ライフサイエンスコーパス: transcription control

1 tion and DOT1L-mediated H3K79 methylation in transcription control.

2 djacent to a CpG-islands implicated in TERRA transcription control.

3 s MLL fusion partners belies a dependency on transcription control.

4 ing, a recently recognized important step of transcription control.

5 s, including Gli2 and Gli3, that function in transcription control.

6 ication of ligand binding is central to LacI transcription control.

7 l integration at the level of cis-regulatory transcription control.

8 nd AT8 within proximity is important for the transcription control.

9 t is most likely, however, to be involved in transcription control.

10 exes, thereby regulating their activities in transcription control.

11 that OriP enhancer shares aspects of HSV IE transcription control.

12 of various domains of the leader RNA in this transcription control.

13 y molecule by uridylation-induced, antisense transcription-controlled 3'-5' exonucleolytic degradatio

14 sigma(54)-dependent transcription controls a wide range of stress-related ge

15 of ENL in leukaemia pathogenesis and dynamic transcription control, a chemical genetic strategy was d

16 a richly detailed tapestry of signaling and transcription, controlling an important T cell developme

17 chromatin remodeling is a necessary step in transcription control and its memory, genome integrity,

18 Transcription control and RNA binding are the primary fu

19 regulatory modules as units of developmental transcription control, and also of evolution, in the ass

20 chinery governing cell cycle progression and transcription control are often homologous in yeast and

21 Transcription control at the melting step is not yet und

22 accessibility model is that cis-elements and transcription control binding of the recombination-activ

23 7 which was an indirect effect of c-myc gene transcription control by Ada3.

24 NA strand might be an essential component of transcription control by ppGpp.

25 nor did Stat1 and c-Jun cooperate in driving transcription controlled by the alpha(2)-macroglobulin e

26 c/Rho signalling pathways that regulate gene transcription controlled by the c-fos promoter, the c-fo

27 ated, which led to the dysregulation of gene transcription controlled by these pathways.

28 ral proteins involved in translation, global transcription control, cell-cycle control, stress respon

29 Dopamine receptor genes are under complex transcription control, determining their unique regional

30 However, the key domains by which CASZ1 transcription controls developmental processes and neuro

31 hich are helicases, perform diverse roles in transcription control, DNA repair, and chromosome segreg

32 Positive transcription control elements associated with two DNase

33 n close proximity to consensus sequences for transcription control elements within the thrombomodulin

34 Our analysis suggests that many complex transcription-control functions of the type encountered

35 ch strongly resembles the kor (kil override) transcription control genes identified previously on Str

36 a telomeric reporter gene, a rare example of transcription control in an organism with widespread and

37 limiting the genome-wide adoption of complex transcription control in bacteria.

38 plications of our findings for combinatorial transcription control in eukaryotes are discussed.

39 s on the transcript and the implications for transcription control in other regulatory systems are di

40 ly the consequence of E2F-dependent negative transcription control in quiescent cells.

41 racts with the Pax6 gene in Rb cells through transcription control in the 5'-flanking region upstream

42 teins provide a basis for the specificity of transcription control in the Rb/E2F pathway.

43 These results suggest that transcription control is relatively inexact but that the

44 signaling and a potent modulator of hormonal transcription control, is one candidate for regulating t

45 In most organisms, transcription control makes a major contribution to diff

46 nal conservation of a DPE-dependent, general transcription control mechanism between Drosophila and h

47 ated gene network might result from a non-AR transcription control mechanism common to these genes.

48 , it was found that transcriptional and post-transcription control mechanisms determine potencies and

49 regulation involves many different types of transcription control mechanisms, including mechanisms b

50 15 genes have complex genomic structures and transcription control mechanisms.

51 ct to mutation constrain the organization of transcription control networks?

52 work has provided evidence for E2F-dependent transcription control of both G1/S- and G2/M-regulated g

53 holipid synthesis regulation by zinc and the transcription control of the PIS1 gene.

54 to uncover evidence for much higher upstream transcription control of transcription factors themselve

55 uire specific cellular functions such as RNA transcription control or even become part of protein cod

56 implicate sympathetic nervous system-linked transcription control pathways as candidate mediators of

57 it is often of interest to identify upstream transcription control pathways mediating observed change

58 le, rapid and sensitive tool for identifying transcription control pathways mediating observed gene e

59 is the interaction site for many enzymes and transcription control proteins and as a result, developm

60 CTC-binding factor was enriched at the EBNA2 transcription control region in type I but not type III

61 first exon of E1a and a deletion within the transcription control region of E1b.

62 The transcription control region of the archetype strain of

63 shed through binding of the repressor to the transcription control region of the biotin biosynthetic

64 was performed using specific primers for the transcription control regions of BKV, JCV, and SV40, res

65 e novel repressor sites is highly present in transcription control regions of FeS genes.

66 potential binding sites are identified from transcription control regions of genes of interest.

67 scribed to identify regulatory motifs in the transcription control regions of genes that exhibit simi

68 ed that identify sequence motifs enriched in transcription control regions of genes that share simila

69 ence features (words) present in presumptive transcription control regions.

70 of all genes that contain the motif in their transcription control regions.

71 Indirect readout mechanisms of transcription control rely on the recognition of DNA sha

72 Also, unique sequences, including transcription control sequences, are often subject to ca

73 lex region that spans a variety of potential transcription control signals.

74 arcinogenic mechanisms such as altering gene transcription, controlling stem cell differentiation to

75 eport here a robust, tunable, and reversible transcription control system for endogenous genes.

76 al benefits and mechanistic differences this transcription control system offers.

77 l, and also of evolution, in the assembly of transcription control systems.

78 n3 and Swi4 levels mediated by ECB-dependent transcription controls the timing of the G(1)-to-S phase

79 .2 and to find chromatin landmarks there for transcription control, unannotated genes and chromatin s

80 Included are only examples in which transcription control was modified by the insert.

81 ing, small molecule sensing, and integrative transcription control were amplified selectively.

82 is addressed, the full impact of research on transcription control will be realized throughout the fi