(Q42917954)

11 November 2017

title

Cellular and molecular characterization of abnormal brain development in protein o-mannose N-acetylglucosaminyltransferase 1 knockout mice (English)

1 reference

11 November 2017

Cellular and Molecular Characterization of Abnormal Brain Development in Protein O-Mannose N-Acetylglucosaminyltransferase 1 Knockout Mice (English)

1 reference

10.1016/S0076-6879(10)79020-0

DOI

https://api.crossref.org/works/10.1016/S0076-6879(10)79020-0

6 July 2024

0 references

Jianmin Liu

1

1 reference

11 November 2017

Yuan Yang

2

1 reference

11 November 2017

Xiaofeng Li

3

1 reference

11 November 2017

Peng Zhang

4

1 reference

11 November 2017

Yue Qi

5

1 reference

11 November 2017

Huaiyu Hu

6

1 reference

11 November 2017

language of work or name

English

0 references

publication date

1 January 2010

1 reference

11 November 2017

published in

Methods in Enzymology

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11 November 2017

volume

479

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11 November 2017

page(s)

353-366

1 reference

POMGnT1 mutations in congenital muscular dystrophy: genotype-phenotype correlation and expanded clinical spectrum

11 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2810%2979020-0

7 January 2021

Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2810%2979020-0

7 January 2021

Effects of fukutin deficiency in the developing mouse brain

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2810%2979020-0

7 January 2021

Mild POMGnT1 mutations underlie a novel limb-girdle muscular dystrophy variant.

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2810%2979020-0

7 January 2021

Dystroglycan in development and disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2810%2979020-0

7 January 2021

A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin.

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2810%2979020-0

7 January 2021

Imaging neuronal subsets in transgenic mice expressing multiple spectral variants of GFP

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2810%2979020-0

7 January 2021

Mutant glycosyltransferase and altered glycosylation of alpha-dystroglycan in the myodystrophy mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2810%2979020-0

7 January 2021

Novel POMGnT1 mutations define broader phenotypic spectrum of muscle-eye-brain disease

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2810%2979020-0

7 January 2021

Breaches of the pial basement membrane and disappearance of the glia limitans during development underlie the cortical lamination defect in the mouse model of muscle-eye-brain disease

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2810%2979020-0

7 January 2021

A genetic model for muscle-eye-brain disease in mice lacking protein O-mannose 1,2-N-acetylglucosaminyltransferase (POMGnT1)

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2810%2979020-0

7 January 2021

Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2810%2979020-0

7 January 2021

Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2810%2979020-0

7 January 2021

Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function.

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2810%2979020-0

7 January 2021

Reduced proliferative activity of primary POMGnT1-null myoblasts in vitro.

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2810%2979020-0

7 January 2021

Targeting dystroglycan in the brain.

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2810%2979020-0

7 January 2021

Novel synonymous substitution in POMGNT1 promotes exon skipping in a patient with congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2810%2979020-0

7 January 2021

Pikachurin, a dystroglycan ligand, is essential for photoreceptor ribbon synapse formation

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2810%2979020-0

7 January 2021

A new beta-1,2-N-acetylglucosaminyltransferase that may play a role in the biosynthesis of mammalian O-mannosyl glycans

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2810%2979020-0

7 January 2021

Worldwide distribution and broader clinical spectrum of muscle-eye-brain disease

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2810%2979020-0

7 January 2021

Ectopia of meningeal fibroblasts and reactive gliosis in the cerebral cortex of the mouse model of muscle-eye-brain disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2810%2979020-0

7 January 2021

Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1

1 reference

https://api.crossref.org/works/10.1016%2FS0076-6879%2810%2979020-0

7 January 2021

10.1016/S0076-6879(10)79020-0

Identifiers

DOI

1 reference

release_2epceyruzrcinn2fqvmlw7aqdu

11 November 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/2epceyruzrcinn2fqvmlw7aqdu

24 November 2022

mapped directly with Wikidata item

1 reference