137 related articles for article (PubMed ID: 37084484)
1. Novel dentin sialophosphoprotein gene frameshift mutations affect dentin mineralization.
Zhang Z; Huang G; Huang Y; Liu S; Chen F; Gao X; Dong Y; Tian H
Arch Oral Biol; 2023 Jul; 151():105701. PubMed ID: 37084484
[TBL] [Abstract][Full Text] [Related]
2. Dental properties, ultrastructure, and pulp cells associated with a novel DSPP mutation.
Porntaveetus T; Osathanon T; Nowwarote N; Pavasant P; Srichomthong C; Suphapeetiporn K; Shotelersuk V
Oral Dis; 2018 May; 24(4):619-627. PubMed ID: 29117466
[TBL] [Abstract][Full Text] [Related]
3. Frameshift mutations in dentin phosphoprotein and dependence of dentin disease phenotype on mutation location.
Nieminen P; Papagiannoulis-Lascarides L; Waltimo-Siren J; Ollila P; Karjalainen S; Arte S; Veerkamp J; Tallon Walton V; Chimenos Küstner E; Siltanen T; Holappa H; Lukinmaa PL; Alaluusua S
J Bone Miner Res; 2011 Apr; 26(4):873-80. PubMed ID: 20949630
[TBL] [Abstract][Full Text] [Related]
4. Novel dentin phosphoprotein frameshift mutations in dentinogenesis imperfecta type II.
Lee KE; Kang HY; Lee SK; Yoo SH; Lee JC; Hwang YH; Nam KH; Kim JS; Park JC; Kim JW
Clin Genet; 2011 Apr; 79(4):378-84. PubMed ID: 20618350
[TBL] [Abstract][Full Text] [Related]
5. Identification of DSPP novel variants and phenotype analysis in dentinogenesis dysplasia Shields type II patients.
Du Q; Cao L; Yan N; Kang S; Lin M; Cao P; Jia R; Wang C; Qi H; Yu Y; Zou J; Yang J
Clin Oral Investig; 2023 Jul; 27(7):3885-3894. PubMed ID: 37017752
[TBL] [Abstract][Full Text] [Related]
6. Mouse Dspp frameshift model of human dentinogenesis imperfecta.
Liang T; Hu Y; Zhang H; Xu Q; Smith CE; Zhang C; Kim JW; Wang SK; Saunders TL; Lu Y; Hu JC; Simmer JP
Sci Rep; 2021 Oct; 11(1):20653. PubMed ID: 34667213
[TBL] [Abstract][Full Text] [Related]
7. Compromised alveolar bone cells in a patient with dentinogenesis imperfecta caused by DSPP mutation.
Porntaveetus T; Nowwarote N; Osathanon T; Theerapanon T; Pavasant P; Boonprakong L; Sanon K; Srisawasdi S; Suphapeetiporn K; Shotelersuk V
Clin Oral Investig; 2019 Jan; 23(1):303-313. PubMed ID: 29679229
[TBL] [Abstract][Full Text] [Related]
8. A novel DSPP frameshift mutation causing dentin dysplasia type 2 and disease management strategies.
Yuan M; Zheng X; Xue Y; He Z; Song G; Song Y
Oral Dis; 2023 Sep; 29(6):2394-2400. PubMed ID: 36597617
[TBL] [Abstract][Full Text] [Related]
9. Isolated dentinogenesis imperfecta and dentin dysplasia: revision of the classification.
de La Dure-Molla M; Philippe Fournier B; Berdal A
Eur J Hum Genet; 2015 Apr; 23(4):445-51. PubMed ID: 25118030
[TBL] [Abstract][Full Text] [Related]
10. Enamel malformations associated with a defined dentin sialophosphoprotein mutation in two families.
Wang SK; Chan HC; Rajderkar S; Milkovich RN; Uston KA; Kim JW; Simmer JP; Hu JC
Eur J Oral Sci; 2011 Dec; 119 Suppl 1(Suppl 1):158-67. PubMed ID: 22243242
[TBL] [Abstract][Full Text] [Related]
11. Mutant Dentin Sialophosphoprotein Causes Dentinogenesis Imperfecta.
Liang T; Zhang H; Xu Q; Wang S; Qin C; Lu Y
J Dent Res; 2019 Jul; 98(8):912-919. PubMed ID: 31173534
[TBL] [Abstract][Full Text] [Related]
12. A novel splice acceptor mutation in the DSPP gene causing dentinogenesis imperfecta type II.
Kim JW; Nam SH; Jang KT; Lee SH; Kim CC; Hahn SH; Hu JC; Simmer JP
Hum Genet; 2004 Aug; 115(3):248-54. PubMed ID: 15241678
[TBL] [Abstract][Full Text] [Related]
13. Rough endoplasmic reticulum trafficking errors by different classes of mutant dentin sialophosphoprotein (DSPP) cause dominant negative effects in both dentinogenesis imperfecta and dentin dysplasia by entrapping normal DSPP.
von Marschall Z; Mok S; Phillips MD; McKnight DA; Fisher LW
J Bone Miner Res; 2012 Jun; 27(6):1309-21. PubMed ID: 22392858
[TBL] [Abstract][Full Text] [Related]
14. Phenotype and genotype analyses in seven families with dentinogenesis imperfecta or dentin dysplasia.
Li F; Liu Y; Liu H; Yang J; Zhang F; Feng H
Oral Dis; 2017 Apr; 23(3):360-366. PubMed ID: 27973701
[TBL] [Abstract][Full Text] [Related]
15. Dentin defects caused by a Dspp
Liang T; Smith CE; Hu Y; Zhang H; Zhang C; Xu Q; Lu Y; Qi L; Hu JC; Simmer JP
Sci Rep; 2023 Apr; 13(1):6393. PubMed ID: 37076504
[TBL] [Abstract][Full Text] [Related]
16. Physicochemical properties of dentinogenesis imperfecta with a known DSPP mutation.
Park H; Hyun HK; Woo KM; Kim JW
Arch Oral Biol; 2020 Sep; 117():104815. PubMed ID: 32585446
[TBL] [Abstract][Full Text] [Related]
17. Soundbites.
Patel P
Nat Genet; 2001 Feb; 27(2):129-30. PubMed ID: 11175770
[TBL] [Abstract][Full Text] [Related]
18. Dentin sialophosphoprotein knockout mouse teeth display widened predentin zone and develop defective dentin mineralization similar to human dentinogenesis imperfecta type III.
Sreenath T; Thyagarajan T; Hall B; Longenecker G; D'Souza R; Hong S; Wright JT; MacDougall M; Sauk J; Kulkarni AB
J Biol Chem; 2003 Jul; 278(27):24874-80. PubMed ID: 12721295
[TBL] [Abstract][Full Text] [Related]
19. Phenotypes and genotypes in 2 DGI families with different DSPP mutations.
Song Y; Wang C; Peng B; Ye X; Zhao G; Fan M; Fu Q; Bian Z
Oral Surg Oral Med Oral Pathol Oral Radiol Endod; 2006 Sep; 102(3):360-74. PubMed ID: 16920545
[TBL] [Abstract][Full Text] [Related]
20. [Mutation of dentin sialophosphoprotein and hereditary malformations of dentin].
Zhu QL; Duan XH; Yu Q
Zhonghua Kou Qiang Yi Xue Za Zhi; 2023 Jan; 58(1):17-24. PubMed ID: 36642448
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]