Results 91 to 100 of about 217 (107)

Genes controlling postural changes in blood pressure: comprehensive association analysis of ATP-sensitive potassium channel genes KCNJ8 and ABCC9

Physiological Genomics, 2010
Buffering of blood pressure during change of posture such as standing is controlled largely by the baroreflex. In our population-based Victorian Family Heart Study (VFHS), we previously demonstrated that, on average, systolic blood pressure (SBP) changes very little on standing; however, interindividual variation is substantial and shows familial ...
Justine A, Ellis, Angela, Lamantia, Raul, Chavez, Katrina J, Scurrah, Colin G, Nichols, Stephen B, Harrap   +5 more
openaire   +2 more sources

Physical mapping of the KCNJ8 gene to bovine chromosome 5q3.2–q3.4

Animal Genetics, 2004
C, Drögemüller, S, Mömke, A, Spötter, H, Kuiper, J L, Williams, O, Distl   +5 more
openaire   +2 more sources

Cantù syndrome: Report of a patient with a novel variant in KCNJ8 and revision of literature

American Journal of Medical Genetics, Part A, 2022
Erika Solansh Apuril Velgara, Milena Mariani, Annalaura Torella   +2 more
exaly  

Mixing genome annotation methods in a comparative analysis inflates the apparent number of lineage-specific genes

Current Biology, 2022
Caroline M Weisman, Andrew W Murray, Sean R Eddy   +2 more
exaly  

A novel mutation in the KCNJ8 gene encoding the Kir6.1 subunit of an ATP‐sensitive potassium channel in a Japanese patient with Cantú syndrome

Journal of the European Academy of Dermatology and Venereology, 2020
M. Chihara, A. Asahina, M. Itoh
openaire   +2 more sources

A KCNJ8 mutation associated with early repolarization and atrial fibrillation

Europace, 2012
Jessica T Delaney, Raafia Muhammad, Frank A Fish   +2 more
exaly  

A novel mutation in the KCNJ8 gene encoding the Kir6.1 subunit of an ATP‐sensitive potassium channel in a Japanese patient with Cantú syndrome

Journal of the European Academy of Dermatology and Venereology, 2020
Mami Chihara, A Asahina, Munenari Itoh   +2 more
exaly  

Cantú Syndrome Resulting from Activating Mutation in theKCNJ8Gene

Human Mutation, 2014
Heiko Reutter, Joachim Woelfle, Hartmut Engels   +2 more
exaly  

Loss-of-Function Mutations in the KCNJ8 -Encoded Kir6.1 K ATP Channel and Sudden Infant Death Syndrome

Circulation: Cardiovascular Genetics, 2011
David J Tester, Bi-Hua Tan, Argelia Medeiros-Domingo   +2 more
exaly  

Molecular genetic and functional association of Brugada and early repolarization syndromes with S422L missense mutation in KCNJ8

Heart Rhythm, 2012
Hector Barajas-Martinez, Dan Hu, Tania Ferrer   +2 more
exaly