170 related articles for article (PubMed ID: 34201399)
1. Non-Syndromic Dentinogenesis Imperfecta Caused by Mild Mutations in
Lee Y; Kim YJ; Hyun HK; Lee JC; Lee ZH; Kim JW
J Pers Med; 2021 Jun; 11(6):. PubMed ID: 34201399
[TBL] [Abstract][Full Text] [Related]
2. Novel PAX9 and COL1A2 missense mutations causing tooth agenesis and OI/DGI without skeletal abnormalities.
Wang SK; Chan HC; Makovey I; Simmer JP; Hu JC
PLoS One; 2012; 7(12):e51533. PubMed ID: 23227268
[TBL] [Abstract][Full Text] [Related]
3. Translated Mutant
Kim YJ; Lee Y; Zhang H; Seymen F; Koruyucu M; Bayrak S; Tuloglu N; Simmer JP; Hu JC; Kim JW
J Pers Med; 2022 Jun; 12(6):. PubMed ID: 35743786
[TBL] [Abstract][Full Text] [Related]
4. The Modified Shields Classification and 12 Families with Defined
Simmer JP; Zhang H; Moon SJH; Donnelly LA; Lee YL; Seymen F; Koruyucu M; Chan HC; Lee KY; Wu S; Hsiang CL; Tsai ATP; Slayton RL; Morrow M; Wang SK; Shields ED; Hu JC
Genes (Basel); 2022 May; 13(5):. PubMed ID: 35627243
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Mutational hot spot in the DSPP gene causing dentinogenesis imperfecta type II.
Kim JW; Hu JC; Lee JI; Moon SK; Kim YJ; Jang KT; Lee SH; Kim CC; Hahn SH; Simmer JP
Hum Genet; 2005 Feb; 116(3):186-91. PubMed ID: 15592686
[TBL] [Abstract][Full Text] [Related]
8. Hereditary dentin defects.
Kim JW; Simmer JP
J Dent Res; 2007 May; 86(5):392-9. PubMed ID: 17452557
[TBL] [Abstract][Full Text] [Related]
9. A novel DSPP mutation is associated with type II dentinogenesis imperfecta in a Chinese family.
Zhang X; Chen L; Liu J; Zhao Z; Qu E; Wang X; Chang W; Xu C; Wang QK; Liu M
BMC Med Genet; 2007 Aug; 8():52. PubMed ID: 17686168
[TBL] [Abstract][Full Text] [Related]
10. Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia.
Barron MJ; McDonnell ST; Mackie I; Dixon MJ
Orphanet J Rare Dis; 2008 Nov; 3():31. PubMed ID: 19021896
[TBL] [Abstract][Full Text] [Related]
11. Novel COL1A1 mutation (G559C) [correction of G599C] associated with mild osteogenesis imperfecta and dentinogenesis imperfecta.
Pallos D; Hart PS; Cortelli JR; Vian S; Wright JT; Korkko J; Brunoni D; Hart TC
Arch Oral Biol; 2001 May; 46(5):459-70. PubMed ID: 11286811
[TBL] [Abstract][Full Text] [Related]
12. Clinical characteristics and the identification of novel mutations of COL1A1 and COL1A2 in 61 Chinese patients with osteogenesis imperfecta.
Zhang H; Yue H; Wang C; Hu W; Gu J; He J; Fu W; Hu Y; Li M; Zhang Z
Mol Med Rep; 2016 Nov; 14(5):4918-4926. PubMed ID: 27748872
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Splicing site mutations in dentin sialophosphoprotein causing dentinogenesis imperfecta type II.
Holappa H; Nieminen P; Tolva L; Lukinmaa PL; Alaluusua S
Eur J Oral Sci; 2006 Oct; 114(5):381-4. PubMed ID: 17026502
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Phenotypic variation in dentinogenesis imperfecta/dentin dysplasia linked to 4q21.
Beattie ML; Kim JW; Gong SG; Murdoch-Kinch CA; Simmer JP; Hu JC
J Dent Res; 2006 Apr; 85(4):329-33. PubMed ID: 16567553
[TBL] [Abstract][Full Text] [Related]
17. Dentin dysplasia type I-A dental disease with genetic heterogeneity.
Chen D; Li X; Lu F; Wang Y; Xiong F; Li Q
Oral Dis; 2019 Mar; 25(2):439-446. PubMed ID: 29575674
[TBL] [Abstract][Full Text] [Related]
18. A novel DSPP mutation causes dentinogenesis imperfecta type II in a large Mongolian family.
Bai H; Agula H; Wu Q; Zhou W; Sun Y; Qi Y; Latu S; Chen Y; Mutu J; Qiu C
BMC Med Genet; 2010 Feb; 11():23. PubMed ID: 20146806
[TBL] [Abstract][Full Text] [Related]
19. Haploinsufficiency of
Shi C; Ma N; Zhang W; Ye J; Shi H; Xiang D; Wu C; Song L; Zhang N; Liu Q
Front Physiol; 2020; 11():593626. PubMed ID: 33240110
[TBL] [Abstract][Full Text] [Related]
20. Mutational spectrum of type I collagen genes in Korean patients with osteogenesis imperfecta.
Lee KS; Song HR; Cho TJ; Kim HJ; Lee TM; Jin HS; Park HY; Kang S; Jung SC; Koo SK
Hum Mutat; 2006 Jun; 27(6):599. PubMed ID: 16705691
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
