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Mark A Corbett

Showing results (11-20 of 68) with videos related to

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Plos One|March 20, 2015
shRNA off-target effects in vivo: impaired endogenous siRNA expression and spermatogenic defectsHye-Won Song, Anilkumar Bettegowda, Daniel Oliver, et al.
Experimental Eye Research|July 6, 2021
Differential gene expression analysis of corneal endothelium indicates involvement of phagocytic activity in Fuchs' endothelial corneal dystrophyAbraham Kuot, Mark A Corbett, Richard A Mills, et al.
Annals of Neurology|November 25, 2004
An alphaTropomyosin mutation alters dimer preference in nemaline myopathyMark A Corbett, P Anthony Akkari, Ana Domazetovska, et al.
Translational Psychiatry|April 24, 2018
Analysis of 182 cerebral palsy transcriptomes points to dysregulation of trophic signalling pathways and overlap with autismClare L van Eyk, Mark A Corbett, Alison Gardner, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 23, 2024
Application of multiple mosaic callers improves post-zygotic mutation detection from exome sequencing dataNandini G Sandran, Dani L Fornarino, Mark A Corbett, et al.
Neurobiology of Disease|May 16, 2018
PCDH19 regulation of neural progenitor cell differentiation suggests asynchrony of neurogenesis as a mechanism contributing to PCDH19 Girls Clustering EpilepsyClaire C Homan, Stephen Pederson, Thu-Hien To, et al.
Nature|August 10, 2018
Large deletions induced by Cas9 cleavageFatwa Adikusuma, Sandra Piltz, Mark A Corbett, et al.
Human Molecular Genetics|March 24, 2017
Protocadherin 19 (PCDH19) interacts with paraspeckle protein NONO to co-regulate gene expression with estrogen receptor alpha (ERα)Duyen H Pham, Chuan C Tan, Claire C Homan, et al.
Human Molecular Genetics|March 27, 2021
Transgenic mice with an R342X mutation in Phf6 display clinical features of Börjeson-Forssman-Lehmann SyndromeRaies Ahmed, Shihab Sarwar, Jinghua Hu, et al.
Developmental Medicine and Child Neurology|June 17, 2020
Definition and diagnosis of cerebral palsy in genetic studies: a systematic reviewRyan Pham, Ben W Mol, Jozef Gecz, et al.
Pageof 7

Showing results (11-20 of 68) with videos related to

Sort By:
Pageof 7
Plos One|March 20, 2015
shRNA off-target effects in vivo: impaired endogenous siRNA expression and spermatogenic defectsHye-Won Song, Anilkumar Bettegowda, Daniel Oliver, et al.
Experimental Eye Research|July 6, 2021
Differential gene expression analysis of corneal endothelium indicates involvement of phagocytic activity in Fuchs' endothelial corneal dystrophyAbraham Kuot, Mark A Corbett, Richard A Mills, et al.
Annals of Neurology|November 25, 2004
An alphaTropomyosin mutation alters dimer preference in nemaline myopathyMark A Corbett, P Anthony Akkari, Ana Domazetovska, et al.
Translational Psychiatry|April 24, 2018
Analysis of 182 cerebral palsy transcriptomes points to dysregulation of trophic signalling pathways and overlap with autismClare L van Eyk, Mark A Corbett, Alison Gardner, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 23, 2024
Application of multiple mosaic callers improves post-zygotic mutation detection from exome sequencing dataNandini G Sandran, Dani L Fornarino, Mark A Corbett, et al.
Neurobiology of Disease|May 16, 2018
PCDH19 regulation of neural progenitor cell differentiation suggests asynchrony of neurogenesis as a mechanism contributing to PCDH19 Girls Clustering EpilepsyClaire C Homan, Stephen Pederson, Thu-Hien To, et al.
Nature|August 10, 2018
Large deletions induced by Cas9 cleavageFatwa Adikusuma, Sandra Piltz, Mark A Corbett, et al.
Human Molecular Genetics|March 24, 2017
Protocadherin 19 (PCDH19) interacts with paraspeckle protein NONO to co-regulate gene expression with estrogen receptor alpha (ERα)Duyen H Pham, Chuan C Tan, Claire C Homan, et al.
Human Molecular Genetics|March 27, 2021
Transgenic mice with an R342X mutation in Phf6 display clinical features of Börjeson-Forssman-Lehmann SyndromeRaies Ahmed, Shihab Sarwar, Jinghua Hu, et al.
Developmental Medicine and Child Neurology|June 17, 2020
Definition and diagnosis of cerebral palsy in genetic studies: a systematic reviewRyan Pham, Ben W Mol, Jozef Gecz, et al.
Pageof 7