Tayyeb Bahrami

发表

Genetics and immunodysfunction underlying Behçet’s disease and immunomodulant treatment approaches

Arash Salmaninejad, Meysam Yousefi, S. Aslani, 2017, Journal of immunotoxicology.

Association of PTPN22 Gene Polymorphisms with Susceptibility to Juvenile Idiopathic Arthritis in Iranian Population

Arash Salmaninejad, M. Yekaninejad, N. Rezaei, 2017, Fetal and pediatric pathology.

Screening for intermediate CGG alleles of FMR1 gene in male Iranian patients with Parkinsonism

M. Khaniani, S. M. Derakhshan, H. Darvish, 2016, Neurological Sciences.

A novel variant of SLC26A4 and first report of the c.716T>A variant in Iranian pedigrees with non-syndromic sensorineural hearing loss.

E. Farrokhi, M. Tabatabaiefar, M. Hashemzadeh-Chaleshtori, 2018, American journal of otolaryngology.

PDCD1 single nucleotide genes polymorphisms confer susceptibility to juvenile-onset systemic lupus erythematosus

Arash Salmaninejad, N. Rezaei, F. Tahghighi, 2015, Autoimmunity.

PTPN22 Gene Polymorphisms in Pediatric Systemic Lupus Erythematosus

Arash Salmaninejad, M. Yekaninejad, N. Rezaei, 2020, Fetal and pediatric pathology.

Mutation analysis of GJB2 and GJB6 genes and screening of nine common dfnb loci in iranian pedigrees with autosomal recessive nonsyndromic hearing loss

E. Farrokhi, M. Tabatabaiefar, M. Hashemzadeh-Chaleshtori, 2019, Indian Journal of Otology.

Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of c.299-300delAT Mutation in Kurdish Population of Iran

E. Farrokhi, M. Tabatabaiefar, M. Hashemzadeh-Chaleshtori, 2018, Journal of audiology & otology.

Altered Expression of MicroRNAs Following Chronic Allograft Dysfunction with Interstitial Fibrosis and Tubular Atrophy.

M. Yekaninejad, A. Amirzargar, M. H. Nicknam, 2015, Iranian journal of allergy, asthma, and immunology.

Differential expression of microRNAs in renal transplant patients with acute T-cell mediated rejection.

M. Yekaninejad, A. Amirzargar, M. H. Nicknam, 2015, Transplant immunology.

PTPN22 Single-Nucleotide Polymorphisms in Iranian Patients with Type 1 Diabetes Mellitus

N. Rezaei, A. Saghazadeh, A. Amirzargar, 2017, Immunological investigations.

Specific Distribution of GJB2 Mutations in Kurdistan Province of Iran; Report of a Relatively Isolated Population

Tayyeb Bahrami, M. N. Daloii, G. Karbasi, 2017 .

Lung cancer-associated brain metastasis: Molecular mechanisms and therapeutic options

Arash Salmaninejad, R. Nosrati, Meysam Yousefi, 2017, Cellular Oncology.

Lung cancer-associated brain metastasis: Molecular mechanisms and therapeutic options

Arash Salmaninejad, R. Nosrati, Meysam Yousefi, 2017, Cellular Oncology.

Immunotherapeutic targets in non‐small cell lung cancer

M. Warkiani, Hassan Yousefi, Meysam Rezaei, 2022, Immunology.

Expression Analysis of Long Non-coding RNA Lnc-DC in HLA-DRB1*15:01-Negative Patients with Multiple Sclerosis: A Probable Cause for Gender Differences in Multiple Sclerosis Susceptibility?

M. Taheri, M. Omrani, M. Karimipour, 2020, Journal of Molecular Neuroscience.

Associations Between Genomic Variants in lncRNA-TRPM2-AS and lncRNA-HNF1A-AS1 Genes and Risk of Multiple Sclerosis

M. Taheri, M. Omrani, M. Karimipoor, 2020, Journal of Molecular Neuroscience.

The molecular signature of breast cancer metastasis to bone

Arash Salmaninejad, M. Estiar, Tayyeb Bahrami, 2016, Anti-cancer drugs.

Crosstalk between breast cancer stem cells and metastatic niche: emerging molecular metastasis pathway?

B. Behnam, Arash Salmaninejad, H. Fazilaty, 2013, Tumor Biology.

A Comprehensive Genetic and Clinical Evaluation of Waardenburg Syndrome Type II in a Set of Iranian Patients

A. Zekri, M. Tabatabaiefar, M. Noori-Daloii, 2018, International journal of molecular and cellular medicine.

A Novel Pathogenic Variant in the MITF Gene Segregating with a Unique Spectrum of Ocular Findings in an Extended Iranian Waardenburg Syndrome Kindred

M. Tabatabaiefar, M. Noori-Daloii, Mohammad Amin Tabatabaiefar, 2017, Molecular Syndromology.

Organotropism of breast cancer metastasis: A comprehensive approach to the shared gene network

Tayyeb Bahrami, Muhammadhosein Moradi, Bayazid Ghaderi, 2023, Gene Reports.

BCL-1 Gene Rearrangements in Iranian Non-Hodgkin Lymphoma Patients

M. Estiar, E. Sakhinia, A. Rezamand, 2015, Global journal of health science.

Investigating the Frequency of the ERCC1 Gene C8092A Polymorphism in Iranian Patients with Advanced Gastric Cancer Receiving Platinum-based Chemotherapy.

R. Zamiri, Tayyeb Bahrami, G. A. Tehrani, 2016, Asian Pacific journal of cancer prevention : APJCP.

PDCD1 Single Nucleotide Polymorphisms in Iranian Patients With Juvenile Idiopathic Arthritis.

Arash Salmaninejad, N. Rezaei, V. Ziaee, 2017, Acta medica Iranica.

A novel mutation in the PAX3 gene causes Waardenburg syndrome type I in an Iranian family.

M. Farhadi, M. Noori-Daloii, Mohammad Amin Tabatabaiefar, 2015, International journal of pediatric otorhinolaryngology.

PTPN22 Single-Nucleotide Polymorphisms in Iranian Patients with Type 1 Diabetes Mellitus

N. Rezaei, A. Saghazadeh, A. Amirzargar, 2017, Immunological investigations.