Golgi alpha-mannosidase II deficiency in vertebrate systems: implications for asparagine-linked oligosaccharide processing in mammals (Q34989525)

5 August 2017

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title

Golgi alpha-mannosidase II deficiency in vertebrate systems: implications for asparagine-linked oligosaccharide processing in mammals (English)

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5 August 2017

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1

Kelley W Moremen

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PubMed ID

12417404

5 August 2017

language of work or name

English

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publication date

1 December 2002

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Biochimica et Biophysica Acta

5 August 2017

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5 August 2017

1573

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5 August 2017

3

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5 August 2017

225-235

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Biological roles of oligosaccharides: all of the theories are correct

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

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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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Glycosidases of the asparagine-linked oligosaccharide processing pathway

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Assembly of asparagine-linked oligosaccharides

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The dolichol pathway of N-linked glycosylation

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Insect cells encode a class II alpha-mannosidase with unique properties

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7 January 2021

Human lysosomal and jack bean alpha-mannosidases are retaining glycosidases

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7 January 2021

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Crystal structure of a class I α1,2-mannosidase involved in N-glycan processing and endoplasmic reticulum quality control

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Mutation of Arg(273) to Leu alters the specificity of the yeast N-glycan processing class I alpha1,2-mannosidase

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Molecular and genetic analysis of the Drosophila mas-1 (mannosidase-1) gene which encodes a glycoprotein processing alpha 1,2-mannosidase.

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7 January 2021

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Identifiers

DOI

1 reference

5 August 2017

1 reference

PubMed ID

12417404