Biosynthesis and deficiencies of glycosylphosphatidylinositol - Test2 - elhamkhani - TriplyDB

Biosynthesis and deficiencies of glycosylphosphatidylinositol

Biosynthesis and deficiencies of glycosylphosphatidylinositol

http://www.wikidata.org/entity/Q26998348

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Plant protein glycosylation Glycosyl-Phosphatidyl-Inositol (GPI)-Anchors and Metalloproteases: Their Roles in the Regulation of Exosome Composition and NKG2D-Mediated Immune Recognition Analysis of zwitterionic and anionic N-linked glycans from invertebrates and protists by mass spectrometry A homozygous PIGN missense mutation in Soft-Coated Wheaten Terriers with a canine paroxysmal dyskinesia.TEX101, a glycoprotein essential for sperm fertility, is required for stable expression of Ly6k on testicular germ cells.Analysis of exome data for 4293 trios suggests GPI-anchor biogenesis defects are a rare cause of developmental disorders.Biosynthesis of GPI-anchored proteins: special emphasis on GPI lipid remodeling.The Impact of Glycosyl-Phosphatidyl-Inositol Anchored MICA Alleles on Novel NKG2D-Based Therapies.Labeling Cell Surface GPIs and GPI-Anchored Proteins through Metabolic Engineering with Artificial Inositol Derivatives.pigk Mutation underlies macho behavior and affects Rohon-Beard cell excitability.HSV1 MicroRNA Modulation of GPI Anchoring and Downstream Immune Evasion.GPI-anchored protein organization and dynamics at the cell surface.GPI-AP release in cellular, developmental, and reproductive biology.Chromosomal microarray testing identifies a 4p terminal region associated with seizures in Wolf-Hirschhorn syndrome.Pathogenic Variants in PIGG Cause Intellectual Disability with Seizures and Hypotonia.Flow cytometry in hematological nonmalignant disorders.Monkeypox Virus Host Factor Screen Using Haploid Cells Identifies Essential Role of GARP Complex in Extracellular Virus Formation.Lipid topogenesis--35years on.Fryns Syndrome Associated with Recessive Mutations in PIGN in two Separate Families.Aspergillus fumigatus Cap59-like protein A is involved in α1,3-mannosylation of GPI-anchors.PGAP3-related hyperphosphatasia with mental retardation syndrome: Report of 10 new patients and a homozygous founder mutation.PIGO deficiency: palmoplantar keratoderma and novel mutations Compound heterozygous mutations in the gene PIGP are associated with early infantile epileptic encephalopathy.Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia.Glycosylphosphatidylinositol (GPI) anchored protein deficiency serves as a reliable reporter of Pig-a gene Mutation: Support from an in vitro assay based on L5178Y/Tk+/- cells and the CD90.2 antigen.Identification of a Golgi GPI-N-acetylgalactosamine transferase with tandem transmembrane regions in the catalytic domain.Recessive loss of function PIGN alleles, including an intragenic deletion with founder effect in La Réunion Island, in patients with Fryns syndrome.Reduced cell surface levels of GPI-linked markers in a new case with PIGG loss of function.Ameliorative effect of myo-inositol on red blood cell alterations in polycystic ovary syndrome: in vitro study.A recurrent germline mutation in the PIGA gene causes Simpson-Golabi-Behmel syndrome type 2.A novel PGAP3 mutation in a Croatian boy with brachytelephalangy and a thin corpus callosum.A case for cannabidiol in Wolf-Hirschhorn syndrome seizure management.Recurrent aseptic meningitis with mutations: a novel pathogenesis of recurrent meningitis successfully treated by eculizumab Nuclear envelope localization of PIG-B is essential for GPI-anchor synthesis in

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Biosynthesis and deficiencies of glycosylphosphatidylinositol

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2014 nî lūn-bûn

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2014 թուականին հրատարակուած գիտական յօդուած

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2014 թվականին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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Biosynthesis and deficiencies of glycosylphosphatidylinositol

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Biosynthesis and deficiencies of glycosylphosphatidylinositol

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Biosynthesis and deficiencies of glycosylphosphatidylinositol

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Biosynthesis and deficiencies of glycosylphosphatidylinositol

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Biosynthesis and deficiencies of glycosylphosphatidylinositol

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Biosynthesis and deficiencies of glycosylphosphatidylinositol

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Biosynthesis and deficiencies of glycosylphosphatidylinositol

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Biosynthesis and deficiencies of glycosylphosphatidylinositol

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Biosynthesis and deficiencies of glycosylphosphatidylinositol

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Biosynthesis and deficiencies of glycosylphosphatidylinositol

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Kinoshita T

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Mammalian PIG-L and its yeast homologue Gpi12p are N-acetylglucosaminylphosphatidylinositol de-N-acetylases essential in glycosylphosphatidylinositol biosynthesis

Gaa1p and gpi8p are components of a glycosylphosphatidylinositol (GPI) transamidase that mediates attachment of GPI to proteins

Human dolichol-phosphate-mannose synthase consists of three subunits, DPM1, DPM2 and DPM3

Initial enzyme for glycosylphosphatidylinositol biosynthesis requires PIG-P and is regulated by DPM2

PIG-S and PIG-T, essential for GPI anchor attachment to proteins, form a complex with GAA1 and GPI8

Two subunits of glycosylphosphatidylinositol transamidase, GPI8 and PIG-T, form a functionally important intermolecular disulfide bridge

Human Smp3p adds a fourth mannose to yeast and human glycosylphosphatidylinositol precursors in vivo

Structural requirements for the recruitment of Gaa1 into a functional glycosylphosphatidylinositol transamidase complex

Human PIG-U and yeast Cdc91p are the fifth subunit of GPI transamidase that attaches GPI-anchors to proteins

DPM2 regulates biosynthesis of dolichol phosphate-mannose in mammalian cells: correct subcellular localization and stabilization of DPM1, and binding of dolichol phosphate

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