142 related articles for article (PubMed ID: 27870457)
1. Single-nucleotide polymorphism rs948854 in human galanin gene and multiple sclerosis: a gender-specific risk factor.
Lioudyno V; Abdurasulova I; Bisaga G; Skulyabin D; Klimenko V
J Neurosci Res; 2017 Jan; 95(1-2):644-651. PubMed ID: 27870457
[TBL] [Abstract][Full Text] [Related]
2. The effect of galanin gene polymorphism rs948854 on the severity of multiple sclerosis: A significant association with the age of onset.
Lioudyno V; Abdurasulova I; Tatarinov A; Nikiforova I; Ilves A; Ivashkova E; Stoliarov I; Bisaga G; Klimenko V
Mult Scler Relat Disord; 2020 Jan; 37():101439. PubMed ID: 32173003
[TBL] [Abstract][Full Text] [Related]
3. Implication of galanin gene rs948854 polymorphism in depressive symptoms in adolescents.
da Conceição Machado F; de Souza LV; Rangel M; Jara ZP; do Carmo Franco M
Horm Behav; 2018 Jan; 97():14-17. PubMed ID: 28987550
[TBL] [Abstract][Full Text] [Related]
4. Gender-specific influence of the chromosome 16 chemokine gene cluster on the susceptibility to Multiple Sclerosis.
Galimberti D; Scalabrini D; Fenoglio C; De Riz M; Comi C; Venturelli E; Cortini F; Piola M; Leone M; Dianzani U; D'Alfonso S; Monaco F; Bresolin N; Scarpini E
J Neurol Sci; 2008 Apr; 267(1-2):86-90. PubMed ID: 17967467
[TBL] [Abstract][Full Text] [Related]
5. ApaI, BsmI and TaqI VDR gene polymorphisms in association with multiple sclerosis in Slovaks.
Čierny D; Michalik J; Škereňová M; Kantorová E; Sivák Š; Javor J; Kurča E; Dobrota D; Lehotský J
Neurol Res; 2016 Aug; 38(8):678-84. PubMed ID: 27338176
[TBL] [Abstract][Full Text] [Related]
6. Single nucleotide polymorphism in the MMP-9 gene is associated with susceptibility to develop multiple sclerosis in an Italian case-control study.
La Russa A; Cittadella R; De Marco EV; Valentino P; Andreoli V; Trecroci F; Latorre V; Gambardella A; Quattrone A
J Neuroimmunol; 2010 Aug; 225(1-2):175-9. PubMed ID: 20471697
[TBL] [Abstract][Full Text] [Related]
7. Association of CYP2R1 rs10766197 with MS risk and disease progression.
Scazzone C; Agnello L; Ragonese P; Lo Sasso B; Bellia C; Bivona G; Schillaci R; Salemi G; Ciaccio M
J Neurosci Res; 2018 Feb; 96(2):297-304. PubMed ID: 28834557
[TBL] [Abstract][Full Text] [Related]
8. Genetic association between polymorphisms in the ADAMTS14 gene and multiple sclerosis.
Goertsches R; Comabella M; Navarro A; Perkal H; Montalban X
J Neuroimmunol; 2005 Jul; 164(1-2):140-7. PubMed ID: 15913795
[TBL] [Abstract][Full Text] [Related]
9. Association study of two functional single nucleotide polymorphisms of neuropeptide y gene with multiple sclerosis.
Mohammadi SM; Shirvani Farsani Z; Dosti R; Sahraian MA; Behmanesh M
Neuropeptides; 2016 Dec; 60():45-50. PubMed ID: 27559040
[TBL] [Abstract][Full Text] [Related]
10. Gene polymorphism at position -308 of the tumor necrosis factor alpha promotor is not associated with disease progression in multiple sclerosis patients.
Mäurer M; Kruse N; Giess R; Kyriallis K; Toyka KV; Rieckmann P
J Neurol; 1999 Oct; 246(10):949-54. PubMed ID: 10552245
[TBL] [Abstract][Full Text] [Related]
11. Genetic variants in interleukin 7 receptor α chain (IL-7Ra) are associated with multiple sclerosis risk and disability progression in Central European Slovak population.
Čierny D; Hányšová S; Michalik J; Kantorová E; Kurča E; Škereňová M; Lehotský J
J Neuroimmunol; 2015 May; 282():80-4. PubMed ID: 25903732
[TBL] [Abstract][Full Text] [Related]
12. Apolipoprotein E genotype does not associate with disease severity measured by Multiple Sclerosis Severity Score.
Guerrero AL; Laherrán E; Gutiérrez F; Martín-Polo J; Iglesias F; Alcázar C; Peralta J; Rostami P
Acta Neurol Scand; 2008 Jan; 117(1):21-5. PubMed ID: 17883422
[TBL] [Abstract][Full Text] [Related]
13. 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
[TBL] [Abstract][Full Text] [Related]
14. Interferon gamma allelic variants: sex-biased multiple sclerosis susceptibility and gene expression.
Kantarci OH; Hebrink DD; Schaefer-Klein J; Sun Y; Achenbach S; Atkinson EJ; Heggarty S; Cotleur AC; de Andrade M; Vandenbroeck K; Pelfrey CM; Weinshenker BG
Arch Neurol; 2008 Mar; 65(3):349-57. PubMed ID: 18332247
[TBL] [Abstract][Full Text] [Related]
15. Catechol-O-methyltransferase Val158Met polymorphism (rs4680) is associated with pain in multiple sclerosis.
Fernández-de-las-Peñas C; Ambite-Quesada S; Ortíz-Gutiérrez R; Ortega-Santiago R; Gil-Crujera A; Caminero AB
J Pain; 2013 Dec; 14(12):1719-23. PubMed ID: 24290452
[TBL] [Abstract][Full Text] [Related]
16. Genetic association between polymorphisms in the BTG1 gene and multiple sclerosis.
Camiña-Tato M; Morcillo-Suárez C; Navarro A; Fernández M; Horga A; Montalban X; Comabella M
J Neuroimmunol; 2009 Aug; 213(1-2):142-7. PubMed ID: 19515430
[TBL] [Abstract][Full Text] [Related]
17. Fractalkine gene receptor polymorphism in patients with multiple sclerosis.
Arli B; Irkec C; Menevse S; Yilmaz A; Alp E
Int J Neurosci; 2013 Jan; 123(1):31-7. PubMed ID: 22916723
[TBL] [Abstract][Full Text] [Related]
18. Candidate gene analysis of SPARCL1 gene in patients with multiple sclerosis.
Scalabrini D; Fenoglio C; Scarpini E; De Riz M; Comi C; Venturelli E; Cortini F; Piola M; Villa C; Naldi P; Monaco F; Bresolin N; Galimberti D
Neurosci Lett; 2007 Oct; 425(3):173-6. PubMed ID: 17825989
[TBL] [Abstract][Full Text] [Related]
19. IL-8 (-251 A/T) and CXCR2 (+1208 C/T) gene polymorphisms and risk of multiple sclerosis in Iranian patients.
Kamali-Sarvestani E; Nikseresht AR; Aliparasti MR; Vessal M
Neurosci Lett; 2006 Aug; 404(1-2):159-62. PubMed ID: 16793206
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
