Restoration of correct splicing in IVSI-110 mutation of β-globin gene with antisense oligonucleotides: implications and applications in functional assay development

por Derakhshan, Sima Mansoori, Khaniani, Mahmoud Shekari
Publicado 2017

Evaluation of a newly discovered breast cancer susceptibility locus at 6q25.1 in Iranian Azari-Turkish women

por Garehdaghchi, Ziba, Derakhshan, Siam Mansoori, Khaniani, Mahmoud Shekari
Publicado 2016

An improved Diagnostic PCR Assay for identification of Cryptic Heterozygosity for CGG Triplet Repeat Alleles in the Fragile X Gene (FMR1)

por Khaniani, Mahmoud S, Kalitsis, Paul, Burgess, Trent, Slater, Howard R
Publicado 2008

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

Molecular Evaluation of Ex3 VNTR Polymorphism of the DRD4 Gene in Patients With Autism Spectrum Disorder

por AMIRI, Shahrokh, SHEKARI KHANIANI, Mahmoud, MOHAMMADI, Arman, ASADIAN, Mahan, MEHDIZADEH FANID, Leila, SHAFIEE-KANDJANI, Ali Reza
Publicado 2022