Lu T - Search Results

1

Vacuolar protein sorting 4B regulates the proliferation and odontoblastic differentiation of human dental pulp stem cells through the Wnt-β-catenin signalling pathway.

Pan Y, Lu T, Peng L, Chen Z, Li M, Zhang K, Xiong F, Wu B. Pan Y, et al. Among authors: lu t. Artif Cells Nanomed Biotechnol. 2019 Dec;47(1):2575-2584. doi: 10.1080/21691401.2019.1629950. Artif Cells Nanomed Biotechnol. 2019. PMID: 31218890 Free article.

2

A 3-year clinical evaluation of endodontically treated posterior teeth restored with two different materials using the CEREC AC chair-side system.

Lu T, Peng L, Xiong F, Lin XY, Zhang P, Lin ZT, Wu BL. Lu T, et al. J Prosthet Dent. 2018 Mar;119(3):363-368. doi: 10.1016/j.prosdent.2017.04.022. Epub 2017 Jul 8. J Prosthet Dent. 2018. PMID: 28689915

3

[Analysis of DSPP gene mutation in a Chinese pedigree affected with hereditary dentinogenesis imperfecta].

Hu A, Li X, Chen D, Lu T, Huang J, Xu X, Chen D, Xiong F. Hu A, et al. Among authors: lu t. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Aug 10;35(4):511-514. doi: 10.3760/cma.j.issn.1003-9406.2018.04.011. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 30098245 Chinese.

4

Whole exome sequencing identifies an AMBN missense mutation causing severe autosomal-dominant amelogenesis imperfecta and dentin disorders.

Lu T, Li M, Xu X, Xiong J, Huang C, Zhang X, Hu A, Peng L, Cai D, Zhang L, Wu B, Xiong F. Lu T, et al. Int J Oral Sci. 2018 Sep 3;10(3):26. doi: 10.1038/s41368-018-0027-9. Int J Oral Sci. 2018. PMID: 30174330 Free PMC article.

5

Vps4b heterozygous mice do not develop tooth defects that replicate human dentin dysplasia I.

Hu A, Lu T, Chen D, Huang J, Feng W, Li Y, Guo D, Xu X, Chen D, Xiong F. Hu A, et al. Among authors: lu t. BMC Genet. 2019 Jan 11;20(1):7. doi: 10.1186/s12863-018-0699-3. BMC Genet. 2019. PMID: 30634912 Free PMC article.

6

[Structural characteristics of the deciduous teeth of Tibetan miniature pigs].

Lu T, Zheng Y, Yang H, Wu B, Xiong J, Huang C, Pan Y, Li M, He F, Xiong F. Lu T, et al. Nan Fang Yi Ke Da Xue Xue Bao. 2019 Sep 30;39(9):1113-1117. doi: 10.12122/j.issn.1673-4254.2019.09.18. Nan Fang Yi Ke Da Xue Xue Bao. 2019. PMID: 31640964 Free PMC article. Chinese.

7

The gain-of-function FAM83H mutation caused hypocalcification amelogenesis imperfecta in a Chinese family.

Zheng Y, Lu T, Chen J, Li M, Xiong J, He F, Gan Z, Guo Y, Zhang L, Xiong F. Zheng Y, et al. Among authors: lu t. Clin Oral Investig. 2021 May;25(5):2915-2923. doi: 10.1007/s00784-020-03609-6. Epub 2020 Oct 2. Clin Oral Investig. 2021. PMID: 33009625

8

VPS4B deficiency causes early embryonic lethality and induces signal transduction disorders of cell endocytosis.

Chen D, He F, Lu T, Huang J, Li M, Cai D, Huang C, Chen D, Xiong F. Chen D, et al. Among authors: lu t. Genesis. 2021 Apr;59(4):e23415. doi: 10.1002/dvg.23415. Epub 2021 Mar 7. Genesis. 2021. PMID: 33682352

9

Functional Analysis of Ectodysplasin-A Mutations in X-Linked Nonsyndromic Hypodontia and Possible Involvement of X-Chromosome Inactivation.

Pan Y, Lu T, Peng L, Zeng Q, Huang X, Yao X, Wu B, Xiong F. Pan Y, et al. Among authors: lu t. Stem Cells Int. 2021 Sep 9;2021:7653013. doi: 10.1155/2021/7653013. eCollection 2021. Stem Cells Int. 2021. PMID: 34545288 Free PMC article.

10

Double heterozygous pathogenic mutations in KIF3C and ZNF513 cause hereditary gingival fibromatosis.

Chen J, Xu X, Chen S, Lu T, Zheng Y, Gan Z, Shen Z, Ma S, Wang D, Su L, He F, Shang X, Xu H, Chen D, Zhang L, Xiong F. Chen J, et al. Among authors: lu t. Int J Oral Sci. 2023 Sep 26;15(1):46. doi: 10.1038/s41368-023-00244-1. Int J Oral Sci. 2023. PMID: 37752101 Free PMC article.

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