PubMed (GeneRIF) for id: 3757

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Results by year

Year	Number of Results
2001	4
2002	15
2003	18
2004	25
2005	21
2006	24
2007	33
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2009	56
2010	62
2011	48
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Liu Z, Wang F, Yuan H, Tian F, Yang C, Hu F, Liu Y, Tang M, Ping M, Kang C, Luo T, Yang G, Hu M, Gao Z, Li P. Liu Z, et al. BMC Biol. 2024 Feb 5;22(1):29. doi: 10.1186/s12915-024-01833-0. BMC Biol. 2024. PMID: 38317233 Free article.

Dissecting the associations of KCNH2 genetic polymorphisms with various types of cardiac arrhythmias.

Li S, Zhang Z, Ding Y, Yu T, Qin Z, Guo S. Li S, et al. Gene. 2024 Mar 20;899:148132. doi: 10.1016/j.gene.2024.148132. Epub 2024 Jan 3. Gene. 2024. PMID: 38181928

Identification and characterization of two novel KCNH2 mutations contributing to long QT syndrome.

Owusu-Mensah A, Treat J, Bernardi J, Pfeiffer R, Goodrow R, Tsevi B, Lam V, Audette M, Cordeiro JM, Deo M. Owusu-Mensah A, et al. PLoS One. 2024 Jan 5;19(1):e0287206. doi: 10.1371/journal.pone.0287206. eCollection 2024. PLoS One. 2024. PMID: 38181028 Free PMC article.

Functional and clinical characterization of a novel homozygous KCNH2 missense variant in the pore region of Kv11.1 leading to a viable but severe long-QT syndrome.

Delinière A, Jaupart L, Janin A, Millat G, Boulin T, Andrini O, Chevalier P. Delinière A, et al. Gene. 2024 Mar 1;897:148076. doi: 10.1016/j.gene.2023.148076. Epub 2023 Dec 10. Gene. 2024. PMID: 38086455

KCNH2A561V Heterozygous Mutation Inhibits KCNH2 Protein Expression via The Activation of UPR Mediated by ATF6.

Chen B, Tan L, Chen D, Wang X, Liu J, Huang X, Wang Y, Huang S, Mao F, Lian J. Chen B, et al. Physiol Res. 2023 Nov 28;72(5):621-631. doi: 10.33549/physiolres.935095. Physiol Res. 2023. PMID: 38015761 Free PMC article.

Integrins regulate hERG1 dynamics by girdin-dependent Gαi3: signaling and modeling in cancer cells.

Duranti C, Iorio J, Bagni G, Chioccioli Altadonna G, Fillion T, Lulli M, D'Alessandro FN, Montalbano A, Lastraioli E, Fanelli D, Coppola S, Schmidt T, Piazza F, Becchetti A, Arcangeli A. Duranti C, et al. Life Sci Alliance. 2023 Nov 3;7(1):e202302135. doi: 10.26508/lsa.202302135. Print 2024 Jan. Life Sci Alliance. 2023. PMID: 37923359 Free PMC article.

KCNH2 mutation c.3099_3112del causes congenital long QT syndrome type 2 with gender differences.

Ke Z, Li C, Bai G, Tan L, Wang J, Zhou M, Zhou J, Chen SY, Dong X. Ke Z, et al. Clinics (Sao Paulo). 2023 Sep 30;78:100285. doi: 10.1016/j.clinsp.2023.100285. eCollection 2023. Clinics (Sao Paulo). 2023. PMID: 37783170 Free PMC article.

Translation reinitiation in c.453delC frameshift mutation of KCNH2 producing functional hERG K+ channels with mild dominant negative effect in the heterozygote patient-derived iPSC cardiomyocytes.

Park NK, Park SJ, Park YG, Moon SH, Woo J, Kim HJ, Kim SJ, Choi SW. Park NK, et al. Hum Mol Genet. 2024 Jan 7;33(2):110-121. doi: 10.1093/hmg/ddad165. Hum Mol Genet. 2024. PMID: 37769355

Mechanisms of fever-induced QT prolongation and torsades de pointes in patients with KCNH2 mutation.

Usuda K, Hayashi K, Nakajima T, Kurata Y, Cui S, Kusayama T, Tsuda T, Tada H, Kato T, Sakata K, Usui S, Fujino N, Tanaka Y, Kaneko Y, Kurabayashi M, Tange S, Saito T, Ohta K, Yamagishi M, Takamura M. Usuda K, et al. Europace. 2023 Jun 2;25(6):euad161. doi: 10.1093/europace/euad161. Europace. 2023. PMID: 37386841 Free PMC article.

Hydroxychloroquine Attenuates hERG Channel by Promoting the Membrane Channel Degradation: Computational Simulation and Experimental Evidence for QT-Interval Prolongation with Hydroxychloroquine Treatment.

Wang X, Feng Y, Liu S, Liu J, Pan S, Wei L, Ma Y, Liu Z, Xing Y, Wang J, Cui Q, Zhang Y, Wang T, Cai C. Wang X, et al. Cardiology. 2023;148(4):310-323. doi: 10.1159/000531132. Epub 2023 May 22. Cardiology. 2023. PMID: 37231805 Free article.

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