Minor role of BRCA2 mutation (Exon2 and Exon11) in patients with early-onset breast cancer amongst Iranian Azeri-Turkish women

por Karimian Fathi, Nahid, Shekari Khaniani, Mahmood, Montazeri, Vahid, Mansoori Derakhshan, Sima
Publicado 2014

A novel missense variant in ESRRB gene causing autosomal recessive non-syndromic hearing loss: in silico analysis of a case

por Ghasemnejad, Tohid, Shekari Khaniani, Mahmoud, Nouri Nojadeh, Jafar, Mansoori Derakhshan, Sima
Publicado 2022

The Association between Human Leukocyte Antigen Class II DR3–DQ2 Haplotype and Type 1 Diabetes in Children of the East Azerbaijan State of Iran

por Mansoori Derakhshan, Sima, Zeinali Sehrig, Fatemeh, Sohrabi, Nasrin, Shiva, Siamak, Baradaran, Behzad, Shekari Khaniani, Mahmoud
Publicado 2015

Association study of IL2RA and CTLA4 Gene Variants with Type I Diabetes Mellitus in children in the northwest of Iran

por Ranjouri, Mohammad Reza, Aob, Parisa, Mansoori Derakhshan, Sima, Shekari Khaniani, Mahmoud, Chiti, Hossein, Ramazani, Ali
Publicado 2016

Differential Expression Pattern of Epithelial Mesenchymal Transition Gens: AXL, GAS6, Claudin-1, and Cofilin-1, in Different Stages of Epithelial Ovarian Cancer

por HASSANI, Elham, SHEKARI KHANIANI, Mahmood, SAFFARI, Mojtaba, EMAMI RAZAVI, Amirnader, SHIRKOOHI, Reza, MANSOORI DERAKHSHAN, Sima
Publicado 2019

The worldwide frequency of MYO15A gene mutations in patients with non-syndromic hearing loss: A meta-analysis

por Farjami, Mahsa, Assadi, Reza, Afzal Javan, Fahimeh, Alimardani, Malihe, Eslami, Saeid, Mansoori Derakhshan, Sima, Eslahi, Atieh, Mojarrad, Majid
Publicado 2020