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Physiology & Behavior|November 3, 2019
MgO and ZnO nanoparticles anti-nociceptive effect modulated by glutamate level and NMDA receptor expression in the hippocampus of stressed and non-stressed ratsMozhgan Torabi, Mahnaz Kesmati, Hamid Galehdari, et al.
Life Sciences|April 22, 2018
Neurobehavioral and biochemical modulation following administration of MgO and ZnO nanoparticles in the presence and absence of acute stressMozhgan Torabi, Mahnaz Kesmati, Nahid Pourreza, et al.
Iranian Journal of Pharmaceutical Research : IJPR|December 21, 2018
First Transcriptome Analysis of Iranian Scorpion, Mesobuthus Eupeus Venom GlandMasoumeh Baradaran, Amir Jalali, Maryam Naderi-Soorki, et al.
Iranian Journal of Immunology : IJI|July 27, 2007
Perforin gene analaysis in an Iranian family with familial hemophagocytic lymphohistiocytosisHamid Galehdari, Ebrahim Mohammadi, Behnaz Andashti, et al.
Clinical Case Reports|October 19, 2022
Pemphigus vegetans misdiagnosed as condylomata acuminata: A case reportAmir Hossein Siadat, Reza Moeine, Fariba Iraji, et al.
Bioinformation|September 27, 2014
VMD-SS: A graphical user interface plug-in to calculate the protein secondary structure in VMD programMasoumeh Yahyavi, Sajad Falsafi-Zadeh, Zahra Karimi, et al.
Gene|February 25, 2012
Complement C3 gene polymorphism in renal transplantation (an Iranian experience)Najmeh Bazyar, Negar Azarpira, Saeid Reza Khatami, et al.
Pakistan Journal of Biological Sciences : PJBS|February 12, 2014
Meta-analysis of genetic polymorphisms and ophthalmologic disease risk in Asian populations: a case of DNA repair XRCC1 geneNajmaldin Saki, Hamid Galehdari, Mostafa Feghhi, et al.
Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion|July 16, 2021
Design and Development of Reverse Slot Blot for the Simultaneous Detection of Rare and Regional Specific Mutations in the Beta Globin Gene in Khuzestan Province of IranHamid Galehdari, Mehdi Bijanzadeh, Seyedeh Zohreh Azarshin, et al.
Indian Journal of Human Genetics|May 30, 2013
Molecular analysis of exons 6 and 7 of phenylalanine hydroxylase gene mutations in Phenylketonuria patients in Western IranKeyvan Moradi, Reza Alibakhshi, Keyghobad Ghadiri, et al.
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