Daniel E. Michele, Ph.D. - Publications

2000 University of Michigan, Ann Arbor, Ann Arbor, MI 
muscle gene therapy, DMD

52 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
2022 Michele DE. Mechanisms of skeletal muscle repair and regeneration in health and disease. The Febs Journal. PMID 35929418 DOI: 10.1111/febs.16577  0.467
2020 McDade JR, Naylor MT, Michele DE. Sarcolemma Wounding Activates Dynamin-Dependent Endocytosis in Striated Muscle. The Febs Journal. PMID 32893434 DOI: 10.1111/Febs.15556  0.431
2020 Garbincius JF, Merz LE, Cuttitta AJ, Bayne KV, Schrade S, Armstead EA, Converso-Baran KL, Whitesall SE, D'Alecy LG, Michele DE. Enhanced dimethylarginine degradation improves coronary flow reserve and exercise tolerance in Duchenne muscular dystrophy carrier mice. American Journal of Physiology. Heart and Circulatory Physiology. PMID 32762558 DOI: 10.1152/Ajpheart.00333.2019  0.434
2019 Eisen B, Ben Jehuda R, Cuttitta AJ, Mekies LN, Shemer Y, Baskin P, Reiter I, Willi L, Freimark D, Gherghiceanu M, Monserrat L, Scherr M, Hilfiker-Kleiner D, Arad M, Michele DE, et al. Electrophysiological abnormalities in induced pluripotent stem cell-derived cardiomyocytes generated from Duchenne muscular dystrophy patients. Journal of Cellular and Molecular Medicine. PMID 30618214 DOI: 10.1111/Jcmm.14124  0.328
2018 Buras ED, Converso-Baran K, Davis CS, Akama T, Hikage F, Michele DE, Brooks SV, Chun TH. Fibro-Adipogenic Remodeling of the Diaphragm in Obesity-Associated Respiratory Dysfunction. Diabetes. PMID 30361289 DOI: 10.2337/Db18-0209  0.319
2018 Eisen B, Ben Jehuda R, Cuttitta AJ, Mekies LN, Reiter I, Ramchandren S, Arad M, Michele DE, Binah O. Generation of Duchenne muscular dystrophy patient-specific induced pluripotent stem cell line lacking exons 45-50 of the dystrophin gene (IITi001-A). Stem Cell Research. 29: 111-114. PMID 29653394 DOI: 10.1016/J.Scr.2018.03.023  0.367
2018 Sahinoz M, Khairi S, Cuttitta A, Brady GF, Rupani A, Meral R, Tayeh MK, Thomas P, Riebschleger M, Camelo-Piragua S, Innis JW, Bishr Omary M, Michele DE, Oral EA. Potential association of LMNA-associated generalized lipodystrophy with juvenile dermatomyositis. Clinical Diabetes and Endocrinology. 4: 6. PMID 29610677 DOI: 10.1186/s40842-018-0058-3  0.352
2017 Eisen B, Ben Jehuda R, Mekies L, Shemer Y, Cuttitta A, Monserrat L, Gherghiceanu M, Arad M, Freimark D, Michele D, Binah O. P3248Investigating dilated cardiomyopathy caused by dystrophin mutations using duchenne muscular dystrophy-patients induced pluripotent stem cell-derived cardiomyocytes European Heart Journal. 38. DOI: 10.1093/Eurheartj/Ehx504.P3248  0.303
2016 Campbell M, Witcher M, Gopal A, Michele DE. Dilated cardiomyopathy mutations in delta sarcoglycan exert a dominant negative effect on cardiac myocyte mechanical stability. American Journal of Physiology. Heart and Circulatory Physiology. ajpheart.00521.2015. PMID 26968544 DOI: 10.1152/Ajpheart.00521.2015  0.302
2015 Garbincius JF, Michele DE. Dystrophin-glycoprotein complex regulates muscle nitric oxide production through mechanoregulation of AMPK signaling. Proceedings of the National Academy of Sciences of the United States of America. 112: 13663-8. PMID 26483453 DOI: 10.1073/Pnas.1512991112  0.454
2014 McDade JR, Archambeau A, Michele DE. Rapid actin-cytoskeleton-dependent recruitment of plasma membrane-derived dysferlin at wounds is critical for muscle membrane repair. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 28: 3660-70. PMID 24784578 DOI: 10.1096/Fj.14-250191  0.429
2014 Reifler A, Li X, Archambeau AJ, McDade JR, Sabha N, Michele DE, Dowling JJ. Conditional knockout of pik3c3 causes a murine muscular dystrophy. The American Journal of Pathology. 184: 1819-30. PMID 24726497 DOI: 10.1016/J.Ajpath.2014.02.012  0.548
2014 Raeker MÖ, Shavit JA, Dowling JJ, Michele DE, Russell MW. Membrane-myofibril cross-talk in myofibrillogenesis and in muscular dystrophy pathogenesis: lessons from the zebrafish. Frontiers in Physiology. 5: 14. PMID 24478725 DOI: 10.3389/Fphys.2014.00014  0.416
2014 McDade JR, Michele DE. Membrane damage-induced vesicle-vesicle fusion of dysferlin-containing vesicles in muscle cells requires microtubules and kinesin. Human Molecular Genetics. 23: 1677-86. PMID 24203699 DOI: 10.1093/Hmg/Ddt557  0.451
2013 Muñoz-Cánoves P, Michele D. Special Issue: Myogenesis Febs Journal. 280: 3979-3979. PMID 23889759 DOI: 10.1111/Febs.12454  0.508
2013 Cirak S, Foley AR, Herrmann R, Willer T, Yau S, Stevens E, Torelli S, Brodd L, Kamynina A, Vondracek P, Roper H, Longman C, Korinthenberg R, Marrosu G, Nürnberg P, ... ... Michele DE, et al. ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies. Brain : a Journal of Neurology. 136: 269-81. PMID 23288328 DOI: 10.1093/Brain/Aws312  0.412
2013 Gumerson JD, Davis CS, Kabaeva ZT, Hayes JM, Brooks SV, Michele DE. Muscle-specific expression of LARGE restores neuromuscular transmission deficits in dystrophic LARGE(myd) mice. Human Molecular Genetics. 22: 757-68. PMID 23222475 DOI: 10.1093/Hmg/Dds483  0.765
2013 Reifler A, Michele D, Archambeau A, Li X, Dowling J. P.4.1 PIP kinases, muscle development, and the pathogenesis of myotubular myopathy Neuromuscular Disorders. 23: 759-760. DOI: 10.1016/J.Nmd.2013.06.439  0.532
2011 Gumerson JD, Michele DE. The dystrophin-glycoprotein complex in the prevention of muscle damage. Journal of Biomedicine & Biotechnology. 2011: 210797. PMID 22007139 DOI: 10.1155/2011/210797  0.759
2011 Kabaeva Z, Meekhof KE, Michele DE. Sarcolemma instability during mechanical activity in Largemyd cardiac myocytes with loss of dystroglycan extracellular matrix receptor function. Human Molecular Genetics. 20: 3346-55. PMID 21628317 DOI: 10.1093/Hmg/Ddr240  0.376
2011 Labelle-Dumais C, Dilworth DJ, Harrington EP, de Leau M, Lyons D, Kabaeva Z, Manzini MC, Dobyns WB, Walsh CA, Michele DE, Gould DB. COL4A1 mutations cause ocular dysgenesis, neuronal localization defects, and myopathy in mice and Walker-Warburg syndrome in humans. Plos Genetics. 7: e1002062. PMID 21625620 DOI: 10.1371/Journal.Pgen.1002062  0.361
2011 Ramaswamy KS, Palmer ML, van der Meulen JH, Renoux A, Kostrominova TY, Michele DE, Faulkner JA. Lateral transmission of force is impaired in skeletal muscles of dystrophic mice and very old rats. The Journal of Physiology. 589: 1195-208. PMID 21224224 DOI: 10.1113/Jphysiol.2010.201921  0.526
2011 Mathews KD, Stephan CM, Laubenthal K, Winder TL, Michele DE, Moore SA, Campbell KP. Myoglobinuria and muscle pain are common in patients with limb-girdle muscular dystrophy 2I. Neurology. 76: 194-5. PMID 21220724 DOI: 10.1212/Wnl.0B013E3182061Ad4  0.373
2010 Gumerson JD, Kabaeva ZT, Davis CS, Faulkner JA, Michele DE. Soleus muscle in glycosylation-deficient muscular dystrophy is protected from contraction-induced injury. American Journal of Physiology. Cell Physiology. 299: C1430-40. PMID 20844247 DOI: 10.1152/Ajpcell.00192.2010  0.762
2010 Salazar JJ, Michele DE, Brooks SV. Inhibition of calpain prevents muscle weakness and disruption of sarcomere structure during hindlimb suspension. Journal of Applied Physiology (Bethesda, Md. : 1985). 108: 120-7. PMID 19892928 DOI: 10.1152/Japplphysiol.01080.2009  0.52
2010 Suzuki N, Hozumi K, Urushibata S, Yoshimura T, Kikkawa Y, Gumerson JD, Michele DE, Hoffman MP, Yamada Y, Nomizu M. Identification of alpha-dystroglycan binding sequences in the laminin alpha2 chain LG4-5 module. Matrix Biology : Journal of the International Society For Matrix Biology. 29: 143-51. PMID 19800000 DOI: 10.1016/J.Matbio.2009.09.006  0.677
2009 Michele DE, Kabaeva Z, Davis SL, Weiss RM, Campbell KP. Dystroglycan matrix receptor function in cardiac myocytes is important for limiting activity-induced myocardial damage. Circulation Research. 105: 984-93. PMID 19797173 DOI: 10.1161/Circresaha.109.199489  0.494
2009 Han R, Kanagawa M, Yoshida-Moriguchi T, Rader EP, Ng RA, Michele DE, Muirhead DE, Kunz S, Moore SA, Iannaccone ST, Miyake K, McNeil PL, Mayer U, Oldstone MB, Faulkner JA, et al. Basal lamina strengthens cell membrane integrity via the laminin G domain-binding motif of alpha-dystroglycan. Proceedings of the National Academy of Sciences of the United States of America. 106: 12573-9. PMID 19633189 DOI: 10.1073/Pnas.0906545106  0.559
2008 Kabaeva Z, Zhao M, Michele DE. Blebbistatin extends culture life of adult mouse cardiac myocytes and allows efficient and stable transgene expression. American Journal of Physiology. Heart and Circulatory Physiology. 294: H1667-74. PMID 18296569 DOI: 10.1152/Ajpheart.01144.2007  0.307
2006 Moore SA, Shilling CJ, Westra S, Wall C, Wicklund MP, Stolle C, Brown CA, Michele DE, Piccolo F, Winder TL, Stence A, Barresi R, King N, King W, Florence J, et al. Limb-girdle muscular dystrophy in the United States. Journal of Neuropathology and Experimental Neurology. 65: 995-1003. PMID 17021404 DOI: 10.1097/01.Jnen.0000235854.77716.6C  0.388
2006 Bhosle RC, Michele DE, Campbell KP, Li Z, Robson RM. Interactions of intermediate filament protein synemin with dystrophin and utrophin. Biochemical and Biophysical Research Communications. 346: 768-77. PMID 16777071 DOI: 10.1016/J.Bbrc.2006.05.192  0.452
2005 Yasuda S, Townsend D, Michele DE, Favre EG, Day SM, Metzger JM. Dystrophic heart failure blocked by membrane sealant poloxamer. Nature. 436: 1025-9. PMID 16025101 DOI: 10.1038/Nature03844  0.506
2004 Michele DE, Szatkowski ML, Albayya FP, Metzger JM. Parvalbumin gene delivery improves diastolic function in the aged myocardium in vivo. Molecular Therapy : the Journal of the American Society of Gene Therapy. 10: 399-403. PMID 15294186 DOI: 10.1016/J.Ymthe.2004.05.011  0.37
2004 Kanagawa M, Saito F, Kunz S, Yoshida-Moriguchi T, Barresi R, Kobayashi YM, Muschler J, Dumanski JP, Michele DE, Oldstone MB, Campbell KP. Molecular recognition by LARGE is essential for expression of functional dystroglycan. Cell. 117: 953-64. PMID 15210115 DOI: 10.1016/J.Cell.2004.06.003  0.439
2004 Barresi R, Michele DE, Kanagawa M, Harper HA, Dovico SA, Satz JS, Moore SA, Zhang W, Schachter H, Dumanski JP, Cohn RD, Nishino I, Campbell KP. LARGE can functionally bypass alpha-dystroglycan glycosylation defects in distinct congenital muscular dystrophies. Nature Medicine. 10: 696-703. PMID 15184894 DOI: 10.1038/Nm1059  0.374
2004 Kim DS, Hayashi YK, Matsumoto H, Ogawa M, Noguchi S, Murakami N, Sakuta R, Mochizuki M, Michele DE, Campbell KP, Nonaka I, Nishino I. POMT1 mutation results in defective glycosylation and loss of laminin-binding activity in alpha-DG. Neurology. 62: 1009-11. PMID 15037715 DOI: 10.1212/01.Wnl.0000115386.28769.65  0.325
2004 Dylla DE, Hickey MA, Michele DE, Davidson BL, Campbell KP, McCray PB. 491. Improved Apical Airway Epithelia Targeting Properties of FIV Vector Pseudotyped with Envelopes from LCMV Molecular Therapy. 9. DOI: 10.1016/J.Ymthe.2004.06.405  0.304
2003 Durbeej M, Sawatzki SM, Barresi R, Schmainda KM, Allamand V, Michele DE, Campbell KP. Gene transfer establishes primacy of striated vs. smooth muscle sarcoglycan complex in limb-girdle muscular dystrophy. Proceedings of the National Academy of Sciences of the United States of America. 100: 8910-5. PMID 12851463 DOI: 10.1073/Pnas.1537554100  0.56
2003 Metzger JM, Michele DE, Rust EM, Borton AR, Westfall MV. Sarcomere thin filament regulatory isoforms. Evidence of a dominant effect of slow skeletal troponin I on cardiac contraction. The Journal of Biological Chemistry. 278: 13118-23. PMID 12551900 DOI: 10.1074/Jbc.M212601200  0.412
2002 Cohn RD, Henry MD, Michele DE, Barresi R, Saito F, Moore SA, Flanagan JD, Skwarchuk MW, Robbins ME, Mendell JR, Williamson RA, Campbell KP. Disruption of DAG1 in differentiated skeletal muscle reveals a role for dystroglycan in muscle regeneration. Cell. 110: 639-48. PMID 12230980 DOI: 10.1016/S0092-8674(02)00907-8  0.565
2002 Michele DE, Gomez CA, Hong KE, Westfall MV, Metzger JM. Cardiac dysfunction in hypertrophic cardiomyopathy mutant tropomyosin mice is transgene-dependent, hypertrophy-independent, and improved by beta-blockade. Circulation Research. 91: 255-62. PMID 12169652 DOI: 10.1161/01.Res.0000027530.58419.82  0.403
2002 Moore SA, Saito F, Chen J, Michele DE, Henry MD, Messing A, Cohn RD, Ross-Barta SE, Westra S, Williamson RA, Hoshi T, Campbell KP. Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy. Nature. 418: 422-5. PMID 12140559 DOI: 10.1038/Nature00838  0.375
2002 Michele DE, Barresi R, Kanagawa M, Saito F, Cohn RD, Satz JS, Dollar J, Nishino I, Kelley RI, Somer H, Straub V, Mathews KD, Moore SA, Campbell KP. Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies. Nature. 418: 417-22. PMID 12140558 DOI: 10.1038/Nature00837  0.482
2002 Michele DE, Coutu P, Metzger JM. Divergent abnormal muscle relaxation by hypertrophic cardiomyopathy and nemaline myopathy mutant tropomyosins. Physiological Genomics. 9: 103-11. PMID 12006676 DOI: 10.1152/Physiolgenomics.00099.2001  0.542
2001 Szatkowski ML, Westfall MV, Gomez CA, Wahr PA, Michele DE, DelloRusso C, Turner II, Hong KE, Albayya FP, Metzger JM. In vivo acceleration of heart relaxation performance by parvalbumin gene delivery. The Journal of Clinical Investigation. 107: 191-8. PMID 11160135 DOI: 10.1172/Jci9862  0.739
2000 Michele DE, Metzger JM. Contractile dysfunction in hypertrophic cardiomyopathy: elucidating primary defects of mutant contractile proteins by gene transfer. Trends in Cardiovascular Medicine. 10: 177-82. PMID 11239799 DOI: 10.1016/S1050-1738(00)00067-0  0.488
2000 Michele DE, Metzger JM. Physiological consequences of tropomyosin mutations associated with cardiac and skeletal myopathies. Journal of Molecular Medicine (Berlin, Germany). 78: 543-53. PMID 11199327 DOI: 10.1007/S001090000161  0.531
1999 Michele DE, Albayya FP, Metzger JM. A nemaline myopathy mutation in alpha-tropomyosin causes defective regulation of striated muscle force production. The Journal of Clinical Investigation. 104: 1575-81. PMID 10587521 DOI: 10.1172/Jci7842  0.543
1999 Michele DE, Albayya FP, Metzger JM. Direct, convergent hypersensitivity of calcium-activated force generation produced by hypertrophic cardiomyopathy mutant alpha-tropomyosins in adult cardiac myocytes. Nature Medicine. 5: 1413-7. PMID 10581085 DOI: 10.1038/70990  0.368
1999 Wahr PA, Michele DE, Metzger JM. Parvalbumin gene transfer corrects diastolic dysfunction in diseased cardiac myocytes. Proceedings of the National Academy of Sciences of the United States of America. 96: 11982-5. PMID 10518562 DOI: 10.1073/Pnas.96.21.11982  0.361
1999 Michele DE, Albayya FP, Metzger JM. Thin filament protein dynamics in fully differentiated adult cardiac myocytes: toward a model of sarcomere maintenance. The Journal of Cell Biology. 145: 1483-95. PMID 10385527 DOI: 10.1083/Jcb.145.7.1483  0.321
1999 Metzger JM, Wahr PA, Michele DE, Albayya F, Westfall MV. Effects of myosin heavy chain isoform switching on Ca2+-activated tension development in single adult cardiac myocytes. Circulation Research. 84: 1310-7. PMID 10364569 DOI: 10.1161/01.Res.84.11.1310  0.372
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