Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Laura C. Armstrong"'
Autor:
John P. Snow, Grant Westlake, Lindsay K. Klofas, Soyoun Jeon, Laura C. Armstrong, Kathryn J. Swoboda, Alfred L. George, Jr, Kevin C. Ess
Publikováno v:
Neurobiology of Disease, Vol 141, Iss , Pp 104881- (2020)
Alternating hemiplegia of childhood (AHC) is a rare neurodevelopmental disease caused by heterozygous de novo missense mutations in the ATP1A3 gene that encodes the neuronal specific α3 subunit of the Na,K-ATPase (NKA) pump. Mechanisms underlying pa
Externí odkaz:
https://doaj.org/article/179161d1b68b4de4ad48c56e56d5d6ad
Autor:
Mary-Bronwen L Chalkley, Rachel B Mersfelder, Maria Sundberg, Laura C Armstrong, Mustafa Sahin, Rebecca A Ihrie, Kevin C Ess
Publikováno v:
PLoS ONE, Vol 18, Iss 10, p e0292086 (2023)
Tuberous Sclerosis Complex (TSC) is a debilitating developmental disorder characterized by a variety of clinical manifestations. TSC is caused by mutations in the TSC1 or TSC2 genes, which encode the hamartin/tuberin proteins respectively. These prot
Externí odkaz:
https://doaj.org/article/d45f6b6c25b340218f4d2f8d48a9b3ea
Autor:
David K. Schaffer, Frank E. Block, M. Diana Neely, Jennifer R. McKenzie, John P. Wikswo, David E. Cliffel, Dusty R. Miller, Dmitry A. Markov, Erik M. Werner, Kevin C. Ess, Ethan S. McClain, Laura C. Armstrong, Aaron B. Bowman, Adam R. Travis
Publikováno v:
Sens Actuators B Chem
There is a need for valves and pumps that operate at the microscale with precision and accuracy, are versatile in their application, and are easily fabricated. To that end, we developed a new rotary planar multiport valve to faithfully select solutio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ecc64658fa4c13ff94f2640dd50d797
https://pubmed.ncbi.nlm.nih.gov/34092923
https://pubmed.ncbi.nlm.nih.gov/34092923
Autor:
Laura C. Armstrong, Kevin C. Ess, Alfred L. George, Lindsay K. Klofas, Grant Westlake, John P. Snow, Kathryn J. Swoboda, Soyoun Jeon
Publikováno v:
Neurobiology of Disease, Vol 141, Iss, Pp 104881-(2020)
Alternating hemiplegia of childhood (AHC) is a rare neurodevelopmental disease caused by heterozygous de novo missense mutations in the ATP1A3 gene that encodes the neuronal specific α3 subunit of the Na,K-ATPase (NKA) pump. Mechanisms underlying pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e665e8dc211a8cc1b4f85db7307c1a44
Autor:
Aaron B. Bowman, Kevin C. Ess, Laura C. Armstrong, Grant Westlake, Eric A Armour, Bryan Cawthon, John P. Snow
Publikováno v:
Human molecular genetics. 26(23)
Tuberous sclerosis complex (TSC) is a pediatric disorder of dysregulated growth and differentiation caused by loss of function mutations in either the TSC1 or TSC2 genes, which regulate mTOR kinase activity. To study aberrations of early development
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::452337d109fd03139d4492f020d1a5d1
https://pubmed.ncbi.nlm.nih.gov/28973543
https://pubmed.ncbi.nlm.nih.gov/28973543