Mehri Khatami
Mehri Khatami
Associate Professor of Molecular Genetics
Verified email at - Homepage
Cited by
Cited by
Complex I and ATP content deficiency in lymphocytes from Friedreich's ataxia
MM Heidari, M Houshmand, S Hosseinkhani, S Nafissi, M Khatami
Canadian journal of neurological sciences 36 (1), 26-31, 2009
Polymorphisms in NOS3, MTHFR, APOB and TNF-α genes and risk of coronary atherosclerotic lesions in Iranian patients
MM Heidari, M Khatami, M Hadadzadeh, M Kazemi, S Mahamed, ...
Research in cardiovascular medicine 5 (1), 2016
Upregulation of miR-222 in both Helicobacter pylori-infected and noninfected gastric cancer patients
M Noormohammad, S Sadeghi, H Tabatabaeian, K Ghaedi, A Talebi, ...
Journal of genetics 95 (4), 991-995, 2016
A novel mitochondrial heteroplasmic C13806A point mutation associated with Iranian Friedreich’s ataxia
MM Heidari, M Houshmand, S Hosseinkhani, S Nafissi, ...
Cellular and molecular neurobiology 29 (2), 225, 2009
Novel and heteroplasmic mutations in mitochondrial tRNA genes in Brugada syndrome
M FallahTafti, M Khatami, S Rezaei, MM Heidari, M Hadadzadeh
Cardiology Journal 25 (1), 113–119, 2018
Mitochondrial genetic variation in Iranian infertile men with varicocele
MM Heidari, M Khatami, A Danafar, T Dianat, G Farahmand, AR Talebi
International journal of fertility & sterility 10 (3), 303, 2016
Mutation analysis of TNP1 gene in infertile men with varicocele
MM Heidari, M Khatami, AR Talebi, F Moezzi
Iranian journal of reproductive medicine 12 (4), 257, 2014
The POLG gene polymorphism in Iranian varicocele-associated infertility patients
MM Heidari, M Khatami, AR Talebi
Iranian journal of basic medical sciences 15 (2), 739, 2012
Common rs5918 (PlA1/A2) polymorphism in the ITGB3 gene and risk of coronary artery disease
M Khatami, MM Heidari, S Soheilyfar
Archives of medical sciences. Atherosclerotic diseases 1 (1), e9, 2016
Apolipoprotein E gene polymorphism in Iranian coronary atherosclerosis patients candidate for coronary artery bypass graft
MM Heidari, SK Foruzannia, M Khatami, M Hadadzadeh, ME Meybodi
Iranian journal of basic medical sciences 16 (7), 841, 2013
Rapid Detection of Escherichia coli O157: H7 by Fluorescent Amplification–Based Specific Hybridization (FLASH) PCR
F Khatami, M Heidari, M Khatami
Iranian Red Crescent Medical Journal 14 (9), 594, 2012
Accumulation of mitochondrial genome variations in Persian LQTS patients: a possible risk factor?
M Khatami, M Houshmand, M Sadeghizadeh, M Eftekharzadeh, ...
Cardiovascular Pathology 19 (2), e21-e27, 2010
Association between trinucleotide CAG repeats of the DNA polymerase gene (POLG) with age of onset of Iranian Friedreich’s ataxia patients
MM Heidari, M Houshmand, S Hosseinkhani, S Nafissi, ...
Neurological Sciences 29 (6), 489-493, 2008
Molecular Analysis of rs2070744 and rs1799983 Polymorphisms of NOS3 Gene in Iranian Patients With Multiple Sclerosis
MM Heidari, M Khatami, Y Tahamtan
Basic and Clinical Neuroscience 8 (4), 279-284, 2017
The association of renin–angiotensinogen system genes polymorphisms and idiopathic recurrent pregnancy loss
MM Heidari, M Sheikholeslami, M Yavari, M Khatami, SM Seyedhassani
Human Fertility 22 (3), 164-170, 2019
Simultaneous Genotyping of the Rs4762 and Rs699 Polymor-phisms in Angiotensinogen Gene and Correlation with Iranian CAD Patients with Novel Hexa-primer ARMS-PCR
Khatami M, Heidari M, Hadadzadeh M, Schiber-Mojdehkar B, Bitaraf Sani M ...
Iranian Journal of Public Health 46 (6), 811-819, 2017
Novel point mutations in frataxin gene in Iranian patients with Friedreich’s ataxia
MM Heidari, M Khatami, J Pourakrami
Iranian journal of child neurology 8 (1), 32, 2014
Novel Point Mutations in the NKX2.5 Gene in Pediatric Patients with Non-Familial Congenital Heart Disease
M Khatami, M Mazidi, S Taher, MM Heidari, M Hadadzadeh
Medicina 53 (3), 1-11, 2018
Designing and validation of one-step T-ARMS-PCR for genotyping the eNOS rs1799983 SNP
MM Heidar, M Khatami
Iranian journal of biotechnology 15 (3), 208, 2017
Mutation analysis in exons 22 and 24 of SCN4A gene in Iranian patients with non-dystrophic myotonia
MM Heidari, M Khatami, S Nafissi, F Hesami-Zokai, A Khorrami
Iranian journal of neurology 14 (4), 190, 2015
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