Author = Heidari, Mansour
Identification of a novel homozygous mutation in the DDR2 gene from a patient with spondylo-meta-epiphyseal dysplasia by whole exome sequencing

Volume 24, Issue 2, February 2021, Pages 191-195

10.22038/ijbms.2020.44487.10405

Masoud Heidari; Morteza Soleyman-Nejad; Alireza Isazadeh; Mohammad Hossein Taskiri; Manzar Bolhassani; Nahid Sadighi; Zahra Shiri; Zahra Karimi; Mansour Heidari


Thalidomide attenuates the hyporesponsiveness of isolated atria to chronotropic stimulation in BDL rats: The involvement of TNF-α, IL-6 inhibition, and SOCS1 activation

Volume 22, Issue 11, November 2019, Pages 1259-1266

10.22038/ijbms.2019.32256.7742

Ali Hosseini-chegeni; farahnaz Jazaeri; Aliakbar Yousefi-Ahmadipour; Mansour Heidari; Alireza Abdollahi; Ahmad Reza Dehpour


Mutation analysis of connexin 50 gene among Iranian families with autosomal dominant cataracts

Volume 20, Issue 3, March 2017, Pages 288-293

10.22038/ijbms.2017.8358

Masoumeh Mohebi; Saeed Chenari; Abolfazl Akbari; Fariba Ghassemi; Mehran Zarei-Ghanavati; Ghasem Fakhraie; Nahid Babaie; Mansour Heidari


Down-regulation of miR-135b in colon adenocarcinoma induced by a TGF-β receptor I kinase inhibitor (SD-208)

Volume 18, Issue 9, September 2015, Pages 856-861

10.22038/ijbms.2015.5206

Abolfazl Akbari; Mohammad Hossein Ghahremani; Gholam Reza Mobini; Mahdi Abastabar; Javad Akhtari; Manzar Bolhassani; Mansour Heidari