Elizabeth M. McNally - Publications

Affiliations: 
Human Genetics University of Chicago, Chicago, IL 
Area:
Genetics

121 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
2019 Kramerova I, Kumagai-Cresse C, Ermolova N, Mokhonova E, Marinov M, Capote J, Becerra D, Quattrocelli M, Crosbie RH, Welch E, McNally EM, Spencer MJ. Spp1 (osteopontin) promotes TGFβ processing in fibroblasts of dystrophin deficient muscles through matrix metalloproteinases. Human Molecular Genetics. PMID 31411676 DOI: 10.1093/hmg/ddz181  0.52
2019 Aubert G, Barefield DY, Demonbreun AR, Ramratnam M, Fallon KS, Warner JL, Rossi AE, Hadhazy M, Makielski JC, McNally EM. Deletion of Sulfonylurea Receptor 2 in the Adult Myocardium Enhances Cardiac Glucose Uptake and Is Cardioprotective. Jacc. Basic to Translational Science. 4: 251-268. PMID 31061927 DOI: 10.1016/j.jacbts.2018.11.012  0.88
2019 Zelikovich AS, Quattrocelli M, Salamone IM, Kuntz NL, McNally EM. Moderate exercise improves function and increases adiponectin in the mdx mouse model of muscular dystrophy. Scientific Reports. 9: 5770. PMID 30962487 DOI: 10.1038/s41598-019-42203-z  0.52
2019 Kim EY, Barefield DY, Vo AH, Gacita AM, Schuster EJ, Wyatt EJ, Davis JL, Dong B, Sun C, Page P, Dellefave-Castillo L, Demonbreun A, Zhang HF, McNally EM. Distinct pathological signatures in human cellular models of myotonic dystrophy subtypes. Jci Insight. PMID 30730308 DOI: 10.1172/jci.insight.122686  0.52
2018 Vo AH, Swaggart KA, Woo A, Gao QQ, Demonbreun AR, Fallon KS, Quattrocelli M, Hadhazy M, Page PGT, Chen Z, Eskin A, Squire K, Nelson SF, McNally EM. Dusp6 is a genetic modifier of growth through enhanced ERK activity. Human Molecular Genetics. PMID 30289454 DOI: 10.1093/hmg/ddy349  1
2018 Ramratnam M, Kenny B, Kyle JW, Wiedmeyer B, Hacker TA, Barefield DY, McNally EM, Makielski JC. Transgenic overexpression of the SUR2A-55 splice variant in mouse heart reduces infract size and promotes protective mitochondrial function. Heliyon. 4: e00677. PMID 29998196 DOI: 10.1016/j.heliyon.2018.e00677  0.44
2018 Wyatt EJ, Demonbreun AR, Kim EY, Puckelwartz MJ, Vo AH, Dellefave-Castillo LM, Gao QQ, Vainzof M, Pavanello RCM, Zatz M, McNally EM. Efficient exon skipping of SGCG mutations mediated by phosphorodiamidate morpholino oligomers. Jci Insight. 3. PMID 29720576 DOI: 10.1172/jci.insight.99357  0.88
2018 Ohiri JC, McNally EM. Gene Editing and Gene-Based Therapeutics for Cardiomyopathies. Heart Failure Clinics. 14: 179-188. PMID 29525646 DOI: 10.1016/j.hfc.2017.12.006  0.44
2018 Aartsma-Rus A, Ferlini A, McNally EM, Spitali P, Sweeney HL. 226th ENMC International Workshop:: Towards validated and qualified biomarkers for therapy development for Duchenne muscular dystrophy 20-22 January 2017, Heemskerk, The Netherlands. Neuromuscular Disorders : Nmd. 28: 77-86. PMID 29203356 DOI: 10.1016/j.nmd.2017.10.002  0.6
2017 Quattrocelli M, Capote J, Ohiri JC, Warner JL, Vo AH, Earley JU, Hadhazy M, Demonbreun AR, Spencer MJ, McNally EM. Genetic modifiers of muscular dystrophy act on sarcolemmal resealing and recovery from injury. Plos Genetics. 13: e1007070. PMID 29065150 DOI: 10.1371/journal.pgen.1007070  0.88
2017 Quattrocelli M, Salamone IM, Page P, Warner JL, Demonbreun AR, McNally EM. Intermittent Glucocorticoid Dosing Improves Muscle Repair and Function in Mice with Limb Girdle Muscular Dystrophy. The American Journal of Pathology. PMID 28823869 DOI: 10.1016/j.ajpath.2017.07.017  0.88
2017 Barefield DY, Puckelwartz MJ, Kim EY, Wilsbacher LD, Vo AH, Waters EA, Earley JU, Hadhazy M, Dellefave-Castillo LM, Pesce LL, McNally EM. Experimental Modeling Supports a Role for MyBP-HL as a Novel Myofilament Component in Arrhythmia and Dilated Cardiomyopathy. Circulation. PMID 28778945 DOI: 10.1161/CIRCULATIONAHA.117.028585  0.8
2017 Quattrocelli M, Barefield DY, Warner JL, Vo AH, Hadhazy M, Earley JU, Demonbreun AR, McNally EM. Intermittent glucocorticoid steroid dosing enhances muscle repair without eliciting muscle atrophy. The Journal of Clinical Investigation. PMID 28481224 DOI: 10.1172/JCI91445  0.88
2017 Demonbreun AR, McNally EM. Muscle cell communication in development and repair. Current Opinion in Pharmacology. 34: 7-14. PMID 28419894 DOI: 10.1016/j.coph.2017.03.008  0.88
2016 Quattrocelli M, Spencer MJ, McNally EM. Outside in: The matrix as a modifier of muscular dystrophy. Biochimica Et Biophysica Acta. PMID 28011285 DOI: 10.1016/j.bbamcr.2016.12.020  0.52
2016 Kim EY, Page P, Dellefave-Castillo LM, McNally EM, Wyatt EJ. Direct reprogramming of urine-derived cells with inducible MyoD for modeling human muscle disease. Skeletal Muscle. 6: 32. PMID 27906098 DOI: 10.1186/s13395-016-0103-9  0.52
2016 Vanhoutte D, Schips TG, Kwong JQ, Davis J, Tjondrokoesoemo A, Brody MJ, Sargent MA, Kanisicak O, Yi H, Gao QQ, Rabinowitz JE, Volk T, McNally EM, Molkentin JD. Thrombospondin expression in myofibers stabilizes muscle membranes. Elife. 5. PMID 27669143 DOI: 10.7554/eLife.17589  0.8
2016 Kim EY, Page P, Dellefave-Castillo LM, McNally EM, Wyatt EJ. Direct reprogramming of urine-derived cells with inducible MyoD for modeling human muscle disease. Skeletal Muscle. 6: 32. PMID 27651888 DOI: 10.1186/s13395-016-0103-9  0.8
2016 Nadadur RD, Broman MT, Boukens B, Mazurek SR, Yang X, van den Boogaard M, Bekeny J, Gadek M, Ward T, Zhang M, Qiao Y, Martin JF, Seidman CE, Seidman J, Christoffels V, ... ... McNally EM, et al. Pitx2 modulates a Tbx5-dependent gene regulatory network to maintain atrial rhythm. Science Translational Medicine. 8: 354ra115. PMID 27582060 DOI: 10.1126/scitranslmed.aaf4891  0.8
2016 Quattrocelli M, McNally EM. BMP and WNT: the road to cardiomyocytes is paved with precise modulation. Stem Cell Investigation. 3: 21. PMID 27488191 DOI: 10.21037/sci.2016.06.02  0.52
2016 Demonbreun AR, Quattrocelli M, Barefield DY, Allen MV, Swanson KE, McNally EM. An actin-dependent annexin complex mediates plasma membrane repair in muscle. The Journal of Cell Biology. PMID 27298325 DOI: 10.1083/jcb.201512022  0.8
2016 Lamar KM, Bogdanovich S, Gardner BB, Gao QQ, Miller T, Earley JU, Hadhazy M, Vo AH, Wren L, Molkentin JD, McNally EM. Overexpression of Latent TGFβ Binding Protein 4 in Muscle Ameliorates Muscular Dystrophy through Myostatin and TGFβ. Plos Genetics. 12: e1006019. PMID 27148972 DOI: 10.1371/journal.pgen.1006019  0.8
2016 Demonbreun AR, Allen MV, Warner JL, Barefield DY, Krishnan S, Swanson KE, Earley JU, McNally EM. Enhanced Muscular Dystrophy from Loss of Dysferlin Is Accompanied by Impaired Annexin A6 Translocation after Sarcolemmal Disruption. The American Journal of Pathology. PMID 27070822 DOI: 10.1016/j.ajpath.2016.02.005  0.8
2016 McNally EM, Wyatt EJ. Welcome to the splice age: antisense oligonucleotide-mediated exon skipping gains wider applicability. The Journal of Clinical Investigation. 126: 1236-8. PMID 26999602 DOI: 10.1172/JCI86799  0.8
2016 Lamar KM, Miller T, Dellefave-Castillo L, McNally EM. Genotype-Specific Interaction of Latent TGFβ Binding Protein 4 with TGFβ. Plos One. 11: e0150358. PMID 26918958 DOI: 10.1371/journal.pone.0150358  0.36
2016 Demonbreun AR, McNally EM. Plasma Membrane Repair in Health and Disease. Current Topics in Membranes. 77: 67-96. PMID 26781830 DOI: 10.1016/bs.ctm.2015.10.006  0.88
2016 Duan D, Rafael-Fortney JA, Blain A, Kass DA, McNally EM, Metzger JM, Spurney CF, Kinnett K. Standard Operating Procedures (SOPs) for Evaluating the Heart in Preclinical Studies of Duchenne Muscular Dystrophy. Journal of Cardiovascular Translational Research. 9: 85-6. PMID 26718928 DOI: 10.1007/s12265-015-9669-6  0.8
2015 Demonbreun AR, McNally EM. DNA Electroporation, Isolation and Imaging of Myofibers. Journal of Visualized Experiments : Jove. e53551. PMID 26780499 DOI: 10.3791/53551  0.88
2015 Demonbreun AR, Biersmith BH, McNally EM. Membrane fusion in muscle development and repair. Seminars in Cell & Developmental Biology. PMID 26537430 DOI: 10.1016/j.semcdb.2015.10.026  0.88
2015 Gao QQ, Wyatt E, Goldstein JA, LoPresti P, Castillo LM, Gazda A, Petrossian N, Earley JU, Hadhazy M, Barefield DY, Demonbreun AR, Bönnemann C, Wolf M, McNally EM. Reengineering a transmembrane protein to treat muscular dystrophy using exon skipping. The Journal of Clinical Investigation. PMID 26457733 DOI: 10.1172/JCI82768  0.92
2015 Demonbreun AR, Swanson KE, Rossi AE, Deveaux HK, Earley JU, Allen MV, Arya P, Bhattacharyya S, Band H, Pytel P, McNally EM. Eps 15 Homology Domain (EHD)-1 Remodels Transverse Tubules in Skeletal Muscle. Plos One. 10: e0136679. PMID 26325203 DOI: 10.1371/journal.pone.0136679  0.8
2015 Lenhart KC, O'Neill TJ, Cheng Z, Dee R, Demonbreun AR, Li J, Xiao X, McNally EM, Mack CP, Taylor JM. GRAF1 deficiency blunts sarcolemmal injury repair and exacerbates cardiac and skeletal muscle pathology in dystrophin-deficient mice. Skeletal Muscle. 5: 27. PMID 26301073 DOI: 10.1186/s13395-015-0054-6  0.88
2015 Vo AH, McNally EM. Modifier genes and their effect on Duchenne muscular dystrophy. Current Opinion in Neurology. 28: 528-34. PMID 26263473 DOI: 10.1097/WCO.0000000000000240  0.8
2015 Lee YS, Lehar A, Sebald S, Liu M, Swaggart KA, Talbot CC, Pytel P, Barton ER, McNally EM, Lee SJ. Muscle hypertrophy induced by myostatin inhibition accelerates degeneration in dysferlinopathy. Human Molecular Genetics. PMID 26206886 DOI: 10.1093/hmg/ddv288  1
2015 Gao QQ, McNally EM. The Dystrophin Complex: Structure, Function, and Implications for Therapy. Comprehensive Physiology. 5: 1223-39. PMID 26140716 DOI: 10.1002/cphy.c140048  0.32
2015 Gardner BB, Swaggart KA, Kim G, Watson S, McNally EM. Cardiac function in muscular dystrophy associates with abdominal muscle pathology. Journal of Neuromuscular Diseases. 2: 39-49. PMID 26029630 DOI: 10.3233/JND-140062  1
2015 McNally EM, Kaltman JR, Benson DW, Canter CE, Cripe LH, Duan D, Finder JD, Hoffman EP, Judge DP, Kertesz N, Kinnett K, Kirsch R, Metzger JM, Pearson GD, Rafael-Fortney JA, et al. Contemporary cardiac issues in Duchenne muscular dystrophy. Working Group of the National Heart, Lung, and Blood Institute in collaboration with Parent Project Muscular Dystrophy. Circulation. 131: 1590-8. PMID 25940966 DOI: 10.1161/CIRCULATIONAHA.114.015151  0.8
2015 McNally EM, George AL. New approaches to establish genetic causality. Trends in Cardiovascular Medicine. PMID 25864169 DOI: 10.1016/j.tcm.2015.02.013  0.8
2015 McNally EM, Barefield DY, Puckelwartz MJ. The genetic landscape of cardiomyopathy and its role in heart failure. Cell Metabolism. 21: 174-82. PMID 25651172 DOI: 10.1016/j.cmet.2015.01.013  0.44
2014 Wyatt EJ, Sweeney HL, McNally EM. Meeting Report: New Directions in Biology and Disease of Skeletal Muscle 2014. Journal of Neuromuscular Diseases. 1: 197-206. PMID 27858776  0.6
2014 Wyatt EJ, Sweeney HL, McNally EM. Meeting Report: New Directions in the Biology and Disease of Skeletal Muscle 2014. Journal of Neuromuscular Diseases. 1: 197-206. PMID 26207203 DOI: 10.3233/JND-149003  0.6
2014 Lamar KM, McNally EM. Genetic Modifiers for Neuromuscular Diseases. Journal of Neuromuscular Diseases. 1: 3-13. PMID 25729645 DOI: 10.3233/JND-140023  0.36
2014 Ceco E, Bogdanovich S, Gardner B, Miller T, DeJesus A, Earley JU, Hadhazy M, Smith LR, Barton ER, Molkentin JD, McNally EM. Targeting latent TGFβ release in muscular dystrophy. Science Translational Medicine. 6: 259ra144. PMID 25338755 DOI: 10.1126/scitranslmed.3010018  0.8
2014 Golbus JR, Puckelwartz MJ, Dellefave-Castillo L, Fahrenbach JP, Nelakuditi V, Pesce LL, Pytel P, McNally EM. Targeted analysis of whole genome sequence data to diagnose genetic cardiomyopathy. Circulation. Cardiovascular Genetics. 7: 751-9. PMID 25179549 DOI: 10.1161/CIRCGENETICS.113.000578  0.44
2014 Accornero F, Kanisicak O, Tjondrokoesoemo A, Attia AC, McNally EM, Molkentin JD. Myofiber-specific inhibition of TGFβ signaling protects skeletal muscle from injury and dystrophic disease in mice. Human Molecular Genetics. 23: 6903-15. PMID 25106553 DOI: 10.1093/hmg/ddu413  0.32
2014 Goldstein JA, Bogdanovich S, Beiriger A, Wren LM, Rossi AE, Gao QQ, Gardner BB, Earley JU, Molkentin JD, McNally EM. Excess SMAD signaling contributes to heart and muscle dysfunction in muscular dystrophy. Human Molecular Genetics. 23: 6722-31. PMID 25070948 DOI: 10.1093/hmg/ddu390  0.92
2014 Lenhart KC, Becherer AL, Li J, Xiao X, McNally EM, Mack CP, Taylor JM. GRAF1 promotes ferlin-dependent myoblast fusion. Developmental Biology. 393: 298-311. PMID 25019370 DOI: 10.1016/j.ydbio.2014.06.025  0.8
2014 Wissing ER, Boyer JG, Kwong JQ, Sargent MA, Karch J, McNally EM, Otsu K, Molkentin JD. P38α MAPK underlies muscular dystrophy and myofiber death through a Bax-dependent mechanism. Human Molecular Genetics. 23: 5452-63. PMID 24876160 DOI: 10.1093/hmg/ddu270  0.8
2014 Swaggart KA, Demonbreun AR, Vo AH, Swanson KE, Kim EY, Fahrenbach JP, Holley-Cuthrell J, Eskin A, Chen Z, Squire K, Heydemann A, Palmer AA, Nelson SF, McNally EM. Annexin A6 modifies muscular dystrophy by mediating sarcolemmal repair. Proceedings of the National Academy of Sciences of the United States of America. 111: 6004-9. PMID 24717843 DOI: 10.1073/pnas.1324242111  0.8
2014 Fahrenbach JP, Stoller D, Kim G, Aggarwal N, Yerokun B, Earley JU, Hadhazy M, Shi NQ, Makielski JC, McNally EM. Abcc9 is required for the transition to oxidative metabolism in the newborn heart. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 28: 2804-15. PMID 24648545 DOI: 10.1096/fj.13-244459  0.8
2014 Fahrenbach JP, Andrade J, McNally EM. The CO-Regulation Database (CORD): a tool to identify coordinately expressed genes. Plos One. 9: e90408. PMID 24599084 DOI: 10.1371/journal.pone.0090408  0.4
2014 Demonbreun AR, McNally EM. Dynamin 2 the rescue for centronuclear myopathy. The Journal of Clinical Investigation. 124: 976-8. PMID 24569368 DOI: 10.1172/JCI74434  0.88
2014 Puckelwartz MJ, Pesce LL, Nelakuditi V, Dellefave-Castillo L, Golbus JR, Day SM, Cappola TP, Dorn GW, Foster IT, McNally EM. Supercomputing for the parallelization of whole genome analysis. Bioinformatics (Oxford, England). 30: 1508-13. PMID 24526712 DOI: 10.1093/bioinformatics/btu071  0.8
2014 Posey AD, Swanson KE, Alvarez MG, Krishnan S, Earley JU, Band H, Pytel P, McNally EM, Demonbreun AR. EHD1 mediates vesicle trafficking required for normal muscle growth and transverse tubule development. Developmental Biology. 387: 179-90. PMID 24440153 DOI: 10.1016/j.ydbio.2014.01.004  0.8
2014 Swaggart KA, McNally EM. Modifiers of heart and muscle function: where genetics meets physiology. Experimental Physiology. 99: 621-6. PMID 24213858 DOI: 10.1113/expphysiol.2013.075887  1
2014 Demonbreun AR, Rossi AE, Alvarez MG, Swanson KE, Deveaux HK, Earley JU, Hadhazy M, Vohra R, Walter GA, Pytel P, McNally EM. Dysferlin and myoferlin regulate transverse tubule formation and glycerol sensitivity. The American Journal of Pathology. 184: 248-59. PMID 24177035 DOI: 10.1016/j.ajpath.2013.09.009  0.8
2013 Ceco E, McNally EM. Modifying muscular dystrophy through transforming growth factor-β. The Febs Journal. 280: 4198-209. PMID 23551962 DOI: 10.1111/febs.12266  0.84
2013 Flanigan KM, Ceco E, Lamar KM, Kaminoh Y, Dunn DM, Mendell JR, King WM, Pestronk A, Florence JM, Mathews KD, Finkel RS, Swoboda KJ, Gappmaier E, Howard MT, Day JW, ... ... McNally EM, et al. LTBP4 genotype predicts age of ambulatory loss in Duchenne muscular dystrophy. Annals of Neurology. 73: 481-8. PMID 23440719 DOI: 10.1002/ana.23819  0.8
2012 Heydemann A, Swaggart KA, Kim GH, Holley-Cuthrell J, Hadhazy M, McNally EM. The superhealing MRL background improves muscular dystrophy. Skeletal Muscle. 2: 26. PMID 23216833 DOI: 10.1186/2044-5040-2-26  1
2012 Golbus JR, Puckelwartz MJ, Fahrenbach JP, Dellefave-Castillo LM, Wolfgeher D, McNally EM. Population-based variation in cardiomyopathy genes. Circulation. Cardiovascular Genetics. 5: 391-9. PMID 22763267 DOI: 10.1161/CIRCGENETICS.112.962928  0.4
2012 Arnolds DE, Liu F, Fahrenbach JP, Kim GH, Schillinger KJ, Smemo S, McNally EM, Nobrega MA, Patel VV, Moskowitz IP. TBX5 drives Scn5a expression to regulate cardiac conduction system function. The Journal of Clinical Investigation. 122: 2509-18. PMID 22728936 DOI: 10.1172/JCI62617  0.8
2012 Lorts A, Schwanekamp JA, Baudino TA, McNally EM, Molkentin JD. Deletion of periostin reduces muscular dystrophy and fibrosis in mice by modulating the transforming growth factor-β pathway. Proceedings of the National Academy of Sciences of the United States of America. 109: 10978-83. PMID 22711826 DOI: 10.1073/pnas.1204708109  0.32
2012 McNally EM, Goldstein JA. Interplay between heart and skeletal muscle disease in heart failure: the 2011 George E. Brown Memorial Lecture. Circulation Research. 110: 749-54. PMID 22383709 DOI: 10.1161/CIRCRESAHA.111.256776  0.92
2011 Posey AD, Demonbreun A, McNally EM. Ferlin proteins in myoblast fusion and muscle growth. Current Topics in Developmental Biology. 96: 203-30. PMID 21621072 DOI: 10.1016/B978-0-12-385940-2.00008-5  0.44
2011 McNally EM, Patel AR. Cardiac magnetic resonance of left ventricular trabeculation: the new normal. Circulation. Cardiovascular Imaging. 4: 84-6. PMID 21406661 DOI: 10.1161/CIRCIMAGING.110.962472  0.8
2011 Posey AD, Pytel P, Gardikiotes K, Demonbreun AR, Rainey M, George M, Band H, McNally EM. Endocytic recycling proteins EHD1 and EHD2 interact with fer-1-like-5 (Fer1L5) and mediate myoblast fusion. The Journal of Biological Chemistry. 286: 7379-88. PMID 21177873 DOI: 10.1074/jbc.M110.157222  0.88
2011 Goldstein JA, Kelly SM, LoPresti PP, Heydemann A, Earley JU, Ferguson EL, Wolf MJ, McNally EM. SMAD signaling drives heart and muscle dysfunction in a Drosophila model of muscular dystrophy. Human Molecular Genetics. 20: 894-904. PMID 21138941 DOI: 10.1093/hmg/ddq528  0.92
2011 Demonbreun AR, Fahrenbach JP, Deveaux K, Earley JU, Pytel P, McNally EM. Impaired muscle growth and response to insulin-like growth factor 1 in dysferlin-mediated muscular dystrophy. Human Molecular Genetics. 20: 779-89. PMID 21127009 DOI: 10.1093/hmg/ddq522  0.88
2011 Hofmann Bowman MA, Gawdzik J, Bukhari U, Husain AN, Toth PT, Kim G, Earley J, McNally EM. S100A12 in vascular smooth muscle accelerates vascular calcification in apolipoprotein E-null mice by activating an osteogenic gene regulatory program. Arteriosclerosis, Thrombosis, and Vascular Biology. 31: 337-44. PMID 20966394 DOI: 10.1161/ATVBAHA.110.217745  0.44
2011 Swaggart KA, Heydemann A, Palmer AA, McNally EM. Distinct genetic regions modify specific muscle groups in muscular dystrophy. Physiological Genomics. 43: 24-31. PMID 20959497 DOI: 10.1152/physiolgenomics.00172.2010  0.8
2010 Stoller DA, Fahrenbach JP, Chalupsky K, Tan BH, Aggarwal N, Metcalfe J, Hadhazy M, Shi NQ, Makielski JC, McNally EM. Cardiomyocyte sulfonylurea receptor 2-KATP channel mediates cardioprotection and ST segment elevation. American Journal of Physiology. Heart and Circulatory Physiology. 299: H1100-8. PMID 20656890 DOI: 10.1152/ajpheart.00084.2010  0.8
2010 Goldstein JA, McNally EM. Mechanisms of muscle weakness in muscular dystrophy. The Journal of General Physiology. 136: 29-34. PMID 20584890 DOI: 10.1085/jgp.201010436  0.92
2010 Demonbreun AR, Lapidos KA, Heretis K, Levin S, Dale R, Pytel P, Svensson EC, McNally EM. Myoferlin regulation by NFAT in muscle injury, regeneration and repair. Journal of Cell Science. 123: 2413-22. PMID 20571050 DOI: 10.1242/jcs.065375  0.88
2010 Lakdawala NK, Dellefave L, Redwood CS, Sparks E, Cirino AL, Depalma S, Colan SD, Funke B, Zimmerman RS, Robinson P, Watkins H, Seidman CE, Seidman JG, McNally EM, Ho CY. Familial dilated cardiomyopathy caused by an alpha-tropomyosin mutation: the distinctive natural history of sarcomeric dilated cardiomyopathy. Journal of the American College of Cardiology. 55: 320-9. PMID 20117437 DOI: 10.1016/j.jacc.2009.11.017  0.8
2010 Demonbreun AR, Posey AD, Heretis K, Swaggart KA, Earley JU, Pytel P, McNally EM. Myoferlin is required for insulin-like growth factor response and muscle growth. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 24: 1284-95. PMID 20008164 DOI: 10.1096/fj.09-136309  1
2010 Puckelwartz MJ, Kessler EJ, Kim G, Dewitt MM, Zhang Y, Earley JU, Depreux FF, Holaska J, Mewborn SK, Pytel P, McNally EM. Nesprin-1 mutations in human and murine cardiomyopathy. Journal of Molecular and Cellular Cardiology. 48: 600-8. PMID 19944109 DOI: 10.1016/j.yjmcc.2009.11.006  0.8
2010 Hofmann Bowman M, Wilk J, Heydemann A, Kim G, Rehman J, Lodato JA, Raman J, McNally EM. S100A12 mediates aortic wall remodeling and aortic aneurysm. Circulation Research. 106: 145-54. PMID 19875725 DOI: 10.1161/CIRCRESAHA.109.209486  0.6
2010 Pytel P, Husain A, Moskowitz I, Raman J, MacLeod H, Anderson AS, Burke M, McNally EM. Ventricular fibrillation following autologous intramyocardial cell therapy for inherited cardiomyopathy. Cardiovascular Pathology : the Official Journal of the Society For Cardiovascular Pathology. 19: e33-6. PMID 19026577 DOI: 10.1016/j.carpath.2008.09.004  0.44
2009 Dellefave LM, Pytel P, Mewborn S, Mora B, Guris DL, Fedson S, Waggoner D, Moskowitz I, McNally EM. Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation. Circulation. Cardiovascular Genetics. 2: 442-9. PMID 20031619 DOI: 10.1161/CIRCGENETICS.109.861955  0.44
2009 Heydemann A, Ceco E, Lim JE, Hadhazy M, Ryder P, Moran JL, Beier DR, Palmer AA, McNally EM. Latent TGF-beta-binding protein 4 modifies muscular dystrophy in mice. The Journal of Clinical Investigation. 119: 3703-12. PMID 19884661 DOI: 10.1172/JCI39845  0.8
2009 Millay DP, Maillet M, Roche JA, Sargent MA, McNally EM, Bloch RJ, Molkentin JD. Genetic manipulation of dysferlin expression in skeletal muscle: novel insights into muscular dystrophy. The American Journal of Pathology. 175: 1817-23. PMID 19834057 DOI: 10.2353/ajpath.2009.090107  0.32
2009 Stoller D, Pytel P, Katz S, Earley JU, Collins K, Metcalfe J, Lang RM, McNally EM. Impaired exercise tolerance and skeletal muscle myopathy in sulfonylurea receptor-2 mutant mice. American Journal of Physiology. Regulatory, Integrative and Comparative Physiology. 297: R1144-53. PMID 19675276 DOI: 10.1152/ajpregu.00081.2009  0.52
2009 Puckelwartz MJ, Kessler E, Zhang Y, Hodzic D, Randles KN, Morris G, Earley JU, Hadhazy M, Holaska JM, Mewborn SK, Pytel P, McNally EM. Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in mice. Human Molecular Genetics. 18: 607-20. PMID 19008300 DOI: 10.1093/hmg/ddn386  0.8
2008 Doherty KR, Demonbreun AR, Wallace GQ, Cave A, Posey AD, Heretis K, Pytel P, McNally EM. The endocytic recycling protein EHD2 interacts with myoferlin to regulate myoblast fusion. The Journal of Biological Chemistry. 283: 20252-60. PMID 18502764 DOI: 10.1074/jbc.M802306200  1
2008 Bogdanovich S, McNally EM, Khurana TS. Myostatin blockade improves function but not histopathology in a murine model of limb-girdle muscular dystrophy 2C. Muscle & Nerve. 37: 308-16. PMID 18041051 DOI: 10.1002/mus.20920  0.32
2007 McNally EM, Pytel P. Muscle diseases: the muscular dystrophies. Annual Review of Pathology. 2: 87-109. PMID 18039094 DOI: 10.1146/annurev.pathol.2.010506.091936  0.44
2007 Allikian MJ, Bhabha G, Dospoy P, Heydemann A, Ryder P, Earley JU, Wolf MJ, Rockman HA, McNally EM. Reduced life span with heart and muscle dysfunction in Drosophila sarcoglycan mutants. Human Molecular Genetics. 16: 2933-43. PMID 17855453 DOI: 10.1093/hmg/ddm254  0.8
2007 Stoller D, Kakkar R, Smelley M, Chalupsky K, Earley JU, Shi NQ, Makielski JC, McNally EM. Mice lacking sulfonylurea receptor 2 (SUR2) ATP-sensitive potassium channels are resistant to acute cardiovascular stress. Journal of Molecular and Cellular Cardiology. 43: 445-54. PMID 17765261 DOI: 10.1016/j.yjmcc.2007.07.058  0.52
2007 Bernatchez PN, Acevedo L, Fernandez-Hernando C, Murata T, Chalouni C, Kim J, Erdjument-Bromage H, Shah V, Gratton JP, McNally EM, Tempst P, Sessa WC. Myoferlin regulates vascular endothelial growth factor receptor-2 stability and function. The Journal of Biological Chemistry. 282: 30745-53. PMID 17702744 DOI: 10.1074/jbc.M704798200  0.8
2007 MacLeod H, Pytel P, Wollmann R, Chelmicka-Schorr E, Silver K, Anderson RB, Waggoner D, McNally EM. A novel FKRP mutation in congenital muscular dystrophy disrupts the dystrophin glycoprotein complex. Neuromuscular Disorders : Nmd. 17: 285-9. PMID 17336067 DOI: 10.1016/j.nmd.2007.01.005  0.8
2007 Heydemann A, McNally EM. Consequences of disrupting the dystrophin-sarcoglycan complex in cardiac and skeletal myopathy. Trends in Cardiovascular Medicine. 17: 55-9. PMID 17292047 DOI: 10.1016/j.tcm.2006.12.002  0.6
2007 Parsons SA, Millay DP, Sargent MA, Naya FJ, McNally EM, Sweeney HL, Molkentin JD. Genetic disruption of calcineurin improves skeletal muscle pathology and cardiac disease in a mouse model of limb-girdle muscular dystrophy. The Journal of Biological Chemistry. 282: 10068-78. PMID 17289669 DOI: 10.1074/jbc.M609368200  0.8
2007 Allikian MJ, McNally EM. Processing and assembly of the dystrophin glycoprotein complex. Traffic (Copenhagen, Denmark). 8: 177-83. PMID 17274800 DOI: 10.1111/j.1600-0854.2006.00519.x  0.8
2007 Heydemann A, Demonbreun A, Hadhazy M, Earley JU, McNally EM. Nuclear sequestration of delta-sarcoglycan disrupts the nuclear localization of lamin A/C and emerin in cardiomyocytes. Human Molecular Genetics. 16: 355-63. PMID 17164264 DOI: 10.1093/hmg/ddl453  0.8
2007 Heydemann A, Doherty KR, McNally EM. Genetic modifiers of muscular dystrophy: implications for therapy. Biochimica Et Biophysica Acta. 1772: 216-28. PMID 16916601 DOI: 10.1016/j.bbadis.2006.06.013  1
2006 Parsons SA, Millay DP, Sargent MA, McNally EM, Molkentin JD. Age-dependent effect of myostatin blockade on disease severity in a murine model of limb-girdle muscular dystrophy. The American Journal of Pathology. 168: 1975-85. PMID 16723712 DOI: 10.2353/ajpath.2006.051316  0.8
2006 Kakkar R, Ye B, Stoller DA, Smelley M, Shi NQ, Galles K, Hadhazy M, Makielski JC, McNally EM. Spontaneous coronary vasospasm in KATP mutant mice arises from a smooth muscle-extrinsic process. Circulation Research. 98: 682-9. PMID 16456098 DOI: 10.1161/01.RES.0000207498.40005.e7  0.8
2005 Doherty KR, Cave A, Davis DB, Delmonte AJ, Posey A, Earley JU, Hadhazy M, McNally EM. Normal myoblast fusion requires myoferlin. Development (Cambridge, England). 132: 5565-75. PMID 16280346 DOI: 10.1242/dev.02155  0.8
2005 Firoved AM, Miller GF, Moayeri M, Kakkar R, Shen Y, Wiggins JF, McNally EM, Tang WJ, Leppla SH. Bacillus anthracis edema toxin causes extensive tissue lesions and rapid lethality in mice. The American Journal of Pathology. 167: 1309-20. PMID 16251415 DOI: 10.1016/S0002-9440(10)61218-7  0.8
2005 Heydemann A, Huber JM, Demonbreun A, Hadhazy M, McNally EM. Genetic background influences muscular dystrophy. Neuromuscular Disorders : Nmd. 15: 601-9. PMID 16084087 DOI: 10.1016/j.nmd.2005.05.004  0.8
2005 Pare GC, Easlick JL, Mislow JM, McNally EM, Kapiloff MS. Nesprin-1alpha contributes to the targeting of mAKAP to the cardiac myocyte nuclear envelope. Experimental Cell Research. 303: 388-99. PMID 15652351 DOI: 10.1016/j.yexcr.2004.10.009  0.8
2004 Lapidos KA, Chen YE, Earley JU, Heydemann A, Huber JM, Chien M, Ma A, McNally EM. Transplanted hematopoietic stem cells demonstrate impaired sarcoglycan expression after engraftment into cardiac and skeletal muscle. The Journal of Clinical Investigation. 114: 1577-85. PMID 15578090 DOI: 10.1172/JCI23071  0.6
2004 Heydemann A, McNally EM. Regenerating more than muscle in muscular dystrophy. Circulation. 110: 3290-2. PMID 15557384 DOI: 10.1161/01.CIR.0000149847.84152.0B  0.6
2004 Allikian MJ, Hack AA, Mewborn S, Mayer U, McNally EM. Genetic compensation for sarcoglycan loss by integrin alpha7beta1 in muscle. Journal of Cell Science. 117: 3821-30. PMID 15252120 DOI: 10.1242/jcs.01234  0.8
2004 Wheeler MT, Allikian MJ, Heydemann A, Hadhazy M, Zarnegar S, McNally EM. Smooth muscle cell-extrinsic vascular spasm arises from cardiomyocyte degeneration in sarcoglycan-deficient cardiomyopathy. The Journal of Clinical Investigation. 113: 668-75. PMID 14991064 DOI: 10.1172/JCI20410  0.8
2004 Wheeler MT, Korcarz CE, Collins KA, Lapidos KA, Hack AA, Lyons MR, Zarnegar S, Earley JU, Lang RM, McNally EM. Secondary coronary artery vasospasm promotes cardiomyopathy progression. The American Journal of Pathology. 164: 1063-71. PMID 14982859 DOI: 10.1016/S0002-9440(10)63193-8  0.8
2004 Heydemann A, Huber JM, Kakkar R, Wheeler MT, McNally EM. Functional nitric oxide synthase mislocalization in cardiomyopathy. Journal of Molecular and Cellular Cardiology. 36: 213-23. PMID 14871549 DOI: 10.1016/j.yjmcc.2003.09.020  0.6
2003 Doherty KR, McNally EM. Repairing the tears: dysferlin in muscle membrane repair. Trends in Molecular Medicine. 9: 327-30. PMID 12928033  1
2003 MacLeod HM, Culley MR, Huber JM, McNally EM. Lamin A/C truncation in dilated cardiomyopathy with conduction disease. Bmc Medical Genetics. 4: 4. PMID 12854972 DOI: 10.1186/1471-2350-4-4  0.8
2002 Mislow JM, Holaska JM, Kim MS, Lee KK, Segura-Totten M, Wilson KL, McNally EM. Nesprin-1alpha self-associates and binds directly to emerin and lamin A in vitro. Febs Letters. 525: 135-40. PMID 12163176  0.36
2002 Zhu X, Wheeler MT, Hadhazy M, Lam MY, McNally EM. Cardiomyopathy is independent of skeletal muscle disease in muscular dystrophy. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 16: 1096-8. PMID 12039854 DOI: 10.1096/fj.01-0954fje  0.8
2002 Davis DB, Doherty KR, Delmonte AJ, McNally EM. Calcium-sensitive phospholipid binding properties of normal and mutant ferlin C2 domains. The Journal of Biological Chemistry. 277: 22883-8. PMID 11959863 DOI: 10.1074/jbc.M201858200  0.8
2002 Mislow JM, Kim MS, Davis DB, McNally EM. Myne-1, a spectrin repeat transmembrane protein of the myocyte inner nuclear membrane, interacts with lamin A/C. Journal of Cell Science. 115: 61-70. PMID 11801724  0.8
2001 Porter JD, Merriam AP, Hack AA, Andrade FH, McNally EM. Extraocular muscle is spared despite the absence of an intact sarcoglycan complex in gamma- or delta-sarcoglycan-deficient mice. Neuromuscular Disorders : Nmd. 11: 197-207. PMID 11257478 DOI: 10.1016/S0960-8966(00)00171-1  0.8
2001 Cordier L, Gao GP, Hack AA, McNally EM, Wilson JM, Chirmule N, Sweeney HL. Muscle-specific promoters may be necessary for adeno-associated virus-mediated gene transfer in the treatment of muscular dystrophies. Human Gene Therapy. 12: 205-15. PMID 11177557 DOI: 10.1089/104303401750061267  0.8
2000 Cordier L, Hack AA, Scott MO, Barton-Davis ER, Gao G, Wilson JM, McNally EM, Sweeney HL. Rescue of skeletal muscles of gamma-sarcoglycan-deficient mice with adeno-associated virus-mediated gene transfer. Molecular Therapy : the Journal of the American Society of Gene Therapy. 1: 119-29. PMID 10933922 DOI: 10.1006/mthe.1999.0019  0.8
2000 Hack AA, Lam MY, Cordier L, Shoturma DI, Ly CT, Hadhazy MA, Hadhazy MR, Sweeney HL, McNally EM. Differential requirement for individual sarcoglycans and dystrophin in the assembly and function of the dystrophin-glycoprotein complex. Journal of Cell Science. 113: 2535-44. PMID 10862711  0.8
2000 Hack AA, Groh ME, McNally EM. Sarcoglycans in muscular dystrophy. Microscopy Research and Technique. 48: 167-80. PMID 10679964 DOI: 10.1002/(SICI)1097-0029(20000201/15)48:3/4<167::AID-JEMT5>3.0.CO;2-T  0.8
2000 Thompson TG, Chan YM, Hack AA, Brosius M, Rajala M, Lidov HG, McNally EM, Watkins S, Kunkel LM. Filamin 2 (FLN2): A muscle-specific sarcoglycan interacting protein. The Journal of Cell Biology. 148: 115-26. PMID 10629222 DOI: 10.1083/jcb.148.1.115  0.8
1999 Hack AA, Cordier L, Shoturma DI, Lam MY, Sweeney HL, McNally EM. Muscle degeneration without mechanical injury in sarcoglycan deficiency. Proceedings of the National Academy of Sciences of the United States of America. 96: 10723-8. PMID 10485893 DOI: 10.1073/pnas.96.19.10723  0.8
1998 Hack AA, Ly CT, Jiang F, Clendenin CJ, Sigrist KS, Wollmann RL, McNally EM. Gamma-sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin. The Journal of Cell Biology. 142: 1279-87. PMID 9732288 DOI: 10.1083/jcb.142.5.1279  0.8
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