Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 182

1.

Non-syndromic oligodontia with a novel mutation of PAX9.

Suda N, Ogawa T, Kojima T, Saito C, Moriyama K.

J Dent Res. 2011 Mar;90(3):382-6. doi: 10.1177/0022034510390042. Epub 2010 Nov 22.

PMID:
21098475
2.

Novel PAX9 mutations cause non-syndromic tooth agenesis.

Mitsui SN, Yasue A, Masuda K, Watanabe K, Horiuchi S, Imoto I, Tanaka E.

J Dent Res. 2014 Mar;93(3):245-9. doi: 10.1177/0022034513519801. Epub 2014 Jan 16.

PMID:
24436340
3.

A novel missense mutation in the paired domain of human PAX9 causes oligodontia.

Zhao J, Hu Q, Chen Y, Luo S, Bao L, Xu Y.

Am J Med Genet A. 2007 Nov 1;143A(21):2592-7.

PMID:
17910065
4.

A novel nonsense mutation in PAX9 is associated with marked variability in number of missing teeth.

Hansen L, Kreiborg S, Jarlov H, Niebuhr E, Eiberg H.

Eur J Oral Sci. 2007 Aug;115(4):330-3.

PMID:
17697174
5.

Identification of a nonsense mutation in the PAX9 gene in molar oligodontia.

Nieminen P, Arte S, Tanner D, Paulin L, Alaluusua S, Thesleff I, Pirinen S.

Eur J Hum Genet. 2001 Oct;9(10):743-6.

6.

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. Epub 2003 Nov 7.

7.

A novel mutation in PAX9 causes familial form of molar oligodontia.

Mostowska A, Biedziak B, Trzeciak WH.

Eur J Hum Genet. 2006 Feb;14(2):173-9.

8.

Novel PAX9 mutation associated with syndromic tooth agenesis.

Mostowska A, Zadurska M, Rakowska A, Lianeri M, Jagodziński PP.

Eur J Oral Sci. 2013 Oct;121(5):403-11. doi: 10.1111/eos.12071. Epub 2013 Jul 13.

PMID:
24028587
9.

Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes.

Bergendal B, Klar J, Stecksén-Blicks C, Norderyd J, Dahl N.

Am J Med Genet A. 2011 Jul;155A(7):1616-22. doi: 10.1002/ajmg.a.34045. Epub 2011 May 27.

PMID:
21626677
10.

A novel mutation in human PAX9 causes molar oligodontia.

Frazier-Bowers SA, Guo DC, Cavender A, Xue L, Evans B, King T, Milewicz D, D'Souza RN.

J Dent Res. 2002 Feb;81(2):129-33.

PMID:
11827258
11.

Mutational analysis of families affected with molar oligodontia.

Frazier-Bowers SA, Scott MR, Cavender A, Mensah J, D'Souza RN.

Connect Tissue Res. 2002;43(2-3):296-300.

PMID:
12489173
12.

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
13.

Novel mutation of the initiation codon of PAX9 causes oligodontia.

Klein ML, Nieminen P, Lammi L, Niebuhr E, Kreiborg S.

J Dent Res. 2005 Jan;84(1):43-7.

PMID:
15615874
14.

[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;22(4):419-22. Chinese.

PMID:
16086281
15.

Novel nonsense mutation in MSX1 causes tooth agenesis with cleft lip in a Chinese family.

Liang J, Zhu L, Meng L, Chen D, Bian Z.

Eur J Oral Sci. 2012 Aug;120(4):278-82. doi: 10.1111/j.1600-0722.2012.00965.x. Epub 2012 Jun 25.

PMID:
22813217
16.

Reduction of Pax9 gene dosage in an allelic series of mouse mutants causes hypodontia and oligodontia.

Kist R, Watson M, Wang X, Cairns P, Miles C, Reid DJ, Peters H.

Hum Mol Genet. 2005 Dec 1;14(23):3605-17. Epub 2005 Oct 19.

PMID:
16236760
17.

[Identification of mutation in PAX9 gene in a Mongolian family with non-syndromic oligodontia].

Chen YJ, Liu YJ, Bai HH, Su YL, Feng ML, Wu QZ.

Zhonghua Kou Qiang Yi Xue Za Zhi. 2013 Aug;48(8):490-3. Chinese.

PMID:
24238416
18.

Clinical, radiographic, and genetic evaluation of a novel form of autosomal-dominant oligodontia.

Goldenberg M, Das P, Messersmith M, Stockton DW, Patel PI, D'Souza RN.

J Dent Res. 2000 Jul;79(7):1469-75.

PMID:
11005730
19.

A novel initiation codon mutation of PAX9 in a family with oligodontia.

Liang J, Qin C, Yue H, He H, Bian Z.

Arch Oral Biol. 2016 Jan;61:144-8. doi: 10.1016/j.archoralbio.2015.10.022. Epub 2015 Oct 30.

PMID:
26571067
20.

A novel nonsense mutation in PAX9 is associated with sporadic hypodontia.

Zhu J, Yang X, Zhang C, Ge L, Zheng S.

Mutagenesis. 2012 May;27(3):313-7. doi: 10.1093/mutage/ger080. Epub 2011 Nov 3.

PMID:
22058014

Supplemental Content

Support Center