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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 3
2003 7
2004 5
2005 2
2006 2
2007 4
2008 5
2009 5
2010 5
2011 2
2012 7
2013 2
2014 2
2015 3
2016 7
2017 5
2018 10
2019 11
2020 10
2021 8
2022 4
2023 4
2024 1

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93 results

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Page 1
Functional genetics.
Marchetti G, Pinotti M, Lunghi B, Casari C, Bernardi F. Marchetti G, et al. Among authors: pinotti m. Thromb Res. 2012 Mar;129(3):336-40. doi: 10.1016/j.thromres.2011.10.028. Epub 2011 Nov 17. Thromb Res. 2012. PMID: 22100315 Review.
Translation termination codons in protein synthesis and disease.
Lombardi S, Testa MF, Pinotti M, Branchini A. Lombardi S, et al. Among authors: pinotti m. Adv Protein Chem Struct Biol. 2022;132:1-48. doi: 10.1016/bs.apcsb.2022.06.001. Epub 2022 Jul 30. Adv Protein Chem Struct Biol. 2022. PMID: 36088072
Exploring Splicing-Switching Molecules For Seckel Syndrome Therapy.
Scalet D, Balestra D, Rohban S, Bovolenta M, Perrone D, Bernardi F, Campaner S, Pinotti M. Scalet D, et al. Among authors: pinotti m. Biochim Biophys Acta Mol Basis Dis. 2017 Jan;1863(1):15-20. doi: 10.1016/j.bbadis.2016.09.011. Epub 2016 Sep 14. Biochim Biophys Acta Mol Basis Dis. 2017. PMID: 27639833 Free article.
A recoded view on the F9 p.Cys178Ter pathogenic mechanism.
Branchini A, Pinotti M. Branchini A, et al. Among authors: pinotti m. Thromb Res. 2020 Mar;187:88-90. doi: 10.1016/j.thromres.2020.01.016. Epub 2020 Jan 15. Thromb Res. 2020. PMID: 31978811 No abstract available.
F9 missense mutations impairing factor IX activation are associated with pleiotropic plasma phenotypes.
Branchini A, Morfini M, Lunghi B, Belvini D, Radossi P, Bury L, Serino ML, Giordano P, Cultrera D, Molinari AC, Napolitano M, Bigagli E, Castaman G, Pinotti M, Bernardi F; GePKHIS Study Group of AICE. Branchini A, et al. Among authors: pinotti m. J Thromb Haemost. 2022 Jan;20(1):69-81. doi: 10.1111/jth.15552. Epub 2021 Oct 24. J Thromb Haemost. 2022. PMID: 34626083 Free PMC article.
93 results