باقری, مرتضی
دانشگاه علوم پزشکی ارومیه
[ 1 ] - بررسی ارتباط بین وضعیت ویتامین D و پلی مورفیسم BsmI ژن گیرنده ویتامین D با بیماری هاشیموتو در شهر ارومیه
Background & Aims: The hashimoto thyroiditis as a common autoimmune thyroid disease have a multifactorial etiology. Vitamin D status and vitamin D receptor gene BsmI polymorphism are involved in hashimoto developing. The aim of this research was to study the association between 25hydroxy vitamin D serum levels and BsmI polymorphism with hashimoto. Materials & Methods: We conducted a case-contr...
[ 2 ] - فراوانی آلل‌ها و ژنوتایپ‌های ApaI ژن رسپتور ویتامین D در زنان آذری ایرانی با بیماری سندرم تخمدان پلی‌کیستیک و کنترل سالم
Received: 19 Oct, 2012 Accepted: 22 Dec, 2012 Background & Aims : Polycystic Ovary Syndrome (PCOS) as a heterogeneous disease is one of the most usual women endocrine disorders and the leading causes of infertility by reason of unovulation. PCOS affecting about between 5 and 10 percent of females. The results of recent studies indicated that vitamin D has an important role in calcium home...
[ 3 ] - چند شکلی ژنتیکی4G/5G در پروموتور ژن مهارکننده فعال کننده پلاسمینوژن-1 در زنان با سابقه سقط‌های خود به خودی مکرر و افراد کنترل سالم
Background & Aims: Deletion/insertion of a single guanosine in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene, resulting in two alleles containing either 4 or 5 guanosines (G). Results of recent studies showed that presence of PAI-1 4G allele may increase the risk of human disease. The aim of present study was to determine the 4G/5G genetic variation in the promoter of PAI-...
[ 4 ] - 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 fusi...
[ 5 ] - فاقدعنوان فارسی است
Background & Aims: Spinal muscular atrophy (SMA) is a common disorder with autosomal recessive inheritance pattern. The frequency of carriers of this disease is one in forty to one in sixty. SMA occurs in 98% of cases due to the homozygous deletion of SMN1 exons 7 and 8. The purpose of this study was to evaluating the deletion and point mutations of the SMN1 gene in patients with SMA in west Az...
[ 6 ] - MOLECULAR STUDY OF E148Q MUTATION IN EXON 2 OF MEFV GENE IN PATIENTS WITH PREMATURE CORONARY ARTERY DISEASE
Background & Aims: Recent studies have shown that some of the MEFV gene mutations are common in patients with coronary artery disease. The present study was designed to investigate the presence or absence of E148Q mutation in exon 2 of MEFV gene in patients with premature coronary artery disease. Materials & Methods: In this study, 90 patients with coronary artery disease were voluntarily sele...
[ 7 ] - Prenatal stress increased γ2 GABAA receptor subunit gene expression in hippocampus and potentiated pentylenetetrazol-induced seizure in rats
Objective(s): Stress during pregnancy is able to bring extensive effects on neurobehavioral development in offspring. The GABAergic system plays a pivotal role in neuronal excitability, which can be affected by prenatal stress (PS). This study aimed to evaluate impact of the PS on γ2 subunit of gamma-aminobutyric acid A (GABAA) receptor gene expression in the hippocamp...
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