Literature DB >> 9348651

Molecular genetics of familial cardiomyopathies.

A S Coonar1, W J McKenna.   

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Year:  1997        PMID： 9348651     DOI： 10.1016/s0065-2660(08)60453-8

Source DB:  PubMed          Journal:  Adv Genet        ISSN： 0065-2660            Impact factor:   1.944


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  5 in total

1.  A locus for autosomal dominant mitral valve prolapse on chromosome 11p15.4.

Authors:  Lisa A Freed; James S Acierno; Daisy Dai; Maire Leyne; Jane E Marshall; Francesca Nesta; Robert A Levine; Susan A Slaugenhaupt
Journal:  Am J Hum Genet       Date:  2003-04-21       Impact factor: 11.025

2.  A tropomyosin-2 mutation suppresses a troponin I myopathy in Drosophila.

Authors:  B Naimi; A Harrison; M Cummins; U Nongthomba; S Clark; I Canal; A Ferrus; J C Sparrow
Journal:  Mol Biol Cell       Date:  2001-05       Impact factor: 4.138

Review 3.  The family history: reemergence of an established tool.

Authors:  Robert B Hinton
Journal:  Crit Care Nurs Clin North Am       Date:  2008-06       Impact factor: 1.326

4.  Suppression of muscle hypercontraction by mutations in the myosin heavy chain gene of Drosophila melanogaster.

Authors:  Upendra Nongthomba; Mark Cummins; Samantha Clark; Jim O Vigoreaux; John C Sparrow
Journal:  Genetics       Date:  2003-05       Impact factor: 4.562

5.  Transcription of Drosophila troponin I gene is regulated by two conserved, functionally identical, synergistic elements.

Authors:  María-Cruz Marín; José-Rodrigo Rodríguez; Alberto Ferrús
Journal:  Mol Biol Cell       Date:  2004-01-12       Impact factor: 4.138
  5 in total

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