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Massoud Houshmand

Showing results (61-70 of 161) with videos related to

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Iranian Journal of Child Neurology|December 5, 2017
Glutaric AciduriaType 1: Clinical and Molecular Study in Iranian Patients, 3 Novel MutationsZahra Pirzadeh, Massoud Houshmand, Jafar Nasiri, et al.
Current Molecular Medicine|March 1, 2019
Diagnostic Value of Non-Invasive Prenatal Screening of β-thalassemia by Cell Free Fetal DNA and Fetal NRBCNadia Shafei, Mohammad Saeed Hakhamaneshi, Massoud Houshmand, et al.
Iranian Journal of Pediatrics|October 12, 2012
mtDNA Deletion in an Iranian Infant with Pearson Marrow SyndromeMohammad Taghi Arzanian, Aziz Eghbali, Parvaneh Karimzade, et al.
Iranian Biomedical Journal|February 13, 2014
Three novel mutations in Iranian patients with Tay-Sachs diseaseSolmaz Jamali, Nasim Eskandari, Omid Aryani, et al.
Molecular Biology Reports|October 1, 2013
Association of fibroblast growth factor (FGF-21) as a biomarker with primary mitochondrial disorders, but not with secondary mitochondrial disorders (Friedreich Ataxia)Mohammad Hossein Salehi, Behnam Kamalidehghan, Massoud Houshmand, et al.
Fetal and Pediatric Pathology|June 20, 2019
Role of <i>GJB2</i> and <i>GJB6</i> in Iranian Nonsyndromic Hearing Impairment: From Molecular Analysis to Literature ReviewsMasoumeh Falah, Massoud Houshmand, Maryam Balali, et al.
Iranian Journal of Biotechnology|July 17, 2020
Association of Obesity-Related Genetic Variants (FTO and MC4R) with Breast Cancer Risk: A Population-Based Case-Control Study in IranMina Mozafarizadeh, Sima Parvizi Omran, Zeinab Kordestani, et al.
Archives of Medical Research|July 11, 2006
Delta mtDNA4977 is more common in non-tumoral cells from gastric cancer sampleBehnam Kamalidehghan, Massoud Houshmand, Patimah Ismail, et al.
Cellular and Molecular Neurobiology|September 23, 2008
A novel mitochondrial heteroplasmic C13806A point mutation associated with Iranian Friedreich's ataxiaMohammad Mehdi Heidari, Massoud Houshmand, Saman Hosseinkhani, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 2, 2008
Association between trinucleotide CAG repeats of the DNA polymerase gene (POLG) with age of onset of Iranian Friedreich's ataxia patientsMohammad Mehdi Heidari, Massoud Houshmand, Saman Hosseinkhani, et al.
Pageof 17

Showing results (61-70 of 161) with videos related to

Sort By:
Pageof 17
Iranian Journal of Child Neurology|December 5, 2017
Glutaric AciduriaType 1: Clinical and Molecular Study in Iranian Patients, 3 Novel MutationsZahra Pirzadeh, Massoud Houshmand, Jafar Nasiri, et al.
Current Molecular Medicine|March 1, 2019
Diagnostic Value of Non-Invasive Prenatal Screening of β-thalassemia by Cell Free Fetal DNA and Fetal NRBCNadia Shafei, Mohammad Saeed Hakhamaneshi, Massoud Houshmand, et al.
Iranian Journal of Pediatrics|October 12, 2012
mtDNA Deletion in an Iranian Infant with Pearson Marrow SyndromeMohammad Taghi Arzanian, Aziz Eghbali, Parvaneh Karimzade, et al.
Iranian Biomedical Journal|February 13, 2014
Three novel mutations in Iranian patients with Tay-Sachs diseaseSolmaz Jamali, Nasim Eskandari, Omid Aryani, et al.
Molecular Biology Reports|October 1, 2013
Association of fibroblast growth factor (FGF-21) as a biomarker with primary mitochondrial disorders, but not with secondary mitochondrial disorders (Friedreich Ataxia)Mohammad Hossein Salehi, Behnam Kamalidehghan, Massoud Houshmand, et al.
Fetal and Pediatric Pathology|June 20, 2019
Role of <i>GJB2</i> and <i>GJB6</i> in Iranian Nonsyndromic Hearing Impairment: From Molecular Analysis to Literature ReviewsMasoumeh Falah, Massoud Houshmand, Maryam Balali, et al.
Iranian Journal of Biotechnology|July 17, 2020
Association of Obesity-Related Genetic Variants (FTO and MC4R) with Breast Cancer Risk: A Population-Based Case-Control Study in IranMina Mozafarizadeh, Sima Parvizi Omran, Zeinab Kordestani, et al.
Archives of Medical Research|July 11, 2006
Delta mtDNA4977 is more common in non-tumoral cells from gastric cancer sampleBehnam Kamalidehghan, Massoud Houshmand, Patimah Ismail, et al.
Cellular and Molecular Neurobiology|September 23, 2008
A novel mitochondrial heteroplasmic C13806A point mutation associated with Iranian Friedreich's ataxiaMohammad Mehdi Heidari, Massoud Houshmand, Saman Hosseinkhani, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|December 2, 2008
Association between trinucleotide CAG repeats of the DNA polymerase gene (POLG) with age of onset of Iranian Friedreich's ataxia patientsMohammad Mehdi Heidari, Massoud Houshmand, Saman Hosseinkhani, et al.
Pageof 17