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For: Gripp KW, Smithson SF, Scurr IJ, Baptista J, Majumdar A, Pierre G, Williams M, Henderson LB, Wentzensen IM, McLaughlin H, Leeuwen L, Simon MEH, van Binsbergen E, Dinulos MBP, Kaplan JD, McRae A, Superti-Furga A, Good JM, Kutsche K. Syndromic disorders caused by gain-of-function variants in KCNH1, KCNK4, and KCNN3-a subgroup of K+ channelopathies. Eur J Hum Genet 2021;29:1384-95. [PMID: 33594261 DOI: 10.1038/s41431-021-00818-9] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 8.0] [Reference Citation Analysis]
Number Citing Articles
1 Tian M, Li R, Yang F, Shu X, Li J, Chen J, Peng L, Yu X, Yang C. Phenotypic expansion of KCNH1 ‐associated disorders to include isolated epilepsy and its associations with genotypes and molecular sub‐regional locations. CNS Neurosci Ther 2022. [DOI: 10.1111/cns.14001] [Reference Citation Analysis]
2 Sahoo N, Yang K, Coburger I, Bernert A, Swain SM, Gessner G, Kappl R, Kühl T, Imhof D, Hoshi T, Schönherr R, Heinemann SH. Intracellular hemin is a potent inhibitor of the voltage-gated potassium channel Kv10.1. Sci Rep 2022;12:14645. [PMID: 36030326 DOI: 10.1038/s41598-022-18975-2] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Bauer CK, Holling T, Horn D, Laço MN, Abdalla E, Omar OM, Alawi M, Kutsche K. Clinically Relevant KCNQ1 Variants Causing KCNQ1-KCNE2 Gain-of-Function Affect the Ca2+ Sensitivity of the Channel. IJMS 2022;23:9690. [DOI: 10.3390/ijms23179690] [Reference Citation Analysis]
4 Nagaraj H, Narayanan R. Plasticity manifolds and ion-channel degeneracy govern circadian oscillations of neuronal intrinsic properties in the suprachiasmatic nucleus.. [DOI: 10.1101/2022.07.22.501115] [Reference Citation Analysis]
5 Nam YW, Downey M, Rahman MA, Cui M, Zhang M. Channelopathy of small- and intermediate-conductance Ca2+-activated K+ channels. Acta Pharmacol Sin 2022. [PMID: 35715699 DOI: 10.1038/s41401-022-00935-1] [Reference Citation Analysis]
6 Napoli G, Panzironi N, Traversa A, Catalanotto C, Pace V, Petrizzelli F, Giovannetti A, Lazzari S, Cogoni C, Tartaglia M, Carella M, Mazza T, Pizzuti A, Parisi C, Caputo V. Potassium Channel KCNH1 Activating Variants Cause Altered Functional and Morphological Ciliogenesis. Mol Neurobiol 2022. [PMID: 35639255 DOI: 10.1007/s12035-022-02886-4] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Happ HC, Sadleir LG, Zemel M, de Valles-ibáñez G, Hildebrand MS, Mcconkie-rosell A, Mcdonald M, May H, Sands T, Aggarwal V, Elder C, Feyma T, Bayat A, Møller RS, Fenger CD, Nielsen JEK, Datta AN, Gorman KM, King MD, Linhares N, Burton BK, Paras A, Ellard S, Rankin J, Shukla A, Majethia P, Olson RJ, Muthusamy K, Schimmenti LA, Starnes K, Sedláčková L, Štěrbová K, Vlčková M, Laššuthová P, Jahodová A, Porter BE, Couque N, Colin E, Prouteau C, Collet C, Smol T, Caumes R, Vansenne F, Bisulli F, Licchetta L, Person R, Torti E, Mcwalter K, Webster R, Lesca G, Szepetowski P, Scheffer IE, Mefford HC, Carvill GL. Missense variants in the voltage sensing and pore domain of KCNH5 cause neurodevelopmental phenotypes including epilepsy.. [DOI: 10.1101/2022.04.26.22274147] [Reference Citation Analysis]
8 Orfali R, Nam Y, Nguyen HM, Rahman MA, Yang G, Cui M, Wulff H, Zhang M. Channelopathy-causing mutations in the S45A/S45B and HA/HB helices of KCa2.3 and KCa3.1 channels alter their apparent Ca2+ sensitivity. Cell Calcium 2022;102:102538. [DOI: 10.1016/j.ceca.2022.102538] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
9 Schwarz M, Ryba L, Křepelová A, Moslerová V, Zelinová M, Turnovec M, Martinková J, Kratochvílová L, Drahanský M, Macek M Jr, Havlovicová M. Zimmermann-Laband syndrome in monozygotic twins with a mild neurobehavioral phenotype lacking gingival overgrowth-A case report of a novel KCNN3 gene variant. Am J Med Genet A 2021. [PMID: 34907639 DOI: 10.1002/ajmg.a.62616] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]