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Hemoglobin|June 19, 2015
Interaction of an α-Globin Gene Triplication with β-Globin Gene Mutations in Iranian Patients with β-Thalassemia IntermediaSamaneh Farashi, Nooshin Bayat, Negin Faramarzi Garous, et al.
International Journal of Molecular and Cellular Medicine|November 9, 2023
Mutational Analysis and Genotype Investigation of Less Known Gaucher Mutations through Haplotype Analysis in Iranian Gaucher PatientsNegar Sardarpour, Hamideh Bagherian, Fatemeh Zafarghandi Motlagh, et al.
Iranian Biomedical Journal|October 14, 2024
Mutations in COL6A Gene Family Responsible for Muscular Dystrophies in Three Unrelated FamiliesNasibeh Soltani, Zahra Shahbazi, Morteza Karimipoor, et al.
Archives of Iranian Medicine|January 11, 2022
The Spectrum of Pathogenic Variants in Iranian Families with Hemophilia ASarah Azadmehr, Faezeh Rahiminejad, Fatemeh Zafarghandi Motlagh, et al.
Clinical Laboratory|September 25, 2012
Design of a biological method for rapid detection of presence of PCR inhibitors in aged bone DNAAkram Ghasemi, Nejat Mahdieh, Mahmood Tavallaei, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|July 12, 2014
GJB2 c.-23+1G>A mutation is second most common mutation among Iranian individuals with autosomal recessive hearing lossSirous Zeinali, Elham Davoudi-Dehaghani, Sarah Azadmehr, et al.
Current Pharmaceutical Design|March 14, 2024
Specific Targeting of Zinc Transporter LIV-1 with Immunocytokine Containing Anti-LIV-1 VHH and Human IL-2 and Evaluation of its <i>In vitro</i> Antitumor ActivityRada Dehghan, Arezoo Beig Parikhani, Reza Ahangari Cohan, et al.
Advanced Biomedical Research|December 12, 2017
<i>In Vitro</i> Evaluation of Vegf-Pseudomonas Exotoxin: A Conjugated on Tumor CellsJahangir Langari, Morteza Karimipoor, Majid Golkar, et al.
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