Søgeresultater - Ronald D. Cohn
- Showing 1 - 20 results of 48
- Go to Next Page
-
1
Molecular basis of muscular dystrophies af Ronald D. Cohn, Kevin P. Campbell
Udgivet 2000Revisão -
2
-
3
-
4
-
5
-
6
-
7
-
8
-
9
-
10
Disruption of the β-Sarcoglycan Gene Reveals Pathogenetic Complexity of Limb-Girdle Muscular Dystrophy Type 2E af Madeleine Durbeej, Ronald D. Cohn, Ronald F. Hrstka, Steven A. Moore, Valérie Allamand, Beverly L. Davidson, Roger A. Williamson, Kevin P. Campbell
Udgivet 2000Artigo -
11
-
12
-
13
Denervation atrophy is independent from Akt and mTOR activation and is not rescued by myostatin inhibition af 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
Udgivet 2014Artigo -
14
Genotype–phenotype correlation of congenital anomalies in multiple congenital anomalies hypotonia seizures syndrome (MCAHS1)/<i>PIGN</i>‐related epilepsy af 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
Udgivet 2015Artigo -
15
Disruption of Dag1 in Differentiated Skeletal Muscle Reveals a Role for Dystroglycan in Muscle Regeneration af 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
Udgivet 2002Artigo -
16
Identification and characterization of a functional mitochondrial angiotensin system af 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
Udgivet 2011Artigo -
17
Genome sequencing as a platform for pharmacogenetic genotyping: a pediatric cohort study af 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
Udgivet 2017Artigo -
18
Disruption of the Sarcoglycan–Sarcospan Complex in Vascular Smooth Muscle af 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
Udgivet 1999Artigo -
19
<scp>RNA</scp> seq analysis for the diagnosis of muscular dystrophy af 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
Udgivet 2015Artigo -
20
Clinically relevant copy number variations detected in cerebral palsy af 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
Udgivet 2015Artigo
Søgeredskaber:
Relaterede emner
Biology
Medicine
Genetics
Gene
Internal medicine
Computational biology
Skeletal muscle
Cell biology
Endocrinology
Genome
Muscular dystrophy
Mutation
Pathology
Exome sequencing
Phenotype
Bioinformatics
Pediatrics
Whole genome sequencing
DNA sequencing
Genetic testing
Anatomy
Computer science
Muscle atrophy
Atrophy
Biochemistry
Dystroglycan
Extracellular matrix
Laminin
Muscle hypertrophy
Angiotensin II