Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Shelby E. Hamm"'
Autor:
Shelby E. Hamm, Daniel D. Fathalikhani, Katherine E. Bukovec, Adele K. Addington, Haiyan Zhang, Justin B. Perry, Ryan P. McMillan, Michael W. Lawlor, Mariah J. Prom, Mark A. Vanden Avond, Suresh N. Kumar, Kirsten E. Coleman, J.B. Dupont, David L. Mack, David A. Brown, Carl A. Morris, J. Patrick Gonzalez, Robert W. Grange
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 21, Iss , Pp 144-160 (2021)
We tested the hypothesis that voluntary wheel running would complement microdystrophin gene therapy to improve muscle function in young mdx mice, a model of Duchenne muscular dystrophy. mdx mice injected with a single dose of AAV9-CK8-microdystrophin
Externí odkaz:
https://doaj.org/article/d1cbb7f0e57f48a4854b84e1f8896a3a
Autor:
Brittney Knott, Matthew A. Kocher, Henry A. Paz, Shelby E. Hamm, William Fink, Jordan Mason, Robert W. Grange, Umesh D. Wankhade, Deborah J. Good
Publikováno v:
Nutrients, Vol 14, Iss 4, p 860 (2022)
Prader–Willi Syndrome (PWS) is a human genetic condition that affects up to 1 in 10,000 live births. Affected infants present with hypotonia and developmental delay. Hyperphagia and increasing body weight follow unless drastic calorie restriction i
Externí odkaz:
https://doaj.org/article/3a165ee0f45f4721895a1ea0af20056f
Autor:
Brittney, Knott, Matthew A, Kocher, Henry A, Paz, Shelby E, Hamm, William, Fink, Jordan, Mason, Robert W, Grange, Umesh D, Wankhade, Deborah J, Good
Publikováno v:
Nutrients. 14(4)
Prader-Willi Syndrome (PWS) is a human genetic condition that affects up to 1 in 10,000 live births. Affected infants present with hypotonia and developmental delay. Hyperphagia and increasing body weight follow unless drastic calorie restriction is
Autor:
Jean-Baptiste Dupont, Daniel D. Fathalikhani, Haiyan Zhang, Michael W. Lawlor, Justin B. Perry, Ryan P. McMillan, Shelby E. Hamm, Carl Morris, David Brown, J. Patrick Gonzalez, Robert W. Grange, Mark A. Vanden Avond, Katherine E. Bukovec, Kirsten E. Coleman, Suresh Kumar, David L. Mack, Mariah J. Prom, Adele K. Addington
Publikováno v:
Molecular Therapy. Methods & Clinical Development
Molecular Therapy: Methods & Clinical Development, Vol 21, Iss, Pp 144-160 (2021)
Molecular Therapy: Methods & Clinical Development, Vol 23, Iss, Pp 460-(2021)
Molecular Therapy: Methods & Clinical Development, Vol 21, Iss, Pp 144-160 (2021)
Molecular Therapy: Methods & Clinical Development, Vol 23, Iss, Pp 460-(2021)
We tested the hypothesis that voluntary wheel running would complement microdystrophin gene therapy to improve muscle function in young mdx mice, a model of Duchenne muscular dystrophy. mdx mice injected with a single dose of AAV9-CK8-microdystrophin