Congenital disorders of glycosylation type Ig is defined by a deficiency in dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl mannosyltransferase (Q24296242)

dolichol-linked oligosaccharide biosynthetic process

GOA release 2020-03-11

1 reference

Asparagine-linked glycosylation 12 (alpha-1,6-mannosyltransferase)

GOA release 2020-03-11

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GOA release 2020-03-11

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14

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Nathalie Seta

Nathalie Seta

11

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Isabelle Chantret

Isabelle Chantret

1

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Brigitte Bader-Meunier

Brigitte Bader-Meunier

9

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Delphine Héron

8

Delphine Heron

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author name string

Thierry Dupré

2

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Christophe Delenda

3

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Stéphanie Bucher

4

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Julia Dancourt

5

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Anne Barnier

6

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Aude Charollais

7

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Olivier Danos

10

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Geneviève Durand

12

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Rafael Oriol

13

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Stuart E H Moore

Journal of Biological Chemistry

15

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language of work or name

English

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publication date

12 July 2002

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published in

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volume

277

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issue

28

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page(s)

25815-22

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cites work

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Protein glucosylation and its role in protein folding

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Intracellular functions of N-linked glycans

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Htm1p, a mannosidase-like protein, is involved in glycoprotein degradation in yeast

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Lectins and traffic in the secretory pathway

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Biological roles of oligosaccharides: all of the theories are correct

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Congenital disorders of glycosylation: genetic model systems lead the way.

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Update and perspectives on congenital disorders of glycosylation

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The carbohydrate-deficient glycoprotein syndromes: an overview

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Diseases of abnormal protein glycosylation: an emerging area

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Congenital disorders involving defective N-glycosylation of proteins

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Mutations in PMM2, a phosphomannomutase gene on chromosome 16p13, in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome)

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Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy

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Carbohydrate-deficient glycoprotein syndrome type V: deficiency of dolichyl-P-Glc:Man9GlcNAc2-PP-dolichyl glucosyltransferase

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A mutation in the human ortholog of the Saccharomyces cerevisiae ALG6 gene causes carbohydrate-deficient glycoprotein syndrome type-Ic

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Carbohydrate deficient glycoprotein syndrome type IV: deficiency of dolichyl-P-Man:Man(5)GlcNAc(2)-PP-dolichyl mannosyltransferase

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Dolichol phosphate mannose synthase (DPM1) mutations define congenital disorder of glycosylation Ie (CDG-Ie)

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Deficiency of dolichol-phosphate-mannose synthase-1 causes congenital disorder of glycosylation type Ie

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MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If

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Human glycosylation disorders and sugar supplement therapy.

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Northern blot normalization with a 28S rRNA oligonucleotide probe.

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Model SV40-transformed fibroblast lines for metabolic studies of human prosaposin and acid ceramidase deficiencies

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Use of lectins in analysis of glycoconjugates

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Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences

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Fate mapping of the mouse midbrain-hindbrain constriction using a site-specific recombination system

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GPI anchor biosynthesis in yeast: phosphoethanolamine is attached to the alpha1,4-linked mannose of the complete precursor glycophospholipid

21 January 2018

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Degradation of misfolded endoplasmic reticulum glycoproteins in Saccharomyces cerevisiae is determined by a specific oligosaccharide structure

21 January 2018

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The yeast ALG11 gene specifies addition of the terminal alpha 1,2-Man to the Man5GlcNAc2-PP-dolichol N-glycosylation intermediate formed on the cytosolic side of the endoplasmic reticulum

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The dolichol pathway of N-linked glycosylation

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CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice

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Processing by endoplasmic reticulum mannosidases partitions a secretion-impaired glycoprotein into distinct disposal pathways

21 January 2018

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The pathology of N-glycosylation--stay the middle, avoid the risks

21 January 2018

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Disorders in protein glycosylation and potential therapy: tip of an iceberg?

21 January 2018

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Diagnostic value of Western blotting in carbohydrate-deficient glycoprotein syndrome

21 January 2018

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Abnormal synthesis of mannose 1-phosphate derived carbohydrates in carbohydrate-deficient glycoprotein syndrome type I fibroblasts with phosphomannomutase deficiency

21 January 2018

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Congenital hepatic fibrosis in 3 siblings with phosphomannose isomerase deficiency

21 January 2018

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A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If)

21 January 2018

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Defect in N-glycosylation of proteins is tissue-dependent in Congenital Disorders of Glycosylation Ia

21 January 2018

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HIV-1 genome nuclear import is mediated by a central DNA flap

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Recognition of the oligosaccharide and protein moieties of glycoproteins by the UDP-Glc:glycoprotein glucosyltransferase

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Inhibitors of the Biosynthesis and Processing of N-Linked Oligosaccharide

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inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1074/JBC.M203285200

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

11983712

1 reference

Consolidated OpenCitations Corpus – April 2017