Showing results (101-110 of 282) with videos related to

Sort By:
Pageof 29
Human Genetics|September 30, 2005
Examination of ancestry and ethnic affiliation using highly informative diallelic DNA markers: application to diverse and admixed populations and implications for clinical epidemiology and forensic medicineNan Yang, Hongzhe Li, Lindsey A Criswell, et al.
Molecular Medicine (Cambridge, Mass.)|May 23, 2007
An interferon signature in the peripheral blood of dermatomyositis patients is associated with disease activityEmily C Baechler, Jason W Bauer, Catherine A Slattery, et al.
Molecular Medicine (Cambridge, Mass.)|July 7, 2017
Dense Genotyping of Immune-Related Regions Identifies Loci for Rheumatoid Arthritis Risk and Damage in African AmericansMaria I Danila, Vincent Albert Laufer, Richard J Reynolds, et al.
Plos Medicine|December 21, 2006
Elevated serum levels of interferon-regulated chemokines are biomarkers for active human systemic lupus erythematosusJason W Bauer, Emily C Baechler, Michelle Petri, et al.
Arthritis and Rheumatism|June 26, 2008
A broad analysis of IL1 polymorphism and rheumatoid arthritisAlyssa K Johnsen, Robert M Plenge, Vincent Butty, et al.
The Journal of Rheumatology|March 17, 2009
Plasma 25,OH vitamin D concentrations are not associated with rheumatoid arthritis (RA)-related autoantibodies in individuals at elevated risk for RAMarie Feser, Lezlie A Derber, Kevin D Deane, et al.
BMC Proceedings|December 19, 2009
Data for Genetic Analysis Workshop 16 Problem 1, association analysis of rheumatoid arthritis dataChristopher I Amos, Wei Vivien Chen, Michael F Seldin, et al.
Arthritis and Rheumatism|March 24, 2010
Rheumatoid arthritis risk allele PTPRC is also associated with response to anti-tumor necrosis factor alpha therapyJing Cui, Saedis Saevarsdottir, Brian Thomson, et al.
Annals of the Rheumatic Diseases|December 22, 2018
Genome-wide meta-analysis reveals shared new loci in systemic seropositive rheumatic diseasesMarialbert Acosta-Herrera, Martin Kerick, David González-Serna, et al.
American Journal of Hematology|March 6, 2012
Genome-wide association study of N370S homozygous Gaucher disease reveals the candidacy of CLN8 gene as a genetic modifier contributing to extreme phenotypic variationClarence K Zhang, Philip B Stein, Jun Liu, et al.
Pageof 29