Results 1 -
10
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93
for
".2" Potassium Channel
- ... potassium channel protein TASK-3 K2p9.1 KT3.2 potassium channel subfamily K member 9 potassium channel, two pore ... channel 3 two pore K(+) channel KT3.2 two pore potassium channel KT3.2 Tests of KCNK9 PubMed POTASSIUM CHANNEL, ...
- ... Czirjak G. Molecular background of leak K+ currents: two-pore domain potassium channels. Physiol Rev. 2010 Apr;90(2):559-605. doi: 10.1152/physrev.00029.2009. ...
- ... 2 inwardly rectifying potassium channel KIR6.2 KIR6.2 MGC133230 potassium channel, inwardly rectifying subfamily J member 11 potassium channel, ... member 11 TNDM3 Tests of KCNJ11 PubMed TYPE 2 DIABETES MELLITUS; T2D POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, MEMBER 11; KCNJ11 DIABETES ...
- ... HNSPC KCNA11 KCNQ2_HUMAN KQT-like 2 KV7.2 KVEBN1 potassium channel, voltage gated KQT-like subfamily Q, member 2 ... potassium voltage-gated channel, KQT-like subfamily, member 2 voltage-gated potassium channel subunit Kv7.2 Tests of KCNQ2 PubMed POTASSIUM ...
- ... voltage-gated channel, subfamily H (eag-related), member 2 Tests of KCNH2 PubMed POTASSIUM CHANNEL, VOLTAGE-GATED, SUBFAMILY H, MEMBER 2; KCNH2 NCBI Gene ClinVar Brugada R, Hong K, ...
- ... J2 potassium inwardly-rectifying channel, subfamily J, member 2 Tests of KCNJ2 PubMed POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, MEMBER 2; KCNJ2 NCBI ...
- ... potassium channel, subfamily T, member 1 SLACK Slo2.2 Tests of KCNT1 PubMed POTASSIUM CHANNEL, SUBFAMILY T, MEMBER 1; KCNT1 NCBI Gene ClinVar ... Dibbens LM. Missense mutations in the sodium-gated potassium channel gene KCNT1 ... mutation in two sporadic cases with malignant migrating partial seizures in ...
- ... convulsions caused by altered gating of KCNQ2/KCNQ3 potassium channels. J Neurosci. 2002 Jan 15;22(2):RC199. doi: 10.1523/JNEUROSCI.22-02-j0003. ... Benign Familial Neonatal Convulsions. Neurosci Lett. 2009 Oct 2;462(1):24-9. doi: ... potassium channel subunits: molecular correlates of the M-channel. Science. ...
- ... is associated with point mutations in the human potassium channel gene, KCNA1. Nat Genet. 1994 Oct;8(2):136-40. doi: 10.1038/ng1094-136. Citation ... BR, Hisama FM. Functional analysis of a novel potassium channel (KCNA1) ... myokymia. Neurogenetics. 2007 Apr;8(2):131-5. doi: 10.1007/s10048-006-0071- ...
- ... usually unknown. These cases are classified as type 2 (ATS2). Studies suggest that variations in at least one other potassium channel gene may underlie the disorder in some of ...