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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
July 25, 2003
Abnormal dysbindin expression in cerebellar mossy fiber synapses in the mdx mouse model of Duchenne muscular dystrophy
Roy V Sillitoe, Matthew A Benson, Derek J Blake, et al.
Molecular Neuropsychiatry
|
June 14, 2019
Transcriptional Changes following Cellular Knockdown of the Schizophrenia Risk Gene <i>SETD1A</i> Are Enriched for Common Variant Association with the Disorder
Darren Cameron, Derek J Blake, Nicholas J Bray, et al.
Human Molecular Genetics
|
April 8, 2009
TRIM32 is an E3 ubiquitin ligase for dysbindin
Matthew Locke, Caroline L Tinsley, Matthew A Benson, et al.
Physiological Reviews
|
March 28, 2002
Function and genetics of dystrophin and dystrophin-related proteins in muscle
Derek J Blake, Andrew Weir, Sarah E Newey, et al.
Circulation Research
|
July 7, 2018
Meta-Analysis of Cell Therapy Studies in Heart Failure and Acute Myocardial Infarction
Mariann Gyöngyösi, Paul M Haller, Derek J Blake, et al.
Human Mutation
|
July 29, 2011
A gain-of-glycosylation mutation associated with myoclonus-dystonia syndrome affects trafficking and processing of mouse ε-sarcoglycan in the late secretory pathway
Adrian Waite, Maria Cristina De Rosa, Andrea Brancaccio, et al.
Lancet (London, England)
|
November 9, 2002
Defective glycosylation in muscular dystrophy
Francesco Muntoni, Martin Brockington, Derek J Blake, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 19, 2016
Myoclonus dystonia and muscular dystrophy: ɛ-sarcoglycan is part of the dystrophin-associated protein complex in brain
Adrian J Waite, Francesca A Carlisle, Yiumo Michael Chan, et al.
Plos One
|
September 24, 2013
Knockdown of human TCF4 affects multiple signaling pathways involved in cell survival, epithelial to mesenchymal transition and neuronal differentiation
Marc P Forrest, Adrian J Waite, Enca Martin-Rendon, et al.
Advances in Experimental Medicine and Biology
|
January 13, 2006
Glycosylation defects and muscular dystrophy
Derek J Blake, Christopher T Esapa, Enca Martin-Rendon, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 60) with videos related to
Sort By:
Page
of 6
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
July 25, 2003
Abnormal dysbindin expression in cerebellar mossy fiber synapses in the mdx mouse model of Duchenne muscular dystrophy
Roy V Sillitoe, Matthew A Benson, Derek J Blake, et al.
Molecular Neuropsychiatry
|
June 14, 2019
Transcriptional Changes following Cellular Knockdown of the Schizophrenia Risk Gene <i>SETD1A</i> Are Enriched for Common Variant Association with the Disorder
Darren Cameron, Derek J Blake, Nicholas J Bray, et al.
Human Molecular Genetics
|
April 8, 2009
TRIM32 is an E3 ubiquitin ligase for dysbindin
Matthew Locke, Caroline L Tinsley, Matthew A Benson, et al.
Physiological Reviews
|
March 28, 2002
Function and genetics of dystrophin and dystrophin-related proteins in muscle
Derek J Blake, Andrew Weir, Sarah E Newey, et al.
Circulation Research
|
July 7, 2018
Meta-Analysis of Cell Therapy Studies in Heart Failure and Acute Myocardial Infarction
Mariann Gyöngyösi, Paul M Haller, Derek J Blake, et al.
Human Mutation
|
July 29, 2011
A gain-of-glycosylation mutation associated with myoclonus-dystonia syndrome affects trafficking and processing of mouse ε-sarcoglycan in the late secretory pathway
Adrian Waite, Maria Cristina De Rosa, Andrea Brancaccio, et al.
Lancet (London, England)
|
November 9, 2002
Defective glycosylation in muscular dystrophy
Francesco Muntoni, Martin Brockington, Derek J Blake, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 19, 2016
Myoclonus dystonia and muscular dystrophy: ɛ-sarcoglycan is part of the dystrophin-associated protein complex in brain
Adrian J Waite, Francesca A Carlisle, Yiumo Michael Chan, et al.
Plos One
|
September 24, 2013
Knockdown of human TCF4 affects multiple signaling pathways involved in cell survival, epithelial to mesenchymal transition and neuronal differentiation
Marc P Forrest, Adrian J Waite, Enca Martin-Rendon, et al.
Advances in Experimental Medicine and Biology
|
January 13, 2006
Glycosylation defects and muscular dystrophy
Derek J Blake, Christopher T Esapa, Enca Martin-Rendon, et al.
Page
of 6