ライフサイエンスコーパス: mare

1 ons accompanying sleep paralysis (SP; "night-mare").

2 n focal areas between endometrial folds (6/6 mares).

3 ivators, including Maf-recognition elements (MAREs).

4 es of the Thoroughbred from a British-native mare.

5 expression and if this might be mediated by MAREs.

6 rs, even though the promoters do not contain MAREs.

7 nsurgically from two pairs of identical twin mares.

8 Da that was recognized by mouse anti-rat IgE-MARE-1 in Western blots.

9 alphaCE2 site or half Maf response element (MARE), adjacent to the Pax6 site.

10 In the chronically instrumented pony mare and fetus, this study investigated how changes in f

11 bedo markings on the Moon that occur in both mare and highland terrains; their origin remains a point

12 of these spots is distinct from surrounding mare and highlands material and from regions composed of

13 A truncated zeta promoter containing Nrl-MARE and Pax6 sites has a high level of expression in le

14 nlymphoid cells, a function that maps to the MARE and Th2-specific footprint.

15 lm-regulatory molecule) were detected in 6/6 mares and 5/6 mares, respectively, from endometrial samp

16 peripheral blood lymphocytes from both horse mares and donkey jennets carrying intraspecies pregnanci

17 ined an overlapping Maf recognition element (MARE) and antioxidant responsive element (ARE) that was

18 ntaining overlapping MafA response elements (MARE) and CAAT enhancer binding (CEB) elements regulate

19 rochete group with a late-term abortion in a mare are described.

20 The HS2 MAREs are required for nucleosome mobilization and histo

21 Putative Maf recognition elements (MAREs) are found in the 3' enhancer region of the immuno

22 Combining the ferritin-L MARE/ARE and IRE produced a response to hemin that was 3

23 Regulation of ferritin-L by a MARE/ARE DNA sequence emphasizes the importance of ferri

24 old greater than the sum of responses of the MARE/ARE or IRE alone.

25 uctase (ARE regulator) or quinone reductase (MARE/ARE regulator).

26 The data demonstrate that a stable MARE-associated footprint in LCR HS2 is important for th

27 set of MITF-associated regulatory elements (MAREs) at active enhancers.

28 Leaching experiments on mare basalt 14053 demonstrate that isotopically light Zn

29 are sample-return sites and is a new type of mare basalt not previously sampled, but consistent with

30 try measurements on the 3.7-billion-year-old mare basalt sample 10020.

31 l changes in hydration that were greater for mare basalts (approximately 70%) than for highlands (app

32 ally light Zn condensates also occur on some mare basalts after their crystallization, confirming a v

33 Here, we report analyses of two 3.56-Gy-old mare basalts demonstrating that they were magnetized in

34 Mare basalts may contain hydrogen-rich apatite, but luna

35 eruption of thorium- and titanium-rich lunar mare basalts, plausibly results in a core heat flux suff

36 ARE caused a reduction in the association of MARE-binding proteins and transcription complexes at LCR

37 Maf with MafG rescued the MafG repression of MARE but not ARE-mediated gene expression.

38 ed strongly with sera from recently infected mares but not with sera from horses vaccinated with comm

39 Surprisingly, mares carrying interspecies hybrid mule conceptuses did

40 NA-binding domain (ZF-DBD) to the HS2 tandem MARE caused a reduction in the association of MARE-bindi

41 The MARE-CEB is repressed by MafA, whereas the CEB-MARE site

42 One site (MARE-CEB), from -320 to -300 bp in the promoter, repress

43 stry from high rates of abortion in pregnant mares, death in young foals, establishment of the carrie

44 F-E2 binding sequence, in a TATA box and HS2/MARE-dependent fashion.

45 ersensitive 2 (HS2)-Maf recognition element (MARE) DNA in a sequence-specific manner and remodels nuc

46 chius, where the latter basin has no visible mare fill.

47 eritis virus (EAV), as venereal infection of mares frequently occurs after breeding to such stallions

48 tic fibrosacroma (Maf) recognition elements (MAREs) from the sequence in the proximal promoter region

49 The other site (CEB-MARE), from +2,628 to +2,641 bp in the first intron of t

50 arside of the moon beneath the impact basins Mare Humboltianum, Mendel-Ryberg, and Schiller-Zucchius,

51 unar magnetic fields are strong antipodal to Mare Imbrium and Mare Serenitatis and has discovered the

52 oves, lineations and elongate craters around Mare Imbrium shape much of the nearside Moon.

53 Complexes binding the MARE in lens nuclear extracts are antigenically related

54 al stage-restricted negative effector of the MARE in the IgH 3' enhancer region.

55 hese factors can activate transcription from MAREs in co-transfection assays, mouse germline mutation

56 show that a tandem Maf recognition element (MARE) in locus control region (LCR) hypersensitive site

57 c-Maf binds to a c-Maf response element (MARE) in the proximal IL-4 promoter adjacent to a site f

58 ription factors can elicit responses through MAREs, including not only the AP-1 family proteins, but

59 whose consensus target site in vitro, the T-MARE, is an extended version of an AP-1 site normally re

60 However, mares lack detectable progesterone in the latter half of

61 he chemical compositions of relatively young mare lava flows have implications for the late volcanism

62 ft assays demonstrated that Mafs bind to the MARE-like sequences in the PL1 and PL2 elements, whereas

63 Low-titanium mare lunar dust is minimally irritating to the eyes and

64 rolling erythroid gene regulation implicated MARE (Maf recognition element) cis-elements as crucial t

65 d IL-10 gene expression through binding to a MARE (Maf recognition element) motif in the IL-10 promot

66 The mean MARE (mean absolute relative error) value taken over all

67 n the activation of Maf recognition element (MARE) mediated p53 gene expression.

68 MafG in Hep-G2 cells repressed both ARE and MARE-mediated genes expression.

69 of c-Maf (c-Maf) led to significant loss of MARE-mediated p53 gene expression but had no effect on t

70 the phylogeny corresponding to the Ancestral Mare Mitogenome at ~130-160 thousand years ago.

71 t species (human HM, cow CoM, camel CaM, and mare MM) using an optimised (31)P NMR spectroscopy proce

72 ng, Coulomb-Sarton, Freundlich-Sharonov, and Mare Moscoviense.

73 assays of antibody in convalescent sera from mares naturally infected with L. interrogans suggest tha

74 d whether NF-E2 binds directly to the tandem MAREs of HS2 in intact cells.

75 molecule) were detected in 6/6 mares and 5/6 mares, respectively, from endometrial samples with tissu

76 values of fatty acids, reveals processing of mare's milk and carcass products in ceramics, indicating

77 this region's composition differs from other mare sample-return sites and is a new type of mare basal

78 lds are strong antipodal to Mare Imbrium and Mare Serenitatis and has discovered the smallest known m

79 rostaglandin F2alpha(PGF2alpha) and pregnant mare serum gonadotrophin (PMSG).

80 treatment of prepubertal rats with pregnant mare serum gonadotropin (PMSG).

81 lture medium from mice treated with pregnant mare serum gonadotropin alone had no effect.

82 dium from immature mice primed with pregnant mare serum gonadotropin followed by human chorionic gona

83 rats received a single injection of pregnant mare serum gonadotropin followed by progesterone or vehi

84 sis in intact follicles primed with pregnant mare serum gonadotropin.

85 reased in mutant mice injected with pregnant mare serum gonadotropins.

86 RE-CEB is repressed by MafA, whereas the CEB-MARE site, which is homologous to the A2C1 component of

87 ociate with MAFB and MAFG in the presence of MARE-site DNA, and this interaction is dependent on the

88 A promoter fragment containing Pax6 and MARE sites gives lens-preferred induction of a heterolog

89 Recombinant Maf protein binds to T-MARE sites in the (alpha)A-, (beta)B2-, and (beta)A4-cry

90 CNC family proteins for binding in vitro to MARE sites, have been implicated in the regulation of bo

91 The results emphasize MARE-TATA box interactions in the recruitment of complex

92 ning a genomic DNA library with serum from a mare that had recently aborted due to leptospiral infect

93 The best achieved MARE value is at 4.8%, whereas the worst lies at 25.8%,

94 in this region resulted in the bulk of lunar mare volcanism and altered the density structure of the

95 gma plumbing system for much of the nearside mare volcanism.

96 role of biofilms in equine endometritis, six mares were inoculated with lux-engineered Pseudomonas ae

97 been demonstrated in the pineal gland from a mare with active uveitis and is suspected in some human

98 tected only in the pineal gland from the one mare with active uveitis in which T and B lymphocytes we

99 pendent on the presence of p45 and on intact MAREs within HS2.

100 ends on the tandem Maf-recognition elements (MAREs) within the beta-globin locus control region HS2 e

101 Tandem Maf recognition elements (MAREs) within the hypersensitive site 2 (HS2) subregion