| Year |
Citation |
Score |
| 2024 |
O'Brien JG, Willis AB, Long AM, Kwon JM, Lee G, Li FW, Page PG, Vo AH, Hadhazy M, Spencer MJ, Crosbie RH, Demonbreun AR, McNally EM. The super-healing MRL strain promotes muscle growth in muscular dystrophy through a regenerative extracellular matrix. Jci Insight. PMID 38175727 DOI: 10.1172/jci.insight.173246 |
0.693 |
|
| 2023 |
Fullenkamp DE, Willis AB, Curtin JL, Amaral AP, Dittloff KT, Harris SI, Chychula IA, Holgren CW, Burridge PW, Russell B, Demonbreun AR, McNally EM. Physiological stress improves stem cell modeling of dystrophic cardiomyopathy. Disease Models & Mechanisms. PMID 38050701 DOI: 10.1242/dmm.050487 |
0.621 |
|
| 2023 |
Long AM, Lee G, Demonbreun A, McNally EM. Extracellular matrix contribution to disease progression and dysfunction in myopathy. American Journal of Physiology. Cell Physiology. PMID 37746696 DOI: 10.1152/ajpcell.00182.2023 |
0.718 |
|
| 2023 |
O'Brien JG, Willis AB, Long AM, Kwon J, Lee G, Li F, Page PGT, Vo AH, Hadhazy M, Crosbie RH, Demonbreun AR, McNally EM. The super-healing MRL strain promotes muscle growth in muscular dystrophy through a regenerative extracellular matrix. Biorxiv : the Preprint Server For Biology. PMID 37425960 DOI: 10.1101/2023.06.29.547098 |
0.69 |
|
| 2023 |
Waters EA, Haney CR, Vaught LA, McNally EM, Demonbreun AR. New semi-automated tool for the quantitation of MR imaging to estimate in vivo muscle disease severity in mice. Biorxiv : the Preprint Server For Biology. PMID 37293050 DOI: 10.1101/2023.05.23.541310 |
0.724 |
|
| 2022 |
Wintzinger M, Miz K, York A, Demonbreun AR, Molkentin JD, McNally EM, Quattrocelli M. Effects of Glucocorticoids in Murine Models of Duchenne and Limb-Girdle Muscular Dystrophy. Methods in Molecular Biology (Clifton, N.J.). 2587: 467-478. PMID 36401044 DOI: 10.1007/978-1-0716-2772-3_24 |
0.722 |
|
| 2022 |
Demonbreun AR, Bogdanovic E, Vaught LA, Reiser NL, Fallon KS, Long AM, Oosterbaan CC, Hadhazy M, Page PG, Joseph PRB, Cowen G, Telenson AM, Khatri A, Sadleir KR, Vassar R, ... McNally EM, et al. A conserved annexin A6-mediated membrane repair mechanism in muscle, heart, and nerve. Jci Insight. 7. PMID 35866481 DOI: 10.1172/jci.insight.158107 |
0.681 |
|
| 2022 |
Sancilio A, Schrock JM, Demonbreun AR, D'Aquila RT, Mustanski B, Vaught LA, Reiser NL, Velez MP, Hsieh RR, Ryan DT, Saber R, McNally EM, McDade TW. COVID-19 symptom severity predicts neutralizing antibody activity in a community-based serological study. Scientific Reports. 12: 12269. PMID 35851303 DOI: 10.1038/s41598-022-15791-6 |
0.593 |
|
| 2022 |
McDade TW, Sancilio A, D'Aquila R, Mustanski B, Vaught LA, Reiser NL, Velez ME, Hsieh RR, Ryan DT, Saber R, McNally EM, Demonbreun AR. Low Levels of Neutralizing Antibodies After Natural Infection With Severe Acute Respiratory Syndrome Coronavirus 2 in a Community-Based Serological Study. Open Forum Infectious Diseases. 9: ofac055. PMID 35252468 DOI: 10.1093/ofid/ofac055 |
0.584 |
|
| 2022 |
Simons LM, Lorenzo-Redondo R, Gibson M, Kinch SL, Vandervaart JP, Reiser NL, Eren M, Lux E, McNally EM, Tambur AR, Vaughan DE, Bachta KER, Demonbreun AR, Satchell KJF, Achenbach CJ, et al. Assessment of Virological Contributions to COVID-19 Outcomes in a Longitudinal Cohort of Hospitalized Adults. Open Forum Infectious Diseases. 9: ofac027. PMID 35198645 DOI: 10.1093/ofid/ofac027 |
0.584 |
|
| 2022 |
Quattrocelli M, Wintzinger M, Miz K, Levine DC, Peek CB, Bass J, McNally EM. Muscle mitochondrial remodeling by intermittent glucocorticoid drugs requires an intact circadian clock and muscle PGC1α. Science Advances. 8: eabm1189. PMID 35179955 DOI: 10.1126/sciadv.abm1189 |
0.383 |
|
| 2022 |
Salamone IM, Quattrocelli M, Barefield DY, Page PG, Tahtah I, Hadhazy M, Tomar G, McNally EM. Intermittent glucocorticoid treatment enhances skeletal muscle performance through sexually dimorphic mechanisms. The Journal of Clinical Investigation. 132. PMID 35143417 DOI: 10.1172/JCI149828 |
0.816 |
|
| 2022 |
Zelikovich AS, Joslin BC, Casey P, McNally EM, Ajroud-Driss S. An Open Label Exploratory Clinical Trial Evaluating Safety and Tolerability of Once-Weekly Prednisone in Becker and Limb-Girdle Muscular Dystrophy. Journal of Neuromuscular Diseases. PMID 35124660 DOI: 10.3233/JND-210741 |
0.368 |
|
| 2021 |
Glazer AM, Davogustto GE, Shaffer CM, Vanoye CG, Desai RR, Farber-Eger E, Dikilitas O, Shang N, Pacheco JA, Yang T, Muhammad A, Mosley JD, Van Driest SL, Wells QS, Shaffer LL, ... ... McNally EM, et al. Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study. Circulation. PMID 34930020 DOI: 10.1161/CIRCULATIONAHA.121.055562 |
0.43 |
|
| 2021 |
Demonbreun AR, Velez MP, Saber R, Ryan DT, Sancilio A, McDade TW, McNally EM. mRNA intramuscular vaccination produces a robust IgG antibody response in advanced neuromuscular disease. Neuromuscular Disorders : Nmd. 32: 33-35. PMID 34920929 DOI: 10.1016/j.nmd.2021.11.006 |
0.624 |
|
| 2021 |
Johnston JR, McNally EM. Genetic correction strategies for Duchenne Muscular Dystrophy and their impact on the heart. Progress in Pediatric Cardiology. 63. PMID 34898968 DOI: 10.1016/j.ppedcard.2021.101460 |
0.395 |
|
| 2021 |
Mustanski B, Saber R, Ryan DT, Benbow N, Madkins K, Hayford C, Newcomb ME, Schrock JM, Vaught LA, Reiser NL, Velez MP, Hsieh RR, Demonbreun AR, D'Aquila R, McNally EM, et al. Geographic disparities in COVID-19 case rates are not reflected in seropositivity rates using a neighborhood survey in Chicago. Annals of Epidemiology. PMID 34728335 DOI: 10.1016/j.annepidem.2021.10.006 |
0.579 |
|
| 2021 |
McNally EM, Demonbreun AR. Resealing and rebuilding injured muscle. Science (New York, N.Y.). 374: 262-263. PMID 34648349 DOI: 10.1126/science.abm2240 |
0.732 |
|
| 2021 |
Demonbreun AR, Fallon KS, Oosterbaan CC, Vaught LA, Reiser NL, Bogdanovic E, Velez MP, Salamone IM, Page PGT, Hadhazy M, Quattrocelli M, Barefield DY, Wood LD, Gonzalez JP, Morris C, ... McNally EM, et al. Anti-latent TGFβ binding protein 4 antibody improves muscle function and reduces muscle fibrosis in muscular dystrophy. Science Translational Medicine. 13: eabf0376. PMID 34516828 DOI: 10.1126/scitranslmed.abf0376 |
0.831 |
|
| 2021 |
McDade TW, Demonbreun AR, Sancilio A, Mustanski B, D'Aquila RT, McNally EM. Durability of antibody response to vaccination and surrogate neutralization of emerging variants based on SARS-CoV-2 exposure history. Scientific Reports. 11: 17325. PMID 34462501 DOI: 10.1038/s41598-021-96879-3 |
0.592 |
|
| 2021 |
Barefield DY, Sell JJ, Tahtah I, Kearns SD, McNally EM, Demonbreun AR. Loss of dysferlin or myoferlin results in differential defects in excitation-contraction coupling in mouse skeletal muscle. Scientific Reports. 11: 15865. PMID 34354129 DOI: 10.1038/s41598-021-95378-9 |
0.723 |
|
| 2021 |
Sancilio AE, D'Aquila RT, McNally EM, Velez MP, Ison MG, Demonbreun AR, McDade TW. A surrogate virus neutralization test to quantify antibody-mediated inhibition of SARS-CoV-2 in finger stick dried blood spot samples. Scientific Reports. 11: 15321. PMID 34321523 DOI: 10.1038/s41598-021-94653-z |
0.588 |
|
| 2021 |
Schrock JM, Ryan DT, Saber R, Benbow N, Vaught LA, Reiser N, Velez MP, Hsieh R, Newcomb M, Demonbreun AR, Mustanski B, McNally EM, D'Aquila R, McDade TW. Cohabitation With a Known Coronavirus Disease 2019 Case Is Associated With Greater Antibody Concentration and Symptom Severity in a Community-Based Sample of Seropositive Adults. Open Forum Infectious Diseases. 8: ofab244. PMID 34316503 DOI: 10.1093/ofid/ofab244 |
0.597 |
|
| 2021 |
Demonbreun AR, Sancilio A, Velez MP, Ryan DT, Saber R, Vaught LA, Reiser NL, Hsieh RR, D'Aquila RT, Mustanski B, McNally EM, McDade TW. Comparison of IgG and neutralizing antibody responses after one or two doses of COVID-19 mRNA vaccine in previously infected and uninfected individuals. Eclinicalmedicine. 38: 101018. PMID 34278286 DOI: 10.1016/j.eclinm.2021.101018 |
0.585 |
|
| 2021 |
Demonbreun AR, Sancilio A, Velez ME, Ryan DT, Pesce L, Saber R, Vaught LA, Reiser NL, Hsieh RR, D'Aquila RT, Mustanski B, McDade TW, McNally EM. COVID-19 mRNA vaccination generates greater IgG levels in women compared to men. The Journal of Infectious Diseases. PMID 34117873 DOI: 10.1093/infdis/jiab314 |
0.575 |
|
| 2021 |
Schrock JM, Ryan DT, Saber R, Benbow N, Vaught LA, Reiser N, Velez MP, Hsieh R, Newcomb M, Demonbreun AR, Mustanski B, McNally EM, D'Aquila R, McDade TW. Exposure to SARS-CoV-2 within the household is associated with greater symptom severity and stronger antibody responses in a community-based sample of seropositive adults. Medrxiv : the Preprint Server For Health Sciences. PMID 33758903 DOI: 10.1101/2021.03.11.21253421 |
0.588 |
|
| 2021 |
Demonbreun AR, McDade TW, Pesce LL, Vaught LA, Reiser NL, Bogdanovic E, Velez MP, Hsieh RR, Simons LM, Saber R, Ryan DT, Ison MG, Hultquist JF, Wilkins JT, D'Aquila RT, ... ... McNally EM, et al. Patterns and persistence of SARS-CoV-2 IgG antibodies in Chicago to monitor COVID-19 exposure. Jci Insight. PMID 33755598 DOI: 10.1172/jci.insight.146148 |
0.582 |
|
| 2021 |
Gacita AM, Fullenkamp DE, Ohiri J, Pottinger T, Puckelwartz MJ, Nobrega MA, McNally EM. Genetic Variation in Enhancers Modifies Cardiomyopathy Gene Expression and Progression. Circulation. PMID 33478249 DOI: 10.1161/CIRCULATIONAHA.120.050432 |
0.599 |
|
| 2020 |
Demonbreun AR, McDade TW, Pesce L, Vaught LA, Reiser NL, Bogdanovic E, Velez ME, Hsieh RR, Klaisner CN, Simons LM, Saber R, Ryan DT, Ison MG, Hultquist JF, Wilkins JT, ... ... McNally EM, et al. Patterns and persistence of SARS-CoV-2 IgG antibodies in a US metropolitan site. Medrxiv : the Preprint Server For Health Sciences. PMID 33236031 DOI: 10.1101/2020.11.17.20233452 |
0.58 |
|
| 2020 |
Liu J, Campagna J, John V, Damoiseaux R, Mokhonova E, Becerra D, Meng H, McNally EM, Pyle AD, Kramerova I, Spencer MJ. A Small-Molecule Approach to Restore a Slow-Oxidative Phenotype and Defective CaMKIIβ Signaling in Limb Girdle Muscular Dystrophy. Cell Reports. Medicine. 1: 100122. PMID 33205074 DOI: 10.1016/j.xcrm.2020.100122 |
0.383 |
|
| 2020 |
Quattrocelli M, Zelikovich AS, Salamone IM, Fischer JA, McNally EM. Mechanisms and Clinical Applications of Glucocorticoid Steroids in Muscular Dystrophy. Journal of Neuromuscular Diseases. PMID 33104035 DOI: 10.3233/JND-200556 |
0.799 |
|
| 2020 |
Gacita AM, Dellefave-Castillo L, Page PGT, Barefield DY, Wasserstrom JA, Puckelwartz MJ, Nobrega MA, McNally EM. Altered Enhancer and Promoter Usage Leads to Differential Gene Expression in the Normal and Failed Human Heart. Circulation. Heart Failure. CIRCHEARTFAILURE1200. PMID 32993371 DOI: 10.1161/CIRCHEARTFAILURE.120.006926 |
0.574 |
|
| 2020 |
McDade TW, McNally EM, Zelikovich AS, D'Aquila R, Mustanski B, Miller A, Vaught LA, Reiser NL, Bogdanovic E, Fallon KS, Demonbreun AR. High seroprevalence for SARS-CoV-2 among household members of essential workers detected using a dried blood spot assay. Plos One. 15: e0237833. PMID 32797108 DOI: 10.1371/Journal.Pone.0237833 |
0.616 |
|
| 2020 |
Nuckolls GH, Kinnett K, Dayanidhi S, Domenighetti AA, Duong T, Hathout Y, Lawlor MW, Lee S, Magnusson SP, McDonald CM, McNally EM, Miller NF, Olwin BB, Raghavan P, Roberts T, et al. Conference Report on Contractures in Musculoskeletal and Neurological Conditions. Muscle & Nerve. PMID 32108365 DOI: 10.1002/Mus.26845 |
0.462 |
|
| 2020 |
McNally EM, Mann DL, Pinto Y, Bhakta D, Tomaselli G, Nazarian S, Groh WJ, Tamura T, Duboc D, Itoh H, Hellerstein L, Mammen PPA. Clinical Care Recommendations for Cardiologists Treating Adults With Myotonic Dystrophy. Journal of the American Heart Association. 9: e014006. PMID 32067592 DOI: 10.1161/Jaha.119.014006 |
0.345 |
|
| 2019 |
Quattrocelli M, Zelikovich AS, Jiang Z, Peek CB, Demonbreun AR, Kuntz NL, Barish GD, Haldar SM, Bass J, McNally EM. Pulsed glucocorticoids enhance dystrophic muscle performance through epigenetic-metabolic reprogramming. Jci Insight. 4. PMID 31852847 DOI: 10.1172/Jci.Insight.132402 |
0.728 |
|
| 2019 |
Demonbreun AR, Wyatt EJ, Fallon KS, Oosterbaan CC, Page P, Hadhazy M, Quattrocelli M, Barefield DY, McNally EM. A gene-edited mouse model of Limb-Girdle muscular dystrophy 2C for testing exon skipping. Disease Models & Mechanisms. PMID 31582396 DOI: 10.1242/Dmm.040832 |
0.727 |
|
| 2019 |
McNally E. At the heart of genetic disease: an interview with Elizabeth McNally. Disease Models & Mechanisms. 13. PMID 31548216 DOI: 10.1242/Dmm.041566 |
0.352 |
|
| 2019 |
Demonbreun AR, Fallon KS, Oosterbaan CC, Bogdanovic E, Warner JL, Sell JJ, Page PG, Quattrocelli M, Barefield DY, McNally EM. Recombinant annexin A6 promotes membrane repair and protects against muscle injury. The Journal of Clinical Investigation. PMID 31545299 DOI: 10.1172/Jci128840 |
0.705 |
|
| 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 |
0.444 |
|
| 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 |
0.635 |
|
| 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 |
0.796 |
|
| 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 |
0.676 |
|
| 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 |
0.825 |
|
| 2018 |
Levy Y, Ross JA, Niglas M, Snetkov VA, Lynham S, Liao CY, Puckelwartz MJ, Hsu YM, McNally EM, Alsheimer M, Harridge SD, Young SG, Fong LG, Español Y, Lopez-Otin C, et al. Prelamin A causes aberrant myonuclear arrangement and results in muscle fiber weakness. Jci Insight. 3. PMID 30282816 DOI: 10.1172/Jci.Insight.120920 |
0.447 |
|
| 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 |
0.33 |
|
| 2018 |
Montefiori LE, Sobreira DR, Sakabe NJ, Aneas I, Joslin AC, Hansen GT, Bozek G, Moskowitz IP, McNally EM, Nóbrega MA. A promoter interaction map for cardiovascular disease genetics. Elife. 7. PMID 29988018 DOI: 10.7554/Elife.35788 |
0.611 |
|
| 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 |
0.682 |
|
| 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 |
0.348 |
|
| 2018 |
Fallon JR, McNally EM. Biglycan and LTBP4: Leveraging the extracellular matrix for Duchenne Muscular Dystrophy therapeutics. Matrix Biology : Journal of the International Society For Matrix Biology. PMID 29481844 DOI: 10.1016/J.Matbio.2018.02.016 |
0.534 |
|
| 2018 |
Montefiori LE, Sobreira DR, Sakabe NJ, Aneas I, Joslin AC, Hansen GT, Bozek G, Moskowitz IP, McNally EM, Nóbrega MA. Author response: A promoter interaction map for cardiovascular disease genetics Elife. DOI: 10.7554/Elife.35788.103 |
0.584 |
|
| 2017 |
Giacomazzi G, Holvoet B, Trenson S, Caluwé E, Kravic B, Grosemans H, Cortés-Calabuig Á, Deroose CM, Huylebroeck D, Hashemolhosseini S, Janssens S, McNally E, Quattrocelli M, Sampaolesi M. MicroRNAs promote skeletal muscle differentiation of mesodermal iPSC-derived progenitors. Nature Communications. 8: 1249. PMID 29093487 DOI: 10.1038/S41467-017-01359-W |
0.498 |
|
| 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 |
0.764 |
|
| 2017 |
Puckelwartz MJ, McNally EM. Hypertrophic Cardiomyopathy Gene Testing: Go Big? Circulation. Cardiovascular Genetics. 10. PMID 29030407 DOI: 10.1161/Circgenetics.117.001951 |
0.334 |
|
| 2017 |
McNally EM. Gene Editing for the Heart: Correcting Dystrophin Mutations. Circulation Research. 121: 896-898. PMID 28963182 DOI: 10.1161/Circresaha.117.311865 |
0.414 |
|
| 2017 |
McNally EM, Wyatt EJ. Mutation-Based Therapy for Duchenne Muscular Dystrophy: Antisense Treatment Arrives in the Clinic. Circulation. 136: 979-981. PMID 28893959 DOI: 10.1161/Circulationaha.117.028382 |
0.328 |
|
| 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 |
0.839 |
|
| 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 |
0.364 |
|
| 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 |
0.753 |
|
| 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 |
0.764 |
|
| 2017 |
Zhou C, Li C, Zhou B, Sun H, Koullourou V, Holt I, Puckelwartz MJ, Warren DT, Hayward R, Lin Z, Zhang L, Morris GE, McNally EM, Shackleton S, Rao L, et al. Novel nesprin-1 mutations associated with dilated cardiomyopathy cause nuclear envelope disruption and defects in myogenesis. Human Molecular Genetics. PMID 28398466 DOI: 10.1093/Hmg/Ddx116 |
0.466 |
|
| 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 |
0.498 |
|
| 2016 |
McNally EM. Cardiomyopathy in Muscular Dystrophy: When to Treat? Jama Cardiology. PMID 27926775 DOI: 10.1001/Jamacardio.2016.4910 |
0.373 |
|
| 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 |
0.337 |
|
| 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 |
0.522 |
|
| 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 |
0.446 |
|
| 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 |
0.317 |
|
| 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 |
0.737 |
|
| 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 |
0.524 |
|
| 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 |
0.718 |
|
| 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 |
0.338 |
|
| 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 |
0.324 |
|
| 2016 |
McNally EM. Questions and Answers About Myostatin, GDF11, and the Aging Heart. Circulation Research. 118: 6-8. PMID 26837737 DOI: 10.1161/Circresaha.115.307861 |
0.49 |
|
| 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 |
0.756 |
|
| 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. Author response: Thrombospondin expression in myofibers stabilizes muscle membranes Elife. DOI: 10.7554/Elife.17589.028 |
0.453 |
|
| 2015 |
Demonbreun AR, McNally EM. DNA Electroporation, Isolation and Imaging of Myofibers. Journal of Visualized Experiments : Jove. e53551. PMID 26780499 DOI: 10.3791/53551 |
0.701 |
|
| 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 |
0.762 |
|
| 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 |
0.806 |
|
| 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 |
0.754 |
|
| 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 |
0.733 |
|
| 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 |
0.323 |
|
| 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 |
0.847 |
|
| 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 |
0.403 |
|
| 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 |
0.844 |
|
| 2015 |
Depreux FF, Puckelwartz MJ, Augustynowicz A, Wolfgeher D, Labno CM, Pierre-Louis D, Cicka D, Kron SJ, Holaska J, McNally EM. Disruption of the lamin A and matrin-3 interaction by myopathic LMNA mutations. Human Molecular Genetics. 24: 4284-95. PMID 25948554 DOI: 10.1093/Hmg/Ddv160 |
0.38 |
|
| 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 |
0.375 |
|
| 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 |
0.333 |
|
| 2015 |
Ferlini A, Flanigan KM, Lochmuller H, Muntoni F, 't Hoen PA, McNally E. 204th ENMC International Workshop on Biomarkers in Duchenne Muscular Dystrophy 24-26 January 2014, Naarden, The Netherlands. Neuromuscular Disorders : Nmd. 25: 184-98. PMID 25529833 DOI: 10.1016/J.Nmd.2014.09.004 |
0.319 |
|
| 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. DOI: 10.1186/s13395-015-0054-6 |
0.71 |
|
| 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 |
0.356 |
|
| 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 |
0.463 |
|
| 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 |
0.831 |
|
| 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 |
0.531 |
|
| 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 |
0.781 |
|
| 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 |
0.483 |
|
| 2014 |
Dorn GW, McNally EM. Two strikes and you're out: gene-gene mutation interactions in HCM. Circulation Research. 115: 208-10. PMID 24989488 DOI: 10.1161/Circresaha.114.304383 |
0.323 |
|
| 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 |
0.489 |
|
| 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 |
0.787 |
|
| 2014 |
Puckelwartz MJ, McNally EM. Genetic profiling for risk reduction in human cardiovascular disease. Genes. 5: 214-34. PMID 24705294 DOI: 10.3390/Genes5010214 |
0.3 |
|
| 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 |
0.67 |
|
| 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 |
0.759 |
|
| 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 |
0.84 |
|
| 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 |
0.855 |
|
| 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 |
0.772 |
|
| 2014 |
Zhou C, Li C, Zhou B, Rao L, McNally E, Shanahan C, Zhang Q. NOVEL NESPRIN-1 MUTATIONS DISRUPT NE ORGANIZATION AND INDUCE DILATED CARDIOMYOPATHY Heart. 100: A19.1-A19. DOI: 10.1136/Heartjnl-2014-306916.56 |
0.345 |
|
| 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 |
0.832 |
|
| 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 |
0.797 |
|
| 2013 |
McNally EM, Golbus JR, Puckelwartz MJ. Genetic mutations and mechanisms in dilated cardiomyopathy. The Journal of Clinical Investigation. 123: 19-26. PMID 23281406 DOI: 10.1172/Jci62862 |
0.351 |
|
| 2013 |
McNally E. M.I.2 The matrix as a modifier for muscular dystrophy Neuromuscular Disorders. 23: 738. DOI: 10.1016/J.Nmd.2013.06.376 |
0.434 |
|
| 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 |
0.852 |
|
| 2012 |
Hofmann Bowman MA, McNally EM. Genetic pathways of vascular calcification. Trends in Cardiovascular Medicine. 22: 93-8. PMID 23040839 DOI: 10.1016/J.Tcm.2012.07.002 |
0.348 |
|
| 2012 |
McNally EM. The attachment disorders of muscle: failure to carb-load. The Journal of Clinical Investigation. 122: 3046-8. PMID 22922262 DOI: 10.1172/Jci65483 |
0.439 |
|
| 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 |
0.632 |
|
| 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 |
0.419 |
|
| 2012 |
McNally EM. Genetics: broken giant linked to heart failure. Nature. 483: 281-2. PMID 22422258 DOI: 10.1038/483281A |
0.398 |
|
| 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 |
0.773 |
|
| 2012 |
McNally E. Novel Targets and Approaches to Treating Skeletal Muscle Disease Musclefundamental Biology and Mechanisms of Disease. 1095-1103. DOI: 10.1016/B978-0-12-381510-1.00081-8 |
0.519 |
|
| 2011 |
Puckelwartz MJ, Depreux FF, McNally EM. Gene expression, chromosome position and lamin A/C mutations. Nucleus (Austin, Tex.). 2: 162-7. PMID 21818408 DOI: 10.4161/Nucl.2.3.16003 |
0.351 |
|
| 2011 |
Townsend D, Yasuda S, McNally E, Metzger JM. Distinct pathophysiological mechanisms of cardiomyopathy in hearts lacking dystrophin or the sarcoglycan complex. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 25: 3106-14. PMID 21665956 DOI: 10.1096/Fj.10-178913 |
0.477 |
|
| 2011 |
McNally EM, Sparano D. Mechanisms and management of the heart in myotonic dystrophy. Heart (British Cardiac Society). 97: 1094-100. PMID 21642660 DOI: 10.1136/Hrt.2010.214197 |
0.418 |
|
| 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 |
0.84 |
|
| 2011 |
Arnolds DE, Chu A, McNally EM, Nobrega MA, Moskowitz IP. The emerging genetic landscape underlying cardiac conduction system function. Birth Defects Research. Part a, Clinical and Molecular Teratology. 91: 578-85. PMID 21538814 DOI: 10.1002/Bdra.20800 |
0.619 |
|
| 2011 |
Puckelwartz M, McNally EM. Emery-Dreifuss muscular dystrophy. Handbook of Clinical Neurology. 101: 155-66. PMID 21496632 DOI: 10.1016/B978-0-08-045031-5.00012-8 |
0.462 |
|
| 2011 |
Liang GH, Adebiyi A, Leo MD, McNally EM, Leffler CW, Jaggar JH. Hydrogen sulfide dilates cerebral arterioles by activating smooth muscle cell plasma membrane KATP channels. American Journal of Physiology. Heart and Circulatory Physiology. 300: H2088-95. PMID 21421823 DOI: 10.1152/Ajpheart.01290.2010 |
0.315 |
|
| 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 |
0.796 |
|
| 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 |
0.807 |
|
| 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 |
0.753 |
|
| 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 |
0.435 |
|
| 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 |
0.848 |
|
| 2011 |
Ferrier A, Ryan SD, Kothary R, McNally EM. New Directions in Biology and Disease of Skeletal Muscle, Meeting Report, 5–8 May 2010, Ottawa, Canada Neuromuscular Disorders. 21: 157-159. DOI: 10.1016/J.Nmd.2010.08.009 |
0.457 |
|
| 2010 |
Mewborn SK, Puckelwartz MJ, Abuisneineh F, Fahrenbach JP, Zhang Y, MacLeod H, Dellefave L, Pytel P, Selig S, Labno CM, Reddy K, Singh H, McNally E. Altered chromosomal positioning, compaction, and gene expression with a lamin A/C gene mutation. Plos One. 5: e14342. PMID 21179469 DOI: 10.1371/Journal.Pone.0014342 |
0.341 |
|
| 2010 |
Romfh A, McNally EM. Cardiac assessment in duchenne and becker muscular dystrophies. Current Heart Failure Reports. 7: 212-8. PMID 20857240 DOI: 10.1007/S11897-010-0028-2 |
0.468 |
|
| 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 |
0.676 |
|
| 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 |
0.76 |
|
| 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 |
0.759 |
|
| 2010 |
Dellefave L, McNally EM. The genetics of dilated cardiomyopathy. Current Opinion in Cardiology. 25: 198-204. PMID 20186049 DOI: 10.1097/Hco.0B013E328337Ba52 |
0.317 |
|
| 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 |
0.313 |
|
| 2010 |
Randles KN, Lam le T, Sewry CA, Puckelwartz M, Furling D, Wehnert M, McNally EM, Morris GE. Nesprins, but not sun proteins, switch isoforms at the nuclear envelope during muscle development. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 239: 998-1009. PMID 20108321 DOI: 10.1002/Dvdy.22229 |
0.443 |
|
| 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 |
0.823 |
|
| 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 |
0.417 |
|
| 2010 |
Heydemann A, Ceco E, Lim JE, Hadhazy M, Ryder P, Moran JL, Beier DR, Palmer AA, McNally EM. Latent TGF-β-binding protein 4 modifies muscular dystrophy in mice (The Journal of Clinical Investigation (2010) 120, 2, (645) DOI: 10.1172/JCI39845) Journal of Clinical Investigation. 120: 645. DOI: 10.1172/Jci39845C1 |
0.781 |
|
| 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 |
0.781 |
|
| 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 |
0.81 |
|
| 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 |
0.558 |
|
| 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 |
0.716 |
|
| 2009 |
Attali R, Warwar N, Israel A, Gurt I, McNally E, Puckelwartz M, Glick B, Nevo Y, Ben-Neriah Z, Melki J. Mutation of SYNE-1, encoding an essential component of the nuclear lamina, is responsible for autosomal recessive arthrogryposis. Human Molecular Genetics. 18: 3462-9. PMID 19542096 DOI: 10.1093/Hmg/Ddp290 |
0.335 |
|
| 2009 |
McNally E, Dellefave L. Sarcomere mutations in cardiogenesis and ventricular noncompaction. Trends in Cardiovascular Medicine. 19: 17-21. PMID 19467449 DOI: 10.1016/J.Tcm.2009.03.003 |
0.333 |
|
| 2009 |
Heydemann A, McNally E. NO more muscle fatigue Journal of Clinical Investigation. 119: 448-450. PMID 19306501 DOI: 10.1172/Jci38618 |
0.488 |
|
| 2009 |
McNally EM, Svensson EC. Setting the pace: Tbx3 and Tbx18 in cardiac conduction system development. Circulation Research. 104: 285-7. PMID 19213963 DOI: 10.1161/Circresaha.109.193680 |
0.301 |
|
| 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 |
0.461 |
|
| 2009 |
Wallace GQ, McNally EM. Mechanisms of muscle degeneration, regeneration, and repair in the muscular dystrophies. Annual Review of Physiology. 71: 37-57. PMID 18808326 DOI: 10.1146/Annurev.Physiol.010908.163216 |
0.534 |
|
| 2008 |
Wallace GQ, Lapidos KA, Kenik JS, McNally EM. Long-term survival of transplanted stem cells in immunocompetent mice with muscular dystrophy. The American Journal of Pathology. 173: 792-802. PMID 18711004 DOI: 10.2353/Ajpath.2008.080259 |
0.42 |
|
| 2008 |
McNally EM. Duchenne muscular dystrophy: how bad is the heart? Heart (British Cardiac Society). 94: 976-7. PMID 18625791 DOI: 10.1136/Hrt.2007.138461 |
0.556 |
|
| 2008 |
Dellefave L, McNally EM. Sarcomere mutations in cardiomyopathy, noncompaction, and the developing heart. Circulation. 117: 2847-9. PMID 18519860 DOI: 10.1161/Circulationaha.108.781518 |
0.321 |
|
| 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 |
0.799 |
|
| 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 |
0.519 |
|
| 2008 |
Pu JL, Ye B, Kroboth SL, McNally EM, Makielski JC, Shi NQ. Cardiac sulfonylurea receptor short form-based channels confer a glibenclamide-insensitive KATP activity. Journal of Molecular and Cellular Cardiology. 44: 188-200. PMID 18001767 DOI: 10.1016/J.Yjmcc.2007.09.010 |
0.325 |
|
| 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 |
0.552 |
|
| 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 |
0.496 |
|
| 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 |
0.666 |
|
| 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 |
0.344 |
|
| 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 |
0.393 |
|
| 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 |
0.456 |
|
| 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 |
0.555 |
|
| 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 |
0.515 |
|
| 2007 |
McNally EM. New approaches in the therapy of cardiomyopathy in muscular dystrophy. Annual Review of Medicine. 58: 75-88. PMID 17217326 DOI: 10.1146/Annurev.Med.58.011706.144703 |
0.331 |
|
| 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 |
0.709 |
|
| 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 |
0.8 |
|
| 2007 |
Dellefave LM, McNally EM. Cardiomyopathy in neuromuscular disorders Progress in Pediatric Cardiology. 24: 35-46. DOI: 10.1016/J.Ppedcard.2007.08.005 |
0.453 |
|
| 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 |
0.503 |
|
| 2006 |
McNally EM. Hypertrophic cardiomyopathy: exercise and eat right. Circulation Research. 98: 443-5. PMID 16514074 DOI: 10.1161/01.Res.0000214328.16941.70 |
0.347 |
|
| 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 |
0.738 |
|
| 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 |
0.84 |
|
| 2005 |
McNally EM, MacLeod H. Therapy insight: cardiovascular complications associated with muscular dystrophies. Nature Clinical Practice. Cardiovascular Medicine. 2: 301-8. PMID 16265534 DOI: 10.1038/Ncpcardio0213 |
0.443 |
|
| 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 |
0.701 |
|
| 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 |
0.317 |
|
| 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 |
0.443 |
|
| 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 |
0.564 |
|
| 2004 |
McNally EM, Towbin JA. Cardiomyopathy in muscular dystrophy workshop. 28-30 September 2003, Tucson, Arizona. Neuromuscular Disorders : Nmd. 14: 442-8. PMID 15266661 DOI: 10.1016/J.Nmd.2004.04.003 |
0.433 |
|
| 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 |
0.841 |
|
| 2004 |
McNally EM. Powerful genes--myostatin regulation of human muscle mass. The New England Journal of Medicine. 350: 2642-4. PMID 15215479 DOI: 10.1056/Nejmp048124 |
0.427 |
|
| 2004 |
Lapidos KA, Kakkar R, McNally EM. The dystrophin glycoprotein complex: signaling strength and integrity for the sarcolemma. Circulation Research. 94: 1023-31. PMID 15117830 DOI: 10.1161/01.Res.0000126574.61061.25 |
0.497 |
|
| 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 |
0.423 |
|
| 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 |
0.785 |
|
| 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 |
0.33 |
|
| 2003 |
Doherty KR, McNally EM. Repairing the tears: dysferlin in muscle membrane repair. Trends in Molecular Medicine. 9: 327-30. PMID 12928033 DOI: 10.1016/S1471-4914(03)00136-9 |
0.845 |
|
| 2003 |
Wheeler MT, McNally EM. Sarcoglycans in vascular smooth and striated muscle. Trends in Cardiovascular Medicine. 13: 238-43. PMID 12922020 DOI: 10.1016/S1050-1738(03)00101-4 |
0.506 |
|
| 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 |
0.354 |
|
| 2003 |
McNally E, Allikian M, Wheeler MT, Mislow JM, Heydemann A. Cytoskeletal defects in cardiomyopathy. Journal of Molecular and Cellular Cardiology. 35: 231-41. PMID 12676538 DOI: 10.1016/S0022-2828(03)00018-X |
0.352 |
|
| 2003 |
Wheeler MT, Collins KA, Korcarz CE, Hack AA, Zarnegar S, Lyons M, McNally EM. Reduction of secondary vasospasm limits cardiomyopathy progression Journal of the American College of Cardiology. 41: 218. DOI: 10.1016/S0735-1097(03)81599-1 |
0.743 |
|
| 2002 |
Wheeler MT, Allikian MJ, Heydemann A, McNally EM. The sarcoglycan complex in striated and vascular smooth muscle Cold Spring Harbor Symposia On Quantitative Biology. 67: 389-397. PMID 12858564 DOI: 10.1101/Sqb.2002.67.389 |
0.444 |
|
| 2002 |
Wheeler MT, Zarnegar S, McNally EM. Zeta-sarcoglycan, a novel component of the sarcoglycan complex, is reduced in muscular dystrophy. Human Molecular Genetics. 11: 2147-54. PMID 12189167 DOI: 10.1093/Hmg/11.18.2147 |
0.472 |
|
| 2002 |
Chutkow WA, Pu J, Wheeler MT, Wada T, Makielski JC, Burant CF, McNally EM. Episodic coronary artery vasospasm and hypertension develop in the absence of Sur2 K(ATP) channels. The Journal of Clinical Investigation. 110: 203-8. PMID 12122112 DOI: 10.1172/Jci15672 |
0.57 |
|
| 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 |
0.566 |
|
| 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 |
0.804 |
|
| 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 |
0.709 |
|
| 2002 |
McNally EM. β-Myosin Heavy Chain Gene Mutations in Familial Hypertrophic Cardiomyopathy The Usual Suspect? Circulation Research. 90: 246-247. DOI: 10.1161/Res.90.3.246 |
0.364 |
|
| 2001 |
Vainzof M, Anderson LV, McNally EM, Davis DB, Faulkner G, Valle G, Moreira ES, Pavanello RC, Passos-Bueno MR, Zatz M. Dysferlin protein analysis in limb-girdle muscular dystrophies. Journal of Molecular Neuroscience : Mn. 17: 71-80. PMID 11665864 DOI: 10.1385/Jmn:17:1:71 |
0.674 |
|
| 2001 |
Heydemann A, Wheeler MT, McNally EM. Cardiomyopathy in animal models of muscular dystrophy. Current Opinion in Cardiology. 16: 211-7. PMID 11357018 DOI: 10.1097/00001573-200105000-00009 |
0.515 |
|
| 2001 |
Zhu X, Hadhazy M, Groh ME, Wheeler MT, Wollmann R, McNally EM. Overexpression of gamma-sarcoglycan induces severe muscular dystrophy. Implications for the regulation of Sarcoglycan assembly. The Journal of Biological Chemistry. 276: 21785-90. PMID 11287429 DOI: 10.1074/Jbc.M101877200 |
0.51 |
|
| 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 |
0.841 |
|
| 2001 |
de Paula F, Vainzof M, Bernardino AL, McNally E, Kunkel LM, Zatz M. Mutations in the caveolin-3 gene: When are they pathogenic? American Journal of Medical Genetics. 99: 303-7. PMID 11251997 DOI: 10.1002/1096-8628(2001)9999:9999<::Aid-Ajmg1168>3.0.Co;2-O |
0.368 |
|
| 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 |
0.825 |
|
| 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 |
0.84 |
|
| 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 |
0.82 |
|
| 2000 |
Zhu X, Hadhazy M, Wehling M, Tidball JG, McNally EM. Dominant negative myostatin produces hypertrophy without hyperplasia in muscle. Febs Letters. 474: 71-5. PMID 10828454 DOI: 10.1016/S0014-5793(00)01570-2 |
0.531 |
|
| 2000 |
McNally EM, Ly CT, Rosenmann H, Mitrani Rosenbaum S, Jiang W, Anderson LV, Soffer D, Argov Z. Splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammation. American Journal of Medical Genetics. 91: 305-12. PMID 10766988 DOI: 10.1002/(Sici)1096-8628(20000410)91:4<305::Aid-Ajmg12>3.0.Co;2-S |
0.399 |
|
| 2000 |
Nowak KJ, Walsh P, Jacob RL, Johnsen RD, Peverall J, McNally EM, Wilton SD, Kakulas BA, Laing NG. Severe gamma-sarcoglycanopathy caused by a novel missense mutation and a large deletion. Neuromuscular Disorders : Nmd. 10: 100-7. PMID 10714584 DOI: 10.1016/S0960-8966(99)00063-2 |
0.397 |
|
| 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 |
0.831 |
|
| 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 |
0.823 |
|
| 2000 |
Davis DB, Delmonte AJ, Ly CT, McNally EM. Myoferlin, a candidate gene and potential modifier of muscular dystrophy. Human Molecular Genetics. 9: 217-26. PMID 10607832 DOI: 10.1093/Hmg/9.2.217 |
0.768 |
|
| 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 |
0.837 |
|
| 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 |
0.834 |
|
| 1998 |
McNally EM, de Sá Moreira E, Duggan DJ, Bönnemann CG, Lisanti MP, Lidov HG, Vainzof M, Passos-Bueno MR, Hoffman EP, Zatz M, Kunkel LM. Caveolin-3 in muscular dystrophy. Human Molecular Genetics. 7: 871-7. PMID 9536092 DOI: 10.1093/Hmg/7.5.871 |
0.502 |
|
| 1998 |
McNally EM, Ly CT, Kunkel LM. Human epsilon-sarcoglycan is highly related to alpha-sarcoglycan (adhalin), the limb girdle muscular dystrophy 2D gene. Febs Letters. 422: 27-32. PMID 9475163 DOI: 10.1016/S0014-5793(97)01593-7 |
0.401 |
|
| 1997 |
Messina DN, Speer MC, Pericak-Vance MA, McNally EM. Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23 American Journal of Human Genetics. 61: 909-917. PMID 9382102 DOI: 10.1086/514896 |
0.434 |
|
| 1996 |
Bönnemann CG, Passos-Bueno MR, McNally EM, Vainzof M, de Sá Moreira E, Marie SK, Pavanello RC, Noguchi S, Ozawa E, Zatz M, Kunkel LM. Genomic screening for beta-sarcoglycan gene mutations: missense mutations may cause severe limb-girdle muscular dystrophy type 2E (LGMD 2E). Human Molecular Genetics. 5: 1953-61. PMID 8968749 DOI: 10.1093/Hmg/5.12.1953 |
0.369 |
|
| 1996 |
McNally EM, Duggan D, Gorospe JR, Bönnemann CG, Fanin M, Pegoraro E, Lidov HG, Noguchi S, Ozawa E, Finkel RS, Cruse RP, Angelini C, Kunkel LM, Hoffman EP. Mutations that disrupt the carboxyl-terminus of gamma-sarcoglycan cause muscular dystrophy. Human Molecular Genetics. 5: 1841-7. PMID 8923014 DOI: 10.1093/Hmg/5.11.1841 |
0.422 |
|
| 1996 |
Bönnemann CG, McNally EM, Kunkel LM. Beyond dystrophin Current Opinion in Pediatrics. 8: 569-582. DOI: 10.1097/00008480-199612000-00005 |
0.307 |
|
| 1995 |
Ljunggren A, Duggan D, McNally E, Boylan KB, Gama CH, Kunkel LM, Hoffman EP. Primary adhalin deficiency as a cause of muscular dystrophy in patients with normal dystrophin. Annals of Neurology. 38: 367-72. PMID 7668821 DOI: 10.1002/Ana.410380305 |
0.379 |
|
| 1995 |
Bönnemann CG, Modi R, Noguchi S, Mizuno Y, Yoshida M, Gussoni E, McNally EM, Duggan DJ, Angelini C, Hoffman EP. Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex. Nature Genetics. 11: 266-73. PMID 7581449 DOI: 10.1038/Ng1195-266 |
0.381 |
|
| 1995 |
Noguchi S, McNally EM, Ben Othmane K, Hagiwara Y, Mizuno Y, Yoshida M, Yamamoto H, Bönnemann CG, Gussoni E, Denton PH, Kyriakides T, Middleton L, Hentati F, Ben Hamida M, Nonaka I, et al. Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy. Science (New York, N.Y.). 270: 819-22. PMID 7481775 DOI: 10.1126/Science.270.5237.819 |
0.37 |
|
| 1994 |
McNally EM, Yoshida M, Mizuno Y, Ozawa E, Kunkel LM. Human adhalin is alternatively spliced and the gene is located on chromosome 17q21. Proceedings of the National Academy of Sciences of the United States of America. 91: 9690-4. PMID 7937874 DOI: 10.1073/Pnas.91.21.9690 |
0.409 |
|
| 1991 |
Kitsis RN, Buttrick PM, Mcnally EM, Kaplan ML, Leinwand LA. Hormonal modulation of a gene injected into rat heart in vivo Proceedings of the National Academy of Sciences of the United States of America. 88: 4138-4142. PMID 2034660 DOI: 10.1073/Pnas.88.10.4138 |
0.355 |
|
| 1991 |
McNally E, Sohn R, Frankel S, Leinwand L. Expression of myosin and actin in Escherichia coli. Methods in Enzymology. 196: 368-389. PMID 2034131 DOI: 10.1016/0076-6879(91)96033-N |
0.301 |
|
| 1987 |
Saez LJ, Gianola KM, McNally EM, Feghali R, Eddy R, Shows TB, Leinwand LA. Human cardiac myosin heavy chain genes and their linkage in the genome Nucleic Acids Research. 15: 5443-5459. PMID 3037493 DOI: 10.1093/Nar/15.13.5443 |
0.385 |
|
| 1987 |
Toyoshima YY, Kron SJ, McNally EM, Niebling KR, Toyoshima C, Spudich JA. Myosin subfragment-1 is sufficient to move actin filaments in vitro Nature. 328: 536-539. PMID 2956522 DOI: 10.1038/328536A0 |
0.323 |
|
| 1986 |
Schwartz CE, McNally E, Leinwand L, Skolnick MH. A polymorphic human myosin heavy chain locus is linked to an anonymous single copy locus (D17S1) at 17p13. Cytogenetic and Genome Research. 43: 117-120. PMID 2877813 DOI: 10.1159/000132307 |
0.32 |
|
| 1983 |
Leinwand LA, Saez L, McNally E, Nadal-Ginard B. Isolation and characterization of human myosin heavy chain genes Proceedings of the National Academy of Sciences of the United States of America. 80: 3716-3720. PMID 6304733 DOI: 10.1073/Pnas.80.12.3716 |
0.374 |
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