Martin Tristani-Firouzi
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hERG potassium channels and cardiac arrhythmia
MC Sanguinetti, M Tristani-Firouzi
Nature 440 (7083), 463-469, 2006
Mutations in Kir2. 1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome
NM Plaster, R Tawil, M Tristani-Firouzi, S Canún, S Bendahhou, ...
Cell 105 (4), 511-519, 2001
Mutations in the hminK gene cause long QT syndrome and suppress lKs function
I Splawski, M Tristani-Firouzi, MH Lehmann, MC Sanguinetti, MT Keating
Nature genetics 17 (3), 338-340, 1997
Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)
M Tristani-Firouzi, JL Jensen, MR Donaldson, V Sansone, G Meola, ...
The Journal of clinical investigation 110 (3), 381-388, 2002
Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands
SC Jin, J Homsy, S Zaidi, Q Lu, S Morton, SR DePalma, X Zeng, H Qi, ...
Nature genetics 49 (11), 1593-1601, 2017
An Fgf8 mouse mutant phenocopies human 22q11 deletion syndrome
DU Frank, LK Fotheringham, JA Brewer, LJ Muglia, M Tristani-Firouzi, ...
Oxford University Press for The Company of Biologists Limited 129 (19), 4591 …, 2002
The primary periodic paralyses: diagnosis, pathogenesis and treatment
SL Venance, SC Cannon, D Fialho, B Fontaine, MG Hanna, LJ Ptacek, ...
Brain 129 (1), 8-17, 2006
Electrocardiographic Features in Andersen-Tawil Syndrome Patients With KCNJ2 Mutations: Characteristic T-U–Wave Patterns Predict the KCNJ2 Genotype
L Zhang, DW Benson, M Tristani-Firouzi, LJ Ptacek, R Tawil, PJ Schwartz, ...
Circulation 111 (21), 2720-2726, 2005
Genetic and physiologic dissection of the vertebrate cardiac conduction system
NC Chi, RM Shaw, B Jungblut, J Huisken, T Ferrer, R Arnaout, I Scott, ...
PLoS biology 6 (5), e109, 2008
Zebrafish model for human long QT syndrome
R Arnaout, T Ferrer, J Huisken, K Spitzer, DYR Stainier, M Tristani-Firouzi, ...
Proceedings of the National Academy of Sciences 104 (27), 11316-11321, 2007
PIP2 binding residues of Kir2. 1 are common targets of mutations causing Andersen syndrome
MR Donaldson, JL Jensen, M Tristani–Firouzi, R Tawil, S Bendahhou, ...
Neurology 60 (11), 1811-1816, 2003
Defective potassium channel Kir2. 1 trafficking underlies Andersen-Tawil syndrome
S Bendahhou, MR Donaldson, NM Plaster, M Tristani-Firouzi, YH Fu, ...
Journal of Biological Chemistry 278 (51), 51779-51785, 2003
Voltage‐dependent inactivation of the human K+ channel KvLQT1 is eliminated by association with minimal K+ channel (minK) subunits
M Tristani‐Firouzi, MC Sanguinetti
The Journal of physiology 510 (1), 37-45, 1998
Interactions between S4-S5 linker and S6 transmembrane domain modulate gating of HERG K+ channels
M Tristani-Firouzi, J Chen, MC Sanguinetti
Journal of Biological Chemistry 277 (21), 18994-19000, 2002
A new oral therapy for long QT syndrome: Long-term oral potassium improves repolarization in patients with HERGmutations
SP Etheridge, SJ Compton, M Tristani-Firouzi, JW Mason
Journal of the American College of Cardiology 42 (10), 1777-1782, 2003
The S4–S5 linker couples voltage sensing and activation of pacemaker channels
J Chen, JS Mitcheson, M Tristani-Firouzi, M Lin, MC Sanguinetti
Proceedings of the National Academy of Sciences 98 (20), 11277-11282, 2001
Structural determinants of HERG channel block by clofilium and ibutilide
M Perry, MJ de Groot, R Helliwell, D Leishman, M Tristani-Firouzi, ...
Molecular pharmacology 66 (2), 240-249, 2004
Molecular biology of K+ channels and their role in cardiac arrhythmias
M Tristani-Firouzi, J Chen, JS Mitcheson, MC Sanguinetti
The American journal of medicine 110 (1), 50-59, 2001
Oxygen-induced constriction of rabbit ductus arteriosus occurs via inhibition of a 4-aminopyridine-, voltage-sensitive potassium channel.
M Tristani-Firouzi, HL Reeve, S Tolarova, EK Weir, SL Archer
The Journal of clinical investigation 98 (9), 1959-1965, 1996
The molecular basis of chloroquine block of the inward rectifier Kir2. 1 channel
AA Rodríguez-Menchaca, RA Navarro-Polanco, T Ferrer-Villada, J Rupp, ...
Proceedings of the National Academy of Sciences 105 (4), 1364-1368, 2008
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