Sanguinetti MC - Search Results

1

Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism.

Splawski I, Timothy KW, Sharpe LM, Decher N, Kumar P, Bloise R, Napolitano C, Schwartz PJ, Joseph RM, Condouris K, Tager-Flusberg H, Priori SG, Sanguinetti MC, Keating MT. Splawski I, et al. Among authors: sanguinetti mc. Cell. 2004 Oct 1;119(1):19-31. doi: 10.1016/j.cell.2004.09.011. Cell. 2004. PMID: 15454078 Free article.

2

Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations.

Splawski I, Timothy KW, Decher N, Kumar P, Sachse FB, Beggs AH, Sanguinetti MC, Keating MT. Splawski I, et al. Among authors: sanguinetti mc. Proc Natl Acad Sci U S A. 2005 Jun 7;102(23):8089-96; discussion 8086-8. doi: 10.1073/pnas.0502506102. Epub 2005 Apr 29. Proc Natl Acad Sci U S A. 2005. PMID: 15863612 Free PMC article.

3

Molecular and cellular mechanisms of cardiac arrhythmias.

Keating MT, Sanguinetti MC. Keating MT, et al. Among authors: sanguinetti mc. Cell. 2001 Feb 23;104(4):569-80. doi: 10.1016/s0092-8674(01)00243-4. Cell. 2001. PMID: 11239413 Free article. Review. No abstract available.

4

Molecular genetic insights into cardiovascular disease.

Keating MT, Sanguinetti MC. Keating MT, et al. Among authors: sanguinetti mc. Science. 1996 May 3;272(5262):681-5. doi: 10.1126/science.272.5262.681. Science. 1996. PMID: 8614827 Review.

5

Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia.

Sanguinetti MC, Curran ME, Spector PS, Keating MT. Sanguinetti MC, et al. Proc Natl Acad Sci U S A. 1996 Mar 5;93(5):2208-12. doi: 10.1073/pnas.93.5.2208. Proc Natl Acad Sci U S A. 1996. PMID: 8700910 Free PMC article.

6

Pathophysiology of ion channel mutations.

Keating MT, Sanguinetti MC. Keating MT, et al. Among authors: sanguinetti mc. Curr Opin Genet Dev. 1996 Jun;6(3):326-33. doi: 10.1016/s0959-437x(96)80010-4. Curr Opin Genet Dev. 1996. PMID: 8791523 Review.

7

A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel.

Sanguinetti MC, Jiang C, Curran ME, Keating MT. Sanguinetti MC, et al. Cell. 1995 Apr 21;81(2):299-307. doi: 10.1016/0092-8674(95)90340-2. Cell. 1995. PMID: 7736582 Free article.

8

Long QT syndrome-associated mutations in the Per-Arnt-Sim (PAS) domain of HERG potassium channels accelerate channel deactivation.

Chen J, Zou A, Splawski I, Keating MT, Sanguinetti MC. Chen J, et al. Among authors: sanguinetti mc. J Biol Chem. 1999 Apr 9;274(15):10113-8. doi: 10.1074/jbc.274.15.10113. J Biol Chem. 1999. PMID: 10187793 Free article.

9

Long-QT syndrome-associated missense mutations in the pore helix of the HERG potassium channel.

Huang FD, Chen J, Lin M, Keating MT, Sanguinetti MC. Huang FD, et al. Among authors: sanguinetti mc. Circulation. 2001 Aug 28;104(9):1071-5. doi: 10.1161/hc3501.093815. Circulation. 2001. PMID: 11524404

10

Long QT syndrome-associated mutations in the S4-S5 linker of KvLQT1 potassium channels modify gating and interaction with minK subunits.

Franqueza L, Lin M, Shen J, Splawski I, Keating MT, Sanguinetti MC. Franqueza L, et al. Among authors: sanguinetti mc. J Biol Chem. 1999 Jul 23;274(30):21063-70. doi: 10.1074/jbc.274.30.21063. J Biol Chem. 1999. PMID: 10409658 Free article.

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