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1 ing the photoreceptor-specific expression of nocturnin.
2  cells, in a pattern identical to endogenous nocturnin.
3                     A deletion series of the nocturnin 5'-flanking sequence driving the green fluores
4 nvolved in such circadian control identified nocturnin, a novel gene that displays high-amplitude cir
5  distinct spatial and temporal expression of nocturnin and PARN suggests that there may be specific m
6 mal triglyceride transfer protein (MTP), and nocturnin are involved in the circadian regulation of in
7 re we report that the targeted disruption of Nocturnin (Ccrn4l) in mice, a gene that encodes a circad
8 /or translational silencing, we propose that nocturnin deadenylates clock-related transcripts in a no
9          Our data support a pivotal role for Nocturnin downstream of the circadian clockwork in the p
10  nocturnin promoter, which we designated the nocturnin element (NE).
11 e 388 amino acid protein that we have named "nocturnin" (for night-factor).
12 t the PCE II in the proximal promoter of the nocturnin gene is sufficient for driving the photorecept
13 is precise spatial expression pattern of the nocturnin gene.
14                                              Nocturnin is a clock-regulated deadenylase that controls
15                                              Nocturnin is a vertebrate circadian clock-regulated gene
16       Substrate preference studies show that nocturnin is an exonuclease that specifically degrades t
17 ter homolog of the vertebrate circadian gene nocturnin is expressed in a subset of dorsal neurons and
18                            Here we show that nocturnin is expressed rhythmically in the small intesti
19   The deadenylase and leucine zipper protein Nocturnin is now shown to play a central role.
20                                        While nocturnin is rhythmically expressed in the cytoplasm of
21                                     The gene nocturnin is rhythmically transcribed in Xenopus retinal
22            Gene expression data suggest that Nocturnin knockout mice have deficits in lipid metabolis
23                Our observations suggest that nocturnin may function through protein-protein interacti
24                                Expression of nocturnin mRNA is confined to the clock-containing photo
25                                              Nocturnin mRNA levels exhibit a high amplitude circadian
26                                 Mice lacking nocturnin (Noc(-/-) mice) are resistant to diet-induced
27                                              Nocturnin (NOC) is a circadian-regulated protein related
28                                              Nocturnin (NOC) is a unique deadenylase with robustly rh
29                                              Nocturnin nuclease activity is magnesium dependent, as t
30                             Transcription of nocturnin peaks in these cells in the middle of the nigh
31                   Therefore, we propose that nocturnin plays an important role in the trafficking of
32 ied a novel protein-binding motif within the nocturnin promoter, which we designated the nocturnin el
33                                 Mice lacking Nocturnin remain lean on high-fat diets, with lower body
34               In these studies, we show that nocturnin removes the poly(A) tail from a synthetic RNA
35 t P-CREB controls the rhythmic regulation of nocturnin transcription and perhaps that of other night
36 toreceptors, with a phase similar to that of nocturnin transcription.

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