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1  enamel knot, but remained at the tip of the enamel organ.
2 , the enamel knot, appears at the tip of the enamel organ.
3 ple attempts at invagination and an expanded enamel organ.
4 y reduced Tgf-beta1 transcript levels in rat enamel organ.
5 atrix acidic phosphoprotein expressed in the enamel organ.
6 irm the expression of Ctrc in the developing enamel organ.
7 here report on the expression of Ctrc in the enamel organ.
8 ed to almost undetectable levels in the null enamel organ.
9 y spliced amelogenin found in the developing enamel organ.
10 ance a new model for Ca(2+) transport by the enamel organ.
11 was not localized in any of the cells of the enamel organ.
12 t of cell types which combined represent the enamel organ.
13 transcripts which were expressed only in the enamel organ.
14 , 9, 10, 15, 17, 19) were expressed in mouse enamel organs.
15 ed to overexpress either Dsp or Dpp in their enamel organs.
16 support the hair shaft, are expressed in the enamel organ and are essential organic components of mat
17 e sought to examine DPPI expression in mouse enamel organ and determine if DPPI could activate KLK4.
18 n healthy tissues, MMP-20 is observed in the enamel organ and pulp organ of developing teeth and is p
19 oss from nonrenal sites (such as the eye and enamel organ) and therefore require separate therapy.
20 thin a region we have called the body of the enamel organ, and proliferate in concert with the epithe
21 that are not located between the body of the enamel organ, and therefore are at a distance from the p
22 scripts for Dra and Slc26a6 in mouse incisor enamel organs, and Western blotting confirmed their tran
23 oblast-lineage cells, derived from the human enamel organ, are directly affected by micromolar concen
24 ibles confirmed localization of GPR68 in the enamel organ at all stages of amelogenesis.
25 s most highly amplified from wild-type mouse enamel organs at the secretory stage.
26              Mmp20(+/+)Tg mice had decreased enamel organ cadherin levels compared to the Mmp20 ablat
27 le-genome microarray analysis of rat incisor enamel organ cells derived from the secretory and matura
28 a indicate that Ca2+ influx in LS8 cells and enamel organ cells is mediated by CRAC channels and that
29 that stimulating LS8 cells or murine primary enamel organ cells with thapsigargin to activate SOCE le
30 cementoblasts, and a morphologically correct enamel organ containing fully formed enamel.
31 teins are secreted by ameloblasts within the enamel organ during tooth development.
32  attachments that may cause maturation-stage enamel organ dysplasia.
33 hat served as probes for screening a porcine enamel organ epithelia-specific cDNA library.
34  sequences of clones isolated from a porcine enamel organ epithelia-specific cDNA library.
35 enamel matrix, we have constructed a porcine enamel organ epithelia-specific cDNA library.
36 elopment, TGF-beta inhibits proliferation of enamel organ epithelial cells but the underlying molecul
37  development with increased proliferation of enamel organ epithelial cells, while attenuation of Smad
38 this study is that LRAP also regulates human enamel organ epithelial cells.
39  that rH58 promotes differentiation of human enamel organ epithelial cells.
40 ent with increased apoptotic activity within enamel organ epithelium.
41 , Car6, Cftr) was significantly decreased in enamel organs from Mmp20(-/-) mice.
42 besides the pig, and EMSP1 expression in the enamel organ has never been specifically demonstrated in
43 l proteinase cathepsin K is expressed in the enamel organ in a developmentally defined manner that su
44 e, and intensified Ae2 immunostaining in the enamel organ in comparison with non-fluorotic mutant tee
45 can adversely impact on the formation of the enamel organ is by disturbing self-assembly of the organ
46             The ameloblast cell layer of the enamel organ is in contact with the forming enamel as it
47 ponent of pharyngeal teeth in zebrafish (the enamel organ) is derived from medial endoderm, as hither
48 tes from the dentin, and has a deteriorating enamel organ morphology as development progresses.
49             Strikingly, the Mmp20 null mouse enamel organ morphology is noticeably dysplastic during
50 e amount of Slc26a6 protein was unchanged in enamel organs of Ae2a,b- and Cftr-null mice but reduced
51                                           In enamel organs of Slc26a6-null mice, Dra and pendrin prot
52             In this respect, the rat incisor enamel organ provides a unique tissue for studying the r
53                       The means by which the enamel organ regulates pH during amelogenesis is largely
54 d cells; however, its effect on cells of the enamel organ remains unclear.
55 n, the early asymmetrical development of the enamel organ seems to be a plesiomorphic character for a
56 proteinase (MMP) was isolated from a porcine enamel organ-specific cDNA library.
57 ly and its expression appears limited to the enamel organ, we have named it enamelysin.
58 t was mislocated to the upper portion of the enamel organ, where it remained devoid of proliferating