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Resident PW1+ Progenitor Cells Participate in Vascular Remodeling During Pulmonary Arterial Hypertension.
Circ Res. 2016 Mar 4;118(5):822-33. doi: 10.1161/CIRCRESAHA.115.307035. Epub 2016 Jan 12.
Circ Res. 2016.
PMID: 26838788
Plasticity-related gene-1 inhibits lysophosphatidic acid-induced vascular smooth muscle cell migration and proliferation and prevents neointima formation.
Gaaya A, Poirier O, Mougenot N, Hery T, Atassi F, Marchand A, Saulnier-Blache JS, Amour J, Vogt J, Lompré AM, Soubrier F, Nadaud S.
Gaaya A, et al. Among authors: hery t.
Am J Physiol Cell Physiol. 2012 Nov 15;303(10):C1104-14. doi: 10.1152/ajpcell.00051.2012. Epub 2012 Sep 26.
Am J Physiol Cell Physiol. 2012.
PMID: 23015549
Free article.
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Desmoglein-2 mutations in propeptide cleavage-site causes arrhythmogenic right ventricular cardiomyopathy/dysplasia by impairing extracellular 1-dependent desmosomal interactions upon cellular stress.
Vite A, Gandjbakhch E, Hery T, Fressart V, Gary F, Simon F, Varnous S, Hidden Lucet F, Charron P, Villard E.
Vite A, et al. Among authors: hery t.
Europace. 2020 Feb 1;22(2):320-329. doi: 10.1093/europace/euz329.
Europace. 2020.
PMID: 31845994
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Rare germline heterozygous missense variants in BRCA1-associated protein 1, BAP1, cause a syndromic neurodevelopmental disorder.
Küry S, Ebstein F, Mollé A, Besnard T, Lee MK, Vignard V, Hery T, Nizon M, Mancini GMS, Giltay JC, Cogné B, McWalter K, Deb W, Mor-Shaked H, Li H, Schnur RE, Wentzensen IM, Denommé-Pichon AS, Fourgeux C, Verheijen FW, Faurie E, Schot R, Stevens CA, Smits DJ, Barr E, Sheffer R, Bernstein JA, Stimach CL, Kovitch E, Shashi V, Schoch K, Smith W, van Jaarsveld RH, Hurst ACE, Smith K, Baugh EH, Bohm SG, Vyhnálková E, Ryba L, Delnatte C, Neira J, Bonneau D, Toutain A, Rosenfeld JA; Undiagnosed Diseases Network; Audebert-Bellanger S, Gilbert-Dussardier B, Odent S, Laumonnier F, Berger SI, Smith ACM, Bourdeaut F, Stern MH, Redon R, Krüger E, Margueron R, Bézieau S, Poschmann J, Isidor B.
Küry S, et al. Among authors: hery t.
Am J Hum Genet. 2022 Feb 3;109(2):361-372. doi: 10.1016/j.ajhg.2021.12.011. Epub 2022 Jan 19.
Am J Hum Genet. 2022.
PMID: 35051358
Free PMC article.
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Contribution of exome sequencing for genetic diagnostic in arrhythmogenic right ventricular cardiomyopathy/dysplasia.
Fedida J, Fressart V, Charron P, Surget E, Hery T, Richard P, Donal E, Keren B, Duthoit G, Hidden-Lucet F, Villard E, Gandjbakhch E.
Fedida J, et al. Among authors: hery t.
PLoS One. 2017 Aug 2;12(8):e0181840. doi: 10.1371/journal.pone.0181840. eCollection 2017.
PLoS One. 2017.
PMID: 28767663
Free PMC article.
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A cis-acting mechanism mediates transcriptional memory at Polycomb target genes in mammals.
Holoch D, Wassef M, Lövkvist C, Zielinski D, Aflaki S, Lombard B, Héry T, Loew D, Howard M, Margueron R.
Holoch D, et al. Among authors: hery t.
Nat Genet. 2021 Dec;53(12):1686-1697. doi: 10.1038/s41588-021-00964-2. Epub 2021 Nov 15.
Nat Genet. 2021.
PMID: 34782763
Free article.
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XIST loss impairs mammary stem cell differentiation and increases tumorigenicity through Mediator hyperactivation.
Richart L, Picod-Chedotel ML, Wassef M, Macario M, Aflaki S, Salvador MA, Héry T, Dauphin A, Wicinski J, Chevrier V, Pastor S, Guittard G, Le Cam S, Kamhawi H, Castellano R, Guasch G, Charafe-Jauffret E, Heard E, Margueron R, Ginestier C.
Richart L, et al. Among authors: hery t.
Cell. 2022 Jun 9;185(12):2164-2183.e25. doi: 10.1016/j.cell.2022.04.034. Epub 2022 May 20.
Cell. 2022.
PMID: 35597241
Free article.
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Ad hoc hybrid synaptic junctions to detect nerve stimulation and its application to detect onset of diabetic polyneuropathy.
Gupta S, Ghatak S, Hery T, Khanna S, El Masry M, Sundaresan VB, Sen CK.
Gupta S, et al. Among authors: hery t.
Biosens Bioelectron. 2020 Dec 1;169:112618. doi: 10.1016/j.bios.2020.112618. Epub 2020 Sep 21.
Biosens Bioelectron. 2020.
PMID: 33007616
Free PMC article.
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