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Genetics Research International|September 3, 2013
Regression Modeling and Meta-Analysis of Diagnostic Accuracy of SNP-Based Pathogenicity Detection Tools for UGT1A1 Gene MutationFakher Rahim, Hamid Galehdari, Javad Mohammadi-Asl, et al.International Journal of Molecular Epidemiology and Genetics|July 23, 2013
Meta-analysis diagnostic accuracy of SNP-based pathogenicity detection tools: a case of UTG1A1 gene mutationsHamid Galehdari, Najmaldin Saki, Javad Mohammadi-Asl, et al.Bioinformation|June 21, 2012
Homology modeling and molecular dynamics simulation of odonthubuthus doriae (Od1) scorpion toxin in comparison to the BmK M1Zahra Karimi, Sajad Falsafi-Zadeh, Hamid Galehdari, et al.Molecular Biology Reports|June 22, 2012
The investigation of allele and genotype frequencies of human C3 (rs2230199) in south Iranian populationNajmeh Bazyar, Negar Azarpira, Saied Reza Khatami, et al.Iranian Biomedical Journal|October 31, 2016
A Novel Defensin-Like Peptide Associated with Two Other New Cationic Antimicrobial Peptides in Transcriptome of the Iranian Scorpion VenomMasoumeh Baradaran, Amir Jalali, Maryam Naderi Soorki, et al.Hepatitis Monthly|January 12, 2012
Possible down regulation of the p16 gene promoter in individuals with hepatocellular carcinomaOranous Bashti Shiraz, Hamid Galehdari, Majid Yavarian, et al.Iranian Journal of Neurology|November 26, 2014
Association of interleukin 7 receptor gene polymorphism rs6897932 with multiple sclerosis patients in KhuzestanNastaran Majdinasab, Mahshid Hosseini Behbahani, Hamid Galehdari, et al.Jundishapur Journal of Microbiology|April 3, 2015
Cloning and Expression of Poly 3-Hydroxybutyrate Operon Into Escherichia coliMaryam Jari, Saeid Reza Khatami, Hamid Galehdari, et al.Cell Biochemistry and Biophysics|March 18, 2021
Terminal Peptide Extensions Augment the Retinal IMPDH1 Catalytic Activity and Attenuate the ATP-induced Fibrillation EventsBehnaz Andashti, Razieh Yazdanparast, Maede Motahar, et al.Journal of Medical Case Reports|June 29, 2011
Identification of a novel de novo mutation in the NIPBL gene in an Iranian patient with Cornelia de Lange syndrome: A case reportHamid Galehdari, Roya Monajemzadeh, Habibolah Nazem, et al.Pageof 17