Search Results - Vahidi, Aida

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  1. 1
    Metformin and long non-coding RNAs in breast cancer

    Metformin and long non-coding RNAs in breast cancer by Gholami, Morteza, Klashami, Zeynab Nickhah, Ebrahimi, Pirooz, Mahboobipour, Amir Ali, Farid, Amir Salehi, Vahidi, Aida, Zoughi, Marziyeh, Asadi, Mojgan, Amoli, Mahsa M

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  2. 2
    Vascular Endothelial Growth Factor Genetic Variant Is Associated with in-Stent Restenosis after Percutaneous Coronary Intervention

    Vascular Endothelial Growth Factor Genetic Variant Is Associated with in-Stent Restenosis after Percutaneous Coronary Intervention by Asgarbeik, Saeedeh, Vahidi, Aida, Hasanzad, Mandana, Asadi, Mojgan, Mohammad Amoli, Mahsa

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  3. 3
    Association of microRNA gene polymorphisms with Type 2 diabetes mellitus: A systematic review and meta-analysis

    Association of microRNA gene polymorphisms with Type 2 diabetes mellitus: A systematic review and meta-analysis by Gholami, Morteza, Asgarbeik, Saeedeh, Razi, Farideh, Esfahani, Ensieh, Zoughi, Marzieh, Vahidi, Aida, Larijani, Bagher, Amoli, Mahsa

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  4. 4
    Genetic research in Immunogenetics Group of Endocrinology and Metabolism Research Institute

    Genetic research in Immunogenetics Group of Endocrinology and Metabolism Research Institute by Asgarbeik, Saeedeh, Amoli, Mahsa M., Vahidi, Aida, Klashami, Zeynab Nickhah

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  5. 5
    Evaluation of ERRFI1 +808 T/G variant and its mRNA expression in coronary artery in-stent restenosis

    Evaluation of ERRFI1 +808 T/G variant and its mRNA expression in coronary artery in-stent restenosis by Mehrpooya, Maryam, Asgarbeik, Saeedeh, Vahidi, Aida, Amoli, Mahsa Mohammad, Hosseini, Seyed Kianoosh

    Published in Gene reports
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  6. 6
    VEGFA gene haplotypes in Meniere's disease

    VEGFA gene haplotypes in Meniere's disease by Asgarbeik, Saeedeh, Vahidi, Aida, Yazdani, Nasrin, Tajdini, Ardavan, Amoli, Mahsa M.

    Published in Gene reports
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  7. 7
    eNOS gene Glu298Asp variant confer risk in sudden sensorineural hearing loss

    eNOS gene Glu298Asp variant confer risk in sudden sensorineural hearing loss by Yazdani, Nasrin, Kakavand Hamidi, Armita, Soroush, Negin, Jalili, Neda, Vahidi, Aida, Zarabi Ahrabi, Nakisa, Tajdini, Ardavan, Amoli, Mahsa

    Published in Acta oto-laryngologica
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  8. 8
    Sex-dependent association of ACE (I/D) polymorphism with Meniere's disease

    Sex-dependent association of ACE (I/D) polymorphism with Meniere's disease by Mohseni, Mohammad, Yazdani, Nasrin, Asgarbeik, Saeedeh, Daneshi, Ahmad, Farhadi, Mohammad, Asghari, Alimohamad, Mohebbi, Saleh, Vahidi, Aida, Amoli, Mahsa Mohammad

    Published in Meta Gene
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  9. 9
    Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy

    Recessive mutations in ATP8A2 cause severe hypotonia, cognitive impairment, hyperkinetic movement disorders and progressive optic atrophy by McMillan, Hugh J, Telegrafi, Aida, Singleton, Amanda, Cho, Megan T, Lelli, Daniel, Lynn, Francis C, Griffin, Julie, Asamoah, Alexander, Rinne, Tuula, Erasmus, Corrie E, Koolen, David A, Haaxma, Charlotte A, Keren, Boris, Doummar, Diane, Mignot, Cyril, Thompson, Islay, Velsher, Lea, Dehghani, Mohammadreza, Vahidi Mehrjardi, Mohammad Yahya, Maroofian, Reza, Tchan, Michel, Simons, Cas, Christodoulou, John, Martín-Hernández, Elena, Guillen Sacoto, Maria J, Henderson, Lindsay B, McLaughlin, Heather, Molday, Laurie L, Molday, Robert S, Yoon, Grace

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  10. 10
    Association of Lymphopenia with Short Term Outcomes of Sepsis Patients; a Brief Report

    Association of Lymphopenia with Short Term Outcomes of Sepsis Patients; a Brief Report by Sheikh Motahar Vahedi, Hojat, Bagheri, Aida, Jahanshir, Amirhosein, Seyedhosseini, Javad, Vahidi, Elnaz

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