N. Gaborit

发表

Regional and tissue specific transcript signatures of ion channel genes in the non‐diseased human heart

Stanley Nattel, Denis Escande, Andras Varro, 2007, The Journal of physiology.

Human model of IRX5 mutations reveals key role for this transcription factor in ventricular conduction.

H. Kayserili, Céline Marionneau, F. Charpentier, 2020, Cardiovascular research.

Deciphering Transcriptional Networks during Human Cardiac Development

R. Redon, J. Poschmann, P. Lemarchand, 2022, bioRxiv.

Mental stress test: a rapid, simple, and efficient test to unmask long QT syndrome

R. Redon, F. Charpentier, V. Probst, 2018, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Generation of human induced pluripotent stem cell lines from two patients affected by catecholamine-induced QT prolongation (CIQTP).

R. Redon, V. Probst, P. Lemarchand, 2021, Stem cell research.

RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome.

R. Redon, E. Génin, C. Dina, 2018, European heart journal.

FACS-assisted CRISPR-Cas9 genome editing of human induced pluripotent stem cells

J. Barc, C. Le May, B. Cariou, 2022, STAR protocols.

Gene expression profile associated with chronic atrial fibrillation and underlying valvular heart disease in man.

Nolwenn Le Meur, Stanley Nattel, Marja Steenman, 2006, Journal of molecular and cellular cardiology.

Urine-derived cells provide a readily accessible cell type for feeder-free mRNA reprogramming

C. Chariau, A. Gaignerie, L. Flippe, 2018, Scientific Reports.

Toward Personalized Medicine: Using Cardiomyocytes Differentiated From Urine-Derived Pluripotent Stem Cells to Recapitulate Electrophysiological Characteristics of Type 2 Long QT Syndrome

F. Charpentier, G. Loussouarn, I. Baró, 2015, Journal of the American Heart Association.

In vitro differentiation of W8B2+ human cardiac stem cells: gene expression of ionic channels and spontaneous calcium activity

C. Jayle, P. Bois, J. Faivre, 2020, Cellular & Molecular Biology Letters.

Generation of human induced pluripotent stem cell lines from four unrelated healthy control donors carrying European genetic background

R. Redon, F. Charpentier, V. Probst, 2021, Stem Cell Research.

Generation of three human induced pluripotent stem cell lines with IRX5 knockout and knockin genetic editions using CRISPR-Cas9 system.

C. Bonnard, J. Poschmann, P. Lemarchand, 2021, Stem cell research.

HIV-Tat induces a decrease in IKr and IKsvia reduction in phosphatidylinositol-(4,5)-bisphosphate availability.

Bruno Beaumelle, Isabelle Baró, Gildas Loussouarn, 2016, Journal of molecular and cellular cardiology.

Cooperative and antagonistic roles for Irx3 and Irx5 in cardiac morphogenesis and postnatal physiology

B. Bruneau, Kyoung-Han Kim, C. Hui, 2012, Development.

Iroquois homeobox gene 3 establishes fast conduction in the cardiac His–Purkinje network

James W. Smyth, B. Bruneau, R. Henkelman, 2011, Proceedings of the National Academy of Sciences.

A consistent arrhythmogenic trait in Brugada syndrome cellular phenotype

R. Redon, F. Charpentier, V. Probst, 2021, Clinical and translational medicine.

OP-EHEA190316_online 3081..3094

R. Redon, C. Dina, Céline Marionneau, 2021 .

Human Atrial Ion Channel and Transporter Subunit Gene-Expression Remodeling Associated With Valvular Heart Disease and Atrial Fibrillation

Nolwenn Le Meur, Stanley Nattel, Marja Steenman, 2005, Circulation.

Loss of Iroquois homeobox transcription factors 3 and 5 in osteoblasts disrupts cranial mineralization

B. Bruneau, E. Hsiao, H. Kayserili, 2016, Bone reports.

Extensive enteric nervous system abnormalities in mice transgenic for artificial chromosomes containing Parkinson disease-associated alpha-synuclein gene mutations precede central nervous system changes.

R. Nussbaum, B. Bruneau, Richard J Smeyne, 2010, Human molecular genetics.

Transcriptional profiling of ion channel genes in Brugada syndrome and other right ventricular arrhythmogenic diseases.

G. Breithardt, L. Eckardt, E. Schulze-Bahr, 2009, European heart journal.

Ion-channel mRNA-expression profiling: Insights into cardiac remodeling and arrhythmic substrates.

S. Nattel, S. Demolombe, N. Gaborit, 2010, Journal of molecular and cellular cardiology.

S. Nattel, V. Szűts, D. Escande, 2010, Journal of molecular and cellular cardiology.

Maurocalcin and its analogue MCaE12A facilitate Ca2+ mobilization in cardiomyocytes.

M. Ronjat, M. De Waard, J. Montnach, 2020, The Biochemical journal.

In vitro differentiation of W8B2+ human cardiac stem cells: gene expression of ionic channels and spontaneous calcium activity

C. Jayle, P. Bois, J. Faivre, 2020, Cellular & molecular biology letters.

The β4 subunit of the voltage-gated calcium channel (Cacnb4) regulates the rate of cell proliferation in Chinese Hamster Ovary cells.

Y. Mori, M. Ronjat, J. Brusés, 2017, The international journal of biochemistry & cell biology.

Regional Ion Channel Gene Expression Heterogeneity and Ventricular Fibrillation Dynamics in Human Hearts

T. Farid, S. Nattel, S. Massé, 2014, PloS one.

S. Nattel, V. Szűts, D. Escande, 2010, Journal of molecular and cellular cardiology.

Iroquois homeobox gene 3 establishes fast conduction in the cardiac His–Purkinje network

James W. Smyth, B. Bruneau, R. Henkelman, 2011, Proceedings of the National Academy of Sciences.

RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome.

R. Redon, E. Génin, C. Dina, 2019, European heart journal.