The gene defective in leukocyte adhesion deficiency II encodes a putative GDP-fucose transporter.
about
Modification of epidermal growth factor-like repeats with O-fucose. Molecular cloning and expression of a novel GDP-fucose protein O-fucosyltransferaseComposition of Drosophila melanogaster proteome involved in fucosylated glycan metabolismSlc35c2 promotes Notch1 fucosylation and is required for optimal Notch signaling in mammalian cellsA new type of congenital disorders of glycosylation (CDG-Ii) provides new insights into the early steps of dolichol-linked oligosaccharide biosynthesisThe human solute carrier gene SLC35B4 encodes a bifunctional nucleotide sugar transporter with specificity for UDP-xylose and UDP-N-acetylglucosamineDeficiency of dolichyl-P-Man:Man7GlcNAc2-PP-dolichyl mannosyltransferase causes congenital disorder of glycosylation type IgNeutrophils: Between host defence, immune modulation, and tissue injuryIdentification of a missense mutation (G329A;Arg(110)--> GLN) in the human FUT7 geneRegulation of PSGL-1 interactions with L-selectin, P-selectin, and E-selectin: role of human fucosyltransferase-IV and -VIIGolgi nucleotide sugar transport and leukocyte adhesion deficiency IIReactive oxygen species in inflammation and tissue injuryImpairment of skin wound healing in beta-1,4-galactosyltransferase-deficient mice with reduced leukocyte recruitmentDysregulation of TGF-beta1 receptor activation leads to abnormal lung development and emphysema-like phenotype in core fucose-deficient miceDeletion of core fucosylation on alpha3beta1 integrin down-regulates its functionsMetabolic manipulation of glycosylation disorders in humans and animal modelsThe Concise Guide to PHARMACOLOGY 2013/14: transporters.Congenital disorder of fucosylation type 2c (LADII) presenting with short stature and developmental delay with minimal adhesion defectBiosynthesis in vitro of Caenorhabditis elegans phosphorylcholine oligosaccharides.Naïve T cells re-distribute to the lungs of selectin ligand deficient mice.Neural and synaptic defects in slytherin, a zebrafish model for human congenital disorders of glycosylation.Two by two: the pairings of P-selectin and P-selectin glycoprotein ligand 1.Role of glycans and glycosyltransferases in the regulation of Notch signalingThe role of nucleotide sugar transporters in development of eukaryotes.Expression of cutaneous lymphocyte-associated antigen and E-selectin ligand by circulating human memory CD4+ T lymphocytes specific for herpes simplex virus type 2.The human milk oligosaccharide disialyllacto-N-tetraose prevents necrotising enterocolitis in neonatal rats.Update and perspectives on congenital disorders of glycosylation.Wound-healing defect of CD18(-/-) mice due to a decrease in TGF-beta1 and myofibroblast differentiation.C-mannosylation and o-fucosylation of thrombospondin type 1 repeats.Fucose: biosynthesis and biological function in mammals.Substrate recognition by nucleotide sugar transporters: further characterization of substrate recognition regions by analyses of UDP-galactose/CMP-sialic acid transporter chimeras and biochemical analysis of the substrate specificity of parental andNotch deficiency implicated in the pathogenesis of congenital disorder of glycosylation IIcNeural-specific α3-fucosylation of N-linked glycans in the Drosophila embryo requires fucosyltransferase A and influences developmental signaling associated with O-glycosylationEarly myoclonic encephalopathy caused by a disruption of the neuregulin-1 receptor ErbB4Gene flow and biological conflict systems in the origin and evolution of eukaryotes.A missense mutation in the bovine SLC35A3 gene, encoding a UDP-N-acetylglucosamine transporter, causes complex vertebral malformation.The CMP-sialic acid transporter is localized in the medial-trans Golgi and possesses two specific endoplasmic reticulum export motifs in its carboxyl-terminal cytoplasmic tail.Molecular aspects of primary immunodeficiencies: lessons from cytokine and other signaling pathways.Negative feedback regulation of Wnt signaling via N-linked fucosylation in zebrafish.Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId.Mutation of GDP-mannose-4,6-dehydratase in colorectal cancer metastasis
P2860
Q24291613-499FF654-504F-4792-AE5B-FA5B141330A5Q24291882-14463314-956C-43C9-B843-D7300345F9E2Q24299571-F810BEF8-5E0E-4B3A-B8FC-B16B229947F3Q24299581-C4533B99-AA03-4B2A-850B-1DE881B496BDQ24303481-5F205AD3-EE4D-445E-B7CB-AF40DD1BCED3Q24534595-900BCFA1-A4FB-4E6B-B1FF-65BC404F4C56Q28087227-9DDAB548-CC0E-43A2-88C5-BA1F8E56F987Q28201648-6F56E75D-B300-4F7E-9CD2-5ACC6EF61FADQ28296574-08DD394A-40C0-4E25-A264-427F7973A5B0Q28343407-2FBB6DF7-40A4-45BD-AC4F-C57309714CBCQ28396273-122445E7-A829-4753-9A0D-C28392B995A1Q28513469-6AE4CF93-2FDC-469C-B90A-2278B1B44914Q28585434-73B03342-F78D-4C0A-99E2-B894D7C11D45Q28593539-64C245F6-CEA7-4151-988D-13A01F20C08AQ28749888-BF10482A-DFDC-4A0C-A78C-AFEC09B8FE0EQ30486743-7425EC82-0523-46B1-A58D-14F94C4995D1Q30577686-6569EE24-1A1F-41A4-9B98-9668B5922F7DQ30753910-D2804CAB-A3C9-4DCC-AD47-4547D19B5FBAQ33598397-E73D50D6-3D17-4963-ACFC-00D0B32D9C64Q33741917-CCF764A5-8BA7-4B70-B6CA-DBF40AD43CACQ33942883-5DB9C634-DB36-4545-9AA0-2387EFE6D300Q34030111-4EB45590-3325-4143-8CE1-40C4F512F917Q34049992-E7C01EFF-0B9A-4B1D-8431-DE9607F9D136Q34081662-124226D8-C621-41B4-8CB9-4835B30735A6Q34090141-F9B31FFA-A107-4FD8-AD00-96B218BA04C1Q34110629-77D321A7-8EAF-4A97-9505-2266E3968C30Q34116215-70A43DB9-C876-4B59-BEE4-50EC33075ADCQ34136787-5B308F93-A179-430F-B479-D61E295A76A7Q34185452-678F7853-F364-4DAF-8241-97F1ACF5BA05Q34189085-A06239F7-AADB-430F-997C-AAB0ABAB06AAQ34234413-A2C33061-24F7-4B15-AE91-5F0F80E9DBC4Q34308024-CAFE4B27-1630-4F47-A029-6086F80D8F65Q34325839-6E201644-52D6-4274-96EB-A9E54CBD20BDQ34392545-13026EA5-A5F9-464C-85C5-0124987F5FBAQ34475345-D8258106-94B1-40B3-AC17-2255D975BFDBQ34559314-B99D125E-02AE-4DF6-9B4C-EF4ACA2ACAFEQ34647002-A78781FB-B23E-4182-B1AB-D8C82FAEA211Q34651389-1D2DE42F-2FEF-4FBB-AF6E-57E4E0F7F823Q34789899-457FA7E2-02DD-4FCA-9A8B-59970441CCA7Q34906724-413B0FBA-7B18-4252-9EB6-CF577852FAAD
P2860
The gene defective in leukocyte adhesion deficiency II encodes a putative GDP-fucose transporter.
description
2001 nî lūn-bûn
@nan
2001 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
The gene defective in leukocyt ...... tative GDP-fucose transporter.
@ast
The gene defective in leukocyt ...... tative GDP-fucose transporter.
@en
type
label
The gene defective in leukocyt ...... tative GDP-fucose transporter.
@ast
The gene defective in leukocyt ...... tative GDP-fucose transporter.
@en
prefLabel
The gene defective in leukocyt ...... tative GDP-fucose transporter.
@ast
The gene defective in leukocyt ...... tative GDP-fucose transporter.
@en
P2093
P356
P1433
P1476
The gene defective in leukocyt ...... tative GDP-fucose transporter.
@en
P2093
Eckhardt M
Gerardy-Schahn R
P356
10.1038/88289
P407
P577
2001-05-01T00:00:00Z