|1.||Ferreiro, A: 2 articles (12/2000 - 12/2000)|
|2.||Guicheney, P: 2 articles (12/2000 - 12/2000)|
|3.||Sloan, Andrew E: 1 article (11/2012)|
|4.||Rich, Jeremy N: 1 article (11/2012)|
|5.||Lathia, Justin D: 1 article (11/2012)|
|6.||Phillips, Heidi S: 1 article (11/2012)|
|7.||Li, Meizhang: 1 article (11/2012)|
|8.||Bredel, Markus: 1 article (11/2012)|
|9.||Hale, James S: 1 article (11/2012)|
|10.||Huang, Ping: 1 article (11/2012)|
|1.||Muscular Dystrophies (Muscular Dystrophy)
02/01/2003 - "Clinical and molecular study in congenital muscular dystrophy with partial laminin alpha 2 (LAMA2) deficiency."
12/01/1997 - "Further studies should be performed on patients affected by congenital muscular dystrophy associated with laminin alpha 2 deficiency to test this hypothesis."
07/01/2002 - "We investigated the dy mouse model, which has congenital muscular dystrophy due to a defect in laminin alpha 2, for evidence of cochlear dysfunction. "
02/01/2000 - "When compared with the dystrophies with a primary sarcolemmal defect, it appears that those with primary basal lamina abnormalities (WWS, laminin-alpha-2-deficient, and Fukuyama congenital muscular dystrophies) present early in life, and the phenotype is more severe."
05/01/1999 - "The laminin alpha 2 chain is absent or drastically reduced in a subgroup of congenital muscular dystrophy patients, and in the severely affected dystrophic dy/dy mouse. "
|2.||Small Cell Carcinoma
09/01/1995 - "This study evaluated the expression of a panel of integrin subunits that included subunits that form receptors that bind to collagen and laminin (alpha 2, alpha 3, alpha 6 beta 4) and subunits that form receptors that bind to fibronectin and fibrinogen (alpha 5, alpha V, beta 3, beta 6) in 51 specimens of non-small cell carcinoma (NSCCA) of the lung by use of immunohistochemistry. "
12/01/2000 - "The laminin alpha(2) chain (6q2), Fukuyama type congenital muscular dystrophy (9q31-q33) and muscle-eye-brain disease (1p32-p34) loci were all excluded by linkage analysis. "
02/01/1999 - "Linkage analysis excluded all the known loci for CMD, including laminin alpha 2 on chromosome 6q2, the Fukuyama congenital muscular dystrophy locus on 9q3, the integrin alpha 7 locus on chromosome 12q13 and the recently identified locus on 1p35-36. "
06/01/1995 - "Laminin-alpha 2 expression was also found to be significantly reduced in Fukuyama congenital muscular dystrophy which links to chromosome 9q3. "
04/07/2006 - "Expression profiling of muscles from Fukuyama-type congenital muscular dystrophy and laminin-alpha 2 deficient congenital muscular dystrophy; is congenital muscular dystrophy a primary fibrotic disease?"
12/01/2000 - "Linkage analysis in the only informative family excluded the known loci for congenital muscular dystrophy, including laminin alpha 2 chain on chromosome 6q2, the Fukuyama congenital muscular dystrophy locus on 9q3 and the muscle-eye-brain disease on chromosome 1p3. "
|4.||Limb-Girdle Muscular Dystrophies (Limb-Girdle Muscular Dystrophy)
10/01/1998 - "Partial laminin alpha 2 deficiency should be considered in the differential diagnosis of limb-girdle muscular dystrophy."
11/01/2011 - "In noncharacterized or partially characterized patients, we found deletions in the SETX (senataxin), SGCG [sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein)], and LAMA2 (laminin, alpha 2) genes, as well as duplications involving LAMA2 and the DYSF [dysferlin, limb girdle muscular dystrophy 2B (autosomal recessive)] locus. "
06/01/1995 - "We report consistently preserved laminin-2 expression, including laminin-alpha 2, as detected by immunofluorescence in skeletal muscle from five patients with Walker-Warburg syndrome which is characterized by congenital muscular dystrophy and, in addition, type II lissencephaly or pachygyria, defective CNS myelination, and ocular dysgenesis. "
|2.||Fibrinogen (Factor I)
|8.||merosin negative Muscular dystrophy congenital