Genetics and Multiple Sclerosis

• MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction
• An array of possibilities for the study of autoimmunity
• The presence of glutamic acid at positions 71 or 74 in pocket 4 of the HLA-DRβ1 chain is associated with the clinical course of multiple sclerosis
• Clinical characteristics of African Americans vs Caucasian Americans with multiple sclerosis
• Parental Age, Family Size, and Risk of Multiple Sclerosis
• Multiple sclerosis as a generalized CNS disease—comparative microarray analysis of normal appearing white matter and lesions in secondary progressive MS
• Susceptibility and outcome in MS
• Maternal effect in multiple sclerosis
• Parent-of-origin effect in multiple sclerosis: observations in half-siblings
• Do hyporesponsive genetic variants of the melanocortin 1 receptor contribute to the etiology of multiple sclerosis?
• Genomic Effects of IFN-β in Multiple Sclerosis Patients
• The natural history of multiple sclerosis: a geographically based study
• Gene therapy in autoimmune, demyelinating disease of the central nervous system
• An array of sunshine in multiple sclerosis
• Evectins: Vesicular proteins that carry a pleckstrin homology domain and localize to post-Golgi membranes
• Gene-microarray analysis of multiple sclerosis lesions yields new targets validated in autoimmune encephalomyelitis