Rafael-Fortney JA - Search Results

1

The lack of Troponin I Ser-23/24 phosphorylation is detrimental to in vivo cardiac function and exacerbates cardiac disease.

Salhi HE, Shettigar V, Salyer L, Sturgill S, Brundage EA, Robinett J, Xu Z, Abay E, Lowe J, Janssen PML, Rafael-Fortney JA, Weisleder N, Ziolo MT, Biesiadecki BJ. Salhi HE, et al. Among authors: rafael fortney ja. J Mol Cell Cardiol. 2023 Mar;176:84-96. doi: 10.1016/j.yjmcc.2023.01.010. Epub 2023 Jan 29. J Mol Cell Cardiol. 2023. PMID: 36724829 Free PMC article.

2

Utrophin deficiency worsens cardiac contractile dysfunction present in dystrophin-deficient mdx mice.

Janssen PM, Hiranandani N, Mays TA, Rafael-Fortney JA. Janssen PM, et al. Am J Physiol Heart Circ Physiol. 2005 Dec;289(6):H2373-8. doi: 10.1152/ajpheart.00448.2005. Epub 2005 Jul 15. Am J Physiol Heart Circ Physiol. 2005. PMID: 16024571 Free article.

3

Claudin-5 levels are reduced in human end-stage cardiomyopathy.

Mays TA, Binkley PF, Lesinski A, Doshi AA, Quaile MP, Margulies KB, Janssen PM, Rafael-Fortney JA. Mays TA, et al. J Mol Cell Cardiol. 2008 Jul;45(1):81-7. doi: 10.1016/j.yjmcc.2008.04.005. Epub 2008 Apr 25. J Mol Cell Cardiol. 2008. PMID: 18513742

4

Truncated CASK does not alter skeletal muscle or protein interactors.

Sanford JL, Mays TA, Varian KD, Wilson JB, Janssen PM, Rafael-Fortney JA. Sanford JL, et al. Muscle Nerve. 2008 Sep;38(3):1116-27. doi: 10.1002/mus.20993. Muscle Nerve. 2008. PMID: 18642383

5

Impairment of diastolic function by lack of frequency-dependent myofilament desensitization rabbit right ventricular hypertrophy.

Varian KD, Kijtawornrat A, Gupta SC, Torres CA, Monasky MM, Hiranandani N, Delfin DA, Rafael-Fortney JA, Periasamy M, Hamlin RL, Janssen PM. Varian KD, et al. Circ Heart Fail. 2009 Sep;2(5):472-81. doi: 10.1161/CIRCHEARTFAILURE.109.853200. Epub 2009 Jul 21. Circ Heart Fail. 2009. PMID: 19808378 Free PMC article.

6

Lengthening-contractions in isolated myocardium impact force development and worsen cardiac contractile function in the mdx mouse model of muscular dystrophy.

Xu Y, Delfín DA, Rafael-Fortney JA, Janssen PM. Xu Y, et al. J Appl Physiol (1985). 2011 Feb;110(2):512-9. doi: 10.1152/japplphysiol.00253.2010. Epub 2010 Dec 2. J Appl Physiol (1985). 2011. PMID: 21127205 Free PMC article.

7

Improvement of cardiac contractile function by peptide-based inhibition of NF-κB in the utrophin/dystrophin-deficient murine model of muscular dystrophy.

Delfín DA, Xu Y, Peterson JM, Guttridge DC, Rafael-Fortney JA, Janssen PM. Delfín DA, et al. J Transl Med. 2011 May 17;9:68. doi: 10.1186/1479-5876-9-68. J Transl Med. 2011. PMID: 21586145 Free PMC article.

8

Early treatment with lisinopril and spironolactone preserves cardiac and skeletal muscle in Duchenne muscular dystrophy mice.

Rafael-Fortney JA, Chimanji NS, Schill KE, Martin CD, Murray JD, Ganguly R, Stangland JE, Tran T, Xu Y, Canan BD, Mays TA, Delfín DA, Janssen PM, Raman SV. Rafael-Fortney JA, et al. Circulation. 2011 Aug 2;124(5):582-8. doi: 10.1161/CIRCULATIONAHA.111.031716. Epub 2011 Jul 18. Circulation. 2011. PMID: 21768542 Free PMC article.

9

Sustaining cardiac claudin-5 levels prevents functional hallmarks of cardiomyopathy in a muscular dystrophy mouse model.

Delfín DA, Xu Y, Schill KE, Mays TA, Canan BD, Zang KE, Barnum JA, Janssen PM, Rafael-Fortney JA. Delfín DA, et al. Mol Ther. 2012 Jul;20(7):1378-83. doi: 10.1038/mt.2012.81. Epub 2012 May 1. Mol Ther. 2012. PMID: 22547149 Free PMC article.

10

Cardiomyopathy in the dystrophin/utrophin-deficient mouse model of severe muscular dystrophy is characterized by dysregulation of matrix metalloproteinases.

Delfín DA, Zang KE, Schill KE, Patel NT, Janssen PM, Raman SV, Rafael-Fortney JA. Delfín DA, et al. Neuromuscul Disord. 2012 Nov;22(11):1006-14. doi: 10.1016/j.nmd.2012.05.002. Epub 2012 Jun 29. Neuromuscul Disord. 2012. PMID: 22749475 Free PMC article.

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