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Neurology. Genetics

Showing results (491-500 of 842) with videos related to

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Neurology. Genetics|May 27, 2022
DNA Methylation of the Natriuretic Peptide System Genes and Ischemic Stroke: Gene-Based and Gene Set AnalysesHao Peng, Yiming Fan, Jing Li, et al.
Neurology. Genetics|May 27, 2022
Expanding Clinical Spectrum of <i>C9ORF72</i>-Related Disorders and Promising Therapeutic Strategies: A ReviewSarah Breevoort, Summer Gibson, Karla Figueroa, et al.
Neurology. Genetics|May 27, 2022
Progress in Amyotrophic Lateral Sclerosis Gene Discovery: Reflecting on Classic Approaches and Leveraging Emerging TechnologiesSamuel N Smukowski, Heather Maioli, Caitlin S Latimer, et al.
Neurology. Genetics|July 22, 2021
Autosomal Dominant ANO5-Related Disorder Associated With Myopathy and Gnathodiaphyseal DysplasiaAziz Shaibani, Shaida Khan, Marwan Shinawi
Neurology. Genetics|June 14, 2019
Loss-of-function mutations in Lysyl-tRNA synthetase cause various leukoencephalopathy phenotypesChong Sun, Jie Song, Yanjun Jiang, et al.
Neurology. Genetics|June 14, 2019
Hybrid gel electrophoresis using skin fibroblasts to aid in diagnosing mitochondrial diseaseChristopher Newell, Aneal Khan, David Sinasac, et al.
Neurology. Genetics|May 9, 2017
African American exome sequencing identifies potential risk variants at Alzheimer disease lociAurelie N'Songo, Minerva M Carrasquillo, Xue Wang, et al.
Neurology. Genetics|September 24, 2016
Novel TK2 mutations as a cause of delayed muscle maturation in mtDNA depletion syndromeThanes Termglinchan, Seito Hisamatsu, Junko Ohmori, et al.
Neurology. Genetics|May 24, 2017
HSP and deafness: Neurocristopathy caused by a novel mosaic <i>SOX10</i> mutationSandra Donkervoort, Diana Bharucha-Goebel, Pomi Yun, et al.
Neurology. Genetics|May 24, 2017
Genetic analysis of age at onset variation in spinocerebellar ataxia type 2K P Figueroa, Hilary Coon, Nieves Santos, et al.
Pageof 85

Showing results (491-500 of 842) with videos related to

Sort By:
Pageof 85
Neurology. Genetics|May 27, 2022
DNA Methylation of the Natriuretic Peptide System Genes and Ischemic Stroke: Gene-Based and Gene Set AnalysesHao Peng, Yiming Fan, Jing Li, et al.
Neurology. Genetics|May 27, 2022
Expanding Clinical Spectrum of <i>C9ORF72</i>-Related Disorders and Promising Therapeutic Strategies: A ReviewSarah Breevoort, Summer Gibson, Karla Figueroa, et al.
Neurology. Genetics|May 27, 2022
Progress in Amyotrophic Lateral Sclerosis Gene Discovery: Reflecting on Classic Approaches and Leveraging Emerging TechnologiesSamuel N Smukowski, Heather Maioli, Caitlin S Latimer, et al.
Neurology. Genetics|July 22, 2021
Autosomal Dominant ANO5-Related Disorder Associated With Myopathy and Gnathodiaphyseal DysplasiaAziz Shaibani, Shaida Khan, Marwan Shinawi
Neurology. Genetics|June 14, 2019
Loss-of-function mutations in Lysyl-tRNA synthetase cause various leukoencephalopathy phenotypesChong Sun, Jie Song, Yanjun Jiang, et al.
Neurology. Genetics|June 14, 2019
Hybrid gel electrophoresis using skin fibroblasts to aid in diagnosing mitochondrial diseaseChristopher Newell, Aneal Khan, David Sinasac, et al.
Neurology. Genetics|May 9, 2017
African American exome sequencing identifies potential risk variants at Alzheimer disease lociAurelie N'Songo, Minerva M Carrasquillo, Xue Wang, et al.
Neurology. Genetics|September 24, 2016
Novel TK2 mutations as a cause of delayed muscle maturation in mtDNA depletion syndromeThanes Termglinchan, Seito Hisamatsu, Junko Ohmori, et al.
Neurology. Genetics|May 24, 2017
HSP and deafness: Neurocristopathy caused by a novel mosaic <i>SOX10</i> mutationSandra Donkervoort, Diana Bharucha-Goebel, Pomi Yun, et al.
Neurology. Genetics|May 24, 2017
Genetic analysis of age at onset variation in spinocerebellar ataxia type 2K P Figueroa, Hilary Coon, Nieves Santos, et al.
Pageof 85