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

Year Number of Results
1995 1
2002 1
2004 1
2005 4
2007 3
2008 1
2009 2
2010 3
2012 1
2013 4
2014 2
2015 4
2016 5
2021 0
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Cited Articles for PMCID: 5207508

29 results
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Page 1
OVOL2 Maintains the Transcriptional Program of Human Corneal Epithelium by Suppressing Epithelial-to-Mesenchymal Transition.
Kitazawa K, Hikichi T, Nakamura T, Mitsunaga K, Tanaka A, Nakamura M, Yamakawa T, Furukawa S, Takasaka M, Goshima N, Watanabe A, Okita K, Kawasaki S, Ueno M, Kinoshita S, Masui S. Kitazawa K, et al. Cell Rep. 2016 May 10;15(6):1359-68. doi: 10.1016/j.celrep.2016.04.020. Epub 2016 Apr 28. Cell Rep. 2016. PMID: 27134177 Free article.
Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2.
Davidson AE, Liskova P, Evans CJ, Dudakova L, Nosková L, Pontikos N, Hartmannová H, Hodaňová K, Stránecký V, Kozmík Z, Levis HJ, Idigo N, Sasai N, Maher GJ, Bellingham J, Veli N, Ebenezer ND, Cheetham ME, Daniels JT, Thaung CM, Jirsova K, Plagnol V, Filipec M, Kmoch S, Tuft SJ, Hardcastle AJ. Davidson AE, et al. Am J Hum Genet. 2016 Jan 7;98(1):75-89. doi: 10.1016/j.ajhg.2015.11.018. Epub 2015 Dec 31. Am J Hum Genet. 2016. PMID: 26749309 Free PMC article.
IC3D classification of corneal dystrophies--edition 2.
Weiss JS, Møller HU, Aldave AJ, Seitz B, Bredrup C, Kivelä T, Munier FL, Rapuano CJ, Nischal KK, Kim EK, Sutphin J, Busin M, Labbé A, Kenyon KR, Kinoshita S, Lisch W. Weiss JS, et al. Cornea. 2015 Feb;34(2):117-59. doi: 10.1097/ICO.0000000000000307. Cornea. 2015. PMID: 25564336 Free article.
29 results
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