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Journal Abstract Search

319 related items for PubMed ID: 25604634

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  • 5. Analysis of ICAM1 gene polymorphism in Slovak multiple sclerosis patients.
    Shawkatová I, Javor J, Párnická Z, Bucová M, Čopíková-Cudráková D, Michalík J, Gmitterová K, Čierny D, Buc M, Ďurmanová V.
    Folia Microbiol (Praha); 2017 Jul; 62(4):287-293. PubMed ID: 28130760
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  • 7. ALCAM--novel multiple sclerosis locus interfering with HLA-DRB1*1501.
    Wagner M, Wiśniewski A, Bilińska M, Pokryszko-Dragan A, Nowak I, Kuśnierczyk P, Jasek M.
    J Neuroimmunol; 2013 May 15; 258(1-2):71-6. PubMed ID: 23507476
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  • 8. 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, South Japan Multiple Sclerosis Genetics Consortium.
    Mult Scler; 2013 Nov 15; 19(13):1696-703. PubMed ID: 23549433
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  • 9. 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 15; 61(6):259-63. PubMed ID: 23849771
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  • 11. Lack of association between monocyte protein-1 (MCP-1) -2518 A>G chemoattractant and C-C chemokine receptor 2 (CCR2) Val64Ile polymorphisms and multiple sclerosis in a Tunisian population.
    Messadi A, Fekih-Mrissa N, Kallel A, Bouguerra C, Sediri Y, Zaweli J, Laayouni S, Nciri B, Yedeas M, Mrissa R, Jemaa R, Kaabachi N, Gritli N.
    J Clin Neurosci; 2010 Oct 15; 17(10):1311-3. PubMed ID: 20637631
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  • 12. [Association of CCR2 gene rs1799864 polymorphism with hemophagocytic lymphohistiocytosis in children].
    Ou DY, Luo JM, Tang LJ.
    Zhongguo Dang Dai Er Ke Za Zhi; 2015 Feb 15; 17(2):164-7. PubMed ID: 25760842
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  • 15. 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 15; 18(5):569-77. PubMed ID: 22127897
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  • 16. Association of polymorphisms in MCP-1, CCR2, and CCR5 genes with the risk and clinicopathological characteristics of prostate cancer.
    Kucukgergin C, Isman FK, Cakmakoglu B, Sanli O, Seckin S.
    DNA Cell Biol; 2012 Aug 15; 31(8):1418-24. PubMed ID: 22612293
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  • 17. 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 15; 45(10):912-918. PubMed ID: 37581270
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  • 18. Association of HLA-DRB1*15 allele and CSF oligoclonal bands in a Spanish multiple sclerosis cohort.
    Romero-Pinel L, Martínez-Yélamos S, Bau L, Matas E, Gubieras L, María Pujal J, Morandeira F, Bas J, Arbizu T.
    Eur J Neurol; 2011 Oct 15; 18(10):1258-62. PubMed ID: 21418440
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  • 19. 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 15; 73(4):283-8. PubMed ID: 25992516
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  • 20. A common haplotype of the C-C chemokine receptor 2 gene and HLA-DRB1*0301 are independent genetic risk factors for Löfgren's syndrome.
    Spagnolo P, Sato H, Grunewald J, Brynedal B, Hillert J, Mañá J, Wells AU, Eklund A, Welsh KI, du Bois RM.
    J Intern Med; 2008 Nov 15; 264(5):433-41. PubMed ID: 18513341
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