-
1
-
-
33749059726
-
The neurobiology of multiple sclerosis: Genes, inflammation, and neurodegeneration
-
Hauser SL, Oksenberg JR: The neurobiology of multiple sclerosis: genes, inflammation, and neurodegeneration. Neuron 2006; 52: 61-76.
-
(2006)
Neuron
, vol.52
, pp. 61-76
-
-
Hauser, S.L.1
Oksenberg, J.R.2
-
3
-
-
67049172406
-
Multiple sclerosis and the major histocompati-bility complex
-
Ramagopalan SV, Knight JC, Ebers GC: Multiple sclerosis and the major histocompati-bility complex. Curr Opin Neurol 2009; 22: 219-225.
-
(2009)
Curr Opin Neurol
, vol.22
, pp. 219-225
-
-
Ramagopalan, S.V.1
Knight, J.C.2
Ebers, G.C.3
-
4
-
-
34249030885
-
IL2RA/CD25 polymorphisms contribute to multiple sclerosis susceptibility
-
Matesanz F, Caro-Maldonado A, Fedetz M et al: IL2RA/CD25 polymorphisms contribute to multiple sclerosis susceptibility. J Neurol 2007; 254: 682-684.
-
(2007)
J Neurol
, vol.254
, pp. 682-684
-
-
Matesanz, F.1
Caro-Maldonado, A.2
Fedetz, M.3
-
5
-
-
34548299105
-
International Multiple Sclerosis Genetics Consortium: Risk alleles for multiple sclerosis identified by a genomewide study
-
International Multiple Sclerosis Genetics Consortium: Risk alleles for multiple sclerosis identified by a genomewide study. N Engl J Med 2007; 357: 851-862.
-
(2007)
N Engl J Med
, vol.357
, pp. 851-862
-
-
-
6
-
-
34548351247
-
Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis
-
Gregory SG, Schmidt S, Seth P et al: Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis. Nat Genet 2007; 39: 1083-1091.
-
(2007)
Nat Genet
, vol.39
, pp. 1083-1091
-
-
Gregory, S.G.1
Schmidt, S.2
Seth, P.3
-
7
-
-
34548368541
-
Variation in interleukin 7 receptor alpha chain (IL7R) influences risk of multiple sclerosis
-
Lundmark F, Duvefelt K, Iacobaeus E et al: Variation in interleukin 7 receptor alpha chain (IL7R) influences risk of multiple sclerosis. Nat Genet 2007; 39: 1108-1113.
-
(2007)
Nat Genet
, vol.39
, pp. 1108-1113
-
-
Lundmark, F.1
Duvefelt, K.2
Iacobaeus, E.3
-
8
-
-
56749098072
-
Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis
-
Aulchenko YS, Hoppenbrouwers IA, Ramagopalan SV et al: Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis. Nat Genet 2008; 40: 1402-1403.
-
(2008)
Nat Genet
, vol.40
, pp. 1402-1403
-
-
Aulchenko, Y.S.1
Hoppenbrouwers, I.A.2
Ramagopalan, S.V.3
-
9
-
-
45249112573
-
Interferon regulatory factor 5 (IRF5) gene variants are associated with multiple sclerosis in three distinct populations
-
Kristjansdottir G, Sandling JK, Bonetti A et al: Interferon regulatory factor 5 (IRF5) gene variants are associated with multiple sclerosis in three distinct populations. J Med Genet 2008; 45: 362-369.
-
(2008)
J Med Genet
, vol.45
, pp. 362-369
-
-
Kristjansdottir, G.1
Sandling, J.K.2
Bonetti, A.3
-
11
-
-
59149098926
-
CD226 Gly307Ser association with multiple autoimmune diseases
-
Hafler JP, Maier LM, Cooper JD et al: CD226 Gly307Ser association with multiple autoimmune diseases. Genes Immun 2009; 10: 5-10.
-
(2009)
Genes Immun
, vol.10
, pp. 5-10
-
-
Hafler, J.P.1
Maier, L.M.2
Cooper, J.D.3
-
12
-
-
59149093148
-
International Multiple Sclerosis Genetics Consortium (IMSGC): The expanding genetic overlap between multiple sclerosis and type i diabetes
-
International Multiple Sclerosis Genetics Consortium (IMSGC): The expanding genetic overlap between multiple sclerosis and type I diabetes. Genes Immun 2009; 10: 11-14.
-
(2009)
Genes Immun
, vol.10
, pp. 11-14
-
-
-
13
-
-
35748981184
-
Wellcome Trust Case Control Consortium: Association scan of 14 500 nonsynonymous SNPs in four diseases identifies autoimmunity variants
-
Wellcome Trust Case Control Consortium: Association scan of 14 500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Nat Genet 2007; 39: 1329-1337.
-
(2007)
Nat Genet
, vol.39
, pp. 1329-1337
-
-
-
14
-
-
70349629969
-
Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor
-
Ban M, Goris A, Lorentzen AR et al: Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor. Eur J Hum Genet 2009; 17: 1309-1313.
-
(2009)
Eur J Hum Genet
, vol.17
, pp. 1309-1313
-
-
Ban, M.1
Goris, A.2
Lorentzen, A.R.3
-
15
-
-
0020686503
-
New diagnostic criteria for multiple sclerosis: Guidelines for research protocols
-
Poser CM, Paty DW, Scheinberg L et al: New diagnostic criteria for multiple sclerosis: guidelines for research protocols. Ann Neurol 1983; 13: 227-231.
-
(1983)
Ann Neurol
, vol.13
, pp. 227-231
-
-
Poser, C.M.1
Paty, D.W.2
Scheinberg, L.3
-
16
-
-
0031870438
-
Canadian collaborative project on genetic susceptibility to MS, phase 2: Rationale and method. Canadian Collaborative Study Group
-
Sadovnick AD, Risch NJ, Ebers GC: Canadian collaborative project on genetic susceptibility to MS, phase 2: rationale and method. Canadian Collaborative Study Group. Can J Neurol Sci 1998; 25: 216-221.
-
(1998)
Can J Neurol Sci
, vol.25
, pp. 216-221
-
-
Sadovnick, A.D.1
Risch, N.J.2
Ebers, G.C.3
-
17
-
-
67649874745
-
Kif1b is essential for mRNA localization in oligodendrocytes and development of myelinated axons
-
Lyons DA, Naylor SG, Scholze A, Talbot WS: Kif1b is essential for mRNA localization in oligodendrocytes and development of myelinated axons. Nat Genet 2009; 41: 854-858.
-
(2009)
Nat Genet
, vol.41
, pp. 854-858
-
-
Lyons, D.A.1
Naylor, S.G.2
Scholze, A.3
Talbot, W.S.4
-
18
-
-
0028176627
-
Glucose-6-phosphate dehydrogenase: A housekeeping enzyme subject to tissue-specific regulation by hormones, nutrients, and oxidant stress
-
Kletzien RF, Harris PKV, Foellmi LA: Glucose-6-phosphate dehydrogenase: a housekeeping enzyme subject to tissue-specific regulation by hormones, nutrients, and oxidant stress. FASEB J 1994; 8: 174-181.
-
(1994)
FASEB J
, vol.8
, pp. 174-181
-
-
Kletzien, R.F.1
Harris, P.K.V.2
Foellmi, L.A.3
-
19
-
-
57049132739
-
Glucose metabolism inhibits apoptosis in neurons and cancer cells by redox inactivation of cytochrome C
-
Vaughn AE, Deshmukh M: Glucose metabolism inhibits apoptosis in neurons and cancer cells by redox inactivation of cytochrome C. Nat Cell Biol 2008; 10: 1477-1483.
-
(2008)
Nat Cell Biol
, vol.10
, pp. 1477-1483
-
-
Vaughn, A.E.1
Deshmukh, M.2
-
20
-
-
0042667127
-
Mutations in the genes encoding 11beta-hydroxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase interact to cause cortisone reductase deficiency
-
Draper N, Walker EA, Bujalska IJ et al: Mutations in the genes encoding 11beta-hydroxysteroid dehydrogenase type 1 and hexose-6-phosphate dehydrogenase interact to cause cortisone reductase deficiency. Nat Genet 2003; 34: 434-439.
-
(2003)
Nat Genet
, vol.34
, pp. 434-439
-
-
Draper, N.1
Walker, E.A.2
Bujalska, I.J.3
|