Search research articles
Contact Us
Filters
Showing results (51-60 of 152) with videos related to
Page
of 16
Sort By:
Plos One
|
February 25, 2017
Association of IFIH1 and pro-inflammatory mediators: Potential new clues in SLE-associated pathogenesis
Melissa E Munroe, Nathan Pezant, Michael A Brown, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 5, 2014
Activating mutations in STIM1 and ORAI1 cause overlapping syndromes of tubular myopathy and congenital miosis
Vasyl Nesin, Graham Wiley, Maria Kousi, et al.
Journal of Autoimmunity
|
December 14, 2011
Sex chromosome aneuploidies among men with systemic lupus erythematosus
Skyler P Dillon, Biji T Kurien, Shibo Li, et al.
Public Health Genomics
|
August 23, 2022
Communicating Precision Medicine Research: Multidisciplinary Teams and Diverse Communities
Julie A Beans, Susan B Trinidad, Erika Blacksher, et al.
Translational Psychiatry
|
September 7, 2018
Identification and replication of RNA-Seq gene network modules associated with depression severity
Trang T Le, Jonathan Savitz, Hideo Suzuki, et al.
Translational Psychiatry
|
August 14, 2020
Correction: Identification and replication of RNA-Seq gene network modules associated with depression severity
Trang T Le, Jonathan Savitz, Hideo Suzuki, et al.
Nature Genetics
|
December 7, 2007
Polymorphism at the TNF superfamily gene TNFSF4 confers susceptibility to systemic lupus erythematosus
Deborah S Cunninghame Graham, Robert R Graham, Harinder Manku, et al.
Journal of Biomedicine & Biotechnology
|
April 14, 2012
Effects of IRF5 lupus risk haplotype on pathways predicted to influence B cell functions
Joel M Guthridge, Daniel N Clark, Amanda Templeton, et al.
ACR Open Rheumatology
|
June 16, 2022
A Human MSH6 Germline Variant Associated With Systemic Lupus Erythematosus Induces Lupus-like Disease in Mice
Rithy Meas, Joanne Nititham, Kimberly E Taylor, et al.
American Journal of Human Genetics
|
June 5, 2018
βIV Spectrinopathies Cause Profound Intellectual Disability, Congenital Hypotonia, and Motor Axonal Neuropathy
Chih-Chuan Wang, Xilma R Ortiz-González, Sabrina W Yum, et al.
Page
of 16
Search research articles
Search
Showing results (51-60 of 152) with videos related to
Sort By:
Page
of 16
Plos One
|
February 25, 2017
Association of IFIH1 and pro-inflammatory mediators: Potential new clues in SLE-associated pathogenesis
Melissa E Munroe, Nathan Pezant, Michael A Brown, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 5, 2014
Activating mutations in STIM1 and ORAI1 cause overlapping syndromes of tubular myopathy and congenital miosis
Vasyl Nesin, Graham Wiley, Maria Kousi, et al.
Journal of Autoimmunity
|
December 14, 2011
Sex chromosome aneuploidies among men with systemic lupus erythematosus
Skyler P Dillon, Biji T Kurien, Shibo Li, et al.
Public Health Genomics
|
August 23, 2022
Communicating Precision Medicine Research: Multidisciplinary Teams and Diverse Communities
Julie A Beans, Susan B Trinidad, Erika Blacksher, et al.
Translational Psychiatry
|
September 7, 2018
Identification and replication of RNA-Seq gene network modules associated with depression severity
Trang T Le, Jonathan Savitz, Hideo Suzuki, et al.
Translational Psychiatry
|
August 14, 2020
Correction: Identification and replication of RNA-Seq gene network modules associated with depression severity
Trang T Le, Jonathan Savitz, Hideo Suzuki, et al.
Nature Genetics
|
December 7, 2007
Polymorphism at the TNF superfamily gene TNFSF4 confers susceptibility to systemic lupus erythematosus
Deborah S Cunninghame Graham, Robert R Graham, Harinder Manku, et al.
Journal of Biomedicine & Biotechnology
|
April 14, 2012
Effects of IRF5 lupus risk haplotype on pathways predicted to influence B cell functions
Joel M Guthridge, Daniel N Clark, Amanda Templeton, et al.
ACR Open Rheumatology
|
June 16, 2022
A Human MSH6 Germline Variant Associated With Systemic Lupus Erythematosus Induces Lupus-like Disease in Mice
Rithy Meas, Joanne Nititham, Kimberly E Taylor, et al.
American Journal of Human Genetics
|
June 5, 2018
βIV Spectrinopathies Cause Profound Intellectual Disability, Congenital Hypotonia, and Motor Axonal Neuropathy
Chih-Chuan Wang, Xilma R Ortiz-González, Sabrina W Yum, et al.
Page
of 16