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 (Q48179008)

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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

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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

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Europe PubMed Central

PubMed publication ID

9 February 2018

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

Yuan Yang

2

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Europe PubMed Central

PubMed publication ID

9 February 2018

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

Amber Eade

3

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Europe PubMed Central

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9 February 2018

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

Yufang Xiong

4

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Europe PubMed Central

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9 February 2018

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

Yue Qi

5

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9 February 2018

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

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1 May 2007

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Europe PubMed Central

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9 February 2018

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

The Journal of Comparative Neurology

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9 February 2018

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

502

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Europe PubMed Central

PubMed publication ID

9 February 2018

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

2

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Europe PubMed Central

PubMed publication ID

9 February 2018

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

168-183

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

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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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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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