(Q52567524)

English

Neuronal migration defects in cerebellum of the Largemyd mouse are associated with disruptions in Bergmann glia organization and delayed migration of granule neurons.

scientific article published in January 2005

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 May 2018

http://europepmc.org/abstract/MED/16321882

Neuronal migration defects in cerebellum of the Largemyd mouse are associated with disruptions in Bergmann glia organization and delayed migration of granule neurons. (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 May 2018

http://europepmc.org/abstract/MED/16321882

1 reference

based on heuristic

inferred from title

author name string

Qiang Qu

1

1 reference

Europe PubMed Central

PubMed publication ID

3 May 2018

http://europepmc.org/abstract/MED/16321882

Frances I Smith

2

1 reference

Europe PubMed Central

PubMed publication ID

3 May 2018

http://europepmc.org/abstract/MED/16321882

publication date

1 January 2005

1 reference

Europe PubMed Central

PubMed publication ID

3 May 2018

http://europepmc.org/abstract/MED/16321882

1 reference

Europe PubMed Central

PubMed publication ID

3 May 2018

http://europepmc.org/abstract/MED/16321882

4

1 reference

Europe PubMed Central

PubMed publication ID

3 May 2018

http://europepmc.org/abstract/MED/16321882

4

1 reference

Europe PubMed Central

PubMed publication ID

3 May 2018

http://europepmc.org/abstract/MED/16321882

261-270

1 reference

Europe PubMed Central

PubMed publication ID

3 May 2018

http://europepmc.org/abstract/MED/16321882

https://scigraph.springernature.com/pub.10.1080/14734220500358351

0 references

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://pubmed.ncbi.nlm.nih.gov/16321882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The intrinsic specification of gamma-aminobutyric acid type A receptor alpha6 subunit gene expression in cerebellar granule cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/16321882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dystroglycan inside and out.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16321882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of Pax6 in development of the cerebellar system

1 reference

https://pubmed.ncbi.nlm.nih.gov/16321882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Postnatal effects of retinoic acid on cerebellar development

1 reference

https://pubmed.ncbi.nlm.nih.gov/16321882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular cloning of rat alpha1,3-fucosyltransferase IX (Fuc-TIX) and comparison of the expression of Fuc-TIV and Fuc-TIX genes during rat postnatal cerebellum development

1 reference

https://pubmed.ncbi.nlm.nih.gov/16321882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The human LARGE gene from 22q12.3-q13.1 is a new, distinct member of the glycosyltransferase gene family

1 reference

https://pubmed.ncbi.nlm.nih.gov/16321882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cell intrinsic mechanisms regulate mouse cerebellar granule neuron differentiation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16321882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Viral vector-mediated delivery of competing glycosyltransferases modifies epitope expression cell specifically

1 reference

https://pubmed.ncbi.nlm.nih.gov/16321882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16321882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16321882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular recognition by LARGE is essential for expression of functional dystroglycan

1 reference

https://pubmed.ncbi.nlm.nih.gov/16321882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16321882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distinct modes of neuronal migration in different domains of developing cerebellar cortex.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16321882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebellar granule cells in vitro recapitulate the in vivo pattern of GABAA-receptor subunit expression.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16321882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alpha-dystroglycan interactions affect cerebellar granule neuron migration

1 reference

https://pubmed.ncbi.nlm.nih.gov/16321882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Skeletal, cardiac and tongue muscle pathology, defective retinal transmission, and neuronal migration defects in the Large(myd) mouse defines a natural model for glycosylation-deficient muscle - eye - brain disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/16321882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/16321882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/16321882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of dystroglycan, fukutin and POMGnT1 during mouse cerebellar development

1 reference

https://pubmed.ncbi.nlm.nih.gov/16321882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dystroglycan is involved in laminin-1-stimulated motility of Müller glial cells: combined velocity and directionality analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16321882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dystroglycan is essential for early embryonic development: disruption of Reichert's membrane in Dag1-null mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/16321882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pax6 regulates granule cell polarization during parallel fiber formation in the developing cerebellum

1 reference

https://pubmed.ncbi.nlm.nih.gov/16321882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structures of sialylated O-linked oligosaccharides of bovine peripheral nerve alpha-dystroglycan. The role of a novel O-mannosyl-type oligosaccharide in the binding of alpha-dystroglycan with laminin

1 reference

https://pubmed.ncbi.nlm.nih.gov/16321882

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1080/14734220500358351

1 reference

Europe PubMed Central

PubMed publication ID

3 May 2018

http://europepmc.org/abstract/MED/16321882

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 May 2018

http://europepmc.org/abstract/MED/16321882

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=Q52567524&oldid=1395106563"