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1 llular responses including the activation of scleraxis.
2 boxes that overlaps with the closely related scleraxis.
3                           We have found that Scleraxis, a bHLH transcription factor, is a highly spec
4 n part by the association between Sirt-1 and scleraxis and deacetylation of NF-kappaB and PI3K.
5 /flox)) results in microglossia with reduced Scleraxis and Fgf10 expression as well as decreased myog
6 ing somite are crucial for the expression of scleraxis and Mkp3.
7 rs, and the neotendon transcription factors, Scleraxis and Mohawk.
8 lets, in contrast to tendon-associated genes scleraxis and tenascin, present in the chordae tendineae
9 (dpERK) signaling and promotes expression of scleraxis and tenascin.
10 hat promote tendon fibroblast proliferation: scleraxis and tenomodulin.
11 he level of some markers [e.g., mtwist, mf1, scleraxis, and alpha1(II) collagen] is seen in the anter
12 f biglycan, collagen V, collagen XII, PAI-1, Scleraxis, and Mohawk by TGF-beta1.
13 increased the expression of type I collagen, scleraxis, and tenomodulin.
14 nducer of the tendon progenitor (TNP) marker scleraxis both in organ culture and in cultured cells, a
15  Col5a1(flox/flox) mouse model was bred with Scleraxis-Cre mice to create a targeted tendon and ligam
16  show that tendon development is arrested in Scleraxis-Cre::Mmp14 lox/lox mice that are unable to rel
17                             The induction of scleraxis-expressing TNPs is not affected in mutant embr
18 ascade and in particular, ERK1/2 to activate scleraxis expression in a population of mesenchymal prog
19         Finally, TGF-beta signaling-mediated Scleraxis expression is required for tendonogenesis in t
20 luding the limb tendons, and show that early scleraxis expression marks the progenitor cell populatio
21  endogenous BMP activity and induces ectopic scleraxis expression.
22                                    Using the scleraxis gene as a marker we show that these progenitor
23 d a Col2.3GFP transgene, while expression of Scleraxis-GFP was used to follow differentiation into pe
24 udes both transcriptional activators such as scleraxis, Hand2, and Dermo-1 and repressors such as Twi
25 e results reveal an essential early role for scleraxis in mesoderm formation, as well as a later role
26                                      Loss of scleraxis in mice leads to geometric and structural chan
27          Paraxis expression precedes that of scleraxis in the region of the somite fated to form the
28 e, TGF-beta2 beads induced the expression of Scleraxis in tongue explant cultures.
29                                              Scleraxis is a basic helix-loop-helix (bHLH) transcripti
30                               Loss of EP4 in Scleraxis-lineage cells did not alter gliding function,
31 e three embryonic germ layers confirmed that scleraxis mutant embryos were unable to form mesoderm.
32 nerating chimeric embryos, using lacZ-marked scleraxis-null and wild-type embryonic stem cells, we ex
33                                              Scleraxis-null cells were specifically excluded from the
34         At the time of developmental arrest, scleraxis-null embryos consisted of ectodermal and primi
35 nction in embryonic development, we produced scleraxis-null mice by gene targeting.
36 ect transcription from an E-box found in the scleraxis promoter.
37 ct by identifying two proepicardial markers, Scleraxis (Scx) and Semaphorin3D (Sema3D), that genetica
38  at different stages of development based on scleraxis (Scx) expression.
39                                          The scleraxis (Scx) gene, encoding a bHLH transcription fact
40 ed to determine how the transcription factor Scleraxis (Scx) influences the development and maturatio
41                                              Scleraxis (Scx) is a known regulator of tendon developme
42                                              Scleraxis (scx) is a transcription factor required for t
43                                              Scleraxis (Scx), a bHLH transcription factor, marks this
44 mad2/3-mediated signaling, the expression of Scleraxis (Scx), a transcription factor specific for ten
45 n mammalian tendons and ligaments, including scleraxis (scx), collagen 1a2 (col1a2) and tenomodulin (
46 eted from the myotome induces formation of a scleraxis (Scx)-expressing tendon progenitor population
47 ived chondrogenic lineages, and suggest that scleraxis target genes mediate these processes.
48 steogenic (Runx2, OCN) and ligament-related (scleraxis transcription factor (SCXA), ELN) genes were d
49  of phosphorylated ERK result in the loss of scleraxis transcripts and the loss of distal rib develop
50 sistent with this early embryonic phenotype, scleraxis was found to be expressed throughout the embry
51 omodulin, and tenogenic transcription factor scleraxis, whereas it inhibited gene products involved i

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