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Page 1
The transcriptome profile of human trisomy 21 blood cells.
Antonaros F, Zenatelli R, Guerri G, Bertelli M, Locatelli C, Vione B, Catapano F, Gori A, Vitale L, Pelleri MC, Ramacieri G, Cocchi G, Strippoli P, Caracausi M, Piovesan A. Antonaros F, et al. Among authors: caracausi m. Hum Genomics. 2021 May 1;15(1):25. doi: 10.1186/s40246-021-00325-4. Hum Genomics. 2021. PMID: 33933170 Free PMC article.
Improving mRNA 5' coding sequence determination in the mouse genome.
Piovesan A, Caracausi M, Pelleri MC, Vitale L, Martini S, Bassani C, Gurioli A, Casadei R, Soldà G, Strippoli P. Piovesan A, et al. Among authors: caracausi m. Mamm Genome. 2014 Apr;25(3-4):149-59. doi: 10.1007/s00335-013-9498-3. Epub 2014 Feb 7. Mamm Genome. 2014. PMID: 24504701
Systematic reanalysis of partial trisomy 21 cases with or without Down syndrome suggests a small region on 21q22.13 as critical to the phenotype.
Pelleri MC, Cicchini E, Locatelli C, Vitale L, Caracausi M, Piovesan A, Rocca A, Poletti G, Seri M, Strippoli P, Cocchi G. Pelleri MC, et al. Among authors: caracausi m. Hum Mol Genet. 2016 Jun 15;25(12):2525-2538. doi: 10.1093/hmg/ddw116. Epub 2016 Apr 22. Hum Mol Genet. 2016. PMID: 27106104 Free PMC article.
Difficulty in obtaining the complete mRNA coding sequence at 5' region (5' end mRNA artifact): Causes, consequences in biology and medicine and possible solutions for obtaining the actual amino acid sequence of proteins (Review).
Vitale L, Caracausi M, Casadei R, Pelleri MC, Piovesan A. Vitale L, et al. Among authors: caracausi m. Int J Mol Med. 2017 May;39(5):1063-1071. doi: 10.3892/ijmm.2017.2942. Epub 2017 Apr 6. Int J Mol Med. 2017. PMID: 28393177 Review.
37 results