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Items: 1 to 20 of 27

1.

Genetic interactions between Pax9 and Msx1 regulate lip development and several stages of tooth morphogenesis.

Nakatomi M, Wang XP, Key D, Lund JJ, Turbe-Doan A, Kist R, Aw A, Chen Y, Maas RL, Peters H.

Dev Biol. 2010 Apr 15;340(2):438-49. doi: 10.1016/j.ydbio.2010.01.031. Epub 2010 Feb 1.

2.

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 1;18(15):2863-74. doi: 10.1093/hmg/ddp221. Epub 2009 May 9.

3.

Apc inhibition of Wnt signaling regulates supernumerary tooth formation during embryogenesis and throughout adulthood.

Wang XP, O'Connell DJ, Lund JJ, Saadi I, Kuraguchi M, Turbe-Doan A, Cavallesco R, Kim H, Park PJ, Harada H, Kucherlapati R, Maas RL.

Development. 2009 Jun;136(11):1939-49. doi: 10.1242/dev.033803.

4.

Identification of an ancient Bmp4 mesoderm enhancer located 46 kb from the promoter.

Chandler KJ, Chandler RL, Mortlock DP.

Dev Biol. 2009 Mar 15;327(2):590-602. doi: 10.1016/j.ydbio.2008.12.033. Epub 2009 Jan 3.

5.

Identification and functional analysis of two novel PAX9 mutations.

Wang Y, Wu H, Wu J, Zhao H, Zhang X, Mues G, D'Souza RN, Feng H, Kapadia H.

Cells Tissues Organs. 2009;189(1-4):80-7. doi: 10.1159/000151448. Epub 2008 Aug 14.

6.

Identification of a novel missense mutation of MSX1 gene in Chinese family with autosomal-dominant oligodontia.

Xuan K, Jin F, Liu YL, Yuan LT, Wen LY, Yang FS, Wang XJ, Wang GH, Jin Y.

Arch Oral Biol. 2008 Aug;53(8):773-9. doi: 10.1016/j.archoralbio.2008.02.012. Epub 2008 Mar 28.

PMID:
18374898
7.

Wnt/beta-catenin signaling directs multiple stages of tooth morphogenesis.

Liu F, Chu EY, Watt B, Zhang Y, Gallant NM, Andl T, Yang SH, Lu MM, Piccolo S, Schmidt-Ullrich R, Taketo MM, Morrisey EE, Atit R, Dlugosz AA, Millar SE.

Dev Biol. 2008 Jan 1;313(1):210-24. Epub 2007 Oct 23.

8.

Expression survey of genes critical for tooth development in the human embryonic tooth germ.

Lin D, Huang Y, He F, Gu S, Zhang G, Chen Y, Zhang Y.

Dev Dyn. 2007 May;236(5):1307-12.

9.

A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families.

Chishti MS, Muhammad D, Haider M, Ahmad W.

J Hum Genet. 2006;51(10):872-8. Epub 2006 Aug 24.

PMID:
16932841
10.
11.

Functional consequences of interactions between Pax9 and Msx1 genes in normal and abnormal tooth development.

Ogawa T, Kapadia H, Feng JQ, Raghow R, Peters H, D'Souza RN.

J Biol Chem. 2006 Jul 7;281(27):18363-9. Epub 2006 May 1.

12.

Molecular characterization of a novel PAX9 missense mutation causing posterior tooth agenesis.

Kapadia H, Frazier-Bowers S, Ogawa T, D'Souza RN.

Eur J Hum Genet. 2006 Apr;14(4):403-9.

13.

A novel missense mutation in the paired domain of PAX9 causes non-syndromic oligodontia.

Jumlongras D, Lin JY, Chapra A, Seidman CE, Seidman JG, Maas RL, Olsen BR.

Hum Genet. 2004 Feb;114(3):242-9. Epub 2003 Dec 19.

PMID:
14689302
14.

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;11(11):866-71.

15.

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;111(3):272-6.

PMID:
12786960
16.

Novel missense mutations and a 288-bp exonic insertion in PAX9 in families with autosomal dominant hypodontia.

Das P, Hai M, Elcock C, Leal SM, Brown DT, Brook AH, Patel PI.

Am J Med Genet A. 2003 Apr 1;118A(1):35-42.

PMID:
12605438
17.

The role of MSX1 in human tooth agenesis.

Lidral AC, Reising BC.

J Dent Res. 2002 Apr;81(4):274-8.

18.

Crystal structure of the Msx-1 homeodomain/DNA complex.

Hovde S, Abate-Shen C, Geiger JH.

Biochemistry. 2001 Oct 9;40(40):12013-21.

PMID:
11580277
19.

BMP4 rescues a non-cell-autonomous function of Msx1 in tooth development.

Bei M, Kratochwil K, Maas RL.

Development. 2000 Nov;127(21):4711-8.

20.

Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification.

Wilkie AO, Tang Z, Elanko N, Walsh S, Twigg SR, Hurst JA, Wall SA, Chrzanowska KH, Maxson RE Jr.

Nat Genet. 2000 Apr;24(4):387-90.

PMID:
10742103

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