Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jesse L. Mull"'
Autor:
Natalia Rodriguez-Muela, Nadia K. Litterman, Erika M. Norabuena, Jesse L. Mull, Maria José Galazo, Chicheng Sun, Shi-Yan Ng, Nina R. Makhortova, Andrew White, Maureen M. Lynes, Wendy K. Chung, Lance S. Davidow, Jeffrey D. Macklis, Lee L. Rubin
Publikováno v:
Cell Reports, Vol 18, Iss 6, Pp 1484-1498 (2017)
The mechanism underlying selective motor neuron (MN) death remains an essential question in the MN disease field. The MN disease spinal muscular atrophy (SMA) is attributable to reduced levels of the ubiquitous protein SMN. Here, we report that SMN l
Externí odkaz:
https://doaj.org/article/d7739ee812554562919f40e4b8e6e2b2
Autor:
Maureen M. Lynes, Chicheng Sun, Nina R. Makhortova, Lance S. Davidow, Maria J. Galazo, Nadia K. Litterman, Wendy K. Chung, Jeffrey D. Macklis, Natalia Rodriguez-Muela, Lee L. Rubin, Jesse L. Mull, Erika M. Norabuena, Andrew P. White, Shi-Yan Ng
Publikováno v:
Cell Reports, Vol 18, Iss 6, Pp 1484-1498 (2017)
The mechanism underlying selective motor neuron (MN) death remains an essential question in the MN disease field. The MN disease spinal muscular atrophy (SMA) is attributable to reduced levels of the ubiquitous protein SMN. Here, we report that SMN l
Autor:
Chien-Ping Ko, Luca Santarelli, Hasane Ratni, Roland Schmucki, Maureen S. Lynes, Josephine Sheedy, Sergey Paushkin, Chang-Sun Lee, Irene Gerlach, Jesse L. Mull, Nanjing Zhang, Zhihua Feng, Anthony Turpoff, Anuradha Bhattacharyya, Paulo Fontoura, Priya Vazirani, Panayiota Trifillis, Gary Mitchell Karp, Joseph M. Colacino, Martin Ebeling, Kathleen D. McCarthy, John Babiak, Woll Matthew G, Hongyan Qi, Nikolai Naryshkin, Manaswini Sivaramakrishnan, Lee L. Rubin, Jana Narasimhan, Neil Gregory Almstead, Vijayalakshmi Gabbeta, Amal Dakka, Loren A. Eng, Xin Zhao, Nicole Risher, Young-Choon Moon, Marla Weetall, Jiyuan Ma, Karen K. Y. Ling, Stuart W. Peltz, Ellen Welch, Friedrich Metzger, Guangming Chen, Bansri Furia, Daniel Haehnke, Ronald Kong, Anirvan Ghosh, Xiaoyan Zhang, Karen S. Chen
Publikováno v:
Science. 345:688-693
Drugs that provide the splice of life Motor neurons relay signals from the nervous system to muscle fibers. In patients with spinal muscular atrophy, a protein required for the survival of these neurons is deficient or missing altogether, so the neur
Autor:
Nikolai A, Naryshkin, Marla, Weetall, Amal, Dakka, Jana, Narasimhan, Xin, Zhao, Zhihua, Feng, Karen K Y, Ling, Gary M, Karp, Hongyan, Qi, Matthew G, Woll, Guangming, Chen, Nanjing, Zhang, Vijayalakshmi, Gabbeta, Priya, Vazirani, Anuradha, Bhattacharyya, Bansri, Furia, Nicole, Risher, Josephine, Sheedy, Ronald, Kong, Jiyuan, Ma, Anthony, Turpoff, Chang-Sun, Lee, Xiaoyan, Zhang, Young-Choon, Moon, Panayiota, Trifillis, Ellen M, Welch, Joseph M, Colacino, John, Babiak, Neil G, Almstead, Stuart W, Peltz, Loren A, Eng, Karen S, Chen, Jesse L, Mull, Maureen S, Lynes, Lee L, Rubin, Paulo, Fontoura, Luca, Santarelli, Daniel, Haehnke, Kathleen D, McCarthy, Roland, Schmucki, Martin, Ebeling, Manaswini, Sivaramakrishnan, Chien-Ping, Ko, Sergey V, Paushkin, Hasane, Ratni, Irene, Gerlach, Anirvan, Ghosh, Friedrich, Metzger
Publikováno v:
Science (New York, N.Y.). 345(6197)
Spinal muscular atrophy (SMA) is a genetic disease caused by mutation or deletion of the survival of motor neuron 1 (SMN1) gene. A paralogous gene in humans, SMN2, produces low, insufficient levels of functional SMN protein due to alternative splicin
Autor:
Jesse L. Mull, Atsushi Asakura
Publikováno v:
Journal of stem cell research & therapy
Copyright: © 2012 Mull JL, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and