ライフサイエンスコーパス: atm

1 r frequency of 360 h(-1) at 25 degrees C/1.0 atm H(2).

2 Under the optimal conditions of 1.0 atm H2 using n-BuNH2 as a base and with added water, a t

3 Air at an inlet pressure of 1.0 atm is used as carrier gas, and a vacuum pump is used to

4 he MOF is remarkable because at 78 K and 1.0 atm it sorbs hydrogen at a density near that of liquid h

5 ear that of liquid hydrogen (at 20 K and 1.0 atm) when considering H2 density in the pores.

6 assigned to receive either moderate FPI (2.0 atm) only, moderate FPI+severe HH (40 mm Hg for 45 min)

7 mized to sham, mild (1.2 atm), moderate (2.0 atm) or severe (2.3 atm) TBI.

8 -10 degrees to +60 degrees C and at 1.0-5.0 atm propylene pressure (at 60 degrees C) reveal that act

9 alized only under ultrahigh pressure (20,000 atm, 160 degrees C) and only produces oligomers.

10 ts a pressure difference of -0.036 +/- 0.004 atm (pressure higher in the matrix) and a surface tensio

11 oscopy, and had the same Km constants (0.022 atm, 5.4 mM).

12 nimum outward pressure of approximately 0.06 atm.

13 concentration (10(-5)-1 M), and PCO(2) (0-1 atm).

14 ndency at low pressures and maximized at 0.1 atm C(2)H(2) with a subsequent decrease in steady-state

15 fluid percussion (FP) brain injury (1.8-2.1 atm) was induced in male Sprague-Dawley rats.

16 ted to mild (1.1-1.4 atm), moderate (1.8-2.1 atm), or severe (2.2-2.7 atm) fluid percussion (FP) inju

17 osmolality of growth, from approximately 3.1 atm at 0.03 Osm to approximately 1.5 at 0.1 Osm and to l

18 ed in acidic aqueous solutions (pH = 0-6), 1 atm 25% H2/Ar, and elevated temperatures (tested from 29

19 ilize the 2-iodophenol, 5 equiv of alkyne, 1 atm of CO, 5 mol % Pd(OAc)2, 2 equiv of pyridine, and 1

20 Increasing pressure from ambient (1 atm) pressure to pressures as high as 9 atm leads to a i

21 Consequently, at 298 K and 1 atm [Cu(bpy-1)(2)(SiF(6))] exhibits a relative uptake of

22 d one effective at ambient temperature and 1 atm air or O(2).

23 est uptake for CO(2) yet seen at 298 K and 1 atm by a PCP that does not contain open metal sites.

24 iron dicarbyne at ambient temperature and 1 atm H2 results in release of a CO-derived olefin.

25 ency of 3400 h(-1) at room temperature and 1 atm of 1:1 CO2:H2 (74,000 h(-1) at 20 atm) in tetrahydro

26 iates using a copper chloride catalyst and 1 atm of air as the terminal oxidant is described.

27 ltriaz-1-enes in the presence of DABCO and 1 atm of carbon monoxide in toluene at 80 degrees C gave t

28 iments were performed at (298 +/- 2) K and 1 atm of NOx-free air in a 1080 L photoreactor with in sit

29 ient conditions (i.e., at 20 degrees C and 1 atm pressure), air- and moisture-stable, and recyclable;

30 a, at CO partial pressure between 0.25 and 1 atm under thermophilic conditions.

31 under mild conditions (<400 degrees C and 1 atm) was demonstrated using germanium 2,6-dibutylphenoxi

32 K and 1 atm; 98 cm(3)/g CO(2) at 273 K and 1 atm), even in the absence of open metal sites.

33 t pressure and temperature (NPT, 300 K and 1 atm).

34 ambient conditions (i.e., 25 degrees C and 1 atm).

35 5 cm(3) g(-1) , respectively, at 273 K and 1 atm, is exceptionally high among cationic framework mate

36 etween 0.82 and 1.46 wt % H(2) at 77 K and 1 atm, with enthalpies of adsorption in the range 6.0-8.8

37 reaction time of 1 min at 25 degrees C and 1 atm.

38 with an uptake of 201 cm(3)/g at 295 K and 1 atm.

39 drogen uptake of up to 2.5 wt% at 77 K and 1 atm.

40 ake of 196 cm(3) (STP) cm(-3) at 295 K and 1 atm.

41 at can activate H2 at room temperature and 1 atm.

42 e capacity (ca. 1.89 wt % H(2) at 77 K and 1 atm; 98 cm(3)/g CO(2) at 273 K and 1 atm), even in the a

43 unprecedentedly mild conditions-as low as 1 atm of H(2) and 25 degrees C.

44 capacity (e.g., 70.6 cm(3)/g for CO(2) at 1 atm and 273 K), suggesting that the charged anionic fram

45 he reaction of MSA and methylamine (MA) at 1 atm and 294 K in the presence and absence of water vapor

46 nsertion of CO2 gas to give Pd-OC(O)CH3 at 1 atm and 298 K.

47 Additionally, at 1 atm and 77 K, uptake (at least with low Li(+) loading) i

48 Accurate (+/-2%) values of D(T) at 1 atm are obtained with the contact-free, laser-flash meth

49 CO, 8.5% CO(2), 22% H(2)O, and 37% H(2) at 1 atm for Au/Al(2)O(3) catalysts at 180 degrees C and Au/T

50 degrees C, isobutylene (IB) polymerizes at 1 atm in weakly coordinating solvents containing 10 wt % L

51 tion in a physiological buffer solution at 1 atm O(2) pressure.

52 and relatively fast (complete in <1 h) at 1 atm of dinitrogen.

53 O2 with alpha carbon-centered radicals at 1 atm of N2 are estimated as r(CH2NH2) = 0.79 +/- 0.15, r(

54 earing a pyridine bisimidazoline ligand at 1 atm of O2, alpha- and beta-substituted styrenes were cle

55 At 1 atm pressure and 298 K, Li forms a body-centered cubic l

56 mmediate hydrogenation if exposed to H2 at 1 atm pressure in benzene, affording the silane borane 5-H

57 h the atmosphere over the drop was O(2) at 1 atm pressure, the wired BOD disk scavenged the O(2) so e

58 ted partial pressures of CO(2) (pCO(2)) at 1 atm total pressure, on the carbonation rate of brucite [

59 tively facile (t(1/2) approximately 1 h at 1 atm) and depends upon dinitrogen pressure, in contrast t

60 pability ( approximately 90 cm(3) g(-1) at 1 atm, 273 K, among the highest in Zr-MOFs) but also high

61 f the NC is insensitive to oxygen, even at 1 atm, whereas excited states of both osmium complexes are

62 when the solution is purged with O2 gas at 1 atm.

63 2O, 2,2'-bipyridine, and an O2 atmosphere (1 atm), allows the rapid assembly of either benzimidazoles

64 C, Fe/220 degrees C, or Rh/190 degrees C (1 atm, CO:H(2) 1:1, "mild conditions") contain terminal (1

65 under very mild conditions (-78 degrees C, 1 atm ethylene, 4 mol % catalyst) to give the correspondin

66 Under mild conditions (25 degrees C, 1 atm H2), the supported Cp*ZrMe3, Cp*ZrBz3, and Cp*ZrPh3

67 Exposure of 1 to ca. 1 atm of CO(2) results in the production of methylene diol

68 rature over 24 h but reacted with CO2 (ca. 1 atm) to generate [Zn3(mu-H)2(mu-1,1-O2CH)] (3).

69 3 reacted with CO (1 atm) and various isonitriles under ambient condition, an

70 uantitative oxygen-atom transfer from CO2 (1 atm) at ambient temperature to generate t-butyl formate

71 under atmospherically relevant conditions (1 atm and 30% relative humidity).

72 d benzenes in water under mild conditions (1 atm H2, ambient temperature) with degradation half-lives

73 uorobenzene under mild aqueous conditions (1 atm of H(2), ambient temperature) was developed and the

74 se trialkylsiloxy-1,3-dienes and ethylene (1 atm) as precursors and readily available (bis-phosphine)

75 inylation (HV) when treated with ethylene (1 atm) at room temperature in the presence of [(S,S)-2,4-b

76 and in the case of cyclohexane, ethylene (1 atm) can trap the [(PNP)Ti(CH2(t)Bu)] fragment to form 1

77 e unstable but can exchange with ethylene (1 atm) to form 1 and the free alpha-olefin.

78 (15) to Li(5)B, over a pressure range from 1 atm to 300 GPa.

79 Elevated N2 pressures (>1 atm) have a dramatic effect on catalysis, increasing N2

80 reversibly with a second equivalent of H2 (1 atm) and serves as an olefin hydrogenation catalyst unde

81 to 10(13) molecules of ozone per cm(3) in 1 atm helium to model ozone-limited and ozone-rich troposp

82 xide and carbon dioxide, active under just 1 atm of carbon dioxide pressure, are reported.

83 At 298 K (1 atm), tunneling is predicted to enhance the thermal deca

84 and 20 s(-1) H2 oxidation; pH = 1, 348 K, 1 atm 25% H2/Ar) than the other two derivatives.

85 U-Bai 43 reaches 198 cm(3) (STP: 273.15 K, 1 atm) cm(-3) at 298 K and 65 bar, which is amongst the hi

86 with H2, D2, or NH3 under identical, mild (1 atm, 65 degrees C) conditions showed that SnAr2' reacted

87 pidly and reversibly with carbon monoxide (1 atm) at 25 degrees C to form [Ni(CO)(PCy2NBz2)2](BF4)2,

88 urred when 1a-f were exposed to air or N2 (1 atm), yielding {mer-kappaC,N,C'-(Ar-2-yl)CH2N horizontal

89 equiv of pyridine, 1 equiv of n-Bu(4)NCl, 1 atm of CO, a reaction temperature of 100 degrees C, and

90 e dependence of air breakdown voltage near 1 atm is sublinear, allowing higher E/N values to be reach

91 rption is driven by H2(g) at a pressure of 1 atm in a non-irradiated dry system.

92 OFs), measured at 77 K up to a pressure of 1 atm, have been examined for correlations with their stru

93 of 50 degrees C and a constant pressure of 1 atm.

94 ally simple conditions (1 equiv of olefin, 1 atm O2 or air) with reduced Pd(II)/bis-sulfoxide catalys

95 ysts in toluene at 60 degrees C under only 1 atm of hydrogen gas.

96 Notably, an ethylene pressure of only 1 atm was required.

97 als are already marginally metallic at P = 1 atm and the combination of high and low phonon frequenci

98 ase diagram, the only stable phases at P = 1 atm are the numerous polytypes of the simplest 1:1 stoic

99 The P = 1 atm structures are all semiconducting.

100 Several competitive ground-state P = 1 atm structures are found, perforce with Si-Si bonds, and

101 te and amorphous structures for SiO at P = 1 atm, and crystalline phases also at pressures up to 200

102 ecular units and are semiconducting at P = 1 atm, and some form metallic and superconducting symmetri

103 At P = 1 atm, stability is found for the experimentally known LiB

104 /mol for the barriers at T = 310 K and p = 1 atm.

105 perature (100 degrees C) and low pressure (1 atm).

106 t under mild conditions (room temperature, 1 atm H2).

107 nitrous oxide (uptake at room temperature, 1 atm; release at 323 K).

108 ds 3 equiv of hydrogen at room temperature/1 atm to form the series of compounds Pt3Re2(CO)6(PBut3)3(

109 f reactions conducted with air rather than 1 atm O2.

110 uroprotectants when applied in addition to 1 atm of air.

111 e eta5,eta3-4,5-dihydroindenediyl rings to 1 atm of dihydrogen afforded the tetrahydroindenyl zirconi

112 Exposure of the N2 compounds to 1 atm of dihydrogen resulted in rapid N H bond formation t

113 Upon exposure to 1 atm of O(2) at 100% RH, the SAMs become less densely pac

114 onduction over a pO2 range from 10(-20) to 1 atm with a bulk conductivity of 2.2 x 10(-3) S cm(-1) at

115 Fe(2)(S(2)C(2)H(4))(CNMe)(3)(CO)(3) under 1 atm CO gives the deep pink tricarbonyl [Fe(2)(S(2)C(2)H(

116 gy efficiency (180 mV overpotential) under 1 atm H2 , and 144,000 s(-1) (460 mV overpotential) under

117 2+), oxidizes H2 at 60 s(-1) in MeCN under 1 atm H2 with an unoptimized overpotential of ca. 500 mV u

118 ectrons and protons at -78 degrees C under 1 atm N2 (4.6 equiv NH3/Fe).

119 can be generated at room temperature under 1 atm N2 and are shown to react with E-H bonds from PhSiH3

120 s N2 silylation with Me3SiCl and KC8 under 1 atm N2 at ambient temperature.

121 Under 1 atm of carbon monoxide and at room temperature in methan

122 ynes by N-substituted o-iodoanilines under 1 atm of carbon monoxide results in the formation of 3,4-d

123 H3N; X = Cl, Br) with sodium amalgam under 1 atm of dinitrogen afforded the square pyramidal, high sp

124 variously substituted benzoic acids under 1 atm of O(2) or air is achieved under nonacidic condition

125 ss balance and high turnover numbers under 1 atm of O2 with no need for any additives.

126 yclic carbonates at room temperature under 1 atm pressure.

127 uptake (201.6 cm(3) g(-1) at 196 K, under 1 atm) and acetone (5 wt %), a sorption property that was

128 MR relaxographic data were collected under 1 atm.

129 Both 1-N(2) and 2-N(2) react with 1 atm H(2) to generate thermally stable H(2) complexes 1-H

130 On the other hand, xenon (1 atm) stabilized myoglobin.

131 riving force did not exceed 70 g m(-2) s(-1) atm(-1).

132 ent coronary stent deployment starting at 10 atm and increased serially by 2 atm until the FFR was >/

133 blast wave with incident overpressure of 10 atm.

134 ith osmotic pressures in the range of 10-100 atm or lower.

135 arbon sequestration (GCS) environment at 100 atm of CO(2) and 90 degrees C.

136 t mineral precipitation at 90 degrees C, 100 atm CO2, and 1 M NaCl, conditions relevant to GCS sites.

137 magnetic effects at partial pressures of 100 atm (PO(2)), which may be used to probe membrane protein

138 approximately 0.001 at pressures to over 100 atm, has a frictional behaviour resembling that of artic

139 levant to GCS sites (55-95 degrees C and 102 atm CO(2)).

140 relevant to GCS sites (95 degrees C and 102 atm CO2).

141 as a vapor pressure of approximately 10(-11) atm.

142 ercritical CO2 at high pressures (90 and 110 atm) and low temperatures (35 and 50 degrees C).

143 H2Cl2 solution under 0.30 atm of H2 and 0.13 atm of O2 converted to H2O in the presence of 1 and 10 m

144 unts of analytes and at low pressure, 80-130 atm, typically below the range of other methods.

145 4,000 s(-1) (460 mV overpotential) under 133 atm H2.

146 roken Macondo riser stub ( approximately 153 atm and 4.3 degrees C).

147 lly by 2 atm until the FFR was >/=0.94 or 16 atm was achieved.

148 in 32 patients after deployment at 14 to 16 atm with their delivery balloon system.

149 ible addition of hydrogen to 3b (K(eq) = 190 atm(-1) at 25 degrees C).

150 original FeMo cofactor signal at > or = 0.2 atm N2.

151 ventilated and randomized to sham, mild (1.2 atm), moderate (2.0 atm) or severe (2.3 atm) TBI.

152 arting at 10 atm and increased serially by 2 atm until the FFR was >/=0.94 or 16 atm was achieved.

153 yl bromides that proceeds at low pressure (2 atm CO) under mild conditions.

154 ixed p(CO2(g)) values (from 10(-5) to 10(-2) atm).

155 rge (1,000s of ppmV) fluctuations in [CO(2)](atm) did not characterize ancient climates and that past

156 Empirical estimates of [CO(2)](atm) during Paleozoic and Mesozoic greenhouse climates a

157 We report that greenhouse [CO(2)](atm) have been significantly overestimated because previ

158 ng atmospheric CO(2) concentrations ([CO(2)](atm)) during Earth's ancient greenhouse episodes is esse

159 More accurate [CO(2)](atm), resulting from better constraints on soil CO(2), i

160 nst a pressure difference of up to 40 +/- 20 atm.

161 ckage DNA, generating up to approximately 20 atm of internal capsid pressure.

162 ould be carried out with a TON of 5800 at 20 atm (58% yield).

163 ld be carried out with a TON of 22,500 at 20 atm (75% yield), while ethenolysis of 10,000 equiv of cy

164 and 1 atm of 1:1 CO2:H2 (74,000 h(-1) at 20 atm) in tetrahydrofuran.

165 asingly built-up internal pressure (up to 20 atm) in the capsid.

166 ic solvents at 80-100 degrees C and under 20 atm (at 25 degrees C) of a 4:1 mixture of CO-air, in the

167 -3.0 mol % catalyst at 22 degrees C under 20 atm ethylene.

168 ite such as P(OEt)(3) and P(OPh)(3) under 20 atm of CO, affords the corresponding 2-formylmethyl-1-si

169 2000 atm but changes dramatically for P>2000 atm.

170 lowly upon increasing pressures P up to 2000 atm but changes dramatically for P>2000 atm.

171 ditions (pH 7, 22 degrees C, and PO2 of 0.21 atm), which were about 60 and 350 times of the oxidation

172 With the collection vial at 25 atm, the trapping efficiencies of different solvents wer

173 The best results were obtained at 25 atm.

174 peratures and pressures (2 degrees C and 250 atm), we estimate that the metabolic lifespan for a larv

175 cedures, high-pressure angioplasty (up to 27 atm) was unsuccessful.

176 (1.2 atm), moderate (2.0 atm) or severe (2.3 atm) TBI.

177 Six rates of glucose (3 atm% (13) C) addition (in the range 0-1 mg glucose g(-1)

178 ure and was complete at a H(2) pressure of 3 atm; SO(4)(2-) reduction began at H(2) >/= 3.4 atm.

179 s have an air leak rate of 1.1 x 10(-3) cm(3)atm/m(2)/day, and a mechanical shear strength higher tha

180 A CH2Cl2 solution under 0.30 atm of H2 and 0.13 atm of O2 converted to H2O in the pre

181 reaction conditions (ethylene pressure 5-30 atm and 20-70 degrees C).

182 lar flow reactor at elevated pressures (5-30 atm) and temperatures (800-950 degrees C).

183 manufacturer recommended burst pressure (30 atm) for the treatment of resistant hemodialysis-related

184 the median inflation pressure was 20 (8-30) atm.

185 supercritical CO(2) at 35 degrees C and 300 atm.

186 nreactive molecule at 650 degrees C and 3000 atm pressure, a small fraction of the fullerene molecule

187 inserted into C(60) by heating C(60) in 3000 atm of xenon gas at 650 degrees C.

188 ined in a hypobaric chamber at 290 Torr (0.4 atm) for 21 days and allowed to recover at normoxia (roo

189 oups of rats were subjected to mild (1.1-1.4 atm), moderate (1.8-2.1 atm), or severe (2.2-2.7 atm) fl

190 erwent daily treatment: HBO (90 minutes, 2.4 atm); systemic administration of the free radical scaven

191 ir affinities (b) of 2-5 atm(-1) (median 3.4 atm(-1)).

192 m; SO(4)(2-) reduction began at H(2) >/= 3.4 atm.

193 ero- and carbocycles with 5 mol % iron and 4 atm H(2) at 23 degrees C.

194 At 22 degrees C and 4 atm of H2 pressure, ((iPr)CNC)CoCH3 is an effective prec

195 ts at a sustained hydrodynamic pressure of 4 atm for 10 s.

196 Monitoring the addition of 4 atm of CO by NMR spectroscopy allowed observation of an

197 is(indenyl)zirconium sandwich complexes to 4 atm of H2 resulted in facile oxidative addition to furni

198 d related amides at room temperature under 4 atm H2 pressure to give chiral alcohols with up to 99% y

199 ng a bench-stable cobalt precatalyst under 4 atm of H2 is reported herein.

200 hosphabenzene is shown to be reduced under 4 atm of H2 to give [3.1.0]bicylo reduction products, with

201 heric pCO2 must have been less than 10(-1.4) atm--about 100 times today's level of 360 p.p.m., and at

202 of added water and a large excess of CO2 (40 atm), in addition to CuCl2 and TsOH, caused a significan

203 vely mild conditions (100 degrees C under 40 atm of a 4/1 mixture of CO and air).

204 nd divide in a wide range of pressure (1-400 atm) and temperature (23-40 degrees C).

205 al behavior at pressures between 250 and 400 atm for all the temperatures studied in our experiments.

206 ate to be packaged to a pressure of about 45 atm, factors that are likely to be important during memb

207 oximately 10%) SFCO2 at 70 degrees C and 477 atm, with 0.083 mg of Re/g of SFCO2 extracted.

208 ximately 1.5 at 0.1 Osm and to less than 0.5 atm above 0.5 Osm.

209 h equilibrium binding pressures of below 0.5 atm of CO.

210 loxane operated at an outlet pressure of 0.5 atm provides up to 4 x 10(4) theoretical plates and a pe

211 study examined the effects of mild (1.4-1.5 atm) parasagittal fluid-percussion injury on the electro

212 g(-1)), with Langmuir affinities (b) of 2-5 atm(-1) (median 3.4 atm(-1)).

213 Carotid artery dilation (2.5 atm) and complete endothelial denudation were performed

214 resolving power of 102 when operated at 2.5 atm.

215 rocedure, rats were treated with HBO2 at 3.5 atm absolute (ATA) for 60 min and exhibited an anti-allo

216 lvent with added KOtBu at 50 degrees C and 5 atm H2.

217 nors via exposure to high pressures of NO (5 atm) under basic conditions.

218 functionalities with high pressures of NO (5 atm).

219 Applying osmotic gradients of +/-5 atm, when assuming a fixed trans-bilayer lipid mass dist

220 The calculated pressure (~5 atm) shows that the ejection of DNA into Gram-negative b

221 Rats were exposed to 5 atm (gauge pressure) 100% O(2) until seizures recorded b

222 When the mixture of 5- 7 is exposed to 5 atm H 2 for 1 h (the conditions used for catalyst preact

223 ing a chalcogen partial pressure <6 x 10(-5) atm.

224 hromosome fusions in fifth generation (G(5)) atm tert mutants required the presence of only one criti

225 gorous conditions of 50-100 degrees C and 50 atm H2.

226 ith added Et(3)N and at 100 degrees C and 50 atm initial H(2) pressure.

227 50 to 125 degrees C and at a pressure of 50 atm.

228 hat ultimately are able to withstand over 50 atm of pressure during genome packaging.

229 ensing under hydrostatic pressures up to 510 atm, a range suitable for studying a wide variety of cel

230 pressure is increased from 0 to 800 psi (54 atm) at 23 degrees C, the physical diffusion coefficient

231 lity spectrometer operating from 0.4 to 1.55 atm in a supporting atmosphere of purified air was used

232 e process even at a pressure as high as 1.58 atm inside the HFM, due to the low dissolved CO concentr

233 sequence (NF-SC) TFD for 45 min at 78 psi (6 atm).

234 essure differences of up to approximately 60 atm during replication.

235 function at high pressures (up to about 680 atm).

236 cm(3) g(-1)); b 0.4-1.7 atm(-1) (median 0.7 atm(-1))].

237 m(3) g(-1) (median 7 cm(3) g(-1)); b 0.4-1.7 atm(-1) (median 0.7 atm(-1))].

238 , moderate (1.8-2.1 atm), or severe (2.2-2.7 atm) fluid percussion (FP) injury (or sham surgery) and

239 he milder conditions of 22 degrees C and 3.7 atm H2 is a nonnanocluster, homogeneous catalyst, most l

240 ng platinum(IV) oxide as the catalyst at 3.7 atm, providing the aminoindolizidines in modest-to-high

241 r pressure (p'L,eff) of approximately 10(-7) atm and an enthalpy of vaporization (DeltaHvap,eff) of a

242 , T = 150 degrees C and P(H)2 = 1.0 x 10(-7) atm), DeltaG(+ +) for C-H addition to ((Me)PCP)Ir (plus

243 egrees C under a 5/2 mixture of CO-CO2 at 70 atm in the presence of the PdI2/KI catalytic system.

244 n CH3CN under hydrogen pressures of up to 70 atm.

245 ip with high sensitivity (K(SV) = 584 +/- 71 atm(-1)).

246 n the system outlet pressure from 0.1 to 0.8 atm lead to proportional increases in detector sensitivi

247 is implemented at outlet pressures up to 0.8 atm using a low-dead-volume polymer-coated surface acous

248 vessels, low-pressure balloon dilation to 8 atm was performed, and if it was not successful, the ves

249 t (1 atm) pressure to pressures as high as 9 atm leads to a increase in transfection efficiency from

250 um hydroxide) reduced the p'L,eff to <10(-9) atm and increased the DeltaHvap,eff to >80 kJ/mol, at le

251 ite) in a multiphase water/scCO2 fluid at 90 atm pressure and 50 degrees C was studied in situ, with

252 p to a pressure of 400 MPa (0.1 MPa = 0.9869 atm).

253 In contrast, mre-11 and atm-1 are dispensable for ATL-1 recruitment to stalled r

254 ases ataxia telangiectasia mutated (ATM) and atm and rad3-related (ATR).

255 ssion, the combination of defects in atr and atm exacerbates the fragmentation observed in the atm si

256 Arabidopsis atr and atm mutants display hypersensitivity to gamma-irradiatio

257 cs aspects of the phenotypes of both atr and atm mutants in Arabidopsis, suggesting that SOG1 partici

258 Mutant atr and atm seeds are highly resistant to aging, establishing AT

259 0 human lenses were imaged at 2 atmospheres (atm) pressure and the T(1) (spin-lattice) and T(2) (spin

260 cing the fragmentation seen in atm or in atr atm.

261 bination of either the atm single or the atr atm double mutant with a spo11 defect eliminates the ect

262 d interacting effects of water availability, atm.

263 ow climate change, elevated atmospheric CO2 (atm.

264 f the atmospheric concentration of CO2 ([CO2]atm) during warm periods of Earth's history is important

265 High Eocene [CO2]atm is established from sodium carbonate minerals formed

266 ning of fossil fuels may produce future [CO2]atm approaching 1000 parts per million by volume (ppm).

267 ncentrations), which confirms that high [CO2]atm coincided with Eocene warmth.

268 n contact with the atmosphere indicates [CO2]atm > 1125 ppm (four times preindustrial concentrations)

269 enetic and cytological studies on Drosophila atm and mre11 knockout mutants and discovered a telomere

270 n homologous chromosome ends are greater for atm tert than tert plants.

271 activity (up to 4.2x10(2) kg mol(-1) h(-1>) atm(-1>) ) and AO incorporation (up to 12 % at 0.2 m [AO

272 n biology, with pressures in the few-hundred-atm range having significant effects on cellular morphol

273 chromosome end protection is compromised in atm atr mutants.

274 The most dramatic TRD was detected in atm tert mutants that had undergone meiosis.

275 at which the spontaneous events occurred in atm and trp53 mutant mice.

276 The frequency of homologous recombination in atm mutant mice was increased later during development.

277 unrearranged Sgamma3 segment are reduced in atm(-/-) cells.

278 ificantly reducing the fragmentation seen in atm or in atr atm.

279 am acceptor S regions during CSR and that in atm(-/-) cells Smu DSBs accumulate as they lack a recomb

280 We find that in atm(-/-) cells Smu DSBs are increased, whereas DSBs in d

281 ivities (up to 10(7) g of polymer/(mol of Ln.atm ethylene.h)) and narrow product polymer polydispersi

282 ass in the dark (kH* = (2.09-4.17) x 10(6) M atm(-1)), and the presence of an OH source increased the

283 ve Henry's Law constant of 1.3-5.5 x 10(7) M atm(-1).

284 ClO as DeltaG(s) of -2.9 kcal/mol and 5.5 M/atm, respectively.

285 ive stress, is measured to be 56.9 +/- 2.6 M/atm (n = 3) at 37.4 degrees C with 1 mg of the material

286 high Henry's law coefficient (1.7 x 10(8) M/atm).

287 Moreover, atm tert Arabidopsis experience an abrupt, early onset o

288 highest in an area at mean pH 7.6 (1,827 (mu)atm p(CO(2))) where coralline algal biomass was signific

289 Mice homozygous for null alleles of atm reproduce the radiation sensitivity and high-tumor i

290 g, when the total vapor pressure reaches one atm, and the difference in pK(a) value for the acid and

291 235 versus 620+/-103 and 526+/-104 L/min per atm CO(2); P:=0.0001 and P:<0.0001, respectively) and ch

292 m is engaged that cell autonomously requires atm (ataxia telangiectasia mutated), atr (ATM and Rad3-r

293 rammed breaks: the combination of either the atm single or the atr atm double mutant with a spo11 def

294 xacerbates the fragmentation observed in the atm single mutant, prevents complete synapsis of chromos

295 cycle activity in the Purkinje cells of the atm+/- heterozygote mouse.

296 ctivities (up to 107 g of polymer/(mol of Ti.atm ethylene.h)), narrow product copolymer polydispersit

297 se to aging, ATM delays germination, whereas atm mutant seeds germinate with extensive chromosomal ab

298 e S-phase checkpoint and also cooperate with atm-1 in the checkpoint response to DSBs after ionizing

299 transformation frequencies was detected with atm, atr, lig4, xrcc1, or parp1 mutants.

300 ated by replication stress and function with atm-1 following DSB resection.