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For: De Zio R, Gerbino A, Forleo C, Pepe M, Milano S, Favale S, Procino G, Svelto M, Carmosino M. Functional study of a KCNH2 mutant: Novel insights on the pathogenesis of the LQT2 syndrome. J Cell Mol Med 2019;23:6331-42. [PMID: 31361068 DOI: 10.1111/jcmm.14521] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 1.7] [Reference Citation Analysis]
Number Citing Articles
1 Chen J, Li H, Guo S, Yang Z, Sun S, Zeng J, Gou H, Chen Y, Wang F, Lin Y, Huang K, Yue H, Ma Y, Lin Y. Whole exome sequencing in Brugada and long QT syndromes revealed novel rare and potential pathogenic mutations related to the dysfunction of the cardiac sodium channel. Orphanet J Rare Dis 2022;17:394. [PMID: 36303204 DOI: 10.1186/s13023-022-02542-z] [Reference Citation Analysis]
2 De Zio R, Pietrafesa G, Milano S, Procino G, Bramerio M, Pepe M, Forleo C, Favale S, Svelto M, Gerbino A, Carmosino M. Role of Nuclear Lamin A/C in the Regulation of Nav1.5 Channel and Microtubules: Lesson From the Pathogenic Lamin A/C Variant Q517X. Front Cell Dev Biol 2022;10:918760. [DOI: 10.3389/fcell.2022.918760] [Reference Citation Analysis]
3 Lou J, Chen H, Huang S, Chen P, Yu Y, Chen F. Update on risk factors and biomarkers of sudden unexplained cardiac death. Journal of Forensic and Legal Medicine 2022. [DOI: 10.1016/j.jflm.2022.102332] [Reference Citation Analysis]
4 Mondéjar-Parreño G, Jahng JWS, Belbachir N, Wu BC, Zhang X, Perez MV, Badhwar N, Wu JC. Generation of three heterozygous KCNH2 mutation-carrying human induced pluripotent stem cell lines for modeling LQT2 syndrome. Stem Cell Res 2021;54:102402. [PMID: 34051449 DOI: 10.1016/j.scr.2021.102402] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
5 Khiatah B, Dukes J, Desai C, Frugoli A. Torsades De Pointes Electrical Storm Induced by H1N1 in a Patient with KCNH2 Variant of Unknown Significance. Case Rep Cardiol 2020;2020:8889769. [PMID: 32774932 DOI: 10.1155/2020/8889769] [Reference Citation Analysis]
6 Ahmed Awan Z, Bima A, Rashidi OM, Jamil K, Khan IA, Almukadi HS, Bilgrami AL, Ahmad Shaik N, Banaganapalli B. Low resolution protein mapping and KB-R7943 drug-protein molecular interaction analysis of long-QT syndrome linked KCNH2 mutations. All Life 2020;13:183-193. [DOI: 10.1080/26895293.2020.1737249] [Cited by in Crossref: 3] [Article Influence: 1.5] [Reference Citation Analysis]
7 De Zio R, Gerbino A, Forleo C, Pepe M, Milano S, Favale S, Procino G, Svelto M, Carmosino M. Functional study of a KCNH2 mutant: Novel insights on the pathogenesis of the LQT2 syndrome. J Cell Mol Med 2019;23:6331-42. [PMID: 31361068 DOI: 10.1111/jcmm.14521] [Cited by in Crossref: 5] [Cited by in F6Publishing: 7] [Article Influence: 1.7] [Reference Citation Analysis]