Morteza Bagheri
Cellular and Molecular Research Center, Urmia University of Medical Sciences, Urmia, Iran.
[ 1 ] - The association of FokI and ApaI polymorphisms in vitamin D receptor gene with autoimmune thyroid diseases in the northwest of Iran
Background: Some genetic factors are involved in the etiology of Hashimoto thyroiditis and Graves’ disease as autoimmune thyroid diseases (AITDs). Effects of vitamin D receptor gene polymorphisms in AITDs development have already been investigated in some previous studies. However, no study has been done on the association between VDR FokI and ApaI polymorphisms and AITDs in an Iranian popu…
[ 2 ] - Frequency of BCR-ABL Fusion Transcripts in Iranian Azeri Turkish patients with Chronic Myeloid Leukemia
Background: The Philadelphia chromosome (Ph) characterized by t (9; 22) (q34; q11.2) is a reciprocal translocation giving rise to a chimeric BCR-ABL fusion gene. Incidence of Ph chromosome is over 98% in Patients with Chronic Myeloid Leukemia (CML) and around 20% in acute lymphoblastic leukemia (ALL). The finding of this fusion gene is essential for diagnosis of CML by detection of various fusion…
[ 3 ] - بررسی اثر گروه‌های خونی والدین بر محل لانه‌گزینی جنین و نسبت جنسی ثانویه در کودکان متولد شده در بیمارستان الزهرای میاندوآب
پیش‌زمینه و هدف: با توجه به وجود شواهدی مبنی بر ارتباط محل لانه‌گزینی و جنسیت جنین، هدف این تحقیق بررسی ارتباط گروه‌های خونی ABO و Rh والدین بر نسبت جنسی ثانویه و محل جفت (به‌عنوان عامل واسطه‌ای بین گروه‌های خونی و نسبت جنسی) بود. مواد و روش‌کار: برای انجام این تحقیق توصیفی، اطلاعات 200 نوزاد تک قلوی متولدشده در طی سال‌های 1393 تا 1395 در بیمارستان الزهرای میاندوآب از طریق مراجعه به پرونده مادران…
[ 4 ] - C677T and A1298C Mutations in the Methylenetetrahydrofolate Reductase Gene in Patients with Recurrent Abortion from the Iranian Azeri Turkish
Background To assess whether the C677T and A1298C mutations in the methylenetetrahydrofolate reductase (MTHER) gene are associated with recurrent abortion (RA), we determined the frequencies of the T677 and C1298 mutations in patients and controls. MaterialsAndMethods Mutations were determined by a RFLP-PCR method in 53 patients and 61 matched controls. Results The frequencies of T alleles were 0…
Co-Authors