Laminin alpha 2 (merosin)-deficient muscular dystrophy and demyelinating neuropathy in two cats (Q74458818)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11535231%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

title

Laminin alpha 2 (merosin)-deficient muscular dystrophy and demyelinating neuropathy in two cats (English)

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10 November 2019

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D P O'Brien

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10 November 2019

G C Johnson

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10 November 2019

L A Liu

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10 November 2019

L T Guo

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10 November 2019

E Engvall

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10 November 2019

H C Powell

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10 November 2019

G D Shelton

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10 November 2019

publication date

1 August 2001

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Journal of the Neurological Sciences

10 November 2019

published in

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10 November 2019

volume

189

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10 November 2019

issue

1-2

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10 November 2019

page(s)

37-43

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The homologue of the Duchenne locus is defective in X-linked muscular dystrophy of dogs

10 November 2019

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Normal expression of adhalin and merosin in ovine congenital progressive muscular dystrophy

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Positive immunostaining of ovine congenital progressive muscular dystrophy with antibody against N- and C-terminal dystrophin

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Merosin/laminin-2 and muscular dystrophy

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Muscular dystrophies and the dystrophin-glycoprotein complex

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Absence of integrin α7 causes a novel form of muscular dystrophy

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Merosin, a protein specific for basement membranes of Schwann cells, striated muscle, and trophoblast, is expressed late in nerve and muscle development

7 January 2021

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Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy

7 January 2021

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Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mapping

7 January 2021

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An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

7 January 2021

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Somatosensory and visual evoked potentials in congenital muscular dystrophy: correlation with MRI changes and muscle merosin status

7 January 2021

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Demyelinating peripheral neuropathy in merosin-deficient congenital muscular dystrophy

7 January 2021

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Familial concordance of brain magnetic resonance imaging changes in congenital muscular dystrophy

7 January 2021

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Merosin-deficient congenital muscular dystrophy: the spectrum of brain involvement on magnetic resonance imaging

7 January 2021

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Merosin-negative congenital muscular dystrophy associated with extensive brain abnormalities

7 January 2021

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Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency

7 January 2021

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Deficiency of merosin (laminin M or alpha 2) in congenital muscular dystrophy associated with cerebral white matter alterations

7 January 2021

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Dystrophia Muscularis: A HEREDITARY PRIMARY MYOPATHY IN THE HOUSE MOUSE.

7 January 2021

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Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse

7 January 2021

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Murine muscular dystrophy caused by a mutation in the laminin alpha 2 (Lama2) gene

7 January 2021

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Sarcoglycan isoforms in skeletal muscle

7 January 2021

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The sarcoglycan complex in limb-girdle muscular dystrophy

7 January 2021

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Dystrophin deficiency causes lethal muscle hypertrophy in cats

7 January 2021

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Muscular dystrophy in the mouse caused by an allele at the dy-locus

7 January 2021

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Merosin-deficient congenital muscular dystrophy. Partial genetic correction in two mouse models

7 January 2021

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Laminin alpha2 chain-null mutant mice by targeted disruption of the Lama2 gene: a new model of merosin (laminin 2)-deficient congenital muscular dystrophy.

7 January 2021

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Laminin alpha2 chain-deficient congenital muscular dystrophy: variable epitope expression in severe and mild cases

7 January 2021

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Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathy

7 January 2021

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Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse

7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Identifiers

DOI

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10 November 2019

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