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Jill Rafael-Fortney - Publications

Affiliations: 
Ohio State University, Columbus, Columbus, OH 
Area:
Biochemistry
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34 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Krishna S, Piepho AB, Lake DM, Cumby LR, Lortz KK, Lowe J, Chamberlain JS, Rafael-Fortney JA. Gene therapy delivered micro-dystrophins co-localize with transgenic utrophin in dystrophic skeletal muscle fibers. Neuromuscular Disorders : Nmd. 36: 1-5. PMID 38301403 DOI: 10.1016/j.nmd.2024.01.004  0.407
2022 Howard ZM, Gomatam CK, Rabolli CP, Lowe J, Piepho AB, Bansal SS, Accornero F, Rafael-Fortney JA. Mineralocorticoid receptor antagonists and glucocorticoids differentially affect skeletal muscle inflammation and pathology in muscular dystrophy. Jci Insight. PMID 36040807 DOI: 10.1172/jci.insight.159875  0.335
2022 Howard ZM, Gomatam CK, Piepho AB, Rafael-Fortney JA. Mineralocorticoid Receptor Signaling in the Inflammatory Skeletal Muscle Microenvironments of Muscular Dystrophy and Acute Injury. Frontiers in Pharmacology. 13: 942660. PMID 35837290 DOI: 10.3389/fphar.2022.942660  0.41
2022 Peczkowski KK, Rastogi N, Lowe J, Floyd KT, Schultz EJ, Karaze T, Davis JP, Rafael-Fortney JA, Janssen PML. Corrigendum: Muscle Twitch Kinetics Are Dependent on Muscle Group, Disease State, and Age in Duchenne Muscular Dystrophy Mouse Models. Frontiers in Physiology. 12: 820245. PMID 35069268 DOI: 10.3389/fphys.2021.820245  0.316
2022 Howard ZM, Rastogi N, Lowe J, Hauck JS, Ingale P, Gomatam C, Gomez-Sanchez CE, Gomez-Sanchez EP, Bansal SS, Rafael-Fortney JA. Myeloid mineralocorticoid receptors contribute to skeletal muscle repair in muscular dystrophy and acute muscle injury. American Journal of Physiology. Cell Physiology. 322: C354-C369. PMID 35044859 DOI: 10.1152/ajpcell.00411.2021  0.354
2021 Bal NC, Gupta SC, Pant M, Sopariwala DH, Gonzalez-Escobedo G, Turner J, Gunn JS, Pierson CR, Harper SQ, Rafael-Fortney JA, Periasamy M. Is Upregulation of Sarcolipin Beneficial or Detrimental to Muscle Function? Frontiers in Physiology. 12: 633058. PMID 33732165 DOI: 10.3389/fphys.2021.633058  0.333
2020 Peczkowski KK, Rastogi N, Lowe J, Floyd KT, Schultz EJ, Karaze T, Davis JP, Rafael-Fortney JA, Janssen PML. Muscle Twitch Kinetics Are Dependent on Muscle Group, Disease State, and Age in Duchenne Muscular Dystrophy Mouse Models. Frontiers in Physiology. 11: 568909. PMID 33101056 DOI: 10.3389/fphys.2020.568909  0.354
2020 Tyree C, Peczkowski K, Janssen PM, Rafael-Fortney J, Davis JP. The Role of Thin Filament Calcium Sensitivity in Modulating Relaxation Time of Soleus and EDL Skeletal Muscle Biophysical Journal. 118: 122a. DOI: 10.1016/J.Bpj.2019.11.804  0.407
2019 Hauck JS, Howard ZM, Lowe J, Rastogi N, Pico MG, Swager SA, Petrosino JM, Gomez-Sanchez CE, Gomez-Sanchez EP, Accornero F, Rafael-Fortney JA. Mineralocorticoid Receptor Signaling Contributes to Normal Muscle Repair After Acute Injury. Frontiers in Physiology. 10: 1324. PMID 31736768 DOI: 10.3389/fphys.2019.01324  0.345
2019 Hauck JS, Lowe J, Rastogi N, McElhanon KE, Petrosino JM, Peczkowski KK, Chadwick AN, Zins JG, Accornero F, Janssen PML, Weisleder NL, Rafael-Fortney JA. Mineralocorticoid Receptor Antagonists Improve Membrane Integrity Independent of Muscle Force in Muscular Dystrophy. Human Molecular Genetics. PMID 30759207 DOI: 10.1093/hmg/ddz039  0.402
2018 Lowe J, Kadakia FK, Zins JG, Haupt M, Peczkowski KK, Rastogi N, Floyd KT, Gomez-Sanchez EP, Gomez-Sanchez CE, Elnakish MT, Rafael-Fortney JA, Janssen PML. Mineralocorticoid Receptor Antagonists in Muscular Dystrophy Mice During Aging and Exercise. Journal of Neuromuscular Diseases. PMID 30010143 DOI: 10.3233/JND-180323  0.356
2017 Chadwick JA, Hauck JS, Gomez-Sanchez CE, Gomez-Sanchez EP, Rafael-Fortney JA. Gene expression effects of glucocorticoid and mineralocorticoid receptor agonists and antagonists on normal human skeletal muscle. Physiological Genomics. physiolgenomics.0012. PMID 28432191 DOI: 10.1152/physiolgenomics.00128.2016  0.328
2016 Chadwick JA, Bhattacharya S, Lowe J, Weisleder N, Rafael-Fortney JA. Renin-angiotensin-aldosterone system inhibitors improve membrane stability and change gene expression profiles in dystrophic skeletal muscles. American Journal of Physiology. Cell Physiology. ajpcell.00269.2016. PMID 27881412 DOI: 10.1152/ajpcell.00269.2016  0.385
2016 Lowe J, Floyd KT, Rastogi N, Schultz EJ, Chadwick JA, Swager SA, Zins JG, Kadakia FK, Smart S, Gomez-Sanchez EP, Gomez-Sanchez CE, Raman SV, Janssen PM, Rafael-Fortney JA. Similar efficacy from specific and non-specific mineralocorticoid receptor antagonist treatment of muscular dystrophy mice. Journal of Neuromuscular Diseases. 3: 395-404. PMID 27822449 DOI: 10.3233/JND-160173  0.38
2016 Chadwick JA, Swager SA, Lowe J, Welc SS, Tidball JG, Gomez-Sanchez CE, Gomez-Sanchez EP, Rafael-Fortney JA. Myeloid cells are capable of synthesizing aldosterone to exacerbate damage in muscular dystrophy. Human Molecular Genetics. PMID 27798095 DOI: 10.1093/Hmg/Ddw331  0.407
2015 Lowe J, Wodarcyk AJ, Floyd KT, Rastogi N, Schultz EJ, Swager SA, Chadwick JA, Tran T, Raman SV, Janssen PM, Rafael-Fortney JA. The Angiotensin Converting Enzyme Inhibitor Lisinopril Improves Muscle Histopathology but not Contractile Function in a Mouse Model of Duchenne Muscular Dystrophy. Journal of Neuromuscular Diseases. 2: 257-268. PMID 27110493 DOI: 10.3233/JND-150099  0.336
2015 Chadwick JA, Hauck JS, Lowe J, Shaw JJ, Guttridge DC, Gomez-Sanchez CE, Gomez-Sanchez EP, Rafael-Fortney JA. Mineralocorticoid receptors are present in skeletal muscle and represent a potential therapeutic target. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. PMID 26178166 DOI: 10.1096/fj.15-276782  0.401
2015 Pant M, Sopariwala DH, Bal NC, Lowe J, Delfín DA, Rafael-Fortney J, Periasamy M. Metabolic dysfunction and altered mitochondrial dynamics in the utrophin-dystrophin deficient mouse model of duchenne muscular dystrophy. Plos One. 10: e0123875. PMID 25859846 DOI: 10.1371/Journal.Pone.0123875  0.434
2015 Schill K, Altenburger A, Fultz A, Lowe J, Periasamy M, Villamena F, Rafael-Fortney J, Devor S. Muscle Damage And Oxidative Stress In The Mdx Mouse Medicine & Science in Sports & Exercise. 47: 646. DOI: 10.1249/01.Mss.0000466127.45084.26  0.364
2014 Schill K, Altenburger A, Ostler J, Ziolo M, Rafael-Fortney J, Devor S. Oxygen Consumption And Muscle Fibrosis In The Mdx Mouse Medicine & Science in Sports & Exercise. 46: 353. DOI: 10.1249/01.Mss.0000494235.00417.Db  0.405
2012 Rafael-Fortney JA, Chimanji NS, Schill KE, Martin CD, Murray JD, Stangland JE, Xu Y, Canan BD, Ganguly R, Mays TA, Delfín DA, Tran T, Janssen PML, Raman SV. Response to letter regarding article, "Early treatment with lisinopril and spironolactone preserves cardiac and skeletal muscle in duchenne muscular dystrophy mice" Circulation. 125: e430. DOI: 10.1161/Circulationaha.111.072165  0.352
2011 Delfín DA, Xu Y, Peterson JM, Guttridge DC, Rafael-Fortney JA, Janssen PM. Improvement of cardiac contractile function by peptide-based inhibition of NF-κB in the utrophin/dystrophin-deficient murine model of muscular dystrophy. Journal of Translational Medicine. 9: 68. PMID 21586145 DOI: 10.1186/1479-5876-9-68  0.318
2009 Mays TA, Sanford JL, Hanada T, Chishti AH, Rafael-Fortney JA. Glutamate receptors localize postsynaptically at neuromuscular junctions in mice. Muscle & Nerve. 39: 343-9. PMID 19208409 DOI: 10.1002/Mus.21099  0.667
2008 Sanford JL, Mays TA, Varian KD, Wilson JB, Janssen PM, Rafael-Fortney JA. Truncated CASK does not alter skeletal muscle or protein interactors. Muscle & Nerve. 38: 1116-27. PMID 18642383 DOI: 10.1002/Mus.20993  0.71
2008 Mays TA, Binkley PF, Lesinski A, Doshi AA, Quaile MP, Margulies KB, Janssen PM, Rafael-Fortney JA. Claudin-5 levels are reduced in human end-stage cardiomyopathy. Journal of Molecular and Cellular Cardiology. 45: 81-7. PMID 18513742 DOI: 10.1016/J.Yjmcc.2008.04.005  0.314
2008 Zhou L, Rafael-Fortney JA, Huang P, Zhao XS, Cheng G, Zhou X, Kaminski HJ, Liu L, Ransohoff RM. Haploinsufficiency of utrophin gene worsens skeletal muscle inflammation and fibrosis in mdx mice. Journal of the Neurological Sciences. 264: 106-11. PMID 17889902 DOI: 10.1016/j.jns.2007.08.029  0.338
2007 Acharyya S, Villalta SA, Bakkar N, Bupha-Intr T, Janssen PM, Carathers M, Li ZW, Beg AA, Ghosh S, Sahenk Z, Weinstein M, Gardner KL, Rafael-Fortney JA, Karin M, Tidball JG, et al. Interplay of IKK/NF-kappaB signaling in macrophages and myofibers promotes muscle degeneration in Duchenne muscular dystrophy. The Journal of Clinical Investigation. 117: 889-901. PMID 17380205 DOI: 10.1172/Jci30556  0.334
2006 Hanft LM, Rybakova IN, Patel JR, Rafael-Fortney JA, Ervasti JM. Cytoplasmic gamma-actin contributes to a compensatory remodeling response in dystrophin-deficient muscle. Proceedings of the National Academy of Sciences of the United States of America. 103: 5385-90. PMID 16565216 DOI: 10.1073/Pnas.0600980103  0.4
2006 Baker PE, Kearney JA, Gong B, Merriam AP, Kuhn DE, Porter JD, Rafael-Fortney JA. Analysis of gene expression differences between utrophin/dystrophin-deficient vs mdx skeletal muscles reveals a specific upregulation of slow muscle genes in limb muscles. Neurogenetics. 7: 81-91. PMID 16525850 DOI: 10.1007/s10048-006-0031-7  0.403
2006 Gardner KL, Kearney JA, Edwards JD, Rafael-Fortney JA. Restoration of all dystrophin protein interactions by functional domains in trans does not rescue dystrophy. Gene Therapy. 13: 744-51. PMID 16307000 DOI: 10.1038/sj.gt.3302686  0.38
2006 Gardner KL, Sanford JL, Mays TA, Rafael-Fortney JA. CASK localizes to nuclei in developing skeletal muscle and motor neuron culture models and is agrin-independent. Journal of Cellular Physiology. 206: 196-202. PMID 15965905 DOI: 10.1002/Jcp.20449  0.696
2005 Acharyya S, Butchbach ME, Sahenk Z, Wang H, Saji M, Carathers M, Ringel MD, Skipworth RJ, Fearon KC, Hollingsworth MA, Muscarella P, Burghes AH, Rafael-Fortney JA, Guttridge DC. Dystrophin glycoprotein complex dysfunction: a regulatory link between muscular dystrophy and cancer cachexia. Cancer Cell. 8: 421-32. PMID 16286249 DOI: 10.1016/J.Ccr.2005.10.004  0.348
2005 Sanford JL, Edwards JD, Mays TA, Gong B, Merriam AP, Rafael-Fortney JA. Claudin-5 localizes to the lateral membranes of cardiomyocytes and is altered in utrophin/dystrophin-deficient cardiomyopathic mice. Journal of Molecular and Cellular Cardiology. 38: 323-32. PMID 15698839 DOI: 10.1016/J.Yjmcc.2004.11.025  0.679
2004 Sanford JL, Mays TA, Rafael-Fortney JA. CASK and Dlg form a PDZ protein complex at the mammalian neuromuscular junction. Muscle & Nerve. 30: 164-71. PMID 15266631 DOI: 10.1002/Mus.20073  0.71
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