These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
158 related articles for article (PubMed ID: 34584155)
1. Expression and clinical significance of IL7R, NFATc2, and RNF213 in familial and sporadic multiple sclerosis. Imani SZH; Hojati Z; Khalilian S; Dehghanian F; Kheirollahi M; Khorrami M; Shaygannejad V; Mirmosayyeb O Sci Rep; 2021 Sep; 11(1):19260. PubMed ID: 34584155 [TBL] [Abstract][Full Text] [Related]
2. Gene expression profiles of YAP1, TAZ, CRB3, and VDR in familial and sporadic multiple sclerosis among an Iranian population. Khalilian S; Hojati Z; Dehghanian F; Shaygannejad V; Imani SZH; Kheirollahi M; Khorrami M; Mirmosayyeb O Sci Rep; 2021 Apr; 11(1):7713. PubMed ID: 33833274 [TBL] [Abstract][Full Text] [Related]
3. Association Between IL7R Promoter Polymorphisms and Multiple Sclerosis in Turkish Population. Simsek H; Geckin H; Sensoz NP; List EO; Arman A J Mol Neurosci; 2019 Jan; 67(1):38-47. PubMed ID: 30443838 [TBL] [Abstract][Full Text] [Related]
4. Clinical and diagnostic features of patients with familial multiple sclerosis. Andrijauskis D; Balnyte R; Keturkaite I; Vaitkus A Med Hypotheses; 2019 Oct; 131():109310. PubMed ID: 31443766 [TBL] [Abstract][Full Text] [Related]
5. Rare variants of RNF213 and moyamoya/non-moyamoya intracranial artery stenosis/occlusion disease risk: a meta-analysis and systematic review. Liao X; Deng J; Dai W; Zhang T; Yan J Environ Health Prev Med; 2017 Nov; 22(1):75. PubMed ID: 29165161 [TBL] [Abstract][Full Text] [Related]
6. Association of Multiple Sclerosis Phenotypes with Single Nucleotide Polymorphisms of Al-Eitan L; Qudah MA; Qawasmeh MA Biomolecules; 2020 Feb; 10(3):. PubMed ID: 32111053 [TBL] [Abstract][Full Text] [Related]
7. Familial multiple sclerosis patients have a shorter delay in diagnosis than sporadic cases. Steenhof M; Stenager E; Nielsen NM; Kyvik K; Möller S; Hertz JM Mult Scler Relat Disord; 2019 Jul; 32():97-102. PubMed ID: 31078918 [TBL] [Abstract][Full Text] [Related]
8. Investigating SNHG3 and BCYRN1 lncRnas expression in the peripheral blood cells of multiple sclerosis patients. Tayefeh-Gholami S; Akbarzadeh S; Rajabi A; Najari P; Ghasemzadeh T; HosseinpourFeizi M; Safaralizadeh R Neurol Res; 2024 Sep; 46(9):876-882. PubMed ID: 38832630 [TBL] [Abstract][Full Text] [Related]
9. Genetic variants in IL2RA and IL7R affect multiple sclerosis disease risk and progression. Traboulsee AL; Bernales CQ; Ross JP; Lee JD; Sadovnick AD; Vilariño-Güell C Neurogenetics; 2014 Aug; 15(3):165-9. PubMed ID: 24770783 [TBL] [Abstract][Full Text] [Related]
10. Analysis of STAT1, STAT2 and STAT3 mRNA expression levels in the blood of patients with multiple sclerosis. Manoochehrabadi S; Arsang-Jang S; Mazdeh M; Inoko H; Sayad A; Taheri M Hum Antibodies; 2019; 27(2):91-98. PubMed ID: 30412483 [TBL] [Abstract][Full Text] [Related]
11. Homozygous c.14576G>A variant of RNF213 predicts early-onset and severe form of moyamoya disease. Miyatake S; Miyake N; Touho H; Nishimura-Tadaki A; Kondo Y; Okada I; Tsurusaki Y; Doi H; Sakai H; Saitsu H; Shimojima K; Yamamoto T; Higurashi M; Kawahara N; Kawauchi H; Nagasaka K; Okamoto N; Mori T; Koyano S; Kuroiwa Y; Taguri M; Morita S; Matsubara Y; Kure S; Matsumoto N Neurology; 2012 Mar; 78(11):803-10. PubMed ID: 22377813 [TBL] [Abstract][Full Text] [Related]
12. Candidate gene association analysis of multiple sclerosis in the Jordanian Arab population: A case-control study. Al-Eitan L; Al Qudah M; Al Qawasmeh M Gene; 2020 Oct; 758():144959. PubMed ID: 32683075 [TBL] [Abstract][Full Text] [Related]
13. Gene expression and genotyping studies implicate the interleukin 7 receptor in the pathogenesis of primary progressive multiple sclerosis. Booth DR; Arthur AT; Teutsch SM; Bye C; Rubio J; Armati PJ; Pollard JD; Heard RN; Stewart GJ; J Mol Med (Berl); 2005 Oct; 83(10):822-30. PubMed ID: 16075257 [TBL] [Abstract][Full Text] [Related]
14. The investigation of relevancy between Kouchaki E; Nikoueinejad H; Akbari H; Azimi S; Behnam M J Immunoassay Immunochem; 2019; 40(4):396-406. PubMed ID: 31084243 [No Abstract] [Full Text] [Related]
15. Identification of RNF213 as a susceptibility gene for moyamoya disease and its possible role in vascular development. Liu W; Morito D; Takashima S; Mineharu Y; Kobayashi H; Hitomi T; Hashikata H; Matsuura N; Yamazaki S; Toyoda A; Kikuta K; Takagi Y; Harada KH; Fujiyama A; Herzig R; Krischek B; Zou L; Kim JE; Kitakaze M; Miyamoto S; Nagata K; Hashimoto N; Koizumi A PLoS One; 2011; 6(7):e22542. PubMed ID: 21799892 [TBL] [Abstract][Full Text] [Related]
16. Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of disease. Vilariño-Güell C; Zimprich A; Martinelli-Boneschi F; Herculano B; Wang Z; Matesanz F; Urcelay E; Vandenbroeck K; Leyva L; Gris D; Massaad C; Quandt JA; Traboulsee AL; Encarnacion M; Bernales CQ; Follett J; Yee IM; Criscuoli MG; Deutschländer A; Reinthaler EM; Zrzavy T; Mascia E; Zauli A; Esposito F; Alcina A; Izquierdo G; Espino-Paisán L; Mena J; Antigüedad A; Urbaneja-Romero P; Ortega-Pinazo J; Song W; Sadovnick AD PLoS Genet; 2019 Jun; 15(6):e1008180. PubMed ID: 31170158 [TBL] [Abstract][Full Text] [Related]
17. Glial and neuroaxonal biomarkers in a multiple sclerosis (MS) cohort. Kalatha T; Hatzifilippou E; Arnaoutoglou M; Balogiannis S; Koutsouraki E Hell J Nucl Med; 2019; 22 Suppl 2():113-121. PubMed ID: 31802051 [TBL] [Abstract][Full Text] [Related]
18. Mutations of Lin J; Liang J; Wen J; Luo M; Li J; Sun X; Xu X; Li J; Wang D; Wang J; Chen H; Lai R; Liang F; Li C; Ye F; Zhang J; Zeng J; Yang S; Sheng W J Cereb Blood Flow Metab; 2021 Jun; 41(6):1251-1263. PubMed ID: 32248732 [TBL] [Abstract][Full Text] [Related]
19. Sibling disability risk at onset and during disease progression in familial multiple sclerosis. Wellek A; Korsukewitz C; Bach JP; Schock S; Eienbröker C; Seitz F; Spengler A; Hemmer B; Schlegel K; Oertel WH; Sommer N; Tackenberg B Mult Scler; 2011 Sep; 17(9):1060-6. PubMed ID: 21561958 [TBL] [Abstract][Full Text] [Related]
20. Epidemiology of familial multiple sclerosis and its comparison to sporadic form in Markazi Province, Iran. Faraji F; Mohaghegh P; Talaie A Mult Scler Relat Disord; 2022 Dec; 68():104231. PubMed ID: 36270251 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]