Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Allison P, Berg"'
Autor:
Wendi Gosliner, Celeste Felix, Ron Strochlic, Shana Wright, Allison Yates-Berg, Hannah R Thompson, Hao Tang, Blanca Melendrez
Publikováno v:
Journal of Medical Internet Research, Vol 25, p e41021 (2023)
BackgroundThe Supplemental Nutrition Assistance Program (SNAP) provides over 40 million Americans with money for food without typically providing participants with food or nutrition information. Educational SMS text messages can reach large numbers o
Externí odkaz:
https://doaj.org/article/fd9c950c07884a8f867e47c6e1ea009a
Autor:
Thomas J. McCorvie, Paula M. Loria, Meihua Tu, Seungil Han, Leela Shrestha, D. Sean Froese, Igor M. Ferreira, Allison P. Berg, Wyatt W. Yue
Publikováno v:
Nature Structural & Molecular Biology. 29:628-638
Glycogen synthase (GYS1) is the central enzyme in muscle glycogen biosynthesis. GYS1 activity is inhibited by phosphorylation of its amino (N) and carboxyl (C) termini, which is relieved by allosteric activation of glucose-6-phosphate (Glc6P). We pre
Autor:
Marko Pregel, Jia Liu, Edward B. Stevens, Yiting Wang, David N. Sheppard, Walailak Jantarajit, Lishuang Cao, Allison P. Berg, Katy J. Sutcliffe
Publikováno v:
British Journal of Pharmacology. 179:1319-1337
BACKGROUND AND PURPOSE Cystic fibrosis transmembrane conductance regulator (CFTR) potentiators are small molecules developed to treat the genetic disease cystic fibrosis (CF). They interact directly with CFTR Cl- channels at the plasma membrane to en
Autor:
Thomas J, McCorvie, Paula M, Loria, Meihua, Tu, Seungil, Han, Leela, Shrestha, D Sean, Froese, Igor M, Ferreira, Allison P, Berg, Wyatt W, Yue
Publikováno v:
Nature structuralmolecular biology. 29(7)
Glycogen synthase (GYS1) is the central enzyme in muscle glycogen biosynthesis. GYS1 activity is inhibited by phosphorylation of its amino (N) and carboxyl (C) termini, which is relieved by allosteric activation of glucose-6-phosphate (Glc6P). We pre
Autor:
Ole Wiskow, Clifford J. Woolf, Kasper C. D. Roet, Jackie Klug-McLeod, Devlin Frost, Karen L. Leach, Kevin Eggan, Hongying Yang, Anthony J. Coyle, Allison P. Berg, Amy Brault, Anne B. Jefferson, Liying Zhang, Seungkyu Lee, Mary K. Dornon, Joseph R. Klim, Dongyi Zhao, Fabien Vincent, Rie Maeda, Kuchuan Chen, Xuan Huang, Alyssa Grantham
Publikováno v:
SSRN Electronic Journal.
Drug development is hampered by poor target selection. Phenotypic screens using cells differentiated from patient stem cells offer the possibility to validate known and discover novel disease targets in an unbiased fashion. To identify targets for ma
Autor:
Mary K. Dornon, Joseph R. Klim, Ole Wiskow, Allison P. Berg, Kevin Eggan, Clifford J. Woolf, Devlin Frost, Kuchuan Chen, Liying Zhang, Hongying Yang, Marco T. Siekmann, Karen L. Leach, Anthony J. Coyle, Seungkyu Lee, Jackie Klug-McLeod, Alyssa Grantham, Anne B. Jefferson, Dongyi Zhao, Xuan Huang, Lyn H. Jones, Fabien Vincent, Rie Maeda, Amy Brault, Kasper C.D. Roet
Publikováno v:
Cell reports
SUMMARY Drug development is hampered by poor target selection. Phenotypic screens using neurons differentiated from patient stem cells offer the possibility to validate known and discover novel disease targets in an unbiased fashion. To identify targ
Publikováno v:
The Journal of Neuroscience. 27:8845-8856
Large aspiny cholinergic interneurons provide the sole source of striatal acetylcholine, a neurotransmitter critical for basal ganglia function; these tonically active interneurons receive excitatory inputs from corticostriatal glutamatergic afferent
Autor:
Douglas A. Bayliss, Allison P. Berg
Publikováno v:
Journal of Neurophysiology. 97:1546-1552
Large aspiny cholinergic interneurons provide the sole source of striatal acetylcholine, a neurotransmitter essential for normal basal ganglia function. Cholinergic interneurons engage in multiple firing patterns that depend on interactions among var
Autor:
Douglas A. Bayliss, Brian W. Jeffries, Allison P. Berg, Chris J. McBain, Christine L. Torborg
Publikováno v:
The Journal of Neuroscience. 26:7362-7367
TASK-1 (KCNK3) and TASK-3 (KCNK9) are members of the two-pore domain potassium channel family and form either homomeric or heteromeric open-rectifier (leak) channels. Recent evidence suggests that these channels contribute to the resting potential an
Publikováno v:
The Journal of Neuroscience. 24:6693-6702
Background potassium currents carried by the KCNK family of two-pore-domain K+channels are important determinants of resting membrane potential and cellular excitability. TWIK-related acid-sensitive K+1 (TASK-1, KCNK3) and TASK-3 (KCNK9) are pH-sensi