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

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

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

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

7 -10 degrees to +60 degrees C and at 1.0-5.0 atm propylene pressure (at 60 degrees C) reveal that act

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

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

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

11 nimum outward pressure of approximately 0.06 atm.

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

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

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

15 yde, and arylamine in water medium under a 1 atm carbon dioxide (CO(2)) atmosphere.

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

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

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

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

20 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

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

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

23 reaction free energy profile at 300 K and 1 atm of CH(4) shows no effective energy barriers in the s

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

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

26 eakthrough studies at room temperature and 1 atm show a C(2) H(2) /CO(2) breakthrough time up to 79 m

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

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

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

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

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

32 5 cm(3) g(-1) , respectively, at 273 K and 1 atm, is exceptionally high among cationic framework mate

33 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

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

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

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

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

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

39 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

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

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

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

43 ptake capacity as high as 166.8 cm(3)/g at 1 atm and 298 K, more than twice that of peroxo-MOF-74-Fe,

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

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

46 as capable of heterolytic H(2) cleavage at 1 atm and room temperature, representing, for the first ti

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

48 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

49 -1) (298 K) and 330 cm(3) g(-1) (273 K) at 1 atm for CPM-733-dps (the Co(2) V-BDC form, BDC=1,4-benze

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 ate with high activity (up to 364 h(-1) at 1 atm or 3330 h(-1) at 20 atm of 1:1 H(2):CO(2)).

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

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

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

59 The C(2) H(2) uptake capacity at 1 atm reaches 193.0 cm(3) g(-1) (8.6 mmol g(-1) ) at 273 K

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

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

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

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

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

65 for type A or B species that dominated at 1 atm.

66 2O, 2,2'-bipyridine, and an O2 atmosphere (1 atm), allows the rapid assembly of either benzimidazoles

67 depressurized (i.e., system pressure below 1 atm) batch cultures, nitrogen (or other inert gases) is

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

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

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

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

72 3 reacted with CO (1 atm) and various isonitriles under ambient condition, an

73 lting anionic methylidene couples with CO (1 atm) at low temperature (-78 degrees C) to release ethen

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

89 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

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

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

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

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

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

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

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

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

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

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

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

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

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

103 The P = 1 atm structures are all semiconducting.

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

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

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

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

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

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

110 agents under mild reaction conditions (RT, 1 atm), affording the corresponding disilylketenes, Xant(L

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

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

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

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

115 ses) is used to repressurize the system to 1 atm before taking sample; while for continuous cultures,

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

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

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

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

120 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

121 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(

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

123 2+), oxidizes H2 at 60 s(-1) in MeCN under 1 atm H2 with an unoptimized overpotential of ca. 500 mV u

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

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

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

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

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

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

130 loying an excess of (t) Bu(3) ArO(.) under 1 atm of NH(3) gas at 23 degrees C resulted in up to ten t

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

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

133 yclic carbonates at room temperature under 1 atm pressure.

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

135 cluding difluoro- and fluorobenzene, using 1 atm of H(2), alkoxide bases, and moderate temperatures (

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

137 es up to 3400 Kg copolymer mol(-1) -Zr h(-1) atm(-1) , and with comonomer enchainment up to 5.5 mol %

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

139 blast wave with incident overpressure of 10 atm.

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

141 es (200-300 degrees C) and pressures (50-100 atm) using a copper-zinc-based heterogeneous catalyst.

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

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

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

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

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

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

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

149 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

150 4,000 s(-1) (460 mV overpotential) under 133 atm H2.

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

152 en further controlling the pressure to ~0.17 atm in the steaming-collection unisystem, the water coll

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

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

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

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

157 ramping of xenon-rich gas mixtures (up to 2 atm partial pressure).

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

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

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

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

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

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

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

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

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

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

168 up to 364 h(-1) at 1 atm or 3330 h(-1) at 20 atm of 1:1 H(2):CO(2)).

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

170 ncrease in TOF under ideal HB conditions (20 atm reactant pressure and 400 degrees C) for the Si-dope

171 at a much decreased reactant pressure of 20 atm at 500 degrees C, or alternatively at temperature an

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

173 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

174 -3.0 mol % catalyst at 22 degrees C under 20 atm ethylene.

175 t can achieve the same TOF of pure Fe at 200 atm/500 degrees C under much milder conditions, e.g. at

176 OF) under typical extreme HB conditions (200 atm reactant pressure and 500 degrees C) and a ~43-fold

177 2000 atm but changes dramatically for P>2000 atm.

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

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

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

181 (1.2 atm), moderate (2.0 atm) or severe (2.3 atm) TBI.

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

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

184 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

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

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

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

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

189 ethylamine at 80 degrees C for 24 h under 30 atm of a 1:4 mixture of CO-air.

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

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

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

193 multistep gated sorption of CO(2) below 0.33 atm.

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

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

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

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

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

199 of the phenylimine rhodium precatalyst and 4 atm of H(2) in THF, the manganese nitride ((tBu)Salen)Mn

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

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

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

203 CH(2) Ph, which upon hydrogenolysis under 4 atm H(2) produced the corresponding aldehyde and cobalt

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

227 icon at extreme pressures of ~ 50 MPa (~ 500 atm) have been observed to generate remarkably smooth su

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

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

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

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

232 t pressure decreased to 400 degrees C and 60 atm, respectively.

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

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

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

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

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

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

239 ions between 1,700 and 2,100 K and 4 and 4.7 atm using shock tube and ultrafast, time-resolve laser a

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

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

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

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

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

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

246 mperature (>125 degrees C) and pressure (>80 atm).

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

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

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

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

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

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

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

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

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

256 0 human lenses were imaged at 2 atmospheres (atm) pressure and the T(1) (spin-lattice) and T(2) (spin

257 tand water pressure of about 20 atmospheres (atm) for the species Sepia officinalis Currently, our kn

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

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

260 d interacting effects of water availability, atm.

261 ow climate change, elevated atmospheric CO2 (atm.

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

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

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

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

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

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

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

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

270 rees C are as high as 4208 and 535 kg/(mol h atm) with AO incorporation up to 4.0 mol % and 1.6 mol %

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

272 171-fold phosphorylation that was absent in atm mutant lines.

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 Cs with C* < 10(8) mug m(-3) and H > 10(2) M atm(-1).

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

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

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

286 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

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

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

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

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

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

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.