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1 ested the molar explant morphogenesis at the bud stage.
2 ocks normal myogenic differentiation at tail bud stage.
3 results in arrested tooth development at the bud stage.
4 oth and mammary gland development before the bud stage.
5 bular molar teeth fail to develop beyond the bud stage.
6 post-stratification placode invagination to bud stage.
7 rest in molar tooth development at the E13.5 bud stage.
8 om stratified epithelium through placode and bud stages.
9 st morphologically distinct through to later bud stages.
10 ng in the posterior limb through mid-to-late bud stages.
11 erior limb margins over a wide range of limb bud stages.
12 used to examine expression patterns at later bud stages.
13 uring gastrulation, neurulation, and in tail bud stages.
14 C) conditions for 4 h across several floral bud stages.
15 nhibition is specific to the COPII-dependent budding stage.
16 chalcogen bonding catalysis (ChB) is in the budding stage.
20 rs lack mesenchymal Notch1 expression at the bud stage and exhibit abnormal ameloblast differentiatio
21 ressed in the lateral plate mesoderm at tail bud stage and in the intermediate cell mass (ICM, the lo
22 ts in arrested tooth development at the late bud stage and LEF1 is required for a relay of a Wnt sign
23 mandibular molar development arrested at the bud stage and maxillary molar development arrested at th
25 Tbx2 expression in the dental mesenchyme at bud stage and show that this can be induced by epithelia
27 is expressed by distal mesenchyme during the budding stage and localizes to periductal mesenchymal ce
31 begins in utero and proceeds via a quiescent bud stage before the initial outgrowth and subsequent br
32 mandibular molar developmental arrest at the bud stage but allowed maxillary molars and incisors to d
35 tion of Bmp4 ( Bmp4(ncko/ncko)) both exhibit bud-stage developmental arrest of the mandibular molar t
36 ription factor Hand2 within the PSG from the bud stage (E12.5) of mouse embryonic salivary gland deve
37 e endoderm in Xenopus using neurula and tail-bud-stage embryos and we show that the current hypothesi
40 Whereas all tooth germs were arrested at the bud stage in Msx1(-/-) mice, we show that depleting func
42 of molar mesenchymal Dlx2 expression at the bud stage is Msx1-dependent, both the maintenance of Dlx
43 in the dental epithelium prior to the E12.5 bud stage, is a key player during odontogenesis, being r
44 derm is isolated alone from neurula and tail bud stages, it remains fully viable but will not express
47 dynamin is required for its function in the budding stages of receptor-mediated endocytosis and syna
48 epithelium arrests tooth development at the bud stage, secondary to a lack of cell proliferation in
54 evelop in a coordinated way from the primary bud stage to the generation of millions of alveolar gas
57 the result of this increased cell death, the bud stage tooth germ fails to advance to the cap stage i
58 the mandibular incisor arrested as a single, bud-stage tooth germ and Meckel's cartilage was absent.
59 f each level do not come together until tail bud stages, we conclude that stable regional specificati
60 cient mice, tooth development arrests at the bud stage when Msx1 is required for the expression of Bm
62 nes sad, ear, acp and cyb5 was at the 3-5 mm bud stages, with the SAD and EAR gene products detected