Search Results - "Bonyadi, Morteza"
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Associations of the ANKK1 and DRD2 gene polymorphisms with overweight, obesity and hedonic hunger among women from the Northwest of Iran
Published in Eating and weight disorders (01-02-2021)“…Background Pleasure from palatable foods can stimulate hedonic eating and, therefore, might be a major culprit for obesity. Dopamine receptor polymorphisms,…”
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Exploring the Heterogeneity of Non-Syndromic Hearing Loss: A Comprehensive Review of Implicated Genes and the Role of Whole Exome Sequencing
Published in مجلة علوم ذي قار (27-12-2023)“…Background: Hereditary hearing loss (HHL) accounts for approximately 50-60% of all hearing loss (HL) cases, highlighting the significant role genetics play in…”
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Whole-exome sequencing analysis in a case of primary congenital glaucoma due to the partial uniparental isodisomy
Published in Genomics & informatics (2022)“…We described a clinical, laboratory, and genetic presentation of a pathogenic variant of the CYP1B1 gene through a report of a case of primary congenital…”
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The effect of complement factor B gene variation on age-related macular degeneration in Iranian patients
Published in Iranian journal of ophthalmology (01-09-2019)“…To determine the possible association of rs4151667 (L9H) complement factor B (CFB) gene with age-related macular degeneration (AMD). The L9H is one of the…”
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Common chemotherapeutic agents modulate fatty acid distribution in human hepatocellular carcinoma and colorectal cancer cells
Published in Bioimpacts (01-01-2017)“…Introduction: Cancer cells are critically correlated with lipid molecules, particularly fatty acids, as structural blocks for membrane building, energy…”
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Relationship of Serum Klotho Level With ACE Gene Polymorphism in Stable Kidney Allograft Recipients
Published in Iranian journal of kidney diseases (01-03-2017)“…The kidney is the main source of serum Klotho production. Immunosuppressive agents could affect the kidney in this regard. The effect of the ACE gene…”
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Assessment of MEFV Gene Mutations in Exon 10 in Familial Mediterranean Fever Patients from Iranian Azeri and Turkish Population
Published in Iranian journal of public health (01-01-2016)“…Dear Editor-in-Chief Familial Mediterranean fever (FMF), the most frequent of the periodic fever syndromes, is an autosomal recessive disease, predominantly…”
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Molecular analysis of the SMN and NAIP genes in Iranian spinal muscular atrophy patients
Published in Pediatrics international (01-04-2009)“…Background: Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder characterized by degeneration of spinal cord anterior horn cells,…”
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Genotype-Phenotype Correlation for Cystic Fibrosis According to Registry Center of Cystic Fibrosis
Published in Crescent journal of medical and biological sciences (01-01-2020)“…Objectives: The present study aimed to investigate the correlation of genotype-phenotype in patients with cystic fibrosis (CF) in the Azeri-Turkish population,…”
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FMF Genotype-phenotype correlation in Iranian Azeri Turks: Association between M694V/R761H mutation and amyloidosis
Published in Iranian journal of basic medical sciences (01-07-2015)“…Familial Mediterranean fever (FMF), an inherited autosomal recessive disorder, is frequently present among individuals of Mediterranean origin. Differences in…”
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Helicobacter pylori vacA d1 genotype predicts risk of gastric adenocarcinoma and peptic ulcers in northwestern Iran
Published in Asian Pacific journal of cancer prevention : APJCP (01-01-2014)“…There is a close relationship between Helicobacter pylori (H pylori)-specific factors and different gastroduodenal diseases. The present study aimed to…”
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Tumor Necrosis Factor Gene Polymorphisms in Advanced Non-exudative Age-related Macular Degeneration
Published in Journal of ophthalmic & vision research (01-04-2015)“…To investigate tumor necrosis factor (TNF)-α gene polymorphisms in advanced dry-type age-related macular degeneration (AMD) in a population from Northeastern…”
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Tumour necrosis factor-alpha gene polymorphisms in Iranian patients with biliary atresia
Published in African journal of paediatric surgery (01-07-2014)“…Biliary atresia (BA) is a progressive inflammatory destructive process of the bile ducts. This study evaluated the relationship between single-nucleotide…”
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Helicobacter pylori vacA d1 Genotype Predicts Risk of Gastric Adenocarcinoma and Peptic Ulcers in Northwestern Iran
Published in Asian Pacific journal of cancer prevention : APJCP (2014)“…Background: There is a close relationship between Helicobacter pylori (H pylori)-specific factors and different gastroduodenal diseases. The present study…”
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Genetic pattern of cystic fibrosis patients in Azeri Turkish population
Published in Russian open medical journal (01-01-2017)“…Objective ― This study was designed to analyze the genetic pattern of cystic fibrosis and effects on age, sex and mortality in the Azeri Turkish population in…”
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Gender Differences in Clinical Presentations of Cystic Fibrosis Patients in Azeri Turkish Population
Published in Tuberculosis and respiratory diseases (01-10-2016)“…Cystic fibrosis (CF) is an autosomal recessive disorder with several clinical presentations. This study was undertaken in the Azeri Turkish population in Iran,…”
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Gender Differences in Clinical Presentations of Cystic Fibrosis Patients in Azeri Turkish Population
Published in Tuberculosis and respiratory diseases (01-10-2016)“…Background: Cystic fibrosis (CF) is an autosomal recessive disorder with several clinical presentations. This study was undertaken in the Azeri Turkish…”
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MEFV mutations in Northwest of Iran: a cross sectional study
Published in Iranian journal of basic medical sciences (01-01-2015)“…Familial Mediterranean Fever (FMF) is an autosomal recessive disorder characterized by recurrent episodes of fever accompanied by peritonitis, pleurisy, and…”
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Whole-exome sequencing analysis in a case of primary congenital glaucoma due to the partial uniparental isodisomy
Published in Genomics & informatics (01-09-2022)“…We described a clinical, laboratory, and genetic presentation of a pathogenic variant of the CYP1B1 gene through a report of a case of primary congenital…”
Get full text
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