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Cell Biology International|January 31, 2023
Human umbilical cord mesenchymal stem cells: Heralding an effective treatment against esophageal cancer?Reza ArefNezhad, Fatemeh Rezaei-Tazangi, Hossein Roghani-Shahraki, et al.
Current Molecular Pharmacology|March 25, 2022
Immunomodulatory Therapeutic Effects of Curcumin on M1/M2 Macrophage Polarization in Inflammatory DiseasesElham Abdollahi, Thomas P Johnston, Zahra Ghaneifar, et al.
International Journal of Biological Macromolecules|August 1, 2020
Synthesis of PLGA/chitosan/zeolites and PLGA/chitosan/metal organic frameworks nanofibers for targeted delivery of Paclitaxel toward prostate cancer cells deathBabak Faraji Dizaji, Mohammadreza Hasani Azerbaijan, Niloofar Sheisi, et al.
Cancer Medicine|December 30, 2022
Chimeric antigen receptor T (CAR-T) cells: Novel cell therapy for hematological malignanciesSamane Abbasi, Milad Asghari Totmaj, Masoumeh Abbasi, et al.
Carbohydrate Polymers|February 17, 2021
Magnetic bioactive glasses/Cisplatin loaded-chitosan (CS)-grafted- poly (ε-caprolactone) nanofibers against bone cancer treatmentZahra Amini, Sam Shekofte Rudsary, Seyed Sadegh Shahraeini, et al.
Progress in Molecular Biology and Translational Science|February 15, 2024
Types of RNA therapeuticsPouya Goleij, Mehregan Babamohamadi, Aryan Rezaee, et al.
Discover Oncology|October 15, 2025
Blood expression of CTLA-4, PD-1, and PD-L1 as potential prognostic and diagnostic markers for breast cancer: a systematic reviewMina Niusha, Saba Hajazimian, Nayemeh Soltani, et al.
Cardiovascular Toxicology|July 3, 2025
Epigenetic Alterations Induced by Air Pollution: A Key Driver in Atherosclerosis DevelopmentPouya Goleij, Mohammad Amin Khazeei Tabari, Pantea Majma Sanaye, et al.
Inflammopharmacology|July 22, 2025
Therapeutic potential of melatonin-induced mitophagy in the pathogenesis of Alzheimer's diseasePouya Goleij, Mohammad Amin Khazeei Tabari, Mohadeseh Poudineh, et al.
Journal of Clinical Laboratory Analysis|September 16, 2021
Identification of a compound heterozygous missense mutation in LAMA2 gene from a patient with merosin-deficient congenital muscular dystrophy type 1AAfshin Khorrami, Pouya Goleij, Vahidreza Karamad, et al.
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