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Molecular Biology Reports
|
October 26, 2013
Fifteen novel mutations in the mitochondrial NADH dehydrogenase subunit 1, 2, 3, 4, 4L, 5 and 6 genes from Iranian patients with Leber's hereditary optic neuropathy (LHON)
Zahra Rezvani, Elmira Didari, Ahoura Arastehkani, et al.
Therapeutics and Clinical Risk Management
|
January 6, 2017
Identification of a new mutation in an Iranian family with hereditary multiple osteochondromas
Susan Akbaroghli, Maryam Balali, Behnam Kamalidehghan, et al.
Iranian Journal of Allergy, Asthma, and Immunology
|
December 6, 2016
A Novel CYBB Mutation in Chronic Granulomatous Disease in Iran
Shaghayegh Tajik, Mohsen Badalzadeh, Mohammad Reza Fazlollahi, et al.
Neurology India
|
June 29, 2006
Investigation on mtDNA deletions and twinkle gene mutation (G1423C) in Iranian patients with chronic progressive external opthalmoplagia
Massoud Houshmand, M Shafa Shariat Panahi, B N Hosseini, et al.
Iranian Journal of Public Health
|
August 23, 2017
Simultaneous Genotyping of the rs4762 and rs699 Polymorphisms in Angiotensinogen Gene and Correlation with Iranian CAD Patients with Novel Hexa-primer ARMS-PCR
Mehri Khatami, Mohammad Mehdi Heidari, Mehdi Hadadzadeh, et al.
Cancer Cell International
|
October 31, 2012
Establishment and characterization of two human breast carcinoma cell lines by spontaneous immortalization: Discordance between Estrogen, Progesterone and HER2/neu receptors of breast carcinoma tissues with derived cell lines
Behnam Kamalidehghan, Massoud Houshmand, Fereydoun Kamalidehghan, et al.
Turkish Journal of Medical Sciences
|
May 2, 2018
Analysis of partial AZFc (gr/gr, b1/b3, and b2/b3) deletions in Iranian oligozoospermia candidates for intracytoplasmic sperm injection (ICSI)
Mitra Ataei, Fatemeh Akbarian, Mahba Ataei Talebi, et al.
Journal of the Neurological Sciences
|
January 18, 2006
Complex I deficiency in Persian multiple sclerosis patients
Hassan H Kumleh, Gholam H Riazi, Massoud Houshmand, et al.
Mitochondrial DNA
|
September 18, 2012
Novel human mitochondrial tRNA phe mutation in a patient with hearing impairment: a case study
Mohammad Ali Dowlati, Pupak Derakhshandeh-Peykar, Massoud Houshmand, et al.
Cellular and Molecular Neurobiology
|
July 10, 2007
Investigation on mitochondrial tRNA(Leu/Lys), NDI and ATPase 6/8 in Iranian multiple sclerosis patients
Solmaz Etemad Ahari, Massoud Houshmand, Mehdi Shafa Shariat Panahi, et al.
Page
of 17
Search research articles
Search
Showing results (71-80 of 161) with videos related to
Sort By:
Page
of 17
Molecular Biology Reports
|
October 26, 2013
Fifteen novel mutations in the mitochondrial NADH dehydrogenase subunit 1, 2, 3, 4, 4L, 5 and 6 genes from Iranian patients with Leber's hereditary optic neuropathy (LHON)
Zahra Rezvani, Elmira Didari, Ahoura Arastehkani, et al.
Therapeutics and Clinical Risk Management
|
January 6, 2017
Identification of a new mutation in an Iranian family with hereditary multiple osteochondromas
Susan Akbaroghli, Maryam Balali, Behnam Kamalidehghan, et al.
Iranian Journal of Allergy, Asthma, and Immunology
|
December 6, 2016
A Novel CYBB Mutation in Chronic Granulomatous Disease in Iran
Shaghayegh Tajik, Mohsen Badalzadeh, Mohammad Reza Fazlollahi, et al.
Neurology India
|
June 29, 2006
Investigation on mtDNA deletions and twinkle gene mutation (G1423C) in Iranian patients with chronic progressive external opthalmoplagia
Massoud Houshmand, M Shafa Shariat Panahi, B N Hosseini, et al.
Iranian Journal of Public Health
|
August 23, 2017
Simultaneous Genotyping of the rs4762 and rs699 Polymorphisms in Angiotensinogen Gene and Correlation with Iranian CAD Patients with Novel Hexa-primer ARMS-PCR
Mehri Khatami, Mohammad Mehdi Heidari, Mehdi Hadadzadeh, et al.
Cancer Cell International
|
October 31, 2012
Establishment and characterization of two human breast carcinoma cell lines by spontaneous immortalization: Discordance between Estrogen, Progesterone and HER2/neu receptors of breast carcinoma tissues with derived cell lines
Behnam Kamalidehghan, Massoud Houshmand, Fereydoun Kamalidehghan, et al.
Turkish Journal of Medical Sciences
|
May 2, 2018
Analysis of partial AZFc (gr/gr, b1/b3, and b2/b3) deletions in Iranian oligozoospermia candidates for intracytoplasmic sperm injection (ICSI)
Mitra Ataei, Fatemeh Akbarian, Mahba Ataei Talebi, et al.
Journal of the Neurological Sciences
|
January 18, 2006
Complex I deficiency in Persian multiple sclerosis patients
Hassan H Kumleh, Gholam H Riazi, Massoud Houshmand, et al.
Mitochondrial DNA
|
September 18, 2012
Novel human mitochondrial tRNA phe mutation in a patient with hearing impairment: a case study
Mohammad Ali Dowlati, Pupak Derakhshandeh-Peykar, Massoud Houshmand, et al.
Cellular and Molecular Neurobiology
|
July 10, 2007
Investigation on mitochondrial tRNA(Leu/Lys), NDI and ATPase 6/8 in Iranian multiple sclerosis patients
Solmaz Etemad Ahari, Massoud Houshmand, Mehdi Shafa Shariat Panahi, et al.
Page
of 17