Hasil Pencarian - Marzieh Mojbafan

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  1. 1
    Hints From the Cellular Functions to the Practical Outlook of Circular RNAs

    Hints From the Cellular Functions to the Practical Outlook of Circular RNAs oleh Liora Yesharim, Marzieh Mojbafan, Marzieh Mojbafan, Maryam Abiri, Maryam Abiri

    Diterbitkan 2021-06-01
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  2. 2
    An evaluation of gastric adenocarcinoma-associated CircRNAs based on microarray meta-analysis and ceRNA networks

    An evaluation of gastric adenocarcinoma-associated CircRNAs based on microarray meta-analysis and ceRNA networks oleh Liora Yesharim, Saeed Talebi, Marzieh Mojbafan, Mahdi Alemrajabi, Shahram Teimourian

    Diterbitkan 2023-02-01
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  3. 3
    Genetic analysis of nephrogenic diabetes insipidus patients: A study on the Iranian population

    Genetic analysis of nephrogenic diabetes insipidus patients: A study on the Iranian population oleh Saeed Ghasemi, Marzieh Mojbafan, Saeed Talebi, Nakysa Hooman, Rozita Hoseini

    Diterbitkan 2024-04-01
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  4. 4
    Bethlem myopathy: A novel homozygous variant of c.385C>T (p.Arg129Cys) in the COL6A2 gene

    Bethlem myopathy: A novel homozygous variant of c.385C>T (p.Arg129Cys) in the COL6A2 gene oleh Maryam Kachuei, Kiana Orangi, Aynaz Mohammadi, Mohammad Mohammadi, Marzieh Mojbafan

    Diterbitkan 2024-08-01
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  5. 5
    Mutational spectrum of autosomal recessive limb-girdle muscular dystrophies in a cohort of 112 Iranian patients and reporting of a possible founder effect

    Mutational spectrum of autosomal recessive limb-girdle muscular dystrophies in a cohort of 112 Iranian patients and reporting of a possible founder effect oleh Marzieh Mojbafan, Reza Bahmani, Samira Dabbagh Bagheri, Zohreh Sharifi, Sirous Zeinali

    Diterbitkan 2020-01-01
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  6. 6
    Genetic diagnosis of Bartter syndrome in Iranian patients and detection of a novel homozygous CLCNKB mutation

    Genetic diagnosis of Bartter syndrome in Iranian patients and detection of a novel homozygous CLCNKB mutation oleh Somayeh Takrim Nojehdeh, Marzieh Mojbafan, Nakysa Hooman, Rozita Hoseini, Hasan Otukesh

    Diterbitkan 2022-12-01
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  7. 7
    A Systematic Review of the Possibility of Determining Age Based on DNA Methylation of the ELOVL2 Gene in Human Samples

    A Systematic Review of the Possibility of Determining Age Based on DNA Methylation of the ELOVL2 Gene in Human Samples oleh Foroozan Faress, Maryam Ameri, Marzieh Mojbafan, Mohammad Aminifard, Sayed Mahdi Marashi

    Diterbitkan 2023-01-01
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  8. 8
    Genetic variability in Iranian limb‐girdle muscular dystrophy type 2B patients: An evidence of a founder effect

    Genetic variability in Iranian limb‐girdle muscular dystrophy type 2B patients: An evidence of a founder effect oleh Marzieh Mojbafan, Shirzadeh Tina, Fatemeh Zafarghandi Motlagh, Andrei Surguchov, Yalda Nilipour, Sirous Zeinali

    Diterbitkan 2019-12-01
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  9. 9
    Reporting a rare form of myopathy, myopathy with extrapyramidal signs, in an Iranian family using next generation sequencing: a case report

    Reporting a rare form of myopathy, myopathy with extrapyramidal signs, in an Iranian family using next generation sequencing: a case report oleh Marzieh Mojbafan, Somayeh Takrim Nojehdeh, Faezeh Rahiminejad, Yalda Nilipour, Seyed Hasan Tonekaboni, Sirous Zeinali

    Diterbitkan 2020-04-01
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  10. 10
    A decade of molecular preimplantation genetic diagnosis of 350 blastomeres for beta-thalassemia combined with HLA typing, aneuploidy screening and sex selection in Iran

    A decade of molecular preimplantation genetic diagnosis of 350 blastomeres for beta-thalassemia combined with HLA typing, aneuploidy screening and sex selection in Iran oleh Yeganeh Keshvar, Solmaz Sabeghi, Zohreh Sharifi, Kiyana Sadat Fatemi, Panti Fouladi, Shahrzad Younesi Khah, Faezeh Rahiminejad, Atefeh Joudaki, Masoume Amini, Hamideh Bagherian, Marefat Ghaffari Novin, Mansoureh Movahedin, Marzieh Mojbafan, Sirous Zeinali

    Diterbitkan 2022-04-01
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