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International Journal of Molecular Epidemiology and Genetics
|
April 12, 2012
Genetic variation in MME in relation to neprilysin protein and enzyme activity, Aβ levels, and Alzheimer's disease risk
Scott Miners, Zoë van Helmond, Rachel Barker, et al.
Brain : a Journal of Neurology
|
December 24, 2016
Reply: Atherosclerosis and vascular cognitive impairment neuropathological guideline
Olivia A Skrobot, Johannes Attems, Margaret Esiri, et al.
Human Mutation
|
March 17, 2004
Genetic variants of ABCA1 modify Alzheimer disease risk and quantitative traits related to beta-amyloid metabolism
Hagit Katzov, Katy Chalmers, Juni Palmgren, et al.
Journal of Alzheimer'S Disease : JAD
|
June 18, 2016
A Validation Study of Vascular Cognitive Impairment Genetics Meta-Analysis Findings in an Independent Collaborative Cohort
Olivia Anna Skrobot, Amy Jayne McKnight, Peter Anthony Passmore, et al.
Antioxidants & Redox Signaling
|
October 8, 2013
The branched-chain aminotransferase proteins: novel redox chaperones for protein disulfide isomerase--implications in Alzheimer's disease
Maya El Hindy, Mohammed Hezwani, David Corry, et al.
Nature Communications
|
August 22, 2022
Epigenome-wide association study of human frontal cortex identifies differential methylation in Lewy body pathology
Lasse Pihlstrøm, Gemma Shireby, Hanneke Geut, et al.
Nature Communications
|
September 24, 2022
DNA methylation signatures of Alzheimer's disease neuropathology in the cortex are primarily driven by variation in non-neuronal cell-types
Gemma Shireby, Emma L Dempster, Stefania Policicchio, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 14, 2016
The Vascular Impairment of Cognition Classification Consensus Study
Olivia A Skrobot, John O'Brien, Sandra Black, et al.
Brain : a Journal of Neurology
|
December 10, 2020
Recalibrating the epigenetic clock: implications for assessing biological age in the human cortex
Gemma L Shireby, Jonathan P Davies, Paul T Francis, et al.
Molecular Neurodegeneration
|
August 27, 2015
Distinct clinical and neuropathological features of G51D SNCA mutation cases compared with SNCA duplication and H50Q mutation
Aoife P Kiely, Helen Ling, Yasmine T Asi, et al.
Page
of 21
Search research articles
Search
Showing results (171-180 of 208) with videos related to
Sort By:
Page
of 21
International Journal of Molecular Epidemiology and Genetics
|
April 12, 2012
Genetic variation in MME in relation to neprilysin protein and enzyme activity, Aβ levels, and Alzheimer's disease risk
Scott Miners, Zoë van Helmond, Rachel Barker, et al.
Brain : a Journal of Neurology
|
December 24, 2016
Reply: Atherosclerosis and vascular cognitive impairment neuropathological guideline
Olivia A Skrobot, Johannes Attems, Margaret Esiri, et al.
Human Mutation
|
March 17, 2004
Genetic variants of ABCA1 modify Alzheimer disease risk and quantitative traits related to beta-amyloid metabolism
Hagit Katzov, Katy Chalmers, Juni Palmgren, et al.
Journal of Alzheimer'S Disease : JAD
|
June 18, 2016
A Validation Study of Vascular Cognitive Impairment Genetics Meta-Analysis Findings in an Independent Collaborative Cohort
Olivia Anna Skrobot, Amy Jayne McKnight, Peter Anthony Passmore, et al.
Antioxidants & Redox Signaling
|
October 8, 2013
The branched-chain aminotransferase proteins: novel redox chaperones for protein disulfide isomerase--implications in Alzheimer's disease
Maya El Hindy, Mohammed Hezwani, David Corry, et al.
Nature Communications
|
August 22, 2022
Epigenome-wide association study of human frontal cortex identifies differential methylation in Lewy body pathology
Lasse Pihlstrøm, Gemma Shireby, Hanneke Geut, et al.
Nature Communications
|
September 24, 2022
DNA methylation signatures of Alzheimer's disease neuropathology in the cortex are primarily driven by variation in non-neuronal cell-types
Gemma Shireby, Emma L Dempster, Stefania Policicchio, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 14, 2016
The Vascular Impairment of Cognition Classification Consensus Study
Olivia A Skrobot, John O'Brien, Sandra Black, et al.
Brain : a Journal of Neurology
|
December 10, 2020
Recalibrating the epigenetic clock: implications for assessing biological age in the human cortex
Gemma L Shireby, Jonathan P Davies, Paul T Francis, et al.
Molecular Neurodegeneration
|
August 27, 2015
Distinct clinical and neuropathological features of G51D SNCA mutation cases compared with SNCA duplication and H50Q mutation
Aoife P Kiely, Helen Ling, Yasmine T Asi, et al.
Page
of 21