Author Title Type [ Year(Asc)]
Filters: Author is Taheri, Mohammad  [Clear All Filters]
Mirzajani S, Ghafouri-Fard S, Habibabadi JMehvari, Arsang-Jang S, Omrani MDavood, Fesharaki SSohrab Has, Sayad A, Taheri M. Expression Analysis of lncRNAs in Refractory and Non-Refractory Epileptic Patients. J Mol Neurosci. 2020.
Bahrami T, Taheri M, Javadi S, Omrani MDavood, Karimipour M. Expression Analysis of Long Non-coding RNA Lnc-DC in HLA-DRB1*15:01-Negative Patients with Multiple Sclerosis: A Probable Cause for Gender Differences in Multiple Sclerosis Susceptibility?. J Mol Neurosci. 2020.
Mohebi M, Ghafouri-Fard S, Modarressi MHossein, Dashti S, Zekri A, Kholghi-Oskooei V, Taheri M. Expression analysis of vimentin and the related lncRNA network in breast cancer. Exp Mol Pathol. 2020:104439.
Liaghati P, Momeni P, Oskooei VKholghi, Ghafouri-Fard S, Taheri M. Expression levels of ABCG2 and CD61 genes in breast cancer tissues of Iranian population. Breast Dis. 2020.
Ghafouri-Fard S, Esmaeili M, Taheri M. Expression of non-coding RNAs in hematological malignancies. Eur J Pharmacol. 2020:172976.
Taheri M, Shirvani-Farsani Z, Ghafouri-Fard S, Omrani MDavood. Expression profile of microRNAs in bladder cancer and their application as biomarkers. Biomed Pharmacother. 2020;131:110703.
Mohebi M, Sattari A, Ghafouri-Fard S, Modarressi MHossein, Kholghi-Oskooei V, Taheri M. Expression profiling revealed up-regulation of three lncRNAs in breast cancer samples. Exp Mol Pathol. 2020:104544.
Gharesouran J, Jalaiei A, Hosseinzadeh A, Ghafouri-Fard S, Mokhtari Z, Ghahremanzadeh K, Rezazadeh N, Shiva S, Sadeghvand S, Taheri M, et al. GAA gene mutation detection following clinical evaluation and enzyme activity analysis in Azeri Turkish patients with Pompe disease. Metab Brain Dis. 2020.
Ghafouri-Fard S, Dashti S, Taheri M. The HOTTIP (HOXA transcript at the distal tip) lncRNA: Review of oncogenic roles in human. Biomed Pharmacother. 2020;127:110158.
Ghafouri-Fard S, Dashti S, Farsi M, Taheri M. HOX transcript antisense RNA: An oncogenic lncRNA in diverse malignancies. Exp Mol Pathol. 2020:104578.
Sayad A, Akbari MTaghi, Hesami O, Ghafouri-Fard S, Taheri M. Identification of a Mutation in SPG11 in an Iranian Patient with Spastic Paraplegia and Ears of the Lynx Sign. J Mol Neurosci. 2020.
Maleki P, Sheida SValeh, Mowla SJavad, Soleimani V, Taheri M, Raheb J. LINK-A long non-coding RNA and VEGF RNA expression in epithelial ovarian cancer patients. Hum Antibodies. 2020.
Ghafouri-Fard S, Vafaee R, Shoorei H, Taheri M. microRNAs in gastric cancer: biomarkers and therapeutic targets. Gene. 2020:144937.
Safa A, Bahroudi Z, Shoorei H, Majidpoor J, Abak A, Taheri M, Ghafouri-Fard S. miR-1: A comprehensive review of its role in normal development and diverse disorders. Biomed Pharmacother. 2020;132:110903.
Ghafouri-Fard S, Shoorei H, Taheri M. miRNA profile in ovarian cancer. Exp Mol Pathol. 2020:104381.
Rezaei O, Honarmand K, Nateghinia S, Taheri M, Ghafouri-Fard S. miRNA signature in glioblastoma: Potential biomarkers and therapeutic targets. Exp Mol Pathol. 2020:104550.
Maleki P, Sadeghi Z, Rahpeyma SShahryar, Taheri M, Raheb J. MTT assay dataset of Polyethylenimine coated Graphenoxide nanosheets on breast cancer cell lines (MCF7, MDA-MB-231, MDA-MB-468). Hum Antibodies. 2020.
Ghafouri-Fard S, Shoorei H, Branicki W, Taheri M. Non-coding RNA profile in lung cancer. Exp Mol Pathol. 2020:104411.
Ghafouri-Fard S, Shoorei H, Taheri M. Non-coding RNAs participate in the ischemia-reperfusion injury. Biomed Pharmacother. 2020;129:110419.
Rezaei H, Rezaie Z, Seifati SMorteza, Ardeshirylajimi A, Basiri A, Taheri M, Omrani MDavood. Poly-phosphate increases SMC differentiation of mesenchymal stem cells on PLGA-polyurethane nanofibrous scaffold. Cell Tissue Bank. 2020.
Taheri M, Noroozi R, Sadeghpour S, Omrani MDavood, Ghafouri-Fard S. The rs4759314 SNP within Hotair lncRNA is associated with risk of multiple sclerosis. Mult Scler Relat Disord. 2020;40:101986.
Taheri M, Noroozi R, Aghaei K, Omrani MDavood, Ghafouri-Fard S. The rs594445 in MOCOS gene is associated with risk of autism spectrum disorder. Metab Brain Dis. 2020.
Javadlar M, Dastar S, Gharesouran J, Ghafouri-Fard S, Hosseinzadeh H, Moradi M, Mazraeh SAbdi, Ketab FNasiri Gan, Rezamand A, Hiradfar A, et al. RUNX1 variant as a genetic predisposition factor for acute myeloid leukemia. Exp Mol Pathol. 2020:104440.
Safa A, Omrani MDavood, Nicknafs F, Komaki A, Taheri M, Ghafouri-Fard S. A Single Nucleotide Polymorphism Within Molybdenum Cofactor Sulfurase Gene Is Associated With Neuropsychiatric Conditions. Front Mol Biosci. 2020;7:540375.