ライフサイエンスコーパス: shore

1 p to 2 kb distant, which we term 'CpG island shores'.

2 area of 1100 m (alongshore) by 440 m (cross-shore).

3 structure of subtidal communities closer to shore.

4 II) concentrations (up to about 120 nM) near shore.

5 summer on the sea ice or, where it melts, on shore.

6 er deposition, but were near equilibrium off-shore.

7 he upper water column and/or lived closer to shore.

8 tem (GPS) time series at stations located on shore.

9 ng stations 300 m offshore than close to the shore.

10 , primarily within 30 km of the southeastern shore.

11 de contents decreased with distance from the shore.

12 been considered within a few kilometers from shore.

13 1.8 (95% CI: 1.2, 2.7) for the Upper Eastern Shore.

14 he shell-core transition zone, the so-called shore.

15 s conducted along Lake Malawi's southwestern shore.

16 are associated with different heights on the shore.

17 ly-generated eddies extends for 1000 km from shore.

18 phate, and silicate, respectively, along the shore.

19 extended about 30 km beyond its present-day shore.

20 e intertidal communities along Iberian rocky shores.

21 y located in areas distal to CpG islands and shores.

22 actors and are distinct from CpG islands and shores.

23 more likely to overlap with CpG islands and shores.

24 tebrate inhabiting North Atlantic intertidal shores.

25 t of which overlap with genes and CpG island shores.

26 adients between temperate and tropical rocky shores.

27 zers, as these underpin the ecology of rocky shores.

28 in promoters located outside CpG islands and shores.

29 hinder evolving hurricanes from reaching US shores.

30 ade, particularly on O 'ahu's north and west shores.

31 nding sites within their promoter CpG island shores.

32 t structures biodiversity in temperate rocky shores.

33 derstanding heat stresses - rocky intertidal shores.

34 nces in coral reefs, kelp forests, and rocky shores.

35 espond to concerns expressed by Pacifici and Shore (2019) about a recent paper (Lees-Shepard and Gold

36 ridula along the south-eastern Pacific rocky shore (30 degrees S, Chile) in the region occupied by th

37 blend of pigments for incorporation into the Shore 40 silicone elastomer to generate a prosthesis tha

38 most common forms of contamination impacting shores after a major oil spill; and following the Deepwa

39 collected at the microhabitat level, from 15 shores along the Atlantic European coast spanning nearly

40 inental shelf-break but are also common near-shore and 2) in impacted areas, lionfish have reduced to

41 ross elevation gradients, with distance from shore and among habitat and vegetation types.

42 se states varied by vertical position on the shore and appear to be driven by microhabitat conditions

43 tivity is shaped by sodium toxicity near the shore and by sodium deficit farther inland.

44 5alpha-THP labeling in the nucleus accumbens shore and central nucleus of the amygdala, independent o

45 decades, it has yet to be documented in near-shore and coral reef environments.

46 rpoises are most influenced by distance from shore and depth.

47 ation by water reservoirs can reach far from shore and downstream.

48 nes in activity and body temperature of both shore and ice bears in summer, resembling energy expendi

49 the tsunami as an N wave that propagates to shore and impacts the coast directly.

50 lti-scale processes (e.g., wave-driven cross-shore and longshore transport; dune, bluff, and cliff er

51 ical bottleneck', inhabited exclusively near-shore and marine environments; and third, the evolution

52 ferential methylation of probes lying in the shore and shelf and enhancer regions of striatal and cer

53 opper and aluminum due to large distances to shore and thus incurs higher embodied CO(2)-eq per MWh.

54 Distance from shore and vessel traffic are variables affecting mixed d

55 Spat collection efforts from shore and within the water column were unsuccessful; thi

56 G islands from the UCSC database, CpG island shores and additional content selected from whole-genome

57 ry regions such as promoter CpG islands, CpG shores and enhancers show changes in methylation during

58 t DNA methylation of CpG islands, CpG island shores and first exons is known to play a key role in th

59 on; survival was predicted for two different shores and four sampling times using a single recruitmen

60 represented in regions flanking CpG islands (shores and shelves) and gene bodies.

61 h as those surrounding the CpG islands, i.e. shores and shelves.

62 cerebellum samples, enriched in CpG island "shores" and at further distances from CpG islands.

63 lood and the frontal cortex, CpG islands and shores, and exons.

64 B ALL subtypes, and methylation in CGIs, CGI shores, and in regions around the transcription start si

65 single-base resolution confirm that sloping shores are universal for hypomethylated CGIs in sperm an

66 ng from human use of arctic coastal and near-shore areas as sea ice diminishes.

67 treatment upgrades to the most affected near-shore areas, while simultaneously implementing legislati

68 d wave fetch (a measure of the exposure of a shore) as explanatory variables.

69 angles between the wave crest lines and the shore, as has been demonstrated in shoreline models.

70 n minimum zone and not depth or proximity to shore, as might be expected.

71 r personnel in dry dock; and 6.9% (9/131) of shore-based female naval personnel in San Diego.

72 Among shore-based fishers in coastal Alabama, lower household

73 enlisted men; 5.2% (21/406) of male marines shore-based in Okinawa, Japan; 2.7% (5/183) of female en

74 Shore-based sampling revealed that between-site differen

75 iology of "ice" bears in summer is unknown, "shore" bears purportedly minimize energy losses by enter

76 decline has ecological consequences for near shore benthic ecosystems.

77 e to a redirection of production to the near-shore benthic zone, and large lakes may exhibit shifts i

78 king regions of active promoters, CpG island shores, binding sites of the transcription factor CTCF a

79 ations of waterfowl, breeding, and migratory shore birds.

80 vious work has associated with distance from shore, but no genetic structure was associated with blea

81 showed that differential methylation of CGI shores, but not CGIs, significantly regulated Cav1 expre

82 ough December 2011 at the Mass General/North Shore Cancer Center, a community-based cancer center in

83 ight populations from the island and its off-shore cays, and applied the population genetics results

84 ression pattern of genes associated with CGI shore cDMRs was able to discriminate between disease phe

85 predator attack, foraging unusually close to shore, chemical or algal toxin exposure, abnormal weathe

86 ncipal investigators, and more companies off-shoring clinical trials, overcoming such barriers is of

87 ater, reduced subsurface oxygen both in near-shore coastal water and in the open ocean, rising coasta

88 ean 7.8-7.9, minimum 7.4-7.5), typical rocky shore communities with abundant calcareous organisms shi

89 d management solutions have focused on lower shore communities, neglecting the terrestrial-marine tra

90 ny predator species per prey species as near-shore communities.

91 res of primary production from near- and off-shore communities.

92 In annual surveys of rocky shores, communities of animal species in Shetland showed

93 Changes in rocky shore community composition as responses to climatic flu

94 ere, we removed sessile species from a rocky shore community in a way that deliberately mimicked natu

95 le outplants was reduced dramatically at mid shore compared to low shore levels regardless of the pCO

96 , a phenomenon that we described as "sloping shores." Computational analyses of human and mouse methy

97 cific and density-dependent effects of rocky shore consumers (crabs and snails) on community recovery

98 On 16 March, on-shore continuous GPS stations detected a westward motion

99 rom the south and those living higher on the shore coping better with stressful conditions.

100 e fixed-effects summary odds ratio was 1.35 (Shore-corrected 95% confidence interval: 1.23 to 1.47),

101 eciprocity between epigenetic markers at CGI shores corresponding to differential gene expression in

102 ong 40 km of NW Mediterranean subtidal rocky shores (Corsica, France).

103 th environmental perturbation than their low-shore counterparts.

104 Here, we test the hypothesis that the shore crab (Carcinus maenas) can take up microplastics t

105 re, we test the camouflage strategies of the shore crab (Carcinus maenas) in two habitats, being a sp

106 ze on a community comprised of the predator (shore crab Carcinus maenas), various grazing detritivore

107 oplastics may be ingested and inhaled by the shore crab Carcinus maenas, although the biological cons

108 In the shore crab Hemigrapsus nudus, instead of occupying the r

109 Here we examined the invasive Asian shore crab Hemigrapsus sanguineus, a species that reache

110 ctory predator cues (Carcinus maenas, common shore crab).

111 ence of the minor form of CHH from the green shore crab, Carcinus maenas, was determined by automated

112 diments; marine invertebrates (snails, green shore crab, great spider crab, and edible crab); and tel

113 outhern New England (USA) the invasive Asian shore crab, Hemigrapsus sanguineus, preys on mussels (My

114 migrapsus takanoi, the Japanese brush-clawed shore crab, is a highly successful invader in European s

115 e to human antidepressant drugs; the striped shore crab, Pachygrapsus crassipes, was studied using an

116 n of serotonin than is aggressiveness in the shore crab.

117 conditions using behavioural bioassays with shore crabs (Carcinus maenas) as a model system.

118 compared to the physiological resilience of shore crabs in maintaining osmoregulatory and respirator

119 In shore crabs, color change to improve camouflage and pred

120 e hemiellipsoid body (HB) of the eyestalk of shore crabs.

121 2015 field campaign generate large-scale on-shore currents that hit the coast, generating strong nar

122 A simulation study based on CpG Shore data suggested that in terms of detection of diffe

123 SHORE data were retrospectively analyzed to identify bas

124 high-dimensional methylation data sets (CpG Shore data, THREE data and NIH Roadmap Epigenomics data)

125 se inhibitor induced Cav1 expression via CGI shore demethylation.

126 Finally, by tracing sloping shore dynamics through embryonic and germ cell reprogram

127 A new study on rocky shore ecosystems now offers a test of warning indicators

128 the highest activities associated with near-shore eddies and the Kuroshio Current acting as a southe

129 arise over 14 degrees of latitude and 1 m of shore elevation.

130 ethylation was overrepresented in CpG island shores, enriched within gene bodies but not in intergeni

131 the USA that was also deposited under a near-shore environment.

132 ially reflect a change from nektonic to near-shore environmental niches.

133 In the intertidal zone, high-shore environments experience more environmental fluctua

134 lambeosaurines had less preference for near-shore environments than hadrosaurines in both Arctic and

135 the GOE there was pervasive suboxia in near-shore environments, allowing nonquantitative Se reductio

136 The global flux is dominated by shallow near-shore environments, where CH(4) released from the seaflo

137 Lower shore epiphytes were dominated by filamentous diatoms (B

138 Upper shore epiphytes were dominated by green algae (Chlorophy

139 dditionally, dynamic processes such as cross-shore equilibrium processes and alongshore sediment tran

140 ave evaluated the effects of the oil on near-shore estuarine fish species such as red drum (Sciaenops

141 Eleanor and Miles Harvard Medical School Shore Fellowship Grant, and Massachusetts General Hospit

142 nalysis were enriched in non-CpG islands and shores ([Formula: see text]) and depleted in promoter re

143 mass of aerosols arriving at North American shores from overseas is comparable with the total mass o

144 Patients who enrolled in SHORE fulfilled eligibility criteria per protocol (N = 2

145 e richness gradient of eastern Pacific rocky shore gastropods (spanning c.

146 Regions of high rocky shore habitat continuity are located towards the centres

147 Rocky shore habitat continuity is generally low within tropica

148 mulative ecosystem stress is highest in near-shore habitats, but also extends offshore in Lakes Erie,

149 ht environment resulting from differences in shore height and shading within the host macroalga, like

150 o different morphotypes from three different shore heights.

151 ne and after 1, 3, 6, and 12 months at North Shore Hospital.

152 with Cav1 CGI shore methylation levels, with shore hypermethylation in minimally aggressive, luminal

153 aggressive, luminal breast cancer cells and shore hypomethylation in highly aggressive, basal-like c

154 all ponds, lakes, streams/rivers and the sea shore (i.e. downward QH), with Tw-Ta becoming increasing

155 ake greater use of habitat that is closer to shore in relation to senescent-aged moose.

156 waters also increased in abundances close to shore in southern California during the MHW, a pattern t

157 nter to summer, (iii) and with distance from shore in surface waters only.

158 On rocky shores in Maine, recent experiments suggest that recover

159 n of cytosine-phosphate-guanine (CpG) island shores in nine human iPS cell lines as compared to their

160 ns were situated along the Jubbah palaeolake-shores, in a grassland setting with some trees.

161 l colonization of subantarctic and Antarctic shores, in addition to recent genetic exchange among pop

162 ns, ocean geology, and remote control of off-shore industrial activities.

163 d for marine environmental monitoring of off-shore industrial sites.

164 monitoring threats at sea, both for the off-shore infrastructure and ports.

165 g y(-1) (of mainly higher congeners) to near-shore Lake Ontario compared with volatilization of appro

166 he main route of Sigma5PBDE loadings to near-shore Lake Ontario which acts as a net PBDE sink.

167 tiple private and public values on its North Shore land holdings (Island of O'ahu) of approximately 1

168 However, given the large Mediterranean shore length relative to its surface area, SGD may be a

169 peratures but animals collected from the low-shore lengthened theirs to the greatest degree.

170 onse, the morphotype associated with the low-shore-lengthened response times at high temperatures.

171 ion between the larval carry-over effect and shore level, suggesting little modulation of acidificati

172 ed dramatically at mid shore compared to low shore levels regardless of the pCO2 level that oysters e

173 gh juveniles grew less at mid shore than low shore levels, there was no evidence of an interaction be

174 ion of Infectious Disease Diagnostics, North Shore-LIJ Health System, and now is Vice President for G

175 ication of terrestrial, freshwater, and near-shore marine ecosystems, and comparable increases in pes

176 assess their environmental risk in the near-shore marine environment of Antarctica.

177 where DGT samplers were deployed in the near-shore marine environment of East Antarctica around the o

178 and contaminant monitoring in Antarctic near-shore marine environments need new techniques to overcom

179 ith major implications for riverine and near-shore marine environments.

180 particularly those associated with the lower shore, may exhibit less effective behavioural responses

181 nd Women's, Massachusetts General, and North Shore Medical Center) were evaluated for CMS reporting s

182 adjusted confidence interval (CI) using the Shore method of 95% CI [1.02, 1.45].

183 Recently, other patterns such as CpG island shore methylation and long partially hypomethylated doma

184 hat the increase is a byproduct of island or shore methylation followed by deamination.

185 ncer aggressiveness associated with Cav1 CGI shore methylation levels, with shore hypermethylation in

186 Cav1 CGI shore methylation was also observed in human breast tumo

187 CpG island shore methylation was strongly related to gene expressio

188 rst study of Cav1 (a potential oncogene) CGI shore methylation, we suggest this phenomenon may repres

189 rst study of Cav1 (a potential oncogene) CGI shore methylation, we suggest this phenomenon may repres

190 , and pore-water nutrients) on an intertidal shore near Dublin, Ireland.

191 eastern United States are most prevalent off-shore near the continental shelf-break but are also comm

192 Early invasions of the North American shore occurred mainly via deposition of ballast rock, wh

193 present-day sea level along the southeastern shore of Bermuda contain remains of a former breeding co

194 ocated above the head-of-tide on the western shore of Chesapeake Bay.

195 fibrosis is common in communities along the shore of Lake Albert.

196 ient particles collected on the southeastern shore of Lake Michigan during an event (July 6-8, 2015)

197 ranged from <DL to 2.6 ng/L on the southern shore of Lake Ontario near the mouth of the Oswego River

198 pitation samples were collected close to the shore of Lake Victoria at Entebbe, Uganda, between Octob

199 ely 150 000 residents located on the western shore of Lake Victoria in Tanzania.

200 seawater of Kaneohe Bay on the northeastern shore of Oahu, Hawaii, by extinction culturing in seawat

201 the food chain in shelf waters off the west shore of Oahu, Hawaii.

202 River and adjacent waterways on the eastern shore of the Chesapeake Bay in Maryland, USA.

203 Bioinformatics analysis revealed a CpG shore of the CNTFRalpha gene regulated its mRNA expressi

204 d dollars in three bundles were found on the shore of the Columbia River near Portland, Oregon.

205 heir roots in the populations on the eastern shore of the Mediterranean Sea.

206 e organisms of drift debris deposited on the shores of 30 remote islands from the Arctic to the Antar

207 m coastal climate of Gibraltar, close to the shores of Africa, raises hopes for the future recovery o

208 Flow depths along the shores of Banda Aceh exceeded 9 meters, with inundation

209 s of limpets, found attached to rocks on the shores of Cornwall, Wales and Scotland were explored for

210 a) and Brassica crop species, thrives on the shores of Lake Tuz, Turkey, where soils accumulate high

211 Tar balls collected from the Gulf of Mexico shores of Louisiana and Florida after the BP oil spill h

212 f kilometers across the Pacific Ocean to the shores of North America and Hawai'i.

213 y urbanized estuary, and specifically on the shores of San Mateo County, the county most vulnerable t

214 amples were collected at five sites near the shores of the Great Lakes during the period 2008-2009, i

215 ir samples collected from six sites near the shores of the Great Lakes.

216 amples collected at five sites, all near the shores of the North American Great Lakes during 2008-200

217 protein 2 to the "cytosine-phosphate-guanine shores" of the Kcc2 promoter, and decrease in binding of

218 lted in a shift toward "reshoring" and "near-shoring" of mining processing capabilities as regional p

219 ntries around the Mediterranean Sea with off shore oil production.

220 , but rather in the 3' UTR, gene bodies, CpG shores or 'offshore' sites, and both positive and negati

221 t enrichment of hypermethylated cDMRs in CGI shores (P < 10(-60)), non-CGI-associated promoters (P <

222 rpendicular erosion and 11 m for the maximum shore-perpendicular accretion during the study period.

223 The horizontal, shore-perpendicular change in shoreline position along t

224 we find upper limits of 25 m for the maximum shore-perpendicular erosion and 11 m for the maximum sho

225 n position of the 0.8-m contour sampled from shore-perpendicular profiles spaced at 20-m intervals al

226 ears of monthly profile surveys taken at two shore-perpendicular transects at Duck, North Carolina, U

227 ndomized, open-label, vision examiner-masked SHORE phase 4 study that compared monthly versus pro re

228 nic (10)Be concentrations across a sandstone shore platform in North Yorkshire, UK, to model the chan

229 nce decrease by 38-92% for a near-horizontal shore platform with a low-elevation cliff-platform junct

230 down-wearing and stripping of rock from the shore platform.

231 growth patterns in the western central near-shore portion of Second Connecticut Lake, Pittsburg, New

232 rths at U.S. ports that could be switched to shore power to yield the largest gains for society.

233 NOX, SO2, PM2.5, and CO2 that would occur if shore power were used.

234 require many ships to be equipped to receive shore power, even if doing so would result in a private

235 ves and mandates to encourage a shift toward shore power.

236 thin promoter 'CpG islands' (CGIs) with 'CGI shores', recently described regions that flank CGIs with

237 ment development also now impacting the near-shore region of Lake Baikal, the resilience of the lake'

238 n due to hyper-methylation in the CpG island shore region of mmu-miR-15b in both the spermatozoa of F

239 osystems is more recent in oceanic than near shore regions, yet our understanding of human impacts on

240 The sample locations comprised shore sediment of a large European river (Rhine) and a r

241 cation of pellets, which were separated from shore sediment samples of both rivers.

242 Along shore sediment transport that is driven by waves is gene

243 For this reason, river shore sediments of the rivers Rhine and Main in the Rhin

244 wrinkles are preserved in barely bioturbated shore-shallow lacustrine siliciclastic deposits of the L

245 hylation in CpG islands and demethylation at shore/shelf and open sea.

246 00), 1st exons, 5'UTRs, 3'UTRs, CpG islands, shores, shelves, open seas and FANTOM5 enhancers.

247 ing as a key strategy for decarbonisation of shore-side energy demand at ports.

248 trification, particularly involving electric shore-side vehicles (ESVs), has a significant impact on

249 dulating coseismic subsidence patterns, near-shore slip velocities, and the seismic and tsunami hazar

250 cies responses (for example, changes in near-shore species abundance and predator absence).

251 nced clones revealed that G. duebeni, a high-shore species with the highest thermal tolerance, expres

252 Tigriopus californicus, which inhabits rocky-shore splashpools where diel fluctuations of temperature

253 concentrations than lower bay and New Jersey shore stations.

254 The Mediterranean shores stretching between Sicily, Southern Italy and the

255 nts with retinal vein occlusion (RVO) in the SHORE study.

256 The marine shore sulfidic mine tailings dump at the Chanaral Bay in

257 ement for both species, coincident with near-shore surface currents.

258 compare ecological shifts in subtidal rocky shore systems along CO2 gradients created by volcanic se

259 require a fine-scale assessment of the near-shore temperature changes.

260 Although juveniles grew less at mid shore than low shore levels, there was no evidence of an

261 gene expression more strongly at CpG island shores than CpG islands.

262 DM loci occurred twice as frequently in the shores than in the actual CpG islands.

263 carried out in the late 1990s of open rocky shores that are common along the northern part of the 70

264 On the Upper Eastern Shore, the IRR for arthritis reversed, indicating higher

265 On New Zealand rocky shores, the magnitude of such subsidies differs profound

266 occurs outside of CpG islands and CpG island shores, thus rejecting the hypothesis that the increase

267 ic deep-sea brine pool sited close enough to shore to chronicle floods, yet be otherwise undisturbed

268 habitats ranging from shallow water, to near shore to the open ocean and the deep sea.

269 case study of one measurement drive from the shore to the precoastal mountain range furthest downwind

270 cal study was carried out in Rumonge, a lake-shore town where 318 people were admitted to hospital wi

271 ) Recession due to sea level rise, (3) Cross-shore transport due to waves, and (4) Residual processes

272 , wave-driven processes (longshore and cross-shore transport) still account for 34% of shoreline chan

273 At the shore, ultraviolet (UV) radiation (also present in other

274 t is essential to identify novel pathways to shore up current disease-intervention strategies.

275 tance Laboratory Network (AR Lab Network) to shore up the national capacity for detecting several res

276 fic work has proceeded in a robust manner to shore up the validity of APS as a diagnostic construct.

277 Choosing to shore up those rights, however, will increase the number

278 Shoring up the foundation of academic science will requi

279 onger increase in peak- and late-season near-shore upwelling in the northern limb of the California C

280 onger decrease in peak- and late-season near-shore upwelling in the southern limb.

281 tach themselves to rocks near tide-swept sea shores using byssal threads formed from their extracellu

282 ng along with repeat testing after return to shore was available for 120 of the 122 persons on board

283 e effects on microbiological quality of near-shore water.

284 1.8 +/- 2.7 Tg, is consumed annually in near-shore waters (<50 m), suggesting that aerobic methanotro

285 reported for the first time floating in off-shore waters.

286 d the topshell Gibbula) from a coastal rocky shore, we found that the capacity to predict the combine

287 icinalis on upper and lower zones of a rocky shore were determined.

288 t geographic region, depth, and proximity to shore were significant predictors of community structure

289 Gene bodies, intergenic regions, and CpG shores were preferentially demethylated during erythropo

290 nd other variables (salinity and distance to shore) were much weaker.

291 n its focus of endemicity, the Upper Eastern Shore, were calculated.

292 ion by turbulent shear typical of wave-swept shores where adults of this species live.

293 pment of oscillatory biological reactions at shores where waves impinge on rocks and bring nutrients

294 ithin about 100 km), narwhal moved closer to shore, where they were presumably less vulnerable.

295 s significantly enriched in CpG island (CGI) shores while depleted in CGIs themselves, especially in

296 te concentrations yield maximal biomass near shore, while offshore biomass is positively correlated w

297 combined cycle (without CO2 capture) and on-shore wind power plants, both from a levelized and margi

298 Its genomic location, a CpG island shore within an H3K27ac enhancer mark, and the correlati

299 g to show that subsea permafrost in the near-shore zone of the ESAS has a downward movement of the ic

300 Beyond the near-shore zone, these regions typically have a carbonate con