Update of spectrum c.35delG and c.‐23+1G>A mutations on the GJB2 gene in individuals with autosomal recessive nonsyndromic hearing loss von Azadegan‐Dehkordi, Fatemeh, Ahmadi, Reza, Koohiyan, Mahbobeh, Hashemzadeh‐Chaleshtori, Morteza

Volltext

A Mutation in CABP2, Expressed in Cochlear Hair Cells, Causes Autosomal-Recessive Hearing Impairment von SCHRAUWEN, Isabelle, HELFMANN, Sarah, DHEEDENE, Annelies, CLAES, Charlotte, FRANSEN, Erik, HASHEMZADEH CHALESHTORI, Morteza, COUCKE, Paul, LEE, Amy, MOSER, Tobias, VAN CAMP, Guy, INAGAKI, Akira, PREDOEHL, Friederike, AMIN TABATABAIEFAR, Mohammad, MAGDALENA PICHER, Maria, SOMMEN, Manou, ZAZO SECO, Celia, OOSTRIK, Jaap, KREMER, Hannie

Volltext

Silencing of α‐N‐acetylgalactosaminidase in the gastric cancer cells amplified cell death and attenuated migration, while the multidrug resistance remained unchanged von Jafari, Mahbube, Rahimi, Nasibeh, Jami, Mohammad‐Saeid, Hashemzadeh Chaleshtori, Morteza, Elahian, Fatemeh, Mirzaei, Seyed Abbas

Volltext

Plasma Level Of miR-21 And miR-451 In Primary And Recurrent Breast Cancer Patients von Motamedi, Maryam, Hashemzadeh Chaleshtori, Morteza, Ghasemi, Sorayya, Mokarian, Fariborz

Volltext

A Simple, Rapid, and Efficient Method for Isolating Mesenchymal Stem Cells from the Entire Umbilical Cord von Dehkordi, Mehdi Banitalebi, Madjd, Zahra, Chaleshtori, Morteza Hashemzadeh, Meshkani, Reza, Nikfarjam, Laleh, Kajbafzadeh, Abdol-Mohammad

Volltext

In silico and in vitro effects of the I30T mutation on myelin protein zero instability in the cell membrane von Ghanavatinejad, Fatemeh, Pourteymourfard‐Tabrizi, Zahra, Mahnam, Karim, Doosti, Abbas, Mehri‐Ghahfarrokhi, Ameneh, Pourhadi, Masoumeh, Azimeh Hosseini, Sayedeh, Hashemzadeh Chaleshtori, Morteza, Soltanzadeh, Payam, Jami, Mohammad‐Saeid

Volltext

Molecular diagnosis of SLC26A4-related hereditary hearing loss in a group of patients from two provinces of Iran von Koohiyan, Mahbobeh, Hashemzadeh-Chaleshtori, Morteza, Tabatabaiefar, Mohammad Amin

Volltext

Genetics of hereditary hearing loss in east Iran population: A systematic review of GJB2 mutations von Koohiyan, Mahbobeh, Azadegan-Dehkordi, Fatemeh, Koohian, Farideh, Abolhasani, Marziye, Hashemzadeh-Chaleshtori, Morteza

Volltext

Molecular Mechanisms behind Free Radical Scavengers Function against Oxidative Stress von Ahmadinejad, Fereshteh, Geir Møller, Simon, Hashemzadeh-Chaleshtori, Morteza, Bidkhori, Gholamreza, Jami, Mohammad-Saeid

Volltext

Screening of Myo7A Mutations in Iranian Patients with Autosomal Recessive Hearing Loss from West of Iran von Asgharzade, Samira, Reiisi, Somayeh, Tabatabaiefar, Mohammad Amin, Chaleshtori, Morteza Hashemzadeh

Volltext

The association of VEGF rs833061 and rs2010963 polymorphisms with susceptibility to colorectal cancer in an Iranian population von Bakhshian-Dehkordi, Ehsan, Safaei, Mohsen, Fattahi, Soheila, Faghani, Mostafa, Deris, Fatemeh, Chaleshtori, Morteza Hashemzadeh

Volltext

Lack of Association between ESR1 and CYP1A1 Gene Polymorphisms and Susceptibility to Uterine Leiomyoma in Female Patients of Iranian Descent von Taghizade Mortezaee, Fatemeh, Tabatabaiefar, Mohammad Amin, Hashemzadeh Chaleshtori, Morteza, Miraj, Sepideh

Volltext

An update of spectrum and frequency of GJB2 mutations causing hearing loss in the south of Iran: A literature review von koohiyan, Mahbobeh, Ahmadi, Amirhossein, koohian, Farideh, Aghaei, Shahrzad, Amiri, Beheshteh, Hashemzadeh-Chaleshtori, Morteza

Volltext

Mesenchymal stem cells versus their conditioned medium in the treatment of ischemia/reperfusion injury: Evaluation of efficacy and hepatic specific gene expression in mice von Khosravi-Farsani, Somayeh, Zaminy, Arash

Volltext

Next-generation sequencing reveals a novel pathological mutation in the TMC1 gene causing autosomal recessive non-syndromic hearing loss in an Iranian kindred von Sadeghian, Ladan, Tabatabaiefar, Mohammad Amin, Fattahi, Najmeh, Pourreza, Mohammad Reza, Tahmasebi, Parisa, Alavi, Zahra, Hashemzadeh Chaleshtori, Morteza

Volltext

Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees von Khatami, Somayeh, Askari, Masomeh, Bahreini, Fatemeh, Hashemzadeh-Chaleshtori, Morteza, Hematian, Saeed, Asgharzade, Samira

Volltext

Virulence factors of Helicobacter pylori vacA increase markedly gastric mucosal TGF-β1 mRNA expression in gastritis patients von Rahimian, Ghorbanali, Sanei, Mohammad Hosein, Shirzad, Hedayatollah, Azadegan-Dehkordi, Fatemeh, Taghikhani, Afshin, Salimzadeh, Loghman, Hashemzadeh-Chaleshtori, Morteza, Rafieian-Kopaei, Mahmoud, Bagheri, Nader

Volltext

A Novel Pathologic Variant in OTOF in an Iranian Family Segregating Hereditary Hearing Loss von Tabatabaiefar, Mohammad Amin, Pourreza, Mohammad Reza, Tahmasebi, Parisa, Saki, Nader, Hashemzadeh Chaleshtori, Morteza, Salehi, Rasoul, Mohammadi-asl, Javad

Volltext

GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants von Koohiyan, Mahbobeh, Hashemzadeh-Chaleshtori, Morteza, Salehi, Mansoor, Abtahi, Hamidreza, Reiisi, Somayeh, Pourreza, Mohammad Reza, Noori-Daloii, Mohammad Reza, Tabatabaiefar, Mohammad Amin

Volltext

Identification and Clinical Implications of a Novel MYO15A Variant in a Consanguineous Iranian Family by Targeted Exome Sequencing von Zarepour, Narges, Koohiyan, Mahbobeh, Taghipour-Sheshdeh, Afsaneh, Nemati-Zargaran, Fatemeh, Saki, Nader, Mohammadi-Asl, Javad, Tabatabaiefar, Mohammad Amin, Hashemzadeh-Chaleshtori, Morteza 

Volltext