ライフサイエンスコーパス: satellite

1 n imaging spectroradiometer from NASA's Aqua satellite.

2 d carbon monoxide observations from multiple satellites.

3 particular focus on the 260-bp and Responder satellites.

4 itation to mapping AGV with the latest radar satellites.

5 marks a subtype of PCM1-positive centriolar satellites.

6 and the European Space Agency's Sentinel-1A satellites.

7 of 15 min resolution data from geostationary satellites.

8 s consistent with independent estimates from satellite altimetry, leading to overall acceleration lar

9 In G1, the satellite, an SPB precursor, assembles next to the mothe

10 three Gd ions in one carbon cage, acts as a satellite anchoring on the surface of PDA.

11 We combined satellite and citizen science data to estimate rates of

12 Through integrating satellite and GPS data from five separated populations c

13 ale evaluation of sustainable water use from satellite and ground observations, the established frame

14 y-air mole fraction (XCO2) observations from satellites and ground-based networks are analyzed togeth

15 dangerous solar bursts and prevent damage to satellites and power stations from space weather events.

16 the measurements from aircraft campaigns and satellites, and found a robust association between BC co

17 ral abundance of (13)C is around 1.1%, these satellites appear at 0.54% of the intensity of a parent

18 This work shows that each human alpha satellite array produces a unique set of non-coding tran

19 ost human chromosomes contain multiple alpha satellite arrays that are competent for centromere assem

20 to underlying organization of distinct alpha satellite arrays.

21 nalysis of canopy-scale biophysics rules out satellite artifacts as significant causes of satellite-o

22 and G2 cell cycle phases, the 2-4% of alpha-satellite assembled with CENP-A protects DNA lengths cen

23 gration, the intraparticle coalescence of Au satellites at QD surfaces transforms individual HNCs int

24 Using satellite-based aerosol optical depth (AOD) measurements

25 We find that agreement between satellite-based and traditional field survey-based yield

26 onded sea ice during summer, indicating that satellite-based Arctic annual primary production estimat

27 This establishes a basis to construct a satellite-based column BC approximation (sBC*) over remo

28 verage in China since 2000, however, the new satellite-based dataset Global Forest Change (GFC) finds

29 een field-based biodiversity information and satellite-based Earth system studies, thereby supporting

30 each cohort location using a combination of satellite-based estimates, chemical transport model simu

31 an approximate 11 km x 11 km resolution with satellite-based estimates, chemical transport models, an

32 of East Antarctica, significantly affecting satellite-based estimations close to the ground.

33 n locations) in situ and decadal (2003-2014) satellite-based groundwater storage measurements in west

34 ite monitors, chemical transport models, and satellite-based land use regression models to estimate n

35 We use satellite-based measurements of urban form and nitrogen

36 We further show that satellite-based measures are able to detect positive yie

37 ave the potential to improve the accuracy of satellite-based PM2.5 estimates.

38 Using satellite-based radar imagery for such purposes has been

39 ng pregnancy was estimated using a validated satellite-based spatiotemporally resolved prediction mod

40 of this study demonstrate the potential of a satellite-based vegetation photosynthesis model for diag

41 w NMR experiment (Destruction of Interfering Satellites by Perfect Echo Low-pass filtration, DISPEL)

42 data suggest a mechanism for how centriolar satellites can specifically regulate an ATG8 ortholog, t

43 mation, fibrosis, mitochondrial dysfunction, satellite cell (SC) exhaustion and loss of skeletal and

44 amts1 as a potent extracellular regulator of satellite cell activation and have significant implicati

45 , macrophages secrete Adamts1, which induces satellite cell activation by modulating Notch1 signaling

46 educes Notch signaling, leading to increased satellite cell activation.

47 terstitial fibrogenic cells, which influence satellite cell activity and muscle repair during hypertr

48 ications for understanding the regulation of satellite cell activity and regeneration after muscle in

49 le regrowth following a burn injury requires satellite cell activity, underscoring the therapeutic po

50 assign to Ptpn11 signaling a key function in satellite cell activity.

51 ABSTRACT: Satellite cell contribution to unstressed diaphragm is h

52 Satellite cell depletion did not alter diaphragm mean fi

53 KEY POINTS: Satellite cell depletion does not affect diaphragm adapt

54 Satellite cell depletion early in life (4 months of age)

55 Prolonged satellite cell depletion in the diaphragm does not resul

56 Up-regulation of Pax3 mRNA+ cells after satellite cell depletion in young and aged mice suggests

57 Whether satellite cell depletion negatively impacts diaphragm qu

58 vo diaphragm function was also unaffected by satellite cell depletion.

59 Inhibition of DDR restored satellite cell differentiation ability.

60 Analysis of satellite cell dynamics on myofibers confirmed that HIF1

61 Our insights into a critical mechanism in satellite cell homeostasis during muscle regeneration co

62 PR plays a pivotal role in the regulation of satellite cell homeostasis during regenerative myogenesi

63 We found that short-term CR increased the satellite cell number and collagen VI content of muscle,

64 Focal adhesion kinase activation and satellite cell number are elevated in muscles undergoing

65 Severe burn injury induces satellite cell proliferation and fusion into myofibres w

66 injury induced skeletal muscle regeneration, satellite cell proliferation and fusion.

67 ng muscle regeneration through activation of satellite cell proliferation and migration.

68 vided 5-ethynyl-2'-deoxyuridine to determine satellite cell proliferation, activation and fusion.

69 and regeneration in aged muscles, decreased satellite cell self-renewal and regenerative potential,

70 er normoxia but are required for maintaining satellite cell self-renewal in hypoxic environments.

71 ion of Notch signaling, a key determinant of satellite cell self-renewal.

72 ulated by Notch signaling, a key governor of satellite cell self-renewal.

73 uvenile satellite cell-wild-type (SC-WT) and satellite cell-depleted (SC-Dep) mice (8 weeks of age) w

74 x3 mRNA+ cell density in both young and aged satellite cell-depleted diaphragm muscle (P < 0.05), whi

75 Myonuclear density was maintained in young satellite cell-depleted mice regardless of running, alth

76 , satellite cell-replete) or tamoxifen (Tam, satellite cell-depleted) treated at 4 months of age and

77 Here we have used human primary CD56(Pos) satellite cell-derived myogenic progenitors obtained fro

78 of replicative senescence, decline in muscle satellite cell-mediated regeneration coincides with acti

79 Mice were vehicle (Veh, satellite cell-replete) or tamoxifen (Tam, satellite cel

80 a dKO produced with the tamoxifen-inducible, satellite cell-specific Pax7(CreER) system in postnatal

81 Juvenile satellite cell-wild-type (SC-WT) and satellite cell-depl

82 s in quiescent satellite cells and activated satellite cells (myoblasts) are poorly understood.

83 entary (-7%) and running (-19%) mice without satellite cells (P < 0.05).

84 Previous studies showed porcine muscle satellite cells (PSCs) are important for postnatal skele

85 Satellite cells (SCs) are adult muscle stem cells that a

86 Satellite cells (SCs) are myogenic stem cells required f

87 onse after muscle injury, focusing on muscle satellite cells (SCs), inflammatory reaction, fibrosis,

88 ever, the in vivo roles of HIFs in quiescent satellite cells and activated satellite cells (myoblasts

89 th PDGF-BB showed an increased population of satellite cells and an increase in the number of regener

90 s and the cells that contact them, including satellite cells and motor neurons.

91 ithin skeletal myofibers and in trans within satellite cells and within motor neurons via the neuromu

92 ctivity and regeneration after muscle injury.Satellite cells are crucial for growth and regeneration

93 Muscle satellite cells are myogenic stem cells whose quiescence

94 Conditional depletion of satellite cells attenuates recovery of myofibre area and

95 CD133+ cells and FKRP L276IKI mouse derived satellite cells by a lentiviral vector expressing the wi

96 SC-Dep mice had >93% depletion of satellite cells compared to SC-WT (P < 0.05).

97 ell-specific Pax7(CreER) system in postnatal satellite cells delayed injury-induced muscle repair due

98 ent with this, the in vitro proliferation of satellite cells derived from these muscles was reduced b

99 nt degradation of EZH2 is a prerequisite for satellite cells differentiation and identify PJA1 as a n

100 To determine the necessity of satellite cells during muscle recovery following a burn

101 oncurrent activation and apoptosis of muscle satellite cells following a burn injury in paediatric pa

102 ferentiation on C2C12 myoblasts, and primary satellite cells from mouse and human, we show that culli

103 Depletion of satellite cells impaired post-burn recovery of both musc

104 that allows for the conditional depletion of satellite cells in skeletal muscle.

105 These findings support an integral role for satellite cells in the aetiology of lean tissue recovery

106 x3+ cells may compensate for a loss of Pax7+ satellite cells in the diaphragm.

107 y, underscoring the therapeutic potential of satellite cells in the prevention of prolonged frailty i

108 rvival and differentiation of PERK-deficient satellite cells in vitro and muscle formation in vivo.

109 ctivity in the presence and absence of Pax7+ satellite cells in young and aged mice using an inducibl

110 of PERK, but not the IRE1 arm of the UPR in satellite cells inhibits myofiber regeneration in adult

111 he survival and differentiation of activated satellite cells into the myogenic lineage.

112 tors (myoblasts) that become Pax7(+) MyoD(-) satellite cells prior to birth, but is not detectable in

113 ap1CKO mouse skeletal muscle contained fewer satellite cells than normal and these cells had evidence

114 hat levels of PERK and IRE1 are increased in satellite cells upon muscle injury.

115 sites of muscle injury induce activation of satellite cells via expression of Adamts1.

116 ed activation of muscle stem cells (known as satellite cells) is critical for postnatal muscle growth

117 ates (muscle proteins, lipids, glucose, DNA (satellite cells)) can be monitored simultaneously and fl

118 enewal and maintenance of muscle stem cells (satellite cells).

119 etween muscle tissue compartments, including satellite cells, and infiltrating myeloid cells upon tis

120 ntral for regulating the activation state of satellite cells, but the specific extracellular signals

121 Activity of satellite cells, skeletal muscle stem cells, is altered

122 Strikingly, however, satellite cells, the adult muscle stem cells that are es

123 Satellite cells, the predominant stem cell population in

124 e Drosophila equivalent of vertebrate muscle satellite cells.

125 to birth, but is not detectable in postnatal satellite cells.

126 , which may compensate for the loss of Pax7+ satellite cells.

127 eration due to the differentiation defect of satellite cells.

128 and facilitates the generation of postnatal satellite cells.

129 on cells and a much larger fraction of their satellite cells.

130 enfold differences in abundance of the major satellite CentC, but similar high levels of sequence pol

131 istinct MOF particle-inorganic particle core-satellite clusters were synthesized.

132 urthermore, PCM1-GABARAP-positive centriolar satellites colocalize with forming autophagosomes.

133 ock perturbations that propagate through the satellite constellation at galactic velocities 300 km

134 Analyses of satellite data (1979-2014) and a simplified ice-upper oc

135 from error in anthropogenic emission trends, satellite data and atmospheric transport.

136 Here, we use satellite data and climate observations from 2000 to 201

137 er for sea ice extent, area, and volume from satellite data and realistic coupled climate models.

138 Here, satellite data are used to derive a statistical relation

139 AN exposure was estimated using time-varying satellite data for a composite of persistent nighttime i

140 ssessed long-term fire trends using multiple satellite data sets.

141 We analyze satellite data that document the global diabatic circula

142 12 years (2003 to 2014) of MODIS pantropical satellite data to quantify net annual changes in the abo

143 ational Aeronautics and Space Administration satellite data yielded consistent results.

144 d the Cochrane Eyes and Vision United States Satellite database of systematic reviews.

145 In this study, four satellite datasets are used to investigate this discrepa

146 Among these satellite datasets, forest loss shows much better agreem

147 In two out of three recent satellite datasets, the tropospheric warming from 1979 t

148 In this study, using two satellite datasets, we apply and compare six methods to

149 period 2003 to 2013 were used together with satellite derived data on rainfall, average temperature

150 provided by surface observations and several satellite-derived and reanalysis products, although some

151 Here, we integrate satellite-derived biophysical observations, particle dis

152 ultiple precipitation products (since 1900), satellite-derived data on terrestrial water storage (sin

153 resent observational evidence using multiple satellite-derived datasets that desert amplification is

154 ll unknown due to the large uncertainties in satellite-derived estimates.

155 re confirmed by similar correlations between satellite-derived isoprene emissions and terrain elevati

156 tion in tree mortality could be explained by satellite-derived net primary productivity, suggesting t

157 al regions, but major roads within 100 m and satellite-derived NO2 were consistently the strongest pr

158 ssigned a value for green living space via a satellite-derived normalised difference vegetation index

159 er surveys of Australian reefs combined with satellite-derived sea surface temperatures.

160 an atmospheric model of spectral radiation, satellite-derived spectral water transparency and temper

161 We apply satellite-derived surface irradiance data from the NASA

162 ce-sheet models estimate basal traction from satellite-derived surface velocity, without a priori kno

163 er LSWT to SAT variability using 20 years of satellite-derived temperatures from 144 lakes.

164 antly reconciles current controversies about satellite-detected Amazon phenology, and improves our us

165 Highly repetitive satellite DNA (satDNA) repeats are found in most eukaryo

166 omeres (ENC) are composed of large arrays of satellite DNA and surrounded by segmental duplications.

167 Human centromeres are defined by alpha satellite DNA arrays that are distinct and chromosome sp

168 The overwhelming majority (97%) of alpha-satellite DNA is found to be assembled with histone H3.1

169 intain integrity of the long arrays of alpha-satellite DNA repeats.

170 h for their characteristic repeat sequences (satellite DNA) and for being epigenetically defined.

171 fruit fly Drosophila melanogaster shows that satellite DNA, and corresponding small non-coding RNA, h

172 meres are composed of tandem arrays of alpha-satellite DNA, which spans up to several megabases.

173 rge ( 2 Mb) centromeres are not dominated by satellite DNA.

174 stability is mediated through the centriolar satellite E3 ligase Mib1, which interacts with GABARAP t

175 ent meteorological data sets from the modern satellite era, to examine the temporal characteristics o

176 as a heat engine increased during the modern satellite era.

177 osis suggest that it arises from centromeric satellite expansion and asymmetric modification of micro

178 Prior to the use of GPS satellites, extraordinarily accurate clocks measuring th

179 f the GaAs lattice, resulting in quadrupolar satellites for nuclear [Formula: see text] isotopes, whe

180 e inwardly rectifying K(+) channel Kir4.1 in satellite glial cells.

181 e inwardly rectifying K(+) channel Kir4.1 in satellite glial cells.

182 To address this, we have uncoupled satellite growth from NE insertion.

183 rpretation approach using large databases of satellite imagery at (i) very high spatial resolution an

184 These results suggest that high-resolution satellite imagery can be used to make predictions of sma

185 Our findings are based on satellite imagery from 1973 onwards and aerial photograp

186 st-efficient approach using multi-resolution satellite imagery from Landsat and MODIS during 2009-201

187 les and were combined with optical and radar satellite imagery in a machine learning algorithm to map

188 These data, combined with high-resolution satellite imagery, were used to create new health area a

189 , we correlated annual CUEa , estimated from satellite imagery, with locally determined soil CUEh for

190 imated from PM2.5-prediction models based on satellite imagery.

191 ees, measured by classifying high-resolution satellite imagery.

192 oduce various regular patterns identified in satellite imagery.

193 ngitudinal data derived from high-resolution satellite images to estimate the effect of titling betwe

194 hotosynthesis Model (VPM), climate data, and satellite images to estimate the GPP of terrestrial ecos

195 e Monitoring Instrument (OMI) on NASA's Aura satellite in 2005-2015.

196 phyll-a concentrations from the NASA's MODIS satellite in combination with hourly to daily observatio

197 rvation of these effects by studying exciton satellites in photoemission and tunneling spectroscopy,

198 016 summertime HCHO column data from the OMI satellite instrument, validated with high-quality aircra

199 e structure that separates the mSPB from the satellite is a distance holder that prevents deleterious

200 standing the long-term performance of global satellite leaf area index (LAI) products is important fo

201 kin, thus leading to larger skin lesions and satellite lesions in IL-1R1(-/-) mice.

202 ese conclusions have implications for future satellite lidar Cal/Val efforts, because planned satelli

203 llite lidar Cal/Val efforts, because planned satellite lidars measuring aerosol backscatter, wind vec

204 equal crossing over may differ among complex satellite loci.

205 Here we combine high-resolution (30 m) satellite maps of forest cover with estimates of the edg

206 001-2007 to the 2008-2014 time periods using satellite measurements of CO and CH4, nearly twice the d

207 Using nine years of satellite measurements of surface stress and geostrophic

208 ns inventory derived from global, coincident satellite measurements, made by the Ozone Monitoring Ins

209 eneration Surface Water and Ocean Topography satellite mission will improve the measured sea surface

210 s of the grounding line before the advent of satellite monitoring in the 1990s are poorly dated.

211 A multifunctional core-satellite nanoconstruct is designed by assembling copper

212 zed approach to design high-performance core-satellite nanohybrids that can be easily tailored to com

213 amine (PDA)-gadolinium-metallofullerene core-satellite nanotheranostic agent (denoted as CDPGM) is de

214 Suv39h KMT and suggest a function for major satellite non-coding RNA in the organization of an RNA-n

215 Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) is an elastic backscatte

216 It is, however, hidden from satellite observation, and a lack of globally consistent

217 nvective system (MCS) was studied using both satellite observations and cloud resolving model (CRM) s

218 DCC in climate models and compare them with satellite observations and reanalysis data.

219 We use satellite observations and the Community Land Model (CLM

220 onal regime without significant change since satellite observations began in 1979.

221 gh-resolution information on water supplies, satellite observations can provide essential insight.

222 Recent advances in satellite observations enable estimates of gross losses

223 We combined satellite observations from passive spectrometer, active

224 Here, using satellite observations from the North Pacific Subtropica

225 Here, we use 35 years of satellite observations from the West African Sahel to re

226 Here, using satellite observations in June-August from 2006 to 2011,

227 each other and showed better agreement with satellite observations in pristine clouds, but they show

228 Models based on MODIS satellite observations matched the cross-site spatial pa

229 th a machine-learning approach that combines satellite observations of AGB with climate data across t

230 Here we use satellite observations to show that China and India are

231 ed Amazon phenology, and improves our use of satellite observations to study climate-phenology relati

232 pon examination of in situ data, reanalysis, satellite observations, and land surface models, we find

233 characteristics to test three hypotheses for satellite-observed canopy reflectance seasonality: seaso

234 satellite artifacts as significant causes of satellite-observed seasonal patterns at this site, imply

235 n by these three factors combined, simulated satellite-observed seasonal patterns well, explaining c.

236 g the preferred locations of heterochromatic satellites of different chromosomes, and observations ab

237 These inconsistencies may be due to NOAA satellite orbit changes and MODIS sensor degradation.

238 sphere sea ice concentration trends over the satellite period between observations and CMIP5 multi-mo

239 We show that the centriolar satellite protein PCM1 regulates the recruitment of GABA

240 ests were modeled from the single-date 500 m satellite record and augmented with the 0- to 11-year-ol

241 Over the full 38-year period of the satellite record, the separation between observed warmin

242 rom long-term (1984-2014) spatially complete satellite records, that increased cloudiness and atmosph

243 Satellite remote sensing data have indicated a general '

244 n land use, chemical transport modeling, and satellite remote sensing data.

245 centromeres contain mainly SCEN-like single satellite repeat (Ss1) and several Ty3/gypsy retrotransp

246 ific mechanism that actively maintains alpha-satellite repeat integrity during human cell proliferati

247 of which contained complex arrays of a 14-kb satellite repeat or its 1.2-kb subunit.

248 nd provides an additional affinity for major satellite repeat RNA.

249 Major satellite repeat transcripts remain chromatin-associated

250 tone H3.1 binding within the megabase, alpha-satellite repeat-containing centromeres of 23 human chro

251 pathway and siRNA from a family of X-linked satellite repeats (1.688(X) repeats) promote X recogniti

252 icroscopy implied that CENP-A protects alpha-satellite repeats from extensive rearrangements.

253 Here, we show that centromeres with more satellite repeats house more nucleosomes that confer cen

254 Thus, in this study, both satellite-retrieved and reanalysis data were used to inv

255 st association between BC concentrations and satellite-retrieved CO, tropospheric NO2, and aerosol op

256 V (SLV) kissing loop junction of the Varkud Satellite ribozyme has been experimentally characterized

257 and in cells, SUV39H1 associates with alpha-satellite RNA transcripts.

258 nant-subordinate status and in their nuclear-satellite roles: Carolina chickadees (Poecile carolinens

259 = 0.73, 0.77, and 0.86 at leaf, canopy, and satellite scales, respectively; P < 0.0001).

260 The emergence of satellite sensors that can routinely observe millions of

261 7) show for human centromeres that all alpha-satellite sequences are transcribed into chromatin-bound

262 and is encoded, in part, by repetitive alpha-satellite sequences, which are retained in cis at their

263 scription is linked to underlying repetitive satellite sequences.

264 pport the central importance of high-quality satellite SIF for studying terrestrial carbon cycle dyna

265 range mixtures by suppressing one-bond (13)C satellite signals in (1)H spectra.

266 The new experiment suppresses one-bond (13)C satellite signals, with high efficiency, at negligible c

267 alized SERS-active metal nanoparticles (core/satellite silver nanoparticles, dimers and monomers of g

268 d August 31, 2015 in the Moorfields main and satellite sites.

269 ta, snow data assimilation model output, and satellite spectral data.

270 of skeletal muscle in adults is mediated by satellite stem cells.

271 These flights combined with the previous satellite study suggest CH4 emissions have not changed.

272 How the growing satellite subsequently inserts into the NE is an open qu

273 Here we use a suite of satellite-supported regional climate simulations in Cali

274 the period 2010-2015 using a combination of satellite, surface and aircraft data.

275 ral Italy), using low-cost Global Navigation Satellite System (GNSS) receivers located in the footwal

276 d-based receivers from the Global Navigation Satellite Systems (GNSS).

277 We analysed a multi-year satellite tag dataset to investigate the habitat use of

278 (b) Autumn migration routes of 12 satellite tagged adult European honey buzzards (colour-c

279 (d) Autumn migration routes of 34 satellite tagged adult Montagu's harriers; migratory tra

280 Using GPS tracking of 38 satellite tagged Pacific black ducks (Anas superciliosa)

281 Seventy satellite tags were deployed on basking sharks over four

282 Data from 28 satellite tags with attachment durations of over 165 day

283 Satellite telemetry allows fine tracking of animal movem

284 Here, we combined satellite telemetry and stable isotope analysis to estim

285 e 1990s, using two independent data sources (satellite telemetry data and passive acoustics) for both

286 s (including migration routes) incorporating satellite telemetry data is therefore crucial to develop

287 prey (narwhal, [Formula: see text] = 7) via satellite telemetry in Admiralty Inlet, a large fjord in

288 Satellite temperature measurements do not support the re

289 Using data from the AMSR-E satellite, this metric is evaluated globally based on di

290 vity Recovery and Climate Experiment (GRACE) satellite to evaluate the sustainability of surface wate

291 Satellite tobacco necrosis virus (STNV) is one of the sm

292 ssion rates that are three times higher than satellite top-down estimates and 35% higher than model p

293 We satellite tracked postnatal dispersal in African penguin

294 f the Caribbean Sea and North Atlantic using satellite-tracked drifter trajectory data, the largest c

295 ir migrations; this adult male is carrying a satellite transmitter.

296 ) self-assembled from quantum-dot-Au (QD-Au) satellite-type HNCs.

297 Here we subdivide satellite vegetation data into those from human-unaffect

298 The Varkud satellite (VS) ribozyme catalyzes site-specific RNA clea

299 interiors of the giant icy planets and their satellites, which has motivated their exploration under

300 mpanied by reduced density of the centriolar satellites, with reexpression of C-NAP1 rescuing both ph