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

Year Number of Results
2000 1
2001 1
2003 1
2004 1
2005 2
2006 4
2007 4
2008 5
2009 5
2010 7
2011 12
2012 10
2013 13
2014 9
2015 11
2016 8
2017 9
2018 9
2019 5
2020 16
2021 7
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Similar articles for PMID: 28993503

119 results
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Page 1
Establishment of mouse model of MYH9 disorders: heterozygous R702C mutation provokes macrothrombocytopenia with leukocyte inclusion bodies, renal glomerulosclerosis and hearing disability.
Suzuki N, Kunishima S, Ikejiri M, Maruyama S, Sone M, Takagi A, Ikawa M, Okabe M, Kojima T, Saito H, Naoe T, Matsushita T. Suzuki N, et al. PLoS One. 2013 Aug 20;8(8):e71187. doi: 10.1371/journal.pone.0071187. eCollection 2013. PLoS One. 2013. PMID: 23976996 Free PMC article.
Mouse models of MYH9-related disease: mutations in nonmuscle myosin II-A.
Zhang Y, Conti MA, Malide D, Dong F, Wang A, Shmist YA, Liu C, Zerfas P, Daniels MP, Chan CC, Kozin E, Kachar B, Kelley MJ, Kopp JB, Adelstein RS. Zhang Y, et al. Blood. 2012 Jan 5;119(1):238-50. doi: 10.1182/blood-2011-06-358853. Epub 2011 Sep 8. Blood. 2012. PMID: 21908426 Free PMC article.
Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes.
Heath KE, Campos-Barros A, Toren A, Rozenfeld-Granot G, Carlsson LE, Savige J, Denison JC, Gregory MC, White JG, Barker DF, Greinacher A, Epstein CJ, Glucksman MJ, Martignetti JA. Heath KE, et al. Am J Hum Genet. 2001 Nov;69(5):1033-45. doi: 10.1086/324267. Epub 2001 Oct 4. Am J Hum Genet. 2001. PMID: 11590545 Free PMC article.
119 results
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