225 related articles for article (PubMed ID: 26990204)
1. Common and Low Frequency Variants in MERTK Are Independently Associated with Multiple Sclerosis Susceptibility with Discordant Association Dependent upon HLA-DRB1*15:01 Status.
Binder MD; Fox AD; Merlo D; Johnson LJ; Giuffrida L; Calvert SE; Akkermann R; Ma GZ; ; Perera AA; Gresle MM; Laverick L; Foo G; Fabis-Pedrini MJ; Spelman T; Jordan MA; Baxter AG; Foote S; Butzkueven H; Kilpatrick TJ; Field J
PLoS Genet; 2016 Mar; 12(3):e1005853. PubMed ID: 26990204
[TBL] [Abstract][Full Text] [Related]
2. Polymorphisms in the receptor tyrosine kinase MERTK gene are associated with multiple sclerosis susceptibility.
Ma GZ; Stankovich J; ; Kilpatrick TJ; Binder MD; Field J
PLoS One; 2011 Feb; 6(2):e16964. PubMed ID: 21347448
[TBL] [Abstract][Full Text] [Related]
3. HLA-DRB1*15:01 and the
Binder MD; Nwoke EC; Morwitch E; Dwyer C; Li V; Xavier A; Lea RA; Lechner-Scott J; Taylor BV; Ponsonby AL; Kilpatrick TJ;
Neurol Neuroimmunol Neuroinflamm; 2024 Mar; 11(2):e200190. PubMed ID: 38150649
[TBL] [Abstract][Full Text] [Related]
4. Combination of interleukin-10 gene promoter polymorphisms with HLA-DRB1*15 allele is associated with multiple sclerosis.
Shahbazi M; Abadi JSA; Roshandel D; Koochaki M; Amiri H; Kohansal R; Baghbanian SM; Zamani M
Indian J Med Res; 2017 Jun; 145(6):746-752. PubMed ID: 29067976
[TBL] [Abstract][Full Text] [Related]
5. The association of HLA-DRB1 and HLA-DQB1 alleles with genetic susceptibility to multiple sclerosis in the Slovak population.
Michalik J; Čierny D; Kantorová E; Kantárová D; Juraj J; Párnická Z; Kurča E; Dobrota D; Lehotský J
Neurol Res; 2015; 37(12):1060-7. PubMed ID: 26744784
[TBL] [Abstract][Full Text] [Related]
6. The +190 G/A (rs1799864) polymorphism in the C-C chemokine receptor 2 (CCR2) gene is associated with susceptibility to multiple sclerosis in HLA-DRB1*15:01-negative individuals.
Javor J; Párnická Z; Michalik J; Čopíková-Cudráková D; Shawkatová I; Ďurmanová V; Gmitterová K; Klímová E; Bucová M; Buc M
J Neurol Sci; 2015 Feb; 349(1-2):138-42. PubMed ID: 25604634
[TBL] [Abstract][Full Text] [Related]
7. Relationship between HLA-DRB1* 11/15 genotype and susceptibility to multiple sclerosis in Iran.
Abolfazli R; Samadzadeh S; Sabokbar T; Siroos B; Armaki SA; Aslanbeiki B; Ghelman M; Taheri T; Shakoori A
J Neurol Sci; 2014 Oct; 345(1-2):92-6. PubMed ID: 25064442
[TBL] [Abstract][Full Text] [Related]
8. Analysis of Cdx2 VDR gene polymorphism rs11568820 in association with multiple sclerosis in Slovaks.
Čierny D; Dobrota D; Kantorová E; Malicherová B; Škereňová M; Javor J; Kurča E; Lehotský J
Neurol Res; 2023 Oct; 45(10):912-918. PubMed ID: 37581270
[TBL] [Abstract][Full Text] [Related]
9. HLA-DRB1*15:01 and multiple sclerosis: a female association?
Irizar H; Muñoz-Culla M; Zuriarrain O; Goyenechea E; Castillo-Triviño T; Prada A; Saenz-Cuesta M; De Juan D; Lopez de Munain A; Olascoaga J; Otaegui D
Mult Scler; 2012 May; 18(5):569-77. PubMed ID: 22127897
[TBL] [Abstract][Full Text] [Related]
10. The influence of combined genotypes of the HLADRB1*1501 and CD24 single nucleotide polymorphism on disease severity of Iranian multiple sclerosis patients.
Ghlichnia HA; Kollaee A; Gaffarpoor M; Movafagh A; Ghlichnia B; Zamani M
Acta Med Iran; 2014; 52(6):418-23. PubMed ID: 25130147
[TBL] [Abstract][Full Text] [Related]
11. The CIITA genetic polymorphism rs4774*C in combination with the HLA-DRB1*15:01 allele as a putative susceptibility factor to multiple sclerosis in Brazilian females.
Paradela ER; Alves-Leon SV; Figueiredo AL; Pereira VC; Malfetano F; Mansur LF; Scherpenhuijzen S; Agostinho LA; Rocha CF; Rueda-Lopes F; Gasparetto E; Paiva CL
Arq Neuropsiquiatr; 2015 Apr; 73(4):283-8. PubMed ID: 25992516
[TBL] [Abstract][Full Text] [Related]
12. DNA methylation as a mediator of HLA-DRB1*15:01 and a protective variant in multiple sclerosis.
Kular L; Liu Y; Ruhrmann S; Zheleznyakova G; Marabita F; Gomez-Cabrero D; James T; Ewing E; Lindén M; Górnikiewicz B; Aeinehband S; Stridh P; Link J; Andlauer TFM; Gasperi C; Wiendl H; Zipp F; Gold R; Tackenberg B; Weber F; Hemmer B; Strauch K; Heilmann-Heimbach S; Rawal R; Schminke U; Schmidt CO; Kacprowski T; Franke A; Laudes M; Dilthey AT; Celius EG; Søndergaard HB; Tegnér J; Harbo HF; Oturai AB; Olafsson S; Eggertsson HP; Halldorsson BV; Hjaltason H; Olafsson E; Jonsdottir I; Stefansson K; Olsson T; Piehl F; Ekström TJ; Kockum I; Feinberg AP; Jagodic M
Nat Commun; 2018 Jun; 9(1):2397. PubMed ID: 29921915
[TBL] [Abstract][Full Text] [Related]
13. Combination of Myelin Basic Protein Gene Polymorphisms with HLA-DRB1*1501 in Iranian Patients with Multiple Sclerosis.
Nejati P; Attar M; Rahimian M; Fathi D; Shahbazi M
Iran J Immunol; 2017 Sep; 14(3):231-239. PubMed ID: 28919586
[TBL] [Abstract][Full Text] [Related]
14. Genetic factors and multiple sclerosis in the Moroccan population: a role for HLA class II.
Ouadghiri S; El Alaoui Toussi K; Brick C; Ait Benhaddou EH; Benseffaj N; Benomar A; El Yahyaoui M; Essakalli M
Pathol Biol (Paris); 2013 Dec; 61(6):259-63. PubMed ID: 23849771
[TBL] [Abstract][Full Text] [Related]
15. HLA associations with multiple sclerosis in Greece.
Kouri I; Papakonstantinou S; Bempes V; Vasiliadis HS; Kyritsis AP; Pelidou SH
J Neurol Sci; 2011 Sep; 308(1-2):28-31. PubMed ID: 21741664
[TBL] [Abstract][Full Text] [Related]
16. Multiple sclerosis risk genotypes correlate with an elevated cerebrospinal fluid level of the suggested prognostic marker CXCL13.
Lindén M; Khademi M; Lima Bomfim I; Piehl F; Jagodic M; Kockum I; Olsson T
Mult Scler; 2013 Jun; 19(7):863-70. PubMed ID: 23175382
[TBL] [Abstract][Full Text] [Related]
17. DBA/2J Haplotype on Distal Chromosome 2 Reduces Mertk Expression, Restricts Efferocytosis, and Increases Susceptibility to Atherosclerosis.
Kayashima Y; Makhanova N; Maeda N
Arterioscler Thromb Vasc Biol; 2017 Jul; 37(7):e82-e91. PubMed ID: 28473436
[TBL] [Abstract][Full Text] [Related]
18. Genetic risk factors for pediatric-onset multiple sclerosis.
Gianfrancesco MA; Stridh P; Shao X; Rhead B; Graves JS; Chitnis T; Waldman A; Lotze T; Schreiner T; Belman A; Greenberg B; Weinstock-Guttman B; Aaen G; Tillema JM; Hart J; Caillier S; Ness J; Harris Y; Rubin J; Candee M; Krupp L; Gorman M; Benson L; Rodriguez M; Mar S; Kahn I; Rose J; Roalstad S; Casper TC; Shen L; Quach H; Quach D; Hillert J; Hedstrom A; Olsson T; Kockum I; Alfredsson L; Schaefer C; Barcellos LF; Waubant E;
Mult Scler; 2018 Dec; 24(14):1825-1834. PubMed ID: 28980494
[TBL] [Abstract][Full Text] [Related]
19. A NOTCH4 missense mutation confers resistance to multiple sclerosis in Japanese.
Huang J; Yoshimura S; Isobe N; Matsushita T; Yonekawa T; Sato S; Yamasaki R; Kira J;
Mult Scler; 2013 Nov; 19(13):1696-703. PubMed ID: 23549433
[TBL] [Abstract][Full Text] [Related]
20. The association of rs703842 variants in CYP27B1 with multiple sclerosis susceptibility is influenced by the HLA-DRB1*15:01 allele in Slovaks.
Čierny D; Michalik J; Dubovan P; Škereňová M; Javor J; Kurča E; Dobrota D; Lehotský J
J Neuroimmunol; 2019 May; 330():123-129. PubMed ID: 30875612
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]