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Adrian J Waite

Showing results (1-10 of 16) with videos related to

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Stem Cell Research|October 23, 2020
The generation of an induced pluripotent stem cell line (DCGi001-A) from an individual with FOXG1 syndrome carrying the c.460dupG (p.Glu154fs) variation in the FOXG1 geneAdrian J Waite, David Millar, Angus Clarke
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 brainAdrian 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 differentiationMarc P Forrest, Adrian J Waite, Enca Martin-Rendon, et al.
Current Neurology and Neuroscience Reports|April 6, 2012
Recent advances in the genetics of the ALS-FTLD complexHuw R Morris, Adrian J Waite, Nigel M Williams, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 30, 2011
Psychiatric disorders, myoclonus dystonia, and the epsilon-sarcoglycan gene: a systematic reviewKathryn J Peall, Adrian J Waite, Derek J Blake, et al.
Neurobiology of Aging|February 25, 2014
Reduced C9orf72 protein levels in frontal cortex of amyotrophic lateral sclerosis and frontotemporal degeneration brain with the C9ORF72 hexanucleotide repeat expansionAdrian J Waite, Dirk Bäumer, Simon East, et al.
Journal of Huntington'S Disease|September 24, 2015
Huntingtin Exists as Multiple Splice Forms in Human BrainMatthew Mort, Francesca A Carlisle, Adrian J Waite, et al.
Schizophrenia Bulletin|December 12, 2017
The Psychiatric Risk Gene Transcription Factor 4 (TCF4) Regulates Neurodevelopmental Pathways Associated With Schizophrenia, Autism, and Intellectual DisabilityMarc P Forrest, Matthew J Hill, David H Kavanagh, et al.
Neurobiology of Disease|November 29, 2016
Role of major and brain-specific Sgce isoforms in the pathogenesis of myoclonus-dystonia syndromeJianfeng Xiao, Satya R Vemula, Yi Xue, et al.
Cold Spring Harbor Molecular Case Studies|June 5, 2019
A novel <i>TBK1</i> mutation in a family with diverse frontotemporal dementia spectrum disordersRuth Lamb, Jonathan D Rohrer, Raquel Real, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Stem Cell Research|October 23, 2020
The generation of an induced pluripotent stem cell line (DCGi001-A) from an individual with FOXG1 syndrome carrying the c.460dupG (p.Glu154fs) variation in the FOXG1 geneAdrian J Waite, David Millar, Angus Clarke
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 brainAdrian 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 differentiationMarc P Forrest, Adrian J Waite, Enca Martin-Rendon, et al.
Current Neurology and Neuroscience Reports|April 6, 2012
Recent advances in the genetics of the ALS-FTLD complexHuw R Morris, Adrian J Waite, Nigel M Williams, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 30, 2011
Psychiatric disorders, myoclonus dystonia, and the epsilon-sarcoglycan gene: a systematic reviewKathryn J Peall, Adrian J Waite, Derek J Blake, et al.
Neurobiology of Aging|February 25, 2014
Reduced C9orf72 protein levels in frontal cortex of amyotrophic lateral sclerosis and frontotemporal degeneration brain with the C9ORF72 hexanucleotide repeat expansionAdrian J Waite, Dirk Bäumer, Simon East, et al.
Journal of Huntington'S Disease|September 24, 2015
Huntingtin Exists as Multiple Splice Forms in Human BrainMatthew Mort, Francesca A Carlisle, Adrian J Waite, et al.
Schizophrenia Bulletin|December 12, 2017
The Psychiatric Risk Gene Transcription Factor 4 (TCF4) Regulates Neurodevelopmental Pathways Associated With Schizophrenia, Autism, and Intellectual DisabilityMarc P Forrest, Matthew J Hill, David H Kavanagh, et al.
Neurobiology of Disease|November 29, 2016
Role of major and brain-specific Sgce isoforms in the pathogenesis of myoclonus-dystonia syndromeJianfeng Xiao, Satya R Vemula, Yi Xue, et al.
Cold Spring Harbor Molecular Case Studies|June 5, 2019
A novel <i>TBK1</i> mutation in a family with diverse frontotemporal dementia spectrum disordersRuth Lamb, Jonathan D Rohrer, Raquel Real, et al.
Pageof 2