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Cell Journal|August 4, 2019
Biosimilar Gene Therapy: Investigational Assessment of Secukinumab Gene TherapyAli Fallah, Hajar Estiri, Elizabeth Parrish, et al.
Molecular Genetics and Genomics : MGG|August 10, 2022
Development of a genetic risk score for obesity predisposition evaluationNarges Damavandi, Armin Soleymaniniya, Sobhan Bahrami Zadegan, et al.
Biocell : Official Journal of the Sociedades Latinoamericanas De Microscopia Electronica ... Et. Al|June 9, 2009
Isolation of stem cells from adult rat kidneysYousof Gheisari, Masoud Soleimani, Sirous Zeinali, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|November 16, 2018
Prevalence of factor VIII inhibitors among Afghan patients with hemophilia A: a first reportSayed H Mousavi, Seyed A Mesbah-Namin, Nematullah Rezaie, et al.
Anti-Cancer Drugs|May 30, 2014
TCF4 silencing sensitizes the colon cancer cell line to oxaliplatin as a common chemotherapeutic drugFatemeh Gheidari, Behnaz Bakhshandeh, Ladan Teimoori-Toolabi, et al.
Biochemical and Biophysical Research Communications|October 13, 2010
Unexpected heterogeneity due to recessive and de novo dominant mutations of GJB2 in an Iranian family with nonsyndromic hearing loss: implication for genetic counselingNejat Mahdieh, Atefeh Shirkavand, Marzieh Raeisi, et al.
Acta Oto-Laryngologica|November 26, 2014
Allelic heterogeneity among Iranian DFNB7/11 families: report of a new Iranian deaf family with TMC1 mutation identified by next-generation sequencingElham Davoudi-Dehaghani, Mohammad-Sadegh Fallah, Javad Tavakkoly-Bazzaz, et al.
Molecular Genetics & Genomic Medicine|November 7, 2019
Genetic variability in Iranian limb-girdle muscular dystrophy type 2B patients: An evidence of a founder effectMarzieh Mojbafan, Shirzadeh Tina, Fatemeh Zafarghandi Motlagh, et al.
Hemoglobin|November 17, 2010
Identification of a novel δ-globin gene mutation in an Iranian familyAzam Amirian, Masoomeh Jafarinejad, Alireza R Kordafshari, et al.
Hemoglobin|December 5, 2009
Molecular analysis of gamma-globin promoters, HS-111 and 3'HS1, in beta-thalassemia intermedia patients associated with high levels of Hb FMohammad Hamid, Frouzandeh Mahjoubi, Mohammad T Akbari, et al.
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