سامانه مدیریت نشریات علمی دانشگاه علوم پزشکی مشهد

Mehdizadeh Fanid, Leila, Shahrokhi, Hassan, Adampourezare, Mina, Hosseinpour Feizi, Mohamad Ali, Bonyadi, Mortaza, Eslami, A. (1394). Association between Common Single- nucleotide Polymorphism of Reelin Gene, rs736707 (C/T) with Autism Spectrum Disorder in Iranian-Azeri Patients. , 3(6.1), 1065-1071. doi: 10.22038/ijp.2015.5668
Leila Mehdizadeh Fanid; Hassan Shahrokhi; Mina Adampourezare; Mohamad Ali Hosseinpour Feizi; Mortaza Bonyadi; A Eslami. "Association between Common Single- nucleotide Polymorphism of Reelin Gene, rs736707 (C/T) with Autism Spectrum Disorder in Iranian-Azeri Patients". , 3, 6.1, 1394, 1065-1071. doi: 10.22038/ijp.2015.5668
Mehdizadeh Fanid, Leila, Shahrokhi, Hassan, Adampourezare, Mina, Hosseinpour Feizi, Mohamad Ali, Bonyadi, Mortaza, Eslami, A. (1394). 'Association between Common Single- nucleotide Polymorphism of Reelin Gene, rs736707 (C/T) with Autism Spectrum Disorder in Iranian-Azeri Patients', , 3(6.1), pp. 1065-1071. doi: 10.22038/ijp.2015.5668
Mehdizadeh Fanid, Leila, Shahrokhi, Hassan, Adampourezare, Mina, Hosseinpour Feizi, Mohamad Ali, Bonyadi, Mortaza, Eslami, A. Association between Common Single- nucleotide Polymorphism of Reelin Gene, rs736707 (C/T) with Autism Spectrum Disorder in Iranian-Azeri Patients. , 1394; 3(6.1): 1065-1071. doi: 10.22038/ijp.2015.5668

Association between Common Single- nucleotide Polymorphism of Reelin Gene, rs736707 (C/T) with Autism Spectrum Disorder in Iranian-Azeri Patients

Journal of Pediatric Perspectives
مقاله 9، دوره 3، شماره 6.1، بهمن 2015، صفحه 1065-1071    اصل مقاله (574.93 K)
شناسه دیجیتال (DOI): 10.22038/ijp.2015.5668
نویسندگان
Leila Mehdizadeh Fanid* 1؛ Hassan Shahrokhi2؛ Mina Adampourezare3؛ Mohamad Ali Hosseinpour Feizi4؛ Mortaza Bonyadi5؛ A Eslami6
1Cognitive Neuroscience, PhD, Department of Biology Faculty of Natural Sciences, University of Tabriz, Tabriz, Iran.
2Child and Adolescent Psychiatrist MD, Research Centre of Psychiatry and Behavioral Science, Tabriz University of Medical Science, Tabriz, Iran.
3Physiology, MSc, Department of Biology Faculty of Natural Sciences. University of Tabriz, 29 Bahman Bolvard, Tabriz, Iran.
4Radiobiology, Professor, Department of Biology Faculty of Natural Sciences. University of Tabriz, 29 Bahman Bolvard, Tabriz, Iran.
5Faculty of Natural Sciences. Department of Biology University of Tabriz, 29 Bahman Bolvard, Tabriz, Iran.
6General practitioner, MD. Children`s Hospital of Tabriz Medical University. Tabriz, Iran.
چکیده
Introduction
Reelin gene (RELN) codes a large extracellular matrix glycoprotein with serine protease activity and is implicated in the modulation of neuronal signaling, synaptic transmission and plasticity. The reelin plays a fundamental and pivotal role in the development of laminar structures and may be one of the loci contributing to the positive linkage between chromosome 7q and autistic disorder. This study was performed to examine the association of a frequent genetic variation in reelin gene, rs736707 (C/T), with Autism risk among Iranian-Azeri population.
Materials and Methods
A case–control association study included 74 patients with Autism spectrum disorder (ASD) and 86 healthy subjects. Genomic DNA was extracted from peripheral blood samples by salting-out method. Single nucleotide polymorphisms (SNP) genotyping was carried out by Polymerase chain reaction- restriction fragment length polymorphism (PCR-RFLP) technique. The collected data were analyzed through java stant online statistics software, using Chi-square, with a significance level of 0.05.
Results
Significant differences in the allele and genotype frequencies between cases and controls were not observed (P>0.05). The rs736707SNP was not associated with Autism predisposition in Iranian-Azeri children.
Conclusion
Based on our results, the rs736707 SNP could not be used as a useful molecular biomarker to predict genetic susceptibility for autism spectrum disorder in Iranian-Azeri patients.
کلیدواژه‌ها
Autism؛ Molecular marker, Polymorphism, Reelin gene
آمار
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