A recessive deletion in the GlcNAc-1-phosphotransferase gene results in peri-implantation embryonic lethality
about
Localization of alpha 1,3-fucosyltransferase VI in Weibel-Palade bodies of human endothelial cellsSRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorderA defect in dolichol phosphate biosynthesis causes a new inherited disorder with death in early infancyProtein N-glycosylation in oral cancer: dysregulated cellular networks among DPAGT1, E-cadherin adhesion and canonical Wnt signalingInfection, inflammation and host carbohydrates: a Glyco-Evasion HypothesisThe Integrated Role of Wnt/β-Catenin, N-Glycosylation, and E-Cadherin-Mediated Adhesion in Network DynamicsMetabolic manipulation of glycosylation disorders in humans and animal modelsGlycans - the third revolution in evolution.Ubiquitous Importance of Protein Glycosylation.Evolutional and clinical implications of the epigenetic regulation of protein glycosylation.Congenital myasthenic syndromes due to mutations in ALG2 and ALG14.DPAGT1 myasthenia and myopathy: genetic, phenotypic, and expression studies.Hypoglycosylated E-cadherin promotes the assembly of tight junctions through the recruitment of PP2A to adherens junctions.N-glycosylation gene DPAGT1 is a target of the Wnt/beta-catenin signaling pathway.Congenital disorders of glycosylation: glycosylation defects in man and biological models for their study.Human plasma glycome in attention-deficit hyperactivity disorder and autism spectrum disorders.Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.Improvement of dolichol-linked oligosaccharide biosynthesis by the squalene synthase inhibitor zaragozic acid.Targeted disruption of the mouse phosphomannomutase 2 gene causes early embryonic lethalityHigh throughput isolation and glycosylation analysis of IgG-variability and heritability of the IgG glycome in three isolated human populations.Epigenetic silencing of HNF1A associates with changes in the composition of the human plasma N-glycome.Choline Acetyltransferase Mutations Causing Congenital Myasthenic Syndrome: Molecular Findings and Genotype-Phenotype Correlations.Mutations in DPAGT1 cause a limb-girdle congenital myasthenic syndrome with tubular aggregates.Blastocysts don't go it alone. Extrinsic signals fine-tune the intrinsic developmental program of trophoblast cells.Ogt-dependent X-chromosome-linked protein glycosylation is a requisite modification in somatic cell function and embryo viability.A compound heterozygous mutation in DPAGT1 results in a congenital disorder of glycosylation with a relatively mild phenotypeThe Association Between Glycosylation of Immunoglobulin G and Hypertension: A Multiple Ethnic Cross-Sectional StudyComparative transcriptome analysis reveals a regulatory network of microRNA-29b during mouse early embryonic development.NgBR is essential for endothelial cell glycosylation and vascular development.Mannose supplements induce embryonic lethality and blindness in phosphomannose isomerase hypomorphic mice.Complex genetic regulation of protein glycosylation.Mouse models for congenital disorders of glycosylation.Aberrant PSA glycosylation--a sweet predictor of prostate cancer.The role of glycosylation in IBD.Molecular imaging of N-linked glycosylation suggests glycan biosynthesis is a novel target for cancer therapy.The clinical relevance of glycobiology.Terminal alpha-d-mannosides are critical during sea urchin gastrulation.Null mutations in Drosophila N-acetylglucosaminyltransferase I produce defects in locomotion and a reduced life span.Epigenetic regulation of protein glycosylation.Identification and characterization of transcriptional control region of the human beta 1,4-mannosyltransferase gene.
P2860
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P2860
A recessive deletion in the GlcNAc-1-phosphotransferase gene results in peri-implantation embryonic lethality
description
1999 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 1999
@ast
im November 1999 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 1999/11/01)
@sk
vědecký článek publikovaný v roce 1999
@cs
wetenschappelijk artikel (gepubliceerd op 1999/11/01)
@nl
наукова стаття, опублікована в листопаді 1999
@uk
научни чланак (објављен 1999/11/01)
@sr
name
A recessive deletion in the Gl ...... plantation embryonic lethality
@ast
A recessive deletion in the Gl ...... plantation embryonic lethality
@en
A recessive deletion in the Gl ...... plantation embryonic lethality
@nl
type
label
A recessive deletion in the Gl ...... plantation embryonic lethality
@ast
A recessive deletion in the Gl ...... plantation embryonic lethality
@en
A recessive deletion in the Gl ...... plantation embryonic lethality
@nl
prefLabel
A recessive deletion in the Gl ...... plantation embryonic lethality
@ast
A recessive deletion in the Gl ...... plantation embryonic lethality
@en
A recessive deletion in the Gl ...... plantation embryonic lethality
@nl
P2093
P3181
P356
P1433
P1476
A recessive deletion in the Gl ...... plantation embryonic lethality
@en
P2093
I. K. Vijay
J. D. Marth
K. W. Marek
P304
P3181
P356
10.1093/GLYCOB/9.11.1263
P577
1999-11-01T00:00:00Z