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Noroozi R, Branicki W, Pyrc K, Łabaj PP, Pospiech E, Taheri M, Ghafouri-Fard S. Altered cytokine levels and immune responses in patients with SARS-CoV-2 infection and related conditions. Cytokine. 2020;133:155143.
Mazdeh M, Kordestani H, Komaki A, Eftekharian MMahdi, Arsang-Jang S, Branicki W, Taheri M, Ghafouri-Fard S. Assessment of expression profile of microRNAs in multiple sclerosis patients treated with fingolimod. J Mol Neurosci. 2020.
Sayad A, Badrlou E, Ghafouri-Fard S, Taheri M. Association Analysis Between the rs1899663 Polymorphism of HOTAIR and Risk of Psychiatric Conditions in an Iranian Population. J Mol Neurosci. 2020.
Safa A, Noroozi R, Taheri M, Ghafouri-Fard S. Association Analysis of ANRIL Polymorphisms and Haplotypes with Autism Spectrum Disorders. J Mol Neurosci. 2020.
Ketab FNasiri Gan, Gharesouran J, Ghafouri-Fard S, Dastar S, Mazraeh SAbdi, Hosseinzadeh H, Moradi M, Javadlar M, Hiradfar A, Rezamand A, et al. Dual biomarkers long non-coding RNA GAS5 and its target, NR3C1, contribute to acute myeloid leukemia. Exp Mol Pathol. 2020:104399.
Ghafouri-Fard S, Noroozi R, Vafaee R, Branicki W, Pospiech E, Pyrc K, Łabaj PP, Omrani MDavood, Taheri M, Sanak M. Effects of host genetic variations on response to, susceptibility and severity of respiratory infections. Biomed Pharmacother. 2020;128:110296.
Sayad A, Mirzajani S, Gholami L, Razzaghi P, Ghafouri-Fard S, Taheri M. Emerging role of long non-coding RNAs in the pathogenesis of periodontitis. Biomed Pharmacother. 2020;129:110362.
Ali ZPour Moham, Taheri M, Sangsefidi S, Arsang-Jang S, Mazdeh M, Zamani A, Ghafouri-Fard S, Eftekharian MMahdi. Evaluation of Expression of STAT Genes in Immune-Mediated Polyneuropathies. J Mol Neurosci. 2020.
Ebadi N, Ghafouri-Fard S, Taheri M, Arsang-Jang S, Omrani MDavood. Expression analysis of inflammatory response-associated genes in coronary artery disease. Arch Physiol Biochem. 2020:1-7.
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.
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.
Ghafouri-Fard S, Esmaeili M, Taheri M. Expression of non-coding RNAs in hematological malignancies. Eur J Pharmacol. 2020:172976.
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.
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.
Ghafouri-Fard S, Vafaee R, Shoorei H, Taheri M. microRNAs in gastric cancer: biomarkers and therapeutic targets. Gene. 2020:144937.
Ghafouri-Fard S, Shoorei H, Taheri M. miRNA profile in ovarian cancer. Exp Mol Pathol. 2020:104381.
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.
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.