Hasil Pencarian - Ariane Sadr-Nabavi

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  1. 1
    Chromosome Duplication (14q) and The Genotype Phenotype Correlation

    Chromosome Duplication (14q) and The Genotype Phenotype Correlation oleh Ariane Sadr-Nabavi, Morteza Saeidi

    Diterbitkan 2014-04-01
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  2. 2
    A Novel c.4822>T Mutation on SPG11 in an Iranian Patient Marked by Hereditary Spastic Paraparesis and Skeletal Deformity: An Incidental Finding or a True Association

    A Novel c.4822>T Mutation on SPG11 in an Iranian Patient Marked by Hereditary Spastic Paraparesis and Skeletal Deformity: An Incidental Finding or a True Association oleh Karim Nikkhah, Ali Ghabeli-Juibary, Ariane Sadr-Nabavi

    Diterbitkan 2016-09-01
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  3. 3
    Complications in Diagnosis of Susceptible Cases of Fragile X Syndrome

    Complications in Diagnosis of Susceptible Cases of Fragile X Syndrome oleh Reza JAFARZADEH ESFEHANI, Mahtab DASTPAK, Mohammad Reza MIRINEZHAD, Ariane SADR-NABAVI

    Diterbitkan 2018-07-01
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  4. 4
    Evaluation of COVID-19 trend in Iran; Population response to the recent pandemic overtime

    Evaluation of COVID-19 trend in Iran; Population response to the recent pandemic overtime oleh Reza Jafarzadeh Esfehani, Mohammad Shariati, Ariane Sadr-Nabavi, Hamid Reza Bidkhori

    Diterbitkan 2022-01-01
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  5. 5
    Cardiac Tamponade: A Rare Manifestation of Familial Mediterranean Fever

    Cardiac Tamponade: A Rare Manifestation of Familial Mediterranean Fever oleh Abdolreza Malek, Tina Zeraati, Ariane Sadr-Nabavi, Niloofar Vakili, Mohammad Reza Abbaszadegan

    Diterbitkan 2022-01-01
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  6. 6
    A review of Genetic Etiology and Emerging Molecular Therapies for FSHD in Preclinical Studies

    A review of Genetic Etiology and Emerging Molecular Therapies for FSHD in Preclinical Studies oleh Mohammad Reza Seyyed taghia, Reza Jafarzadeh Esfehani, Reza Boostani, Mohammad Shariati, Ariane Sadr Nabavi

    Diterbitkan 2021-03-01
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  7. 7
    Non-collagenous extracellular matrix protein dermatopontin may play a role as another component of transforming growth factor-β signaling pathway in colon carcinogenesis

    Non-collagenous extracellular matrix protein dermatopontin may play a role as another component of transforming growth factor-β signaling pathway in colon carcinogenesis oleh Ariane Sadr-Nabavi, Samaneh Bouromand-Noughabi, Naser Tayebi-Meybodi, Kimia Dadkhah, Nafiseh Amini, Alfons Meindl, Mohammad Reza Abbaszadegan

    Diterbitkan 2021-04-01
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  8. 8
    Analysis of MTHFR Gene C.677C>T and C.1298A>C Polymorphisms in Iranian Patients with Non-Syndromic Cleft Lip and Palate.

    Analysis of MTHFR Gene C.677C>T and C.1298A>C Polymorphisms in Iranian Patients with Non-Syndromic Cleft Lip and Palate. oleh Arezoo Jahanbin, Nadia Hasanzadeh, Faraneh Abdolhoseinpour, Ariane Sadr-Nabavi, Mohammad-Ali Raisolsadat, Khosro Shamsian, Farnaz Mohajertehran, Hamidreza Kianifar

    Diterbitkan 2014-06-01
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  9. 9
    Evaluation of bax, bcl-2, p21 and p53 genes expression variations on cerebellum of BALB/c mice before and after birth under mobile phone radiation exposure

    Evaluation of bax, bcl-2, p21 and p53 genes expression variations on cerebellum of BALB/c mice before and after birth under mobile phone radiation exposure oleh Najmeh Ghatei, Ariane Sadr Nabavi, Mohammad Hossein Bahreyni Toosi, Hosein Azimian, Mansour Homayoun, Reza Ghasemnezhad Targhi, Hossein Haghir

    Diterbitkan 2017-08-01
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  10. 10
    The effect of platelet-rich plasma on human mesenchymal stem cell-induced bone regeneration of canine alveolar defects with calcium phosphate-based scaffolds

    The effect of platelet-rich plasma on human mesenchymal stem cell-induced bone regeneration of canine alveolar defects with calcium phosphate-based scaffolds oleh Reihaneh Shafieian, Maryam Moghaddam Matin, Amin Rahpeyma, Alireza Fazel, Hamideh Salari Sedigh, Ariane Sadr-Nabavi, Halimeh Hassanzadeh, Alireza Ebrahimzadeh-Bideskan

    Diterbitkan 2017-10-01
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  11. 11
    The prevalence of SMN gene deletion/duplication in spinal muscular atrophy families referred to neuro-genetic centers of Mashhad, Iran

    The prevalence of SMN gene deletion/duplication in spinal muscular atrophy families referred to neuro-genetic centers of Mashhad, Iran oleh Mohammad Shariati, Alireza Davoudi, Reza Boostani, Farah Ashrafzadeh, Mehran Beiraghi Toosi, Nafiseh Todarbary, Javad Akhondian, Narges Hashemi, Ariane Sadr-Nabavi

    Diterbitkan 2024-07-01
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  12. 12
    Renin-Angiotensin A1166C Polymorphism and the Rrisk of Stroke

    Renin-Angiotensin A1166C Polymorphism and the Rrisk of Stroke oleh Peyman Zargari, Mohammad R. Ghasemi, Maryam Pirhoushiaran, Veda Vakili, Javad Hami, Mohammad Taghi Farzadfard, Payam Sasan-Nezhad, Mahmood R. Azarpazhooh, Ariane Sadr-Nabavi

    Diterbitkan 2015-07-01
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  13. 13
    PREVALENCE OF ß-THALASSEMIA MUTATIONS AMONG NORTHEASTERN IRANIAN POPULATION AND THEIR IMPACTS ON HEMATOLOGICAL INDICES AND APPLICATION OF PRENATAL DIAGNOSIS, A SEVEN-YEARS STUDY

    PREVALENCE OF ß-THALASSEMIA MUTATIONS AMONG NORTHEASTERN IRANIAN POPULATION AND THEIR IMPACTS ON HEMATOLOGICAL INDICES AND APPLICATION OF PRENATAL DIAGNOSIS, A SEVEN-YEARS STUDY oleh Mohammad Ehsan Jaripour, Kourosh Hayatigolkhatmi, Vahid Iranmanesh, Farhad Khadivi Zand, Zahra Badiei, Hamid Farhangi, Ali Ghasemi, Abdollah Banihashem, Reza Jafarzadeh Esfehani, Ariane Sadr-Nabavi

    Diterbitkan 2018-07-01
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  14. 14
    Copy number analysis from whole-exome sequencing data revealed a novel homozygous deletion in PARK7 leads to severe early-onset Parkinson's disease

    Copy number analysis from whole-exome sequencing data revealed a novel homozygous deletion in PARK7 leads to severe early-onset Parkinson's disease oleh Mohammad Reza Seyedtaghia, Mohammad Soudyab, Mohammad Shariati, Reza Jafarzadeh Esfehani, Shabnam Vafadar, Neda Shalaei, Vahid Nouri, Michael Zech, Julianne Winkelmann, Ali shoeibi, Ariane Sadr-Nabavi

    Diterbitkan 2023-04-01
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