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searching for Kir6.2 9 found (18 total)

alternate case: kir6.2

Permanent neonatal diabetes (412 words) [view diff] exact match in snippet view article find links to article

caused by activating mutations of the KCNJ11 gene, which codes for the Kir6.2 subunit of the beta cell KATP channel. This disease is considered to be
HMR 1883 (900 words) [view diff] exact match in snippet view article find links to article
selectively the Kir6.2/SUR2A KATP subtype, found mostly in the membranes of cardiac cells. However, data showing that HMR 1098 inhibits the Kir6.2/SUR1 KATP
Hyperinsulinemic hypoglycemia (1,112 words) [view diff] exact match in snippet view article find links to article
11p15 Paternal Kir6.2 mutation with clonal loss of heterozygosity of 11p15 Diffuse hyperinsulinism KATP channel disorders SUR1 mutations Kir6.2 mutations Glucokinase
Plakophilin-2 (3,980 words) [view diff] exact match in snippet view article find links to article
has also shown that plakophilin-2 binds to the K(ATP) channel subunit, Kir6.2, and that in cardiomyocytes from haploinsufficient PKP2 mice, K(ATP) channel
ABCC8 (1,086 words) [view diff] exact match in snippet view article find links to article
"Mutations in the genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) in diabetes mellitus and hyperinsulinism". Hum
Glutamate dehydrogenase 1 (2,962 words) [view diff] exact match in snippet view article find links to article
ABCC8, which encodes the protein SUR1, or KCNJ11, which encodes the protein Kir6.2. In the Ashkenazi Jewish population, two ABCC8 founder mutations are responsible
ANK2 (3,673 words) [view diff] exact match in snippet view article find links to article
TJ; Anderson, ME; Mohler, PJ (10 September 2010). "Ankyrin-B regulates Kir6.2 membrane expression and function in heart". The Journal of Biological Chemistry
Genetic causes of type 2 diabetes (2,221 words) [view diff] exact match in snippet view article find links to article
subfamily J, member 11), encodes the islet ATP-sensitive potassium channel Kir6.2, and TCF7L2 (transcription factor 7–like 2) regulates proglucagon gene expression
Bioelectricity (18,115 words) [view diff] exact match in snippet view article find links to article
Mutations in the Gene Encoding the ATP-Sensitive Potassium-Channel Subunit Kir6.2 and Permanent Neonatal Diabetes" (PDF). New England Journal of Medicine