Hasil Pencarian - Morteza Hashemzadeh

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  1. 1
    Different Types of the Coagulation Disorders in Hamadan and A Comparison of the ABO & Rh Blood Group Distribution in the Patients and the Control Group

    Different Types of the Coagulation Disorders in Hamadan and A Comparison of the ABO & Rh Blood Group Distribution in the Patients and the Control Group oleh Hamid Pour-Jafari, Morteza Hashemzadeh Chaleshtori

    Diterbitkan 2003-12-01
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  2. 2
    Expandable DNA Repeat and Human Hereditary Disorders

    Expandable DNA Repeat and Human Hereditary Disorders oleh Shahin Ramazi, Ali Fasihi, Maryam Godarziyan, Morteza Hashemzadeh-Chaleshtori

    Diterbitkan 2016-03-01
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  3. 3
    Population Data on D7S2425 Marker in Five Ethnic Groups of the Iranian Population: A Highly Informative Marker for Molecular Diagnosis of ARNSHL

    Population Data on D7S2425 Marker in Five Ethnic Groups of the Iranian Population: A Highly Informative Marker for Molecular Diagnosis of ARNSHL oleh Marjan Mojtabavi Naeini, Sadeq Vallian Boroujeni, Morteza Hashemzadeh Chaleshtori

    Diterbitkan 2014-01-01
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  4. 4
    Synthesis of Novel Surface-Modified Hematite Nanoparticles for Lead Ions Removal from Aqueous Solution

    Synthesis of Novel Surface-Modified Hematite Nanoparticles for Lead Ions Removal from Aqueous Solution oleh Morteza Hashemzadeh, Abdolreza Nilchi, Amir Hessam Hassani, Reza Saberi

    Diterbitkan 2019-05-01
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  5. 5
    Correlation of Endothelial Nitric Oxide Synthase Gene Polymorphism (GG, TT and GT Genotype) with Proteinuria and Retinopathy in Type 2 Diabetic Patients

    Correlation of Endothelial Nitric Oxide Synthase Gene Polymorphism (GG, TT and GT Genotype) with Proteinuria and Retinopathy in Type 2 Diabetic Patients oleh Ali Momeni, Morteza Hashemzadeh Chaleshtori, Saeed Saadatmand, Soleiman Kheiri

    Diterbitkan 2016-02-01
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  6. 6
    Screening of Myo7A Mutations in Iranian Patients with Autosomal Recessive Hearing Loss from West of Iran

    Screening of Myo7A Mutations in Iranian Patients with Autosomal Recessive Hearing Loss from West of Iran oleh Samira ASGHARZADE, Somayeh REIISI, Mohammad Amin TABATABAIEFAR, Morteza HASHEMZADEH CHALESHTORI

    Diterbitkan 2017-01-01
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  7. 7
    Analysis of relationship between tumor necrosis factor alpha gene (g308a polymorphism) with preterm labor

    Analysis of relationship between tumor necrosis factor alpha gene (g308a polymorphism) with preterm labor oleh Lobat Jafarzadeh, Azar Danesh, Marzieh Sadeghi, Fateme Heybati, Morteza Hashemzadeh

    Diterbitkan 2013-01-01
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  8. 8
    Clinical Aspects of Microsatellite Instability Testing in Colorectal Cancer

    Clinical Aspects of Microsatellite Instability Testing in Colorectal Cancer oleh Mehrdad Zeinalian, Morteza Hashemzadeh-Chaleshtori, Rasoul Salehi, Mohammad Hassan Emami

    Diterbitkan 2018-01-01
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  9. 9
    Mesenchymal stem cells versus their conditioned medium in the treatment of ischemia/reperfusion injury: Evaluation of efficacy and hepatic specific gene expression in mice

    Mesenchymal stem cells versus their conditioned medium in the treatment of ischemia/reperfusion injury: Evaluation of efficacy and hepatic specific gene expression in mice oleh Somayeh Khosravi-Farsani, Arash Zaminy, Sedigheh Kazemi, Morteza Hashemzadeh-Chaleshtori

    Diterbitkan 2022-07-01
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  10. 10
    Accessing Genetic and Environmental Factors of Hearing Loss in 354 Families in Gom and Markazi Provinces

    Accessing Genetic and Environmental Factors of Hearing Loss in 354 Families in Gom and Markazi Provinces oleh Abdolrahim Sadeghi, Mohammad Hossein San'ati, Fatemeh Alasti, Morteza Hashemzadeh-Chaleshtari

    Diterbitkan 2005-07-01
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  11. 11
    Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked family

    Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked fa... oleh Somayeh Reiisi, Mohammad Amin Tabatabaiefar, Mohammad Hosein Sanati, Morteza Hashemzadeh Chaleshtori

    Diterbitkan 2016-07-01
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  12. 12
    Lack of Association between ESR1 and CYP1A1 Gene Polymorphisms and Susceptibility to Uterine Leiomyoma in Female Patients of Iranian Descent

    Lack of Association between ESR1 and CYP1A1 Gene Polymorphisms and Susceptibility to Uterine Leiomyoma in Female Patients of Iranian Descent oleh Fatemeh Taghizade Mortezaee, Mohammad Amin Tabatabaiefar, Morteza Hashemzadeh Chaleshtori, Sepideh Miraj

    Diterbitkan 2014-06-01
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  13. 13
    Tumor microsatellite instability and clinicopathologic features in Iranian colorectal cancer patients at risk for Lynch syndrome

    Tumor microsatellite instability and clinicopathologic features in Iranian colorectal cancer patients at risk for Lynch syndrome oleh Mehrdad Zeinalian, Morteza Hashemzadeh-Chaleshtori, Rasoul Salehi, Mohammad Kazemi, Mohammad Hassan Emami

    Diterbitkan 2015-01-01
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  14. 14
    Familial Colorectal CancerType X in Central Iran: A New Clinicopathologic Description

    Familial Colorectal CancerType X in Central Iran: A New Clinicopathologic Description oleh Mehrdad Zeinalian, Mahdi Hadian, Morteza Hashemzadeh-Chaleshtori, Rasoul Salehi, Mohammad Hassan Emami

    Diterbitkan 2016-10-01
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  15. 15
    بررسی جهش‌های ژن LRTOMT (لوکوس 63DFNB) در بیماران مبتلا به ناشنوایی غیر سندرمیک مغلوب استان هرمزگان با استفاده از روش‌های PCR-SSCP، PCR-HA و توالی‌یابی DNA

    بررسی جهش‌های ژن LRTOMT (لوکوس 63DFNB) در بیماران مبتلا به ناشنوایی غیر سندرمیک مغلوب استان هرمزگان با استفاده از روش‌های PCR-SSCP، PCR-HA و توالی‌یابی DNA... oleh Shahrbanoo Parchami-Barjui, Somayeh Reiisi, Fatemeh Rezaiean, Fatemeh Heybati, Morteza Hashemzadeh-Chaleshtori

    Diterbitkan 2014-10-01
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  16. 16
    Association of Hypoxia-inducible factor α subunits with TSGA10 transcripts in HeLa, MCF7 and MDA-MB231- cell lines

    Association of Hypoxia-inducible factor α subunits with TSGA10 transcripts in HeLa, MCF7 and MDA-MB231- cell lines oleh Parya Rahmani Rad, Maryam Beigom Mobasheri, Morteza Hashemzadeh-Chaleshtori, Mohammad Hossein Modarressi

    Diterbitkan 2018-01-01
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  17. 17
    MT1XT20 Single Quasi-Monomorphic Mononucleotide Marker for Detection of Microsatellite Instability in Iranian Patients with Hereditary Nonpolyposis Colorectal Cancer (HNPCC)

    MT1XT20 Single Quasi-Monomorphic Mononucleotide Marker for Detection of Microsatellite Instability in Iranian Patients with Hereditary Nonpolyposis Colorectal Cancer (HNPCC) oleh Najmeh Farahani, Parvaneh Nikpour, Mohammad Hassan Emami, Morteza Hashemzadeh, Mehrdad Zeinalian, Rasoul Salehi

    Diterbitkan 2016-02-01
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  18. 18
    Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees

    Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees oleh Somayeh Khatami, Masomeh Askari, Fatemeh Bahreini, Morteza Hashemzadeh-Chaleshtori, Saeed Hematian, Samira Asgharzade

    Diterbitkan 2020-11-01
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  19. 19
    Investigation of Mutations in Exons 15 and 18 of MYBPC3 Gene in Hypertrophic Cardiomyopathy Patients

    Investigation of Mutations in Exons 15 and 18 of MYBPC3 Gene in Hypertrophic Cardiomyopathy Patients oleh Behnaz Sadat Abedi, Seyedeh Zohreh kiyani, Morteza Hashemzadeh Chaleshtori, Shahrbanoo Parchami, Abbas Doosti

    Diterbitkan 2015-08-01
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  20. 20
    Molecular Mechanisms behind Free Radical Scavengers Function against Oxidative Stress

    Molecular Mechanisms behind Free Radical Scavengers Function against Oxidative Stress oleh Fereshteh Ahmadinejad, Simon Geir Møller, Morteza Hashemzadeh-Chaleshtori, Gholamreza Bidkhori, Mohammad-Saeid Jami

    Diterbitkan 2017-07-01
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