Truncated, inactive N-acetylglucosaminyltransferase III (GlcNAc-TIII) induces neurological and other traits absent in mice that lack GlcNAc-TIII. (Q32101334)

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English	Truncated, inactive N-acetylglucosaminyltransferase III (GlcNAc-TIII) induces neurological and other traits absent in mice that lack GlcNAc-TIII.	scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

Truncated, inactive N-acetylglucosaminyltransferase III (GlcNAc-TIII) induces neurological and other traits absent in mice that lack GlcNAc-TIII. (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

author name string

Riddhi Bhattacharyya

1

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

Mantu Bhaumik

2

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Europe PubMed Central

PubMed publication ID

6 July 2017

T Shantha Raju

3

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Europe PubMed Central

PubMed publication ID

6 July 2017

Pamela Stanley

4

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Europe PubMed Central

PubMed publication ID

6 July 2017

language of work or name

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publication date

1 May 2002

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Europe PubMed Central

PubMed publication ID

6 July 2017

Journal of Biological Chemistry

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Europe PubMed Central

PubMed publication ID

6 July 2017

277

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Europe PubMed Central

PubMed publication ID

6 July 2017

29

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

26300-26309

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Europe PubMed Central

PubMed publication ID

6 July 2017

cDNA cloning, expression, and chromosomal localization of human N-acetylglucosaminyltransferase III (GnT-III)

1 reference

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Down-regulation of the alpha-Gal epitope expression in N-glycans of swine endothelial cells by transfection with the N-acetylglucosaminyltransferase III gene. Modulation of the biosynthesis of terminal structures by a bisecting GlcNAc

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Cloning and chromosomal mapping of the mouse Mgat3 gene encoding N-acetylglucosaminyltransferase III

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Isolation, characterization and inactivation of the mouse Mgat3 gene: the bisecting N-acetylglucosamine in asparagine-linked oligosaccharides appears dispensable for viability and reproduction

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Expression of N-acetylglucosaminyltransferase III in hepatic nodules generated by different models of rat liver carcinogenesis.

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Changes of beta-1,4-N-acetylglucosaminyltransferase III (GnT-III) in patients with leukaemia.

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Chinese hamster ovary (CHO) cells may express six beta 4-galactosyltransferases (beta 4GalTs). Consequences of the loss of functional beta 4GalT-1, beta 4GalT-6, or both in CHO glycosylation mutants

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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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Genetic remodeling of protein glycosylation in vivo induces autoimmune disease

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Modeling human congenital disorder of glycosylation type IIa in the mouse: conservation of asparagine-linked glycan-dependent functions in mammalian physiology and insights into disease pathogenesis

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A catalytically inactive beta 1,4-N-acetylglucosaminyltransferase III (GnT-III) behaves as a dominant negative GnT-III inhibitor

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Identifiers

10.1074/JBC.M202276200

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 July 2017

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