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Massoud Houshmand

Showing results (31-40 of 161) with videos related to

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Genes & Genomics|August 18, 2022
The relationship between common mutations in CFTR, AR genes, Y chromosome microdeletions and karyotyping abnormalities with very severe oligozoospermia in Iranian menLeyla Jafari, Kyumars Safinejad, Mahboobeh Nasiri, et al.
Iranian Journal of Public Health|June 18, 2020
<i>Zataria multiflora</i> Boiss. Essential Oil Induce Apoptosis in Two Human Colon Cancer Cell Lines (HCT116 & SW48)Narges Ahani, Mohammad Hossein Sangtarash, Majid Alipour Eskandani, et al.
Journal of Cellular Biochemistry|August 31, 2018
Genipin induces cell death via intrinsic apoptosis pathways in human glioblastoma cellsNarges Ahani, Mohammad Hossein Sangtarash, Massoud Houshmand, et al.
Iranian Biomedical Journal|December 31, 2013
Molecular and clinical investigation of Iranian patients with Friedreich ataxiaMohammad Hossein Salehi, Massoud Houshmand, Omid Aryani, et al.
Mitochondrial DNA. Part A, DNA Mapping, Sequencing, and Analysis|September 19, 2014
Association of genetic variations in the mitochondrial D-loop with β-thalassemiaLeila Jamali, Mohammad Mehdi Banoei, Elham Khalili, et al.
Iranian Journal of Pediatrics|January 16, 2014
Alexander Disease: Report of Two Unrelated Infantile Form Cases, Identified by GFAP Mutation Analysis and Review of Literature; The First Report from IranMahmoud-Reza Ashrafi, Alireza Tavasoli, Omid Aryani, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|March 20, 2009
Complex I and ATP content deficiency in lymphocytes from Friedreich's ataxiaMohammad Mehdi Heidari, Massoud Houshmand, Saman Hosseinkhani, et al.
Mitochondrial DNA. Part A, DNA Mapping, Sequencing, and Analysis|July 9, 2015
Age-related decrease in mtDNA content as a consequence of mtDNA 4977 bp deletionLeila Zabihi Diba, Seyed Mojtaba Mohaddes Ardebili, Jalal Gharesouran, et al.
Chemotherapy|May 14, 2015
Prevalence of the UGT1A1*6 (c.211G>A) Polymorphism and Prediction of Irinotecan Toxicity in Iranian Populations of Different EthnicitiesReyhaneh Shakibi, Behnam Kamalidehghan, Fatemeh Ahmadipour, et al.
Cell Journal|March 20, 2013
Investigation of the Mitochondrial ATPase 6/8 and tRNA(Lys) Genes Mutations in AutismFahimeh Piryaei, Massoud Houshmand, Omid Aryani, et al.
Pageof 17

Showing results (31-40 of 161) with videos related to

Sort By:
Pageof 17
Genes & Genomics|August 18, 2022
The relationship between common mutations in CFTR, AR genes, Y chromosome microdeletions and karyotyping abnormalities with very severe oligozoospermia in Iranian menLeyla Jafari, Kyumars Safinejad, Mahboobeh Nasiri, et al.
Iranian Journal of Public Health|June 18, 2020
<i>Zataria multiflora</i> Boiss. Essential Oil Induce Apoptosis in Two Human Colon Cancer Cell Lines (HCT116 & SW48)Narges Ahani, Mohammad Hossein Sangtarash, Majid Alipour Eskandani, et al.
Journal of Cellular Biochemistry|August 31, 2018
Genipin induces cell death via intrinsic apoptosis pathways in human glioblastoma cellsNarges Ahani, Mohammad Hossein Sangtarash, Massoud Houshmand, et al.
Iranian Biomedical Journal|December 31, 2013
Molecular and clinical investigation of Iranian patients with Friedreich ataxiaMohammad Hossein Salehi, Massoud Houshmand, Omid Aryani, et al.
Mitochondrial DNA. Part A, DNA Mapping, Sequencing, and Analysis|September 19, 2014
Association of genetic variations in the mitochondrial D-loop with β-thalassemiaLeila Jamali, Mohammad Mehdi Banoei, Elham Khalili, et al.
Iranian Journal of Pediatrics|January 16, 2014
Alexander Disease: Report of Two Unrelated Infantile Form Cases, Identified by GFAP Mutation Analysis and Review of Literature; The First Report from IranMahmoud-Reza Ashrafi, Alireza Tavasoli, Omid Aryani, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|March 20, 2009
Complex I and ATP content deficiency in lymphocytes from Friedreich's ataxiaMohammad Mehdi Heidari, Massoud Houshmand, Saman Hosseinkhani, et al.
Mitochondrial DNA. Part A, DNA Mapping, Sequencing, and Analysis|July 9, 2015
Age-related decrease in mtDNA content as a consequence of mtDNA 4977 bp deletionLeila Zabihi Diba, Seyed Mojtaba Mohaddes Ardebili, Jalal Gharesouran, et al.
Chemotherapy|May 14, 2015
Prevalence of the UGT1A1*6 (c.211G>A) Polymorphism and Prediction of Irinotecan Toxicity in Iranian Populations of Different EthnicitiesReyhaneh Shakibi, Behnam Kamalidehghan, Fatemeh Ahmadipour, et al.
Cell Journal|March 20, 2013
Investigation of the Mitochondrial ATPase 6/8 and tRNA(Lys) Genes Mutations in AutismFahimeh Piryaei, Massoud Houshmand, Omid Aryani, et al.
Pageof 17