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Year | Number of Results |
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2005 | 1 |
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2017 | 1 |
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Reduction of Pax9 gene dosage in an allelic series of mouse mutants causes hypodontia and oligodontia.
Hum Mol Genet. 2005 Dec 1;14(23):3605-17. doi: 10.1093/hmg/ddi388. Epub 2005 Oct 19.
Hum Mol Genet. 2005.
PMID: 16236760
Pax9 is required for cardiovascular development and interacts with Tbx1 in the pharyngeal endoderm to control 4th pharyngeal arch artery morphogenesis.
Phillips HM, Stothard CA, Shaikh Qureshi WM, Kousa AI, Briones-Leon JA, Khasawneh RR, O'Loughlin C, Sanders R, Mazzotta S, Dodds R, Seidel K, Bates T, Nakatomi M, Cockell SJ, Schneider JE, Mohun TJ, Maehr R, Kist R, Peters H, Bamforth SD.
Phillips HM, et al.
Development. 2019 Sep 23;146(18):dev177618. doi: 10.1242/dev.177618.
Development. 2019.
PMID: 31444215
Free PMC article.
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A developmental transcriptomic analysis of Pax1 and Pax9 in embryonic intervertebral disc development.
Sivakamasundari V, Kraus P, Sun W, Hu X, Lim SL, Prabhakar S, Lufkin T.
Sivakamasundari V, et al.
Biol Open. 2017 Feb 15;6(2):187-199. doi: 10.1242/bio.023218.
Biol Open. 2017.
PMID: 28011632
Free PMC article.
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Osr2 acts downstream of Pax9 and interacts with both Msx1 and Pax9 to pattern the tooth developmental field.
Zhou J, Gao Y, Zhang Z, Zhang Y, Maltby KM, Liu Z, Lan Y, Jiang R.
Zhou J, et al.
Dev Biol. 2011 May 15;353(2):344-53. doi: 10.1016/j.ydbio.2011.03.012. Epub 2011 Mar 17.
Dev Biol. 2011.
PMID: 21420399
Free PMC article.
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Generation of organized anterior foregut epithelia from pluripotent stem cells using small molecules.
Kearns NA, Genga RM, Ziller M, Kapinas K, Peters H, Brehm MA, Meissner A, Maehr R.
Kearns NA, et al.
Stem Cell Res. 2013 Nov;11(3):1003-12. doi: 10.1016/j.scr.2013.06.007. Epub 2013 Jun 29.
Stem Cell Res. 2013.
PMID: 23917481
Free article.
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Derivation of a mouse model for conditional inactivation of Pax9.
Kist R, Greally E, Peters H.
Kist R, et al.
Genesis. 2007 Jul;45(7):460-4. doi: 10.1002/dvg.20295.
Genesis. 2007.
PMID: 17610273
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Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities.
Peters H, Neubüser A, Kratochwil K, Balling R.
Peters H, et al.
Genes Dev. 1998 Sep 1;12(17):2735-47. doi: 10.1101/gad.12.17.2735.
Genes Dev. 1998.
PMID: 9732271
Free PMC article.
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