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TAD boundary deletion causes PITX2-related cardiac electrical and structural defects.
Published in:
Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-47739-x
By:
- Baudic, Manon;
- Murata, Hiroshige;
- Bosada, Fernanda M.;
- Melo, Uirá Souto;
- Aizawa, Takanori;
- Lindenbaum, Pierre;
- van der Maarel, Lieve E.;
- Guedon, Amaury;
- Baron, Estelle;
- Fremy, Enora;
- Foucal, Adrien;
- Ishikawa, Taisuke;
- Ushinohama, Hiroya;
- Jurgens, Sean J.;
- Choi, Seung Hoan;
- Kyndt, Florence;
- Le Scouarnec, Solena;
- Wakker, Vincent;
- Thollet, Aurélie;
- Rajalu, Annabelle
Publication type:
Article
Erosion Effect in the Degradation of Coated and Uncoated Glass Solar Mirrors Highlighted by Coupled Accelerated Erosion/Aging Tests.
Published in:
Coatings (2079-6412), 2022, v. 12, n. 8, p. 1087, doi. 10.3390/coatings12081087
By:
- Lakhouil, Sara;
- Boukheir, Sofia;
- Bouaouine, Hassane;
- Baron, Estelle Le;
- Disdier, Angela;
- Vuillerme, Valery;
- Naamane, Sanae
Publication type:
Article
Multimodality imaging and transcriptomics to phenotype mitral valve dystrophy in a unique knock-in Filamin-A rat model.
Published in:
Cardiovascular Research, 2023, v. 119, n. 3, p. 759, doi. 10.1093/cvr/cvac136
By:
- Delwarde, Constance;
- Toquet, Claire;
- Aumond, Pascal;
- Kayvanjoo, Amir Hossein;
- Foucal, Adrien;
- Vely, Benjamin Le;
- Baudic, Manon;
- Lauzier, Benjamin;
- Blandin, Stéphanie;
- Véziers, Joëlle;
- Paul-Gilloteaux, Perrine;
- Lecointe, Simon;
- Baron, Estelle;
- Massaiu, Ilaria;
- Poggio, Paolo;
- Rémy, Séverine;
- Anegon, Ignacio;
- Marec, Hervé Le;
- Monassier, Laurent;
- Schott, Jean-Jacques
Publication type:
Article
Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome.
Published in:
2016
By:
- Portero, Vincent;
- Le Scouarnec, Solena;
- Es ‐ Salah ‐ Lamoureux, Zeineb;
- Burel, Sophie;
- Gourraud, Jean ‐ Baptiste;
- Bonnaud, Stéphanie;
- Lindenbaum, Pierre;
- Simonet, Floriane;
- Violleau, Jade;
- Baron, Estelle;
- Moreau, Eléonore;
- Scott, Carol;
- Chatel, Stéphanie;
- Loussouarn, Gildas;
- O'Hara, Thomas;
- Mabo, Philippe;
- Dina, Christian;
- Le Marec, Hervé;
- Schott, Jean ‐ Jacques;
- Probst, Vincent
Publication type:
journal article
Variants of Transient Receptor Potential Melastatin Member 4 in Childhood Atrioventricular Block.
Published in:
2016
By:
- Syam, Ninda;
- Chatel, Stéphanie;
- Ozhathil, Lijo Cherian;
- Sottas, Valentin;
- Rougier, Jean‐Sébastien;
- Baruteau, Alban;
- Baron, Estelle;
- Amarouch, Mohamed‐Yassine;
- Daumy, Xavier;
- Probst, Vincent;
- Schott, Jean‐Jacques;
- Abriel, Hugues
Publication type:
journal article
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome.
Published in:
Human Molecular Genetics, 2015, v. 24, n. 10, p. 2757, doi. 10.1093/hmg/ddv036
By:
- Le Scouarnec, Solena;
- Karakachoff, Matilde;
- Gourraud, Jean-Baptiste;
- Lindenbaum, Pierre;
- Bonnaud, Stéphanie;
- Portero, Vincent;
- Duboscq-Bidot, Laëtitia;
- Daumy, Xavier;
- Simonet, Floriane;
- Teusan, Raluca;
- Baron, Estelle;
- Violleau, Jade;
- Persyn, Elodie;
- Bellanger, Lise;
- Barc, Julien;
- Chatel, Stéphanie;
- Martins, Raphaël;
- Mabo, Philippe;
- Sacher, Frédéric;
- Haïssaguerre, Michel
Publication type:
Article
Burden of rare variants in arrhythmogenic cardiomyopathy with right dominant form‐associated genes provides new insights for molecular diagnosis and clinical management.
Published in:
Human Mutation, 2022, v. 43, n. 9, p. 1333, doi. 10.1002/humu.24436
By:
- Goudal, Adeline;
- Karakachoff, Matilde;
- Lindenbaum, Pierre;
- Baron, Estelle;
- Bonnaud, Stéphanie;
- Kyndt, Florence;
- Arnaud, Marine;
- Minois, Damien;
- Bourcereau, Emmanuelle;
- Thollet, Aurélie;
- Deleuze, Jean‐François;
- Genin, Emmanuelle;
- Wiart, François;
- Pasquié, Jean‐Luc;
- Galand, Vincent;
- Sacher, Frédéric;
- Dina, Christian;
- Redon, Richard;
- Bezieau, Stéphane;
- Schott, Jean‐Jacques
Publication type:
Article

Found: 7

TAD boundary deletion causes PITX2-related cardiac electrical and structural defects.

Erosion Effect in the Degradation of Coated and Uncoated Glass Solar Mirrors Highlighted by Coupled Accelerated Erosion/Aging Tests.

Multimodality imaging and transcriptomics to phenotype mitral valve dystrophy in a unique knock-in Filamin-A rat model.

Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome.

Variants of Transient Receptor Potential Melastatin Member 4 in Childhood Atrioventricular Block.

Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome.

Burden of rare variants in arrhythmogenic cardiomyopathy with right dominant form‐associated genes provides new insights for molecular diagnosis and clinical management.