Alpha-mannosidase-II deficiency results in dyserythropoiesis and unveils an alternate pathway in oligosaccharide biosynthesis. (Q36872019)

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4 November 2019

title

Alpha-mannosidase-II deficiency results in dyserythropoiesis and unveils an alternate pathway in oligosaccharide biosynthesis (English)

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4 November 2019

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7

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4 November 2019

author name string

D Chui

1

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4 November 2019

M Oh-Eda

2

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4 November 2019

Y F Liao

3

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4 November 2019

K Panneerselvam

4

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4 November 2019

A Lal

5

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4 November 2019

K W Marek

6

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4 November 2019

K W Moremen

8

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4 November 2019

M N Fukuda

9

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4 November 2019

J D Marth

10

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4 November 2019

language of work or name

English

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publication date

1 July 1997

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4 November 2019

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4 November 2019

volume

90

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4 November 2019

issue

1

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4 November 2019

page(s)

157-167

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Structural analysis of the N-linked oligosaccharides from murine glycophorin

4 November 2019

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Purification and characterization of a novel broad-specificity (alpha1 2, alpha1 3 and alpha1 6) mannosidase from rat liver

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Subcellular distribution in rat liver of a novel broad-specificity (alpha 1----2, alpha 1----3 and alpha 1----6) mannosidase active on oligomannose glycans

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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)

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Hereditary Erythroblastic Multinuclearity Associated with a Positive Acidified-Serum Test: a Type of Congenital Dyserythropoietic Anaemia

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Inhibition of lysosomal alpha-mannosidase by swainsonine, an indolizidine alkaloid isolated from Swainsona canescens

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Three types of blood group I specificity among monoclonal anti-I autoantibodies revealed by analogues of a branched erythrocyte glycolipid

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Congenital dyserythropoietic anaemia type II (HEMPAS) and its molecular basis

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Defect in glycosylation of erythrocyte membrane proteins in congenital dyserythropoietic anaemia type II (HEMPAS).

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Incomplete synthesis of N-glycans in congenital dyserythropoietic anemia type II caused by a defect in the gene encoding alpha-mannosidase II

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Incompletely processed N-glycans of serum glycoproteins in congenital dyserythropoietic anaemia type II (HEMPAS)

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T-cell-specific deletion of a polypeptide N-acetylgalactosaminyl-transferase gene by site-directed recombination

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Ricin-resistant mutants of baby-hamster-kidney cells deficient in alpha-mannosidase-II-catalyzed processing of asparagine-linked oligosaccharides

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Mice lacking N-acetylglucosaminyltransferase I activity die at mid-gestation, revealing an essential role for complex or hybrid N-linked carbohydrates

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Immobilized lectin columns: useful tools for the fractionation and structural analysis of oligosaccharides

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Assembly of asparagine-linked oligosaccharides

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Cloning, expression, purification, and characterization of the human broad specificity lysosomal acid alpha-mannosidase

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Cloning, expression, purification, and characterization of the murine lysosomal acid alpha-mannosidase

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Molecular cloning and expression of cDNAs encoding human alpha-mannosidase II and a previously unrecognized alpha-mannosidase IIx isozyme

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4 November 2019

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