157 related articles for article (PubMed ID: 27987400)
1. An insertion/deletion polymorphism within 3'UTR of RYR2 modulates sudden unexplained death risk in Chinese populations.
Wang S; Zhang Z; Yang Y; Wang C; Tao R; Hu S; Yin Z; Zhang Q; Li L; He Y; Zhu S; Li C; Zhang S; Zhang J; Sheng L; Wu F; Luo B; Gao Y
Forensic Sci Int; 2017 Jan; 270():165-172. PubMed ID: 27987400
[TBL] [Abstract][Full Text] [Related]
2. A common indel polymorphism of the Desmoglein-2 (DSG2) is associated with sudden cardiac death in Chinese populations.
Zou Y; Zhang Q; Zhang J; Chen X; Zhou W; Yang Z; Yang Q; Yu H; Li L; He Y; Li C; Zhang S; Zhu S; Luo B; Gao Y
Forensic Sci Int; 2019 Aug; 301():382-387. PubMed ID: 31220685
[TBL] [Abstract][Full Text] [Related]
3. Association between an indel polymorphism in the 3'UTR of COL1A2 and the risk of sudden cardiac death in Chinese populations.
Yin Z; Guo Y; Zhang J; Zhang Q; Li L; Wang S; Wang C; He Y; Zhu S; Li C; Zhang S; Zha L; Cai J; Luo B; Gao Y
Leg Med (Tokyo); 2017 Sep; 28():22-26. PubMed ID: 28738217
[TBL] [Abstract][Full Text] [Related]
4. Association between an indel polymorphism within CTH and the risk of sudden cardiac death in a Chinese population.
Zhou W; Yang Q; Yu H; Zhang Q; Zou Y; Chen X; Yang Z; Qu Y; Tan R; Li L; Zhu S; He Y; Luo B; Gao Y
Leg Med (Tokyo); 2020 Sep; 46():101736. PubMed ID: 32563979
[TBL] [Abstract][Full Text] [Related]
5. Genetic association study of a novel indel polymorphism in HSPA1B with the risk of sudden cardiac death in the Chinese populations.
Yang Z; Zhang Q; Yu H; Du H; Li L; He Y; Zhu S; Li C; Zhang S; Luo B; Gao Y
Forensic Sci Int; 2021 Jan; 318():110637. PubMed ID: 33309992
[TBL] [Abstract][Full Text] [Related]
6. A Novel
Yang Z; Zhang Q; Yu H; Li L; He Y; Zhu S; Li C; Zhang S; Luo B; Gao Y
DNA Cell Biol; 2021 Jan; 40(1):10-17. PubMed ID: 33180568
[TBL] [Abstract][Full Text] [Related]
7. Targeted mutational analysis of the RyR2-encoded cardiac ryanodine receptor in sudden unexplained death: a molecular autopsy of 49 medical examiner/coroner's cases.
Tester DJ; Spoon DB; Valdivia HH; Makielski JC; Ackerman MJ
Mayo Clin Proc; 2004 Nov; 79(11):1380-4. PubMed ID: 15544015
[TBL] [Abstract][Full Text] [Related]
8. Exome analysis in 34 sudden unexplained death (SUD) victims mainly identified variants in channelopathy-associated genes.
Neubauer J; Lecca MR; Russo G; Bartsch C; Medeiros-Domingo A; Berger W; Haas C
Int J Legal Med; 2018 Jul; 132(4):1057-1065. PubMed ID: 29350269
[TBL] [Abstract][Full Text] [Related]
9. Modulation of STIM1 by a risk insertion/deletion polymorphism underlying genetics susceptibility to sudden cardiac death originated from coronary artery disease.
Zhang Q; He Y; Xu H; Li L; Guo Y; Zhang J; Cheng L; Yu H; Dai Y; Yang Q; Yang Z; Li C; Zhang S; Zhu S; Luo B; Gao Y
Forensic Sci Int; 2021 Nov; 328():111010. PubMed ID: 34592581
[TBL] [Abstract][Full Text] [Related]
10. Genetic Variations Within METTL16 and Susceptibility to Sudden Cardiac Death in Chinese Populations With Coronary Artery Disease.
Zhen X; Zhao W; Wang J; Li L; He Y; Zhang J; Li C; Zhang S; Huang J; Luo B; Gao Y
Am J Cardiol; 2023 Sep; 202():90-99. PubMed ID: 37423176
[TBL] [Abstract][Full Text] [Related]
11. Postmortem genetic screening of SNPs in RyR2 gene in sudden unexplained nocturnal death syndrome in the southern Chinese Han population.
Huang L; Liu C; Tang S; Su T; Cheng J
Forensic Sci Int; 2014 Feb; 235():14-8. PubMed ID: 24447446
[TBL] [Abstract][Full Text] [Related]
12. Postmortem long QT syndrome genetic testing for sudden unexplained death in the young.
Tester DJ; Ackerman MJ
J Am Coll Cardiol; 2007 Jan; 49(2):240-6. PubMed ID: 17222736
[TBL] [Abstract][Full Text] [Related]
13. Ryanodine receptor-mediated arrhythmias and sudden cardiac death.
Blayney LM; Lai FA
Pharmacol Ther; 2009 Aug; 123(2):151-77. PubMed ID: 19345240
[TBL] [Abstract][Full Text] [Related]
14. Spectrum and prevalence of cardiac ryanodine receptor (RyR2) mutations in a cohort of unrelated patients referred explicitly for long QT syndrome genetic testing.
Tester DJ; Kopplin LJ; Will ML; Ackerman MJ
Heart Rhythm; 2005 Oct; 2(10):1099-105. PubMed ID: 16188589
[TBL] [Abstract][Full Text] [Related]
15. Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia.
Marks AR; Priori S; Memmi M; Kontula K; Laitinen PJ
J Cell Physiol; 2002 Jan; 190(1):1-6. PubMed ID: 11807805
[TBL] [Abstract][Full Text] [Related]
16. Cardiac channelopathy testing in 274 ethnically diverse sudden unexplained deaths.
Wang D; Shah KR; Um SY; Eng LS; Zhou B; Lin Y; Mitchell AA; Nicaj L; Prinz M; McDonald TV; Sampson BA; Tang Y
Forensic Sci Int; 2014 Apr; 237():90-9. PubMed ID: 24631775
[TBL] [Abstract][Full Text] [Related]
17. Impact of NR5A2 and RYR2 3'UTR polymorphisms on the risk of breast cancer in a Chinese Han population.
Wei Y; Wang X; Zhang Z; Zhao C; Chang Y; Bian Z; Zhao X
Breast Cancer Res Treat; 2020 Aug; 183(1):1-8. PubMed ID: 32572717
[TBL] [Abstract][Full Text] [Related]
18. Cardiac channel molecular autopsy: insights from 173 consecutive cases of autopsy-negative sudden unexplained death referred for postmortem genetic testing.
Tester DJ; Medeiros-Domingo A; Will ML; Haglund CM; Ackerman MJ
Mayo Clin Proc; 2012 Jun; 87(6):524-39. PubMed ID: 22677073
[TBL] [Abstract][Full Text] [Related]
19. Common RyR2 variants associate with ventricular arrhythmias and sudden cardiac death in chronic heart failure.
Ran Y; Chen J; Li N; Zhang W; Feng L; Wang R; Hui R; Zhang S; Pu J
Clin Sci (Lond); 2010 Jun; 119(5):215-23. PubMed ID: 20408814
[TBL] [Abstract][Full Text] [Related]
20. Postmortem molecular screening for cardiac ryanodine receptor type 2 mutations in sudden unexplained death: R420W mutated case with characteristics of status thymico-lymphatics.
Nishio H; Iwata M; Suzuki K
Circ J; 2006 Nov; 70(11):1402-6. PubMed ID: 17062961
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
