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

Year Number of Results
1981 1
1983 1
1985 3
1987 7
1988 17
1989 26
1990 35
1991 62
1992 53
1993 64
1994 75
1995 74
1996 73
1997 93
1998 134
1999 143
2000 176
2001 180
2002 168
2003 190
2004 164
2005 201
2006 243
2007 295
2008 307
2009 351
2010 369
2011 420
2012 443
2013 489
2014 477
2015 423
2016 416
2017 410
2018 445
2019 308
2020 16
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6,633 results
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Page 1
Systematic Analysis of Human Protein Phosphatase Interactions and Dynamics.
Yadav L, Tamene F, Göös H, van Drogen A, Katainen R, Aebersold R, Gstaiger M, Varjosalo M. Yadav L, et al. Cell Syst. 2017 Apr 26;4(4):430-444.e5. doi: 10.1016/j.cels.2017.02.011. Epub 2017 Mar 18. Cell Syst. 2017. PMID: 28330616 Free article.
Regulation of Cell Division.
Heim A, Rymarczyk B, Mayer TU. Heim A, et al. Adv Exp Med Biol. 2017;953:83-116. doi: 10.1007/978-3-319-46095-6_3. Adv Exp Med Biol. 2017. PMID: 27975271 Review.
The multiple functions of protein phosphatase 6.
Ohama T. Ohama T. Biochim Biophys Acta Mol Cell Res. 2019 Jan;1866(1):74-82. doi: 10.1016/j.bbamcr.2018.07.015. Epub 2018 Jul 21. Biochim Biophys Acta Mol Cell Res. 2019. PMID: 30036567 Free article. Review.
Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowth.
Loveday C, Tatton-Brown K, Clarke M, Westwood I, Renwick A, Ramsay E, Nemeth A, Campbell J, Joss S, Gardner M, Zachariou A, Elliott A, Ruark E, van Montfort R; Childhood Overgrowth Collaboration, Rahman N. Loveday C, et al. Hum Mol Genet. 2015 Sep 1;24(17):4775-9. doi: 10.1093/hmg/ddv182. Epub 2015 May 13. Hum Mol Genet. 2015. PMID: 25972378 Free PMC article.
De Novo Truncating Mutations in the Last and Penultimate Exons of PPM1D Cause an Intellectual Disability Syndrome.
Jansen S, Geuer S, Pfundt R, Brough R, Ghongane P, Herkert JC, Marco EJ, Willemsen MH, Kleefstra T, Hannibal M, Shieh JT, Lynch SA, Flinter F, FitzPatrick DR, Gardham A, Bernhard B, Ragge N, Newbury-Ecob R, Bernier R, Kvarnung M, Magnusson EA, Wessels MW, van Slegtenhorst MA, Monaghan KG, de Vries P, Veltman JA; Deciphering Developmental Disorders Study, Lord CJ, Vissers LE, de Vries BB. Jansen S, et al. Am J Hum Genet. 2017 Apr 6;100(4):650-658. doi: 10.1016/j.ajhg.2017.02.005. Epub 2017 Mar 23. Am J Hum Genet. 2017. PMID: 28343630 Free PMC article.
The Highly Recurrent PP2A Aα-Subunit Mutation P179R Alters Protein Structure and Impairs PP2A Enzyme Function to Promote Endometrial Tumorigenesis.
Taylor SE, O'Connor CM, Wang Z, Shen G, Song H, Leonard D, Sangodkar J, LaVasseur C, Avril S, Waggoner S, Zanotti K, Armstrong AJ, Nagel C, Resnick K, Singh S, Jackson MW, Xu W, Haider S, DiFeo A, Narla G. Taylor SE, et al. Cancer Res. 2019 Aug 15;79(16):4242-4257. doi: 10.1158/0008-5472.CAN-19-0218. Epub 2019 May 29. Cancer Res. 2019. PMID: 31142515
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