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1 ional regulator involved in human urothelial cytodifferentiation.
2 te the same genes prematurely and accelerate cytodifferentiation.
3 nctioning cell autonomously to promote organ cytodifferentiation.
4 ture and in regulating intestinal epithelial cytodifferentiation.
5 g that Frk/rak is dispensable for intestinal cytodifferentiation.
6 nd initiate, but do not complete, pancreatic cytodifferentiation.
7 nt role for Runx2 in tooth morphogenesis and cytodifferentiation.
8 ically relevant factors that facilitate this cytodifferentiation.
9 association with slow cell proliferation and cytodifferentiation.
10  lineage-specific proliferation, rather than cytodifferentiation.
11 promote intestinal growth, morphogenesis and cytodifferentiation.
12                          Identification of a cytodifferentiation agent target may shed light on the m
13 regulates early gene expression and promotes cytodifferentiation and cell-specific gene expression.
14 , it results in failure of midgut epithelial cytodifferentiation and of the intestine to lengthen and
15 nals can have specific inhibitory effects on cytodifferentiation and suggest that one function of end
16 nical response is associated with incomplete cytodifferentiation and the induction of apoptosis with
17 raction plays an important role in prostatic cytodifferentiation and the maintenance of the different
18 lished that ductal morphogenesis, epithelial cytodifferentiation, and proliferation/apoptosis are reg
19 d the stable acquisition of cell fate direct cytodifferentiation during organogenesis.
20 ion of both lung branching morphogenesis and cytodifferentiation, establishing the mechanistic basis
21 g the period of epithelial morphogenesis and cytodifferentiation fails to disrupt these processes.
22 lation of apoB mRNA editing is an autonomous cytodifferentiation function of small intestine for whic
23 portant developmental stages of normal islet cytodifferentiation in differentiating ES cell cultures.
24 e-stimulating hormone)-induced rat granulosa cytodifferentiation in serum-free medium.
25 re first detected at the beginning of muscle cytodifferentiation in stage 24/25 limbs, shortly after
26 th the hypoplastic phenotype and the delayed cytodifferentiation in TACE-deficient lungs were rescued
27  in both branching and peripheral epithelial cytodifferentiation in the absence of TACE protein.
28 eatic ductal morphogenesis; 3) duct-specific cytodifferentiation, in the form of carbonic anhydrase I
29 eric pattern is established in mesoderm, and cytodifferentiation is apparently normal, but the segmen
30  controlling late morphogenesis and terminal cytodifferentiation is not known.
31 ate that MT-DLX3 acts to disrupt odontoblast cytodifferentiation leading to odontoblast apoptosis, an
32 mentary, with no expression of several early cytodifferentiation markers including GATA4, GATA6, and
33                  These cells expressed early cytodifferentiation markers, including GATA-6 and ApoJ.
34 tion of DSPP by Runx2 is dependent on use of cytodifferentiation of dental ectomesenchymal-derived ce
35          This leads to growth inhibition and cytodifferentiation of mammary tumor cells and a concurr
36                                       During cytodifferentiation of odontoblasts there is a constant
37 o) mutation, which arrests morphogenesis and cytodifferentiation of the gut and exocrine pancreas in
38 ne, and this restriction precedes the normal cytodifferentiation of the intestinal epithelium.
39 nscriptional programs guiding patterning and cytodifferentiation of the lung.
40 mesenchyme, which promotes proliferation and cytodifferentiation of the prostatic epithelium.
41  regulate coordinated cell morphogenesis and cytodifferentiation of the retinal pigmented epithelium.
42 retinal pigment epithelium morphogenesis and cytodifferentiation requires SoxB1 downregulation, which
43 ion is activated at the onset of limb muscle cytodifferentiation, s-actin expression occurs much earl
44  odontogenesis from epithelial thickening to cytodifferentiation stages.
45  period of villus development and epithelial cytodifferentiation, to generate Gata4Gata6 double condi
46 oblast cell proliferation was decreased, and cytodifferentiation was increased in a dose-dependent ma
47 le the subsequent phases are associated with cytodifferentiation within the myotome.

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