R Mohammad-Panah
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Explore the profile of R Mohammad-Panah including associated specialties, affiliations and a list of published articles.
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Recent Articles
1.
Riochet D, Mohammad-Panah R, Hebert S, MacGregor G, Baro I, Guihard G, et al.
Biochem Biophys Res Commun
. 2001 Aug;
286(2):376-80.
PMID: 11500048
Biophysical properties of ROMK2 channel were investigated at physiological temperature, after reexpression of the recombinant ROMK2 protein in a mammalian cell expression system (COS-7). We observed that ROMK2 induced an...
2.
POTET F, Scott J, Mohammad-Panah R, Escande D, Baro I
Am J Physiol Heart Circ Physiol
. 2001 Apr;
280(5):H2038-45.
PMID: 11299204
In cardiac myocytes, the slow component of the delayed rectifier K(+) current (I(Ks)) is regulated by cAMP. Elevated cAMP increases I(Ks) amplitude, slows its deactivation kinetics, and shifts its activation...
3.
Mohammad-Panah R, Gyomorey K, Rommens J, Choudhury M, Li C, Wang Y, et al.
J Biol Chem
. 2000 Nov;
276(11):8306-13.
PMID: 11096079
It has been previously determined that ClC-2, a member of the ClC chloride channel superfamily, is expressed in certain epithelial tissues. These findings fueled speculation that ClC-2 can compensate for...
4.
Mohammad-Panah R, Demolombe S, Neyroud N, Guicheney P, Kyndt F, van den Hoff M, et al.
Am J Hum Genet
. 1999 Mar;
64(4):1015-23.
PMID: 10090886
The long QT syndrome is characterized by prolonged cardiac repolarization and a high risk of sudden death. Mutations in the KCNQ1 gene, which encodes the cardiac KvLQT1 potassium ion (K+)...
5.
Demolombe S, Baro I, Pereon Y, Bliek J, Mohammad-Panah R, Pollard H, et al.
J Biol Chem
. 1998 Apr;
273(12):6837-43.
PMID: 9506986
Mutations in the KvLQT1 gene are the cause of the long QT syndrome 1. KvLQT1 gene product is associated with the regulator protein IsK to produce a component of the...
6.
Mohammad-Panah R, Demolombe S, Riochet D, Leblais V, Loussouarn G, Pollard H, et al.
Am J Physiol
. 1998 Mar;
274(2):C310-8.
PMID: 9486119
We investigated whether high levels of expression of the cystic fibrosis transmembrane conductance regulator (CFTR) would alter the functional properties of newly synthesized recombinant proteins. COS-7, CFPAC-1, and A549 cells...
7.
Loussouarn G, Charpentier F, Mohammad-Panah R, Kunzelmann K, Baro I, Escande D
Mol Pharmacol
. 1997 Dec;
52(6):1131-6.
PMID: 9396783
Mutations in the KvLQT1 gene are the cause for the long QT syndrome [Circulation 94:1996-2012 (1996)]. Coexpression of KvLQT1 in association with the channel regulator protein IsK produces a K+...
8.
Loussouarn G, Demolombe S, Mohammad-Panah R, Escande D, Baro I
Am J Physiol
. 1996 Nov;
271(5 Pt 1):C1565-73.
PMID: 8944640
The perforated-patch configuration of the patch-clamp technique was used to record whole cell currents from human epithelial CFPAC-1 cells defective for functional cystic fibrosis transmembrane conductance regulator (CFTR). In CFPAC-1...