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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