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Identification of MYOM2 as a candidate gene in hypertrophic cardiomyopathy and Tetralogy of Fallot, and its functional evaluation in the Drosophila heart.
Auxerre-Plantié E, Nielsen T, Grunert M, Olejniczak O, Perrot A, Özcelik C, Harries D, Matinmehr F, Dos Remedios C, Mühlfeld C, Kraft T, Bodmer R, Vogler G, Sperling SR. Auxerre-Plantié E, et al. Among authors: perrot a. Dis Model Mech. 2020 Dec 18;13(12):dmm045377. doi: 10.1242/dmm.045377. Dis Model Mech. 2020. PMID: 33033063 Free PMC article.
[No title available]
[No authors listed] [No authors listed] PMID: 34005118
Rare and private variations in neural crest, apoptosis and sarcomere genes define the polygenic background of isolated Tetralogy of Fallot.
Grunert M, Dorn C, Schueler M, Dunkel I, Schlesinger J, Mebus S, Alexi-Meskishvili V, Perrot A, Wassilew K, Timmermann B, Hetzer R, Berger F, Sperling SR. Grunert M, et al. Among authors: perrot a. Hum Mol Genet. 2014 Jun 15;23(12):3115-28. doi: 10.1093/hmg/ddu021. Epub 2014 Jan 23. Hum Mol Genet. 2014. PMID: 24459294
Intrinsic MYH7 expression regulation contributes to tissue level allelic imbalance in hypertrophic cardiomyopathy.
Montag J, Syring M, Rose J, Weber AL, Ernstberger P, Mayer AK, Becker E, Keyser B, Dos Remedios C, Perrot A, van der Velden J, Francino A, Navarro-Lopez F, Ho CY, Brenner B, Kraft T. Montag J, et al. Among authors: perrot a. J Muscle Res Cell Motil. 2017 Aug;38(3-4):291-302. doi: 10.1007/s10974-017-9486-4. Epub 2017 Nov 3. J Muscle Res Cell Motil. 2017. PMID: 29101517 Free PMC article.
Burst-Like Transcription of Mutant and Wildtype MYH7-Alleles as Possible Origin of Cell-to-Cell Contractile Imbalance in Hypertrophic Cardiomyopathy.
Montag J, Kowalski K, Makul M, Ernstberger P, Radocaj A, Beck J, Becker E, Tripathi S, Keyser B, Mühlfeld C, Wissel K, Pich A, van der Velden J, Dos Remedios CG, Perrot A, Francino A, Navarro-López F, Brenner B, Kraft T. Montag J, et al. Among authors: perrot a. Front Physiol. 2018 Apr 9;9:359. doi: 10.3389/fphys.2018.00359. eCollection 2018. Front Physiol. 2018. PMID: 29686627 Free PMC article.
Hypertrophic cardiomyopathy-related beta-myosin mutations cause highly variable calcium sensitivity with functional imbalances among individual muscle cells.
Kirschner SE, Becker E, Antognozzi M, Kubis HP, Francino A, Navarro-López F, Bit-Avragim N, Perrot A, Mirrakhimov MM, Osterziel KJ, McKenna WJ, Brenner B, Kraft T. Kirschner SE, et al. Among authors: perrot a. Am J Physiol Heart Circ Physiol. 2005 Mar;288(3):H1242-51. doi: 10.1152/ajpheart.00686.2004. Epub 2004 Nov 18. Am J Physiol Heart Circ Physiol. 2005. PMID: 15550524 Free article.
Molecular genetics of congenital atrial septal defects.
Posch MG, Perrot A, Berger F, Ozcelik C. Posch MG, et al. Among authors: perrot a. Clin Res Cardiol. 2010 Mar;99(3):137-47. doi: 10.1007/s00392-009-0095-0. Epub 2009 Dec 11. Clin Res Cardiol. 2010. PMID: 20012542 Free PMC article. Review.
315 results