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Steven A Moore

Showing results (61-70 of 141) with videos related to

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Neurology. Genetics|February 12, 2020
A novel noncoding <i>FKRP</i> mutation in early onset limb-girdle muscular dystrophyEzgi Saylam, Steven A Moore, Akilandeswari Aravindhan, et al.
Annals of Neurology|February 29, 2008
Dysferlin-deficient muscular dystrophy features amyloidosisSimone Spuler, Miriam Carl, Joanna Zabojszcza, et al.
Cellular and Molecular Neurobiology|June 1, 2006
Pharmacological characterization of endocannabinoid transport and fatty acid amide hydrolase inhibitorsAmy K Dickason-Chesterfield, Stephanie R Kidd, Steven A Moore, et al.
Clinical Imaging|July 13, 2019
Magnetic Resonance Imaging characteristics in case of TOR1AIP1 muscular dystrophyAashim Bhatia, Bret C Mobley, Joy Cogan, et al.
The Journal of Biological Chemistry|March 29, 2012
Novel mutation in spectrin-like repeat 1 of dystrophin central domain causes protein misfolding and mild Becker muscular dystrophyGyula Acsadi, Steven A Moore, Angélique Chéron, et al.
The Journal of Molecular Diagnostics : JMD|August 13, 2021
Validation of Optical Genome Mapping for the Molecular Diagnosis of Facioscapulohumeral Muscular DystrophyAaron A Stence, Jon G Thomason, Jonathan A Pruessner, et al.
The AAPS Journal|December 20, 2022
Development and Validation of a Western Blot Method to Quantify Mini-Dystrophin in Human Skeletal Muscle BiopsiesCatherine I Soderstrom, Jennifer Larsen, Carolina Owen, et al.
Transgenic Research|November 3, 2004
Overexpression of GSK3betaS9A resulted in tau hyperphosphorylation and morphology reminiscent of pretangle-like neurons in the brain of PDGSK3beta transgenic miceBaolin Li, John Ryder, Yuan Su, et al.
Neuromuscular Disorders : NMD|April 4, 2009
Further evidence of Fukutin mutations as a cause of childhood onset limb-girdle muscular dystrophy without mental retardationRebecca L Puckett, Steven A Moore, Thomas L Winder, et al.
Neurology|January 9, 2015
Urologic and gastrointestinal symptoms in the dystroglycanopathiesCameron D Crockett, Laura A Bertrand, Christopher S Cooper, et al.
Pageof 15

Showing results (61-70 of 141) with videos related to

Sort By:
Pageof 15
Neurology. Genetics|February 12, 2020
A novel noncoding <i>FKRP</i> mutation in early onset limb-girdle muscular dystrophyEzgi Saylam, Steven A Moore, Akilandeswari Aravindhan, et al.
Annals of Neurology|February 29, 2008
Dysferlin-deficient muscular dystrophy features amyloidosisSimone Spuler, Miriam Carl, Joanna Zabojszcza, et al.
Cellular and Molecular Neurobiology|June 1, 2006
Pharmacological characterization of endocannabinoid transport and fatty acid amide hydrolase inhibitorsAmy K Dickason-Chesterfield, Stephanie R Kidd, Steven A Moore, et al.
Clinical Imaging|July 13, 2019
Magnetic Resonance Imaging characteristics in case of TOR1AIP1 muscular dystrophyAashim Bhatia, Bret C Mobley, Joy Cogan, et al.
The Journal of Biological Chemistry|March 29, 2012
Novel mutation in spectrin-like repeat 1 of dystrophin central domain causes protein misfolding and mild Becker muscular dystrophyGyula Acsadi, Steven A Moore, Angélique Chéron, et al.
The Journal of Molecular Diagnostics : JMD|August 13, 2021
Validation of Optical Genome Mapping for the Molecular Diagnosis of Facioscapulohumeral Muscular DystrophyAaron A Stence, Jon G Thomason, Jonathan A Pruessner, et al.
The AAPS Journal|December 20, 2022
Development and Validation of a Western Blot Method to Quantify Mini-Dystrophin in Human Skeletal Muscle BiopsiesCatherine I Soderstrom, Jennifer Larsen, Carolina Owen, et al.
Transgenic Research|November 3, 2004
Overexpression of GSK3betaS9A resulted in tau hyperphosphorylation and morphology reminiscent of pretangle-like neurons in the brain of PDGSK3beta transgenic miceBaolin Li, John Ryder, Yuan Su, et al.
Neuromuscular Disorders : NMD|April 4, 2009
Further evidence of Fukutin mutations as a cause of childhood onset limb-girdle muscular dystrophy without mental retardationRebecca L Puckett, Steven A Moore, Thomas L Winder, et al.
Neurology|January 9, 2015
Urologic and gastrointestinal symptoms in the dystroglycanopathiesCameron D Crockett, Laura A Bertrand, Christopher S Cooper, et al.
Pageof 15