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Page 1
RAF1 mutations in childhood-onset dilated cardiomyopathy.
Dhandapany PS, Razzaque MA, Muthusami U, Kunnoth S, Edwards JJ, Mulero-Navarro S, Riess I, Pardo S, Sheng J, Rani DS, Rani B, Govindaraj P, Flex E, Yokota T, Furutani M, Nishizawa T, Nakanishi T, Robbins J, Limongelli G, Hajjar RJ, Lebeche D, Bahl A, Khullar M, Rathinavel A, Sadler KC, Tartaglia M, Matsuoka R, Thangaraj K, Gelb BD. Dhandapany PS, et al. Nat Genet. 2014 Jun;46(6):635-639. doi: 10.1038/ng.2963. Epub 2014 Apr 28. Nat Genet. 2014. PMID: 24777450 Free PMC article.
Dominant negative Ras attenuates pathological ventricular remodeling in pressure overload cardiac hypertrophy.
Ramos-Kuri M, Rapti K, Mehel H, Zhang S, Dhandapany PS, Liang L, García-Carrancá A, Bobe R, Fischmeister R, Adnot S, Lebeche D, Hajjar RJ, Lipskaia L, Chemaly ER. Ramos-Kuri M, et al. Among authors: dhandapany ps. Biochim Biophys Acta. 2015 Nov;1853(11 Pt A):2870-84. doi: 10.1016/j.bbamcr.2015.08.006. Epub 2015 Aug 8. Biochim Biophys Acta. 2015. PMID: 26260012 Free PMC article.
Myeloid Dysregulation in a Human Induced Pluripotent Stem Cell Model of PTPN11-Associated Juvenile Myelomonocytic Leukemia.
Mulero-Navarro S, Sevilla A, Roman AC, Lee DF, D'Souza SL, Pardo S, Riess I, Su J, Cohen N, Schaniel C, Rodriguez NA, Baccarini A, Brown BD, Cavé H, Caye A, Strullu M, Yalcin S, Park CY, Dhandapany PS, Yongchao G, Edelmann L, Bahieg S, Raynal P, Flex E, Tartaglia M, Moore KA, Lemischka IR, Gelb BD. Mulero-Navarro S, et al. Among authors: dhandapany ps. Cell Rep. 2015 Oct 20;13(3):504-515. doi: 10.1016/j.celrep.2015.09.019. Epub 2015 Oct 8. Cell Rep. 2015. PMID: 26456833 Free PMC article.
Novel mitochondrial DNA mutations implicated in Noonan syndrome.
Dhandapany PS, Sadayappan S, Vanniarajan A, Karthikeyan B, Nagaraj C, Gowrishankar K, Selvam GS, Singh L, Thangaraj K. Dhandapany PS, et al. Int J Cardiol. 2007 Aug 21;120(2):284-5. doi: 10.1016/j.ijcard.2006.07.229. Epub 2006 Nov 7. Int J Cardiol. 2007. PMID: 17092585
Novel Mutations in β-MYH7 Gene in Indian Patients With Dilated Cardiomyopathy.
Rani DS, Vijaya Kumar A, Nallari P, Sampathkumar K, Dhandapany PS, Narasimhan C, Rathinavel A, Thangaraj K. Rani DS, et al. Among authors: dhandapany ps. CJC Open. 2021 Aug 8;4(1):1-11. doi: 10.1016/j.cjco.2021.07.020. eCollection 2022 Jan. CJC Open. 2021. PMID: 35072022 Free PMC article.
Ribosomal protein S6 kinase beta-1 gene variants cause hypertrophic cardiomyopathy.
Jain PK, Jayappa S, Sairam T, Mittal A, Paul S, Rao VJ, Chittora H, Kashyap DK, Palakodeti D, Thangaraj K, Shenthar J, Koranchery R, Rajendran R, Alireza H, Mohanan KS, Rathinavel A, Dhandapany PS. Jain PK, et al. Among authors: dhandapany ps. J Med Genet. 2022 Oct;59(10):984-992. doi: 10.1136/jmedgenet-2021-107866. Epub 2021 Dec 16. J Med Genet. 2022. PMID: 34916228
35 results