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Expression analysis of hsa_circ_0020397, hsa_circ_0005986, hsa_circ_0003028, and hsa_circ_0006990 in renal cell carcinoma.
Mohammadisoleimani E, Firoozi Z, Naghizadeh MM, Asad AG, Jafari A, Pourjafarian MH, Ariafar A, Mansoori H, Dastsooz H, Sabaie H, Zeighami S, Mansoori Y. Mohammadisoleimani E, et al. Among authors: asad ag. Exp Mol Pathol. 2023 Feb;129:104848. doi: 10.1016/j.yexmp.2022.104848. Epub 2022 Dec 7. Exp Mol Pathol. 2023. PMID: 36496205 Free article.
Upregulation of hsa_circ_0004812 promotes COVID-19 cytokine storm via hsa-miR-1287-5p/IL6R, RIG-I axis.
Mohammadisoleimani E, Firoozi Z, Naghizadeh MM, Ghanbari Asad A, Pezeshki B, Gholampour Y, Mirzaei E, Simin M, Saliani M, Moravej A, Armoon Z, Mansoori Y. Mohammadisoleimani E, et al. Among authors: ghanbari asad a. J Clin Lab Anal. 2022 Oct;36(10):e24666. doi: 10.1002/jcla.24666. Epub 2022 Aug 21. J Clin Lab Anal. 2022. PMID: 35989496 Free PMC article.
AutoMap is a high performance homozygosity mapping tool using next-generation sequencing data.
Quinodoz M, Peter VG, Bedoni N, Royer Bertrand B, Cisarova K, Salmaninejad A, Sepahi N, Rodrigues R, Piran M, Mojarrad M, Pasdar A, Ghanbari Asad A, Sousa AB, Coutinho Santos L, Superti-Furga A, Rivolta C. Quinodoz M, et al. Among authors: ghanbari asad a. Nat Commun. 2021 Jan 22;12(1):518. doi: 10.1038/s41467-020-20584-4. Nat Commun. 2021. PMID: 33483490 Free PMC article.
Whole exome sequencing in 17 consanguineous Iranian pedigrees expands the mutational spectrum of inherited retinal dystrophies.
Rehman AU, Sepahi N, Bedoni N, Ravesh Z, Salmaninejad A, Cancellieri F, Peter VG, Quinodoz M, Mojarrad M, Pasdar A, Asad AG, Ghalamkari S, Piran M, Piran M, Superti-Furga A, Rivolta C. Rehman AU, et al. Among authors: asad ag. Sci Rep. 2021 Sep 29;11(1):19332. doi: 10.1038/s41598-021-98677-3. Sci Rep. 2021. PMID: 34588515 Free PMC article.