Resultats de la cerca - Ronald D. Cohn

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  1. 1
    Molecular basis of muscular dystrophies

    Molecular basis of muscular dystrophies per Ronald D. Cohn, Kevin P. Campbell

    Publicat 2000
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  2. 2
    Genetic evaluation of the pediatric patient with hypotonia: perspective from a hypotonia specialty clinic and review of the literature

    Genetic evaluation of the pediatric patient with hypotonia: perspective from a hypotonia specialty clinic and review of the literature per Emily C. Lisi, Ronald D. Cohn

    Publicat 2011
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  3. 3
    Role of TGF-β signaling in inherited and acquired myopathies

    Role of TGF-β signaling in inherited and acquired myopathies per Tyesha N. Burks, Ronald D. Cohn

    Publicat 2011
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  4. 4
    Treating pediatric neuromuscular disorders: The future is now

    Treating pediatric neuromuscular disorders: The future is now per James J. Dowling, Hernán Gonorazky, Ronald D. Cohn, Craig Campbell

    Publicat 2017
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  5. 5
    Genome sequencing as a diagnostic test

    Genome sequencing as a diagnostic test per Gregory Costain, Ronald D. Cohn, Stephen W. Scherer, Christian R. Marshall

    Publicat 2021
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  6. 6
    Myostatin does not regulate cardiac hypertrophy or fibrosis

    Myostatin does not regulate cardiac hypertrophy or fibrosis per Ronald D. Cohn, Hsin-Yueh Liang, Reena Shetty, Theodore P. Abraham, Kathryn R. Wagner

    Publicat 2007
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  7. 7
    Prevention of cardiomyopathy in mouse models lacking the smooth muscle sarcoglycan-sarcospan complex

    Prevention of cardiomyopathy in mouse models lacking the smooth muscle sarcoglycan-sarcospan complex per Ronald D. Cohn, Madeleine Durbeej, Steven A. Moore, Ramón Mauricio Coral‐Vázquez, Sally Prouty, Kevin P. Campbell

    Publicat 2001
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  8. 8
    Hibernating squirrel muscle activates the endurance exercise pathway despite prolonged immobilization

    Hibernating squirrel muscle activates the endurance exercise pathway despite prolonged immobilization per Ran Xu, Eva Andrés‐Mateos, Rebeca Mejı́as, Elizabeth M. MacDonald, Leslie A. Leinwand, Dana K. Merriman, R. Fink, Ronald D. Cohn

    Publicat 2013
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  9. 9
    Regulation of Muscle Mass by Follistatin and Activins

    Regulation of Muscle Mass by Follistatin and Activins per Se‐Jin Lee, Yun‐Sil Lee, Teresa A. Zimmers, Arshia Soleimani, Martin M. Matzuk, Kunihiro Tsuchida, Ronald D. Cohn, Elisabeth R. Barton

    Publicat 2010
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  10. 10
    Disruption of the β-Sarcoglycan Gene Reveals Pathogenetic Complexity of Limb-Girdle Muscular Dystrophy Type 2E

    Disruption of the β-Sarcoglycan Gene Reveals Pathogenetic Complexity of Limb-Girdle Muscular Dystrophy Type 2E per Madeleine Durbeej, Ronald D. Cohn, Ronald F. Hrstka, Steven A. Moore, Valérie Allamand, Beverly L. Davidson, Roger A. Williamson, Kevin P. Campbell

    Publicat 2000
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  11. 11
    Losartan Restores Skeletal Muscle Remodeling and Protects Against Disuse Atrophy in Sarcopenia

    Losartan Restores Skeletal Muscle Remodeling and Protects Against Disuse Atrophy in Sarcopenia per Tyesha N. Burks, Eva Andrés‐Mateos, Ruth Marx, Rebeca Mejı́as, Christel van Erp, Jessica L. Simmers, Jeremy Walston, Christopher W. Ward, Ronald D. Cohn

    Publicat 2011
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  12. 12
    Saturation variant interpretation using CRISPR prime editing

    Saturation variant interpretation using CRISPR prime editing per Steven Erwood, Teija M.I. Bily, Jason Lequyer, Joyce Yan, Nitya Gulati, Reid A. Brewer, Liangchi Zhou, Laurence Pelletier, Evgueni A. Ivakine, Ronald D. Cohn

    Publicat 2022
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  13. 13
    Denervation atrophy is independent from Akt and mTOR activation and is not rescued by myostatin inhibition

    Denervation atrophy is independent from Akt and mTOR activation and is not rescued by myostatin inhibition per Elizabeth M. MacDonald, Eva Andrés‐Mateos, Rebeca Mejı́as, Jessica L. Simmers, Ruifa Mi, Jae-Sung Park, Stephanie Ying, Ahmet Höke, Se‐Jin Lee, Ronald D. Cohn

    Publicat 2014
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  14. 14
    Genotype–phenotype correlation of congenital anomalies in multiple congenital anomalies hypotonia seizures syndrome (MCAHS1)/<i>PIGN</i>‐related epilepsy

    Genotype–phenotype correlation of congenital anomalies in multiple congenital anomalies hypotonia seizures syndrome (MCAHS1)/<i>PIGN</i>‐related epilepsy per Leah R. Fleming, Monica E. Lemmon, Natalie Beck, Maria R. Johnson, Weiyi Mu, David R. Murdock, Joann Bodurtha, Julie Hoover‐Fong, Ronald D. Cohn, Thangamadhan Bosemani, Kristin Barañano, Ada Hamosh

    Publicat 2015
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  15. 15
    Disruption of Dag1 in Differentiated Skeletal Muscle Reveals a Role for Dystroglycan in Muscle Regeneration

    Disruption of Dag1 in Differentiated Skeletal Muscle Reveals a Role for Dystroglycan in Muscle Regeneration per Ronald D. Cohn, Michael D. Henry, Daniel E. Michele, Rita Barresi, Fumiaki Saito, Steven A. Moore, Jason Flanagan, Mark W. Skwarchuk, Michael E. Robbins, Jerry R. Mendell, Roger A. Williamson, Kevin P. Campbell

    Publicat 2002
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  16. 16
    Identification and characterization of a functional mitochondrial angiotensin system

    Identification and characterization of a functional mitochondrial angiotensin system per Peter M. Abadir, D. Brian Foster, Michael T. Crow, Carol Cooke, Jasma Rucker, Alka Jain, Barbara J. Smith, Tyesha N. Burks, Ronald D. Cohn, Neal S. Fedarko, Robert M. Carey, Brian O’Rourke, Jeremy Walston

    Publicat 2011
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  17. 17
    Genome sequencing as a platform for pharmacogenetic genotyping: a pediatric cohort study

    Genome sequencing as a platform for pharmacogenetic genotyping: a pediatric cohort study per Iris Cohn, Tara Paton, Christian R. Marshall, Raveen Basran, Dimitri J. Stavropoulos, Peter N. Ray, Nasim Monfared, Robin Z. Hayeems, M. Stephen Meyn, Sarah Bowdin, Stephen W. Scherer, Ronald D. Cohn, Shinya Ito

    Publicat 2017
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  18. 18
    Disruption of the Sarcoglycan–Sarcospan Complex in Vascular Smooth Muscle

    Disruption of the Sarcoglycan–Sarcospan Complex in Vascular Smooth Muscle per Ramón Mauricio Coral‐Vázquez, Ronald D. Cohn, Steven A. Moore, Joseph A. Hill, Robert M. Weiß, Robin L. Davisson, Volker Straub, Rita Barresi, Dimple Bansal, Ron F. Hrstka, Roger A. Williamson, Kevin P. Campbell

    Publicat 1999
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  19. 19
    <scp>RNA</scp> seq analysis for the diagnosis of muscular dystrophy

    <scp>RNA</scp> seq analysis for the diagnosis of muscular dystrophy per Hernán Gonorazky, Minggao Liang, Beryl B. Cummings, Monkol Lek, Johann Micallef, Cynthia Hawkins, Raveen Basran, Ronald D. Cohn, Michael D. Wilson, Daniel G. MacArthur, Christian R. Marshall, Peter N. Ray, James J. Dowling

    Publicat 2015
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  20. 20
    Clinically relevant copy number variations detected in cerebral palsy

    Clinically relevant copy number variations detected in cerebral palsy per Maryam Oskoui, Matthew J. Gazzellone, Bhooma Thiruvahindrapuram, Mehdi Zarrei, John Andersen, John Wei, Zhuozhi Wang, Richard F. Wintle, Christian R. Marshall, Ronald D. Cohn, Rosanna Weksberg, Dimitri J. Stavropoulos, Darcy Fehlings, Michael Shevell, Stephen W. Scherer

    Publicat 2015
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