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Journal Abstract Search
179 related items for PubMed ID: 14607846
1. Functional analysis of a mutation in PAX9 associated with familial tooth agenesis in humans. Mensah JK, Ogawa T, Kapadia H, Cavender AC, D'Souza RN. J Biol Chem; 2004 Feb 13; 279(7):5924-33. PubMed ID: 14607846 [Abstract] [Full Text] [Related]
3. Pathogenic mechanisms of tooth agenesis linked to paired domain mutations in human PAX9. Wang Y, Groppe JC, Wu J, Ogawa T, Mues G, D'Souza RN, Kapadia H. Hum Mol Genet; 2009 Aug 01; 18(15):2863-74. PubMed ID: 19429910 [Abstract] [Full Text] [Related]
4. [Functional analysis of novel mutations in PAX9 associated with familial oligodontia]. Zhao JL, Chen YX, Bao L, Wu TJ, Zhou L. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Aug 01; 22(4):419-22. PubMed ID: 16086281 [Abstract] [Full Text] [Related]
7. Characterization of PAX9 variant P20L identified in a Japanese family with tooth agenesis. Murakami A, Yasuhira S, Mayama H, Miura H, Maesawa C, Satoh K. PLoS One; 2017 Aug 01; 12(10):e0186260. PubMed ID: 29023497 [Abstract] [Full Text] [Related]
8. Non-syndromic oligodontia with a novel mutation of PAX9. Suda N, Ogawa T, Kojima T, Saito C, Moriyama K. J Dent Res; 2011 Mar 01; 90(3):382-6. PubMed ID: 21098475 [Abstract] [Full Text] [Related]
11. Molecular basis of non-syndromic tooth agenesis: mutations of MSX1 and PAX9 reflect their role in patterning human dentition. Mostowska A, Kobielak A, Trzeciak WH. Eur J Oral Sci; 2003 Oct 01; 111(5):365-70. PubMed ID: 12974677 [Abstract] [Full Text] [Related]
12. Msx1 mutations: how do they cause tooth agenesis? Wang Y, Kong H, Mues G, D'Souza R. J Dent Res; 2011 Mar 01; 90(3):311-6. PubMed ID: 21297014 [Abstract] [Full Text] [Related]
14. Novel mutation in the paired box sequence of PAX9 gene in a sporadic form of oligodontia. Mostowska A, Kobielak A, Biedziak B, Trzeciak WH. Eur J Oral Sci; 2003 Jun 01; 111(3):272-6. PubMed ID: 12786960 [Abstract] [Full Text] [Related]
17. A missense mutation in PAX9 in a family with distinct phenotype of oligodontia. Lammi L, Halonen K, Pirinen S, Thesleff I, Arte S, Nieminen P. Eur J Hum Genet; 2003 Nov 01; 11(11):866-71. PubMed ID: 14571272 [Abstract] [Full Text] [Related]
19. A novel nonsense mutation in PAX9 is associated with sporadic hypodontia. Zhu J, Yang X, Zhang C, Ge L, Zheng S. Mutagenesis; 2012 May 01; 27(3):313-7. PubMed ID: 22058014 [Abstract] [Full Text] [Related]