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Items: 1 to 20 of 154

1.

A case-control study of the association between tooth-development gene polymorphisms and non-syndromic hypodontia in the Chinese Han population.

Liu H, Zhang J, Song S, Zhao H, Han D, Feng H.

Eur J Oral Sci. 2012 Oct;120(5):378-85. doi: 10.1111/j.1600-0722.2012.00986.x. Epub 2012 Aug 18.

PMID:
22984994
2.

rs929387 of GLI3 is involved in tooth agenesis in Chinese Han population.

Liu H, Han D, Wong S, Nan X, Zhao H, Feng H.

PLoS One. 2013 Nov 20;8(11):e80860. doi: 10.1371/journal.pone.0080860. eCollection 2013.

3.

Association between rs11001553 of DKK1 and non-syndromic tooth agenesis in the Chinese Han population.

Liu HC, Zhang J, Wong S, Han D, Zhao HS, Feng HL.

Genet Mol Res. 2014 Apr 3;13(3):7133-9. doi: 10.4238/2014.April.3.4.

4.

Polymorphism of ZBTB17 gene is associated with idiopathic dilated cardiomyopathy: a case control study in a Han Chinese population.

Li X, Luo R, Mo X, Jiang R, Kong H, Hua W, Wu X.

Eur J Med Res. 2013 Apr 9;18:10. doi: 10.1186/2047-783X-18-10.

5.

PAX9 polymorphisms and susceptibility with sporadic tooth agenesis in Turkish populations: a case-control study.

Isman E, Nergiz S, Acar H, Sari Z.

BMC Genomics. 2013 Oct 26;14:733. doi: 10.1186/1471-2164-14-733.

6.

Nucleotide variants of genes encoding components of the Wnt signalling pathway and the risk of non-syndromic tooth agenesis.

Mostowska A, Biedziak B, Zadurska M, Dunin-Wilczynska I, Lianeri M, Jagodzinski PP.

Clin Genet. 2013 Nov;84(5):429-40. doi: 10.1111/cge.12061. Epub 2012 Dec 7.

PMID:
23167694
7.

A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort.

Yu J, He X, Yao D, Li Z, Li H, Zhao Z.

Behav Brain Funct. 2011 May 14;7:13. doi: 10.1186/1744-9081-7-13.

8.

WNT10A variants are associated with non-syndromic tooth agenesis in the general population.

Song S, Zhao R, He H, Zhang J, Feng H, Lin L.

Hum Genet. 2014 Jan;133(1):117-24. doi: 10.1007/s00439-013-1360-x. Epub 2013 Sep 17.

PMID:
24043634
9.

The association analysis of TBX6 polymorphism with susceptibility to congenital scoliosis in a Chinese Han population.

Fei Q, Wu Z, Wang H, Zhou X, Wang N, Ding Y, Wang Y, Qiu G.

Spine (Phila Pa 1976). 2010 Apr 20;35(9):983-8. doi: 10.1097/BRS.0b013e3181bc963c.

PMID:
20228709
10.

Intronic single nucleotide polymorphisms of engrailed homeobox 2 modulate the disease vulnerability of autism in a han chinese population.

Yang P, Shu BC, Hallmayer JF, Lung FW.

Neuropsychobiology. 2010;62(2):104-15. doi: 10.1159/000315441. Epub 2010 Jun 3.

PMID:
20523082
11.

Analysis of 50 SNPs in CYP2D6, CYP2C19, CYP2C9, CYP3A4 and CYP1A2 by MALDI-TOF mass spectrometry in Chinese Han population.

Shi Y, Xiang P, Li L, Shen M.

Forensic Sci Int. 2011 Apr 15;207(1-3):183-7. doi: 10.1016/j.forsciint.2010.10.004. Epub 2010 Nov 10.

PMID:
21071160
12.

Candidate gene studies in hypodontia suggest role for FGF3.

Vieira AR, D'Souza RN, Mues G, Deeley K, Hsin HY, K├╝chler EC, Meira R, Patir A, Tannure PN, Lips A, Costa MC, Granjeiro JM, Seymen F, Modesto A.

Eur Arch Paediatr Dent. 2013 Dec;14(6):405-10. doi: 10.1007/s40368-013-0010-2. Epub 2013 Apr 3.

13.

[Msh homebox-1 polymorphisms and susceptibility to 198 sporadic tooth agenesis: a case-control study].

Wang H, Wang L, Pan YC, Ma JQ, Zhang WB.

Zhonghua Kou Qiang Yi Xue Za Zhi. 2010 Mar;45(3):135-40. Chinese.

PMID:
20450679
14.

PAX9 polymorphisms and susceptibility to sporadic tooth agenesis: a case-control study in southeast China.

Pan Y, Wang L, Ma J, Zhang W, Wang M, Zhong W, Huang Y.

Eur J Oral Sci. 2008 Apr;116(2):98-103. doi: 10.1111/j.1600-0722.2007.00517.x.

PMID:
18353002
15.

Linkage and association of myocilin (MYOC) polymorphisms with high myopia in a Chinese population.

Tang WC, Yip SP, Lo KK, Ng PW, Choi PS, Lee SY, Yap MK.

Mol Vis. 2007 Apr 4;13:534-44.

16.

Association of the homeobox transcription factor gene ENGRAILED 2 with autistic disorder in Chinese children.

Yang P, Lung FW, Jong YJ, Hsieh HY, Liang CL, Juo SH.

Neuropsychobiology. 2008;57(1-2):3-8. doi: 10.1159/000123115. Epub 2008 Apr 18.

PMID:
18424904
17.

Novel EDA mutation resulting in X-linked non-syndromic hypodontia and the pattern of EDA-associated isolated tooth agenesis.

Han D, Gong Y, Wu H, Zhang X, Yan M, Wang X, Qu H, Feng H, Song S.

Eur J Med Genet. 2008 Nov-Dec;51(6):536-46. doi: 10.1016/j.ejmg.2008.06.002. Epub 2008 Jul 9.

PMID:
18657636
18.

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;111(5):365-70. Review.

PMID:
12974677
19.

Association of common PAX9 variants with permanent tooth size variation in non-syndromic East Asian populations.

Lee WC, Yamaguchi T, Watanabe C, Kawaguchi A, Takeda M, Kim YI, Haga S, Tomoyasu Y, Ishida H, Maki K, Park SB, Kimura R.

J Hum Genet. 2012 Oct;57(10):654-9. doi: 10.1038/jhg.2012.90. Epub 2012 Jul 19.

PMID:
22810112
20.

[Association of single nucleotide polymorphisms of MD-1 gene with asthma in adults of Han Nationality in Southern China].

Tan JY, Luo YL, Huang X, Shao JL, Lin L, Yang XX.

Zhonghua Jie He He Hu Xi Za Zhi. 2011 Feb;34(2):104-8. Chinese.

PMID:
21426727
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