Structure of the human laminin alpha2-chain gene (LAMA2), which is affected in congenital muscular dystrophy - Wikidata - wikimedia - TriplyDB

Structure of the human laminin alpha2-chain gene (LAMA2), which is affected in congenital muscular dystrophy

Structure of the human laminin alpha2-chain gene (LAMA2), which is affected in congenital muscular dystrophy

http://www.wikidata.org/entity/Q28296180

about

The zebrafish candyfloss mutant implicates extracellular matrix adhesion failure in laminin alpha2-deficient congenital muscular dystrophy.Mild congenital muscular dystrophy in two patients with an internally deleted laminin alpha2-chain The structural organisation of LAMA4, the gene encoding laminin alpha4 PCR based mutation screening of the laminin alpha2 chain gene (LAMA2): application to prenatal diagnosis and search for founder effects in congenital muscular dystrophy Laminins: structure and genetic regulation.Laminins and human disease.wing blister, a new Drosophila laminin alpha chain required for cell adhesion and migration during embryonic and imaginal development Myoblast transplantations lead to the expression of the laminin alpha 2 chain in normal and dystrophic (dy/dy) mouse muscles.Potential molecular chaperones involved in laminin chain assembly.LAMA2 gene analysis in a cohort of 26 congenital muscular dystrophy patients

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P2860

Structure of the human laminin alpha2-chain gene (LAMA2), which is affected in congenital muscular dystrophy

http://www.wikidata.org/entity/Q28296180

description

1996 nî lūn-bûn

@nan

1996 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

1996 թվականի նոյեմբերին հրատարակված գիտական հոդված

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1996年の論文

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1996年論文

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1996年論文

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1996年論文

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1996年論文

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1996年論文

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1996年论文

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name

Structure of the human laminin ...... congenital muscular dystrophy

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Structure of the human laminin ...... congenital muscular dystrophy

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Structure of the human laminin ...... congenital muscular dystrophy

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type

label

Structure of the human laminin ...... congenital muscular dystrophy

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Structure of the human laminin ...... congenital muscular dystrophy

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Structure of the human laminin ...... congenital muscular dystrophy

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prefLabel

Structure of the human laminin ...... congenital muscular dystrophy

@ast

Structure of the human laminin ...... congenital muscular dystrophy

@en

Structure of the human laminin ...... congenital muscular dystrophy

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JBC.271.44.27664

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Journal of Biological Chemistry

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Structure of the human laminin ...... congenital muscular dystrophy

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P2093

K Tryggvason

http://www.w3.org/2001/XMLSchema#string

R Vuolteenaho

http://www.w3.org/2001/XMLSchema#string

X Zhang

http://www.w3.org/2001/XMLSchema#string

P2860

Molecular heterogeneity of basal laminae: isoforms of laminin and collagen IV at the neuromuscular junction and elsewhere

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

Human beta 2 chain of laminin (formerly S chain): cDNA cloning, chromosomal localization, and expression in carcinomas

Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12

Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

Merosin, a tissue-specific basement membrane protein, is a laminin-like protein

Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity

Localization of the gene (LAMA4) to chromosome 6q21 and isolation of a partial cDNA encoding a variant laminin A chain

Primary structure of the human laminin A chain. Limited expression in human tissues

A truncated laminin chain homologous to the B2 chain: structure, spatial expression, and chromosomal assignment

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