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Items: 1 to 20 of 24

1.

Myocardial calcium signalling and arrhythmia pathogenesis.

Scoote M, Williams AJ.

Biochem Biophys Res Commun. 2004 Oct 1;322(4):1286-309. Review.

PMID:
15336976
2.

Ryanodine receptor channelopathies.

Benkusky NA, Farrell EF, Valdivia HH.

Biochem Biophys Res Commun. 2004 Oct 1;322(4):1280-5. Review.

PMID:
15336975
3.

Calstabin deficiency, ryanodine receptors, and sudden cardiac death.

Lehnart SE, Wehrens XH, Marks AR.

Biochem Biophys Res Commun. 2004 Oct 1;322(4):1267-79. Review.

PMID:
15336974
4.

RyR2 mutations linked to ventricular tachycardia and sudden death reduce the threshold for store-overload-induced Ca2+ release (SOICR).

Jiang D, Xiao B, Yang D, Wang R, Choi P, Zhang L, Cheng H, Chen SR.

Proc Natl Acad Sci U S A. 2004 Aug 31;101(35):13062-7. Epub 2004 Aug 20.

5.

Sudden death in familial polymorphic ventricular tachycardia associated with calcium release channel (ryanodine receptor) leak.

Lehnart SE, Wehrens XH, Laitinen PJ, Reiken SR, Deng SX, Cheng Z, Landry DW, Kontula K, Swan H, Marks AR.

Circulation. 2004 Jun 29;109(25):3208-14. Epub 2004 Jun 14.

6.

Protection from cardiac arrhythmia through ryanodine receptor-stabilizing protein calstabin2.

Wehrens XH, Lehnart SE, Reiken SR, Deng SX, Vest JA, Cervantes D, Coromilas J, Landry DW, Marks AR.

Science. 2004 Apr 9;304(5668):292-6.

7.
8.

FKBP12.6 deficiency and defective calcium release channel (ryanodine receptor) function linked to exercise-induced sudden cardiac death.

Wehrens XH, Lehnart SE, Huang F, Vest JA, Reiken SR, Mohler PJ, Sun J, Guatimosim S, Song LS, Rosemblit N, D'Armiento JM, Napolitano C, Memmi M, Priori SG, Lederer WJ, Marks AR.

Cell. 2003 Jun 27;113(7):829-40.

9.
10.

The binding of the RyR2 calcium channel to its gating protein FKBP12.6 is oppositely affected by ARVD2 and VTSIP mutations.

Tiso N, Salamon M, Bagattin A, Danieli GA, Argenton F, Bortolussi M.

Biochem Biophys Res Commun. 2002 Dec 13;299(4):594-8.

PMID:
12459180
12.

A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel.

Lahat H, Pras E, Olender T, Avidan N, Ben-Asher E, Man O, Levy-Nissenbaum E, Khoury A, Lorber A, Goldman B, Lancet D, Eldar M.

Am J Hum Genet. 2001 Dec;69(6):1378-84. Epub 2001 Oct 25.

13.

Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia.

Priori SG, Napolitano C, Tiso N, Memmi M, Vignati G, Bloise R, Sorrentino V, Danieli GA.

Circulation. 2001 Jan 16;103(2):196-200.

14.

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2).

Tiso N, Stephan DA, Nava A, Bagattin A, Devaney JM, Stanchi F, Larderet G, Brahmbhatt B, Brown K, Bauce B, Muriago M, Basso C, Thiene G, Danieli GA, Rampazzo A.

Hum Mol Genet. 2001 Feb 1;10(3):189-94.

15.

Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia.

Laitinen PJ, Brown KM, Piippo K, Swan H, Devaney JM, Brahmbhatt B, Donarum EA, Marino M, Tiso N, Viitasalo M, Toivonen L, Stephan DA, Kontula K.

Circulation. 2001 Jan 30;103(4):485-90.

16.

PKA phosphorylation dissociates FKBP12.6 from the calcium release channel (ryanodine receptor): defective regulation in failing hearts.

Marx SO, Reiken S, Hisamatsu Y, Jayaraman T, Burkhoff D, Rosemblit N, Marks AR.

Cell. 2000 May 12;101(4):365-76.

17.

Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts.

Swan H, Piippo K, Viitasalo M, Heikkilä P, Paavonen T, Kainulainen K, Kere J, Keto P, Kontula K, Toivonen L.

J Am Coll Cardiol. 1999 Dec;34(7):2035-42.

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19.

Embryonic lethality and abnormal cardiac myocytes in mice lacking ryanodine receptor type 2.

Takeshima H, Komazaki S, Hirose K, Nishi M, Noda T, Iino M.

EMBO J. 1998 Jun 15;17(12):3309-16.

20.

Chromosome mapping of five human cardiac and skeletal muscle sarcoplasmic reticulum protein genes.

Otsu K, Fujii J, Periasamy M, Difilippantonio M, Uppender M, Ward DC, MacLennan DH.

Genomics. 1993 Aug;17(2):507-9.

PMID:
8406504
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