MTHFR polymorphisms and breast cancer risk

by Hosseini, Mojgan, Houshmand, Massoud, Ebrahimi, Ahmad
Published 2011

The mitochondrial DNA mutations associated with cardiac arrhythmia investigated in an LQTS family

by Khatami, Fatemeh, Mehdi Heidari, Mohammad, Houshmand, Massoud
Published 2014

Beta-Thalassemia in Iran: New Insight into the Role of Genetic Admixture and Migration

by Rezaee, Ali Reza, Banoei, Mohammad Mehdi, Khalili, Elham, Houshmand, Massoud
Published 2012

Is Bax/Bcl-2 Ratio Considered as a Prognostic Marker with Age and Tumor Location in Colorectal Cancer?

by Khodapasand, Ehsan, Jafarzadeh, Narges, Farrokhi, Farid, Kamalidehghan, Behnam, Houshmand, Massoud
Published 2015

Expression levels of the BAK1 and BCL2 genes highlight the role of apoptosis in age-related hearing impairment

by Falah, Masoumeh, Najafi, Mohammad, Houshmand, Massoud, Farhadi, Mohammad
Published 2016

New Mutation of Pelizaeus­-Merzbacher-Like Disease; A Report from Iran

by Karimzadeh, Parvaneh, Ahmadabadi, Farzad, Aryani, Omid, Houshmand, Massoud, Khatami, Alireza
Published 2014

Investigation of tRNALys/Leu and ATPase 6/8 gene mutations in Iranian ataxia telangiectasia patients

by Houshmand, Massoud, Kasraie, Sadaf, Etemad Ahari, Solmaz, Moin, Mostafa, Bahar, Mohammadali, Zamani, Akram
Published 2011

Is 8860 variation a rare polymorphism or associated as a secondary effect in HCM disease?

by Houshmand, Massoud, Montazeri, Maryam, Kuchekian, Nafiseh, Noohi, Freidoon, Nozar, Givtaj, Zamani, Akram
Published 2011

Analysis of mitochondrial ND1 gene in human colorectal cancer

by Akouchekian, Mansoureh, Houshmand, Massoud, Akbari, Mohammad Hassan Hosseini, Kamalidehghan, Behnam, Dehghan, Masoumeh
Published 2011

Gene expression profiling of mitochondrial oxidative phosphorylation (OXPHOS) complex I in Friedreich ataxia (FRDA) patients

by Salehi, Mohammad Hossein, Kamalidehghan, Behnam, Houshmand, Massoud, Goh, Yong Meng, Sadeghizadeh, Majid, Aryani, Omid, Nafissi, Shahriar
Published 2014

Establishment and characterization of two human breast carcinoma cell lines by spontaneous immortalization: Discordance between Estrogen, Progesterone and HER2/neu receptors of bre...

by Kamalidehghan, Behnam, Houshmand, Massoud, Kamalidehghan, Fereydoun, Jafarzadeh, Narges, Azari, Shahram, Akmal, Sharifah Noor, Rosli, Rozita
Published 2012

mtDNA Deletion in an Iranian Infant with Pearson Marrow Syndrome

by Arzanian, Mohammad Taghi, Eghbali, Aziz, Karimzade, Parvaneh, Ahmadi, Mitra, Houshmand, Massoud, Rezaei, Nima
Published 2010

New pathogenic variations of mitochondrial DNA in Alzheimer disease!!

by Nia, Samira Sheibani, Azadfar, Parisa, Akbari, Leila, Assarzadegan, Farhad, Kamalidehghan, Behnam, Maroof, Hamid Reza, Houshmand, Massoud
Published 2013

Alexander Disease: Report of Two Unrelated Infantile Form Cases, Identified by GFAP Mutation Analysis and Review of Literature; The First Report from Iran

by Ashrafi, Mahmoud-Reza, Tavasoli, Alireza, Aryani, Omid, Alizadeh, Hooman, Houshmand, Massoud
Published 2013

The mitochondrial ATPase6 gene is more susceptible to mutation than the ATPase8 gene in breast cancer patients

by Ghaffarpour, Massoud, Mahdian, Reza, Fereidooni, Forouzandeh, Kamalidehghan, Behnam, Moazami, Nasrin, Houshmand, Massoud
Published 2014

Association of fibroblast growth factor (FGF-21) as a biomarker with primary mitochondrial disorders, but not with secondary mitochondrial disorders (Friedreich Ataxia)

by Salehi, Mohammad Hossein, Kamalidehghan, Behnam, Houshmand, Massoud, Aryani, Omid, Sadeghizadeh, Majid, Mossalaeie, Mir Majid
Published 2013

Investigation of the Mitochondrial ATPase 6/8 and tRNALys Genes Mutations in Autism

by Piryaei, Fahimeh, Houshmand, Massoud, Aryani, Omid, Dadgar, Sepideh, Soheili, Zahra-Soheila
Published 2012

Gene Expression Profiling of Mitochondrial Oxidative Phosphorylation (OXPHOS) Complex I in Friedreich Ataxia (FRDA) Patients

by Salehi, Mohammad Hossein, Kamalidehghan, Behnam, Houshmand, Massoud, Yong Meng, Goh, Sadeghizadeh, Majid, Aryani, Omid, Nafissi, Shahriar
Published 2014

Association of ABCB1 and SLC22A16 Gene Polymorphisms with Incidence of Doxorubicin-Induced Febrile Neutropenia: A Survey of Iranian Breast Cancer Patients

by Faraji, Abolfazl, Dehghan Manshadi, Hamid Reza, Mobaraki, Maryam, Zare, Mahkameh, Houshmand, Massoud
Published 2016

Identification of a new mutation in an Iranian family with hereditary multiple osteochondromas

by Akbaroghli, Susan, Balali, Maryam, Kamalidehghan, Behnam, Saber, Siamak, Aryani, Omid, Meng, Goh Yong, Houshmand, Massoud
Published 2016