Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Darren Murrey"'
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:
Bartholomew J Naughton, F Jason Duncan, Darren Murrey, Tierra Ware, Aaron Meadows, Douglas M McCarty, Haiyan Fu
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e80142 (2013)
Mucopolysaccharidosis (MPS) IIIB is a devastating neuropathic lysosomal storage disease with complex pathology. This study identifies molecular signatures in peripheral blood that may be relevant to MPS IIIB pathogenesis using a mouse model. Genome-w
Externí odkaz:
https://doaj.org/article/1765de5a86994bc2a248fcd3df484760
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
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
Autor:
Douglas M. McCarty, Haiyan Fu, Kathryn Waligura, Marybeth Camboni, Darren Murrey, Aaron S. Meadows
Publikováno v:
Molecular Genetics and Metabolism. 117:S79
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1d260ab85eb7a2d4bc85199a393f8e6
https://doi.org/10.1016/j.ymgme.2015.12.356
https://doi.org/10.1016/j.ymgme.2015.12.356
Publikováno v:
Molecular Genetics and Metabolism. 111:S75
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bef8689c336282061fb7c8524e4ace9e
https://doi.org/10.1016/j.ymgme.2013.12.173
https://doi.org/10.1016/j.ymgme.2013.12.173
Autor:
F. Jason Duncan, Darren Murrey, Kimberly Zaraspe, Haiyan Fu, Bartholomew Naughton, Douglas M. McCarty, Aaron S. Meadows, Tierra Ware
Publikováno v:
Molecular Genetics and Metabolism. 111:S44
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e71b64d2ce45e7b6373c2e0efb331dfb
https://doi.org/10.1016/j.ymgme.2013.12.089
https://doi.org/10.1016/j.ymgme.2013.12.089