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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
11 following TNF-alpha treatment was G(0)-G(1) switch gene 2 (G0S2), the activation of which also requi
13 ased studies have identified the G0S2 (G0/G1 switch gene 2) as a selective inhibitor of the key intra
14 virus 68 (MHV68, gammaHV68), essential lytic switch gene 50 controls the interchange between lytic an
16 well-characterized modules: one populated by switch genes, all up-regulated in COPD cases and related
17 rm plasticity into environmentally sensitive switch genes and downstream genes that execute the decis
18 r region of the gene for Rta, the main lytic switch gene, and the other is within the promoter region
19 e expression data sets showed that wild-type switch genes are downregulated in ripening-deficient mut
24 aison of several ripening master regulators "switch genes" can play a central role in the induction o
25 In leaves of the booting stage, APA site-switching genes displayed global shortening of 3' untran
27 the circadian transcription factors that can switch gene expression on and off, it is still unclear h
29 differentiation, keratinocytes sequentially switch gene expression programs, resulting in terminal d
31 coded controllers to generate plants able to switch gene expression selectively depending on oxygen a
34 at impairing TCR signals at the CD4 SP stage switched gene expression patterns from CD4- to CD8-linea
35 a given transcription factor and objectively switches gene expression from an OFF state to an ON stat
36 m Borrelia hermsii, a relapsing fever agent, switches gene expression of a surface protein between di
37 en together, our work provides modularity in switching gene-expression patterns by cell geometric con
38 lso show that optix simultaneously acts as a switch gene for blue structural iridescence in some butt
41 in somatic cells serves as the developmental switch gene for somatic sex determination and X-chromoso
43 expression of the putative lymphocyte G0/G1 switch gene (G0S2), heme oxygenase 1 (HMOX1), tumor necr
44 ranscriptional data on reduced expression of switch genes hint towards a disturbed ripening onset.
45 Accessibility changes within compartment switching genes, however, are mainly observed in non-pro
46 t is premature to conclude that Sxl is not a switch gene in germ cells for at least some sex-specific
47 ly that Sxl functions as a sex determination switch gene in most species in the Drosophila genus.
48 hese results highlight a pivotal role of the switch genes in grapevine ripening, as well as their pos
49 e identified and characterized two Imitation Switch genes in Saccharomyces cerevisiae, ISW1 and ISW2,
52 tingly, 70% of AGER negative interactors are switch genes including PRDX4, whose activation strongly
55 nal enhancers are short segments of DNA that switch genes on and off in response to a variety of intr
58 t R. centenum contains two sets of motor and switch genes, one set for the lateral flagella and the o
59 ed number of lytic genes such as lytic cycle switch gene ORF 50 (RTA) and the immediate early (IE) ly
60 quent decline in the expression of the lytic switch gene, ORF50, while latent gene expression persist
61 ring on the berry, a subset of genes, called switch genes previously suggested as master regulators o
63 m biases, highlighting the potential role of switch-gene regulation in the evolution of plasticity.
64 irus (KSHV), the promoter of the viral lytic switch gene, Rta, is organized into bivalent chromatin,
68 the dose of X chromosomes to the regulatory-switch gene Sex-lethal (Sxl) during Drosophila sex deter
74 haromyces pombe, products of two mating-type switching genes, swi1 and swi3, participate in fork arre
75 mination gene Sex-lethal (Sxl) acting on its switch-gene target transformer (tra) to produce Tra(F) p
77 uing not only because it harbours the master-switch gene that determines gender but also because of i
78 icing of xol-1, the master sex-determination switch gene that triggers male development in XO embryos
79 splicing as well as splicing for subordinate switch genes that regulate sex determination and dosage
80 YCN activity maintains the transcription of "switch" genes that are rate-limiting for metabolic activ
81 the FGF family appears to be a prototype of "switch genes" that are endowed with organizational and m
87 pressing the masculinizing sex determination switch gene xol-1 (XO lethal) in a dose-dependent manner
90 , which repress the master sex-determination switch gene xol-1 via two distinct, dose-dependent molec