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Clinical Laboratory|November 20, 2010
Investigation of GJB6 large deletions in Iranian patients using quantitative real-time PCRNejat Mahdieh, Marzieh Raeisi, Atefeh Shirkavand, et al.
Biomed Research International|April 30, 2019
Improvement of K562 Cell Line Transduction by FBS Mediated Attachment to the Cell Culture PlateMaryam Abbasalipour, Mohammad Ali Khosravi, Sirous Zeinali, et al.
Haematologica|June 21, 2006
First report on the co-inheritance of (beta) IVS I-1 (G-->T) Thalassemia with the (gamma) CD85 [Phe-->Ser (F1) (TTT-->TCT)] HbA2 Etolia in IranSirous Zeinali, Seyed Mohammad Eram, Seyed Babak Azimifar, et al.
Journal of Biotechnology|June 22, 2021
Targeted integration into pseudo attP sites of CHO cells using CRISPR/Cas9Sana Pourtabatabaei, Samaneh Ghanbari, Narges Damavandi, et al.
Life Sciences|November 4, 2019
A gene-based anti-angiogenesis therapy as a novel strategy for cancer treatmentAsghar Fallah, Hamid Reza Heidari, Behzad Bradaran, et al.
Advanced Biomedical Research|July 31, 2019
Microsatellite Marker Analysis for Laboratory Mice ProfilingReza Ahangari Cohan, Davoud Nouri Inanlou, Mohammad Hasan Samiee Aref, et al.
International Journal of Pediatric Otorhinolaryngology|March 26, 2013
A transversion mutation in non-coding exon 3 of the TMC1 gene in two ethnically related Iranian deaf families from different geographical regions; evidence for founder effectElham Davoudi-Dehaghani, Sirous Zeinali, Nejat Mahdieh, et al.
Cancer Genetics|October 14, 2017
Potential circulating miRNA signature for early detection of NSCLCAyda Arab, Morteza Karimipoor, Shiva Irani, et al.
BMC Medical Genetics|April 16, 2020
Reporting a rare form of myopathy, myopathy with extrapyramidal signs, in an Iranian family using next generation sequencing: a case reportMarzieh Mojbafan, Somayeh Takrim Nojehdeh, Faezeh Rahiminejad, et al.
Metabolic Brain Disease|May 24, 2019
Maple syrup urine disease mutation spectrum in a cohort of 40 consanguineous patients and insilico analysis of novel mutationsMaryam Abiri, Hassan Saei, Maryam Eghbali, et al.
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