Mohammad Mehdi Heidari (M M Heidari)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 13

Top Topics

Bioinformatics Analysis

Congenital Heart Disease

Coronary Artery

Top Venues

Molecular biology reports

Applied biochemistry and biotechnology

Molecular biotechnology

Physiology international

This page only lists publications with an associated author ORCID identifier.

Publications

Fateme Tabrizi, Mehri Khatami, Mohammad Mehdi Heidari, José Bragança, Hassan Tatari, Mohsen Namnabat, Mehdi Hadadzadeh, Mohammad Ali Navabi Shirazi
Novel and deleterious nucleotide variations in the HAND1 gene probably affect miRNA target sites and protein function in pediatric patients with congenital heart disease. Molecular biology reports 51 (1) (2024)
Mahsa Mirzaei, Shima Mirhoseini, Mohammad Mehdi Heidari, Mehri Khatami
Design and Production of a Novel Anti-PD-1 Nanobody by CDR Grafting and Site-Directed Mutagenesis Approach. Molecular biotechnology (2024)
Mohammad Mehdi Heidari, Elham Anbar Shirazi, Seyedeh Fatemeh Cheraghi, Roghayeh Shahshahani, Tina Rahnama, Mehri Khatami
CDR grafting and site-directed mutagenesis approach for the generation and affinity maturation of Anti-CD20 nanobody. Molecular biology reports 51 (1) (2024)
Mohammad Mehdi Heidari, Elham Anbar Shirazi, Seyedeh Fatemeh Cheraghi, Roghayeh Shahshahani, Tina Rahnama, Mehri Khatami
CDR grafting and site-directed mutagenesis approach for the generation and affinity maturation of Anti-CD20 nanobody. Molecular biology reports 51 (1) (2024)
Fateme Tabrizi, Mehri Khatami, Mohammad Mehdi Heidari, José Bragança, Hassan Tatari, Mohsen Namnabat, Mehdi Hadadzadeh, Mohammad Ali Navabi Shirazi
Novel and deleterious nucleotide variations in the HAND1 gene probably affect miRNA target sites and protein function in pediatric patients with congenital heart disease. Molecular biology reports 51 (1) (2024)
Fateme Tabrizi, Mehri Khatami, Mohammad Mehdi Heidari, José Bragança, Hassan Tatari, Mohsen Namnabat, Mehdi Hadadzadeh, Mohammad Ali Navabi Shirazi
Novel and deleterious nucleotide variations in the HAND1 gene probably affect miRNA target sites and protein function in pediatric patients with congenital heart disease. Molecular biology reports 51 (1) (2024)
Mohammad Mehdi Heidari, Seyed Ali Madani Manshadi, Ahmad Reza Eshghi, Fatemeh Talebi, Mehri Khatami, José Bragança, Mahtab Ordooei, Reyhane Chamani, Farzaneh Ghasemi
Mutational and bioinformatics analysis of the NKX2.1 gene in a cohort of Iranian pediatric patients with congenital hypothyroidism (CH). Physiology international 109 (2) (2022)
Faranak Ghadamyari, Mohammad Mehdi Heidari, Sirous Zeinali, Mehri Khatami, Shahin Merat, Hamideh Bagherian, Leili Rejali, Farzaneh Ghasemi
Mutational screening through comprehensive bioinformatics analysis to detect novel germline mutations in the APC gene in patients with familial adenomatous polyposis (FAP). Journal of clinical laboratory analysis 35 (5) (2021)
Monireh Mohammadpanah, Mohammad Mehdi Heidari, Mehri Khatami, Mehdi Hadadzadeh
Relationship of hypomethylation CpG islands in interleukin-6 gene promoter with IL-6 mRNA levels in patients with coronary atherosclerosis. Journal of cardiovascular and thoracic research 12 (3) (2020)
Mohammad Mehdi Heidari, Fatemeh Sadat Mirfakhradini, Fahime Tayefi, Saghar Ghorbani, Mehri Khatami, Mehdi Hadadzadeh
Novel Point Mutations in Mitochondrial MT-CO2 Gene May Be Risk Factors for Coronary Artery Disease. Applied biochemistry and biotechnology 191 (3) (2020)
E Afkhami, Mohammad Mehdi Heidari, M Khatami, F Ghadamyari, S Dianatpour
Detection of novel mitochondrial mutations in cytochrome C oxidase subunit 1 (COX1) in patients with familial adenomatous polyposis (FAP). Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico 22 (6) (2019)
Sima Dianatpour, Mehri Khatami, Mohammad Mehdi Heidari, Mehdi Hadadzadeh
Novel Point Mutations of CITED2 Gene Are Associated with Non-familial Congenital Heart Disease (CHD) in Sporadic Pediatric Patients. Applied biochemistry and biotechnology 190 (3) (2019)
Mohammad Mehdi Heidari, Abolfazl Keshmirshekan, Mozhgan Bidakhavidi, Azam Khosravi, Zeinab Bandari, Mehri Khatami, Shahriar Nafissi
A novel heteroplasmic mutation in mitochondrial tRNAArg gene associated with non-dystrophic myotonias. Acta neurologica Belgica 120 (3) (2018)