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R Lincoln

Showing results (151-160 of 166) with videos related to

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Science Translational Medicine|August 28, 2024
An autoimmune transcriptional circuit drives FOXP3<sup>+</sup> regulatory T cell dysfunctionTomokazu S Sumida, Matthew R Lincoln, Liang He, et al.
Genome Research|August 26, 2010
A ChIP-seq defined genome-wide map of vitamin D receptor binding: associations with disease and evolutionSreeram V Ramagopalan, Andreas Heger, Antonio J Berlanga, et al.
Brain : a Journal of Neurology|November 22, 2008
Genotype-Phenotype correlations in multiple sclerosis: HLA genes influence disease severity inferred by 1HMR spectroscopy and MRI measuresD T Okuda, R Srinivasan, J R Oksenberg, et al.
Annals of Neurology|June 3, 2004
Linkage and association with the NOS2A locus on chromosome 17q11 in multiple sclerosisLisa F Barcellos, Ann B Begovich, Rebecca L Reynolds, et al.
Nature Genetics|May 13, 2024
Genetic mapping across autoimmune diseases reveals shared associations and mechanismsMatthew R Lincoln, Noah Connally, Pierre-Paul Axisa, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|August 30, 2022
Toward Precision Phenotyping of Multiple SclerosisDavid Pitt, Chih Hung Lo, Susan A Gauthier, et al.
American Journal of Human Genetics|December 12, 2003
Mapping multiple sclerosis susceptibility to the HLA-DR locus in African AmericansJorge R Oksenberg, Lisa F Barcellos, Bruce A C Cree, et al.
Human Molecular Genetics|August 15, 2006
Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosisLisa F Barcellos, Stephen Sawcer, Patricia P Ramsay, 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.
Nature Genetics|September 28, 2005
A whole-genome admixture scan finds a candidate locus for multiple sclerosis susceptibilityDavid Reich, Nick Patterson, Philip L De Jager, et al.
Pageof 17

Showing results (151-160 of 166) with videos related to

Sort By:
Pageof 17
Science Translational Medicine|August 28, 2024
An autoimmune transcriptional circuit drives FOXP3<sup>+</sup> regulatory T cell dysfunctionTomokazu S Sumida, Matthew R Lincoln, Liang He, et al.
Genome Research|August 26, 2010
A ChIP-seq defined genome-wide map of vitamin D receptor binding: associations with disease and evolutionSreeram V Ramagopalan, Andreas Heger, Antonio J Berlanga, et al.
Brain : a Journal of Neurology|November 22, 2008
Genotype-Phenotype correlations in multiple sclerosis: HLA genes influence disease severity inferred by 1HMR spectroscopy and MRI measuresD T Okuda, R Srinivasan, J R Oksenberg, et al.
Annals of Neurology|June 3, 2004
Linkage and association with the NOS2A locus on chromosome 17q11 in multiple sclerosisLisa F Barcellos, Ann B Begovich, Rebecca L Reynolds, et al.
Nature Genetics|May 13, 2024
Genetic mapping across autoimmune diseases reveals shared associations and mechanismsMatthew R Lincoln, Noah Connally, Pierre-Paul Axisa, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|August 30, 2022
Toward Precision Phenotyping of Multiple SclerosisDavid Pitt, Chih Hung Lo, Susan A Gauthier, et al.
American Journal of Human Genetics|December 12, 2003
Mapping multiple sclerosis susceptibility to the HLA-DR locus in African AmericansJorge R Oksenberg, Lisa F Barcellos, Bruce A C Cree, et al.
Human Molecular Genetics|August 15, 2006
Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosisLisa F Barcellos, Stephen Sawcer, Patricia P Ramsay, 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.
Nature Genetics|September 28, 2005
A whole-genome admixture scan finds a candidate locus for multiple sclerosis susceptibilityDavid Reich, Nick Patterson, Philip L De Jager, et al.
Pageof 17