Pages that link to "Q43197113"
Jump to navigation
Jump to search
The following pages link to George C. Ebers (Q43197113):
Displaying 50 items.
- Interferon beta for secondary progressive multiple sclerosis (Q24240509) (← links)
- Reducing the probability of false positive research findings by pre-publication validation - experience with a large multiple sclerosis database (Q24288959) (← links)
- Functional analysis of missense variants in the TRESK (KCNK18) K channel (Q24602232) (← links)
- Congenital Abnormalities and Multiple Sclerosis (Q27496682) (← links)
- Male homosexuality: absence of linkage to microsatellite markers at Xq28 (Q28142177) (← links)
- A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia (Q28261023) (← links)
- High reprint orders in medical journals and pharmaceutical industry funding: case-control study (Q28727838) (← links)
- Crossed cerebral lateralization for verbal and visuo-spatial function in a pair of handedness discordant monozygotic twins: MRI and fMRI brain imaging (Q28754374) (← links)
- Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis (Q28943435) (← links)
- Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci (Q29417047) (← links)
- PRKCA and multiple sclerosis: association in two independent populations (Q33238942) (← links)
- The inheritance of resistance alleles in multiple sclerosis (Q33298407) (← links)
- Methylation of class II transactivator gene promoter IV is not associated with susceptibility to multiple sclerosis (Q33349615) (← links)
- No effect of preterm birth on the risk of multiple sclerosis: a population based study (Q33357046) (← links)
- The Multiple Sclerosis Risk Sharing Scheme Monitoring Study--early results and lessons for the future (Q33397837) (← links)
- Inactive or moderately active human promoters are enriched for inter-individual epialleles (Q33742167) (← links)
- The epidemiology of multiple sclerosis in Scotland: inferences from hospital admissions. (Q33813291) (← links)
- Multiple sclerosis, vitamin D, and HLA-DRB1*15. (Q33899907) (← links)
- The natural history of multiple sclerosis: a geographically based study 10: relapses and long-term disability (Q33944200) (← links)
- A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura (Q34140189) (← links)
- A ChIP-seq defined genome-wide map of vitamin D receptor binding: associations with disease and evolution (Q34153604) (← links)
- Seasonal distribution of psychiatric births in England (Q34230382) (← links)
- Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the TYK2 gene (Q34284850) (← links)
- Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita). (Q34327027) (← links)
- Month of birth, vitamin D and risk of immune-mediated disease: a case control study (Q34327362) (← links)
- Hexose-6-phosphate dehydrogenase: a new risk gene for multiple sclerosis (Q34329046) (← links)
- Genetic, environmental and stochastic factors in monozygotic twin discordance with a focus on epigenetic differences. (Q34381971) (← links)
- Protein-protein interaction analysis highlights additional loci of interest for multiple sclerosis (Q34456223) (← links)
- Twin concordance and sibling recurrence rates in multiple sclerosis. (Q34542659) (← links)
- MHC transmission: insights into gender bias in MS susceptibility. (Q34555282) (← links)
- Association of UV radiation with multiple sclerosis prevalence and sex ratio in France (Q34555392) (← links)
- Microchimerism in autoimmunity and transplantation: potential relevance to multiple sclerosis (Q34646812) (← links)
- HLA-DRB1 confers increased risk of pediatric-onset MS in children with acquired demyelination (Q34647079) (← links)
- Evidence for genetic basis of multiple sclerosis. The Canadian Collaborative Study Group. (Q34733337) (← links)
- Vitamin D receptor ChIP-seq in primary CD4+ cells: relationship to serum 25-hydroxyvitamin D levels and autoimmune disease (Q34815644) (← links)
- Geography of hospital admissions for multiple sclerosis in England and comparison with the geography of hospital admissions for infectious mononucleosis: a descriptive study (Q34954476) (← links)
- Risk alleles for multiple sclerosis in multiplex families. (Q34985640) (← links)
- Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis (Q35008221) (← links)
- Lockhart Clarke's contribution to the description of amyotrophic lateral sclerosis (Q35239032) (← links)
- Survival in MS: a randomized cohort study 21 years after the start of the pivotal IFNβ-1b trial. (Q35909839) (← links)
- Vitamin D receptor binding, chromatin states and association with multiple sclerosis. (Q36122415) (← links)
- Prognostic factors for multiple sclerosis: the importance of natural history studies. (Q36260705) (← links)
- Origins of magic: review of genetic and epigenetic effects (Q36294687) (← links)
- Cause of death in MS: long-term follow-up of a randomised cohort, 21 years after the start of the pivotal IFNβ-1b study (Q36496516) (← links)
- Multiple sclerosis: the environment and causation. (Q36818642) (← links)
- HLA class I alleles tag HLA-DRB1*1501 haplotypes for differential risk in multiple sclerosis susceptibility (Q36861570) (← links)
- Environmental factors and multiple sclerosis. (Q37085108) (← links)
- TRPV1 gates tissue access and sustains pathogenicity in autoimmune encephalitis. (Q37100271) (← links)
- Epistasis among HLA-DRB1, HLA-DQA1, and HLA-DQB1 loci determines multiple sclerosis susceptibility (Q37183035) (← links)
- The genetics of clinical outcome in multiple sclerosis. (Q37218364) (← links)