Site-specific Mtm1 mutagenesis by an AAV-Cre vector reveals that myotubularin is essential in adult muscle

By Joubert Romain   Vignaud Alban   Le Mickaël   Moal Christelle   Messaddeq Nadia   Buj-Bello Anna  

Human Molecular Genetics, Vol. 22, Iss. 9, 2013-05 ,pp. : 1856-1866

Oxford University Press

Access to resources Recommend Favorite

Loss of phosphatase activity in myotubularin-related protein 2 is associated with Charcot–Marie–Tooth disease type 4B1

By Berger P.  

Human Molecular Genetics, Vol. 11, Iss. 13, 2002-06 ,pp. : 1569-1579

Oxford University Press

Access to resources Recommend Favorite

Impaired PGC-1 function in muscle in Huntington's disease

By Chaturvedi Rajnish K.   Adhihetty Peter   Shukla Shubha   Hennessy Thomas   Calingasan Noel   Yang Lichuan   Starkov Anatoly   Kiaei Mahmoud   Cannella Milena   Sassone Jenny   Ciammola Andrea   Squitieri Fernando   Beal M. Flint  

Human Molecular Genetics, Vol. 18, Iss. 16, 2009-08 ,pp. : 3048-3065

Oxford University Press

Access to resources Recommend Favorite

Modification of splicing in the dystrophin gene in cultured Mdx muscle cells by antisense oligoribonucleotides

By Dunckley M.G.  

Human Molecular Genetics, Vol. 7, Iss. 7, 1998-07 ,pp. : 1083-1090

Oxford University Press

Access to resources Recommend Favorite

The product of an oculopharyngeal muscular dystrophy gene, poly(A)-binding protein 2, interacts with SKIP and stimulates muscle-specific gene expression

By Kim Y-J.  

Human Molecular Genetics, Vol. 10, Iss. 11, 2001-05 ,pp. : 1129-1139

Oxford University Press

Access to resources Recommend Favorite