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Andrew Singleton

Showing results (101-110 of 286) with videos related to

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Annals of Neurology|August 1, 2022
Effect Modification between Genes and Environment and Parkinson's Disease RiskMaria Teresa Periñán, Kajsa Brolin, Sara Bandres-Ciga, et al.
Neurobiology of Aging|August 16, 2016
Exome sequencing in a consanguineous family clinically diagnosed with early-onset Alzheimer's disease identifies a homozygous CTSF mutationJose Bras, Ruth Djaldetti, Ana Margarida Alves, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 29, 2018
A paradoxical relationship between family history, onset age, and genetic risk in Parkinson's diseaseMadeleine Kristiansen, Jodi Maple-Grødem, Guido Alves, et al.
Neuroscience Letters|October 7, 2004
The tau H2 haplotype is almost exclusively Caucasian in originWhitney Evans, Hon Chung Fung, John Steele, et al.
Journal of Alzheimer'S Disease : JAD|November 27, 2018
Peripheral GRN mRNA and Serum Progranulin Levels as a Potential Indicator for Both the Presence of Splice Site Mutations and Individuals at Risk for Frontotemporal DementiaGamze Guven, Başar Bilgic, Zeynep Tufekcioglu, et al.
Neurology|September 12, 2014
Identical twins with the C9orf72 repeat expansion are discordant for ALSZhengrui Xi, Yana Yunusova, Marka van Blitterswijk, et al.
Biological Research for Nursing|August 16, 2014
A genomic profile of the immune response to stroke with implications for stroke recoveryTaura L Barr, Reyna VanGilder, Stephanie Rellick, et al.
Plos Genetics|January 17, 2009
Genome-wide association study of plasma polyunsaturated fatty acids in the InCHIANTI StudyToshiko Tanaka, Jian Shen, Gonçalo R Abecasis, et al.
The Lancet. Neurology|June 8, 2015
Targeting α-synuclein for treatment of Parkinson's disease: mechanistic and therapeutic considerationsBenjamin Dehay, Mathieu Bourdenx, Philippe Gorry, et al.
American Journal of Human Genetics|February 29, 2008
Splice mutation in the iron-sulfur cluster scaffold protein ISCU causes myopathy with exercise intoleranceFanny Mochel, Melanie A Knight, Wing-Hang Tong, et al.
Pageof 29

Showing results (101-110 of 286) with videos related to

Sort By:
Pageof 29
Annals of Neurology|August 1, 2022
Effect Modification between Genes and Environment and Parkinson's Disease RiskMaria Teresa Periñán, Kajsa Brolin, Sara Bandres-Ciga, et al.
Neurobiology of Aging|August 16, 2016
Exome sequencing in a consanguineous family clinically diagnosed with early-onset Alzheimer's disease identifies a homozygous CTSF mutationJose Bras, Ruth Djaldetti, Ana Margarida Alves, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 29, 2018
A paradoxical relationship between family history, onset age, and genetic risk in Parkinson's diseaseMadeleine Kristiansen, Jodi Maple-Grødem, Guido Alves, et al.
Neuroscience Letters|October 7, 2004
The tau H2 haplotype is almost exclusively Caucasian in originWhitney Evans, Hon Chung Fung, John Steele, et al.
Journal of Alzheimer'S Disease : JAD|November 27, 2018
Peripheral GRN mRNA and Serum Progranulin Levels as a Potential Indicator for Both the Presence of Splice Site Mutations and Individuals at Risk for Frontotemporal DementiaGamze Guven, Başar Bilgic, Zeynep Tufekcioglu, et al.
Neurology|September 12, 2014
Identical twins with the C9orf72 repeat expansion are discordant for ALSZhengrui Xi, Yana Yunusova, Marka van Blitterswijk, et al.
Biological Research for Nursing|August 16, 2014
A genomic profile of the immune response to stroke with implications for stroke recoveryTaura L Barr, Reyna VanGilder, Stephanie Rellick, et al.
Plos Genetics|January 17, 2009
Genome-wide association study of plasma polyunsaturated fatty acids in the InCHIANTI StudyToshiko Tanaka, Jian Shen, Gonçalo R Abecasis, et al.
The Lancet. Neurology|June 8, 2015
Targeting α-synuclein for treatment of Parkinson's disease: mechanistic and therapeutic considerationsBenjamin Dehay, Mathieu Bourdenx, Philippe Gorry, et al.
American Journal of Human Genetics|February 29, 2008
Splice mutation in the iron-sulfur cluster scaffold protein ISCU causes myopathy with exercise intoleranceFanny Mochel, Melanie A Knight, Wing-Hang Tong, et al.
Pageof 29