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Johnathan Cooper-Knock

Showing results (21-30 of 107) with videos related to

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Molecular Neurodegeneration|April 10, 2013
Simultaneous and independent detection of C9ORF72 alleles with low and high number of GGGGCC repeats using an optimised protocol of Southern blot hybridisationVladimir L Buchman, Johnathan Cooper-Knock, Natalie Connor-Robson, et al.
Bioinformatics (Oxford, England)|July 7, 2026
ProMeta: a meta-learning framework for robust disease diagnosis and prediction from plasma proteomicsHan Li, Haoteng Gu, Lei Hu, et al.
Neuropathology and Applied Neurobiology|June 23, 2015
Motor neurone disease/amyotrophic lateral sclerosis associated with intermediate-length CAG repeat expansions in Ataxin-2 does not have 1C2-positive polyglutamine inclusionsJohn Robin Highley, Alejandro Lorente Pons, Johnathan Cooper-Knock, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 4, 2020
Concurrent sodium channelopathies and amyotrophic lateral sclerosis supports shared pathogenesisJohn P Franklin, Johnathan Cooper-Knock, Aravindhan Baheerathan, et al.
Neuropathology and Applied Neurobiology|October 17, 2014
Invited review: decoding the pathophysiological mechanisms that underlie RNA dysregulation in neurodegenerative disorders: a review of the current state of the artMatthew J Walsh, Johnathan Cooper-Knock, Jennifer E Dodd, et al.
The Journal of Pathology|May 12, 2020
Oligodendrocyte pathology exceeds axonal pathology in white matter in human amyotrophic lateral sclerosisAlejandro Lorente Pons, Adrian Higginbottom, Johnathan Cooper-Knock, et al.
Neurology|October 11, 2013
C9ORF72 transcription in a frontotemporal dementia case with two expanded allelesJohnathan Cooper-Knock, Adrian Higginbottom, Natalie Connor-Robson, et al.
Dermatology Research and Practice|September 4, 2018
Whole Genome Sequencing in an Acrodermatitis Enteropathica Family from the Middle EastFaisel Abu-Duhier, Vivetha Pooranachandran, Andrew J G McDonagh, et al.
BMC Genetics|September 22, 2020
Identification of single nucleotide variants in the Moroccan population by whole-genome sequencingLucy Crooks, Johnathan Cooper-Knock, Paul R Heath, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|August 26, 2015
Oligogenic inheritance of optineurin (OPTN) and C9ORF72 mutations in ALS highlights localisation of OPTN in the TDP-43-negative inclusions of C9ORF72-ALSJoanna J Bury, J Robin Highley, Johnathan Cooper-Knock, et al.
Pageof 11

Showing results (21-30 of 107) with videos related to

Sort By:
Pageof 11
Molecular Neurodegeneration|April 10, 2013
Simultaneous and independent detection of C9ORF72 alleles with low and high number of GGGGCC repeats using an optimised protocol of Southern blot hybridisationVladimir L Buchman, Johnathan Cooper-Knock, Natalie Connor-Robson, et al.
Bioinformatics (Oxford, England)|July 7, 2026
ProMeta: a meta-learning framework for robust disease diagnosis and prediction from plasma proteomicsHan Li, Haoteng Gu, Lei Hu, et al.
Neuropathology and Applied Neurobiology|June 23, 2015
Motor neurone disease/amyotrophic lateral sclerosis associated with intermediate-length CAG repeat expansions in Ataxin-2 does not have 1C2-positive polyglutamine inclusionsJohn Robin Highley, Alejandro Lorente Pons, Johnathan Cooper-Knock, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|July 4, 2020
Concurrent sodium channelopathies and amyotrophic lateral sclerosis supports shared pathogenesisJohn P Franklin, Johnathan Cooper-Knock, Aravindhan Baheerathan, et al.
Neuropathology and Applied Neurobiology|October 17, 2014
Invited review: decoding the pathophysiological mechanisms that underlie RNA dysregulation in neurodegenerative disorders: a review of the current state of the artMatthew J Walsh, Johnathan Cooper-Knock, Jennifer E Dodd, et al.
The Journal of Pathology|May 12, 2020
Oligodendrocyte pathology exceeds axonal pathology in white matter in human amyotrophic lateral sclerosisAlejandro Lorente Pons, Adrian Higginbottom, Johnathan Cooper-Knock, et al.
Neurology|October 11, 2013
C9ORF72 transcription in a frontotemporal dementia case with two expanded allelesJohnathan Cooper-Knock, Adrian Higginbottom, Natalie Connor-Robson, et al.
Dermatology Research and Practice|September 4, 2018
Whole Genome Sequencing in an Acrodermatitis Enteropathica Family from the Middle EastFaisel Abu-Duhier, Vivetha Pooranachandran, Andrew J G McDonagh, et al.
BMC Genetics|September 22, 2020
Identification of single nucleotide variants in the Moroccan population by whole-genome sequencingLucy Crooks, Johnathan Cooper-Knock, Paul R Heath, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|August 26, 2015
Oligogenic inheritance of optineurin (OPTN) and C9ORF72 mutations in ALS highlights localisation of OPTN in the TDP-43-negative inclusions of C9ORF72-ALSJoanna J Bury, J Robin Highley, Johnathan Cooper-Knock, et al.
Pageof 11