x S Structures for Photocatalytic Hydrogen Production. Cadmium 66-69 CD1c molecule Homo sapiens 74-77 28925020-0 2017 One-Pot Synthesis of Size-Controllable Core-Shell CdS and Derived CdS@Znx Cd1-x S Structures for Photocatalytic Hydrogen Production. Hydrogen 112-120 CD1c molecule Homo sapiens 74-77 28925020-3 2017 Herein, a facile one-pot method for the synthesis of monodisperse, size-controllable CdS core-shell and CdS@Znx Cd1-x S core-double shell submicrospheres, which were engineered with respect to structure and size, is reported. Cadmium 104-107 CD1c molecule Homo sapiens 112-115 28925020-3 2017 Herein, a facile one-pot method for the synthesis of monodisperse, size-controllable CdS core-shell and CdS@Znx Cd1-x S core-double shell submicrospheres, which were engineered with respect to structure and size, is reported. znx 108-111 CD1c molecule Homo sapiens 112-115 28925020-6 2017 By introduction of a zinc precursor in the synthetic system, CdS@Znx Cd1-x S core-double shell submicrospheres were obtained by cation exchange of CdS with zinc ions, with a process of diffusion of CdS towards the outside and transformation of Znx Cd1-x S crystallites. Cadmium 61-64 CD1c molecule Homo sapiens 69-72 28925020-6 2017 By introduction of a zinc precursor in the synthetic system, CdS@Znx Cd1-x S core-double shell submicrospheres were obtained by cation exchange of CdS with zinc ions, with a process of diffusion of CdS towards the outside and transformation of Znx Cd1-x S crystallites. Cadmium 61-64 CD1c molecule Homo sapiens 248-251 28925020-6 2017 By introduction of a zinc precursor in the synthetic system, CdS@Znx Cd1-x S core-double shell submicrospheres were obtained by cation exchange of CdS with zinc ions, with a process of diffusion of CdS towards the outside and transformation of Znx Cd1-x S crystallites. znx 65-68 CD1c molecule Homo sapiens 69-72 28925020-6 2017 By introduction of a zinc precursor in the synthetic system, CdS@Znx Cd1-x S core-double shell submicrospheres were obtained by cation exchange of CdS with zinc ions, with a process of diffusion of CdS towards the outside and transformation of Znx Cd1-x S crystallites. znx 65-68 CD1c molecule Homo sapiens 248-251 28925020-6 2017 By introduction of a zinc precursor in the synthetic system, CdS@Znx Cd1-x S core-double shell submicrospheres were obtained by cation exchange of CdS with zinc ions, with a process of diffusion of CdS towards the outside and transformation of Znx Cd1-x S crystallites. Cadmium 147-150 CD1c molecule Homo sapiens 69-72 28925020-6 2017 By introduction of a zinc precursor in the synthetic system, CdS@Znx Cd1-x S core-double shell submicrospheres were obtained by cation exchange of CdS with zinc ions, with a process of diffusion of CdS towards the outside and transformation of Znx Cd1-x S crystallites. Cadmium 147-150 CD1c molecule Homo sapiens 69-72 28925020-6 2017 By introduction of a zinc precursor in the synthetic system, CdS@Znx Cd1-x S core-double shell submicrospheres were obtained by cation exchange of CdS with zinc ions, with a process of diffusion of CdS towards the outside and transformation of Znx Cd1-x S crystallites. znx 244-247 CD1c molecule Homo sapiens 69-72 28925020-8 2017 Furthermore, CdS@Znx Cd1-x S core-double shell structures exhibited excellent stability over 20 h of hydrogen production. Cadmium 13-16 CD1c molecule Homo sapiens 21-24 28925020-8 2017 Furthermore, CdS@Znx Cd1-x S core-double shell structures exhibited excellent stability over 20 h of hydrogen production. Hydrogen 101-109 CD1c molecule Homo sapiens 21-24 29170618-1 2017 We report on the growth and characterization of optical quality multiple quantum well structures of Zn x Cd1-x Se/Zn x Cd y Mg1-x-y Se on an ultra-thin Bi2Se3/CdTe virtual substrate on c-plane Al2O3 (sapphire). Zinc 100-102 CD1c molecule Homo sapiens 105-108 29170618-1 2017 We report on the growth and characterization of optical quality multiple quantum well structures of Zn x Cd1-x Se/Zn x Cd y Mg1-x-y Se on an ultra-thin Bi2Se3/CdTe virtual substrate on c-plane Al2O3 (sapphire). cadmium telluride 159-163 CD1c molecule Homo sapiens 105-108 28463795-8 2017 Western blot analysis indicated remarkable concentration dependent alterations in the expression of proliferation and survival proteins CD1, E2F, CE1, p53, p21, BAX, BCL-2, cytochrome C and cleaved PARP in cisatracurium-treated groups as compared with the untreated group. cisatracurium 206-219 CD1c molecule Homo sapiens 136-139 28587692-2 2017 Energy-dispersive X-ray spectrometry (EDX) in the scanning transmission electron microscope and atom probe tomography (APT) experiments reveal the formation of Cr-rich regions in Cd1-x Cr x Te layers grown by molecular beam epitaxy. Chromium 160-162 CD1c molecule Homo sapiens 179-182 28458670-5 2017 Moreover, physiological concentrations of all-trans retinoic acid (ATRA) are able to re-program the differentiation of moDCs resulting in altered gene expression profiles of the master transcription factors RARalpha and interferon regulatory factor 4, and concomitantly regulate the cell surface expression levels of CD1 proteins and also the mucosa-associated CD103 integrin to different directions. Tretinoin 52-65 CD1c molecule Homo sapiens 317-320 28691226-7 2017 47: 1171-1180] provide intriguing data implying that common small molecule CSs such as dinitrochlorobenzene can also recruit and activate autoreactive CD1-restricted T cells specific for cell-endogenous lipids, which are enriched in human skin. Dinitrochlorobenzene 87-107 CD1c molecule Homo sapiens 151-154 28691226-8 2017 The effects of dinitrochlorobenzene on CD1 T-cell recruitment and function were dependent on newly synthesized CD1 molecules and the presence of endogenous lipids. Dinitrochlorobenzene 15-35 CD1c molecule Homo sapiens 39-42 28691226-8 2017 The effects of dinitrochlorobenzene on CD1 T-cell recruitment and function were dependent on newly synthesized CD1 molecules and the presence of endogenous lipids. Dinitrochlorobenzene 15-35 CD1c molecule Homo sapiens 111-114 28458670-5 2017 Moreover, physiological concentrations of all-trans retinoic acid (ATRA) are able to re-program the differentiation of moDCs resulting in altered gene expression profiles of the master transcription factors RARalpha and interferon regulatory factor 4, and concomitantly regulate the cell surface expression levels of CD1 proteins and also the mucosa-associated CD103 integrin to different directions. Tretinoin 67-71 CD1c molecule Homo sapiens 317-320 28104514-3 2017 We have developed an approach of in vivo expansion of Tregs with RGI-2001, a novel liposomal formulation of a synthetic derivative of alpha-galactosylceramide, a naturally occurring ligand that binds to CD1 and activates and expands invariant natural killer cells. alpha-galactosylceramide 134-158 CD1c molecule Homo sapiens 203-206 28291364-1 2017 The polylactic-co-glycolic acid polyethylene glycol conjugated with cell penetrating peptide R7 (PLGA-PEG-R7)/polysulfadimethoxine-folate nanoparticles loaded with docetaxel (DTX) and GDC0941 (R7/PSD-Fol NPs) were prepared to overcome multidrug resistance (MDR) and enhance the antitumor activity. Polylactic Acid-Polyglycolic Acid Copolymer 4-31 CD1c molecule Homo sapiens 93-95 28291364-1 2017 The polylactic-co-glycolic acid polyethylene glycol conjugated with cell penetrating peptide R7 (PLGA-PEG-R7)/polysulfadimethoxine-folate nanoparticles loaded with docetaxel (DTX) and GDC0941 (R7/PSD-Fol NPs) were prepared to overcome multidrug resistance (MDR) and enhance the antitumor activity. Polylactic Acid-Polyglycolic Acid Copolymer 4-31 CD1c molecule Homo sapiens 97-108 28291364-1 2017 The polylactic-co-glycolic acid polyethylene glycol conjugated with cell penetrating peptide R7 (PLGA-PEG-R7)/polysulfadimethoxine-folate nanoparticles loaded with docetaxel (DTX) and GDC0941 (R7/PSD-Fol NPs) were prepared to overcome multidrug resistance (MDR) and enhance the antitumor activity. Polylactic Acid-Polyglycolic Acid Copolymer 4-31 CD1c molecule Homo sapiens 106-108 28291364-1 2017 The polylactic-co-glycolic acid polyethylene glycol conjugated with cell penetrating peptide R7 (PLGA-PEG-R7)/polysulfadimethoxine-folate nanoparticles loaded with docetaxel (DTX) and GDC0941 (R7/PSD-Fol NPs) were prepared to overcome multidrug resistance (MDR) and enhance the antitumor activity. Polyethylene Glycols 32-51 CD1c molecule Homo sapiens 93-95 28291364-1 2017 The polylactic-co-glycolic acid polyethylene glycol conjugated with cell penetrating peptide R7 (PLGA-PEG-R7)/polysulfadimethoxine-folate nanoparticles loaded with docetaxel (DTX) and GDC0941 (R7/PSD-Fol NPs) were prepared to overcome multidrug resistance (MDR) and enhance the antitumor activity. Polyethylene Glycols 32-51 CD1c molecule Homo sapiens 97-108 28291364-1 2017 The polylactic-co-glycolic acid polyethylene glycol conjugated with cell penetrating peptide R7 (PLGA-PEG-R7)/polysulfadimethoxine-folate nanoparticles loaded with docetaxel (DTX) and GDC0941 (R7/PSD-Fol NPs) were prepared to overcome multidrug resistance (MDR) and enhance the antitumor activity. Polyethylene Glycols 32-51 CD1c molecule Homo sapiens 106-108 28291364-1 2017 The polylactic-co-glycolic acid polyethylene glycol conjugated with cell penetrating peptide R7 (PLGA-PEG-R7)/polysulfadimethoxine-folate nanoparticles loaded with docetaxel (DTX) and GDC0941 (R7/PSD-Fol NPs) were prepared to overcome multidrug resistance (MDR) and enhance the antitumor activity. Docetaxel 164-173 CD1c molecule Homo sapiens 93-95 28291364-1 2017 The polylactic-co-glycolic acid polyethylene glycol conjugated with cell penetrating peptide R7 (PLGA-PEG-R7)/polysulfadimethoxine-folate nanoparticles loaded with docetaxel (DTX) and GDC0941 (R7/PSD-Fol NPs) were prepared to overcome multidrug resistance (MDR) and enhance the antitumor activity. Docetaxel 164-173 CD1c molecule Homo sapiens 97-108 28291364-1 2017 The polylactic-co-glycolic acid polyethylene glycol conjugated with cell penetrating peptide R7 (PLGA-PEG-R7)/polysulfadimethoxine-folate nanoparticles loaded with docetaxel (DTX) and GDC0941 (R7/PSD-Fol NPs) were prepared to overcome multidrug resistance (MDR) and enhance the antitumor activity. Docetaxel 175-178 CD1c molecule Homo sapiens 93-95 28291364-1 2017 The polylactic-co-glycolic acid polyethylene glycol conjugated with cell penetrating peptide R7 (PLGA-PEG-R7)/polysulfadimethoxine-folate nanoparticles loaded with docetaxel (DTX) and GDC0941 (R7/PSD-Fol NPs) were prepared to overcome multidrug resistance (MDR) and enhance the antitumor activity. 2-(1H-indazol-4-yl)-6-(4-methanesulfonylpiperazin-1-ylmethyl)-4-morpholin-4-ylthieno(3,2-d)pyrimidine 184-191 CD1c molecule Homo sapiens 93-95 28291364-4 2017 Due to the pH-sensitive effect of PSD-folate, the releasing of DTX and GDC0941 from the R7/PSD-Fol NPs was lower in pH 7.4 buffer solution than that in pH 5.0 buffer solution. psd-folate 34-44 CD1c molecule Homo sapiens 88-90 28291364-4 2017 Due to the pH-sensitive effect of PSD-folate, the releasing of DTX and GDC0941 from the R7/PSD-Fol NPs was lower in pH 7.4 buffer solution than that in pH 5.0 buffer solution. Docetaxel 63-66 CD1c molecule Homo sapiens 88-90 28291364-4 2017 Due to the pH-sensitive effect of PSD-folate, the releasing of DTX and GDC0941 from the R7/PSD-Fol NPs was lower in pH 7.4 buffer solution than that in pH 5.0 buffer solution. 2-(1H-indazol-4-yl)-6-(4-methanesulfonylpiperazin-1-ylmethyl)-4-morpholin-4-ylthieno(3,2-d)pyrimidine 71-78 CD1c molecule Homo sapiens 88-90 28221804-4 2017 Herein we present a novel synthesis of CdSe/Cd1-xZnxS seeded nanorods with a radially graded composition that show bright and highly polarized green emission with minimal intermittency, as confirmed by ensemble and single nanorods optical measurements. cdse 39-43 CD1c molecule Homo sapiens 44-47 28291364-5 2017 The half maximal inhibitory concentration (IC50) of MCF-7 and resistant to doxorubicin (MCF-7/Adr) cells illustrated the cytotoxicity of R7/PSD-Fol nanoparticles by using the MTT method. Doxorubicin 75-86 CD1c molecule Homo sapiens 137-139 28291364-5 2017 The half maximal inhibitory concentration (IC50) of MCF-7 and resistant to doxorubicin (MCF-7/Adr) cells illustrated the cytotoxicity of R7/PSD-Fol nanoparticles by using the MTT method. monooxyethylene trimethylolpropane tristearate 175-178 CD1c molecule Homo sapiens 137-139 28291364-6 2017 The uptake of R7/PSD-Fol NPs was visualized by using the fluorescence of Rh-123 to detect the targeting effect of folate on the surface of R7/PSD-Fol NPs. Rhodamine 123 73-79 CD1c molecule Homo sapiens 14-16 28291364-6 2017 The uptake of R7/PSD-Fol NPs was visualized by using the fluorescence of Rh-123 to detect the targeting effect of folate on the surface of R7/PSD-Fol NPs. Folic Acid 114-120 CD1c molecule Homo sapiens 14-16 28291364-6 2017 The uptake of R7/PSD-Fol NPs was visualized by using the fluorescence of Rh-123 to detect the targeting effect of folate on the surface of R7/PSD-Fol NPs. Folic Acid 114-120 CD1c molecule Homo sapiens 139-141 28291364-10 2017 It was concluded that R7/PSD-Fol NPs loaded with DTX and GDC0941 could overcome MDR and enhance the antitumor effect further. Docetaxel 49-52 CD1c molecule Homo sapiens 22-24 28291364-10 2017 It was concluded that R7/PSD-Fol NPs loaded with DTX and GDC0941 could overcome MDR and enhance the antitumor effect further. 2-(1H-indazol-4-yl)-6-(4-methanesulfonylpiperazin-1-ylmethyl)-4-morpholin-4-ylthieno(3,2-d)pyrimidine 57-64 CD1c molecule Homo sapiens 22-24 28087664-5 2017 In the present study, we showed that human blood CD1c+ cDCs (cDC2s) can be further separated into two subpopulations according to their CD5 expression status. Chenodeoxycholate 3-sulphate 55-59 CD1c molecule Homo sapiens 49-53 28176522-3 2017 Our results identify that full miscibility of most Cd1-xZnxOyS1-y compositions and even binaries like Zn(O,S) is outside typical photovoltaic processing conditions. Zinc 56-58 CD1c molecule Homo sapiens 51-54 28116384-0 2017 Effect of Zn substitution on the magnetic and magnetocaloric properties of Cd1-xZnxCr2Se4 spinel. Zinc 10-12 CD1c molecule Homo sapiens 75-78 28169376-0 2017 Surface Passivation of CdSe Quantum Dots in All Inorganic Amorphous Solid by Forming Cd1-xZnxSe Shell. cdse 23-27 CD1c molecule Homo sapiens 85-88 28169376-3 2017 In this study, surface passivation of CdSe quantum dots (QDs) by Cd1-xZnxSe shell in silicate glass was reported. cdse 38-42 CD1c molecule Homo sapiens 65-68 28169376-3 2017 In this study, surface passivation of CdSe quantum dots (QDs) by Cd1-xZnxSe shell in silicate glass was reported. Silicates 85-93 CD1c molecule Homo sapiens 65-68 27250804-11 2017 CONCLUSIONS: TARC levels are increased in RA SF and our data indicate that this results from production by SFMCs and in particular CD1c cDCs. Chenodeoxycholate 3-sulphate 136-140 CD1c molecule Homo sapiens 131-135 28243553-2 2017 We performed a study on a range of (Cd1-x Zn x )3As2 mixed crystals undergoing a transition from the Dirac semimetal phase with an inverse electron energy spectrum to trivial a semiconductor with a direct spectrum in the crystal bulk by varying the composition x. dirac 101-106 CD1c molecule Homo sapiens 36-39 27250804-12 2017 TARC attracts T cells and TARC secretion by MCs is crucially dependent on the presence of CD1c cDCs. mcs 44-47 CD1c molecule Homo sapiens 90-94 27250804-12 2017 TARC attracts T cells and TARC secretion by MCs is crucially dependent on the presence of CD1c cDCs. Chenodeoxycholate 3-sulphate 95-99 CD1c molecule Homo sapiens 90-94 27598838-0 2016 Bare Cd1-xZnxS ZB/WZ Heterophase Nanojunctions for Visible Light Photocatalytic Hydrogen Production with High Efficiency. Hydrogen 80-88 CD1c molecule Homo sapiens 5-8 27636008-4 2016 METHODS: In vitro toxicity was investigated in human skin melanoma Sk-Mel-28 cells, and skin squamous cell carcinoma was induced in CD1 mice by dimethylbenzanthracene (DMBA) and 12-O-tetradecanoyl-phorbol-13-acetate (TPA). 9,10-Dimethyl-1,2-benzanthracene 144-166 CD1c molecule Homo sapiens 132-135 27636008-4 2016 METHODS: In vitro toxicity was investigated in human skin melanoma Sk-Mel-28 cells, and skin squamous cell carcinoma was induced in CD1 mice by dimethylbenzanthracene (DMBA) and 12-O-tetradecanoyl-phorbol-13-acetate (TPA). 9,10-Dimethyl-1,2-benzanthracene 168-172 CD1c molecule Homo sapiens 132-135 27636008-4 2016 METHODS: In vitro toxicity was investigated in human skin melanoma Sk-Mel-28 cells, and skin squamous cell carcinoma was induced in CD1 mice by dimethylbenzanthracene (DMBA) and 12-O-tetradecanoyl-phorbol-13-acetate (TPA). Tetradecanoylphorbol Acetate 178-215 CD1c molecule Homo sapiens 132-135 27598838-1 2016 In this work, we report the synthesis of Cd1-xZnxS zinc blende/wurtzite (ZB/WZ) heterophase nanojunctions with highly efficient charge separation by a solvothermal method in a mixed solution of diethylenetriamine (DETA) and distilled water. zinc sulfide 51-62 CD1c molecule Homo sapiens 41-44 27598838-1 2016 In this work, we report the synthesis of Cd1-xZnxS zinc blende/wurtzite (ZB/WZ) heterophase nanojunctions with highly efficient charge separation by a solvothermal method in a mixed solution of diethylenetriamine (DETA) and distilled water. wurtzite 63-71 CD1c molecule Homo sapiens 41-44 27598838-1 2016 In this work, we report the synthesis of Cd1-xZnxS zinc blende/wurtzite (ZB/WZ) heterophase nanojunctions with highly efficient charge separation by a solvothermal method in a mixed solution of diethylenetriamine (DETA) and distilled water. Zoledronic Acid 73-75 CD1c molecule Homo sapiens 41-44 27598838-1 2016 In this work, we report the synthesis of Cd1-xZnxS zinc blende/wurtzite (ZB/WZ) heterophase nanojunctions with highly efficient charge separation by a solvothermal method in a mixed solution of diethylenetriamine (DETA) and distilled water. diethylenetriamine 194-212 CD1c molecule Homo sapiens 41-44 27598838-1 2016 In this work, we report the synthesis of Cd1-xZnxS zinc blende/wurtzite (ZB/WZ) heterophase nanojunctions with highly efficient charge separation by a solvothermal method in a mixed solution of diethylenetriamine (DETA) and distilled water. diethylenetriamine 214-218 CD1c molecule Homo sapiens 41-44 27598838-1 2016 In this work, we report the synthesis of Cd1-xZnxS zinc blende/wurtzite (ZB/WZ) heterophase nanojunctions with highly efficient charge separation by a solvothermal method in a mixed solution of diethylenetriamine (DETA) and distilled water. Water 234-239 CD1c molecule Homo sapiens 41-44 27598838-7 2016 Further, the strong binding between the l-cysteine ligand and Cd1-xZnxS elongated nanocrystals protects and stabilizes NCs; the l-cysteine ligand at the interface could trap holes from Cd1-xZnxS NCs, while photogenerated electrons transfer to Cd1-xZnxS catalytic sites for proton reduction. Cysteine 40-50 CD1c molecule Homo sapiens 62-65 27598838-7 2016 Further, the strong binding between the l-cysteine ligand and Cd1-xZnxS elongated nanocrystals protects and stabilizes NCs; the l-cysteine ligand at the interface could trap holes from Cd1-xZnxS NCs, while photogenerated electrons transfer to Cd1-xZnxS catalytic sites for proton reduction. Cysteine 40-50 CD1c molecule Homo sapiens 185-188 27598838-7 2016 Further, the strong binding between the l-cysteine ligand and Cd1-xZnxS elongated nanocrystals protects and stabilizes NCs; the l-cysteine ligand at the interface could trap holes from Cd1-xZnxS NCs, while photogenerated electrons transfer to Cd1-xZnxS catalytic sites for proton reduction. Cysteine 128-138 CD1c molecule Homo sapiens 62-65 27598838-7 2016 Further, the strong binding between the l-cysteine ligand and Cd1-xZnxS elongated nanocrystals protects and stabilizes NCs; the l-cysteine ligand at the interface could trap holes from Cd1-xZnxS NCs, while photogenerated electrons transfer to Cd1-xZnxS catalytic sites for proton reduction. Cysteine 128-138 CD1c molecule Homo sapiens 185-188 27598838-8 2016 Our results demonstrate that Cd1-xZnxS ZB/WZ heterophase junctions stabilized by l-cysteine molecules can effectively separate charge carriers and achieve highly visible light photocatalytic hydrogen production. Cysteine 81-91 CD1c molecule Homo sapiens 29-32 27598838-8 2016 Our results demonstrate that Cd1-xZnxS ZB/WZ heterophase junctions stabilized by l-cysteine molecules can effectively separate charge carriers and achieve highly visible light photocatalytic hydrogen production. Hydrogen 191-199 CD1c molecule Homo sapiens 29-32 27454933-4 2016 The catalytic activity of CD2 from both species exhibited broad substrate specificity, whereas that of CD1 was highly specific for substrates bearing C-terminal acetyllysine residues. N-epsilon-Acetyl-L-lysine 161-173 CD1c molecule Homo sapiens 103-106 26902728-7 2016 Interestingly, only the 1,800-pRBC dose caused a reduction in the circulating CD1c(+) mDC count with evidence of apoptosis. 1,800-prbc 24-34 CD1c molecule Homo sapiens 78-82 27251953-0 2016 Biomolecule-assisted synthesis of defect-mediated Cd1-xZnxS/MoS2/graphene hollow spheres for highly efficient hydrogen evolution. Graphite 65-73 CD1c molecule Homo sapiens 50-53 27251953-0 2016 Biomolecule-assisted synthesis of defect-mediated Cd1-xZnxS/MoS2/graphene hollow spheres for highly efficient hydrogen evolution. Hydrogen 110-118 CD1c molecule Homo sapiens 50-53 27251953-4 2016 A facile biomolecule-assisted strategy was used to self-assmble Cd1-xZnxS/MoS2/graphene hollow spheres. molybdenum disulfide 74-78 CD1c molecule Homo sapiens 64-67 27251953-4 2016 A facile biomolecule-assisted strategy was used to self-assmble Cd1-xZnxS/MoS2/graphene hollow spheres. Graphite 79-87 CD1c molecule Homo sapiens 64-67 27622063-10 2016 Moreover, upon interaction with platinum-treated tumor cells, CD1c(+) DCs efficiently stimulated allogeneic proliferation of T lymphocytes. Platinum 32-40 CD1c molecule Homo sapiens 62-66 30090283-0 2016 The functional role of the structure of the dioxo-isobacteriochlorin in the catalytic site of cytochrome cd1 for the reduction of nitrite. dioxo-isobacteriochlorin 44-68 CD1c molecule Homo sapiens 105-108 30090283-0 2016 The functional role of the structure of the dioxo-isobacteriochlorin in the catalytic site of cytochrome cd1 for the reduction of nitrite. Nitrites 130-137 CD1c molecule Homo sapiens 105-108 30090283-1 2016 Cytochrome cd1 is a key enzyme in bacterial denitrification and catalyzes one-electron reduction of nitrite (NO2-) to nitric oxide (NO) at the heme d1 center under anaerobic conditions. Nitrites 100-107 CD1c molecule Homo sapiens 11-14 30090283-1 2016 Cytochrome cd1 is a key enzyme in bacterial denitrification and catalyzes one-electron reduction of nitrite (NO2-) to nitric oxide (NO) at the heme d1 center under anaerobic conditions. Nitrogen Dioxide 109-112 CD1c molecule Homo sapiens 11-14 30090283-1 2016 Cytochrome cd1 is a key enzyme in bacterial denitrification and catalyzes one-electron reduction of nitrite (NO2-) to nitric oxide (NO) at the heme d1 center under anaerobic conditions. Nitric Oxide 118-130 CD1c molecule Homo sapiens 11-14 30090283-2 2016 The heme d1 has a unique dioxo-isobacteriochlorin structure and is present only in cytochrome cd1. Heme 4-8 CD1c molecule Homo sapiens 94-97 30090283-3 2016 To reveal the functional role of the unique heme d1 in the catalytic nitrite reduction, we studied effect of the porphyrin macrocycle on each reaction step of the catalytic cycle of cytochrome cd1 using synthetic model complexes. Porphyrins 113-122 CD1c molecule Homo sapiens 193-196 30090283-10 2016 These results suggest that the heme d1 has evolved as the catalytic site of cytochrome cd1 to catalyze the nitrite reduction at the highest possible redox potential while maintaining its catalytic activity. Nitrites 107-114 CD1c molecule Homo sapiens 87-90 26884207-0 2016 Cholesteryl esters stabilize human CD1c conformations for recognition by self-reactive T cells. Cholesterol Esters 0-18 CD1c molecule Homo sapiens 35-39 26959879-4 2016 The postoperative suppressed percentages of pDCs, CD1c+ mDCs, and CD141+ mDCs increased significantly following the perioperative treatment with flurbiprofen. Flurbiprofen 145-157 CD1c molecule Homo sapiens 50-54 26775239-0 2016 Mesoporous Cd1-xZnxS microspheres with tunable bandgap and high specific surface areas for enhanced visible-light-driven hydrogen generation. Hydrogen 121-129 CD1c molecule Homo sapiens 11-14 26775239-3 2016 Herein, we describe a facile one-pot hydrothermal approach toward uniform mesoporous microspheres of Cd1-xZnxS by adopting diethylenetriamine (DETA) as the structure-directing agent. diethylenetriamine 123-141 CD1c molecule Homo sapiens 101-104 26775239-3 2016 Herein, we describe a facile one-pot hydrothermal approach toward uniform mesoporous microspheres of Cd1-xZnxS by adopting diethylenetriamine (DETA) as the structure-directing agent. diethylenetriamine 143-147 CD1c molecule Homo sapiens 101-104 26295903-0 2016 Effects of in Utero Exposure to Arsenic during the Second Half of Gestation on Reproductive End Points and Metabolic Parameters in Female CD-1 Mice. Arsenic 32-39 CD1c molecule Homo sapiens 138-142 26295903-11 2016 CONCLUSION: Our findings revealed unexpected effects of in utero exposure to arsenic: exposure to both a human-relevant low dose and a tumor-inducing level led to early onset of vaginal opening and to obesity in female CD-1 mice. Arsenic 77-84 CD1c molecule Homo sapiens 219-223 26884207-3 2016 Computational simulations exploring different occupancy states of the groove reenacted these different CD1c conformations and suggested cholesteryl esters (CE) and acylated steryl glycosides (ASG) as new ligand classes for CD1c. Cholesterol Esters 136-154 CD1c molecule Homo sapiens 103-107 26884207-3 2016 Computational simulations exploring different occupancy states of the groove reenacted these different CD1c conformations and suggested cholesteryl esters (CE) and acylated steryl glycosides (ASG) as new ligand classes for CD1c. Cholesterol Esters 136-154 CD1c molecule Homo sapiens 223-227 26884207-3 2016 Computational simulations exploring different occupancy states of the groove reenacted these different CD1c conformations and suggested cholesteryl esters (CE) and acylated steryl glycosides (ASG) as new ligand classes for CD1c. steryl glycosides 173-190 CD1c molecule Homo sapiens 223-227 26884207-3 2016 Computational simulations exploring different occupancy states of the groove reenacted these different CD1c conformations and suggested cholesteryl esters (CE) and acylated steryl glycosides (ASG) as new ligand classes for CD1c. N-Acetylgalactosamine 4-sulphate 192-195 CD1c molecule Homo sapiens 223-227 26884207-5 2016 Hence, human CD1c adopts different conformations dependent on ligand occupancy of its groove, with CE and ASG stabilizing CD1c conformations that provide a footprint for binding of CD1c self-reactive T-cell receptors. N-Acetylgalactosamine 4-sulphate 106-109 CD1c molecule Homo sapiens 13-17 26884207-5 2016 Hence, human CD1c adopts different conformations dependent on ligand occupancy of its groove, with CE and ASG stabilizing CD1c conformations that provide a footprint for binding of CD1c self-reactive T-cell receptors. N-Acetylgalactosamine 4-sulphate 106-109 CD1c molecule Homo sapiens 122-126 26884207-5 2016 Hence, human CD1c adopts different conformations dependent on ligand occupancy of its groove, with CE and ASG stabilizing CD1c conformations that provide a footprint for binding of CD1c self-reactive T-cell receptors. N-Acetylgalactosamine 4-sulphate 106-109 CD1c molecule Homo sapiens 122-126 26755823-2 2016 In this study, we report that CD1c tetramers carrying Mycobacterium tuberculosis phosphomycoketide bind gammadelta TCRs. phosphomycoketide 81-98 CD1c molecule Homo sapiens 30-34 26755752-4 2016 The more important aspects investigated pertain to the visible-light-induced generation of hydrogen by using semiconductor heterostructures of the type ZnO/Pt/Cd1-xZnxS and dye-sensitized semiconductors. Hydrogen 91-99 CD1c molecule Homo sapiens 159-162 26755823-5 2016 Surprisingly, TCRs also bind CD1c complexes formed with diverse lipids such as lysophosphatidylcholine, sulfatide, or mannosyl-phosophomycoketide, but not lipopeptide ligands. Lysophosphatidylcholines 79-102 CD1c molecule Homo sapiens 29-33 26755823-5 2016 Surprisingly, TCRs also bind CD1c complexes formed with diverse lipids such as lysophosphatidylcholine, sulfatide, or mannosyl-phosophomycoketide, but not lipopeptide ligands. Sulfoglycosphingolipids 104-113 CD1c molecule Homo sapiens 29-33 26755823-5 2016 Surprisingly, TCRs also bind CD1c complexes formed with diverse lipids such as lysophosphatidylcholine, sulfatide, or mannosyl-phosophomycoketide, but not lipopeptide ligands. mannosyl-phosophomycoketide 118-145 CD1c molecule Homo sapiens 29-33 26978928-2 2015 Then water-soluble Cd1-xZnxSe ternary quantum dots with different component were prepared by colloid chemistry. Water 5-10 CD1c molecule Homo sapiens 19-22 26567872-5 2015 This is realized by controlling the spatial overlap between the carrier wave functions with the manganese ions by adjusting the location, composition, and number of the CdSe, Cd1-xMnxS, and CdS layers. Manganese 96-105 CD1c molecule Homo sapiens 175-178 31973329-2 2015 Crystal-structure analysis reveals 1) in 1, phthalate moieties for L1 link Cd1 centers into a 1D slightly helical chain; Cd2 centers act as bridges, linking 1D helical chains into a 3D network with a (3,5)-connected topology; 2) in 2-4, although Cd2+ centers were further modified by the introduction of organic bases, L1 molecules still link Cd2+ centers into 3D networks, which can all be simplified as pcu topology; 3) in 2-4, phthalate moieties first link Cd2+ centers into an oligomer, in which carboxylate-bridged discrete or rod-shaped secondary building units (SBUs) are found (tetranuclear SBU in 2 and 3, rod-shaped SBU in 4); and 4) in 5, L2 molecules link Cd2+ centers into a 2D (4,4) net; introduced bpp molecules serve as pillar linkers, extending Cd2+ -L2 layers into a 3D network of 5. phthalic acid 44-53 CD1c molecule Homo sapiens 75-78 26451804-2 2015 Here we report a novel strategy to synthesize Zn x Cd1-x S NFs via the synergistic actions of the graphene oxide (GO) confinement effect and oriented cation exchange. Zinc 46-48 CD1c molecule Homo sapiens 51-54 26451804-2 2015 Here we report a novel strategy to synthesize Zn x Cd1-x S NFs via the synergistic actions of the graphene oxide (GO) confinement effect and oriented cation exchange. graphene oxide 98-112 CD1c molecule Homo sapiens 51-54 26451804-2 2015 Here we report a novel strategy to synthesize Zn x Cd1-x S NFs via the synergistic actions of the graphene oxide (GO) confinement effect and oriented cation exchange. graphene oxide 114-116 CD1c molecule Homo sapiens 51-54 26487699-11 2016 We conclude that the lipid-binding groove in ZAG contains at least two distinct fatty acid-binding sites for DAUDA and C16-BODIPY, similar to the multiple lipid binding seen in the structurally related immune protein CD1c. Fatty Acids 80-90 CD1c molecule Homo sapiens 217-221 26107189-0 2015 Influence of Endosomal Escape and Degradation of alpha-Galactosylceramide Loaded Liposomes on CD1d Antigen Presentation. alpha-galactosylceramide 49-73 CD1c molecule Homo sapiens 94-97 25753381-8 2015 The identity of the preferred ligands for gammadelta T cells remains obscure, but it is now known that this receptor can also functionally engage CD1-lipid, or immunoglobulin (Ig) superfamily proteins called butyrophilins in the presence of pyrophosphate intermediates of bacterial lipid biosynthesis. diphosphoric acid 241-254 CD1c molecule Homo sapiens 146-149