Targeting dystroglycan in the brain. (Q35053118)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12546815%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

review article

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title

Targeting dystroglycan in the brain (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12546815%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12546815%20AND%20SRC:MED&resulttype=core&format=json

17 December 2019

S Carbonetto

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17 December 2019

language of work or name

English

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publication date

1 January 2003

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17 December 2019

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17 December 2019

volume

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17 December 2019

issue

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17 December 2019

page(s)

193-196

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

17 December 2019

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Skeletal, cardiac and tongue muscle pathology, defective retinal transmission, and neuronal migration defects in the Large(myd) mouse defines a natural model for glycosylation-deficient muscle - eye - brain disorders

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7 January 2021

Dystroglycan is selectively associated with inhibitory GABAergic synapses but is dispensable for their differentiation.

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

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Laminin and alpha-dystroglycan mediate acetylcholine receptor aggregation via a MuSK-independent pathway

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The O-glycosylated stalk domain is required for apical sorting of neurotrophin receptors in polarized MDCK cells

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