137 related articles for article (PubMed ID: 37084484)
21. DSPP mutation in dentinogenesis imperfecta Shields type II.
Zhang X; Zhao J; Li C; Gao S; Qiu C; Liu P; Wu G; Qiang B; Lo WH; Shen Y
Nat Genet; 2001 Feb; 27(2):151-2. PubMed ID: 11175779
[TBL] [Abstract][Full Text] [Related]
22. [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
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Aug; 35(4):511-514. PubMed ID: 30098245
[TBL] [Abstract][Full Text] [Related]
23. Accelerated enamel mineralization in Dspp mutant mice.
Verdelis K; Szabo-Rogers HL; Xu Y; Chong R; Kang R; Cusack BJ; Jani P; Boskey AL; Qin C; Beniash E
Matrix Biol; 2016; 52-54():246-259. PubMed ID: 26780724
[TBL] [Abstract][Full Text] [Related]
24. Dentin phosphoprotein compound mutation in dentin sialophosphoprotein causes dentinogenesis imperfecta type III.
Dong J; Gu T; Jeffords L; MacDougall M
Am J Med Genet A; 2005 Jan; 132A(3):305-9. PubMed ID: 15690376
[TBL] [Abstract][Full Text] [Related]
25. Transcriptional repression of the Dspp gene leads to dentinogenesis imperfecta phenotype in Col1a1-Trps1 transgenic mice.
Napierala D; Sun Y; Maciejewska I; Bertin TK; Dawson B; D'Souza R; Qin C; Lee B
J Bone Miner Res; 2012 Aug; 27(8):1735-45. PubMed ID: 22508542
[TBL] [Abstract][Full Text] [Related]
26. Transgenic expression of dentin phosphoprotein (DPP) partially rescued the dentin defects of DSPP-null mice.
Zhang H; Xie X; Liu P; Liang T; Lu Y; Qin C
PLoS One; 2018; 13(4):e0195854. PubMed ID: 29672573
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. 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]
29. Withdrawal: A novel DSPP frameshift mutation causing dentin dysplasia type 2 and disease management strategies.
Oral Dis; 2023 Mar; 29(2):855. PubMed ID: 36346235
[No Abstract] [Full Text] [Related]
30. Functional splicing assay of DSPP mutations in hereditary dentin defects.
Lee KE; Lee SK; Jung SE; Lee Zh; Kim JW
Oral Dis; 2011 Oct; 17(7):690-5. PubMed ID: 21736673
[TBL] [Abstract][Full Text] [Related]
31. Overlapping DSPP mutations cause dentin dysplasia and dentinogenesis imperfecta.
McKnight DA; Simmer JP; Hart PS; Hart TC; Fisher LW
J Dent Res; 2008 Dec; 87(12):1108-11. PubMed ID: 19029076
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Hereditary dentine diseases resulting from mutations in DSPP gene.
Maciejewska I; Chomik E
J Dent; 2012 Jul; 40(7):542-8. PubMed ID: 22521702
[TBL] [Abstract][Full Text] [Related]
34. Refined mapping of the human dentin sialophosphoprotein (DSPP) gene within the critical dentinogenesis imperfecta type II and dentin dysplasia type II loci.
MacDougall M
Eur J Oral Sci; 1998 Jan; 106 Suppl 1():227-33. PubMed ID: 9541230
[TBL] [Abstract][Full Text] [Related]
35. A novel splice site mutation in the dentin sialophosphoprotein gene in a Chinese family with dentinogenesis imperfecta type II.
Wang H; Hou Y; Cui Y; Huang Y; Shi Y; Xia X; Lu H; Wang Y; Li X
Mutat Res; 2009 Mar; 662(1-2):22-7. PubMed ID: 19103209
[TBL] [Abstract][Full Text] [Related]
36. A dentin sialophosphoprotein mutation that partially disrupts a splice acceptor site causes type II dentin dysplasia.
Lee SK; Hu JC; Lee KE; Simmer JP; Kim JW
J Endod; 2008 Dec; 34(12):1470-3. PubMed ID: 19026876
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Hereditary dentin defects.
Kim JW; Simmer JP
J Dent Res; 2007 May; 86(5):392-9. PubMed ID: 17452557
[TBL] [Abstract][Full Text] [Related]
39. Role of the NH2 -terminal fragment of dentin sialophosphoprotein in dentinogenesis.
Gibson MP; Liu Q; Zhu Q; Lu Y; Jani P; Wang X; Liu Y; Paine ML; Snead ML; Feng JQ; Qin C
Eur J Oral Sci; 2013 Apr; 121(2):76-85. PubMed ID: 23489896
[TBL] [Abstract][Full Text] [Related]
40. Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP.
Xiao S; Yu C; Chou X; Yuan W; Wang Y; Bu L; Fu G; Qian M; Yang J; Shi Y; Hu L; Han B; Wang Z; Huang W; Liu J; Chen Z; Zhao G; Kong X
Nat Genet; 2001 Feb; 27(2):201-4. PubMed ID: 11175790
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
