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Massoud Houshmand

Showing results (81-90 of 161) with videos related to

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Oman Medical Journal|August 8, 2020
Association of rs12487066, rs12044852, rs10735781, rs3135388, rs6897932, rs1321172, rs10492972, and rs9657904 Polymorphisms with Multiple Sclerosis in Iranian PopulationTakavar Razavian, Mahdieh Ebrahimi Shakib, Kurosh Gharagozli, et al.
Therapeutics and Clinical Risk Management|November 2, 2016
The potential role for use of mitochondrial DNA copy number as predictive biomarker in presbycusisMasoumeh Falah, Massoud Houshmand, Mohammad Najafi, et al.
Archives of Medical Research|September 15, 2006
Tumoral cell mtDNA approximately 8.9 kb deletion is more common than other deletions in gastric cancerBehnam Kamalidehghan, Massoud Houshmand, Mehdi Shafa Shariat Panahi, et al.
Mitochondrial DNA|March 8, 2013
T4216C mutation in NADH dehydrogenase I gene is associated with recurrent pregnancy lossAbasalt Hosseinzadeh Colagar, Elaheh Mosaieby, Seyed Mohammad Seyedhassani, et al.
Cell Journal|September 8, 2016
Mitochondrial Copy Number and D-Loop Variants in Pompe PatientsFatemeh Bahreini, Massoud Houshmand, Mohammad Hossein Modaresi, et al.
Cell Journal|June 19, 2019
Mitochondrial Polymorphisms, in The D-Loop Area, Are Associated with Brain TumorsDonya Altafi, Soha Sadeghi, Hamed Hojatian, et al.
Iranian Journal of Kidney Diseases|November 8, 2011
Recurrence of primary hyperoxaluria after kidney transplantationTahereh Malakoutian, Mojgan Asgari, Massoud Houshmand, et al.
Plos One|April 8, 2014
Gene expression profiling of mitochondrial oxidative phosphorylation (OXPHOS) complex I in Friedreich ataxia (FRDA) patientsMohammad Hossein Salehi, Behnam Kamalidehghan, Massoud Houshmand, et al.
Neurologia I Neurochirurgia Polska|July 25, 2008
An A8296G mutation in the MT-TK gene of a patient with epilepsy - a disease-causing mutation or rare polymorphism?Ali Mohammad Ahadi, Majid Sadeghizadeh, Massoud Houshmand, et al.
The Indian Journal of Medical Research|September 18, 2010
High prevalence of AZFb microdeletion in Iranian patients with idiopathic non-obstructive azoospermiaReza Mirfakhraie, Farzaneh Mirzajani, Sayed Mahdi Kalantar, et al.
Pageof 17

Showing results (81-90 of 161) with videos related to

Sort By:
Pageof 17
Oman Medical Journal|August 8, 2020
Association of rs12487066, rs12044852, rs10735781, rs3135388, rs6897932, rs1321172, rs10492972, and rs9657904 Polymorphisms with Multiple Sclerosis in Iranian PopulationTakavar Razavian, Mahdieh Ebrahimi Shakib, Kurosh Gharagozli, et al.
Therapeutics and Clinical Risk Management|November 2, 2016
The potential role for use of mitochondrial DNA copy number as predictive biomarker in presbycusisMasoumeh Falah, Massoud Houshmand, Mohammad Najafi, et al.
Archives of Medical Research|September 15, 2006
Tumoral cell mtDNA approximately 8.9 kb deletion is more common than other deletions in gastric cancerBehnam Kamalidehghan, Massoud Houshmand, Mehdi Shafa Shariat Panahi, et al.
Mitochondrial DNA|March 8, 2013
T4216C mutation in NADH dehydrogenase I gene is associated with recurrent pregnancy lossAbasalt Hosseinzadeh Colagar, Elaheh Mosaieby, Seyed Mohammad Seyedhassani, et al.
Cell Journal|September 8, 2016
Mitochondrial Copy Number and D-Loop Variants in Pompe PatientsFatemeh Bahreini, Massoud Houshmand, Mohammad Hossein Modaresi, et al.
Cell Journal|June 19, 2019
Mitochondrial Polymorphisms, in The D-Loop Area, Are Associated with Brain TumorsDonya Altafi, Soha Sadeghi, Hamed Hojatian, et al.
Iranian Journal of Kidney Diseases|November 8, 2011
Recurrence of primary hyperoxaluria after kidney transplantationTahereh Malakoutian, Mojgan Asgari, Massoud Houshmand, et al.
Plos One|April 8, 2014
Gene expression profiling of mitochondrial oxidative phosphorylation (OXPHOS) complex I in Friedreich ataxia (FRDA) patientsMohammad Hossein Salehi, Behnam Kamalidehghan, Massoud Houshmand, et al.
Neurologia I Neurochirurgia Polska|July 25, 2008
An A8296G mutation in the MT-TK gene of a patient with epilepsy - a disease-causing mutation or rare polymorphism?Ali Mohammad Ahadi, Majid Sadeghizadeh, Massoud Houshmand, et al.
The Indian Journal of Medical Research|September 18, 2010
High prevalence of AZFb microdeletion in Iranian patients with idiopathic non-obstructive azoospermiaReza Mirfakhraie, Farzaneh Mirzajani, Sayed Mahdi Kalantar, et al.
Pageof 17