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European Journal of Pharmacology|April 12, 2015
The therapeutic potential of berberine against the altered intrinsic properties of the CA1 neurons induced by Aβ neurotoxicityMasoud Haghani, Mohammad Shabani, Mahdi Tondar
Environmental Technology|April 4, 2015
Hydrodynamic modelling of free water-surface constructed storm water wetlands using a finite volume techniqueMohammad Zounemat-Kermani, Miklas Scholz, Mohammad-Mahdi Tondar
In Vitro Cellular & Developmental Biology. Animal|November 28, 2014
Generation of eye field/optic vesicle-like structures from human embryonic stem cells under two-dimensional and chemically defined conditionsMaryam Parvini, Kazem Parivar, Fatemeh Safari, et al.
Behavioural Pharmacology|May 26, 2017
Nitric oxide pathway presumably does not contribute to antianxiety and memory retrieval effects of losartanIraj Aghaei, Shokouh Arjmand, Shahrokh Yousefzadeh Chabok, et al.
Molecular Neurobiology|April 4, 2014
Human pluripotent stem cell-derived retinal pigmented epithelium in retinal treatment: from bench to bedsideMaryam Parvini, Leila Satarian, Kazem Parivar, et al.
Acta Chimica Slovenica|January 1, 2015
Feasibility of clinoptilolite application as a microporous carrier for pH-controlled oral delivery of aspirinMahdi Tondar, Mohammad Javad Parsa, Yaser Yousefpour, et al.
Reviews of Physiology, Biochemistry and Pharmacology|August 13, 2016
Electromagnetic Fields and Stem Cell Fate: When Physics Meets BiologySara Hassanpour Tamrin, Fatemeh Sadat Majedi, Mahdi Tondar, et al.
Colloids and Surfaces. B, Biointerfaces|June 17, 2016
Understanding biophysical behaviours of microfluidic-synthesized nanoparticles at nano-biointerfaceShirin Soleimani, Mohammad Mahdi Hasani-Sadrabadi, Fatemeh Sadat Majedi, et al.
Molecular Biology Reports|July 1, 2014
A newly identified c.1824_1828dupATACG mutation in exon 13 of the GAA gene in infantile-onset glycogen storage disease type II (Pompe disease)Omid Aryani, Masoumeh Dehghan Manshadi, Mahdi Tondar, et al.
Plos One|September 13, 2014
Two novel tyrosinase (TYR) gene mutations with pathogenic impact on oculocutaneous albinism type 1 (OCA1)Vadieh Ghodsinejad Kalahroudi, Behnam Kamalidehghan, Ahoura Arasteh Kani, et al.
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