Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Boguslaw Felczak"'
Autor:
Amber L. Southwell, Sonia Franciosi, Erika B. Villanueva, Yuanyun Xie, Laurie A. Winter, Janaki Veeraraghavan, Alan Jonason, Boguslaw Felczak, Weining Zhang, Vlad Kovalik, Sabine Waltl, George Hall, Mahmoud A. Pouladi, Ernest S. Smith, William J. Bowers, Maurice Zauderer, Michael R. Hayden
Publikováno v:
Neurobiology of Disease, Vol 76, Iss , Pp 46-56 (2015)
Huntington disease (HD) is an inherited, fatal neurodegenerative disease with no disease-modifying therapy currently available. In addition to characteristic motor deficits and atrophy of the caudate nucleus, signature hallmarks of HD include behavio
Externí odkaz:
https://doaj.org/article/99a93dc1282c4cf6b5dc56f2438c4a79
Autor:
Sabine Waltl, Dagmar E. Ehrnhoefer, Boguslaw Felczak, Lorenzo Casal, Amber L. Southwell, Meenalochani Sivasubramanian, Lisa M. Anderson, Anita Fazeli, Xiaofan Qiu, Erika B. Villanueva, Yuanyun Xie, Michelle Tsang, Michael R. Hayden
Publikováno v:
Human Molecular Genetics. 27:239-253
Oxidative stress is a prominent feature of Huntington disease (HD), and we have shown previously that reduced levels of hace1 (HECT domain and Ankyrin repeat containing E3 ubiquitin protein ligase 1) in patient striatum may contribute to the pathogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8162b1e4d2606c1c8c03bb5479382b0d
https://doi.org/10.1093/hmg/ddx394
https://doi.org/10.1093/hmg/ddx394
Autor:
Boguslaw Felczak, Sabine Waltl, George Hall, Erika B. Villanueva, Yuanyun Xie, Michael R. Hayden, Weining Zhang, Ernest S. Smith, Amber L. Southwell, Maurice Zauderer, Vlad Kovalik, Laurie A. Winter, Alan S. Jonason, Sonia Franciosi, William J. Bowers, Mahmoud A. Pouladi, Janaki Veeraraghavan
Publikováno v:
Neurobiology of Disease, Vol 76, Iss, Pp 46-56 (2015)
Huntington disease (HD) is an inherited, fatal neurodegenerative disease with no disease-modifying therapy currently available. In addition to characteristic motor deficits and atrophy of the caudate nucleus, signature hallmarks of HD include behavio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4695d8f490b8ca0232dade08a084827b
https://doi.org/10.1016/j.nbd.2015.01.002
https://doi.org/10.1016/j.nbd.2015.01.002
Autor:
Crystal N. Doty, Eric E. Swayze, Michael R. Hayden, Nicholas S. Caron, Holly Kordasiewicz, Susan M. Freier, C. Frank Bennet, Yuanyun Xie, Amber L. Southwell, Niels H. Skotte, Boguslaw Felczak, Punit P. Seth, Erika B. Villanueva, Michael Oestergaard
Publikováno v:
Molecular Therapy. 23
Huntington disease (HD) is a dominant, genetic neurodegenerative disease characterized by progressive loss of voluntary motor control, psychiatric disturbance, and cognitive decline, for which there is currently no disease-modifying therapy. HD is ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3ca6d18226ecf67b3ce7e1af720b41d