Mice with a homozygous deletion of the Mgat2 gene encoding UDP-N-acetylglucosamine:alpha-6-D-mannoside beta1,2-N-acetylglucosaminyltransferase II: a model for congenital disorder of glycosylation type IIa (Q28589941)

From Wikidata

Jump to navigation Jump to search

scientific journal article

Language	Label	Description	Also known as
English	Mice with a homozygous deletion of the Mgat2 gene encoding UDP-N-acetylglucosamine:alpha-6-D-mannoside beta1,2-N-acetylglucosaminyltransferase II: a model for congenital disorder of glycosylation type IIa	scientific journal article

Statements

scholarly article

1 reference

31 January 2017

1 reference

Europe PubMed Central

Mice with a homozygous deletion of the Mgat2 gene encoding UDP-N-acetylglucosamine:alpha-6-D-mannoside beta1,2-N-acetylglucosaminyltransferase II: a model for congenital disorder of glycosylation type IIa (English)

1 reference

31 January 2017

congenital disorder of glycosylation type IIa

0 references

Mannoside acetylglucosaminyltransferase 2

1 reference

GOA release 2020-03-11

1 reference

based on heuristic

inferred from title

congenital disorder

1 reference

based on heuristic

inferred from title

congenital disorder

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

author name string

Yan Wang

1

1 reference

31 January 2017

Harry Schachter

2

1 reference

31 January 2017

Jamey D. Marth

3

1 reference

31 January 2017

language of work or name

0 references

publication date

19 December 2002

1 reference

31 January 2017

Biochimica et Biophysica Acta

1 reference

31 January 2017

1573

1 reference

31 January 2017

301–311

1 reference

31 January 2017

3

1 reference

31 January 2017

The 'yellow brick road' to branched complex N-glycans

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900397-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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)

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900397-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Carbohydrate deficient glycoprotein syndrome type II: a deficiency in Golgi localised N-acetyl-glucosaminyltransferase II.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900397-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Carbohydrate-deficient glycoprotein syndrome type II.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900397-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Carbohydrate-deficient glycoprotein syndrome type 2

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900397-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Congenital disorders of glycosylation IIa cause growth retardation, mental retardation, and facial dysmorphism

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900397-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900397-5

7 January 2021

based on heuristic

inferred from DOI database lookup

The human UDP-N-acetylglucosamine: alpha-6-D-mannoside-beta-1,2- N-acetylglucosaminyltransferase II gene (MGAT2). Cloning of genomic DNA, localization to chromosome 14q21, expression in insect cells and purification of the recombinant protein

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900397-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular cloning of the porcine beta-1,2-N-acetylglucosaminyltransferase II gene and assignment to chromosome 1q23-q27.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900397-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular cloning and expression of cDNA encoding the rat UDP-N-acetylglucosamine:alpha-6-D-mannoside beta-1,2-N-acetylglucosaminyltransferase II

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900397-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular cloning of cDNA encoding N-acetylglucosaminyltransferase II from Arabidopsis thaliana.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900397-5

7 January 2021

based on heuristic

inferred from DOI database lookup

The O-GlcNAc transferase gene resides on the X chromosome and is essential for embryonic stem cell viability and mouse ontogeny

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900397-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Determination of glycan structures and molecular masses of the glycovariants of serum transferrin from a patient with carbohydrate deficient syndrome type II

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900397-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Structure of serum transferrin in carbohydrate-deficient glycoprotein syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900397-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Electrospray ionization-mass spectrometric analysis of serum transferrin isoforms in patients with carbohydrate-deficient glycoprotein syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900397-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Biosynthetic controls that determine the branching and microheterogeneity of protein-bound oligosaccharides

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900397-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic remodeling of protein glycosylation in vivo induces autoimmune disease

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900397-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900397-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Use of geographutoxin II (mu-conotoxin) for the study of neuromuscular transmission in mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900397-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Germ cell survival through carbohydrate-mediated interaction with Sertoli cells

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900397-5

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900397-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Complex asparagine-linked oligosaccharides are required for morphogenic events during post-implantation development.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900397-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Active suppression of interneuron programs within developing motor neurons revealed by analysis of homeodomain factor HB9.

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900397-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Transcriptional mechanisms in the development of motor control

1 reference

https://api.crossref.org/works/10.1016%2FS0304-4165%2802%2900397-5

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0304-4165(02)00397-5

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q28589941&oldid=2041806170"