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Showing results (291-300 of 428) with videos related to

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Human Molecular Genetics|July 1, 1996
Evidence for locus heterogeneity in the Bethlem myopathy and linkage to 2q37M C Speer, R Tandan, P N Rao, et al.
Brain : a Journal of Neurology|June 9, 2009
Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathyKristl G Claeys, Stephan Züchner, Marina Kennerson, et al.
Neurobiology of Aging|November 12, 2023
Genetic analyses in multiplex families confirms chromosome 5q35 as a risk locus for Alzheimer's Disease in individuals of African AncestryKaren Nuytemans, Farid Rajabli, Melissa Jean-Francois, et al.
Journal of Alzheimer'S Disease & Parkinsonism|November 28, 2017
Exome Sequencing of Extended Families with Alzheimer's Disease Identifies Novel Genes Implicated in Cell Immunity and Neuronal FunctionH N Cukier, B K Kunkle, K L Hamilton, et al.
Human Genetics|February 8, 2011
Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery diseaseMollie A Minear, David R Crosslin, Beth S Sutton, et al.
Archives of Neurology|June 16, 2005
Expression profiling of substantia nigra in Parkinson disease, progressive supranuclear palsy, and frontotemporal dementia with parkinsonismMichael A Hauser, Yi-Ju Li, Hong Xu, et al.
Annals of Neurology|January 27, 2006
Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2Stephan Züchner, Peter De Jonghe, Albena Jordanova, et al.
Genomics|February 9, 2000
Analysis of association at single nucleotide polymorphisms in the APOE regionE R Martin, J R Gilbert, E H Lai, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 28, 2014
Absence of C9ORF72 expanded or intermediate repeats in autopsy-confirmed Parkinson's diseaseKaren Nuytemans, Vanessa Inchausti, Gary W Beecham, et al.
Annals of Human Genetics|March 6, 2008
Polymorphisms of the tumor suppressor gene LSAMP are associated with left main coronary artery diseaseL Wang, E R Hauser, S H Shah, et al.
Pageof 43

Showing results (291-300 of 428) with videos related to

Sort By:
Pageof 43
Human Molecular Genetics|July 1, 1996
Evidence for locus heterogeneity in the Bethlem myopathy and linkage to 2q37M C Speer, R Tandan, P N Rao, et al.
Brain : a Journal of Neurology|June 9, 2009
Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathyKristl G Claeys, Stephan Züchner, Marina Kennerson, et al.
Neurobiology of Aging|November 12, 2023
Genetic analyses in multiplex families confirms chromosome 5q35 as a risk locus for Alzheimer's Disease in individuals of African AncestryKaren Nuytemans, Farid Rajabli, Melissa Jean-Francois, et al.
Journal of Alzheimer'S Disease & Parkinsonism|November 28, 2017
Exome Sequencing of Extended Families with Alzheimer's Disease Identifies Novel Genes Implicated in Cell Immunity and Neuronal FunctionH N Cukier, B K Kunkle, K L Hamilton, et al.
Human Genetics|February 8, 2011
Polymorphic variants in tenascin-C (TNC) are associated with atherosclerosis and coronary artery diseaseMollie A Minear, David R Crosslin, Beth S Sutton, et al.
Archives of Neurology|June 16, 2005
Expression profiling of substantia nigra in Parkinson disease, progressive supranuclear palsy, and frontotemporal dementia with parkinsonismMichael A Hauser, Yi-Ju Li, Hong Xu, et al.
Annals of Neurology|January 27, 2006
Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2Stephan Züchner, Peter De Jonghe, Albena Jordanova, et al.
Genomics|February 9, 2000
Analysis of association at single nucleotide polymorphisms in the APOE regionE R Martin, J R Gilbert, E H Lai, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 28, 2014
Absence of C9ORF72 expanded or intermediate repeats in autopsy-confirmed Parkinson's diseaseKaren Nuytemans, Vanessa Inchausti, Gary W Beecham, et al.
Annals of Human Genetics|March 6, 2008
Polymorphisms of the tumor suppressor gene LSAMP are associated with left main coronary artery diseaseL Wang, E R Hauser, S H Shah, et al.
Pageof 43