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3 ations at EGF6 and EGF36 (added by Manic and Lunatic but not Radical) inhibited Notch1 activation fro
4 used bone morphogenetic protein 4 (BMP4) and lunatic fringe (Fng) as molecular markers to identify th
5 th two other putative sensory organ markers, Lunatic Fringe (L-fng) and chicken Serrate1 (Ser1), both
7 helium, anteroposterior encroachment of alar lunatic fringe (L-fng) expression, and/or basal Shh sign
8 opus homologs of the Drosophila gene fringe, lunatic Fringe (lFng) and radical Fringe (rFng), were id
9 ntrally expressed otic genes such as NeuroD, Lunatic fringe (Lfng) and Six1 are shifted dorsally, whe
14 aevis and Danio rerio, include an absence of lunatic fringe (lfng) expression within the presomitic m
15 mponents of the Notch pathway, including the Lunatic fringe (Lfng) gene, are also expressed during di
16 ce homozygous for a targeted mutation of the lunatic fringe (Lfng) gene, one of the mouse homologues
18 The Notch pathway and the Notch modulator Lunatic fringe (Lfng) play multiple roles during segment
19 narily conserved 2.3 kb region in the murine Lunatic fringe (Lfng) promoter that drives periodic expr
22 d expression of the Notch target genes HEY1, lunatic fringe (LFNG), and ephrin-B2, reduced phosphoryl
23 ifferential regulation of Notch receptors by Lunatic Fringe (Lfng), which encodes an O-fucosylpeptide
26 een a dorsal domain (dorsal roof) expressing lunatic fringe and Notch, and a ventral domain (posterio
27 We also identified pronephric expression of lunatic fringe and radical fringe that is temporally and
28 nge proteins in Chinese hamster ovary cells (Lunatic fringe and Radical fringe) as well as exogenous
29 ted that demonstrate that radical fringe and lunatic fringe are expressed in the granulosa cells of d
30 his study examines the distribution of chick lunatic fringe at sites of neural crest formation and ex
32 further insight into the mechanism by which lunatic fringe controls somite development, we have cond
34 tal plate prior to somite formation and that lunatic fringe expression cycles autonomously with a per
36 nt, we have conducted a thorough analysis of lunatic fringe expression in the unsegmented paraxial me
38 These findings point to a novel role for lunatic fringe in regulating cell division and/or produc
46 sruption in mouse embryos, we show here that lunatic fringe is likewise required for boundary formati
47 hough the beta 3GlcNAcT activity of manic or lunatic fringe is shown to be necessary for inhibition o
49 ic periodic expression pattern suggests that lunatic fringe may function to integrate notch signaling
50 ringe homologue and suggest a model in which lunatic fringe modulates Notch signalling in the segment
56 indirect reporter system, that the 3'UTR of Lunatic Fringe strongly destabilizes transcripts, while
60 Lrrn1 also regulates the glycosyltransferase Lunatic Fringe, a modulator of Notch signalling, maintai
63 ure expression delays for three transcripts [Lunatic fringe, Hes7/her1, and Notch-regulated-ankyrin-r
64 ption in somite 0 requires the expression of lunatic fringe, which modifies the activation of the Not
69 hat expression of mammalian fringe proteins (Lunatic [LFng], Manic [MFng], or Radical [RFng] Fringe)
72 have demonstrated that, similar to Manic and Lunatic, Radical fringe is also a fucose-specific beta1,
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