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Journal Abstract Search

159 related items for 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 28; 11(1):19260. PubMed ID: 34584155
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  • 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 08; 11(1):7713. PubMed ID: 33833274
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  • 6. Association of Multiple Sclerosis Phenotypes with Single Nucleotide Polymorphisms of IL7R, LAG3, and CD40 Genes in a Jordanian Population: A Genotype-Phenotype Study.
    Al-Eitan L, Qudah MA, Qawasmeh MA.
    Biomolecules; 2020 Feb 26; 10(3):. PubMed ID: 32111053
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  • 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 Feb 26; 27(2):91-98. PubMed ID: 30412483
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  • 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 20; 758():144959. PubMed ID: 32683075
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  • 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 20; 15(6):e1008180. PubMed ID: 31170158
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  • 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 Jun 20; 22 Suppl 2():113-121. PubMed ID: 31802051
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  • 18. Mutations of RNF213 are responsible for sporadic cerebral cavernous malformation and lead to a mulberry-like cluster in zebrafish.
    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 20; 41(6):1251-1263. PubMed ID: 32248732
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