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