Abnormal glycosylation of red cell membrane band 3 in the congenital disorder of glycosylation Ig. (Q34195477)

31 July 2017

title

Abnormal glycosylation of red cell membrane band 3 in the congenital disorder of glycosylation Ig. (English)

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congenital disorder of glycosylation Ig

31 July 2017

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Nathalie Seta

5

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Brigitte Bader-Meunier

object named as

Brigitte Bader-Meunier

2

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author name string

Ewa Zdebska

1

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31 July 2017

Pierre-Olivier Schischmanoff

3

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31 July 2017

Thierry Dupré

4

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31 July 2017

Gil Tchernia

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31 July 2017

Jerzy Kościelak

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31 July 2017

Jean Delaunay

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31 July 2017

language of work or name

English

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publication date

7 May 2003

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31 July 2017

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31 July 2017

volume

54

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31 July 2017

issue

2

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31 July 2017

page(s)

224-229

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Congenital disorders of glycosylation

31 July 2017

cites work

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

21 January 2018

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Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane

21 January 2018

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The joys of HexNAc. The synthesis and function of N- and O-glycan branches

21 January 2018

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ABH blood group active glycoconjugates from human red cells

21 January 2018

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Ordered assembly of the asymmetrically branched lipid-linked oligosaccharide in the endoplasmic reticulum is ensured by the substrate specificity of the individual glycosyltransferases

21 January 2018

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Importance of glycosidases in mammalian glycoprotein biosynthesis

21 January 2018

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Processing of asparagine-linked oligosaccharides in insect cells: evidence for alpha-mannosidase II.

21 January 2018

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Purification and properties of α-mannosidase II from Golgi-like membranes of baculovirus-infected Spodoptera frugiperda (IPLB-SF-21AE) cells

21 January 2018

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Structure of Golgi alpha-mannosidase II: a target for inhibition of growth and metastasis of cancer cells

21 January 2018

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Red cell antigens on band 3 and glycophorin A.

21 January 2018

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Glycolipids and glycopeptides of red cell membranes in congenital dyserythropoietic anaemia type II (CDA II).

21 January 2018

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HEMPAS. Hereditary erythroblastic multinuclearity with positive acidified serum lysis test

21 January 2018

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Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q11.2 by genomewide search

21 January 2018

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Hyperinsulinemic hypoglycemia as a presenting sign in phosphomannose isomerase deficiency: A new manifestation of carbohydrate-deficient glycoprotein syndrome treatable with mannose

21 January 2018

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Carbohydrate-deficient glycoprotein syndrome type II. An autosomal recessive N-acetylglucosaminyltransferase II deficiency different from typical hereditary erythroblastic multinuclearity, with a positive acidified-serum lysis test (HEMPAS)

21 January 2018

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A single-sample method for determination of carbohydrate and protein contents glycoprotein bands separated by sodium dodecyl sulfate- polyacrylamide gel electrophoresis

21 January 2018

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Fluorescamine: A Reagent for Assay of Amino Acids, Peptides, Proteins, and Primary Amines in the Picomole Range

21 January 2018

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New method for the isolation of polyglycosylceramides from human erythrocyte membranes

21 January 2018

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Alterations of Globin Chain Synthesis and of Red Cell Membrane Proteins in Congenital Dyserythropoietic Anemia I and II

21 January 2018

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21 January 2018

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21 January 2018

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Glycoconjugate abnormalities in patients with congenital dyserythropoietic anaemia type I, II and III

21 January 2018

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Short report: erythrocyte membranes from a patient with congenital dyserythropoietic anaemia type I (CDA-I) show identical, although less pronounced, glycoconjugate abnormalities to those from patients with CDA-II (HEMPAS)

21 January 2018

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Structure of serum transferrin in carbohydrate-deficient glycoprotein syndrome

21 January 2018

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10.1203/01.PDR.0000072327.55955.F7

21 January 2018

Identifiers

DOI

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Dimensions Publication ID

31 July 2017

1028510865

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