ライフサイエンスコーパス: dentinogenesis imperfecta

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1 tooth disorders such as dentin dysplasia and dentinogenesis imperfecta.

2 oring the Col1a2(oim) mutation (oim) express dentinogenesis imperfecta.

3 Dentinogenesis imperfecta (DGI) and dentin dysplasia (DD

4 Dentinogenesis imperfecta (DGI) and dentin dysplasia (DD

5 Dentinogenesis imperfecta (DGI) is characterized by disc

6 lt in human hereditary dental disorders like dentinogenesis imperfecta II (MIM 125420) and dentin dys

7 otein (dspp), a candidate gene implicated in dentinogenesis imperfecta II (MIM 125420), is significan

8 ations in this gene were identified in human dentinogenesis imperfecta II (Online Mendelian Inheritan

9 that develop tooth defects similar to human dentinogenesis imperfecta III with enlarged pulp chamber

10 nd shares some features of the human disease dentinogenesis imperfecta III.

11 p9-/- teeth displayed a phenotype similar to dentinogenesis imperfecta, including decreased dentin mi

12 s that may be accompanied by bone deformity, dentinogenesis imperfecta, short stature, and shortened

13 Dentinogenesis Imperfecta type II (DGI-II) is a localize

14 ed to determine if DGI-III co-localized with dentinogenesis imperfecta type II (DGI-II), which has be

15 attering (SAXS) were performed on normal and dentinogenesis imperfecta type II (DI-II) teeth.

16 d Dmp2 genes at a position equivalent to the dentinogenesis imperfecta type II location on human 4q21

17 As recent studies have shown that dentinogenesis imperfecta type II results from mutation

18 tween, and shared chromosomal location with, dentinogenesis imperfecta type II, a second disorder of

19 trong candidate gene for the genetic disease dentinogenesis imperfecta type II.

20 Dentinogenesis imperfecta type III (DGI-III) is an autos

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