Showing 1 - 7 results of 7 for search 'Reza Mirfakhraie', query time: 0.07s Refine Results
  1. 1
    Aberrant Wnt/β-Catenin Signaling Pathway in Testis of Azoospermic Men​

    Aberrant Wnt/β-Catenin Signaling Pathway in Testis of Azoospermic Men​ by Marefat Ghaffari Novin, Reza Mirfakhraie, Hamid Nazarian

    Published 2015
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  2. 2
    Effect of Umbelliprenin on HIF-1α- Driven Angiogenesis Induced by EGF and CoCl2 in T47D Cell Line

    Effect of Umbelliprenin on HIF-1α- Driven Angiogenesis Induced by EGF and CoCl2 in T47D Cell Line by Somayeh Mahmoodi Khatonabadi, Roya Atabakhshian, Reza Mirfakhraie, Shiva Ghafghazi, Seyed Ali Ziai*

    Published 2024
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  3. 3
    Contribution of long noncoding RNA HOTAIR variants to preeclampsia susceptibility in Iranian women

    Contribution of long noncoding RNA HOTAIR variants to preeclampsia susceptibility in Iranian women by Sahra Esmkhani, Hossein Sadeghi, Majid Ghasemian, Reihaneh Pirjani, Mona Amin-Beidokhti, Milad Gholami, Fakhrolmolouk Yassaee, Reza Mirfakhraie

    Published 2021
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  4. 4
    Umbelliprenin Suppresses Angiogenesis Signaling in SKBR-3 Cell Line by Downregulation of EGF/CoCl2 -Mediated PI3K/AKT/MAPK

    Umbelliprenin Suppresses Angiogenesis Signaling in SKBR-3 Cell Line by Downregulation of EGF/CoCl2 -Mediated PI3K/AKT/MAPK by Roya Atabakhshian, Siamak Salami, Reza Mirfakhraie, Somayeh Mahmoodi Khatonabadi, Majid Sirati-Sabet, Bahram Gholamali Yaghmaei, Shiva Ghafghazi, Amirreza Dowlati Beirami, Mitra Sadat Rezaei, Seyed Ali Ziai*

    Published 2021
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  5. 5
    Comprehensive review and expanding the genetic landscape of Cornelia-de-Lange spectrum: insights from novel mutations and skin biopsy in exome-negative cases

    Comprehensive review and expanding the genetic landscape of Cornelia-de-Lange spectrum: insights from novel mutations and skin biopsy in exome-negative cases by Sahand Tehrani Fateh, Nadia Mohammad Zadeh, Shadab Salehpour, Farzad Hashemi-Gorji, Ashkan Omidi, Hossein Sadeghi, Reza Mirfakhraie, Parinaz Moghimi, Sepideh Keyvanfar, Sepideh Mohammadi Sarvaleh, Mohammad Miryounesi, Mohammad-Reza Ghasemi

    Published 2024
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  6. 6
    Broadening the phenotype and genotype spectrum of novel mutations in pontocerebellar hypoplasia with a comprehensive molecular literature review

    Broadening the phenotype and genotype spectrum of novel mutations in pontocerebellar hypoplasia with a comprehensive molecular literature review by Mohammad-Reza Ghasemi, Sahand Tehrani Fateh, Aysan Moeinafshar, Hossein Sadeghi, Parvaneh Karimzadeh, Reza Mirfakhraie, Mitra Rezaei, Farzad Hashemi-Gorji, Morteza Rezvani Kashani, Fatemehsadat Fazeli Bavandpour, Saman Bagheri, Parinaz Moghimi, Masoumeh Rostami, Rasoul Madannejad, Hassan Roudgari, Mohammad Miryounesi

    Published 2024
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  7. 7
    Exome sequencing reveals neurodevelopmental genes in simplex consanguineous Iranian families with syndromic autism

    Exome sequencing reveals neurodevelopmental genes in simplex consanguineous Iranian families with syndromic autism by Mohammad-Reza Ghasemi, Hossein Sadeghi, Farzad Hashemi-Gorji, Reza Mirfakhraie, Vijay Gupta, Afif Ben-Mahmoud, Saman Bagheri, Katayoon Razjouyan, Shadab Salehpour, Seyed Hassan Tonekaboni, Mehdi Dianatpour, Davood Omrani, Mi-Hyeon Jang, Lawrence C. Layman, Mohammad Miryounesi, Hyung-Goo Kim

    Published 2024
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