M. Hashemzadeh Chaleshtori

Plasma Level Of miR-21 And miR-451 In Primary And Recurrent Breast Cancer Patients

F. Mokarian, S. Ghasemi, M. Motamedi, 2019, Breast cancer.

The role and spectrum of SLC26A4 mutations in Iranian patients with autosomal recessive hereditary deafness

E. Farrokhi, N. Bagheri, M. Tabatabaiefar, 2015, International journal of audiology.

Molecular Characterization of Iranian Patients with Possible Familial Hypercholesterolemia

E. Farrokhi, M. Chaleshtori, K. Ghatreh Samani, 2011, Indian Journal of Clinical Biochemistry.

Assessment of the Effects of IL9, IL9R, IL17A, and IL17F Gene Polymorphisms on Women with Allergic Rhinitis in Shahrekord, Iran

S. Heydari, M. Hashemzadeh Chaleshtori, F. Zandi, 2016, Annals of medical and health sciences research.

Genetic linkage analysis of DFNB22 in families with autosomal recessive non-syndromic hearing loss in Khuzestan province

Ladan Sadeghian, M. Tabatabaiefar, Mohammad Amin Tabatabaiefar, 2019, Journal of Shahrekord University of Medical Sciences.

Upregulation of Neuroprogenitor and Neural Markers via Enforced miR-124 and Growth Factor Treatment

M. Jami, M. Hashemzadeh Chaleshtori, A. Mehri Ghahfarrokhi, 2020, International journal of molecular and cellular medicine.

A Novel Pathologic Variant in OTOF in an Iranian Family Segregating Hereditary Hearing Loss

R. Salehi, N. Saki, M. Tabatabaiefar, 2018, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

Dermatoglyphics in patients with eczema, psoriasis and alopecia areata

D. Farhud, M. Hashemzadeh Chaleshtori, H. Pour-Jafari, 2003, Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging.

A pathogenic variant in SLC26A4 is associated with Pendred syndrome in a consanguineous Iranian family

M. Tabatabaiefar, J. Mohammadi-Asl, Mohammad Amin Tabatabaiefar, 2019, International journal of audiology.

Novel mutations in the pejvakin gene are associated with autosomal recessive non‐syndromic hearing loss in Iranian families

M. Dolati, E. Farrokhi, M. Hashemzadeh Chaleshtori, 2007, Clinical genetics.

Next-generation sequencing reveals a novel pathological mutation in the TMC1 gene causing autosomal recessive non-syndromic hearing loss in an Iranian kindred.

Ladan Sadeghian, M. Tabatabaiefar, P. Tahmasebi, 2019, International journal of pediatric otorhinolaryngology.

In silico and in vitro effects of the I30T mutation on myelin protein zero instability in the cell membrane

K. Mahnam, A. Doosti, M. Jami, 2019, Cell biology international.

I405V and -629C/A polymorphisms of the cholesteryl ester transfer protein gene in patients with coronary artery disease.

E. Farrokhi, K. Ghatreh Samani, M. Noori, 2009, Iranian biomedical journal.

Lack of Association between ESR1 and CYP1A1 Gene Polymorphisms and Susceptibility to Uterine Leiomyoma in Female Patients of Iranian Descent

S. Miraj, M. Tabatabaiefar, Mohammad Amin Tabatabaiefar, 2014, Cell journal.

Genotyping data and novel haplotype diversity of STR markers in the SLC26A4 gene region in five ethnic groups of the Iranian population.

M. Hashemzadeh Chaleshtori, Hamzeh Mesrian Tanha, Marjan Mojtabavi Naeini, 2014, Genetic testing and molecular biomarkers.

Investigation of LRTOMT gene (locus DFNB63) mutations in Iranian patients with autosomal recessive non-syndromic hearing loss

A. Yousefi, M. Abolhasani, M. Hashemzadeh Chaleshtori, 2013, International journal of molecular and cellular medicine.

Genotyping data and novel haplotype diversity of STR markers in the SLC26A4 gene region in five ethnic groups of the Iranian population.

M. Hashemzadeh Chaleshtori, Hamzeh Mesrian Tanha, Marjan Mojtabavi Naeini, 2014, Genetic testing and molecular biomarkers.