Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy. (Q42524154)

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11 November 2019

title

Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy (English)

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11 November 2019

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1

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11 November 2019

Michael D. Henry

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11 November 2019

Kevin P Campbell

12

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11 November 2019

author name string

Fumiaki Saito

2

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11 November 2019

Jianguo Chen

3

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11 November 2019

Daniel E Michele

4

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11 November 2019

Albee Messing

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11 November 2019

Ronald D Cohn

7

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11 November 2019

Susan E Ross-Barta

8

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11 November 2019

Steve Westra

9

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11 November 2019

Roger A Williamson

10

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11 November 2019

Toshinori Hoshi

11

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11 November 2019

language of work or name

English

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publication date

1 July 2002

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11 November 2019

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11 November 2019

volume

418

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11 November 2019

issue

6896

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11 November 2019

page(s)

422-425

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https://scigraph.springernature.com/pub.10.1038/nature00838

11 November 2019

exact match

0 references

cites work

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

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

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Dystroglycan inside and out.

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Dystroglycan distribution in adult mouse brain: a light and electron microscopy study

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Molecular basis of muscular dystrophies.

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A stoichiometric complex of neurexins and dystroglycan in brain

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hGFAP-cre transgenic mice for manipulation of glial and neuronal function in vivo.

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Role of the basement membrane in neurogenesis and repair of injury in the central nervous system

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Perlecan is essential for cartilage and cephalic development

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Roles for laminin in embryogenesis: exencephaly, syndactyly, and placentopathy in mice lacking the laminin alpha5 chain

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

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Human brain malformations and their lessons for neuronal migration

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

21 January 2018

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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

21 January 2018

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Selective deficiency of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophy

21 January 2018

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

21 January 2018

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

21 January 2018

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Maturation and maintenance of the neuromuscular synapse: genetic evidence for roles of the dystrophin--glycoprotein complex

21 January 2018

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A synaptic model of memory: long-term potentiation in the hippocampus

21 January 2018

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GLIA: listening and talking to the synapse

21 January 2018

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Progressive muscular dystrophy in alpha-sarcoglycan-deficient mice

21 January 2018

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

21 January 2018

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Postsynaptic factors control the duration of synaptic enhancement in area CA1 of the hippocampus

21 January 2018

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Congenital progressive muscular dystrophy of the Fukuyama type - clinical, genetic and pathological considerations

21 January 2018

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inferred from DOI database lookup

7 January 2021

based on heuristic

Muscle-eye-brain disease: a neuropathological study

1 reference

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inferred from DOI database lookup

7 January 2021

based on heuristic

Changes in paired-pulse facilitation suggest presynaptic involvement in long-term potentiation.

1 reference

https://api.crossref.org/works/10.1038%2FNATURE00838

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NATURE00838

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12140559%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

11 November 2019

0 references

1 reference