상아질 형성부전증의 분자병리학적 고찰

키워드

참고문헌 (42)

1. "Hereditary defects of dentin", 19, pp.25~45 (1975)
2. "상아질 형성부전증에 대한 증례 보고", 27, pp.1~6 (2000)
3. "상아질 형성 부전증에 대한 증례 보고", 20, pp.472~479 (1993)
4. "Type II 상아질형성부전증의 임상 증례", 28, pp.654~660 (2001)
5. "상아질 형성부전증에 대한 증례 보고", 33 (2006)
6. "상아질형성부전증에 대한 증례보고", 20, pp.493~499 (1993)
7. "Correlated clinical and structural study of hereditary opalescent dentin", 15, pp.316~ (1936)
8. "A proposed classification for heritable human dentine defects with a description of a new entity", 18, pp.543~553 (1973)
9. "Linkage between dentinogenesis imperfecta and Gc", 46, pp.35~40 (1982)
10. "Histological distribution of phosphophoryn in normal and pathological human dentins", 15, pp.463~467 (1986)
11. "Dentin phosphoprotein gene locus is not associated with dentinogenesis imperfecta types II and III", 50, pp.190~194 (1992)
12. "Dentin phosphoprotein in dentin development:implications in dentinogenesis imperfecta", 88 suppl 1, pp.195~208 (1992)
13. "Presence of dentin phosphoprotein in molars of a patient with dentinogenesis imperfecta type II", 14, pp.26~32 (1994)
14. "Mapping of the human dentin matrix acidic phosphoprotein gene (DMP1) to the dentinogenesis imperfecta type II critical region at chromosome 4q21", 30, pp.347~349 (1995)
15. "Dentin matrix protein-1,a candidate gene for dentinogenesis imperfecta", 35, pp.267~272 (1996)
16. "Elucidation of the sequence and the genomic organization of the human dentin matrix acidic phosphoprotein 1 (DMP1) gene: exclusion of the locus from a causative role in the pathogenesis of dentinogenesis imperfecta type II", 42, pp.38~45 (1997)
17. "Dentin dysplasia,type II linkage to chromosome 4q", 17, pp.172~177 (1997)
18. "Refinement of the dentinogenesis imperfecta type II locus to an interval of less than 2 centiMorgans at chromosome 4q21 and the creation of a yeast artificial chromosome contig of the critical region", 78, pp.1270~1276 (1999)
19. "DSPP mutation in dentinogenesis imperfecta Shields type II", 27, pp.151~152 (2001)
20. "Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP", 27, pp.201~204 (2001)
21. "Dentin sialoprotein, dentin phosphoprotein, enamelysin and ameloblastin: tooth-specific molecules that are distinctively expressed during murine dental differentiation.", 106, pp.963~970 (1998)
22. "The expression of dentin sialophosphoprotein gene in bone", 81, pp.392~394 (2002)
23. "Detection of dentin sialoprotein in rat periodontium", 112, pp.163~170 (2004)
24. "Expression of SIBLINGs and their partner MMPs in salivary glands", 83, pp.664~670 (2004)
25. "Expression of dentin sialophosphoprotein in human prostate cancer and its correlation with tumor aggressiveness", 118, pp.850~856 (2006)
26. "Reduced expression of dentin sialophosphoprotein is associated with dysplastic dentin in mice overexpressing transforming growth factor-beta 1 in teeth", 276, pp.11016~11020 (2001)
27. "TGF beta-1 downregulates DMP-1 and DSPP in odontoblasts", 43, pp.354~358 (2002)
28. "TGF-beta activated Smad signalling leads to a Smad3-mediated down-regulation of DSPP in an odontoblast cell line", 49, pp.911~918 (2004)
29. "Spatial expression of Cbfa1", Runx2 isoforms in teeth and characterization of binding sites in the DSPP gene, 2002, pp.43, 338~344
30. "Deletion of dentin matrix protein-1 leads to a partial failure of maturation of predentin into dentin,hypomineralization,and expanded cavities of pulp and root canal during postnatal tooth development", 279, pp.19141~19148 (2004)
31. "Dentin matrix protein 1 regulates dentin sialophosphoprotein gene transcription during early odontoblast differentiation", 281, pp.19064~19071 (2006)
32. "The carboxyl-terminal domain of phosphophoryn contains unique extended triplet amino acid repeat sequences forming ordered carboxyl-phosphate interaction ridges that may be essential in the biomineralization rocess", 271, pp.32869~32873 (1996)
33. "Dentin sialoprotein and dentin phosphoprotein overexpression during amelogenesis", 280, pp.31991~31998 (2005)
34. "Clinical,histopathologic,and genetic investigation in two large families with dentinogenesis imperfecta type II", 114, pp.491~498 (2004)
35. "Mutation of the signal peptide region of the bicistronic gene DSPP affects translocation to the endoplasmic reticulum and results in defective dentine biomineralization", 11, pp.2559~2565 (2002)
36. "A novel splice acceptor mutation in the DSPP gene causing dentinogenesis imperfecta type II", 115, pp.248~254 (2004)
37. "Mutational hot spot in the DSPP gene causing dentinogenesis imperfecta type II", 116, pp.186~191 (2005)
38. "Dentin phosphoprotein compound mutation in dentin sialophosphoprotein causes dentinogenesis imperfecta type III", 132, pp.305~309 (2005)
39. "An unusual presentation of opalescent dentin and Brandywine isolate hereditary opalescent dentin in an Ashkenazic Jewish family", 59, pp.608~615 (1985)
40. "Dentinogenesis imperfecta:an early treatment strategy", 23, pp.232~237 (2001)
41. "Removable overdentures in the oral rehabilitation of patients with dentinogenesis imperfecta", pp.304~315 (1978)
42. "Dentinogenesis imperfecta:genetic variations in a six-generation family", 48, pp.1196~1199 (1969)

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