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    hOGG1 gene polymorphism and breast cancer risk: A systematic review and meta-analysis study 

    Ali Sanjari Moghaddam; Milad Nazarzadeh; Zeinab Bidel; Aliasghar Karamatinia; Hossein Darvish; Alireza Mosavi Jarrahi; Alireza Mosavi Jarrahi (2017-01-01)
    © 2017 Wiley Periodicals, Inc. To address the effect of hGGO1 (rs1052133) gene polymorphism on the risk of breast cancer, a meta-analysis was performed. We pooled adjusted odds ratios (OR) as overall and three subgroups ...
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    Association study of the vesicular monoamine transporter 1 (VMAT1) gene with autism in an Iranian population 

    Rezvan Noroozi; Soudeh Ghafouri-Fard; Mir Davood Omrani; Mohsen Habibi; Arezou Sayad; Mohammad Taheri (2017-08-20)
    Copyright © 2017 Elsevier B.V. All rights reserved. Autism Spectrum Disorders (ASD) (MIM 209850) are a group of neurodevelopmental disorders distinguished by destructed social interaction and communication abilities along ...
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    In silico dissection of miRNA targetome polymorphisms and their role in regulating miRNA-mediated gene expression in esophageal cancer 

    Ziba Nariman-Saleh-Fam; Milad Bastami; Mohammad Hossein Somi; Naser Samadi; Naser Samadi; Mohammad Reza Abbaszadegan; Farkhondeh Behjati; Hamid Ghaedi; Javad Tavakkoly-Bazzaz; Andrea Masotti (2016-12-01)
    © 2016, Springer Science+Business Media New York. Esophageal cancer is the eighth most common cancer worldwide. Also middle-aged obese adults with higher body mass index during childhood have a greater risk to develop ...
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    SNAP-25 gene variations and attention-deficit hyperactivity disorder in Iranian population 

    Mahjoubeh Zarrabi Alhosseini; Javad Jamshidi; Alireza Zare Bidoki; Saeid Ganji; Mohammad Reza Eslami Amirabadi; Babak Emamalizadeh; Shaghayegh Taghavi; Parasto Shokraeian; Fatemeh Mohajerani; Hossein Darvish (2016-11-01)
    © 2016 Informa UK Limited, trading as Taylor & Francis Group. Objectives: Attention deficit hyperactivity disorder (ADHD) is a common psychiatric condition of childhood characterized by persistent symptoms of hyperactivity, ...
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    SIPA1L2, MIR4697, GCH1 and VPS13C loci and risk of Parkinson's diseases in Iranian population: A case-control study 

    Tannaz Safaralizadeh; Javad Jamshidi; Ehsan Esmaili Shandiz; Abolfazl Movafagh; Atena Fazeli; Babak Emamalizadeh; Navid Manafi; Shaghayegh Taghavi; Abbas Tafakhori; Hossein Darvish (2016-10-15)
    © 2016 Elsevier B.V. Parkinson's disease (PD) is the second most common neurodegenerative disorder. Prevalence of PD increases steadily with age. A recent meta-analysis of genome-wide association studies has identified six ...
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    Genetic variants and expression study of FOXP3 gene in acute coronary syndrome in Iranian patients 

    Milad Gholami; Ali Esfandiary; Masoumeh Vatanparast; Reza Mirfakhraie; Mir Mohsen Hosseini; Soudeh Ghafouri-Fard (2016-04-01)
    © 2016 John Wiley & Sons, Ltd. Acute coronary syndrome (ACS) is the most serious form of coronary artery disease. Inflammatory processes participate in different stages of this disorder. FOXP3 gene plays an important ...
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    Association of XPC gene polymorphisms with prostate cancer risk 

    Shima A. Kahnamouei; Behzad Narouie; Mehdi Sotoudeh; Mohammad J. Mollakouchekian; Nasser Simforoosh; Seyed A M Ziaee; Mohammad Samzadeh; Mohammad Samzadeh; Mahdi Afshari; Seyed H. Jamaldini; Seyed H. Jamaldini; Mahdieh Imeni; Mandana Hasanzad; Mandana Hasanzad (2016-01-01)
    Background: Defective DNA repair capacity caused by inherited polymorphisms could be associated with cancer susceptibility. One of the major repair pathways is Nucleotide Excision Repair (NER). We investigated Xeroderma ...
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    Myxovirus resistance protein A (MxA) polymorphism is associated with IFNβ response in Iranian multiple sclerosis patients 

    Arezou Sayad; Soudeh Ghafouri-Fard; Mir Davood Omrani; Mir Davood Omrani; Rezvan Noroozi; Mohammad Taheri; Mohammad Taheri; Mohammad Taheri (2017-06-01)
    © 2017, Springer-Verlag Italia. Multiple sclerosis (MS) is a heterogeneous immune-related demyelinating disorder of central nervous system with several genetic and environmental factors contributing in its pathogenesis or ...
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    Association between polymorphisms in TP53 and MDM2 genes and susceptibility to prostate cancer 

    Mohammad Hashemi; Mohammad Hashemi; Shadi Amininia; Mahboubeh Ebrahimi; Nasser Simforoosh; Abbas Basiri; Seyed Amir Mohsen Ziaee; Behzad Narouie; Mehdi Sotoudeh; Mohammad Javad Mollakouchekian; Esmaeil Rezghi Maleki; Hamideh Hanafi-Bojd; Maryam Rezaei; Gholamreza Bahari; Mohsen Taheri; Saeid Ghavami (2017-04-01)
    © 2017, Spandidos Publications. All rights reserved. Tumor protein 53 (TP53), a tumor suppressor gene, is a vital cellular cancer suppressor in multicellular organisms. Murine double minute-2 (MDM2) is an oncoprotein that ...
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    Parental cigarette smoking, transforming growth factor-alpha gene variant and the risk of orofacial cleft in Iranian infants 

    Asghar Ebadifar; Roya Hamedi; Hamid Reza Khorramkhorshid; Koorosh Kamali; Fatemeh Aghakhani Moghadam (2016-04-01)
    © 2016, Mashhad University of Medical Sciences. All rights reserved. Objective(s): We investigated the influence of genetic variation of the transforming growth-factor alpha (TGFA) locus on the relationship between smoking ...
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    AuthorArezou Sayad (13)Mohammad Reza Zali (13)Seyed Reza Mohebbi (10)Hossein Darvish (9)Mehdi Hedayati (9)Mohammad Taheri (9)Ahmad Reza Ebadian (8)Babak Emamalizadeh (8)Javad Jamshidi (8)Mahdi Kadkhodazadeh (8)... View MoreSubject
    Polymorphism (139)
    Prostate cancer (10)Peri-implantitis (8)Iran (7)Periodontitis (7)Coronary artery disease (6)Iranian (6)Gene (5)Genetic (5)Iranian population (5)... View MoreDate Issued2010 - 2017 (131)2004 - 2009 (8)Has File(s)No (139)

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