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Results: 1 to 20 of 57

1.

Arrhythmogenesis in a catecholaminergic polymorphic ventricular tachycardia mutation that depresses ryanodine receptor function.

Zhao YT, Valdivia CR, Gurrola GB, Powers PP, Willis BC, Moss RL, Jalife J, Valdivia HH.

Proc Natl Acad Sci U S A. 2015 Mar 31;112(13):E1669-77. doi: 10.1073/pnas.1419795112. Epub 2015 Mar 16.

2.

The mechanism of flecainide action in CPVT does not involve a direct effect on RyR2.

Bannister ML, Thomas NL, Sikkel MB, Mukherjee S, Maxwell C, MacLeod KT, George CH, Williams AJ.

Circ Res. 2015 Apr 10;116(8):1324-35. doi: 10.1161/CIRCRESAHA.116.305347. Epub 2015 Feb 3.

PMID:
25648700
3.

Dysfunction in the βII spectrin-dependent cytoskeleton underlies human arrhythmia.

Smith SA, Sturm AC, Curran J, Kline CF, Little SC, Bonilla IM, Long VP, Makara M, Polina I, Hughes LD, Webb TR, Wei Z, Wright P, Voigt N, Bhakta D, Spoonamore KG, Zhang C, Weiss R, Binkley PF, Janssen PM, Kilic A, Higgins RS, Sun M, Ma J, Dobrev D, Zhang M, Carnes CA, Vatta M, Rasband MN, Hund TJ, Mohler PJ.

Circulation. 2015 Feb 24;131(8):695-708. doi: 10.1161/CIRCULATIONAHA.114.013708. Epub 2015 Jan 28.

PMID:
25632041
4.

Role of Cys³⁶⁰² in the function and regulation of the cardiac ryanodine receptor.

Mi T, Xiao Z, Guo W, Tang Y, Hiess F, Xiao J, Wang Y, Zhang JZ, Zhang L, Wang R, Jones PP, Chen SR.

Biochem J. 2015 Apr 1;467(1):177-90. doi: 10.1042/BJ20141263.

PMID:
25605235
5.

Loss of microRNA-106b-25 cluster promotes atrial fibrillation by enhancing ryanodine receptor type-2 expression and calcium release.

Chiang DY, Kongchan N, Beavers DL, Alsina KM, Voigt N, Neilson JR, Jakob H, Martin JF, Dobrev D, Wehrens XH, Li N.

Circ Arrhythm Electrophysiol. 2014 Dec;7(6):1214-22. doi: 10.1161/CIRCEP.114.001973. Epub 2014 Nov 11.

PMID:
25389315
6.

De novo mutations in moderate or severe intellectual disability.

Hamdan FF, Srour M, Capo-Chichi JM, Daoud H, Nassif C, Patry L, Massicotte C, Ambalavanan A, Spiegelman D, Diallo O, Henrion E, Dionne-Laporte A, Fougerat A, Pshezhetsky AV, Venkateswaran S, Rouleau GA, Michaud JL.

PLoS Genet. 2014 Oct 30;10(10):e1004772. doi: 10.1371/journal.pgen.1004772. eCollection 2014 Oct.

7.

Hypoxia adaptations in the grey wolf (Canis lupus chanco) from Qinghai-Tibet Plateau.

Zhang W, Fan Z, Han E, Hou R, Zhang L, Galaverni M, Huang J, Liu H, Silva P, Li P, Pollinger JP, Du L, Zhang X, Yue B, Wayne RK, Zhang Z.

PLoS Genet. 2014 Jul 31;10(7):e1004466. doi: 10.1371/journal.pgen.1004466. eCollection 2014 Jul.

8.

Gene expression profiles of patients with cerebral hematoma following spontaneous intracerebral hemorrhage.

Yang T, Gu J, Kong B, Kuang Y, Cheng L, Cheng J, Xia X, Ma Y, Zhang J.

Mol Med Rep. 2014 Oct;10(4):1671-8. doi: 10.3892/mmr.2014.2421. Epub 2014 Jul 25.

9.

Altered RyR2 regulation by the calmodulin F90L mutation associated with idiopathic ventricular fibrillation and early sudden cardiac death.

Nomikos M, Thanassoulas A, Beck K, Vassilakopoulou V, Hu H, Calver BL, Theodoridou M, Kashir J, Blayney L, Livaniou E, Rizkallah P, Nounesis G, Lai FA.

FEBS Lett. 2014 Aug 25;588(17):2898-902. doi: 10.1016/j.febslet.2014.07.007. Epub 2014 Jul 15.

PMID:
25036739
10.

RYR2 sequencing reveals novel missense mutations in a Kazakh idiopathic ventricular tachycardia study cohort.

Akilzhanova A, Guelly C, Nuralinov O, Nurkina Z, Nazhat D, Smagulov S, Tursunbekov A, Alzhanova A, Rashbayeva G, Abdrakhmanov A, Dosmagambet S, Trajanoski S, Zhumadilov Z, Sharman A, Bekbosynova M.

PLoS One. 2014 Jun 30;9(6):e101059. doi: 10.1371/journal.pone.0101059. eCollection 2014.

11.

The arrhythmogenic human HRC point mutation S96A leads to spontaneous Ca(2+) release due to an impaired ability to buffer store Ca(2+).

Zhang JZ, McLay JC, Jones PP.

J Mol Cell Cardiol. 2014 Sep;74:22-31. doi: 10.1016/j.yjmcc.2014.04.019. Epub 2014 May 5.

PMID:
24805197
12.

A novel RyR2 mutation in a 2-year-old baby presenting with atrial fibrillation, atrial flutter, and atrial ectopic tachycardia.

Di Pino A, Caruso E, Costanzo L, Guccione P.

Heart Rhythm. 2014 Aug;11(8):1480-3. doi: 10.1016/j.hrthm.2014.04.037. Epub 2014 May 2. No abstract available.

PMID:
24793461
13.

Nonuniform and variable arrangements of ryanodine receptors within mammalian ventricular couplons.

Asghari P, Scriven DR, Sanatani S, Gandhi SK, Campbell AI, Moore ED.

Circ Res. 2014 Jul 7;115(2):252-62. doi: 10.1161/CIRCRESAHA.115.303897. Epub 2014 Apr 30.

PMID:
24786399
14.

Are RYR2 exon-3 deletions truly causative for non-compaction?

Finsterer J, Stöllberger C.

Europace. 2014 Dec;16(12):1864. doi: 10.1093/europace/euu027. Epub 2014 Apr 12. No abstract available.

PMID:
24728420
15.

Genetic basis of atrial fibrillation.

Hong K, Xiong Q.

Curr Opin Cardiol. 2014 May;29(3):220-6. doi: 10.1097/HCO.0000000000000051. Review.

PMID:
24614860
16.

Crystal structure and conformational flexibility of the unligated FK506-binding protein FKBP12.6.

Chen H, Mustafi SM, LeMaster DM, Li Z, Héroux A, Li H, Hernández G.

Acta Crystallogr D Biol Crystallogr. 2014 Mar;70(Pt 3):636-46. doi: 10.1107/S1399004713032112. Epub 2014 Feb 15.

17.

Characterisation of connexin expression and electrophysiological properties in stable clones of the HL-1 myocyte cell line.

Dias P, Desplantez T, El-Harasis MA, Chowdhury RA, Ullrich ND, Cabestrero de Diego A, Peters NS, Severs NJ, MacLeod KT, Dupont E.

PLoS One. 2014 Feb 28;9(2):e90266. doi: 10.1371/journal.pone.0090266. eCollection 2014.

18.

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. doi: 10.1016/j.forsciint.2013.12.007. Epub 2013 Dec 16.

PMID:
24447446
19.

Lobe-specific calmodulin binding to different ryanodine receptor isoforms.

Lau K, Chan MM, Van Petegem F.

Biochemistry. 2014 Feb 11;53(5):932-46. doi: 10.1021/bi401502x. Epub 2014 Jan 30.

PMID:
24447242
20.

The ryanodine receptor store-sensing gate controls Ca2+ waves and Ca2+-triggered arrhythmias.

Chen W, Wang R, Chen B, Zhong X, Kong H, Bai Y, Zhou Q, Xie C, Zhang J, Guo A, Tian X, Jones PP, O'Mara ML, Liu Y, Mi T, Zhang L, Bolstad J, Semeniuk L, Cheng H, Zhang J, Chen J, Tieleman DP, Gillis AM, Duff HJ, Fill M, Song LS, Chen SR.

Nat Med. 2014 Feb;20(2):184-92. doi: 10.1038/nm.3440. Epub 2014 Jan 19.

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