Mina Adampourezare
Physiology, MSc. Department of Biology Faculty of Natural Sciences. University of Tabriz, 29 Bahman Bolvard, Tabriz, Iran, IR.
[ 1 ] - Study of Polymorphism of the DRD2 Gene (-141C Ins/Del, rs1799732) with Attention Deficit Hyperactivity Disorder a Population Sample of Children in Iranian-Azeri
BackgroundAttention deficit hyperactivity disorder (ADHD), is a multifactorial disorder and converging evidence has implicated abnormalities of dopamine neurotransmission. The aim of this study was to examine the association of -141 polymorphisms in DRD2 gene with ADHA among Iranian-Azeri population.Materials and Methods A case–control association study included 153 patients with attention defi...
[ 2 ] - An Association Analysis of Reelin Gene (RELN) Exon 22 (G/C), Rs.362691, Polymorphism with Autism Spectrum Disorder among Iranian-Azeri Population
Background Autism spectrum disorder (ASD) is a intricate childhood neuropsychiatric disorder that is described by deficits in communication of verbal and non-verbal, reciprocal social interactions, stereotypic behaviors, interests, and activities. The studies of post-mortem neuro-anatomical anomalies have indicated that migration alterations could occur early during development (first trimester...
[ 3 ] - The Association of DRD2 Gene TaqI Polymorphism with Attention Deficit Hyperactivity Disorder a Population Sample of Iranian Azeri-children
Background Attention deficit hyperactivity disorder (ADHD) is a multi-factorial disorder that has defined by hyperactivity, impulsivity and attention deficits. Various neurotransmitters such as dopamine can play a role in its pathophysiology. The aim of this study was to examine the association of two common single nucleotide polymorphisms in DRD2 gene, Taq I A (T/C) and Taq I B (G/A), with ADH...
[ 4 ] - بررسی ارتباط پلی مورفیسمی های تک نوکلئوتیدی ( اگزون 22 ، ,rs362691 C>G و اینترون 59 ، rs736707 C>T ) ژنReelin با ناهنجاری طیف اوتیسم در کودکان مبتلای آذری در شمالغرب ایران
اختلاف طیف اتیسم (ASD) اختلال عصبی پیچیده دوران کودکی است که توسط نقص در ارتباطات کلامی و غیر کلامی، تعاملات اجتماعی متقابل، رفتارهای کلیشه ای، علایق و فعالیتها توصیف شده است. در طول رشد مغز جنینی Reelin سیگنالی را برای مهاجرت مناسب نورون های جدید حاصل از تقسیم میتوزی فراهم می کند. از آنجایی که ژن Reelin نقش بسیار مهمی در این فرآیند مهاجرتی دارد بنابراین، این ژن به عنوان یک ژن کاندید بالقوه ...