Results 141 to 144 of about 1,474 (144)

Pharmacological Rescue of Human Disease Mutations in KCNJ10 and KCNJ16 by Novel Kir4.1/5.1 Potentiator, VU0493206

The Journal of Pharmacology and Experimental Therapeutics, 2023
Samantha McClenahan, Dongsoo Lee, Jerod Denton   +2 more
openaire   +1 more source

Type, location and zygosity of KCNJ16 mutations may determine the clinical severity of Hypokalemic Tubulopathy and Deafness (HkTD)

medRxiv
L. Gondra, S. Mora, I. G. Shaikh, A. Garcia-Castano, F. Schilling, G. Ariceta, L. Garcia-Suarez, P. Tejera-Carreno, G. Fernandez-Juarez, A. S. Rodriguez, J. Pujol-Gimenez, M. Garcia-Alonso, S. Gomez-Conde, A. C. Aranaga Decori, M. Koemhoff, V. Renigunta, S. Weber, L. Madariaga, A. Renigunta   +18 more
semanticscholar   +1 more source

Molecular deconstruction of the pre-Bötzinger Complex/Nucleus Ambiguus (preBötC/NA) region: cellular constituencies and transcriptional responses to repeated seizures in the rat hindbrain

bioRxiv
Wasif A. Osmani, Ibrahim Vazirabad, Neil Rhode, G. Mouradian, Anna D. Manis, Matthew R. Hodges   +5 more
semanticscholar   +1 more source

Faculty Opinions recommendation of Renal phenotype in mice lacking the Kir5.1 (Kcnj16) K+ channel subunit contrasts with that observed in SeSAME/EAST syndrome.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature, 2011
openaire   +1 more source