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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2009 | 2 |
2011 | 2 |
2012 | 1 |
2024 | 0 |
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4 results
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A novel mechanism for the transcriptional regulation of Wnt signaling in development.
Genes Dev. 2011 Sep 1;25(17):1783-95. doi: 10.1101/gad.17227011. Epub 2011 Aug 19.
Genes Dev. 2011.
PMID: 21856776
Free PMC article.
The PI3K-PTEN tug-of-war, oxidative stress and retinal degeneration.
Kang KH, Lemke G, Kim JW.
Kang KH, et al.
Trends Mol Med. 2009 May;15(5):191-8. doi: 10.1016/j.molmed.2009.03.005. Epub 2009 Apr 18.
Trends Mol Med. 2009.
PMID: 19380252
Free PMC article.
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VAX1 mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: the first description of a VAX1 phenotype in humans.
Slavotinek AM, Chao R, Vacik T, Yahyavi M, Abouzeid H, Bardakjian T, Schneider A, Shaw G, Sherr EH, Lemke G, Youssef M, Schorderet DF.
Slavotinek AM, et al.
Hum Mutat. 2012 Feb;33(2):364-8. doi: 10.1002/humu.21658. Epub 2011 Dec 27.
Hum Mutat. 2012.
PMID: 22095910
Free PMC article.
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Lack of protein S in mice causes embryonic lethal coagulopathy and vascular dysgenesis.
Burstyn-Cohen T, Heeb MJ, Lemke G.
Burstyn-Cohen T, et al.
J Clin Invest. 2009 Oct;119(10):2942-53. doi: 10.1172/JCI39325.
J Clin Invest. 2009.
PMID: 19729839
Free PMC article.
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