Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Rebecca D Imhoff-Manuel"'
Autor:
María de Lourdes Martínez-Silva, Rebecca D Imhoff-Manuel, Aarti Sharma, CJ Heckman, Neil A Shneider, Francesco Roselli, Daniel Zytnicki, Marin Manuel
Publikováno v:
eLife, Vol 7 (2018)
Hyperexcitability has been suggested to contribute to motoneuron degeneration in amyotrophic lateral sclerosis (ALS). If this is so, and given that the physiological type of a motor unit determines the relative susceptibility of its motoneuron in ALS
Externí odkaz:
https://doaj.org/article/e84ef059e33a431c86730f1b886b6e3d
Publikováno v:
eLife, Vol 3 (2014)
In amyotrophic lateral sclerosis (ALS) the large motoneurons that innervate the fast-contracting muscle fibers (F-type motoneurons) are vulnerable and degenerate in adulthood. In contrast, the small motoneurons that innervate the slow-contracting fib
Externí odkaz:
https://doaj.org/article/534596e862094e00a7ce8fb8399787d4
Autor:
Elma Kajtaz, Matthew C. Tresch, Jody D. Ciolino, Vicki M. Tysseling, Katharina A. Quinlan, Rebecca D Imhoff-Manuel, Charles J. Heckman
Publikováno v:
The Journal of Physiology. 595:5387-5400
To improve our understanding of early disease mechanisms and find reliable biomarkers of amyotrophic lateral sclerosis (ALS), a progressive neurodegenerative disease, we measured electromyogram (EMG) activity in hind limb muscles of SOD1G93A mice. In
Autor:
Marin Manuel, Neil A. Shneider, Aarti Sharma, Daniel Zytnicki, Rebecca D Imhoff-Manuel, Charles J. Heckman, Francesco Roselli, María de Lourdes Martínez-Silva
Publikováno v:
eLife
eLife, eLife Sciences Publication, 2018, 7
eLife, Vol 7 (2018)
eLife, eLife Sciences Publication, 2018, 7
eLife, Vol 7 (2018)
International audience; Hyperexcitability has been suggested to contribute to motoneuron degeneration in amyotrophic lateral sclerosis (ALS). If this is so, and given that the physiological type of a motor unit determines the relative susceptibility
Autor:
Daniel Zytnicki, Francesco Roselli, Charles J. Heckman, María de Lourdes Martínez-Silva, Rebecca D Imhoff-Manuel, Marin Manuel, Neil A. Shneider, Aarti Sharma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::db97a9b18cb7a8c81e114e788e4883d1
https://doi.org/10.7554/elife.30955.019
https://doi.org/10.7554/elife.30955.019
Autor:
Charles J. Heckman, Rebecca D Imhoff-Manuel, Marin Manuel, Matthew C. Tresch, David A. Klein, Vicki M. Tysseling
Publikováno v:
Journal of Neurophysiology
Journal of Neurophysiology, American Physiological Society, 2017, 118 (5), pp.2944-2952. ⟨10.1152/jn.00190.2017⟩
Journal of Neurophysiology, American Physiological Society, 2017, 118 (5), pp.2944-2952. ⟨10.1152/jn.00190.2017⟩
After spinal cord injury (SCI), reflexes become hyperexcitable, leading to debilitating muscle spasms and compromised motor function. Previous work has described adaptations in spinal systems that might underlie this hyperexcitability, including an i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7cd7c550040352788f9dc86c11b4b97e
https://hal.archives-ouvertes.fr/hal-02042414
https://hal.archives-ouvertes.fr/hal-02042414
Publikováno v:
eLife
eLife, Vol 3 (2014)
eLife, Vol 3 (2014)
In amyotrophic lateral sclerosis (ALS) the large motoneurons that innervate the fast-contracting muscle fibers (F-type motoneurons) are vulnerable and degenerate in adulthood. In contrast, the small motoneurons that innervate the slow-contracting fib