ライフサイエンスコーパス: C

1 C. africana was rapidly and reliably identified by micro

2 C. sativa threshing residues were biorefined by consecut

3 absorbed radiation dose from whole-body (11)C-nicotine PET imaging of 11 healthy (5 male and 6 femal

4 uction in mGluR5 availability (that is, [(11)C]ABP688 binding) in both MDD and control subjects (aver

5 centration leading to a 50% reduction of (11)C-BMT-136088 specific binding were 73 +/- 30 nmol/kg and

6 udy assessed the in vivo distribution of (11)C-nicotine and the absorbed radiation dose from whole-bo

7 were studied using the TSPO radioligand (11)C-(R)-PK11195.

8 (PET) and the MOR-selective radioligand [(11)C]carfentanil.

9 It is demonstrated that [(11)C]-(R)-3 readily crosses the blood-brain barrier (BBB) i

10 we investigate whether changes of (13)C/(12)C, (2)H/(1)H, and (15)N/(14)N ratios of NDMA give rise t

11 d fourfold increases (+ c. 4 mug excess (13) C) compared with nonsibling pairs.

12 g pairs exhibited significantly greater (13) C transfer to recipient roots in two of four Douglas-fir

13 (13)C-flux analysis showed that Pkm2 deletion reduced the fl

14 through MR detection of increased HP [1-(13)C]pyruvate-to-lactate conversion.

15 ydroqui noline is reported, the (1)H and (13)C NMR data of which are in excellent agreement with thos

16 constitution elucidated unambiguously by (13)C and (15)N isotopic labeling.

17 f CO2 in air of known but differing delta(13)C and delta(18)O isotopic composition allows standard un

18 .48 per thousand to be achieved for delta(13)C and delta(18)O measurements, respectively.

19 o reassessment of the role that the delta(13)C record plays in reconstructing the oxygenation of eart

20 mits, the carbonate carbon isotope (delta(13)C) record becomes insensitive to changes in organic carb

21 ch (LambdaC-H = Deltadelta(2)H/Deltadelta(13)C approximately epsilonbulk(H)/epsilonbulk(C), where Del

22 k(C), where Deltadelta(2)H and Deltadelta(13)C are changes in isotope ratios during degradation) resu

23 n enhancement using (13)C-diazomethane" ((13)C-TrEnDi), which results in the methyl esterification of

24 In this paper, we dissolve (13)C-labeled calcites in natural seawater.

25 y differentiated from those arising from (13)C-labeled tracers, thereby allowing the enrichment of a

26 awake rats as measured by ex vivo (1)H-[(13)C]-nuclear magnetic resonance spectroscopy.

27 We used (2)H/(13)C metabolic flux analysis to quantify intermediary metab

28 All participants had (13)C-spirulina GE breath test T1/2 values of 79 minutes or

29 This work establishes hyperpolarized [(13)C]-Glyc as a novel agent for clinically relevant (13)C M

30 olved oxygen, high pH, and enrichment of (13)C in CO2) indicate that upwelling of cold, nutrient-rich

31 Here, we investigate whether changes of (13)C/(12)C, (2)H/(1)H, and (15)N/(14)N ratios of NDMA give

32 fragments are detected either by (1)H or (13)C NMR.

33 as a novel agent for clinically relevant (13)C MRS studies of energy metabolism and further provides

34 to as "trimethylation enhancement using (13)C-diazomethane" ((13)C-TrEnDi), which results in the met

35 ermediate, yielding (C5 Me5 )2 Th[kappa(2) -(C,C')-(CH2 )(CH2 )PPh2 ]Cl.

36 ific capacity of about 130 mA h g(-1) at 35 C (fully charged within 100 s) and sustain more than 10

37 insight into the mechanistic details of hm(5)C function to be obtained, the availability of RNAs cont

38 ly disordered C-terminal linker (CTL), and a C-terminal conserved peptide (CTC).

39 -C bonds at a single carbon center bearing a C(sp(3)) organoboron functional group.

40 construct triaryl(heteroaryl)methanes via a C-H functionalization in good to excellent yield, and re

41 entially lost over monovalent cations upon A.C protonation, providing experimental indication of the

42 Here, we show that lamin A/C expressing cells can form an actin cap to resist nucle

43 have been engineered to catalyze abiological C-H bond amination reactions, but the yields of these re

44 Accordingly, C. cohnii was characterised by a high level of sulfur co

45 riction mimetics are mainly effective across C. elegans strains, indicating species and strain-specif

46 um-magnesium and lithium-zinc amides affords C-2 or C-8 functionalized derivatives in a regioselectiv

47 heal administration of DEPs activated airway C-fibers.

48 rica and has potential to dramatically alter C cycling and accumulation in these ecosystems.

49 However, on microarray analysis C-82 treatment strongly up-regulated two clusters of gen

50 erved sortase A-dependent cell wall-anchored C terminus, whereas the surface-exposed N terminus is hi

51 .9 nA/mug mL(-1), T = 1.4 nA/mug mL(-1), and C = 15.1 9 nA/mug mL(-1)), low limit of detection (G, A

52 viral replicative capacity of subtypes A and C may paradoxically contribute to their more efficient s

53 prenylated natural products boropinols A and C.

54 roup at day 10, the SAAs of both Adelta- and C-fibers at the "ascending" phase of microcontractions w

55 ds through inter- and intramolecular C-C and C-N bond formation.

56 idation and the construction of both C-C and C-N bonds.

57 5)-10(-6)), whereas C-->G, U-->A, G-->C, and C-->A errors from purine-purine and pyrimidine-pyrimidin

58 ase-3/7) and lung deposition of collagen and C' (C5b-9).

59 s is developed via C-H functionalization and C-N bond formation.

60 ationships between the functional groups and C-H bonds of a substrate has been exploited to achieve m

61 at (IMF) was lower for GSPC than for GSC and C.

62 proteins to test whether DAT and SERT N and C termini contribute to transporter substrate and inhibi

63 We find that both the N- and C-terminal domains of TTP are involved in an interaction

64 f respiratory yeasts such as P. pastoris and C. albicans, and it may have novel moonlighting function

65 ng Drosophila eye, we found that partial APC/C inactivation severely inhibits retinal differentiation

66 Apolipoprotein C-III (apoC-III) is a key regulator of lipoprotein metab

67 adult patients with AML, the response to Ara-C-containing therapy was inversely correlated with SAMHD

68 lective ortho-specific nitration of aromatic C(sp(2))-H bonds using chelation-assisted removable vici

69 Three independent observers (A, B, C) measured PVRs at two different time points during the

70 ased on the trnL gene were designed (A-, B-, C- and D-trnL systems).

71 The enzymatic beta-C-H hydroxylation of the feedstock chemical isobutyric a

72 s on the formation of hydrogen bonds between C-terminal residues of lentil peptides and residues of t

73 omeostasis (PHO) to TORC1 may differ between C. albicans and S. cerevisiae The converse direction of

74 us flow protocol has been developed for bond C-H activation which promotes the alpha-cyanation of sec

75 cular amidation and the construction of both C-C and C-N bonds.

76 s, suppression of bone turnover (assessed by C-terminal telopeptide levels).

77 liable estimates of the total forest carbon (C) pool are lacking due to insufficient information on d

78 r quantifying their impact on forest carbon (C) uptake.

79 Coastal wetlands are sites of rapid carbon (C) sequestration and contain large soil C stocks.

80 an emission line of singly ionized carbon ([C ii] at a wavelength of 158 micrometres) in four galaxi

81 in, we report a silver-free Pd(II)-catalyzed C(sp(3))-H arylation of saturated bicyclic and tricyclic

82 dditionally, many transition-metal-catalyzed C-H bond additions to polarized pi bonds occur within ca

83 summarizes the advancements in Pd-catalyzed C(sp(3))-H activation via various redox manifolds, inclu

84 ces of this challenge, we have characterized C. neoformans GMP synthase, the second enzyme in the gua

85 he benchmark Pt/C catalyst, the optimized Co@C-800 (carbonized at 800 degrees C) exhibited high oxyge

86 of diphenyl sulfide also showed competitive C-S bond cleavage giving phenyl sulfinic acid and ioniza

87 highly Lewis acidic borane with concomitant C-H or C-C bond formation.

88 In contrast, C-strand length decreases continuously, indicating a def

89 frequencies between affecteds and controls (C/TTCTG: gamma(2) value = 0.014; p = 0.904).

90 nnectivity was examined by cross-correlating C-IN discharge.

91 Daily C assimilation was greater at elevated [CO2 ] in both cu

92 s compared to 0-47% degradation at 0 degrees C (1000 m), where the aromatic hydrocarbons fluoranthene

93 y exposed to cold treatment (40 d, 0 degrees C) and an additional group of CH fruits were pre-conditi

94 nd 8.5% (95% CI, 1.5%-15.0%) for a 1 degrees C increase in monthly MIT at <15, 15-64, and >/=65 years

95 The reaction in chloroform at 100 degrees C under Rh2(OAc)4 catalysis provides 4-aminopyrrole-3-ca

96 In the sediment heated up to 100 degrees C, we found unexpectedly low DOC concentrations in the p

97 PCB from phycocyanin and gave at 120 degrees C the same yield within 30min compared to 16h by the con

98 temperature requirement to only 120 degrees C.

99 red with a very slow reaction at 125 degrees C in the absence of NaBAr(F)4.

100 growing season temperatures from 14 degrees C to 33 degrees C.

101 1440 degrees C is a far lower temperature than usual beta --> alpha p

102 ed on a time scale of minutes at -15 degrees C in the presence of (0.4 mM) NaBAr(F)4 as compared with

103 brio infections at a threshold of 16 degrees C revealed a relative risk (RR)=1.14 (95% CI: 1.02, 1.27

104 -fried up to recommended limits (175 degrees C, 8h/day, 28h) in extra-virgin olive oil (EVOO), peanut

105 o significant difference to nearly 2 degrees C warmer than present-day temperatures.

106 Temperatures <2 degrees C were detected in 4 of 19 cold boxes (21%) transporting

107 uits were pre-conditioned 48 h at 20 degrees C prior to low-temperature exposure (pre-conditioning, P

108 at high temperatures (typically 2000 degrees C and above).

109 optimally at pH 7.0, temperature 25 degrees C and 6min of incubation time.

110 ces under two storage conditions: 30 degrees C/23% RH and 30 degrees C/75% RH.

111 nditions: 30 degrees C/23% RH and 30 degrees C/75% RH.

112 CSO remained stable up to 300 degrees C with negligible degradation.

113 p process has been achieved at 1,300 degrees C/900 degrees C by using yttrium-based rare earth mangan

114 temperatures from 14 degrees C to 33 degrees C.

115 e enzyme had optimum temperaturet 35 degrees C and was relatively stable at 77 degrees C, with 59.93%

116 osition temperature of 320.16+/-0.35 degrees C, which indicated that there was good thermal stability

117 stable over prolonged storage at 37 degrees C.

118 ent after ultrasound treatment at 40 degrees C.

119 owders significantly decreased at 45 degrees C and 60 degrees C.

120 A difference threshold of 0.47 degrees C or greater between affected and unaffected skin showed

121 rocarbon degradation was faster at 5 degrees C (500 m) with 65-89% of each component degraded after 5

122 ing of CO2-from 1.5 degrees C to 4.5 degrees C or greater -remains largely unscathed by the onslaught

123 sponse to a doubling of CO2-from 1.5 degrees C to 4.5 degrees C or greater -remains largely unscathed

124 ce temperatures (14.5 degrees C-17.5 degrees C) and high chlorophyll-a ( approximately 11 mg m(-3)).

125 f low sea surface temperatures (14.5 degrees C-17.5 degrees C) and high chlorophyll-a ( approximately

126 se in fungal growth after 7days at 5 degrees C.

127 When stored at 60 degrees C, the use of WPI alone conferred lower stability to the

128 tly decreased at 45 degrees C and 60 degrees C.

129 ions, in isothermal conditions at 60 degrees C.

130 on in a temperature control mode (60 degrees C/50 W) until there was approximately 80% EGM amplitude

131 d 325 mW cm(-2) at 500, 550, and 600 degrees C, respectively.

132 reaching its highest activity at 65 degrees C and that Tfu-FNO is likely to act in vivo as an F420 r

133 d were at column temperature of 61.7 degrees C using tri-distilled water without salt, adjusted pH of

134 with lithium diisopropylamide at -70 degrees C is easy to achieve, whereas reaction with lithium-magn

135 es C and was relatively stable at 77 degrees C, with 59.93% loss of activity.

136 hloromethane and acetonitrile at -78 degrees C in the presence of primary, secondary and tertiary alc

137 ptimized Co@C-800 (carbonized at 800 degrees C) exhibited high oxygen reduction reaction activity wit

138 with 5-mm spatial resolution at 800 degrees C.

139 been achieved at 1,300 degrees C/900 degrees C by using yttrium-based rare earth manganites.

140 mantle conditions (2 GPa and 750-900 degrees C).

141 d temperature within the range 85-95 degrees C.

142 ology parameters, color changes (h degrees , C *, DeltaE) microstructure (optical microscopy), and as

143 n vitro antifungal exposure failed to detect C. glabrata isolates with echinocandin resistance-associ

144 iSiCN nanocomposite films with the different C and Si contents are synthesized by the reactive-magnet

145 atechols, employing an oxyacetamide-directed C-H hydroxylation on phenols.

146 g GTPase domain, an intrinsically disordered C-terminal linker (CTL), and a C-terminal conserved pept

147 ed uptake of tau species, whereas the distal C-terminal-specific antibody (Tau46) had little effect.

148 The dual-element C-H isotope approach (LambdaC-H = Deltadelta(2)H/Deltade

149 By engineering C-terminal charges, we develop CRY2high and CRY2low with

150 , P = 0.07) was primarily driven by enhanced C uptake during spring (129%, P = 0.001) and fall (124%,

151 3)C approximately epsilonbulk(H)/epsilonbulk(C), where Deltadelta(2)H and Deltadelta(13)C are changes

152 ation, emphasizing the importance of the fac-C,N,S-iron(II) motif in promoting enzyme-like reactivity

153 nfecting ultraviolet [UV-C] light except for C difficile, for which bleach and UV-C were used); bleac

154 (quaternary ammonium disinfectant except for C difficile, for which bleach was used); UV (quaternary

155 Patients with testing ordered for C. difficile were enrolled and assigned a high, medium,

156 ts among the mildest conditions reported for C-H cleavage at a Ni center.

157 ir (MMR) pathways to generate mutations at G-C and A-T base pairs, respectively.

158 arylation/intramolecular amidation of gamma-C(sp(3))-H bonds.

159 on period to 48-70 h led to successive gamma-C(sp(3))-H arylation/intramolecular amidation and the co

160 ilized attenuating mutation in the P/C gene (C(Delta170)).

161 Two common polymorphisms, the c. 1298A > C, of the methylene-tetrahydrofolate reductase (MTHFR) g

162 A with rates of approximately 10(-4) The A-->C, G-->A, A-->U, C-->U, G-->U, U-->C, and U-->G errors m

163 t (10(-5)-10(-6)), whereas C-->G, U-->A, G-->C, and C-->A errors from purine-purine and pyrimidine-py

164 ) The A-->C, G-->A, A-->U, C-->U, G-->U, U-->C, and U-->G errors mostly due to pyrimidine-purine mism

165 main through a 37-residue domain and the HCN C terminus through the TPR domains.

166 ], high-density lipoprotein cholesterol [HDL-C], low-density lipoprotein cholesterol [LDL-C], total c

167 Check Hep C successfully supported high-need participants through

168 Hepatitis C virus (HCV) has dominated the field of hepatology for

169 events, particularly among HIV and hepatitis C infected people among whom cardiovascular disease risk

170 cially in individuals with chronic hepatitis C (HCV); however, the impact of nonheavy use is not clea

171 ins AP1 and AP2, are essential for hepatitis C virus (HCV) infection, but the underlying mechanism an

172 human immunodeficiency virus (HIV)/hepatitis C virus (HCV)-coinfected patients treated with interfero

173 cohort (representative of Italian hepatitis C virus-infected patients in care).

174 viruses including human pathogens hepatitis C virus (HCV), Severe acute respiratory syndrome (SARS),

175 Chronic infections with hepatitis C virus (HCV) and HIV are highly prevalent in the USA an

176 who are chronically infected with hepatitis C virus (HCV) and who do not have a sustained virologic

177 ng persons currently infected with hepatitis C virus lived >10 miles from a syringe services program.

178 pective study of 226 patients with hepatitis C virus-associated cirrhosis and CSPH who had SVR to int

179 ular basis of TAD formation, we performed Hi-C experiments on cells depleted for the Forkhead transcr

180 h differential abilities to downmodulate HLA-C.

181 cells were able to sense alterations of HLA-C expression demonstrated by increased antiviral activit

182 total Hg are strongly related to soil humus C accumulation (R(2) = 0.94, p < 0.001).

183 regulated for LTA, LPS, Poly(dT), and Poly(I:C), and 12, 142, 249, and 16 genes were downregulated fo

184 regulated for LTA, LPS, Poly(dT), and Poly(I:C), respectively, with at least a 1-fold change relative

185 Here, oxygen-dependent changes in C. jejuni physiology were studied at constant growth rat

186 ses continuously, indicating a deficiency in C-strand fill-in synthesis.

187 ious roles in floral and leaf development in C. hirsuta than in A. thaliana.

188 floral regulators that act nonredundantly in C. hirsuta, such that LFY has more obvious roles in flor

189 ed in S. cerevisiae was genetically shown in C. albicans using conditional TOR1 alleles.

190 he maximal number of fucose substitutions in C. elegans, which in part may be due to different method

191 nse variants identified in the intracellular C-terminal domain of the GluN2B NMDAR subunit.

192 n proceeds through inter- and intramolecular C-C and C-N bond formation.

193 t and hydrophobic spacer peptide (SP) at its C-terminus early in the maturation process, which is pro

194 ugh a novel dynein interacting site near its C terminus.

195 ype II implanted by 2 surgeons (C.H.D. and J.C.).

196 results suggest that S-palmitoylation of JAM-C can be potentially targeted to control cancer metastas

197 Finally, we demonstrated that JAM-C controls Src family kinase (SFK) activation in LSC and

198 activation was uniquely found within the JAM-C-expressing LSC compartment.

199 Y., Kazimirova, M., Roller, L., Jobichen, C., Swaminathan, K., Mizuguchi, J., Iwanaga, S., Nuttall

200 ependent for co-dependency on protein kinase C delta (PKCdelta).

201 work, we identified the major protein kinase C substrate MARCKS (myristoylated alanine-rich C kinase

202 l cells transduced Gbetagamma-protein kinase C- and Gbetagamma-metalloproteinase/EGFR-dependent MAPK/

203 C], low-density lipoprotein cholesterol [LDL-C], total cholesterol [TC]) were studied as continuous v

204 Among individuals with LDL-C >/=190 mg/dL, pravastatin reduced the risk of coronary

205 llowed by the bronchi, endocrine glands-like C cells of the thyroid (medullary carcinoma), the parasy

206 est deficient 2 (O-MAD2) into "closed" MAD2 (C-MAD2).

207 the analogous complex with a pincer-type mer-C,N,S ligation, emphasizing the importance of the fac-C,

208 The high performance of rGO@MgO/C nanocomposite can be ascribed to the hierarchical arch

209 of the human and murine forms of the myeloid C-type lectin receptor langerin for simple and complex l

210 erent olfactory neuron types in the nematode C. elegans.

211 Casein kinase 2 (CK2) binds to the NHE3 C-terminus and constitutively phosphorylates a downstrea

212 Notably, neither H2 activation nor C-H hydride abstraction was observed in the analogous co

213 eterocyclic carbene (NHC) chemistry, a novel C-N bond activation and ring-opening process is describe

214 ain associated with DSD activity and a novel C-terminal hydroxyphenylpyruvate dioxygenase-like domain

215 We report novel C. jejuni factors essential throughout its life cycle.

216 by low chemoselectivity for the amination of C-H bonds over competing reduction of the azide substrat

217 te tau toxicity, we screened a collection of C. elegans mutations in dopamine-related genes (n = 45)

218 could affect the distribution and density of C. finmarchicus.

219 due to Ndep has enhanced detrital inputs of C to soils, causing an average increase of 1.2 kgCm(-2)

220 ent and suggest that alternative splicing of C-Src in the developing vertebrate nervous system evolve

221 esium and lithium-zinc amides affords C-2 or C-8 functionalized derivatives in a regioselective fashi

222 Lewis acidic borane with concomitant C-H or C-C bond formation.

223 In addition to the Orai C terminus, the main coupling site for STIM1, the Orai N

224 g a stabilized attenuating mutation in the P/C gene (C(Delta170)).

225 important differences in how the Rb and p107 C-terminal domains (CTDs) associate with the coiled-coil

226 r, we propose a new approach to use Parylene C as a versatile template for patterning soft materials

227 agonist-induced activation of phospholipase C beta or with a rapamycin-inducible system in which var

228 ac) provokes inhibition of the phospholipase C by an as yet unknown mechanism.

229 n colocalize with VERNALIZATION1/PHYTOCHROME C and VERNALIZATION2, loci identified as flowering regul

230 Platelet C-type lectin-like receptor 2 (CLEC-2) is known to maint

231 no acid substitution mutations within a PMS2 C-terminal (721)QRLIAP motif attenuate or abolish human

232 ted that alpha-1 antitrypsin (AAT; Prolastin-C), a serine protease inhibitor used for the treatment o

233 glycoprotein called the prion protein or PrP(C) The current work tests a new hypothesis that sialylat

234 Compared to the benchmark Pt/C catalyst, the optimized Co@C-800 (carbonized at 800 de

235 ty for the oxygen reduction reaction than Pt/C, and twice the mass activity of the hollow nanoframe.

236 A cutoff of RAI-C of at least 21 classified 18.3% patients as "frail" wi

237 ), classifying only 3.7% as "frail." The RAI-C and RAI-A represent effective tools for measuring frai

238 e insulin receptor (IR) and mannose receptor C-type 1 (MR), which functions to clear endogenous manno

239 enic zebrafish that uses a mannose receptor, C type 1 (mrc1a) promoter to drive strong EGFP expressio

240 substrate MARCKS (myristoylated alanine-rich C kinase substrate) as a potential target molecule for k

241 Rs910083-C is also associated with increased risk of squamous cel

242 05]; effect size, 0.21), mean (SD) total SAC-C score (boys, 23.9 [3.9] vs girls, 24.9 [3.5]; mean dif

243 has been exploited to achieve meta-selective C-H activation by using a covalently attached, U-shaped

244 istent with predictions of conventional soil C models and suggest that elevated CO2 might increase tu

245 bon (C) sequestration and contain large soil C stocks.

246 O2 might increase turnover rates of new soil C.

247 By expressing the target protein with SpyTag C-terminal to the SrtA recognition motif, it can be cova

248 rmediary steps as well as direct, late stage C-7 hydroxylation provides both natural products in six

249 The subfamily C ATP-binding cassette (ABCC) transporters mediate multi

250 C-B downregulation function in HIV-1 subtype C and show that carriage of Nef variants with enhanced M

251 In summary, C. neoformans harvests lipids from macrophages, and the

252 MEAN suppressed C-MYC expression and increased expression of several tum

253 oprosthesis type II implanted by 2 surgeons (C.H.D. and J.C.).

254 ute HCV in HIV-1 infected individuals (SWIFT-C) is an open-label, 2-cohort clinical trial in which th

255 immune reconstitution inflammatory syndrome (C-IRIS), upon initiation of antiretroviral therapy (ART)

256 imit of detection (G, A = 0.5 mug mL(-1); T, C = 1.0 mug mL(-1)), and high selectivity in the presenc

257 [from 10microM to 50nM] in comparison to ta-C thin film electrodes and (ii) the coating method signi

258 Tenascin-C is an extracellular matrix molecule that drives progre

259 The C-statistics were 0.662 for ADA fasting glucose clinical

260 The C-terminal DSP domain induced phosphorylation of occludi

261 The C-terminal extension of capsid protein VP3 folds into a

262 ns harvests lipids from macrophages, and the C. neoformans-macrophage interaction is modulated by exo

263 thiomethyl and extended functionality at the C(4) position.

264 and hydrophobic and polar amino acids at the C-terminal end.

265 show that a unique, conserved domain at the C-terminus of Swc5, called Bucentaur (BCNT), is essentia

266 ecies, MAF1L and MAF1S, are regulated by the C-box YSY motif, which, when mutated, alters species sto

267 Secreted MSPds derived from the C. elegans VAPB homolog VPR-1 promote mitochondrial loca

268 ) permits positively charged residues in the C-terminal helix to engage in DNA binding, triggering a

269 lable procedure was developed to install the C-3 amido group.

270 recognizes the C-2-amino group, but not the C-6-oxo group, N-1-hydrogen, or N-7-nitrogen, of GDP for

271 m both N-domain twisting and rotation of the C domain (up to 30 degrees ) at the end of the relativel

272 -Hartwig reactions involving cleavage of the C(acyl)-O bond of aryl esters that proceed under mild co

273 Metalation of the C-3 position of the quinolinic ring with lithium diisopr

274 The intensity of the C-D band is proportional to the extent of deuteration in

275 Experimental and theoretical studies of the C-H amination reaction mediated by the iron dipyrrinato

276 of Cp*RhCl to accelerate the cleavage of the C-H bond of N-pentafluorophenylbenzamides, providing a n

277 of ubiquitin, two interhelical loops of the C-terminal four-helix bundle appear to penetrate the mem

278 cid replacements on lipid association of the C-terminal peptide fully recapitulated their effects on

279 Many members of the C-type lectin receptor family serve as pattern recogniti

280 In particular, the C terminus functions as a toggle switch, which affects a

281 cated that the PRNTase domain recognizes the C-2-amino group, but not the C-6-oxo group, N-1-hydrogen

282 2' sugar modifications and revealed that the C-terminal region of FUS is sufficient to retain ASOs in

283 Here, we show that the C-type lectin receptor CD69 controls tTreg cell developm

284 signalling events have been misattributed to C-Src because they cannot be distinguished by convention

285 adiation Facility to check whether the O- to C-state transition in fully activated fibers of fast ske

286 itive, 866 of 1447 (60%) contained toxigenic C. difficile, and fecal toxin was detected in 511 of 866

287 of 683 subjects were positive for toxigenic C. difficile by direct toxigenic culture, and 141 of 682

288 BB) in rodents and selectively binds to TrkB/C receptors in vivo, as evidenced by entrectinib blockin

289 e reagent, resulting in the formation of two C-C bonds at a single carbon center bearing a C(sp(3)) o

290 pproximately 10(-4) The A-->C, G-->A, A-->U, C-->U, G-->U, U-->C, and U-->G errors mostly due to pyri

291 We identify a conserved region in the Ulp2 C terminus that mediates its specificity for rDNA-associ

292 d a weak base, lysine amino groups underwent C-N bond formation at room temperature.

293 ept for C difficile, for which bleach and UV-C were used); bleach; and bleach and UV-C.

294 d UV-C were used); bleach; and bleach and UV-C.

295 isinfectant and disinfecting ultraviolet [UV-C] light except for C difficile, for which bleach and UV

296 nd vascular endothelial growth factor (VEGF)-C expression were measured.

297 naphthylamines with azoles is developed via C-H functionalization and C-N bond formation.

298 inct differences in anthocyanins and vitamin C contents, on human intestinal Caco-2 cells exposed to

299 SmI2(H2O)n should be able to form very weak C-H bonds.

300 relatively frequent (10(-5)-10(-6)), whereas C-->G, U-->A, G-->C, and C-->A errors from purine-purine