Sahar Moghbelinejad

Department of Biochemistry and Genetic, School of Medicine, Qazvin University of Medical Sciences, Qazvin, Iran

[ 1 ] - CRISPR/Cas9, a new approach to successful knockdown of ABCB1/P-glycoprotein and reversal of chemosensitivity in human epithelial ovarian cancer cell line

Objective(s): Multidrug resistance (MDR) is a major obstacle in the successful chemotherapy of ovarian cancer. Inhibition of P-glycoprotein (P-gp), a member of ATP-binding cassette (ABC) transporters, is a well-known strategy to overcome MDR in cancer. The aim of this study was to investigate the efficiency and ability of CRISPR/Cas9 genome editing technology to knockdown ABCB1 gene expression ...

[ 2 ] - افزایش میزان حیات، تعداد و تحرک اسپرم مردان با اسپرماتوژنزیس طبیعی تحت تأثیر عصاره زعفران پس از پدیده انجماد- ذوب

زمینه: امروزه در استفاده از روش­های کمک باروری شاهد به کار بردن روش انجماد اسپرم به میزان زیادی هستیم از طرفی در مطالعه­های مختلف، تأثیر منفی انجماد بر شاخص­های مختلف اسپرم نشان داده شده است. هدف: مطالعه حاضر با هدف تعیین اثر زعفران به عنوان یک ماده آنتی­اکسیدان بر شاخص­های مختلف اسپرم مردان با اسپرماتوژنزیس طبیعی پس از پدیده انجماد- ذوب انجام شد. مواد و روش­ها: این مطالعه مورد- شاهدی در سال 13...

[ 3 ] - Association of the -308G/A Polymorphism of TNF-α Gene with Some Semen and Sperm Parameters in Men with Infertility

Background The tumor necrosis factor alpha (TNF-α) gene is a cytokine involved in systemic inflammation. Results of the association of its polymorphisms with infertility in men are controversial.  Objective The aim of this study was to evaluate the association of -308G/A polymorphism in TNF-α gene with different parameters of semen and sperm in infertile men.  Methods Participants were 210 me...

[ 4 ] - Mutation in Aminoacyl Trna Synthetase 1 In Autosomal Recessive ‎Intellectual Disability ‎

Background: Intellectual disability (ID) is one of the most common neurodevelopment disorders that caused by both environment and genetic factors. Also genetic defects have involving for approximately 50% of ID etiology, it is demonstrated that genetics play significant role in ID development. The important risk factor in most country in ID is consanguinity marriage. Iran has high frequency of ...