ライフサイエンスコーパス: mole

1 in the absolute sensitivity (counts per unit mole).

2 es/mul, equating to atto-molar (or low zepto-mole).

3 or a level of 9.7% or higher (>/=83 mmol per mole).

4 alt bridge strength of ~3.9 kilocalories per mole.

5 n/BSA mixture and sensitivity down to 1 atto-mole.

6 the star-nosed mole and the common, eastern mole.

7 uces ion binding by several kilocalories per mole.

8 for accurate classification of hydatidiform moles.

9 ers in selected cranial nerves in shrews and moles.

10 ion in diverse species and are not unique to moles.

11 A strong binding constant of 0.55x10(6) L mole(-1) between the HSA-AuNC and bilirubin was discerne

12 cule analyte, 3-phenoxybenzoic acid (214.2 g mole(-1)).

13 lobin level of 6.9% or lower (</=52 mmol per mole), 2.38 (95% CI, 2.02 to 2.80) for a level of 7.0 to

14 or a level of 7.0 to 7.8% (53 to 62 mmol per mole), 3.11 (95% CI, 2.66 to 3.62) for a level of 7.9 to

15 or a level of 7.9 to 8.7% (63 to 72 mmol per mole), 3.65 (95% CI, 3.11 to 4.30) for a level of 8.8 to

16 In this study, upper extremity moles, a higher ability to achieve a tan, and history of

17 the last decade to attain sub-kilojoule per mole accuracy, an order-of-magnitude improvement in cert

18 benzene was predicted with sub-kilojoule per mole accuracy.

19 ally measured value of 45.8 kilocalories per mole (agreeing closely with a value of 45.1 kilocalories

20 led individual sample is mixed with an equal mole amount of a (13)C-labeled pool or control for relat

21 oximately 10(10) and sub-zeptomole (<10(-21) mole) analyte detection were accomplished by coating the

22 01 Gb in African elephant, 3.69 Gb in golden mole and 3.31 Gb in manatee, whereas published results s

23 sn-glycero-3-phospho-L-serine (POPS) 3:1 mol/mole and at neutral pH, the peptide adopts transmembrane

24 h had DeltaDeltaG values less than -6.0 Kcal/mole and for all of them the edited adenosines mis-paire

25 LRP2, cause familial biparental hydatidiform mole and multilocus imprinting disturbance, respectively

26 ous melanomas or traits of familial atypical mole and multiple melanoma syndrome had a higher frequen

27 yndrome), CDKN2 mutations (familial atypical mole and multiple melanoma), or DNA repair gene mutation

28 ory specializations - such as the star-nosed mole and the common, eastern mole.

29 purely androgenetic in complete hydatidiform moles and diandric triploid in partial hydatidiform mole

30 We found that moles and shrews have tiny optic nerves with fiber count

31 TnT with PNIPAAm at 25 (DeltaGcoil=-6.0 Kcal/mole) and 37 degrees C (DeltaGglobular=-41.0 kcal/mole)

32 or a level of 8.8 to 9.6% (73 to 82 mmol per mole), and 8.51 (95% CI, 7.24 to 10.01) for a level of 9

33 xtrapolated DeltaGfold > 60 kilocalories per mole), and their crystal structures are close to those o

34 sts of hantaviruses include rodents, shrews, moles, and bats.

35 hantaviruses in multiple species of shrews, moles, and insectivorous bats from widely separated geog

36 However, the glabrous noses of moles are an exception.

37 Hydatidiform moles are intriguing pathologic entities representing ab

38 DNs), also known as Clark's nevi or atypical moles, are distinguished from common melanocytic nevi by

39 n-butane was 10 times higher than methane by mole at 2 bar, followed by iso-butane and propane.

40 On a per mole basis, amines are much more effective than AS at pr

41 the aromatic ring rather than on a classical mole basis.

42 The first mole-borne hantavirus isolate will facilitate long-overd

43 this hypertrophied cranial nerve, star-nosed mole brains were not larger than predicted from body siz

44 losely with a value of 45.1 kilocalories per mole calculated by density functional theory).

45 ophila melanogaster and a human hydatidiform mole cell line (CHM1) from SMRT sequencing.

46 tellite containing reads in the hydatidiform mole (CHM1, haploid-like) genome.

47 DNA from an essentially haploid hydatidiform mole, CHM1.

48 By mole, cholesterol is the most abundant component of anim

49 ate heating selectively amplifies minor (<25 mole %) components of these solution-phase mixtures.

50 Like mice and rats, the star-nosed mole (Condylura cristata) is a somatosensory specialist.

51 ensory star on the rostrum of the star-nosed mole (Condylura cristata).

52 utine morphologic assessment of hydatidiform moles continues to suffer from interobserver diagnostic

53 ar pattern in preparations of the star-nosed mole cortex and the principal sensory nucleus, we hypoth

54 Rare familial biparental hydatidiform moles (due to NLRP7 or KHDC3L mutations) share such glob

55 nsforms signal intensity values into percent mole enrichment for each isotopologue measured.

56 (47 mole % of Klason lignin for beech and 78 mole % for a high-syringyl transgenic poplar).

57 ately, monomer yields were between 76 and 90 mole % for these three major biomass fractions.

58 etrievals of the column-averaged CO2 dry-air mole fraction ([Formula: see text]) as well as the fluor

59 The column-averaged CO2 dry-air mole fraction (XCO2) observations from satellites and gr

60 twork near the lipid membrane at a bulk DMSO mole fraction (XDMSO) of <0.1, regardless of the lipid c

61 14)CO2) to quantify the recently added CO2ff mole fraction at surface sites surrounding a point sourc

62 ition that is dependent on the subunit/lipid mole fraction density and follows an equilibrium dimeriz

63 y prepare the PSMs, adjusting the calculated mole fraction for the loss bias and an uncertainty calcu

64 oved by up to approximately 3.5x using 0.046 mole fraction heptane in the methanol acceptor.

65 A cPLA2, exhibiting an XI(50) value of 0.011 mole fraction in a mixed micelle assay and an IC50 of 30

66 ixtures are the dominant PBDE input (>99% in mole fraction in AED and ACL, and 94.7% in AMW).

67 DOPE bilayers show that increase of the DOPE mole fraction in general stabilizes interfacial orientat

68 Ambient mole fraction levels were obtained through six levels of

69 N2O) in a dry-natural air balance at ambient mole fraction levels.

70 per thousand, respectively, at a nominal CO2 mole fraction of 400 mumol mol(-1) in air.

71 To this aim, the (30)Si mole fraction of a sample of the new material was measur

72 t the rapid increase of about 50 per cent in mole fraction of atmospheric methane at the Younger Drya

73 ncentration of ATV decreased linearly as the mole fraction of ATV in the formulation decreased and a

74 th 24% of SSA particles containing chloride (mole fraction of Cl/Na >/= 0.1, 90% chloride depletion).

75 Cadaverine mole fraction of lysine plus cadaverine (CF) indicated b

76 K(+) channels, consideration of the membrane mole fraction of PI(4,5)P2 lipids with different acyl ch

77 1 in diacylphosphatidylcholine), but not the mole fraction of POPG (>0.25) in the bilayer-forming pho

78 nge of green to violet by varying the indium mole fraction of the InxGa1-xN MQWs in the range 0.13 </

79 However, the mole fraction of the key monoterpene beta-pinene decreas

80 tates are observed, the mutant increases the mole fraction of the S complex (increasing the duty rati

81 with whole air or synthetic air covered the mole fraction range of (378-420) mumol mol(-1) and were

82 air or synthetic air as the matrix over the mole fraction range of 1600-2100 nmol mol(-1).

83 onmethane hydrocarbon compounds covering the mole fraction range of 60 picomoles per mol to 230 picom

84 The mole fraction solubility of crystalline vanillin was rec

85 The mole fraction solubility of vanillin was observed highes

86 To accurately establish mole fraction trends and to relate measurement records f

87 bilayers (partitioning coefficient ~1200 in mole fraction units), and this is highly unusual for a h

88 The 2011 global mean tropospheric dry air mole fraction was 0.86 +/- 0.04 parts per trillion, resu

89 ateral growth rate occurred when the methane mole fraction was approximately 0.6.

90 work, an independent estimate of the (30)Si mole fraction was obtained by applying a relative measur

91 betagamma, GIRK2 opens as a function of PIP2 mole fraction with Hill coefficient 2.5 and an affinity

92 l measurements of methane and carbon dioxide mole fraction, and isotopic values at King's College Lon

93 d lipid bilayer as a function of cholesterol mole fraction.

94 orespiration and responds to atmospheric CO2 mole fraction.

95 HFC-1234yf was undetectable at Jungfraujoch (mole fractions <0.003 ppt, parts-per-trillion, 10(-12))

96 HCFC-1233zd(E) is present at very low mole fractions (typically <0.03 ppt) at both stations, a

97 Accurate measurements of NO, NO2, and O3 mole fractions allow the calculation of ozone absorption

98 d top-down approaches (measuring atmospheric mole fractions and isotopes) for constraining these geol

99 y two standards of CO2 in air with different mole fractions but identical isotopic composition was de

100 Elevated atmospheric NMHC mole fractions coincided with build-up of ambient 1-h oz

101 c values from preparation and the analytical mole fractions determined from regression illustrate the

102 of C2-C5 nonmethane hydrocarbon (NMHC) mean mole fractions during temperature inversion events in 20

103 surements, retrievals of column-averaged CH4 mole fractions from GOSAT, new wetland inundation estima

104 e percentage of measurements with detectable mole fractions has steadily increased to 4.5% in 2014.

105 We show that phosphoinositide mole fractions in the lipid membrane reach physiological

106 sted significant enhancements in atmospheric mole fractions measured near Houston and surrounding are

107 nts diluted down from standards with nominal mole fractions of 50 mumol/mol.

108 monoterpene beta-pinene decreased, while the mole fractions of alpha-pinene, d-limonene (R-(+)-limone

109 Understanding the effects of small mole fractions of cholesterol should help resolve the co

110 ntal Air, were certified by NIST for ambient mole fractions of CO2, CH4, and N2O relative to NIST PSM

111 hase (H II ) is observed occurring at higher mole fractions of DOPE than in pure water.

112 hosphomimetic mutants and also by increasing mole fractions of DOPS in the proteoliposomes.

113 conductor Cu2Zn(1-x)Fe(x)SnS4 with different mole fractions of iron (x(Fe)) were synthesized by the d

114 o two coexisting micelle populations at high mole fractions of the FC maltoside.

115 e to within about +/-5% with the gravimetric mole fractions of the hydrocarbons.

116 ane hydrocarbons (NMHCs) suggest atmospheric mole fractions ranging from low picomoles per mol (ppt)

117 ents of key monoterpenes suggest atmospheric mole fractions ranging from low pmol/mol (parts-per-tril

118 ide bandgap MgZnO thin films with various Mg mole fractions were grown on c-sapphire substrate using

119 pecific compositions (i.e., Si, Al, and NaOH mole fractions) using colloidal silica and sodium alumin

120 AlxCrCoFeNi for Al ranging from 0 </= x </=2 mole fractions, and find that the HEA shows large chemic

121 At low mole fractions, cholesterol segregates into 10- to 100-n

122 networks started monitoring atmospheric CH4 mole fractions.

123 appear at the 0.18-0.26 range of cholesterol mole fractions.

124 of relative fluorescence signals to absolute mole fractions.

125 eaching task (a variant of the arcade whac-a-mole game) in which money could be earned if players hit

126 d data generated from a haploid hydatidiform mole genome (CHM1) and a diploid human genome (NA12878)

127 However, clinically atypical moles have not been previously recognized as a component

128 l ratios from 0.25 x 10(-19) to 25 x 10(-19) moles-Hg/cell (equivalent to Hg/cell-SH of 0.71 to 71) s

129 red hair colors, higher number of extremity moles, higher susceptibility to sunburn as a child/adole

130 s an energy between 15 and 35 kilojoules per mole, hydrogen bonding can be a strong driver of molecul

131 nd infers amphibious ancestries of echidnas, moles, hyraxes, and elephants, offering a fresh perspect

132 It is similar to extant subterranean golden moles in having reduced digit segments as compared to th

133 nd diandric triploid in partial hydatidiform moles) is a fundamental genetic event leading to global

134 thane C-H bond cleavage is 9.5 kilojoule per mole (kJ/mol) lower than the binding energy of the adsor

135 isk was higher in women who had at least one mole larger than 3 mm in diameter on their left arms (ha

136 ote that the tactile fovea of the star-nosed mole, located on the medial ventral ray, does not have i

137 For example, the familial atypical multiple mole melanoma (FAMMM) syndrome, related to a gene mutati

138 ncreased, whereas the stabilizing effect per mole of all saccharides decreased.

139 ecreased, whereas the stabilizing effect per mole of all saccharides increased, and that the absolute

140 mounts with 2 mol of AgNPs oxidized for each mole of chlorine added.

141 es at 230 kelvin are about 14 kilojoules per mole of crystallite more stable than hexagonal crystalli

142 used by a higher electron release (3e(-) per mole of Fe(0)) from Pd-NZVI in the butanol organic phase

143 ion with TCE in the aqueous phase (2e(-) per mole of Fe(0)).

144 0.9 mbar CO2, the amount of captured CO2 per mole of IL in the near-surface region is quantified to ~

145 o 0.93 +/- 0.04 moles of ritonavir bound per mole of inactivated CYP3A4.

146 rate is more effective than nitrate on a per mole of inhibitor basis.

147 ation is two mole of TEMPOL consumed for one mole of LH and one mole of LOOH.

148 f TEMPOL consumed for one mole of LH and one mole of LOOH.

149 3.2 mol of succinic anhydride/mole of lysine content gave maximum degree of succinylat

150 before fragmenting by at least 600 kcal per mole of monomer.

151 globin level of 6.9% or less (</=52 mmol per mole of nonglycated hemoglobin) was 1.92 (95% CI, 1.75 t

152 ar (*)OH yields (moles of (*)OH produced per mole of ozone consumed) were 21 +/- 3% for g O3/g DOC =

153 quency reaching 18,046 moles of hydrogen per mole of platinum per hour.

154 energy-efficient fuel and yield more ATP per mole of substrate than pyruvate and increase the free en

155 er of moles of ozone required to oxidize one mole of sulfide to sulfate) of 2.91, which is comparable

156 stoichiometry of the adduct formation is two mole of TEMPOL consumed for one mole of LH and one mole

157 e energies of activation of viscous flow per mole of the solvents (Deltamu1(0 not equal)) and of the

158 and the values range from -56 to -177 kJ per mole of TMAAI.

159 The average molar (*)OH yields (moles of (*)OH produced per mole of ozone consumed) were

160 x 10(9) moles of reduced sulphur and 10(10) moles of CO2, promoting the formation of ca. 1.19 Mt of

161 n average turnover frequency reaching 18,046 moles of hydrogen per mole of platinum per hour.

162 sponds to 2x10(-9) g in 0.5 ml or 23x10(-15) moles of inhibited BChE in 0.5 ml of plasma.

163 radii from 2.5 to 9.5 nm and with up to 10% moles of ions.

164 development providing up to 2.6-18 x 10(18) moles of O2 equivalents to the Earth system.

165 sulted in a stoichiometric factor (number of moles of ozone required to oxidize one mole of sulfide t

166 nic activity has produced around 3.1 x 10(9) moles of reduced sulphur and 10(10) moles of CO2, promot

167 binding stoichiometry equal to 0.93 +/- 0.04 moles of ritonavir bound per mole of inactivated CYP3A4.

168 uses (1)H NMR to quantify both the number of moles of the reference and of the studied compound prese

169 a two-step, one-pot process and requires 2-8 mole % of 3,3'-Ph2 -BINOL as the optimal catalyst.

170 With 1.0 to 5.0 mole % of a molybdenum-based catalyst, which may be deli

171 yields during subsequent hydrogenolysis (47 mole % of Klason lignin for beech and 78 mole % for a hi

172 been identified in five species of fossorial moles (order Eulipotyphla, family Talpidae) from Eurasia

173 rated, with an equimolar feed enriched to 81 mole % para-xylene, without phase change and at ambient

174 and can be performed with as little as 0.25 mole per cent catalyst in less than six hours at room te

175 ied out in high yield with as little as 0.01 mole per cent catalyst with a moisture- and air-tolerant

176 Transformations typically proceed with 5.0 mole per cent of the complex and an inexpensive reaction

177 ontinental lithosphere of 0.36-2.27 x 10(11) moles per year is comparable to estimates from marine sy

178 was thought to be negligible (0.009 x 10(11) moles per year).

179 tions (hydration) are in the range of 10(11) moles per year.

180 Catalyst loadings as low as 0.01 mole percent and preparative scalability (25 grams) are

181 t do not specify how tracer enrichment (i.e. mole percent excess (MPE) or tracer-to-tracee ratio (TTR

182 ian silicate [(Mg,Fe)SiO3] with nominally 10 mole percent Fe.

183 oadings of Earth-abundant initiators (1 to 5 mole percent) and occurs under mild conditions (30 degre

184 d generate olefins at low loadings (0.3 to 2 mole percent) and temperatures (22 degrees to 80 degrees

185 unding membrane, e.g., phospholipid content, mole percentage of cholesterol, and the presence of lipi

186 onent analysis of 27 individual fatty acids (mole percentage) was the main exposure (subsequently cal

187 Apart from the atypical mole phenotype, development of new melanocytic nevi in o

188 325 nmol mol(-1) (ppb) but at micromole per mole (ppm) levels as well.

189 nal and behavioral factors associated with a mole-prone phenotype in adolescents.

190 e (age, 14 years) that are associated with a mole-prone phenotype in late adolescence (age, 17 years)

191 Main Outcome and Measures: Mole-prone phenotype in the 11th grade, defined as total

192 cally recognizable factors associated with a mole-prone phenotype that may facilitate the identificat

193 1.36-13.25; P = .01) were associated with a mole-prone phenotype.

194 rs), 111 participants (26.6%) demonstrated a mole-prone phenotype: 69 students (62.2%) with 1 nevus g

195 re found to be the same as expected from the mole proportions of monomers in polymerizing solutions u

196 the paternal genome in sporadic hydatidiform moles (purely androgenetic in complete hydatidiform mole

197 /MS) is used to determine the identities and mole quantities of mitochondrial metabolites using authe

198 x volume is combined with the aforementioned mole quantities to calculate the matrix concentrations o

199 n of DNA and RNA molecules down to the zepto-mole range.

200 The blind mole rat (BMR), Spalax galili, is an excellent model for

201 The naked mole rat (Heterocephalus glaber) is a long-lived and tum

202 The naked mole rat (Heterocephalus glaber) is an exceptionally lon

203 Recent studies in naked mole rat and long-lived sea urchins showed that these sp

204 campal and olfactory structures of the naked mole rat brain.

205 neuronal migration are not unusual in naked mole rat brains.

206 HMW-HA triggers hypersensitivity of naked mole rat cells to contact inhibition, which is associate

207 ped a freely available web portal, the Naked Mole Rat Genome Resource, featuring the data and results

208 Tumor resistance in the naked mole rat is mediated by the extracellular matrix compone

209 When overexpressed in naked mole rat or human cells, pALT(INK4a/b) has stronger abil

210 is present in both cultured cells and naked mole rat tissues but is absent in human and mouse cells.

211 nsistent with exceptional endurance of naked mole rat tissues to various genotoxic stresses.

212 entify a mechanism responsible for the naked mole rat's cancer resistance.

213 ve contributed to the evolution of the naked mole rat's extraordinary traits, including in regions of

214 erested in the genome and genes of the naked mole rat, and also to facilitate further studies on this

215 bonobo/chimpanzee, guinea pig/degu/tuco-tuco/mole rat, and cattle/yak.

216 T(INK4a/b) of the INK4a/b locus in the naked mole rat, contributes to the increased resistance to tum

217 Here, we show that, in the naked mole rat, the INK4a/b locus encodes an additional produc

218 In naked mole-rat (NMR) colonies, breeding is monopolized by the

219 Here we cloned naked mole-rat ASIC3 (nmrASIC3) and used a cell-surface biotin

220 Furthermore, the naked mole-rat cells are more sensitive to HA signalling, as t

221 essing the HA-degrading enzyme, HYAL2, naked mole-rat cells become susceptible to malignant transform

222 f mouse fibroblasts fails to transform naked mole-rat cells.

223 ersibly inhibits ASIC-like currents in naked mole-rat dorsal root ganglia neurons.

224 We found that naked mole-rat fibroblasts secrete extremely high-molecular-ma

225 sh and amphibians, suggesting that the naked mole-rat is a powerful model for exploring the mechanism

226 t that 28S ribosomal RNA (rRNA) of the naked mole-rat is processed into two smaller fragments of uneq

227 RF and urocortin 3, respectively, in African mole-rat species with diametrically opposed social behav

228 the long lifespans observed in many bat and mole-rat species.

229 During anoxia, the naked mole-rat switches to anaerobic metabolism fueled by fruc

230 ctose-driven glycolytic respiration in naked mole-rat tissues avoids feedback inhibition of glycolysi

231 ay reflect a further adaptation of the naked mole-rat to living in an environment with high-carbon di

232 The African naked mole-rat's (Heterocephalus glaber) social and subterrane

233 The preternaturally long-lived naked mole-rat, like other long-lived species and experimental

234 n time (12 and 36 h), protein:monosaccharide mole ratio (1:1 or 1:3) and moiety type, compared to unp

235 pretargeting parameters: a BsMAb-to-peptide mole ratio of 20 and 30 h pretargeting delay.

236 By altering the mole ratio of sodium citrate/sodium alginate, the degrad

237 3:1 mole ratio of Span 60:Tween 60, 4mg/ml of alpha-TOC and

238 ween 60, 4mg/ml of alpha-TOC and 25:12.5:2.5 mole ratio of surfactant:Chol:DCP was the optimum formul

239 miting value, however, as the sulfur to iron mole ratio was greater than 0.025.

240 In C4, the TF2-to-peptide mole ratio was increased to 40 (delay 30 h), resulting i

241 ds to the production of metgas (H2/CO in 2:1 mole ratio) for exclusive methanol synthesis.

242 The variations in critical packing mole ratios can be explained by global effects of headgr

243 real-time measurements of Ne, Ar, Kr, and Xe mole ratios in natural waters.

244 ometry, I2 was observed in the atmosphere at mole ratios of 0.3-1.0 ppt, and in the snowpack intersti

245 Experiments were carried out at two mole ratios of tocopherols to beta-carotene, i.e. at 1:1

246 ppt, and in the snowpack interstitial air at mole ratios up to 22 ppt under natural sunlit conditions

247 is 0.7% or better and 1.0% or better for all mole ratios when the instrument is installed in a temper

248 urfactants (Span60 and Tween60) in different mole ratios, presence or absence of cholesterol (Chol) a

249 In contrast, some studies of social mole rats (including naked mole rats, Heterocephalus gla

250 Naked mole rats (NMRs) live in sizable colonies where breeding

251 cer-prone mice and almost cancer-proof naked mole rats and blind mole rats.

252 is consistent with the hypothesis that naked mole rats are neotenous, with retention of juvenile char

253 Naked mole rats are the longest-living rodents, whose nervous

254 of nonreproductive individuals in Damaraland mole rats closely resembles that found in other cooperat

255 ial DNA in the control region and ATP6 in 28 mole rats from basalt and in 14 from chalk habitats.

256 We speculate that naked mole rats have evolved a higher concentration of HA in t

257 Overall, we conclude that naked mole rats show an extremely protracted period of brain m

258 rats, Heterocephalus glaber, and Damaraland mole rats, Fukomys damarensis) suggest that individual d

259 studies of social mole rats (including naked mole rats, Heterocephalus glaber, and Damaraland mole ra

260 Here we show that, in Damaraland mole rats, individual contributions to cooperative behav

261 ge from 4 years in mice to 32 years in naked mole rats.

262 lmost cancer-proof naked mole rats and blind mole rats.

263 Naked mole-rats (Heterocephalus glaber) live in groups that ar

264 ranscriptomic data from 26 bat species, five mole-rats and 38 outgroup species.

265 GF1 axis relates to the longevity of African mole-rats and bats, we compared and analysed the homolog

266 udied in species with reduced vision such as mole-rats and bats.

267 nd examined Nrf2-signaling activity in naked mole-rats and nine other rodent species with varying max

268 Cape mole-rats are solitary; they tolerate conspecifics only

269 at which the level of CRF1 binding in naked mole-rats exceeds that in Cape mole-rats include the bas

270 s; in contrast, the level is greater in Cape mole-rats in the shell of the nucleus accumbens and medi

271 ing, the sites with a greater level in naked mole-rats include the basolateral amygdaloid nucleus and

272 ding in naked mole-rats exceeds that in Cape mole-rats include the basolateral amygdaloid nucleus, hi

273 odents were found to be more conserved, with mole-rats lacking uniquely conserved amino acid substitu

274 Naked mole-rats live in large eusocial colonies that are chara

275 RF1 binding in the nucleus accumbens of Cape mole-rats reflects their lack of affiliative behavior.

276 Under experimental conditions, naked mole-rats tolerate hours of extreme hypoxia and survive

277 r binding densities in female and male naked mole-rats varying in breeding status.

278 he neurobiology of social hierarchy in naked mole-rats, and add to a growing body of work that links

279 Naked mole-rats, despite having functional ASICs, are insensit

280 performed optic nerve injury in adult naked mole-rats, the longest living rodent, with a maximum lif

281 kedly from this pattern are bats and African mole-rats, with members of both groups being extremely l

282 ular nucleus display a greater level in Cape mole-rats.

283 s were under purifying selection in bats and mole-rats.

284 The energy used per liquid mole recovered ranges from 920 to 52,000 kJ/mol and is a

285 an previously mapped receptive fields in the mole's principal sensory nucleus.

286 obtained in 85% yield over two steps on a 1-mole scale from commercially available 4-amino-2,2,6,6-t

287 in asymmetric synthesis, we have developed a mole-scale, two-step synthesis of a 1:1 mixture of the d

288 ave therefore named this phenomenon "whack-a-mole" sensitivity, after a popular fun park game.

289 specific phylogenetic pattern of the Chinese mole shrew (Anourosorex squamipes) in southwest China th

290 imum (LIG) was an unfavorable period for the mole shrews because of a high degree of seasonality; A.

291 ceanic mercury inventory by 36-1,313 million moles since the 1500s.

292 s) weighing only a few grams and much larger mole species weighing up to 90 grams.

293 noma-related worry in patients with atypical mole syndrome (AMS).

294 virus (NVAV), from lung tissue of a European mole (Talpa europaea), captured in central Poland in Aug

295 In most species of moles, the skin on the nose is covered with domed mechan

296 wide range of lifestyles, from burrowing in moles to flying in bats.

297 umber-average molar mass 21.4 kilograms per mole) to a mixture of linear poly[7-26]catenanes, branch

298 The star-nosed mole was an outlier, with more than twice the number of

299 and 37 degrees C (DeltaGglobular=-41.0 kcal/mole) were calculated to elucidate the interaction and s

300 in the global ocean to be 290 +/- 80 million moles, with almost two-thirds residing in water shallowe