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Plos One|February 25, 2022
Human IL-2Rɑ subunit binding modulation of IL-2 through a decline in electrostatic interactions: A computational and experimental approachArezoo Beig Parikhani, Kowsar Bagherzadeh, Rada Dehghan, et al.The Journal of Investigative Dermatology|December 1, 2016
Dystrophic Epidermolysis Bullosa: COL7A1 Mutation Landscape in a Multi-Ethnic Cohort of 152 Extended Families with High Degree of Customary Consanguineous MarriagesHassan Vahidnezhad, Leila Youssefian, Sirous Zeinali, et al.Metabolic Brain Disease|July 20, 2018
Autozygosity mapping of methylmalonic acidemia associated genes by short tandem repeat markers facilitates the identification of five novel mutations in an Iranian patient cohortMehdi Shafaat, Mohammad Reza Alaee, Ali Rahmanifar, et al.Stem Cells and Development|May 9, 2012
Genetic modification of mesenchymal stem cells to overexpress CXCR4 and CXCR7 does not improve the homing and therapeutic potentials of these cells in experimental acute kidney injuryYousof Gheisari, Kayhan Azadmanesh, Naser Ahmadbeigi, et al.New Biotechnology|October 4, 2012
Development of VEGFR2-specific Nanobody Pseudomonas exotoxin A conjugated to provide efficient inhibition of tumor cell growthMahdi Behdani, Sirous Zeinali, Morteza Karimipour, et al.Scientific Reports|May 17, 2019
Development and validation of a novel panel of 16 STR markers for simultaneous diagnosis of β-thalassemia, aneuploidy screening, maternal cell contamination detection and fetal sample authenticity in PND and PGD/PGS casesZohreh Sharifi, Faezeh Rahiminejad, Atefeh Joudaki, et al.Clinical Laboratory|February 7, 2017
FLT3 Gene Mutation Profile and Prognosis in Adult Acute Myeloid LeukemiaAileen Azari-Yam, Javad Tavakkoly-Bazzaz, Yousef Semnani, et al.The Journal of Investigative Dermatology|November 26, 2016
Gene-Targeted Next Generation Sequencing Identifies PNPLA1 Mutations in Patients with a Phenotypic Spectrum of Autosomal Recessive Congenital Ichthyosis: The Impact of ConsanguinityHassan Vahidnezhad, Leila Youssefian, Amir Hossein Saeidian, et al.Human Mutation|July 11, 2022
Mutation update: The spectra of PLEC sequence variants and related plectinopathiesHassan Vahidnezhad, Leila Youssefian, Nailah Harvey, et al.Journal of Pediatric Hematology/Oncology|April 7, 2007
Thalassemia in Iran: epidemiology, prevention, and managementHassan Abolghasemi, Ali Amid, Sirous Zeinali, et al.Pageof 18