Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Morgan Myers"'
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
Publikováno v:
ECS Meeting Abstracts. :1560-1560
Skin cancer is a pressing public health issue, especially in rural communities like Appalachia.1 Increasing public awareness about the risk of exposure to UV radiation and its correlation to the prevalence of skin cancer could change public behavior
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84be629db4d86d06032f5abb819a3779
https://doi.org/10.1149/ma2018-01/26/1560
https://doi.org/10.1149/ma2018-01/26/1560