J. Mohammadi Asl

发表

How is the relationship between TWIST-1 and BCR-ABL1 gene expressions in chronic myeloid leukaemia patients?

N. Heidari, N. Saki, T. Vosoughi, 2018, Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals.

Melatonin and Testicular Damage in Busulfan Treated Mice

A. Khodadadi, M. Hemadi, G. Saki, 2014, Iranian Red Crescent medical journal.

UGT1A1 Gene Mutation due to Crigler-Najjar Syndrome in Iranian Patients: Identification of a Novel Mutation

F. Rahim, H. Galehdari, M. Tabatabaiefar, 2013, BioMed research international.

A novel infram deletion in MSH6 gene in glioma: Conversation on MSH6 mutations in brain tumors

M. Hajjari, J. Mohammadi Asl, M. Tahmasebi Birgani, 2018, Journal of cellular physiology.

The pattern of gene copy number alteration (CNAs) in hepatocellular carcinoma: an in silico analysis

V. Carloni, Arman Shahrisa, H. Ansari, 2021, Molecular cytogenetics.

Study of the Role of siRNA Mediated Promoter Methylation in DNMT3B Knockdown and Alteration of Promoter Methylation of CDH1, GSTP1 Genes in MDA-MB -453 Cell Line

M. Rabbani, H. Mir Mohammad Sadeghi, A. Jafarian-dehkordi, 2017, Iranian journal of pharmaceutical research : IJPR.

Utilization of Whole Exome Sequencing in Non-Syndromic Premature Ovarian Failure: Ficolin-3 Gene Mutation in an Iranian Family.

P. Ghandil, A. Ghadiri, R. Nikbakht, 2021, Iranian biomedical journal.

Quantitative evaluation of DNMT3B promoter methylation in breast cancer patients using differential high resolution melting analysis

M. Rabbani, H. Mir Mohammad Sadeghi, A. Jafarian-dehkordi, 2013, Research in pharmaceutical sciences.

Upregulation of SNHG7 and FAIM2 Expression Levels in Chronic Myelogenous Leukemia Patients Compared with Normal Subjects

N. Saki, J. Mohammadi Asl, M. Hajari, 2023, Gene, Cell and Tissue.

Identification of Novel PTPRQ and MYO1A Mutations in An Iranian Pedigree with Autosomal Recessive Hearing Loss

J. Mohammadi Asl, Farah Talebi, Farideh Ghanbari Mardasi, 2018, Cell journal.

Identification of a Novel Stop Loss Mutation in P2RX2 Gene in an Iranian Family with Autosomal Nonsyndromic Hearing Loss

J. Mohammadi Asl, F. Ghanbari, Reza Azizi Malamiri, 2021, Iranian biomedical journal.

Exome Sequencing Identifies a Novel SGCA Gene Mutation in an Iranian Family with Limb Girdle Muscular Dystrophy: A Case Report

J. Mohammadi Asl, Z. Khoshnood, Mostafa Neissi, 2023, Gene, Cell and Tissue.

Digenic Mutations in Junctional Epidermolysis Bullosa in An Iranian Family

J. Mohammadi Asl, K. Riahi, Farah Talebi, 2021, Cell journal.

Identification of A Novel Missense Mutation in The Norrie Disease Gene: The First Molecular Genetic Analysis and Prenatal Diagnosis of Norrie Disease in An Iranian Family

J. Mohammadi Asl, Farah Talebi, A. Lashgari, 2018, Cell journal.

How is the relationship between TWIST-1 and BCR-ABL1 gene expressions in chronic myeloid leukaemia patients?

N. Saki, T. Vosoughi, A. Saki Malehi, 2018, Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals.