Ngā hua rapu - Zeinali, Sirous

Whakamahine hua
  1. 1
    Molecular Basis of α-Thalassemia in Iran

    Molecular Basis of α-Thalassemia in Iran mā Valaei, Atefeh, Karimipoor, Morteza, Kordafshari, Alireza, Zeinali, Sirous

    I whakaputaina 2018
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  2. 2
    High-Resolution HLA-A Typing in Normal Iranian Population

    High-Resolution HLA-A Typing in Normal Iranian Population mā Hadadianpour, Azadeh, Aref, Mohammad Hasan Samiee, Zeinali, Sirous

    I whakaputaina 2018
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  3. 3
    Endometriotic Mesenchymal Stem Cells Epigenetic Pathogenesis: Deregulation of miR-200b, miR-145, and let7b in A Functional Imbalanced Epigenetic Disease

    Endometriotic Mesenchymal Stem Cells Epigenetic Pathogenesis: Deregulation of miR-200b, miR-145, and let7b in A Functional Imbalanced Epigenetic Disease mā Mashayekhi, Parisa, Noruzinia, Mehrdad, Zeinali, Sirous, Khodaverdi, Sepideh

    I whakaputaina 2019
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  4. 4
    Induction of apoptosis and cell cycle arrest in colorectal cancer cells by novel anticancer metabolites of Streptomyces sp. 801

    Induction of apoptosis and cell cycle arrest in colorectal cancer cells by novel anticancer metabolites of Streptomyces sp. 801 mā Kouroshnia, Arghavan, Zeinali, Sirous, Irani, Shiva, Sadeghi, Akram

    I whakaputaina 2022
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  5. 5
    Distal Renal Tubular Acidosis in an Iranian Patient with Hereditary Spherocytosis

    Distal Renal Tubular Acidosis in an Iranian Patient with Hereditary Spherocytosis mā Shahab-Movahed, Zahra, Majd, Ahmad, Siasi Torbati, Elham, Zeinali, Sirous

    I whakaputaina 2021
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  6. 6
    Revisiting a Complex Rearrangement Involving a 619 Base Pairs Deletion, 6 Nucleotide Insertion Followed by a A > G Substitution Causing β°-Thalassemia

    Revisiting a Complex Rearrangement Involving a 619 Base Pairs Deletion, 6 Nucleotide Insertion Followed by a A > G Substitution Causing β°-Thalassemia mā DabbaghBagheri, Samira, Ghadami, Shirin, Mollazadeh, Faeze, Saadat, Ameneh, Zeinali, Sirous

    I whakaputaina 2016
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  7. 7
    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 mā Mojbafan, Marzieh, Bahmani, Reza, Bagheri, Samira Dabbagh, Sharifi, Zohreh, Zeinali, Sirous

    I whakaputaina 2020
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  8. 8
    In silico design, construction and cloning of Trastuzumab humanized monoclonal antibody: A possible biosimilar for Herceptin

    In silico design, construction and cloning of Trastuzumab humanized monoclonal antibody: A possible biosimilar for Herceptin mā Akbarzadeh-Sharbaf, Soudabeh, Yakhchali, Bagher, Minuchehr, Zarrin, Shokrgozar, Mohammad Ali, Zeinali, Sirous

    I whakaputaina 2012
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  9. 9
    Expression Enhancement in Trastuzumab Therapeutic Monoclonal Antibody Production using Genomic Amplification with Methotrexate

    Expression Enhancement in Trastuzumab Therapeutic Monoclonal Antibody Production using Genomic Amplification with Methotrexate mā Akbarzadeh-Sharbaf, Soudabeh, Yakhchali, Bagher, Minuchehr, Zarrin, Shokrgozar, Mohammad Ali, Zeinali, Sirous

    I whakaputaina 2013
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  10. 10
    Characterization and haplotype study of 6 novel STR markers related to the KCNQ1 gene in heterogeneous cardiovascular disorders in the Iranian population

    Characterization and haplotype study of 6 novel STR markers related to the KCNQ1 gene in heterogeneous cardiovascular disorders in the Iranian population mā AMIRIAN, Azam, ZAFARI, Zahra, SHARIFI, Zohreh, KORDAFSHARI, Alireza, KARIMIPOOR, Morteza, ZEINALI, Sirous

    I whakaputaina 2019
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  11. 11
    Frequency and Correlation of Common Genes Copy Number Alterations in Childhood Acute Lymphoblastic Leukemia with Prognosis

    Frequency and Correlation of Common Genes Copy Number Alterations in Childhood Acute Lymphoblastic Leukemia with Prognosis mā Hosein Pour Feizi, Abbasali, Zeinali, Sirous, Toporski, Jacek, Sheervalilou, Roghayeh, Mehranfar, Sahar

    I whakaputaina 2020
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  12. 12
    Improvement of K562 Cell Line Transduction by FBS Mediated Attachment to the Cell Culture Plate

    Improvement of K562 Cell Line Transduction by FBS Mediated Attachment to the Cell Culture Plate mā Abbasalipour, Maryam, Khosravi, Mohammad Ali, Zeinali, Sirous, Khanahmad, Hossein, Karimipoor, Morteza, Azadmanesh, Kayhan

    I whakaputaina 2019
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  13. 13
    Biosimilar Gene Therapy: Investigational Assessment of Secukinumab Gene Therapy

    Biosimilar Gene Therapy: Investigational Assessment of Secukinumab Gene Therapy mā Fallah, Ali, Estiri, Hajar, Parrish, Elizabeth, Soleimani, Mansoureh, Zeinali, Sirous, Zadeh-Vakili, Azita

    I whakaputaina 2020
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  14. 14
    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 mā Mojbafan, Marzieh, Tina, Shirzadeh, Zafarghandi Motlagh, Fatemeh, Surguchov, Andrei, Nilipour, Yalda, Zeinali, Sirous

    I whakaputaina 2019
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  15. 15
    Transient expression of anti-VEFGR2 nanobody in Nicotiana tabacum and N. benthamiana

    Transient expression of anti-VEFGR2 nanobody in Nicotiana tabacum and N. benthamiana mā Modarresi, Mostafa, Javaran, Mokhtar Jalali, Shams-bakhsh, Masoud, Zeinali, Sirous, Behdani, Mahdi, Mirzaee, Malihe

    I whakaputaina 2018
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  16. 16
    Microsatellite Marker Analysis for Laboratory Mice Profiling

    Microsatellite Marker Analysis for Laboratory Mice Profiling mā Ahangari Cohan, Reza, Nouri Inanlou, Davoud, Samiee Aref, Mohammad Hasan, Zeinali, Sirous, Farhoudi, Ramin

    I whakaputaina 2019
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  17. 17
    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 mā Mojbafan, Marzieh, Nojehdeh, Somayeh Takrim, Rahiminejad, Faezeh, Nilipour, Yalda, Tonekaboni, Seyed Hasan, Zeinali, Sirous

    I whakaputaina 2020
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  18. 18
    Transient Expression Assay of (A)γ-588 (A/G) Mutations in the K562 Cell Line

    Transient Expression Assay of (A)γ-588 (A/G) Mutations in the K562 Cell Line mā Hamid, Mohammad, Mahjoubi, Frouzandeh, Akbari, Mohammad Taghi, Khanahmad, Hossein, Jamshidi, Fatemeh, Zeinali, Sirous, Karimipoor, Morteza

    I whakaputaina 2011
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  19. 19
    MicroRNA-148b and microRNA-152 reactivate tumor suppressor genes through suppression of DNA methyltransferase-1 gene in pancreatic cancer cell lines

    MicroRNA-148b and microRNA-152 reactivate tumor suppressor genes through suppression of DNA methyltransferase-1 gene in pancreatic cancer cell lines mā Azizi, Masoumeh, Teimoori-Toolabi, Ladan, Arzanani, Mohsen Karimi, Azadmanesh, Kayhan, Fard-Esfahani, Pezhman, Zeinali, Sirous

    I whakaputaina 2014
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  20. 20
    A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome

    A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome mā Youssefian, Leila, Touati, Andrew, Saeidian, Amir Hossein, Zargari, Omid, Zeinali, Sirous, Vahidnezhad, Hassan, Uitto, Jouni

    I whakaputaina 2017
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