Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
My NCBI Filters
Results by year

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

Year Number of Results
1993 1
1998 2
1999 1
2000 1
2001 1
2002 2
2003 3
2004 3
2005 1
2006 2
2007 1
2008 1
2009 1
2010 4
2011 2
2012 3
2013 4
2014 1
2015 1
2016 2
2017 3
2018 2
2019 5
2020 3
2021 1
Text availability
Article attribute
Article type
Publication date

PubMed Links for id: 8799

46 results
Results by year
Filters applied: . Clear all
Page 1
Novel PEX11B Mutations Extend the Peroxisome Biogenesis Disorder 14B Phenotypic Spectrum and Underscore Congenital Cataract as an Early Feature.
Taylor RL, Handley MT, Waller S, Campbell C, Urquhart J, Meynert AM, Ellingford JM, Donnelly D, Wilcox G, Lloyd IC, Mundy H, FitzPatrick DR, Deshpande C, Clayton-Smith J, Black GC. Taylor RL, et al. Invest Ophthalmol Vis Sci. 2017 Jan 1;58(1):594-603. doi: 10.1167/iovs.16-21026. Invest Ophthalmol Vis Sci. 2017. PMID: 28129423 Free PMC article.
Self-interaction of human Pex11pβ during peroxisomal growth and division.
Bonekamp NA, Grille S, Cardoso MJ, Almeida M, Aroso M, Gomes S, Magalhaes AC, Ribeiro D, Islinger M, Schrader M. Bonekamp NA, et al. PLoS One. 2013;8(1):e53424. doi: 10.1371/journal.pone.0053424. Epub 2013 Jan 7. PLoS One. 2013. PMID: 23308220 Free PMC article.
46 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page