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The Journal of Clinical Investigation
|
September 8, 2007
Elevation of RNA-binding protein CUGBP1 is an early event in an inducible heart-specific mouse model of myotonic dystrophy
Guey-Shin Wang, Debra L Kearney, Mariella De Biasi, et al.
Human Molecular Genetics
|
January 7, 2010
Heart-specific overexpression of CUGBP1 reproduces functional and molecular abnormalities of myotonic dystrophy type 1
Misha Koshelev, Satyam Sarma, Roger E Price, et al.
Iscience
|
October 30, 2024
Alternatively spliced MAP4 isoforms have key roles in maintaining microtubule organization and skeletal muscle function
Lathan Lucas, Larissa Nitschke, Brandon Nguyen, et al.
The International Journal of Biochemistry & Cell Biology
|
October 15, 2018
Modulation of alternative splicing of trafficking genes by genome editing reveals functional consequences in muscle biology
R Eric Blue, Amrita Koushik, Nichlas M Engels, et al.
Cell Reports
|
January 14, 2014
The Mef2 transcription network is disrupted in myotonic dystrophy heart tissue, dramatically altering miRNA and mRNA expression
Auinash Kalsotra, Ravi K Singh, Priyatansh Gurha, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 15, 2008
Expanded CTG repeats within the DMPK 3' UTR causes severe skeletal muscle wasting in an inducible mouse model for myotonic dystrophy
James P Orengo, Pierre Chambon, Daniel Metzger, et al.
Human Molecular Genetics
|
August 30, 2007
Expression, localization and tau exon 10 splicing activity of the brain RNA-binding protein TNRC4
J Paul Chapple, Karen Anthony, Teresa Rodriguez Martin, et al.
Elife
|
August 23, 2017
Extensive alternative splicing transitions during postnatal skeletal muscle development are required for calcium handling functions
Amy E Brinegar, Zheng Xia, James Anthony Loehr, et al.
Molecular and Cellular Biology
|
October 17, 2024
Small Molecule Screening Identifies HSP90 as a Modifier of RNA Foci in Myotonic Dystrophy Type 1
Sara J Johnson, Hannah L Johnson, Reid T Powell, et al.
Molecular Cell
|
August 2, 2002
Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing
Nicolas Charlet-B, Rajesh S Savkur, Gopal Singh, et al.
Page
of 11
Search research articles
Search
Showing results (71-80 of 106) with videos related to
Sort By:
Page
of 11
The Journal of Clinical Investigation
|
September 8, 2007
Elevation of RNA-binding protein CUGBP1 is an early event in an inducible heart-specific mouse model of myotonic dystrophy
Guey-Shin Wang, Debra L Kearney, Mariella De Biasi, et al.
Human Molecular Genetics
|
January 7, 2010
Heart-specific overexpression of CUGBP1 reproduces functional and molecular abnormalities of myotonic dystrophy type 1
Misha Koshelev, Satyam Sarma, Roger E Price, et al.
Iscience
|
October 30, 2024
Alternatively spliced MAP4 isoforms have key roles in maintaining microtubule organization and skeletal muscle function
Lathan Lucas, Larissa Nitschke, Brandon Nguyen, et al.
The International Journal of Biochemistry & Cell Biology
|
October 15, 2018
Modulation of alternative splicing of trafficking genes by genome editing reveals functional consequences in muscle biology
R Eric Blue, Amrita Koushik, Nichlas M Engels, et al.
Cell Reports
|
January 14, 2014
The Mef2 transcription network is disrupted in myotonic dystrophy heart tissue, dramatically altering miRNA and mRNA expression
Auinash Kalsotra, Ravi K Singh, Priyatansh Gurha, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 15, 2008
Expanded CTG repeats within the DMPK 3' UTR causes severe skeletal muscle wasting in an inducible mouse model for myotonic dystrophy
James P Orengo, Pierre Chambon, Daniel Metzger, et al.
Human Molecular Genetics
|
August 30, 2007
Expression, localization and tau exon 10 splicing activity of the brain RNA-binding protein TNRC4
J Paul Chapple, Karen Anthony, Teresa Rodriguez Martin, et al.
Elife
|
August 23, 2017
Extensive alternative splicing transitions during postnatal skeletal muscle development are required for calcium handling functions
Amy E Brinegar, Zheng Xia, James Anthony Loehr, et al.
Molecular and Cellular Biology
|
October 17, 2024
Small Molecule Screening Identifies HSP90 as a Modifier of RNA Foci in Myotonic Dystrophy Type 1
Sara J Johnson, Hannah L Johnson, Reid T Powell, et al.
Molecular Cell
|
August 2, 2002
Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing
Nicolas Charlet-B, Rajesh S Savkur, Gopal Singh, et al.
Page
of 11