Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jessica H Myers"'
Autor:
Xueyong Wang, Murad Nawaz, Chris DuPont, Jessica H Myers, Steve RA Burke, Roger A Bannister, Brent D Foy, Andrew A Voss, Mark M Rich
Publikováno v:
eLife, Vol 11 (2022)
Excitation-contraction coupling (ECC) is the process by which electrical excitation of muscle is converted into force generation. Depolarization of skeletal muscle resting potential contributes to failure of ECC in diseases such as periodic paralysis
Externí odkaz:
https://doaj.org/article/ccd1295cc8eb45478225599c31db8d5d
Autor:
Jessica H Myers, Kirsten Denman, Chris DuPont, Ahmed A Hawash, Kevin R Novak, Andrew Koesters, Manfred Grabner, Anamika Dayal, Andrew A Voss, Mark M Rich
Publikováno v:
eLife, Vol 10 (2021)
In addition to the hallmark muscle stiffness, patients with recessive myotonia congenita (Becker disease) experience debilitating bouts of transient weakness that remain poorly understood despite years of study. We performed intracellular recordings
Externí odkaz:
https://doaj.org/article/f201e13c4e5f4c20b08b45b730d90c95
Autor:
Xueyong Wang, Murad Nawaz, Chris DuPont, Jessica H Myers, Steve RA Burke, Roger A Bannister, Brent D Foy, Andrew A Voss, Mark M Rich
Publikováno v:
eLife, Vol 11 (2022)
eLife
eLife
Excitation-contraction coupling (ECC) is the process by which electrical excitation of muscle is converted into force generation. Depolarization of skeletal muscle resting potential contributes to failure of ECC in diseases such as periodic paralysis
Autor:
Kevin R. Novak, Anamika Dayal, Chris DuPont, Jessica H Myers, Mark M. Rich, Andrew Koesters, Kirsten Denman, Andrew A. Voss, Manfred Grabner, Ahmed A. Hawash
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f6215c5c397370bb10183025c7f0aad
https://doi.org/10.7554/elife.65691.sa2
https://doi.org/10.7554/elife.65691.sa2
Autor:
Chris DuPont, Anamika Dayal, Andrew Koesters, Kevin R. Novak, Kirsten Denman, Andrew A. Voss, Jessica H Myers, Ahmed A. Hawash, Mark M. Rich, Manfred Grabner
Publikováno v:
eLife, Vol 10 (2021)
eLife
eLife
In addition to the hallmark muscle stiffness, patients with recessive myotonia congenita (Becker disease) experience debilitating bouts of transient weakness that remain poorly understood despite years of study. We performed intracellular recordings
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93b40765fcf9a44c20c5417a622d7891
https://doi.org/10.1101/2020.12.23.424129
https://doi.org/10.1101/2020.12.23.424129
Autor:
Jeremy M. Sullivan, Charlotte J. Sumner, Cathleen M. Lutz, Laurent P. Bogdanik, Mark M. Rich, Kevin R. Novak, Nicklaus L. Brown, Kirsten Denman, Chris DuPont, Phillip V. Walker, Andrew A. Voss, Jessica H Myers, David R. Ladle
Publikováno v:
Ann Neurol
OBJECTIVE Myotonia is caused by involuntary firing of skeletal muscle action potentials and causes debilitating stiffness. Current treatments are insufficiently efficacious and associated with side effects. Myotonia can be triggered by voluntary move
Publikováno v:
eNeuro
We investigated the calcium dynamics of dorsal root ganglion (DRG) neurons using transgenic mice to target expression of the genetically encoded calcium indicator (GECI), GCaMP6s, to a subset of neurons containing parvalbumin (PV), a calcium-binding