SK Cha, C Huang, Y Ding, X Qi, CL Huang… - Journal of Biological …, 2011 - ASBMB ... or BSND) (1,–,5). The hypocalciuric, hypomagnesemic variant of Bartter syndrome, Gitelman syndrome, is due to loss of function mutations of the thiazide-sensitive NaCl co-transporter (6). The recently described SeSAME (seizures, sensorineural deafness, ataxia, mental ... Related articles - All 4 versions
R Anupam, A Datta, M Kesic… - Journal of Biological …, 2011 - ASBMB ... Our data indicate that p30 specifically binds to cellular ATM (ataxia telangiectasia mutated) and REGγ (a nuclear 20 S proteasome activator). Under conditions of genotoxic stress, p30 expression was associated with reduced levels of ATM and increased cell survival. ... Cited by 2 - Related articles - All 4 versions
M Wang, H Sui, W Li, J Wang… - American Journal of …, 2011 - Am Physiological Soc ... The physiological importance of the basolateral K channels in maintaining transepithelial membrane transport in the TAL and distal nephron is best demonstrated in SeSAME disease (Seizures, Sensorineural deafness, Ataxia, Mental retardation, and Electrolyte imbalance). ... Related articles - All 3 versions
[HTML] from nih.govE Ujházy, M Mach, J Navarová, I Brucknerová… - Interdisciplinary …, 2011 - Versita ... Neuromotor and reflex development Within the neuromotor and reflex development assess- ment, we observed righting reflex (on day 5 PP, the pup´s ability to turn over from supine position), negative geo- taxia (8 PP, the pup´s ability to turn 180° on a 25° inclined placed head ... Related articles - All 4 versions
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