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Biology|July 29, 2025
Identification of Novel Molecular Panel as Potential Biomarkers of PAN-Gastrointestinal Cancer Screening: Bioinformatics and Experimental AnalysisFatemeh Hajibabaie, Parisa Mohamadynejad, Laleh Shariati, et al.
Indian Journal of Clinical Biochemistry : IJCB|January 21, 2025
Differential Impact of VNTR Polymorphism in the CBS Gene on Gastric and Breast Cancers RiskSayedeh Zeinab Sajjadi, Zeinab Alizadeh, Mehdi Moghanibashi, et al.
Biomarkers : Biochemical Indicators of Exposure, Response, and Susceptibility to Chemicals|January 2, 2025
Upregulation of LncRNAs G2E3-AS1 and BACE1-AS as prognostic biomarkers in metastatic colorectal cancerShahrbanoo Nandoust Kenari, Parisa Mohamadynejad, Mehdi Moghanibashi, et al.
Acta Bio-Medica : Atenei Parmensis|January 25, 2022
Association study of polymorphism in Thrombomodulin gene [rs1042579] with cardiovascular diseaseElham Khosravi, Ladan Sadeghian, Parisa Mohamadynejad, et al.
Indian Journal of Clinical Biochemistry : IJCB|February 20, 2020
ErbB4 3'-UTR Variant (c.*3622A>G) is Associated with ER/PR Negativity and Advanced Breast CancerMaryam Tabatabian, Hamzeh Mesrian Tanha, Hossein Tabatabaeian, et al.
Gene|March 24, 2012
Proteomics of a new esophageal cancer cell line established from Persian patientMehdi Moghanibashi, Ferdous Rastgar Jazii, Zahra-Soheila Soheili, et al.
Functional & Integrative Genomics|March 30, 2013
Esophageal cancer alters the expression of nuclear pore complex binding protein Hsc70 and eIF5A-1Mehdi Moghanibashi, Ferdous Rastgar Jazii, Zahra-Soheila Soheili, et al.
Molecular Biology Reports|February 20, 2019
Sexual dimorphism in the expression of GKN2 and FOXA2 genes in the human stomachReza Mohammadi, Zahra Mohammadi, Reza Abedi, et al.
Gene|January 30, 2013
Identification of a novel missense mutation of PEX7 gene in an Iranian patient with rhizomelic chondrodysplasia punctata type 1Parisa Mohamadynejad, Kamran Ghaedi, Yousef Shafeghati, et al.
Annals of Clinical and Laboratory Science|March 7, 2013
C86Y: as a destructive homozygous mutation deteriorating Pex7p function causing rhizomelic chondrodysplasia punctata type IAhmad Salamian, Parisa Mohamadynejad, Kamran Ghaedi, et al.
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