Rezultati - Ronald D. Cohn

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  1. 1
    Molecular basis of muscular dystrophies

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

    Izdano 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 od Emily C. Lisi, Ronald D. Cohn

    Izdano 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 od Tyesha N. Burks, Ronald D. Cohn

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

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

    Izdano 2017
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  5. 5
    Genome sequencing as a diagnostic test

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

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

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

    Izdano 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 od Ronald D. Cohn, Madeleine Durbeej, Steven A. Moore, Ramón Mauricio Coral‐Vázquez, Sally Prouty, Kevin P. Campbell

    Izdano 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 od Ran Xu, Eva Andrés‐Mateos, Rebeca Mejı́as, Elizabeth M. MacDonald, Leslie A. Leinwand, Dana K. Merriman, R. Fink, Ronald D. Cohn

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

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

    Izdano 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 od Madeleine Durbeej, Ronald D. Cohn, Ronald F. Hrstka, Steven A. Moore, Valérie Allamand, Beverly L. Davidson, Roger A. Williamson, Kevin P. Campbell

    Izdano 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 od Tyesha N. Burks, Eva Andrés‐Mateos, Ruth Marx, Rebeca Mejı́as, Christel van Erp, Jessica L. Simmers, Jeremy Walston, Christopher W. Ward, Ronald D. Cohn

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

    Saturation variant interpretation using CRISPR prime editing od 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

    Izdano 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 od 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

    Izdano 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 od 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

    Izdano 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 od 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

    Izdano 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 od 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

    Izdano 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 od 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

    Izdano 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 od 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

    Izdano 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 od 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

    Izdano 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 od 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

    Izdano 2015
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