Wong SW - Search Results

1

BMP4 mutations in tooth agenesis and low bone mass.

Yu M, Wang H, Fan Z, Xie C, Liu H, Liu Y, Han D, Wong SW, Feng H. Yu M, et al. Among authors: wong sw. Arch Oral Biol. 2019 Jul;103:40-46. doi: 10.1016/j.archoralbio.2019.05.012. Epub 2019 May 15. Arch Oral Biol. 2019. PMID: 31128441 Free PMC article.

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. Liu H, et al. PLoS One. 2013 Nov 20;8(11):e80860. doi: 10.1371/journal.pone.0080860. eCollection 2013. PLoS One. 2013. PMID: 24278334 Free PMC article.

3

Novel missense mutations in the AXIN2 gene associated with non-syndromic oligodontia.

Wong S, Liu H, Bai B, Chang H, Zhao H, Wang Y, Han D, Feng H. Wong S, et al. Arch Oral Biol. 2014 Mar;59(3):349-53. doi: 10.1016/j.archoralbio.2013.12.009. Epub 2013 Dec 31. Arch Oral Biol. 2014. PMID: 24581859

4

[Association between AXIN2 polymorphism and oligodontia].

Wong S, Liu HC, Li Y, Han D, Feng HL. Wong S, et al. Beijing Da Xue Xue Bao Yi Xue Ban. 2014 Apr 18;46(2):269-73. Beijing Da Xue Xue Bao Yi Xue Ban. 2014. PMID: 24743819 Free article. Chinese.

5

A novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontia.

Wong SW, Liu HC, Han D, Chang HG, Zhao HS, Wang YX, Feng HL. Wong SW, et al. Mutagenesis. 2014 Sep;29(5):319-23. doi: 10.1093/mutage/geu019. Epub 2014 Jun 9. Mutagenesis. 2014. PMID: 24914010

6

Morphological analyses and a novel de novo DLX3 mutation associated with tricho-dento-osseous syndrome in a Chinese family.

Li Y, Han D, Zhang H, Liu H, Wong S, Zhao N, Qiu L, Feng H. Li Y, et al. Eur J Oral Sci. 2015 Aug;123(4):228-34. doi: 10.1111/eos.12197. Epub 2015 Jun 24. Eur J Oral Sci. 2015. PMID: 26104267

7

Simultaneous Occurence of an Autosomal Dominant Inherited MSX1 Mutation and an X-linked Recessive Inherited EDA Mutation in One Chinese Family with Non-syndromic Oligodontia.

Zhang XX, Wong SW, Han D, Feng HL. Zhang XX, et al. Among authors: wong sw. Chin J Dent Res. 2015;18(4):229-34. doi: 10.3290/j.cjdr.a35147. Chin J Dent Res. 2015. PMID: 26629556 Free article.

8

Mutations in WNT10B Are Identified in Individuals with Oligodontia.

Yu P, Yang W, Han D, Wang X, Guo S, Li J, Li F, Zhang X, Wong SW, Bai B, Liu Y, Du J, Sun ZS, Shi S, Feng H, Cai T. Yu P, et al. Among authors: wong sw. Am J Hum Genet. 2016 Jul 7;99(1):195-201. doi: 10.1016/j.ajhg.2016.05.012. Epub 2016 Jun 16. Am J Hum Genet. 2016. PMID: 27321946 Free PMC article.

9

Senescence: novel insight into DLX3 mutations leading to enhanced bone formation in Tricho-Dento-Osseous syndrome.

Zhao N, Han D, Liu H, Li Y, Wong SW, Cao Z, Xu J, Zhang X, Cai T, Wang Y, Feng H. Zhao N, et al. Among authors: wong sw. Sci Rep. 2016 Dec 7;6:38680. doi: 10.1038/srep38680. Sci Rep. 2016. PMID: 27924851 Free PMC article.

10

Mutant Runx2 regulates amelogenesis and osteogenesis through a miR-185-5p-Dlx2 axis.

Chang H, Wang Y, Liu H, Nan X, Wong S, Peng S, Gu Y, Zhao H, Feng H. Chang H, et al. Cell Death Dis. 2017 Dec 14;8(12):3221. doi: 10.1038/s41419-017-0078-4. Cell Death Dis. 2017. PMID: 29242628 Free PMC article.

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