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Massoud Houshmand

Showing results (51-60 of 161) with videos related to

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Archives of Iranian Medicine|January 3, 2012
The anticipation and inheritance pattern of c.487A>G mutation in the GJB2 geneMasoumeh Falah, Massoud Houshmand, Saeid Mahmoudian, et al.
Iranian Biomedical Journal|November 28, 2012
A novel mutation in the aprataxin (APTX) gene in an Iranian individual suffering early-onset ataxia with oculomotor apraxia type 1(AOA1) diseaseNayereh Nouri, Narges Nouri, Omid Aryani, et al.
Frontiers in Molecular Biosciences|June 22, 2023
Investigation of FGF21 mRNA levels and relative mitochondrial DNA copy number levels and their relation in nonalcoholic fatty liver disease: a case-control studyMassoud Houshmand, Vahide Zeinali, Amirhossein Hosseini, et al.
Journal of Research in Medical Sciences : the Official Journal of Isfahan University of Medical Sciences|March 31, 2011
Analysis of mitochondrial ND1 gene in human colorectal cancerMansoureh Akouchekian, Massoud Houshmand, Mohammad Hassan Hosseini Akbari, et al.
Plos One|December 31, 2016
Association of ABCB1 and SLC22A16 Gene Polymorphisms with Incidence of Doxorubicin-Induced Febrile Neutropenia: A Survey of Iranian Breast Cancer PatientsAbolfazl Faraji, Hamid Reza Dehghan Manshadi, Maryam Mobaraki, et al.
Iranian Journal of Child Neurology|October 25, 2019
Clinical Feature and Genetics in Rett Syndrome: A Report on Iranian PatientsParvaneh Karimzadeh, Majid Kheirollahi, Seyed Massoud Houshmand, et al.
Archives of Medical Science : AMS|February 2, 2012
Investigation of tRNA and ATPase 6/8 gene mutations in Iranian ataxia telangiectasia patientsMassoud Houshmand, Sadaf Kasraie, Solmaz Etemad Ahari, et al.
Mitochondrion|April 4, 2006
Identification and sizing of GAA trinucleotide repeat expansion, investigation for D-loop variations and mitochondrial deletions in Iranian patients with Friedreich's ataxiaMassoud Houshmand, Mehdi Shafa Shariat Panahi, Shahriar Nafisi, et al.
Mitochondrial DNA. Part A, DNA Mapping, Sequencing, and Analysis|December 5, 2019
An A10398G mitochondrial DNA alteration is related to increased risk of breast cancer, and associates with Her2 positive receptorMohammad Mehdi Jahani, Azita Azimi Meibody, Talie Karimi, et al.
Journal of Clinical Microbiology|June 7, 2003
Prevalence of human T-lymphotropic virus type 1 among blood donors from Mashhad, IranMohammad Reza Abbaszadegan, Mehran Gholamin, Abbas Tabatabaee, et al.
Pageof 17

Showing results (51-60 of 161) with videos related to

Sort By:
Pageof 17
Archives of Iranian Medicine|January 3, 2012
The anticipation and inheritance pattern of c.487A>G mutation in the GJB2 geneMasoumeh Falah, Massoud Houshmand, Saeid Mahmoudian, et al.
Iranian Biomedical Journal|November 28, 2012
A novel mutation in the aprataxin (APTX) gene in an Iranian individual suffering early-onset ataxia with oculomotor apraxia type 1(AOA1) diseaseNayereh Nouri, Narges Nouri, Omid Aryani, et al.
Frontiers in Molecular Biosciences|June 22, 2023
Investigation of FGF21 mRNA levels and relative mitochondrial DNA copy number levels and their relation in nonalcoholic fatty liver disease: a case-control studyMassoud Houshmand, Vahide Zeinali, Amirhossein Hosseini, et al.
Journal of Research in Medical Sciences : the Official Journal of Isfahan University of Medical Sciences|March 31, 2011
Analysis of mitochondrial ND1 gene in human colorectal cancerMansoureh Akouchekian, Massoud Houshmand, Mohammad Hassan Hosseini Akbari, et al.
Plos One|December 31, 2016
Association of ABCB1 and SLC22A16 Gene Polymorphisms with Incidence of Doxorubicin-Induced Febrile Neutropenia: A Survey of Iranian Breast Cancer PatientsAbolfazl Faraji, Hamid Reza Dehghan Manshadi, Maryam Mobaraki, et al.
Iranian Journal of Child Neurology|October 25, 2019
Clinical Feature and Genetics in Rett Syndrome: A Report on Iranian PatientsParvaneh Karimzadeh, Majid Kheirollahi, Seyed Massoud Houshmand, et al.
Archives of Medical Science : AMS|February 2, 2012
Investigation of tRNA and ATPase 6/8 gene mutations in Iranian ataxia telangiectasia patientsMassoud Houshmand, Sadaf Kasraie, Solmaz Etemad Ahari, et al.
Mitochondrion|April 4, 2006
Identification and sizing of GAA trinucleotide repeat expansion, investigation for D-loop variations and mitochondrial deletions in Iranian patients with Friedreich's ataxiaMassoud Houshmand, Mehdi Shafa Shariat Panahi, Shahriar Nafisi, et al.
Mitochondrial DNA. Part A, DNA Mapping, Sequencing, and Analysis|December 5, 2019
An A10398G mitochondrial DNA alteration is related to increased risk of breast cancer, and associates with Her2 positive receptorMohammad Mehdi Jahani, Azita Azimi Meibody, Talie Karimi, et al.
Journal of Clinical Microbiology|June 7, 2003
Prevalence of human T-lymphotropic virus type 1 among blood donors from Mashhad, IranMohammad Reza Abbaszadegan, Mehran Gholamin, Abbas Tabatabaee, et al.
Pageof 17