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

Year Number of Results
2003 1
2004 1
2005 1
2007 1
2008 1
2009 3
2010 4
2011 8
2012 4
2013 6
2014 9
2015 10
2016 18
2017 9
2018 10
2019 5
2020 7
2021 15
2022 7
2023 12
2024 3

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113 results

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Page 1
Megakaryocytes in the lung: guests or ghosts?
Malara A, Balduini A. Malara A, et al. Among authors: balduini a. Blood. 2024 Jan 18;143(3):192-193. doi: 10.1182/blood.2023022897. Blood. 2024. PMID: 38236613 No abstract available.
Newly identified roles for PIEZO1 mechanosensor in controlling normal megakaryocyte development and in primary myelofibrosis.
Abbonante V, Karkempetzaki AI, Leon C, Krishnan A, Huang N, Di Buduo CA, Cattaneo D, Ward CM, Matsuura S, Guinard I, Weber J, De Acutis A, Vozzi G, Iurlo A, Ravid K, Balduini A. Abbonante V, et al. Among authors: balduini a. Am J Hematol. 2024 Mar;99(3):336-349. doi: 10.1002/ajh.27184. Epub 2024 Jan 2. Am J Hematol. 2024. PMID: 38165047 Free article.
Unraveling the hormonal pathway to megakaryocyte well-being.
Della Rosa G, Di Buduo CA, Balduini A. Della Rosa G, et al. Among authors: balduini a. J Thromb Haemost. 2023 Nov;21(11):3078-3081. doi: 10.1016/j.jtha.2023.08.006. J Thromb Haemost. 2023. PMID: 37858524 No abstract available.
Inside-to-outside and back to the future of megakaryopoiesis.
Di Buduo CA, Miguel CP, Balduini A. Di Buduo CA, et al. Among authors: balduini a. Res Pract Thromb Haemost. 2023 May 30;7(4):100197. doi: 10.1016/j.rpth.2023.100197. eCollection 2023 May. Res Pract Thromb Haemost. 2023. PMID: 37416054 Free PMC article.
Sirtuin 6 Regulates the Activation of the ATP/Purinergic Axis in Endothelial Cells.
Astigiano C, Piacente F, Laugieri ME, Benzi A, Di Buduo CA, Miguel CP, Soncini D, Cea M, Antonelli A, Magnani M, Balduini A, De Flora A, Bruzzone S. Astigiano C, et al. Among authors: balduini a. Int J Mol Sci. 2023 Apr 4;24(7):6759. doi: 10.3390/ijms24076759. Int J Mol Sci. 2023. PMID: 37047732 Free PMC article.
Bi-allelic variants in the ESAM tight-junction gene cause a neurodevelopmental disorder associated with fetal intracranial hemorrhage.
Lecca M, Pehlivan D, Suñer DH, Weiss K, Coste T, Zweier M, Oktay Y, Danial-Farran N, Rosti V, Bonasoni MP, Malara A, Contrò G, Zuntini R, Pollazzon M, Pascarella R, Neri A, Fusco C, Marafi D, Mitani T, Posey JE, Bayramoglu SE, Gezdirici A, Hernandez-Rodriguez J, Cladera EA, Miravet E, Roldan-Busto J, Ruiz MA, Bauzá CV, Ben-Sira L, Sigaudy S, Begemann A, Unger S, Güngör S, Hiz S, Sonmezler E, Zehavi Y, Jerdev M, Balduini A, Zuffardi O, Horvath R, Lochmüller H, Rauch A, Garavelli L, Tournier-Lasserve E, Spiegel R, Lupski JR, Errichiello E. Lecca M, et al. Among authors: balduini a. Am J Hum Genet. 2023 Apr 6;110(4):681-690. doi: 10.1016/j.ajhg.2023.03.005. Epub 2023 Mar 29. Am J Hum Genet. 2023. PMID: 36996813 Free PMC article.
Inherited Thrombocytopenia Caused by Variants in Crucial Genes for Glycosylation.
Marín-Quílez A, Díaz-Ajenjo L, Di Buduo CA, Zamora-Cánovas A, Lozano ML, Benito R, González-Porras JR, Balduini A, Rivera J, Bastida JM. Marín-Quílez A, et al. Among authors: balduini a. Int J Mol Sci. 2023 Mar 7;24(6):5109. doi: 10.3390/ijms24065109. Int J Mol Sci. 2023. PMID: 36982178 Free PMC article. Review.
113 results