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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.
Archives of Medical Research
|
September 15, 2006
Tumoral cell mtDNA approximately 8.9 kb deletion is more common than other deletions in gastric cancer
Behnam Kamalidehghan, Massoud Houshmand, Mehdi Shafa Shariat Panahi, 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.
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.
Journal of Neurovirology
|
August 11, 2022
The evaluation expression of non-coding RNAs in response to HSV-G47∆ oncolytic virus infection in glioblastoma multiforme cancer stem cells
Reza Vazifehmand, Dhuha Saeed Ali, Zulkefley Othman, et al.
Journal of Tissue Engineering and Regenerative Medicine
|
July 16, 2011
Expansion and long-term maintenance of induced pluripotent stem cells in stirred suspension bioreactors
Mehdi Shafa, Kirsten Sjonnesen, Akihiro Yamashita, et al.
BMC Cell Biology
|
December 16, 2011
Impact of stirred suspension bioreactor culture on the differentiation of murine embryonic stem cells into cardiomyocytes
Mehdi Shafa, Roman Krawetz, Yuan Zhang, et al.
Cellular and Molecular Neurobiology
|
October 24, 2007
Huntington's disease and mitochondrial DNA deletions: event or regular mechanism for mutant huntingtin protein and CAG repeats expansion?!
Mohammad Mehdi Banoei, Massoud Houshmand, Mehdi Shafa Shariat Panahi, et al.
Neuro-Degenerative Diseases
|
December 11, 2008
Mitochondrial tRNALeu/Lys and ATPase 6/8 gene variations in spinocerebellar ataxias
Sepideh Safaei, Massoud Houshmand, Mohammad Mehdi Banoei, et al.
Cellular and Molecular Neurobiology
|
June 10, 2006
Mitochondrial D-loop variation in Persian multiple sclerosis patients: K and A haplogroups as a risk factor!!
Hassan Hassani-Kumleh, Massoud Houshmand, Mehdi Shafa Shariat Panahi, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 27) with videos related to
Sort By:
Page
of 3
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.
Archives of Medical Research
|
September 15, 2006
Tumoral cell mtDNA approximately 8.9 kb deletion is more common than other deletions in gastric cancer
Behnam Kamalidehghan, Massoud Houshmand, Mehdi Shafa Shariat Panahi, 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.
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.
Journal of Neurovirology
|
August 11, 2022
The evaluation expression of non-coding RNAs in response to HSV-G47∆ oncolytic virus infection in glioblastoma multiforme cancer stem cells
Reza Vazifehmand, Dhuha Saeed Ali, Zulkefley Othman, et al.
Journal of Tissue Engineering and Regenerative Medicine
|
July 16, 2011
Expansion and long-term maintenance of induced pluripotent stem cells in stirred suspension bioreactors
Mehdi Shafa, Kirsten Sjonnesen, Akihiro Yamashita, et al.
BMC Cell Biology
|
December 16, 2011
Impact of stirred suspension bioreactor culture on the differentiation of murine embryonic stem cells into cardiomyocytes
Mehdi Shafa, Roman Krawetz, Yuan Zhang, et al.
Cellular and Molecular Neurobiology
|
October 24, 2007
Huntington's disease and mitochondrial DNA deletions: event or regular mechanism for mutant huntingtin protein and CAG repeats expansion?!
Mohammad Mehdi Banoei, Massoud Houshmand, Mehdi Shafa Shariat Panahi, et al.
Neuro-Degenerative Diseases
|
December 11, 2008
Mitochondrial tRNALeu/Lys and ATPase 6/8 gene variations in spinocerebellar ataxias
Sepideh Safaei, Massoud Houshmand, Mohammad Mehdi Banoei, et al.
Cellular and Molecular Neurobiology
|
June 10, 2006
Mitochondrial D-loop variation in Persian multiple sclerosis patients: K and A haplogroups as a risk factor!!
Hassan Hassani-Kumleh, Massoud Houshmand, Mehdi Shafa Shariat Panahi, et al.
Page
of 3