Tristani-Firouzi M - Search Results

1

hERG potassium channels and cardiac arrhythmia.

Sanguinetti MC, Tristani-Firouzi M. Sanguinetti MC, et al. Nature. 2006 Mar 23;440(7083):463-9. doi: 10.1038/nature04710. Nature. 2006. PMID: 16554806 Review.

2

Contribution of Previously Unrecognized RNA Splice-Altering Variants to Congenital Heart Disease.

Jang MY, Patel PN, Pereira AC, Willcox JAL, Haghighi A, Tai AC, Ito K, Morton SU, Gorham JM, McKean DM, DePalma SR, Bernstein D, Brueckner M, Chung WK, Giardini A, Goldmuntz E, Kaltman JR, Kim R, Newburger JW, Shen Y, Srivastava D, Tristani-Firouzi M, Gelb BD, Porter GA Jr, Seidman CE, Seidman JG. Jang MY, et al. Among authors: tristani firouzi m. Circ Genom Precis Med. 2023 Jun;16(3):224-231. doi: 10.1161/CIRCGEN.122.003924. Epub 2023 May 11. Circ Genom Precis Med. 2023. PMID: 37165897 Free PMC article.

3

Mutations in the hminK gene cause long QT syndrome and suppress IKs function.

Splawski I, Tristani-Firouzi M, Lehmann MH, Sanguinetti MC, Keating MT. Splawski I, et al. Nat Genet. 1997 Nov;17(3):338-40. doi: 10.1038/ng1197-338. Nat Genet. 1997. PMID: 9354802

4

Voltage-dependent inactivation of the human K+ channel KvLQT1 is eliminated by association with minimal K+ channel (minK) subunits.

Tristani-Firouzi M, Sanguinetti MC. Tristani-Firouzi M, et al. J Physiol. 1998 Jul 1;510 ( Pt 1)(Pt 1):37-45. doi: 10.1111/j.1469-7793.1998.037bz.x. J Physiol. 1998. PMID: 9625865 Free PMC article.

5

Functional effects of mutations in KvLQT1 that cause long QT syndrome.

Wang Z, Tristani-Firouzi M, Xu Q, Lin M, Keating MT, Sanguinetti MC. Wang Z, et al. J Cardiovasc Electrophysiol. 1999 Jun;10(6):817-26. doi: 10.1111/j.1540-8167.1999.tb00262.x. J Cardiovasc Electrophysiol. 1999. PMID: 10376919

6

Molecular biology of K(+) channels and their role in cardiac arrhythmias.

Tristani-Firouzi M, Chen J, Mitcheson JS, Sanguinetti MC. Tristani-Firouzi M, et al. Am J Med. 2001 Jan;110(1):50-9. doi: 10.1016/s0002-9343(00)00623-9. Am J Med. 2001. PMID: 11152866 Review.

7

The S4-S5 linker couples voltage sensing and activation of pacemaker channels.

Chen J, Mitcheson JS, Tristani-Firouzi M, Lin M, Sanguinetti MC. Chen J, et al. Proc Natl Acad Sci U S A. 2001 Sep 25;98(20):11277-82. doi: 10.1073/pnas.201250598. Epub 2001 Sep 11. Proc Natl Acad Sci U S A. 2001. PMID: 11553787 Free PMC article.

8

Interactions between S4-S5 linker and S6 transmembrane domain modulate gating of HERG K+ channels.

Tristani-Firouzi M, Chen J, Sanguinetti MC. Tristani-Firouzi M, et al. J Biol Chem. 2002 May 24;277(21):18994-9000. doi: 10.1074/jbc.M200410200. Epub 2002 Feb 25. J Biol Chem. 2002. PMID: 11864984 Free article.

9

Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome).

Tristani-Firouzi M, Jensen JL, Donaldson MR, Sansone V, Meola G, Hahn A, Bendahhou S, Kwiecinski H, Fidzianska A, Plaster N, Fu YH, Ptacek LJ, Tawil R. Tristani-Firouzi M, et al. J Clin Invest. 2002 Aug;110(3):381-8. doi: 10.1172/JCI15183. J Clin Invest. 2002. PMID: 12163457 Free PMC article.

10

Structural determinants and biophysical properties of HERG and KCNQ1 channel gating.

Tristani-Firouzi M, Sanguinetti MC. Tristani-Firouzi M, et al. J Mol Cell Cardiol. 2003 Jan;35(1):27-35. doi: 10.1016/s0022-2828(02)00286-9. J Mol Cell Cardiol. 2003. PMID: 12623297 Review.

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