(Q42524154)

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

11 November 2019

title

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

1 reference

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

11 November 2019

0 references

1

1 reference

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11 November 2019

Michael D. Henry

5

1 reference

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11 November 2019

Kevin P Campbell

12

1 reference

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11 November 2019

author name string

Fumiaki Saito

2

1 reference

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11 November 2019

Jianguo Chen

3

1 reference

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11 November 2019

Daniel E Michele

4

1 reference

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

11 November 2019

Albee Messing

6

1 reference

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11 November 2019

Ronald D Cohn

7

1 reference

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11 November 2019

Susan E Ross-Barta

8

1 reference

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11 November 2019

Steve Westra

9

1 reference

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11 November 2019

Roger A Williamson

10

1 reference

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11 November 2019

Toshinori Hoshi

11

1 reference

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11 November 2019

language of work or name

English

0 references

publication date

1 July 2002

1 reference

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11 November 2019

1 reference

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11 November 2019

volume

418

1 reference

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11 November 2019

issue

6896

1 reference

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11 November 2019

page(s)

422-425

1 reference

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An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

11 November 2019

cites work

1 reference

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

Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain disease

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Dystroglycan inside and out.

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Molecular basis of muscular dystrophies.

21 January 2018

1 reference

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

A stoichiometric complex of neurexins and dystroglycan in brain

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Perlecan is essential for cartilage and cephalic development

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

Human brain malformations and their lessons for neuronal migration

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

GLIA: listening and talking to the synapse

21 January 2018

1 reference

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

Progressive muscular dystrophy in alpha-sarcoglycan-deficient mice

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

inferred from DOI database lookup

7 January 2021

based on heuristic

Muscle-eye-brain disease: a neuropathological study

1 reference

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

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

1029768090

0 references

1 reference