Novel Point Mutations in Frataxin Gene in Iranian Patients with Friedreich’s Ataxia

por HEIDARI, Mohammad Mehdi, KHATAMI, Mehri, POURAKRAMI, Jafar
Publicado 2014

Common rs5918 (PlA1/A2) polymorphism in the ITGB3 gene and risk of coronary artery disease

por Khatami, Mehri, Heidari, Mohammad Mehdi, Soheilyfar, Sorour
Publicado 2016

Molecular Analysis of rs2070744 and rs1799983 Polymorphisms of NOS3 Gene in Iranian Patients With Multiple Sclerosis

por Heidari, Mohammad Mehdi, Khatami, Mehri, Tahamtan, Yaser
Publicado 2017

The POLG Gene Polymorphism in Iranian Varicocele-Associated Infertility Patients

por Heidari, Mohammad Mehdi, Khatami, Mehri, Talebi, Ali Reza
Publicado 2012

Protective effect of Berberis vulgaris on Fenton reaction-induced DNA cleavage

por Sadat Asadi, Nooshin, Heidari, Mohammad Mehdi, Khatami, Mehri
Publicado 2019

The POLG Polyglutamine Tract Variants in Iranian Patients with Multiple Sclerosis

por KHATAMI, Mehri, HEIDARI, Mohammad Mehdi, MANSOURI, Reza, MOUSAVI, Fatemeh
Publicado 2015

Relationship of hypomethylation CpG islands in interleukin-6 gene promoter with IL-6 mRNA levels in patients with coronary atherosclerosis

por Mohammadpanah, Monireh, Heidari, Mohammad Mehdi, Khatami, Mehri, Hadadzadeh, Mehdi
Publicado 2020

Mutation analysis of TNP1 gene in infertile men with varicocele

por Heidari, Mohammad Mehdi, Khatami, Mehri, Talebi, Ali Reza, Moezzi, Fahime
Publicado 2014

Identification of a novel non-sense mutation in TBX5 gene in pediatric patients with congenital heart defects

por Khatami, Mehri, Heidari, Mohammad Mehdi, Kazeminasab, Fatemeh, Zare Bidaki, Razieh
Publicado 2018

Novel Point Mutations in the NKX2.5 Gene in Pediatric Patients with Non-Familial Congenital Heart Disease

por Khatami, Mehri, Mazidi, Mansoureh, Taher, Shabnam, Heidari, Mohammad Mehdi, Hadadzadeh, Mehdi
Publicado 2018

Association of Pathogenic Missense and Nonsense Mutations in Mitochondrial COII Gene with Familial Adenomatous Polyposis (FAP)

por Shaker Ardakani, Zahra, Heidari, Mohammad Mehdi, Khatami, Mehri, Bitaraf Sani, Morteza
Publicado 2020

Mutation analysis in exons 22 and 24 of SCN4A gene in Iranian patients with non-dystrophic myotonia

por Heidari, Mohammad Mehdi, Khatami, Mehri, Nafissi, Shahriar, Hesami-Zokai, Faezeh, Khorrami, Afshin
Publicado 2015

The association between TNP2 gene polymorphisms and Iranian infertile men with varicocele: A case-control study

por Heidari, Mohammad Mehdi, Danafar, Amirhossein, Moezzi, Fahime, Khatami, Mehri, Talebi, Ali Reza
Publicado 2019

Apolipoprotein E Gene Polymorphism in Iranian Coronary Atherosclerosis Patients Candidate for Coronary Artery Bypass Graft

por Heidari, Mohammad Mehdi, Foruzannia, Seyed Khalil, Khatami, Mehri, Hadadzadeh, Mehdi, Emami Meybodi, Mahmoud
Publicado 2013

Mitochondrial Genetic Variation in Iranian Infertile Men with Varicocele

por Heidari, Mohammad Mehdi, Khatami, Mehri, Danafar, Amirhossein, Dianat, Tahere, Farahmand, Ghazaleh, Talebi, Ali Reza
Publicado 2016

Polymorphisms in NOS3, MTHFR, APOB and TNF-α Genes and Risk of Coronary Atherosclerotic Lesions in Iranian Patients

por Heidari, Mohammad Mehdi, Khatami, Mehri, Hadadzadeh, Mehdi, Kazemi, Mahbobeh, Mahamed, Sahar, Malekzadeh, Pegah, Mirjalili, Massomeh
Publicado 2015

Simultaneous Genotyping of the rs4762 and rs699 Polymorphisms in Angiotensinogen Gene and Correlation with Iranian CAD Patients with Novel Hexa-primer ARMS-PCR

por KHATAMI, Mehri, HEIDARI, Mohammad Mehdi, HADADZADEH, Mehdi, SCHEIBER-MOJDEHKAR, Barbara, BITARAF SANI, Morteza, HOUSHMAND, Massoud
Publicado 2017

Mutational screening through comprehensive bioinformatics analysis to detect novel germline mutations in the APC gene in patients with familial adenomatous polyposis (FAP)

por Ghadamyari, Faranak, Heidari, Mohammad Mehdi, Zeinali, Sirous, Khatami, Mehri, Merat, Shahin, Bagherian, Hamideh, Rejali, Leili, Ghasemi, Farzaneh
Publicado 2021

Mitochondrial mutations in protein coding genes of respiratory chain including complexes IV, V, and mt-tRNA genes are associated risk factors for congenital heart disease

por Heidari, Mohammad Mehdi, Khatami, Mehri, Kamalipour, Akram, Kalantari, Mustafa, Movahed, Mahsa, Emmamy, Mohammad Hayet, Hadadzadeh, Mehdi, Bragança, José, Namnabat, Mohsen, Mazrouei, Bahareh
Publicado 2022