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 alt bridge strength of ~3.9 kilocalories per mole.

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

5 ate the involvement of LIGHT in hydatidiform moles.

6 for accurate classification of hydatidiform moles.

7 lopment of masculinizing ovotestes in female moles.

8 iderable ring strain (30-50 kilocalories per mole)(2,3) that characterizes these transient intermedia

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

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

11 cetate reduction (2 mole methane formation/1 mole acetate consumption), coupling of acetoclastic meth

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

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

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

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

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

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

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

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

20 e with high palladium (Pd) loading (e.g., 10 mole %) and a need for (super)stoichiometric quantities

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

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

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

24 Hydatidiform moles are intriguing pathologic entities representing ab

25 Hydatidiform moles are known to pose an extremely high risk of severe

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

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

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

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

30 discovery of genetically distinct shrew- and mole-borne viruses belonging to the newly defined family

31 For 13 of the 20 symptoms (abnormal mole, breast lump, post-menopausal bleeding, rectal blee

32 , whereas the opposite was true for abnormal mole, breast lump, postmenopausal bleeding, and rectal b

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

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

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

36 pore sequencing of the complete hydatidiform mole CHM13 genome, combined with complementary technolog

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

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

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

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

41 Transgenic mice with a knock-in mole CYP17A1 enhancer or overexpressing FGF9 showed phen

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

43 l transfer efficiency [100% x moles MCCA-oil moles electrons(-1)] of 74% at 15 A m(-2).

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

45 are familiar with the meandering tunnels of moles, far fewer are familiar with the creatures that ma

46 (47 mole % of Klason lignin for beech and 78 mole % for a high-syringyl transgenic poplar).

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

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

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

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

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

52 We analyzed vertical atmospheric CO(2) mole fraction data obtained onboard commercial aircraft

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

54 or CH(2)Cl(2) and C(2)Cl(4), the majority of mole fraction enhancements were observed from the north,

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

56 (CH(4)) is a potent greenhouse gas, and its mole fraction has more than doubled since the preindustr

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

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

59 The R712G mutant increased the mole fraction in the post-power-stroke conformation in t

60 Ambient mole fraction levels were obtained through six levels of

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

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

63 increasing cholesterol content approaching a mole fraction of 50%.

64 to an accuracy of +/-1 carbon number and the mole fraction of a mixture component to within an averag

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

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

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

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

69 t recently available data on the atmospheric mole fraction of CO(2), measured from six sites across C

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

71 ed and their stability with reference to the mole fraction of oxygen.

72 em can be tailored by simply controlling the mole fraction of PEG lipid, producing bilayers with diff

73 lex rather than a simple way with increasing mole fraction of the acid from 0 to 0.7, reflecting the

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

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

76 ary mixture used for this work had a methane mole fraction of x(methane,grav) = (0.506875 +/- 0.00019

77 grav) = (0.506875 +/- 0.00019) and a propane mole fraction of x(propane,grav) = (0.493125 +/- 0.00019

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

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

80 The mole fraction solubility of crystalline vanillin was rec

81 The mole fraction solubility of vanillin was observed highes

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

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

84 Changes with PGPC mole fraction, X(PGPC), of the area of the shorter wavel

85 orespiration and responds to atmospheric CO2 mole fraction.

86 ilarly, regardless of the ganglioside or its mole fraction.

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

88 fractions are formed by control of PEG lipid mole fraction.

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

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

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

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

93 Direct-to-indirect bandgap crossover Al mole fractions for c-phase AlGaN and AlInN alloys are de

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

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

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

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

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

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

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

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

102 pre- and post-power stroke conformations and mole fractions of these conformations were not altered b

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

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

105 networks started monitoring atmospheric CH4 mole fractions.

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

107 ter uptake of the polymer (as moles of water/mole H(+)) is 5-10x greater than that of Nafion.

108 radation over water (up to 240 moles TCE per mole H(2) O), with an electron efficiency of up to 70%,

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

110 d nevus density at age 21 years (many vs. no moles hazard ratio [95% confidence interval] = 4.91 [2.8

111 ELISA in 17 women with complete hydatidiform mole (HM) and 20 gestational-age-matched normal pregnant

112 h an apparent quantum yield of 1.37 x 10(-3) moles hydrogen per moles incident photons.

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

114 um yield of 1.37 x 10(-3) moles hydrogen per moles incident photons.

115 GHT in the trophoblast cells of hydatidiform mole induces sFlt-1, which might underlie the pathogenic

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

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

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

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

120 1)) and MCCA-oil transfer efficiency [100% x moles MCCA-oil moles electrons(-1)] of 74% at 15 A m(-2)

121 Familial atypical multiple mole melanoma (FAMMM) syndrome is a hereditary cancer sy

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

123 Jeghers syndrome, familial atypical multiple mole melanoma, Lynch syndrome (hereditary nonpolyposis c

124 The complete acetate reduction (2 mole methane formation/1 mole acetate consumption), coup

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

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

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

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

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

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

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

132 3.2 mol of succinic anhydride/mole of lysine content gave maximum degree of succinylat

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

134 , taking advantage of its high ATP yield per mole of O(2).

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

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

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

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

139 te that between 1.2 x 10(8) and 1.3 x 10(10) moles of carbon dioxide per year are released from the s

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

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

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

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

144 The water uptake of the polymer (as moles of water/mole H(+)) is 5-10x greater than that of

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

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

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

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

149 GF9, which is heterochronically expressed in mole ovotestes.

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

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

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

153 limoles per square centimeter per hour (3660 moles per kilogram of catalyst per hour).

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

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

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

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

158 0.002, 0.034 +/- 0.002, and 0.046 +/- 0.003 mole percentage excess, respectively; P < 0.001).

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

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

161 ncapsulation (as high as 114 mol% taxane per mole phospholipid) and subsequent stability (>3 years at

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

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

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

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

166 1.36-13.25; P = .01) were associated with a mole-prone phenotype.

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

168 ) Composition of the imprinted polymer, (the mole proportions of AN and MSAN), and the concentrations

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

184 erriding anti-cancer mechanisms of the naked mole rat.

185 The Ansell's mole-rat (Fukomys anselli) has been the subject of many

186 brain atlas was available only for the naked mole-rat (Heterocephalus glaber).

187 The subterranean-dwelling naked mole-rat (NM-R; Heterocephalus glaber) exhibits prolonge

188 monstrated by us and Liang et al. that naked mole-rat (NMR) cells are more resistant to SV40LT and H-

189 Naked mole-rat (NMR), the longest-living rodent, produces very

190 of HA in the cancer resistance of the naked mole-rat (NMR), we undertook to explore the structural a

191 o a growing list of adaptations in the naked mole-rat and provides a plausible proximate mechanism fo

192 ompertz's law 'uniquely identifies the naked mole-rat as a non-aging mammal'.

193 from the brain of the closely related naked mole-rat as well as from epigeic mammals (rat), with a p

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

195 resent a comprehensive atlas of the Ansell's mole-rat brain based on Nissl and Kluver-Barrera stained

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

197 We found that the p53 protein in naked mole-rat embryonic fibroblasts (NEFs) exhibits a half-li

198 In addition, the AITC-insensitive highveld mole-rat exhibited overexpression of the leak channel NA

199 Analysis of the naked mole-rat genome revealed, uniquely among mammals, a hist

200 unique evolutionary trajectories in African mole-rat hearing and establishes species members as natu

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

202 The naked mole-rat is a subterranean rodent, approximately the siz

203 and human p53, a larger proportion of naked mole-rat p53 protein is constitutively localized in the

204 ermined that the long half-life of the naked mole-rat p53 protein reflects protein-extrinsic regulati

205 l nuclear localization of p53 in NEFs, naked mole-rat p53 retains its canonical tumor suppressive act

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

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

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

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

210 African rodent species related to the naked mole-rat with the painful substances capsaicin, acid (hy

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

212 the p53 protein may contribute to the naked mole-rat's remarkable resistance to cancer.

213 s induced by oncogenic Ras than mouse, blind mole-rat, and human cells, revealing suppressed Ras sign

214 ed in long-lived species including the naked mole-rat, bats, and the bowhead whale, but these adaptat

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

216 nderlying the cancer resistance of the naked mole-rat, we investigated the regulation and function of

217 mutated tumor suppressor, TP53, in the naked mole-rat.

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

219 A mole ratio of hydrogen to carbon monoxide near unity (H(

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

221 3:1 mole ratio of Span 60:Tween 60, 4mg/ml of alpha-TOC and

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

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

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

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

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

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

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

229 Chol:PCer mole ratios were 3:1, 3:2, and 3:3, at a fixed 7:3 phosp

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

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

232 deal bicelles even at low lipid-to-detergent mole ratios.

233 bils (Meriones unguiculatus), and Damaraland mole rats (Fukomys damarensis), another subterranean rod

234 Compared to many other rodent species, naked mole rats (Heterocephalus glaber) have elevated auditory

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

236 Naked mole rats (NMRs) are currently one of the most popular n

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

238 chondria of various tissues from mice, naked mole rats (NMRs), and bats possess two mechanistically s

239 Naked and Damaraland mole rats also showed reduced lateral and medial efferen

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

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

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

243 r innervation in mature and developing naked mole rats compared to mice (Mus musculus), gerbils (Meri

244 Damaraland mole rats showed no evidence of postnatal reorganization

245 Developmentally, naked mole rats showed reduced and prolonged postnatal reorgan

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

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

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

249 conspicuously, in both naked and Damaraland mole rats, inner hair cell (IHC) afferent ribbon density

250 lopmental refinement in naked and Damaraland mole rats.

251 hared similarly between naked and Damaraland mole rats.

252 ed a Kaplan-Meier survival analysis of naked mole-rats (Heterocephalus glaber) and concluded that the

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

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

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

256 hearing in naked and the related Damaraland mole-rats and to examine whether these alterations resul

257 Naked mole-rats are adapted to living in a low-oxygen and high

258 Naked mole-rats are highly vocal, eusocial, subterranean roden

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

260 African mole-rats are subterranean rodents that spend their whol

261 the diminished function of KCC2, adult naked mole-rats demonstrate a reduced efficacy of inhibition t

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

263 pharmacological intervention, in adult naked mole-rats exposed to a simulated hyperthermic surface en

264 e molecular changes likely rendered highveld mole-rats immune to the stings of the Natal droptail ant

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

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

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

268 ings suggest that altered hearing in African mole-rats is adaptive, perhaps tailoring hearing to euso

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

270 neuronal activity, we studied whether naked mole-rats might demonstrate energy savings in GABAergic

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

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

273 African naked mole-rats were likely the first mammals to evolve eusoci

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

275 orical lifespan data on more than 3200 naked mole-rats, collected over a total observation period of

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

277 kely mechanism of altered hearing in African mole-rats, making them the only identified mammals natur

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

279 olony behavioral monitoring of captive naked mole-rats, we found a durable nest, characterized by hig

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

281 tion in outer hair cells isolated from naked mole-rats.

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

283 essing FGF9 showed phenotypes recapitulating mole sexual features.

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

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

286 rption capacity, and the energy released per mole sorbed NH(3)(g) indicated stronger bonds formed wit

287 soil niche has given rise to a diversity of mole species that could be said to resemble the evolutio

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

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

290 omosome-scale genome assembly of the Iberian mole, Talpa occidentalis, with transcriptomic, epigeneti

291 ve for TCE degradation over water (up to 240 moles TCE per mole H(2) O), with an electron efficiency

292 delicate wings were the key innovation, for moles the forelimbs have undergone a similarly dramatic

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

294 s composed of DPPC:DSPC:DSPE-PEG2k (80:15:5, mole%) then reached 12 wt% loading, 4-fold greater than

295 CI 1-3; eight of 584 patients) for abnormal mole to 80% (71-87; 84 of 105 patients) for neck lump.

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

297 pond to changes in absolute nutrient amount (moles) vs. its concentration in water (molarity).

298 identify distinct dose responses to either N-moles, W-volume, N-molarity (N/W), or their synergistic

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

300 es reliably produces benign nevi (pigmented 'moles'), yet the same change is the most common driver m