Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Alicia Ridgley"'
Publikováno v:
Journal of Cachexia, Sarcopenia and Muscle, Vol 14, Iss 5, Pp 2204-2215 (2023)
Abstract Background Sarcopenia, an age‐related loss of muscle mass, is a critical factor that affects the health of the older adults. The SOD1KO mouse is deficient of Cu/Zn superoxide dismutase, used as an accelerated aging model. We previously sho
Externí odkaz:
https://doaj.org/article/53647f224bbf4f64a667f27973577f38
Autor:
Zarife Sahenk, Burcak Ozes, Darren Murrey, Morgan Myers, Kyle Moss, Mehmet E. Yalvac, Alicia Ridgley, Lei Chen, Jerry R. Mendell
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 22, Iss , Pp 401-414 (2021)
Limb girdle muscular dystrophy (LGMD) 2A/R1, caused by mutations in the CAPN3 gene and CAPN3 loss of function, is known to play a role in disease pathogenicity. In this study, AAVrh74.tMCK.CAPN3 was delivered systemically to two different age groups
Externí odkaz:
https://doaj.org/article/dc63800556e54ec48f051843902e5f99
Autor:
Lei Chen, Mehmet E. Yalvac, Alicia Ridgley, Darren Murrey, Kyle Moss, Jerry R. Mendell, Morgan Myers, Zarife Sahenk, Burcak Ozes
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 22, Iss, Pp 401-414 (2021)
Molecular Therapy. Methods & Clinical Development
Molecular Therapy. Methods & Clinical Development
Limb girdle muscular dystrophy (LGMD) 2A/R1, caused by mutations in the CAPN3 gene and CAPN3 loss of function, is known to play a role in disease pathogenicity. In this study, AAVrh74.tMCK.CAPN3 was delivered systemically to two different age groups
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4ed3cc6fa75414170186537cf89b0e8
https://doi.org/10.1016/j.omtm.2021.06.010
https://doi.org/10.1016/j.omtm.2021.06.010
Autor:
Jerry R. Mendell, Alicia Ridgley, Kyle Moss, Shasha Bai, Lei Chen, Morgan Myers, Mona M. Freidin, Burcak Ozes, Jennifer L. McKinney, Charles K. Abrams, Zarife Sahenk
Publikováno v:
Gene Therapy. 29:127-137
X-linked Charcot-Marie-Tooth neuropathy (CMTX) is caused by mutations in the gene encoding Gap Junction Protein Beta-1 (GJB1)/Connexin32 (Cx32) in Schwann cells. Neurotrophin-3 (NT-3) is an important autocrine factor supporting Schwann cell survival
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::884a8fe35edc2f05afb9a259c428e4f2
https://doi.org/10.1038/s41434-021-00231-3
https://doi.org/10.1038/s41434-021-00231-3
Publikováno v:
Brain Communications. 3
Glycyl–tRNA synthetase mutations are associated to the Charcot–Marie–Tooth disease type-2D. The GarsP278KY/+ model for Charcot–Marie–Tooth disease type-2D is known best for its early onset severe neuropathic phenotype with findings includin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2156d53b3e7f39c15768398e7ba37cfd
https://doi.org/10.1093/braincomms/fcab252
https://doi.org/10.1093/braincomms/fcab252