Structure of the human laminin alpha2-chain gene (LAMA2), which is affected in congenital muscular dystrophy (Q28296180)

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

A new nomenclature for the laminins

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

Primary structure and expression of a novel human laminin alpha 4 chain

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

Molecular cloning of a novel laminin chain, alpha 5, and widespread expression in adult mouse tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

Molecular Cloning of the cDNA Encoding Human Laminin A Chain

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

Human laminin M chain (merosin): complete primary structure, chromosomal assignment, and expression of the M and A chain in human fetal tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

The human laminin beta 2 chain (S-laminin): structure, expression in fetal tissues and chromosomal assignment of the LAMB2 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

Structure of the human laminin gamma 2 chain gene (LAMC2): alternative splicing with different tissue distribution of two transcripts

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

Human laminin A chain (LAMA) gene: chromosomal mapping to locus 18p11.3

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

The genes for nicein/kalinin 125- and 100-kDa subunits, candidates for junctional epidermolysis bullosa, map to chromosomes 1q32 and 1q25-q31

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

Isolation of a human laminin B2 (LAMB2) cDNA clone and assignment of the gene to chromosome region 1q25----q31

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

Muscular dystrophies: diseases of the dystrophin-glycoprotein complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

β–sarcoglycan: characterization and role in limb–girdle muscular dystrophy linked to 4q12

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664

YAC contigs mapping the human COL4A5 and COL4A6 genes and DXS118 within Xq21.3–q22

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.271.44.27664