(Q48179008)

English

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

scientific article

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/17479518

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 (English)

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/17479518

1 reference

based on heuristic

inferred from title

author name string

Huaiyu Hu

1

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/17479518

Yuan Yang

2

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/17479518

Amber Eade

3

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/17479518

Yufang Xiong

4

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/17479518

Yue Qi

5

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/17479518

language of work or name

0 references

publication date

1 May 2007

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/17479518

The Journal of Comparative Neurology

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/17479518

502

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/17479518

2

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/17479518

168-183

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/17479518

POMT1 mutation results in defective glycosylation and loss of laminin-binding activity in alpha-DG.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

21 January 2018

RNAi reveals doublecortin is required for radial migration in rat neocortex

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

FAK deficiency in cells contributing to the basal lamina results in cortical abnormalities resembling congenital muscular dystrophies

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the FKRP gene can cause muscle-eye-brain disease and Walker-Warburg syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycan

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Time of origin or corresponding cell classes in the cerebral cortex of normal and reeler mutant mice: an autoradiographic analysis

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

A 295-kDA intermediate filament-associated protein in radial glia and developing muscle cells in vivo and in vitro

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI 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://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Effects of fukutin deficiency in the developing mouse brain

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Close homolog of L1 modulates area-specific neuronal positioning and dendrite orientation in the cerebral cortex

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Reelin binds alpha3beta1 integrin and inhibits neuronal migration.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Periventricular heterotopia and the genetics of neuronal migration in the cerebral cortex

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Reelin controls granule cell migration in the dentate gyrus by acting on the radial glial scaffold

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Dystroglycan-alpha, a dystrophin-associated glycoprotein, is a functional agrin receptor

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Beta1-class integrins regulate the development of laminae and folia in the cerebral and cerebellar cortex

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

A critical function of the pial basement membrane in cortical histogenesis.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Muscle-eye-brain disease: a neuropathological study

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Characterization of CNS precursor subtypes and radial glia

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Reelin signaling directly affects radial glia morphology and biochemical maturation

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

New directions in neuronal migration

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Dystroglycan inside and out.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Polysialic acid regulates chain formation by migrating olfactory interneuron precursors

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Congenital muscular dystrophy: molecular and cellular aspects.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Deficiency of alpha-dystroglycan in muscle-eye-brain disease

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Congenital diaphragmatic hernia, kidney agenesis and cardiac defects associated with Slit3-deficiency in mice

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

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/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

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/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Loss-of-function of an N-acetylglucosaminyltransferase, POMGnT1, in muscle-eye-brain disease

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Cell migration in the forebrain

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Use of bromodeoxyuridine-immunohistochemistry to examine the proliferation, migration and time of origin of cells in the central nervous system.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of radial glial cells within the developing murine central nervous system: studies based upon a new immunohistochemical marker

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

alpha-Dystroglycan is a laminin receptor involved in extracellular matrix assembly on myotubes and muscle cell viability.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Integrin-linked kinase deletion from mouse cortex results in cortical lamination defects resembling cobblestone lissencephaly.

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Novel hippocampal interneuronal subtypes identified using transgenic mice that express green fluorescent protein in GABAergic interneurons

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Principles of neural cell migration

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Role of the reelin signaling pathway in central nervous system development

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Human brain malformations and their lessons for neuronal migration

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Structural analysis of sequences O-linked to mannose reveals a novel Lewis X structure in cranin (dystroglycan) purified from sheep brain

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

The cells of cajal-retzius: still a mystery one century after

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Reelin and brain development

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Reeler/Disabled-like disruption of neuronal migration in knockout mice lacking the VLDL receptor and ApoE receptor 2

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Magnetic resonance imaging in classification of congenital muscular dystrophies with brain abnormalities

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

POMT2 mutations cause alpha-dystroglycan hypoglycosylation and Walker-Warburg syndrome

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Malformation of the radial glial scaffold in the dentate gyrus of reeler mice, scrambler mice, and ApoER2/VLDLR-deficient mice

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Cloning and expression of a novel UDP-GlcNAc:alpha-D-mannoside beta1,2-N-acetylglucosaminyltransferase homologous to UDP-GlcNAc:alpha-3-D-mannoside beta1,2-N-acetylglucosaminyltransferase I

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Reelin is a positional signal for the lamination of dentate granule cells

1 reference

https://api.crossref.org/works/10.1002%2FCNE.21238

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/CNE.21238

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/17479518

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/17479518

reason for deprecated rank

unchecked identifier

0 references

ResearchGate publication ID

0 references

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=Q48179008&oldid=2188712747"