Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Kelly E. Crowe"'
Autor:
Brian J. Paleo, Kevin E. McElhanon, Hannah R. Bulgart, Kassidy K. Banford, Eric X Beck, Kristina M. Sattler, Briana N. Goines, Shelby L. Ratcliff, Kelly E. Crowe, Noah Weisleder
Publikováno v:
Cells, Vol 11, Iss 9, p 1417 (2022)
Duchenne muscular dystrophy (DMD) is a common X-linked degenerative muscle disorder that involves mutations in the DMD gene that frequently reduce the expression of the dystrophin protein, compromising the structural integrity of the sarcolemmal memb
Externí odkaz:
https://doaj.org/article/9a4592bacceb45fbaf358a3bc2e9eaa7
Autor:
Rui Xu, Ying Jia, Deborah A. Zygmunt, Megan L. Cramer, Kelly E. Crowe, Guohong Shao, Agatha E. Maki, Haley N. Guggenheim, Benjamin C. Hood, Danielle A. Griffin, Ellyn Peterson, Brad Bolon, John P. Cheatham, Sharon L. Cheatham, Kevin M. Flanigan, Louise R. Rodino-Klapac, Louis G. Chicoine, Paul T. Martin
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 10, Iss , Pp 89-104 (2018)
Recombinant adeno-associated virus (rAAV)rh74.MCK.GALGT2 is a muscle-specific gene therapy that is being developed to treat forms of muscular dystrophy. Here we report on an isolated limb infusion technique in a non-human primate model, where hindlim
Externí odkaz:
https://doaj.org/article/f9bc6cfb8158407cb2dff2b604340149
Autor:
Kelly E. Crowe, Ajit Varki, Jonathan Okerblom, Paul T. Martin, Kunio Kawanishi, Paul M.L. Janssen, Annie N. Samraj, Bethannie Golden, Hai Yu, Xi Chen, Agatha E. Maki, Deborah A. Zygmunt, Anna Ashbrook, Sandra Diaz
Publikováno v:
Am J Pathol
Humans cannot synthesize the common mammalian sialic acid N-glycolylneuraminic acid (Neu5Gc) because of an inactivating deletion in the cytidine-5'-monophospho-(CMP)–N-acetylneuraminic acid hydroxylase (CMAH) gene responsible for its synthesis. Hum
Autor:
Kara E. Bradley, Kelly E. Crowe
Publikováno v:
The FASEB Journal. 36
Autor:
Mackenzie Roth, Kelly E. Crowe
Publikováno v:
The FASEB Journal. 36
Autor:
Megan E. Gilpin, Kelly E. Crowe
Publikováno v:
The FASEB Journal. 36
Autor:
Megan N. Poynter, Kelly E. Crowe
Publikováno v:
The FASEB Journal. 36
Autor:
Kelly E. Crowe
Publikováno v:
The FASEB Journal. 36
Autor:
Satoru Noguchi, Kelly E. Crowe, Deborah A. Zygmunt, Louise R. Rodino-Klapac, Kristin N. Heller, Ichizo Nishino, Paul T. Martin
Publikováno v:
Journal of neuromuscular diseases. 9(1)
Background GNE myopathy (GNEM) is a rare, adult-onset, inclusion body myopathy that results from partial loss of function mutations in the GNE gene. GNE encodes UDP-GlcNAc epimerase/Mannose-6 kinase, a protein with two enzymatic activities that compr
Autor:
Brian J. Paleo, Kelly E. Crowe
Publikováno v:
The FASEB Journal. 35