165 results on '"Lincoln, Matthew R."'
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2. Genetic mapping across autoimmune diseases reveals shared associations and mechanisms
3. List of contributors
4. Type I interferon transcriptional network regulates expression of coinhibitory receptors in human T cells
5. Author Correction: A systems biology approach uncovers cell-specific gene regulatory effects of genetic associations in multiple sclerosis
6. A systems biology approach uncovers cell-specific gene regulatory effects of genetic associations in multiple sclerosis
7. Epigenetic fine-mapping: identification of causal mechanisms for autoimmunity
8. Toward Precision Phenotyping of Multiple Sclerosis
9. An autoimmune transcriptional circuit drives FOXP3+ regulatory T cell dysfunction.
10. Multiple sclerosis therapies and pregnancy
11. Prenatal planning in multiple sclerosis
12. Candidate gene studies and fine-mapping of the mjor histocompatibilty complex association in multiple sclerosis
13. Activated β-catenin in Foxp3+ regulatory T cells links inflammatory environments to autoimmunity
14. Pearls & Oy-sters: Homozygous Complement Factor I Deficiency Presenting as Fulminant Relapsing Complement-Mediated CNS Vasculitis
15. Postpartum issues with multiple sclerosis
16. Chapter 101 - Vitamin D mechanisms of protection in multiple sclerosis
17. Enhanced astrocyte responses are driven by a genetic risk allele associated with multiple sclerosis
18. A multiple sclerosis–protective coding variant reveals an essential role for HDAC7 in regulatory T cells
19. An Autoimmune Transcriptional Circuit Driving Foxp3+Regulatory T cell Dysfunction
20. Author Correction: Activated β-catenin in Foxp3+ regulatory T cells links inflammatory environments to autoimmunity
21. Postpartum issues with multiple sclerosis
22. Multiple sclerosis therapies and pregnancy
23. Prenatal planning in multiple sclerosis
24. Epistasis among HLA-DRB1, HLA-DQA1, and HLA-DQB1 Loci Determines Multiple Sclerosis Susceptibility
25. HLA Class I Alleles Tag HLA-DRB1 1501 Haplotypes for Differential Risk in Multiple Sclerosis Susceptibility
26. Evidence for genetic regulation of vitamin D status in twins with multiple sclerosis
27. HLA class I alleles tag HLA-DRBI*1501 haplotypes for differential risk in multiple sclerosis susceptibility
28. Joint analysis reveals shared autoimmune disease associations and identifies common mechanisms
29. Vitamin D as disease-modifying therapy for multiple sclerosis?
30. Robert Whytt, Benjamin Franklin, and the first probable case of multiple sclerosis
31. Of mice and men: experimental autoimmune encephalitis and multiple sclerosis
32. Parent-of-origin effects at the major histocompatibility complex in multiple sclerosis
33. Parental transmission of HLA-DRB1*15 in multiple sclerosis
34. List of contributors
35. Epigenetics in multiple sclerosis susceptibility: difference in transgenerational risk localizes to the major histocompatibility complex
36. Transmission of class I/II multi-locus MHC haplotypes and multiple sclerosis susceptibility: accounting for linkage disequilibrium
37. Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistance
38. Methylation of class II transactivator gene promoter IV is not associated with susceptibility to Multiple Sclerosis
39. An autoimmune transcriptional circuit drives FOXP3+regulatory T cell dysfunction
40. PTGER2-β-Catenin Axis Links High Salt Environments to Autoimmunity by Balancing IFNγ and IL-10 in FoxP3+Regulatory T cells
41. Enhanced Astrocyte Responses are Driven by a Genetic Risk Allele Associated with Multiple Sclerosis
42. Select this articleA ChIP-seq defined genome-wide map of vitamin D receptor binding: associations with disease and evolution
43. Clinical Reasoning: A 34-year-old man with headache, diplopia, and hemiparesis
44. Expression of the multiple sclerosis associated MHC class II allele HLA-DRBI*1501 is regulated by vitamin D
45. Activated ß-catenin in Foxp3+regulatory T cells links inflammatory environments to autoimmunity
46. Parental non-inherited HLA resistance alleles do not confer protection against multiple sclerosis
47. A ChIP-seq defined genome-wide map of vitamin D receptor binding: Associations with disease and evolution
48. Chronic cerebrospinal venous insufficiency and multiple sclerosis
49. Expression of the Multiple Sclerosis-Associated MHC Class II Allele HLA-DRB1*1501 Is Regulated by Vitamin D
50. Methylation of class II transactivator gene promoter IV is not associated with susceptibility to Multiple Sclerosis
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