Mehri Khatami

发表

Complex I and ATP Content Deficiency in Lymphocytes from Friedreich's Ataxia

S. Hosseinkhani, M. Houshmand, M. Khatami, 2009, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

In-silico study to identify the pathogenic single nucleotide polymorphisms in the coding region of CDKN2A gene

M. Khatami, M. Heidari, Reyhane Chamani, 2021 .

Heterobimetallic PtII -AuI Complexes Comprising Unsymmetrical 1,1-Bis(diphenylphosphanyl)methane Bridges: Synthesis, Photophysical, and Cytotoxic Studies

H. R. Shahsavari, M. Khatami, Reza Babadi Aghakhanpour, 2019, European Journal of Inorganic Chemistry.

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

M. Khatami, M. Heidari, M. Hadadzadeh, 2018, Medicina.

Novel and heteroplasmic mutations in mitochondrial tRNA genes in Brugada syndrome.

M. Khatami, M. Heidari, Shiva Rezaei, 2013, Cardiology journal.

Mutational Analysis of the VPREB1 Gene of Pre-BCR Complex in a Cohort of Sporadic Pediatric Patients With B-Cell Acute Lymphoblastic Leukemia

A. Hashemi, M. Khatami, Zohreh Khanjarpanah, 2022, Journal of pediatric hematology/oncology.

Novel missense mutation in NKX2.6 gene (c.389 G > C, Arg130Pro) as a potentially pathogenic variant in pediatric patients with congenital heart disease

M. Khatami, M. Heidari, Fatemeh Ahmadi, 2023, Gene Reports.

Mutational and bioinformatics analysis of the NKX2.1 gene in a cohort of Iranian pediatric patients with congenital hypothyroidism (CH).

J. Bragança, M. Khatami, M. Heidari, 2022, Physiology international.

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

M. Khatami, M. Heidari, M. Hadadzadeh, 2015, Research in cardiovascular medicine.

Molecular Study of Nucleotide Changes of ATPase6 and MT-CYB Genes in the Mitochondrial Genome of Patients with Familial Adenomatous Polyposis (FAP)

M. Heidari, F. Ebrahimi, M. Mirzaei, 2023, Journal of Shahid Sadoughi University of Medical Sciences.

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

S. Merat, S. Zeinali, M. Khatami, 2021, Journal of clinical laboratory analysis.

Detection of novel mitochondrial mutations in cytochrome C oxidase subunit 1 (COX1) in patients with familial adenomatous polyposis (FAP)

M. Khatami, M. Heidari, S. Dianatpour, 2019, Clinical and Translational Oncology.

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

M. Khatami, M. Heidari, Morteza Bitaraf Sani, 2021, International journal of molecular and cellular medicine.

A novel heteroplasmic mutation in mitochondrial tRNAArg gene associated with non-dystrophic myotonias

M. Heidari, S. Nafissi, Z. Bandari, 2018, Acta Neurologica Belgica.

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

A. Khorrami, M. Khatami, M. Heidari, 2015, Iranian journal of neurology.

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

M. Heidari, Jafar Pourakrami, Mehri Khatami, 2014, Iranian journal of child neurology.

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

M. Khatami, M. Heidari, M. Hadadzadeh, 2020, Journal of cardiovascular and thoracic research.

Novel Point Mutations in 3′-Untranslated Region of GATA4 Gene Are Associated with Sporadic Non-syndromic Atrial and Ventricular Septal Defects

M. Khatami, M. Heidari, M. Hadadzadeh, 2021, Current Medical Science.

Novel Point Mutations in Mitochondrial MT-CO2 Gene May Be Risk Factors for Coronary Artery Disease

M. Khatami, M. Heidari, M. Hadadzadeh, 2020, Applied Biochemistry and Biotechnology.

Rapid Detection of Escherichia coli O157: H7 by Fluorescent Amplification–Based Specific Hybridization (FLASH) PCR

M. Khatami, M. Heidari, F. Khatami, 2012, Iranian Red Crescent medical journal.

A Novel Nonsense Mutation in Exon 5 of KIND1 Gene in an Iranian Family with Kindler Syndrome.

M. Khatami, M. Heidari, S. Kargar, 2016, Archives of Iranian medicine.

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

M. Houshmand, M. Khatami, M. Heidari, 2017, Iranian journal of public health.

Induced pluripotent stem cells (iPSCs) based approaches for hematopoietic cancer therapy

M. Khatami, M. Heidari, Bardia Khandany, 2019, Iranian Journal of Pediatric Hematology & Oncology.

Design and Production of a Novel Anti-PD-1 Nanobody by CDR Grafting and Site-Directed Mutagenesis Approach.

M. Heidari, Mehri Khatami, Mahsa Mirzaei, 2024, Molecular biotechnology.

Studying the Pathogenic Effect of New Nucleotide Changes in the Promoter Region of the TERT Gene in Patients with Glioblastoma Brain Tumor

M. Heidari, M. Broomand, Mehri Khatami, 2024, Journal of Shahid Sadoughi University of Medical Sciences.

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

J. Bragança, M. Khatami, M. Heidari, 2022, EXCLI journal.

NOVEL NUCLEOTIDE CHANGES IN MITOCHONDRIAL COXII, CYTOCHROME B AND TRNAGLU GENES IN PATIENTS WITH BRUGADA SYNDROME

M. Khatami, Z. G. Yakhdan, Mehri Khatami, 2014 .

Accumulation of mitochondrial genome variations in Persian LQTS patients: a possible risk factor?

M. Houshmand, M. Sadeghizadeh, K. Banihashemi, 2010, Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology.