ライフサイエンスコーパス: mare

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

2 nt (R(2)), and Mean absolute relative error (MARE).

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

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

5 rom sheep, nine from buffalo, and three from mare.

6 one patient may potentially be spared from a MARE.

7 of these molecules in uEVs during MRP in the mare.

8 n of pregnancy (MRP) are still unknow in the mare.

9 p, 466 for goat, 197 for buffalo, and 69 for mare.

10 d hydrocarbons seas Kraken, Ligeia and Punga Mare.

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

12 mares, resulting in parameters similar to NW mares.

13 sexes were sacrificed with 34% identified as mares.

14 letal muscle mitochondrial function in older mares.

15 altered skeletal muscle metabolism in older mares.

16 oxytocinase), a key regulator of oxytocin in mares.

17 fects of dietary oil supplementation in aged mares.

18 expression and if this might be mediated by MAREs.

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

20 nsurgically from two pairs of identical twin mares.

21 (R(2) = 0.96, RMSE = 22.37, MAE = 15.65, and MARE = 0.26).

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

23 d mitochondrial function in aged light-horse mares (23.2 +/- 1.1 year), which are excellent models of

24 in Nitra (n = 10; 4 stallions, 5 geldings, 1 mare, 4 stallions, 5 geldings and 1 mare, consisting of

25 MarE, a heme-dependent enzyme, catalyzes a unique 2-oxin

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

27 While MarE adopts a global structure resembling the homotetram

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

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

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

31 lung and lymph node tissues of two horses (a mare and its foal) from Italy that succumbed to an acute

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

33 strate's alpha-amino nitrogen differ between MarE and TDO, and the substrate's orientation in the bin

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

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

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

37 ometrosis is a major cause of infertility in mares and is characterized by degenerative, functional a

38 f the resident uterine microbiome in healthy mares and to establish the presence of a core microbiome

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

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

41 ventricular arrhythmias and related events (MAREs) and to develop a stratification tool predicting M

42 ich were previously associated to MRP in the mare, and thus bringing added value to the current knowl

43 ), without an embryo (P-, n = 7) in pregnant mares, and both uterine horns of nonbred mares (NB, n =

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

45 The HS2 MAREs are required for nucleosome mobilization and histo

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

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

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

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

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

51 These structures establish MarE as a member of the heme-dependent aromatic oxygenas

52 ts of obesity on the metabolic health of old mares as well as test the ability of diet supplementatio

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

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

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

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

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

58 ng'e-5 mission returned some of the youngest mare basalt samples reported so far, dated at 2.0 billio

59 Mare basalt sources are likely to have originated from p

60 nger model age of ~4.33 Ga for the source of mare basalts (240 My after solar system formation) might

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

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

63 Lunar mare basalts are depleted in F and Cl by approximately a

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

65 The average loss tangent of mare basalts is estimated at 0.0040-0.0061.

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

67 Some of the Apollo mare basalts show evidence for the presence in their sou

68 s at the low end of the range estimated from mare basalts that erupted from around 4.0 Ga to 2.8 Ga (

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

70 unar meteorite, Asuka-881757, and associated mare basalts, represent ancient (~3.9 Ga) partial melts

71 low than those associated with later-erupted mare basalts, suggesting a fundamental shift in melting

72 chemical study of two types of young farside mare basalts, the ~2.8-billion year (Ga) low-Ti and ~2.9

73 res and shallower depths than typical Apollo mare basalts.

74 ilk samples from Basque Mountain Horse breed mares belonging to three different farms and three lacta

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

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

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

78 2 and 13 after ovulation) and cyclic control mares (C; day 10 and 13 after ovulation) were analyzed.

79 Surprisingly, mares carrying interspecies hybrid mule conceptuses did

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

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

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

83 dings, 1 mare, 4 stallions, 5 geldings and 1 mare, consisting of the breeds 3 Slovak warmblood, 4 Cze

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

85 The incidence of MAREs, defined as sudden cardiac death, sustained ventri

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

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

88 Our findings suggest that lunar syn-tectonic mare emplacement along reactivated inherited faults prov

89 superfamily, including PrnB, SfmD, TyrH, and MarE, expand its boundaries and mediate monooxygenation

90 Obese mares fed the complex diet supplement had better insulin

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

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

93 Real-world MAE ranged from 0.09 to 0.13, MARE from 1.3 to 22.7%, with ICCs indicating moderate (0

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

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

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

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

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

99 resent the first X-ray crystal structures of MarE in complex with its prime substrate, (2S,3S)-beta-m

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

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

102 to develop a stratification tool predicting MAREs in adults with a systemic right ventricle (sRV).

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

118 Mare milk has traditionally been attributed a number of

119 This study deeply characterized mare milk proteome accounting for both caseins and prote

120 contributes to the deep characterization of mare milk proteome and provides new insights into the ef

121 scarce, with particularly limited studies on mare milk proteomics.

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

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

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

125 n = 6); and in periparturient and postpartum mares (n = 18).

126 Mares (n = 19, 17.9 +/- 3.7 years) were placed into one

127 a (n = 7) and homogenized tissue of diestrus mares (n = 6) were evaluated using protein determination

128 D21-22 in non-pregnant (n = 5) and pregnant mares (n = 6); and in periparturient and postpartum mare

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

130 ant mares, and both uterine horns of nonbred mares (NB, n = 6).

131 on three intervention periods-(1) state-led Mare Nostrum, (2) private-led search-and-rescue, and (3)

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

133 from uterine lavages collected from pregnant mares (P; day 10, 11, 12 and 13 after ovulation) and cyc

134 albedo and lower iron content than volcanic mare plains, suggesting an origin of ejecta-induced debr

135 We hypothesized that obesity in the mare promotes follicular lipid accumulation and altered

136 uisiana, and Australia as well as that of 19 mares purchased from scattered owners in the Southern Mi

137 Horses present one potential model since mares receive intense gynecological care.

138 eks and completion of sample collections, OB mares received L-carnitine alone for an additional 6 wee

139 K in the nearside mantle that formed surface mare regions 3-4 billion years ago(11) and could influen

140 logical properties of the low-titanium lunar mare regolith simulant JSC-1A are measured using concent

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

142 metabolic changes in the follicles of obese mares, resulting in parameters similar to NW mares.

143 ive ICDs implanted in patients with a 5-year MARE risk >10%, one patient may potentially be spared fr

144 iographic parameters was devised to estimate MARE risk and to identify high-risk patients who may ben

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

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

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

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

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

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

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

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

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

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

155 espite differing oxygen activation outcomes, MarE shares a substrate binding mode similar to IDO and

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

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

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

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

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

161 ate below the heme plane, which is absent in MarE, suggesting mechanistic differences.

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

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

164 We analyzed the microbiomes of 35 healthy mares that are long-time residents of three farms in Okl

165 ternal recognition of pregnancy (MRP) in the mare, the embryo needs to signal its presence to the end

166 considered, stallions were more likely than mares to be WNV seropositive (OR = 2.4, 95% CI 1.6-3.7,

167 ated by covering 17 m diameter crater in the Mare Tranquillitatis with a structure made from a lunar

168 (the youngest radiometric-dated homogeneous mare unit) through both statistics of fresh crater morph

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

170 els, achieving mean absolute relative error (MARE) values of 4.95% for the entire dataset, 5.92% for

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

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

173 The incidence of MAREs was 6.3 per 1000 patient-years.

174 Obesity in mares was significantly associated with insulin dysregul

175 Twenty mares were grouped as: Normal Weight [NW, n = 6, body co

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

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

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

179 The association of MAREs with clinical, electrical, and echocardiographic p

180 mber contribute to PL similarly in women and mares, with triploidy the dominant ploidy type over the

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

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

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