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The Journal of Pharmacology and Experimental Therapeutics
|
March 4, 2010
Implementation of a fluorescence-based screening assay identifies histamine H3 receptor antagonists clobenpropit and iodophenpropit as subunit-selective N-methyl-D-aspartate receptor antagonists
Kasper B Hansen, Praseeda Mullasseril, Sara Dawit, et al.
Neurobiology of Aging
|
September 7, 2023
An Alzheimer's disease risk variant in TTC3 modifies the actin cytoskeleton organization and the PI3K-Akt signaling pathway in iPSC-derived forebrain neurons
Holly N Cukier, Carolina L Duarte, Mayra J Laverde-Paz, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
March 25, 2026
Dissecting Alzheimer's disease heritability across populations
Shiying Liu, William S Bush, Brian W Kunkle, et al.
Plos Genetics
|
October 2, 2010
Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities
Adam C Naj, Gary W Beecham, Eden R Martin, et al.
Biorxiv : the Preprint Server for Biology
|
June 9, 2023
An Alzheimer's disease risk variant in
Holly N Cukier, Carolina L Duarte, Mayra J Laverde-Paz, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 25, 2025
Basic Science and Pathogenesis
Pedro R Mena, Andrew F Zaman, Michael L Cuccaro, et al.
Neuroscience Letters
|
April 13, 2017
Targeted sequencing of ABCA7 identifies splicing, stop-gain and intronic risk variants for Alzheimer disease
B W Kunkle, R M Carney, M A Kohli, et al.
Journal of Alzheimer'S Disease : JAD
|
December 8, 2020
Lower Levels of Education Are Associated with Cognitive Impairment in the Old Order Amish
Jairo Ramos, Aneesa R Chowdhury, Laura J Caywood, et al.
Genomics
|
November 24, 1999
Genetic studies of autistic disorder and chromosome 7
A Ashley-Koch, C M Wolpert, M M Menold, et al.
Human Molecular Genetics
|
August 25, 2000
Myotilin is mutated in limb girdle muscular dystrophy 1A
M A Hauser, S K Horrigan, P Salmikangas, et al.
Page
of 43
Search research articles
Search
Showing results (301-310 of 428) with videos related to
Sort By:
Page
of 43
The Journal of Pharmacology and Experimental Therapeutics
|
March 4, 2010
Implementation of a fluorescence-based screening assay identifies histamine H3 receptor antagonists clobenpropit and iodophenpropit as subunit-selective N-methyl-D-aspartate receptor antagonists
Kasper B Hansen, Praseeda Mullasseril, Sara Dawit, et al.
Neurobiology of Aging
|
September 7, 2023
An Alzheimer's disease risk variant in TTC3 modifies the actin cytoskeleton organization and the PI3K-Akt signaling pathway in iPSC-derived forebrain neurons
Holly N Cukier, Carolina L Duarte, Mayra J Laverde-Paz, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
March 25, 2026
Dissecting Alzheimer's disease heritability across populations
Shiying Liu, William S Bush, Brian W Kunkle, et al.
Plos Genetics
|
October 2, 2010
Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities
Adam C Naj, Gary W Beecham, Eden R Martin, et al.
Biorxiv : the Preprint Server for Biology
|
June 9, 2023
An Alzheimer's disease risk variant in
Holly N Cukier, Carolina L Duarte, Mayra J Laverde-Paz, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 25, 2025
Basic Science and Pathogenesis
Pedro R Mena, Andrew F Zaman, Michael L Cuccaro, et al.
Neuroscience Letters
|
April 13, 2017
Targeted sequencing of ABCA7 identifies splicing, stop-gain and intronic risk variants for Alzheimer disease
B W Kunkle, R M Carney, M A Kohli, et al.
Journal of Alzheimer'S Disease : JAD
|
December 8, 2020
Lower Levels of Education Are Associated with Cognitive Impairment in the Old Order Amish
Jairo Ramos, Aneesa R Chowdhury, Laura J Caywood, et al.
Genomics
|
November 24, 1999
Genetic studies of autistic disorder and chromosome 7
A Ashley-Koch, C M Wolpert, M M Menold, et al.
Human Molecular Genetics
|
August 25, 2000
Myotilin is mutated in limb girdle muscular dystrophy 1A
M A Hauser, S K Horrigan, P Salmikangas, et al.
Page
of 43