Showing 1 - 12 results of 12 for search 'Mehri KHATAMI', query time: 0.04s Refine Results
  1. 1
    Novel Missense Mitochondrial ND4L Gene Mutations in Friedreich's Ataxia

    Novel Missense Mitochondrial ND4L Gene Mutations in Friedreich's Ataxia by Mohammad Mehdi Heidari, Mehri Khatami

    Published 2011-05-01
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  2. 2
    Analysis of Missense Mutations of CX3CR1 Gene in Patients with Recurrent Pregnancy Loss Using Bioinformatics Tools

    Analysis of Missense Mutations of CX3CR1 Gene in Patients with Recurrent Pregnancy Loss Using Bioinformatics Tools by Bahareh Mazrouei, Mohammad Mehdi Heidari, Mehri Khatami

    Published 2022-08-01
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  3. 3
    Molecular Analysis of rs2070744 and rs1799983 Polymorphisms of NOS3 Gene in Iranian Patients With Multiple Sclerosis

    Molecular Analysis of rs2070744 and rs1799983 Polymorphisms of NOS3 Gene in Iranian Patients With Multiple Sclerosis by Mohammad Mehdi Heidari, Mehri Khatami, Yaser Tahamtan

    Published 2017-07-01
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  4. 4
    The Study of Nitric Oxide Synthase 3 (NOS3) T-786C and 4a4b Gene Polymorphism in Iranian Men with Varicocele

    The Study of Nitric Oxide Synthase 3 (NOS3) T-786C and 4a4b Gene Polymorphism in Iranian Men with Varicocele by Seyede Nafise Tabatabaei, Mohammad Mehdi Heidari, Mehri Khatami

    Published 2020-03-01
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  5. 5
    Review of Genetic Changes and Factors Causing Cardiac Arrhythmias

    Review of Genetic Changes and Factors Causing Cardiac Arrhythmias by Mehri Khatami, Mohammad Mehdi Heidari, Bahareh Mazrouei, Rojin Aflaki

    Published 2023-02-01
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  6. 6
    Molecular Mechanisms of Recurrent Pregnancy Loss

    Molecular Mechanisms of Recurrent Pregnancy Loss by Bahareh Mazrouei, , Mohammad Mehdi Heidari, Mehri Khatami, Maryam Tahmasebi

    Published 2020-05-01
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  7. 7
    Identification of a novel non-sense mutation in TBX5 gene in pediatric patients with congenital heart defects

    Identification of a novel non-sense mutation in TBX5 gene in pediatric patients with congenital heart defects by Mehri Khatami, Mohammad Mehdi Heidari, Fatemeh Kazeminasab, Razieh Zare Bidaki

    Published 2018-03-01
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  8. 8
    Genetic Causes of Familial Adenomatous Polyposis (FAP), Risk Factors and Clinical Outcomes

    Genetic Causes of Familial Adenomatous Polyposis (FAP), Risk Factors and Clinical Outcomes by Mohammad Mehdi Heidari, Elham Afkhami aqhda, Maryam Tahmasebi, Mehri Khatami, Zahra Shaker Ardakani

    Published 2024-03-01
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  9. 9
    Molecular Study of Nucleotide Changes of ATPase6 and MT-CYB Genes in the Mitochondrial Genome of Patients with Familial Adenomatous Polyposis (FAP)

    Molecular Study of Nucleotide Changes of ATPase6 and MT-CYB Genes in the Mitochondrial Genome of Patients with Familial Adenomatous Polyposis (FAP) by Mohammad Mehdi Heidari, Fatemeh Ebrahimi, Zahra Shaker Ardakani, Mahsa Mirzaei, Shima Mirhosseini, Mehri Khatami

    Published 2023-08-01
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  10. 10
    Mitochondrial Genetic Variation in Iranian Infertile Men with Varicocele

    Mitochondrial Genetic Variation in Iranian Infertile Men with Varicocele by Mohammad Mehdi Heidari, Mehri Khatami, Amirhossein Danafar, Tahere Dianat, Ghazaleh Farahmand, Ali Reza Talebi

    Published 2016-10-01
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  11. 11
    Simultaneous Genotyping of the Rs4762 and Rs699 Polymorphisms in Angiotensinogen Gene and Correlation with Iranian CAD Patients with Novel Hexa-primer ARMS-PCR

    Simultaneous Genotyping of the Rs4762 and Rs699 Polymorphisms in Angiotensinogen Gene and Correlation with Iranian CAD Patients with Novel Hexa-primer ARMS-PCR by Mehri KHATAMI, Mohammad Mehdi HEIDARI, Mehdi HADADZADEH, Barbara SCHEIBER-MOJDEHKAR, Morteza BITARAF SANI, Massoud HOUSHMAND

    Published 2017-05-01
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  12. 12
    Mitochondrial mutations in protein coding genes of respiratory chain including complexes IV, V, and mt-tRNA genes are associated risk factors for congenital heart disease

    Mitochondrial mutations in protein coding genes of respiratory chain including complexes IV, V, and mt-tRNA genes are associated risk factors for congenital heart disease by Mohammad Mehdi Heidari, Mehri Khatami, Akram Kamalipour, Mustafa Kalantari, Mahsa Movahed, Mohammad Hayet Emmamy, Mehdi Hadadzadeh, José Bragança, Mohsen Namnabat, Bahareh Mazrouei

    Published 2022-11-01
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