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1 ance a new model for Ca(2+) transport by the enamel organ.
2 t of cell types which combined represent the enamel organ.
3 enamel knot, but remained at the tip of the enamel organ.
4 , the enamel knot, appears at the tip of the enamel organ.
5 ple attempts at invagination and an expanded enamel organ.
6 y reduced Tgf-beta1 transcript levels in rat enamel organ.
7 atrix acidic phosphoprotein expressed in the enamel organ.
8 irm the expression of Ctrc in the developing enamel organ.
9 here report on the expression of Ctrc in the enamel organ.
10 ed to almost undetectable levels in the null enamel organ.
11 y spliced amelogenin found in the developing enamel organ.
12 was not localized in any of the cells of the enamel organ.
13 transcripts which were expressed only in the enamel organ.
14 ed to overexpress either Dsp or Dpp in their enamel organs.
15 support the hair shaft, are expressed in the enamel organ and are essential organic components of mat
16 e sought to examine DPPI expression in mouse enamel organ and determine if DPPI could activate KLK4.
17 n healthy tissues, MMP-20 is observed in the enamel organ and pulp organ of developing teeth and is p
18 thin a region we have called the body of the enamel organ, and proliferate in concert with the epithe
19 that are not located between the body of the enamel organ, and therefore are at a distance from the p
20 scripts for Dra and Slc26a6 in mouse incisor enamel organs, and Western blotting confirmed their tran
21 oblast-lineage cells, derived from the human enamel organ, are directly affected by micromolar concen
25 le-genome microarray analysis of rat incisor enamel organ cells derived from the secretory and matura
26 a indicate that Ca2+ influx in LS8 cells and enamel organ cells is mediated by CRAC channels and that
27 that stimulating LS8 cells or murine primary enamel organ cells with thapsigargin to activate SOCE le
34 elopment, TGF-beta inhibits proliferation of enamel organ epithelial cells but the underlying molecul
35 development with increased proliferation of enamel organ epithelial cells, while attenuation of Smad
40 besides the pig, and EMSP1 expression in the enamel organ has never been specifically demonstrated in
41 l proteinase cathepsin K is expressed in the enamel organ in a developmentally defined manner that su
42 e, and intensified Ae2 immunostaining in the enamel organ in comparison with non-fluorotic mutant tee
43 can adversely impact on the formation of the enamel organ is by disturbing self-assembly of the organ
47 e amount of Slc26a6 protein was unchanged in enamel organs of Ae2a,b- and Cftr-null mice but reduced
54 t was mislocated to the upper portion of the enamel organ, where it remained devoid of proliferating
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