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David Mann

Showing results (141-150 of 161) with videos related to

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Human Molecular Genetics|June 29, 2014
Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodiesJose Bras, Rita Guerreiro, Lee Darwent, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 4, 2011
No evidence that extended tracts of homozygosity are associated with Alzheimer's diseaseRebecca Sims, Sarah Dwyer, Denise Harold, et al.
Neurobiology of Aging|December 9, 2015
Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseasesRita Guerreiro, Valentina Escott-Price, Lee Darwent, et al.
The Lancet. Neurology|September 11, 2007
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiativeRosa Rademakers, Matt Baker, Jennifer Gass, et al.
Acta Neuropathologica Communications|January 31, 2020
Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodiesTatiana Orme, Dena Hernandez, Owen A Ross, et al.
Neurobiology of Aging|September 27, 2016
Analysis of C9orf72 repeat expansions in a large international cohort of dementia with Lewy bodiesCelia Kun-Rodrigues, Owen A Ross, Tatiana Orme, et al.
The Lancet. Neurology|December 22, 2017
Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association studyRita Guerreiro, Owen A Ross, Celia Kun-Rodrigues, et al.
Neurobiology of Aging|November 19, 2018
A comprehensive screening of copy number variability in dementia with Lewy bodiesCelia Kun-Rodrigues, Tatiana Orme, Susana Carmona, et al.
Neurobiology of Disease|April 7, 2019
Heritability and genetic variance of dementia with Lewy bodiesRita Guerreiro, Valentina Escott-Price, Dena G Hernandez, et al.
Journal of Alzheimer'S Disease : JAD|September 18, 2010
The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis studyJean-Charles Lambert, Kristel Sleegers, Antonio González-Pérez, et al.
Pageof 17

Showing results (141-150 of 161) with videos related to

Sort By:
Pageof 17
Human Molecular Genetics|June 29, 2014
Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of dementia with Lewy bodiesJose Bras, Rita Guerreiro, Lee Darwent, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 4, 2011
No evidence that extended tracts of homozygosity are associated with Alzheimer's diseaseRebecca Sims, Sarah Dwyer, Denise Harold, et al.
Neurobiology of Aging|December 9, 2015
Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Parkinson's and Alzheimer's diseasesRita Guerreiro, Valentina Escott-Price, Lee Darwent, et al.
The Lancet. Neurology|September 11, 2007
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiativeRosa Rademakers, Matt Baker, Jennifer Gass, et al.
Acta Neuropathologica Communications|January 31, 2020
Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodiesTatiana Orme, Dena Hernandez, Owen A Ross, et al.
Neurobiology of Aging|September 27, 2016
Analysis of C9orf72 repeat expansions in a large international cohort of dementia with Lewy bodiesCelia Kun-Rodrigues, Owen A Ross, Tatiana Orme, et al.
The Lancet. Neurology|December 22, 2017
Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association studyRita Guerreiro, Owen A Ross, Celia Kun-Rodrigues, et al.
Neurobiology of Aging|November 19, 2018
A comprehensive screening of copy number variability in dementia with Lewy bodiesCelia Kun-Rodrigues, Tatiana Orme, Susana Carmona, et al.
Neurobiology of Disease|April 7, 2019
Heritability and genetic variance of dementia with Lewy bodiesRita Guerreiro, Valentina Escott-Price, Dena G Hernandez, et al.
Journal of Alzheimer'S Disease : JAD|September 18, 2010
The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis studyJean-Charles Lambert, Kristel Sleegers, Antonio González-Pérez, et al.
Pageof 17