From proteins to genes: immunoanalysis in the diagnosis of muscular dystrophies. - Wikidata - wikimedia - TriplyDB

From proteins to genes: immunoanalysis in the diagnosis of muscular dystrophies.

From proteins to genes: immunoanalysis in the diagnosis of muscular dystrophies.

http://www.wikidata.org/entity/Q35166268

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Diagnostic approach to the congenital muscular dystrophies.The Classification, Natural History and Treatment of the Limb Girdle Muscular Dystrophies Immunohistochemistry of sarcolemmal membrane-associated proteins in formalin-fixed and paraffin-embedded skeletal muscle tissue: a promising tool for the diagnostic evaluation of common muscular dystrophies.Muscle hypertrophy as the presenting sign in a patient with a complete FHL1 deletion.Exome sequences versus sequential gene testing in the UK highly specialised Service for Limb Girdle Muscular Dystrophy.Exercise-induced alterations and loss of sarcomeric M-line organization in the diaphragm muscle of obscurin knockout mice.The molecular cross talk of the dystrophin-glycoprotein complex.

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From proteins to genes: immunoanalysis in the diagnosis of muscular dystrophies.

http://www.wikidata.org/entity/Q35166268

description

2011 nî lūn-bûn

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2011 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2011 թվականի հունիսին հրատարակված գիտական հոդված

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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name

From proteins to genes: immunoanalysis in the diagnosis of muscular dystrophies.

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From proteins to genes: immunoanalysis in the diagnosis of muscular dystrophies.

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type

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From proteins to genes: immunoanalysis in the diagnosis of muscular dystrophies.

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From proteins to genes: immunoanalysis in the diagnosis of muscular dystrophies.

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From proteins to genes: immunoanalysis in the diagnosis of muscular dystrophies.

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From proteins to genes: immunoanalysis in the diagnosis of muscular dystrophies.

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Skeletal Muscle

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From proteins to genes: immunoanalysis in the diagnosis of muscular dystrophies.

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Rita Barresi

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P2860

Myotilin is mutated in limb girdle muscular dystrophy 1A

Telethonin and other new proteins of the Z-disc of skeletal muscle

Sarcospan, the 25-kDa transmembrane component of the dystrophin-glycoprotein complex

Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A

Identification and characterization of the dystrophin anchoring site on beta-dystroglycan

Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy

A comparative study of alpha-dystroglycan glycosylation in dystroglycanopathies suggests that the hypoglycosylation of alpha-dystroglycan does not consistently correlate with clinical severity

Immunohistochemical analysis of calpain 3: advantages and limitations in diagnosing LGMD2A

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.

Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy.

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