Genetics
Specific to MS
- A genome-scan in a single pedigree with a high prevalence of MS
- Functional epistasis on a common MHC haplotype associated with multiple sclerosis
- Interleukin 7 receptor a chain (IL7R) shows allelic and functional association with multiple sclerosis
- Multiple sclerosis: putting two and two together
- Old Suspects Found Guilty — The First Genome Profile of Multiple Sclerosis
- Risk Alleles for Multiple Sclerosis Identified by a Genomewide Study
- Variation in interleukin 7 receptor a chain (IL7R) influences risk of multiple sclerosis
- An array of possibilities for the study of autoimmunity
- An array of sunshine in multiple sclerosis
- Clinical characteristics of African Americans vs Caucasian Americans with multiple sclerosis
- Do hyporesponsive genetic variants of the melanocortin 1 receptor contribute to the etiology of multiple sclerosis?
- Evectins: Vesicular proteins that carry a pleckstrin homology domain and localize to post-Golgi membranes
- Gene therapy in autoimmune, demyelinating disease of the central nervous system
- Gene-microarray analysis of multiple sclerosis lesions yields new targets validated in autoimmune encephalomyelitis
- Genomic Effects of IFN- in Multiple Sclerosis Patients
- Maternal effect in multiple sclerosis
- MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction
- Multiple sclerosis as a generalized CNS disease—comparative microarray analysis of normal appearing white matter and lesions in secondary progressive MS
- Parent-of-origin effect in multiple sclerosis: observations in half-siblings
- Parental Age, Family Size, and Risk of Multiple Sclerosis
- Susceptibility and outcome in MS
- The natural history of multiple sclerosis: a geographically based study
- The presence of glutamic acid at positions 71 or 74 in pocket 4 of the HLA-DRb1 chain is associated with the clinical course of multiple sclerosis