Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Eric A. Hoffman"'
Autor:
Alan Pittman, Ehsan Ghayoor Karimiani, Isabella Moroni, Yalda Jamshidi, Marina Mora, Reza Boostani, Swati Mummidivarpu, Eric P. Hoffman, M. Chiara Manzini, Samantha Martinez, Daniele Podini, Edmund Cauley
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 8, Iss 11, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine, Vol 8, Iss 11, Pp n/a-n/a (2020)
Background Congenital muscular dystrophy type 1A (MDC1A), also termed merosin‐deficient congenital muscular dystrophy (CMD), is a severe form of CMD caused by mutations in the laminin α2 gene (LAMA2). Of the more than 300 likely pathogenic variant
Autor:
Eric Selinsky, Niall M. Moyna, Linda S. Pescatello, Heather Gordish-Dressman, Paul S. Visich, Robert F. Zoeller, Eric P. Hoffman, Michael Bruneau, Garrett I. Ash, Paul D. Thompson, Joseph M. Devaney, Sean Walsh, Paul M. Gordon, Theodore J. Angelopoulos, Priscilla M. Clarkson
Publikováno v:
Molecular Genetics & Genomic Medicine
Background Interleukin‐15 (IL‐15) is a myokine associated with muscle strength, possibly by attenuating protein breakdown. A variant in the alpha‐receptor (IL‐15Rα 1775 A>C, rs2228059) partially modulates the muscle strength and size respons
Autor:
Paul S. Visich, R L Seip, Niall M. Moyna, Paul M. Gordon, Joseph M. Devaney, Linda S. Pescatello, Theodore J. Angelopoulos, Michael Bruneau, Heather Gordish-Dressman, Paul D. Thompson, Stephen Bilbie, Eric P. Hoffman, Robert F. Zoeller
Publikováno v:
Molecular Genetics & Genomic Medicine
Background The angiotensin-converting enzyme (ACE) insertion/deletion (I/D) polymorphism (rs4340) (ACE DIP) accounts for half of the variability in plasma ACE concentrations. ACE has been widely studied for its influence on sports performance; howeve
Autor:
Edmund S. Cauley, Alan Pittman, Swati Mummidivarpu, Ehsan G. Karimiani, Samantha Martinez, Isabella Moroni, Reza Boostani, Daniele Podini, Marina Mora, Yalda Jamshidi, Eric P. Hoffman, M. Chiara Manzini
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 11, Pp n/a-n/a (2020)
Abstract Background Congenital muscular dystrophy type 1A (MDC1A), also termed merosin‐deficient congenital muscular dystrophy (CMD), is a severe form of CMD caused by mutations in the laminin α2 gene (LAMA2). Of the more than 300 likely pathogeni
Externí odkaz:
https://doaj.org/article/30bb022ab7354e7990f235b44b44dd59