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Page 1
Long-term rescue of a familial hypertrophic cardiomyopathy caused by a mutation in the thin filament protein, tropomyosin, via modulation of a calcium cycling protein.
Gaffin RD, Peña JR, Alves MS, Dias FA, Chowdhury SA, Heinrich LS, Goldspink PH, Kranias EG, Wieczorek DF, Wolska BM. Gaffin RD, et al. Among authors: heinrich ls. J Mol Cell Cardiol. 2011 Nov;51(5):812-20. doi: 10.1016/j.yjmcc.2011.07.026. Epub 2011 Aug 5. J Mol Cell Cardiol. 2011. PMID: 21840315 Free PMC article.
Neonatal gene transfer of Serca2a delays onset of hypertrophic remodeling and improves function in familial hypertrophic cardiomyopathy.
Peña JR, Szkudlarek AC, Warren CM, Heinrich LS, Gaffin RD, Jagatheesan G, del Monte F, Hajjar RJ, Goldspink PH, Solaro RJ, Wieczorek DF, Wolska BM. Peña JR, et al. Among authors: heinrich ls. J Mol Cell Cardiol. 2010 Dec;49(6):993-1002. doi: 10.1016/j.yjmcc.2010.09.010. Epub 2010 Sep 18. J Mol Cell Cardiol. 2010. PMID: 20854827 Free PMC article.
Acute graft dysfunction after living-related renal transplant.
Ellimoottil C, Brandt W, Bernardi K, Evans A, Mehta V, Picken MM, Phelan K, Heinrich L, Milner J, Wai PY, Asolati M, Kuo PC, Lu AD. Ellimoottil C, et al. Urology. 2013 Oct;82(4):764-7. doi: 10.1016/j.urology.2013.06.025. Epub 2013 Aug 12. Urology. 2013. PMID: 23947990 No abstract available.