(Q48179008)

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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

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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)

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Europe PubMed Central

PubMed publication ID

9 February 2018

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

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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

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1 May 2007

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Europe PubMed Central

PubMed publication ID

9 February 2018

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

The Journal of Comparative Neurology

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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.

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RNAi reveals doublecortin is required for radial migration in rat neocortex

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

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

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

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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

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

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

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

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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

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Effects of fukutin deficiency in the developing mouse brain

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

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Reelin binds alpha3beta1 integrin and inhibits neuronal migration.

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

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

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

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

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

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

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

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Muscle-eye-brain disease: a neuropathological study

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Characterization of CNS precursor subtypes and radial glia

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Reelin signaling directly affects radial glia morphology and biochemical maturation

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New directions in neuronal migration

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Dystroglycan inside and out.

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Polysialic acid regulates chain formation by migrating olfactory interneuron precursors

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Congenital muscular dystrophy: molecular and cellular aspects.

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

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An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

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

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

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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

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

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

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

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Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy.

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

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Principles of neural cell migration

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Role of the reelin signaling pathway in central nervous system development

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

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

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

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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

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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

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