Search Results - "Morteza Bonyadi"

Associations of the ANKK1 and DRD2 gene polymorphisms with overweight, obesity and hedonic hunger among women from the Northwest of Iran by Aliasghari, Fereshteh, Nazm, Saba A., Yasari, Sepideh, Mahdavi, Reza, Bonyadi, Morteza

“…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 by Barrak, Mohammed M., Bonyadi, Morteza, Hasan Jasim Hami, Mohammed D. Al Ali, Riam Yousfe Muttair, Rawa Abdulkareem Abd

“…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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The effect of complement factor B gene variation on age-related macular degeneration in Iranian patients by Roshanipour, Nasrin, Bonyadi, Morteza, Jabbarpour Bonyadi, Mohammad Hossein, Soheilian, Masoud

“…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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Identification of Gastric Cancer-Related Strains of Helicobacter pylori: Findings from Single Biopsy Specimens for PCR and Campylobacter-Like Organism Test by Basiri, Zeinab, Safaralizadeh, Reza, Jabbarpour Bonyadi, Morteza, Abdolmohammadi, Reza, Somi, Mohammad Hossein

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Common chemotherapeutic agents modulate fatty acid distribution in human hepatocellular carcinoma and colorectal cancer cells by Mehdizadeh, Amir, Bonyadi, Morteza, Darabi, Masoud, Rahbarghazi, Reza, Montazersaheb, Soheila, Velaei, Kobra, Shaaker, Maghsood, Somi, Mohammad-Hossein

“…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 by Zaare Nahandi, Maryam, Ardalan, Mohamad Reza, Banagozar Mohamadi, Ali, Ghorbani Haghjo, Amir, Jabbarpor Bonyadi, Morteza, Mohamadian, Tahere

“…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 by Bonyadi, Morteza, Niaei, Gholamreza, Abdolmohammadi, Reza

“…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 by Omrani, Omid, Bonyadi, Morteza, Barzgar, Mohammad

“…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 by Mandana Rafeey, Morteza Jabarpoor-Bonyadi, Leila Vahedi

“…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 by Bonyadi, Morteza Jabbarpour, Somi, Mohammad Hossein, Khoshknab, Mir Milad Pourmousavi, Eslami, Forough, Montazam, Mehrdad, Gerami, Sousan Mir Najd

“…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 by Basiri, Zeinab, Safaralizadeh, Reza, Bonyadi, Morteza Jabbarpour, Somi, Mohammad Hossein, Mahdavi, Majid, Latifi-Navid, Saeid

“…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 by Bonyadi, Mohammad Hossein Jabbarpoor, Bonyadi, Morteza, Ahmadieh, Hamid, Fotuhi, Nikoo, Shoeibi, Nasser, Saadat, Saeed, Yagubi, Zakieh

“…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 by Fotouhi, Nikou, Bonyadi, Morteza, Jahanafrooz, Zohreh, Ahmadian, Nahid, Sadeghi-Shabestari, Mahnaz, Aslanabadi, Saeid, Ghergherehchi, Robabeh, Pormosavi, Milad, Rafeey, Mandana

“…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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Genetic pattern of cystic fibrosis patients in Azeri Turkish population by Jabarpoor-Bonyadi, Morteza, Rafeey, Mandana, Vahedi, Amir, Vahedi, Leila

“…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 by Vahedi, Leila, Jabarpoor-Bonyadi, Morteza, Ghojazadeh, Morteza, Vahedi, Amir, Rafeey, Mandana

“…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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MEFV mutations in Northwest of Iran: a cross sectional study by Bonyadi, Morteza Jabbarpour, Gerami, Sousan Mir Najd, Somi, Mohammad Hossein, Dastgiri, Saeed

“…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 by Zavarzadeh, Parisima Ghaffarian, Bonyadi, Morteza, Abedi, Zahra

“…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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Unraveling DREAM-PL: A Case Report on Challenges and Management by Barrak, Mohammed M., Al-Aidy, S. R., Morteza Bonyadi

“…An uncommon autosomal recessive condition called DREAM-PL syndrome is typified by dysmorphic facial features, renal agenesis, male ambiguous genitalia,…”
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Helicobacter pylori vacA i region polymorphism but not babA2 status associated to gastric cancer risk in northwestern Iran by Mottaghi, Batool, Safaralizadeh, Reza, Bonyadi, Morteza, Latifi-Navid, Saeid, Somi, Mohammad Hossein

“…Helicobacter pylori -specific genotypes have been strongly associated with an increased risk of gastric cancer (GC). The aim of the present work was to study…”
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Colorectal cancer in Iran: Molecular epidemiology and screening strategies by Dolatkhah, Roya, Dastgiri, Saeed, Somi, Mohammad hossein, Jabbarpour Bonyadi, Morteza, Kermani, Iraj Asvadi, Farassati, Faris

“…Abstract only…”
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