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L Haines

Showing results (651-660 of 908) with videos related to

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The British Journal of Dermatology|March 25, 2011
Wide spectrum of filaggrin-null mutations in atopic dermatitis highlights differences between Singaporean Chinese and European populationsH Chen, J E A Common, R L Haines, et al.
Plos One|October 7, 2017
Caspase-8, association with Alzheimer's Disease and functional analysis of rare variantsJan Rehker, Johanna Rodhe, Ryan R Nesbitt, et al.
Plos Genetics|August 29, 2006
GATA2 is associated with familial early-onset coronary artery diseaseJessica J Connelly, Tianyuan Wang, Julie E Cox, et al.
American Journal of Human Genetics|October 21, 2004
A second-generation genomic screen for multiple sclerosisS J Kenealy, M-C Babron, Y Bradford, et al.
Annals of Neurology|July 22, 2014
PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylationGyungah Jun, Hirohide Asai, Ella Zeldich, et al.
Medrxiv : the Preprint Server for Health Sciences|January 10, 2024
Missense and Loss of Function Variants at GWAS Loci in Familial Alzheimer's DiseaseTamil Iniyan Gunasekaran, Dolly Reyes-Dumeyer, Kelley M Faber, et al.
Neurology. Genetics|April 12, 2016
Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer diseaseMartin A Kohli, Holly N Cukier, Kara L Hamilton-Nelson, et al.
Human Molecular Genetics|August 12, 2010
Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12,566 individualsFarren B S Briggs, Selena E Bartlett, Benjamin A Goldstein, et al.
Human Molecular Genetics|June 5, 2019
RNA editing alterations in a multi-ethnic Alzheimer disease cohort converge on immune and endocytic molecular pathwaysOlivia K Gardner, Lily Wang, Derek Van Booven, et al.
Neuroscience Letters|July 6, 2004
Analysis of European mitochondrial haplogroups with Alzheimer disease riskJoelle M van der Walt, Yulia A Dementieva, Eden R Martin, et al.
Pageof 91

Showing results (651-660 of 908) with videos related to

Sort By:
Pageof 91
The British Journal of Dermatology|March 25, 2011
Wide spectrum of filaggrin-null mutations in atopic dermatitis highlights differences between Singaporean Chinese and European populationsH Chen, J E A Common, R L Haines, et al.
Plos One|October 7, 2017
Caspase-8, association with Alzheimer's Disease and functional analysis of rare variantsJan Rehker, Johanna Rodhe, Ryan R Nesbitt, et al.
Plos Genetics|August 29, 2006
GATA2 is associated with familial early-onset coronary artery diseaseJessica J Connelly, Tianyuan Wang, Julie E Cox, et al.
American Journal of Human Genetics|October 21, 2004
A second-generation genomic screen for multiple sclerosisS J Kenealy, M-C Babron, Y Bradford, et al.
Annals of Neurology|July 22, 2014
PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylationGyungah Jun, Hirohide Asai, Ella Zeldich, et al.
Medrxiv : the Preprint Server for Health Sciences|January 10, 2024
Missense and Loss of Function Variants at GWAS Loci in Familial Alzheimer's DiseaseTamil Iniyan Gunasekaran, Dolly Reyes-Dumeyer, Kelley M Faber, et al.
Neurology. Genetics|April 12, 2016
Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer diseaseMartin A Kohli, Holly N Cukier, Kara L Hamilton-Nelson, et al.
Human Molecular Genetics|August 12, 2010
Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12,566 individualsFarren B S Briggs, Selena E Bartlett, Benjamin A Goldstein, et al.
Human Molecular Genetics|June 5, 2019
RNA editing alterations in a multi-ethnic Alzheimer disease cohort converge on immune and endocytic molecular pathwaysOlivia K Gardner, Lily Wang, Derek Van Booven, et al.
Neuroscience Letters|July 6, 2004
Analysis of European mitochondrial haplogroups with Alzheimer disease riskJoelle M van der Walt, Yulia A Dementieva, Eden R Martin, et al.
Pageof 91