Search Results - "Bonyadi, Morteza"

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  1. 1

    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

    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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    Journal Article
  2. 2

    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

    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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    Journal Article
  3. 3

    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

    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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    Journal Article
  4. 4

    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

    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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    Journal Article
  5. 5
  6. 6

    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

    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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  7. 7

    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

    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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    Journal Article
  8. 8

    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

    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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    Journal Article
  9. 9

    Molecular analysis of the SMN and NAIP genes in Iranian spinal muscular atrophy patients by Omrani, Omid, Bonyadi, Morteza, Barzgar, Mohammad

    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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    Journal Article
  10. 10

    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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    Journal Article
  11. 11

    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

    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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    Journal Article
  12. 12

    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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    Journal Article
  13. 13

    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

    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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    Journal Article
  14. 14

    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

    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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  15. 15

    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

    “…Background: There is a close relationship between Helicobacter pylori (H pylori)-specific factors and different gastroduodenal diseases. The present study…”
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    Journal Article
  16. 16

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

    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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  17. 17

    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

    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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    Journal Article
  18. 18

    Gender Differences in Clinical Presentations of Cystic Fibrosis Patients in Azeri Turkish Population by Leila Vahedi, Morteza Jabarpoor-bonyadi, Morteza Ghojazadeh, Amir Vahedi, Mandana Rafeey

    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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    Journal Article
  19. 19

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

    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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    Journal Article
  20. 20

    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

    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
    Journal Article