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1 y rewired by the cell-autonomous action of a switch gene.
2 gulate the promoters for the gammaHV68 lytic switch gene.
3   Here we show that let-7 is a heterochronic switch gene.
4 of the ribosome binding sequence of the fliN switch gene.
5 chromatin, similar to cellular developmental switch genes.
6 ranscriptional reprogramming of key meristem switching genes.
7 ical and cell-based studies identified G0/G1 switch gene 2 (G0S2) as an inhibitor of adipose triglyce
8      Methylation-mediated silencing of G0-G1 switch gene 2 (G0S2) has been detected in a variety of s
9                            The protein G0/G1 switch gene 2 (G0S2) is a small basic protein that funct
10  following TNF-alpha treatment was G(0)-G(1) switch gene 2 (G0S2), the activation of which also requi
11 ased studies have identified the G0S2 (G0/G1 switch gene 2) as a selective inhibitor of the key intra
12 virus 68 (MHV68, gammaHV68), essential lytic switch gene 50 controls the interchange between lytic an
13 es transcript levels for the essential lytic switch gene 50.
14 r region of the gene for Rta, the main lytic switch gene, and the other is within the promoter region
15 e expression data sets showed that wild-type switch genes are downregulated in ripening-deficient mut
16                                              Switch genes are involved in multiple processes and incl
17 +-dependent transcription of the lytic cycle switch gene BZLF1.
18           The Epstein-Barr virus (EBV) lytic switch gene, BZLF1, is tightly regulated in latently inf
19                                          All switch genes, expressed at low levels in vegetative/gree
20 the circadian transcription factors that can switch gene expression on and off, it is still unclear h
21              Following injury, keratinocytes switch gene expression programs from the one that promot
22 e developmentally appropriate expression and switch gene expression programs.
23            Further, NFI temporal binding and switch gene expression were upregulated in the developin
24 at impairing TCR signals at the CD4 SP stage switched gene expression patterns from CD4- to CD8-linea
25 m Borrelia hermsii, a relapsing fever agent, switches gene expression of a surface protein between di
26 en together, our work provides modularity in switching gene-expression patterns by cell geometric con
27 lso show that optix simultaneously acts as a switch gene for blue structural iridescence in some butt
28                   In concurrence, the master switch gene for osteoblasts, Cbfa1, was also downregulat
29            Sex-lethal (Sxl) functions as the switch gene for sex-determination in Drosophila melanoga
30 in somatic cells serves as the developmental switch gene for somatic sex determination and X-chromoso
31  expression of the putative lymphocyte G0/G1 switch gene (G0S2), heme oxygenase 1 (HMOX1), tumor necr
32 t is premature to conclude that Sxl is not a switch gene in germ cells for at least some sex-specific
33 ly that Sxl functions as a sex determination switch gene in most species in the Drosophila genus.
34 e identified and characterized two Imitation Switch genes in Saccharomyces cerevisiae, ISW1 and ISW2,
35 gulatory RNAs that function as heterochronic switch genes in the nematode C. elegans.
36  of the coding sequence of the upstream fliM switch gene, in the same operon.
37 mutation in a flagellar basal body, hook, or switch gene is present.
38 nal enhancers are short segments of DNA that switch genes on and off in response to a variety of intr
39 roximity so they can work synergistically to switch genes on and off in time and space.
40     These mechanisms are not responsible for switching genes on and off.
41 t R. centenum contains two sets of motor and switch genes, one set for the lateral flagella and the o
42 ed number of lytic genes such as lytic cycle switch gene ORF 50 (RTA) and the immediate early (IE) ly
43 quent decline in the expression of the lytic switch gene, ORF50, while latent gene expression persist
44 irus (KSHV), the promoter of the viral lytic switch gene, Rta, is organized into bivalent chromatin,
45 ) acts as a positive regulator of the master switch gene Sex lethal (Sxl).
46             The Drosophila sex-determination switch gene Sex-lethal (Sxl) and the X-chromosome signal
47                                   The binary switch gene Sex-lethal (Sxl) controls sexual identity in
48  the dose of X chromosomes to the regulatory-switch gene Sex-lethal (Sxl) during Drosophila sex deter
49                In D. melanogaster the binary switch gene Sex-lethal (Sxl) plays a pivotal role in som
50                                          The switch gene Sex-lethal (Sxl) was thought to elicit all a
51 tive male or female regulatory states of the switch gene Sex-lethal.
52 ex of an individual by regulating the master switch gene, Sex-lethal (Sxl).
53 ic splicing pattern of the sex determination switch gene, sex-lethal.
54 haromyces pombe, products of two mating-type switching genes, swi1 and swi3, participate in fork arre
55 mination gene Sex-lethal (Sxl) acting on its switch-gene target transformer (tra) to produce Tra(F) p
56                              Sxl is a master switch gene that controls its own pre-mRNA splicing as w
57 uing not only because it harbours the master-switch gene that determines gender but also because of i
58 splicing as well as splicing for subordinate switch genes that regulate sex determination and dosage
59 YCN activity maintains the transcription of "switch" genes that are rate-limiting for metabolic activ
60 the FGF family appears to be a prototype of "switch genes" that are endowed with organizational and m
61 d HMVEC through activation of the KSHV lytic switch gene, the open reading frame 50.
62                 Analysis of the prototypical switch gene TOS4 (Target Of SBF 4) reveals its role as a
63 than size dimorphism by controlling only the switch gene transformer (tra).
64                      A special subset named "switch genes" was identified, with the additional proper
65 pressing the masculinizing sex determination switch gene xol-1 (XO lethal) in a dose-dependent manner
66 the activity of the master sex-determination switch gene xol-1 in a dose-dependent manner.
67                                      The sex switch gene xol-1 is the direct molecular target of this
68 , which repress the master sex-determination switch gene xol-1 via two distinct, dose-dependent molec
69 hion to regulate levels of the developmental switch gene xol-1.
70 he sex-determination and dosage-compensation switch gene, xol-1.
71 beta activates the promoter of the EBV lytic switch gene ZTA.

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