Zobrazeno 1 - 10
of 686
pro vyhledávání: '"C. P. Weaver"'
Autor:
Durso, Pamela R.
Publikováno v:
Baptist History & Heritage; Fall2022, Vol. 55 Issue 3, p7-11, 5p
Autor:
Foster, Gaines M.
Publikováno v:
Louisiana History: The Journal of the Louisiana Historical Association, 2000 Jan 01. 41(1), 119-121.
Externí odkaz:
https://www.jstor.org/stable/4233648
Autor:
Amy N Shore, Keyong Li, Mona Safari, Alshaima'a M Qunies, Brittany D Spitznagel, C David Weaver, Kyle Emmitte, Wayne Frankel, Matthew C Weston
Publikováno v:
eLife, Vol 13 (2024)
More than 20 recurrent missense gain-of-function (GOF) mutations have been identified in the sodium-activated potassium (KNa) channel gene KCNT1 in patients with severe developmental and epileptic encephalopathies (DEEs), most of which are resistant
Externí odkaz:
https://doaj.org/article/c400c6aeddf44a7fa69400b6b4b9e3a2
Autor:
Nigam M. Mishra, Brittany D. Spitznagel, Yu Du, Yasmeen K. Mohamed, Ying Qin, C. David Weaver, Kyle A. Emmitte
Publikováno v:
Molecules, Vol 29, Iss 23, p 5494 (2024)
Epilepsy of infancy with migrating focal seizures (EIMFS) is a rare, serious, and pharmacoresistant epileptic disorder often linked to gain-of-function mutations in the KCNT1 gene. KCNT1 encodes the sodium-activated potassium channel known as SLACK,
Externí odkaz:
https://doaj.org/article/97ec9fb835ab49e79c485155658686c3
Autor:
Alshaima’a M. Qunies, Brittany D. Spitznagel, Yu Du, Paul K. Peprah, Yasmeen K. Mohamed, C. David Weaver, Kyle A. Emmitte
Publikováno v:
Molecules, Vol 29, Iss 11, p 2437 (2024)
Gain-of-function mutations in the KCNT1 gene, which encodes the sodium-activated potassium channel known as SLACK, are associated with the rare but devastating developmental and epileptic encephalopathy known as epilepsy of infancy with migrating foc
Externí odkaz:
https://doaj.org/article/0f2c5566b05b4d4bb6e0881d09280aae
Autor:
Emre Fertan, William H. Gendron, Aimée A. Wong, Gabrielle M. Hanson, Richard E. Brown, Ian C. G. Weaver
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-20 (2023)
Abstract Reduced insulin-like growth factor 2 (IGF2) levels in Alzheimer’s disease (AD) may be the mechanism relating age-related metabolic disorders to dementia. Since Igf2 is an imprinted gene, we examined age and sex differences in the relations
Externí odkaz:
https://doaj.org/article/63573e24d4b14e2ba9b4a7f1e2c0f3ff
Autor:
Walker, Randolph Meade
Publikováno v:
The Journal of Negro History, 2000 Jul 01. 85(3), 131-132.
Externí odkaz:
https://www.jstor.org/stable/2649064
Autor:
Wilson, Harold
Publikováno v:
The Journal of Southern History, 2000 Feb 01. 66(1), 135-136.
Externí odkaz:
https://www.jstor.org/stable/2587468