Présentation
Responsable valorisation IPMC
Experte senior en transfert de technologies à la Direction Scientifique de CNRS Innovation
Déléguée Scientifique auprès de la Direction Générale Déléguée à l’Innovation du CNRS
Publications
2019
TMEM33 regulates intracellular calcium homeostasis in renal tubular epithelial cells.,
Nat Commun 2019 May; 10(1): 2024.
2016
Piezo1-dependent regulation of urinary osmolarity.,
Pflugers Arch 2016 Jul; 468(7): 1197-1206.
2016
Smooth muscle filamin A is a major determinant of conduit artery structure and function at the adult stage.,
Pflugers Arch 2016 Jul; 468(7): 1151-1160.
2016
Arterial Myogenic Activation through Smooth Muscle Filamin A.,
Cell Rep 2016 Mar; 14(9): 2050-2058.
2015
Piezo1 in Smooth Muscle Cells Is Involved in Hypertension-Dependent Arterial Remodeling.,
Cell Rep 2015 Nov; 13(6): 1161-1171.
2015
An alternative to force.,
Elife 2015 Jun; 4(): .
2014
Regional ion channel gene expression heterogeneity and ventricular fibrillation dynamics in human hearts.,
PLoS One 2014 ; 9(1): e82179.
2013
Piezo1-dependent stretch-activated channels are inhibited by Polycystin-2 in renal tubular epithelial cells.,
EMBO Rep 2013 Dec; 14(12): 1143-8.
2013
Slower Piezo1 inactivation in dehydrated hereditary stomatocytosis (xerocytosis).,
Biophys J 2013 Aug; 105(4): 833-4.
2012
Circadian rhythms govern cardiac repolarization and arrhythmogenesis.,
Nature 2012 Feb; 483(7387): 96-9.
2011
Early ion-channel remodeling and arrhythmias precede hypertrophy in a mouse model of complete atrioventricular block.,
J Mol Cell Cardiol 2011 Nov; 51(5): 713-21.
2010
Gender-related differences in ion-channel and transporter subunit expression in non-diseased human hearts.,
J Mol Cell Cardiol 2010 Oct; 49(4): 639-46.
2010
Gender disparity in cardiac electrophysiology: implications for cardiac safety pharmacology.,
Pharmacol Ther 2010 Jul; 127(1): 9-18.
2010
Variable Na(v)1.5 protein expression from the wild-type allele correlates with the penetrance of cardiac conduction disease in the Scn5a(+/-) mouse model.,
PLoS One 2010 Feb; 5(2): e9298.
2010
Ion-channel mRNA-expression profiling: Insights into cardiac remodeling and arrhythmic substrates.,
J Mol Cell Cardiol 2010 Jan; 48(1): 96-105.
2009
Transfer of rolf S3-S4 linker to HERG eliminates activation gating but spares inactivation.,
Biophys J 2009 Sep; 97(5): 1323-34.
2009
Haplotype-sharing analysis implicates chromosome 7q36 harboring DPP6 in familial idiopathic ventricular fibrillation.,
Am J Hum Genet 2009 Apr; 84(4): 468-76.
2009
Molecular and functional characterization of a new potassium conductance in mouse ventricular fibroblasts.,
J Mol Cell Cardiol 2009 Apr; 46(4): 508-17.
2009
Transcriptional profiling of ion channel genes in Brugada syndrome and other right ventricular arrhythmogenic diseases.,
Eur Heart J 2009 Feb; 30(4): 487-96.
2008
Marked differences between atrial and ventricular gene-expression remodeling in dogs with experimental heart failure.,
J Mol Cell Cardiol 2008 Dec; 45(6): 821-31.
2008
Dysfunction in ankyrin-B-dependent ion channel and transporter targeting causes human sinus node disease.,
Proc Natl Acad Sci U S A 2008 Oct; 105(40): 15617-22.
2008
Distinct cellular and molecular mechanisms underlie functional remodeling of repolarizing K+ currents with left ventricular hypertrophy.,
Circ Res 2008 Jun; 102(11): 1406-15.
2008
Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans.,
J Clin Invest 2008 Jun; 118(6): 2260-8.
2007
Regional and tissue specific transcript signatures of ion channel genes in the non-diseased human heart.,
J Physiol 2007 Jul; 582(Pt 2): 675-93.
2007
Contrasting gene expression profiles in two canine models of atrial fibrillation.,
Circ Res 2007 Feb; 100(3): 425-33.
2006
Gene expression profile associated with chronic atrial fibrillation and underlying valvular heart disease in man.,
J Mol Cell Cardiol 2006 Jan; 40(1): 173-84.
2005
Chronic heart rate reduction remodels ion channel transcripts in the mouse sinoatrial node but not in the ventricle.,
Physiol Genomics 2005 Dec; 24(1): 4-12.
2005
Targeted deletion of Kv4.2 eliminates I(to,f) and results in electrical and molecular remodeling, with no evidence of ventricular hypertrophy or myocardial dysfunction.,
Circ Res 2005 Dec; 97(12): 1342-50.
2005
In vitro molecular interactions and distribution of KCNE family with KCNQ1 in the human heart.,
Cardiovasc Res 2005 Aug; 67(3): 529-38.
2005
Functional genomics of cardiac ion channel genes.,
Cardiovasc Res 2005 Aug; 67(3): 438-47.
2005
Lonesome Kv4.2 channels.,
J Mol Cell Cardiol 2005 Aug; 39(2): 401-2.
2005
Human atrial ion channel and transporter subunit gene-expression remodeling associated with valvular heart disease and atrial fibrillation.,
Circulation 2005 Jul; 112(4): 471-81.
2005
Conditional mineralocorticoid receptor expression in the heart leads to life-threatening arrhythmias.,
Circulation 2005 Jun; 111(23): 3025-33.
2005
Mouse model of SCN5A-linked hereditary Lenègre’s disease: age-related conduction slowing and myocardial fibrosis.,
Circulation 2005 Apr; 111(14): 1738-46.
2005
Expression of human ERG K+ channels in the mouse heart exerts anti-arrhythmic activity.,
Cardiovasc Res 2005 Jan; 65(1): 128-37.
2005
Specific pattern of ionic channel gene expression associated with pacemaker activity in the mouse heart.,
J Physiol 2005 Jan; 562(Pt 1): 223-34.
2004
DNA chip technology in cardiovascular research.,
Arch Mal Coeur Vaiss 2004 Dec; 97(12): 1251-5.
2004
Long-term amiodarone administration remodels expression of ion channel transcripts in the mouse heart.,
Circulation 2004 Nov; 110(19): 3028-35.
2004
New KCNQ1 mutations leading to haploinsufficiency in a general population; Defective trafficking of a KvLQT1 mutant.,
Cardiovasc Res 2004 Jul; 63(1): 60-8.
2004
Cardiac channelopathies: from men to mice.,
Ann Med 2004 ; 36 Suppl 1(): 28-34.
2003
Na+ channel mutation leading to loss of function and non-progressive cardiac conduction defects.,
J Mol Cell Cardiol 2003 May; 35(5): 549-57.
2003
Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease.,
J Am Coll Cardiol 2003 Feb; 41(4): 643-52.
2003
Microarray analysis reveals complex remodeling of cardiac ion channel expression with altered thyroid status: relation to cellular and integrated electrophysiology.,
Circ Res 2003 Feb; 92(2): 234-42.
2003
Paramyotonia congenita with an SCN4A mutation affecting cardiac repolarization.,
Neurology 2003 Jan; 60(2): 340-2.
2001
Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family.,
Circulation 2001 Dec; 104(25): 3081-6.
2001
Divergent expression of delayed rectifier K(+) channel subunits during mouse heart development.,
Cardiovasc Res 2001 Oct; 52(1): 65-75.
2001
Transgenic mice overexpressing human KvLQT1 dominant-negative isoform. Part I: Phenotypic characterisation.,
Cardiovasc Res 2001 May; 50(2): 314-27.
2001
Transgenic mice overexpressing human KvLQT1 dominant-negative isoform. Part II: Pharmacological profile.,
Cardiovasc Res 2001 May; 50(2): 328-34.
2001
Differential expression of KvLQT1 and its regulator IsK in mouse epithelia.,
Am J Physiol Cell Physiol 2001 Feb; 280(2): C359-72.
2000
Differential expression of KvLQT1 isoforms across the human ventricular wall.,
Am J Physiol Heart Circ Physiol 2000 Jun; 278(6): H1908-15.
1999
Mutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmias.,
Am J Hum Genet 1999 Apr; 64(4): 1015-23.
1999
beta3-adrenoceptor control the cystic fibrosis transmembrane conductance regulator through a cAMP/protein kinase A-independent pathway.,
J Biol Chem 1999 Mar; 274(10): 6107-13.
1998
Cystic fibrosis transmembrane conductance regulator (CFTR) nucleotide-binding domain 1 (NBD-1) and CFTR truncated within NBD-1 target to the epithelial plasma membrane and increase anion permeability.,
Biochemistry 1998 Oct; 37(43): 15222-30.
1998
Targeting of CFTR protein is linked to the polarization of human pancreatic duct cells in culture.,
Eur J Cell Biol 1998 Jul; 76(3): 220-7.
1998
Polyethylenimine but not cationic lipids promotes transgene delivery to the nucleus in mammalian cells.,
J Biol Chem 1998 Mar; 273(13): 7507-11.
1998
A dominant negative isoform of the long QT syndrome 1 gene product.,
J Biol Chem 1998 Mar; 273(12): 6837-43.
1998
Hyperexpression of recombinant CFTR in heterologous cells alters its physiological properties.,
Am J Physiol 1998 Feb; 274(2): C310-8.
1996
Expression of CFTR controls cAMP-dependent activation of epithelial K+ currents.,
Am J Physiol 1996 Nov; 271(5 Pt 1): C1565-73.
1996
ATP-binding cassette proteins as targets for drug discovery.,
Trends Pharmacol Sci 1996 Aug; 17(8): 273-5.
1996
A method for the rapid detection of recombinant CFTR during gene therapy in cystic fibrosis.,
Gene Ther 1996 Aug; 3(8): 685-94.
1996
Adenosine A1 stimulation activates delta-protein kinase C in rat ventricular myocytes.,
Circ Res 1996 Jan; 78(1): 161-5.
1994
Abnormal subcellular localization of mutated CFTR protein in a cystic fibrosis epithelial cell line.,
Eur J Cell Biol 1994 Oct; 65(1): 214-9.
1991
Ifosfamide continuous infusion plus etoposide in the treatment of elderly patients with aggressive lymphoma: a phase II study.,
Hematol Oncol 1991 ; 9(4-5): 225-33.
