ライフサイエンスコーパス: N

1 N isotope compositions of emitted arc gases (9-11 N degr

2 N(6)-methyladenosine (m(6)A) is an essential internal RN

3 N-acetylcysteine accelerates amputation stump healing in

4 N-fixing trees comprise only a slightly smaller fraction

5 N-Linked protein glycosylation is an essential and highl

6 N-termini of several proteases were downregulated in prt

7 N=37 adhered to the exercise, most attending >/=1 sessio

8 ent of age (P < 0.001), T stage (P < 0.001), N stage (P < 0.001), and grade (P = 0.049).

9 In 1 N HBr (aq), the photocatalyst undergoes excited-state el

10 tope compositions of emitted arc gases (9-11 N degrees ) imply less subducted pelagic sediment contri

11 ges of (13)C/(12)C, (2)H/(1)H, and (15)N/(14)N ratios of NDMA give rise to isotope fractionation tren

12 x chemistry with nitrogen isotope ((15)N/(14)N) values from approximately 2.31-billion-year-old shale

13 This study examined the fate of a (15) N-NO3- tracer over 5-6 years in a mixed deciduous stand

14 We used the difference in delta(15) N between 20 ant conspecifics in 10 genera between two p

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

16 r changes of (13)C/(12)C, (2)H/(1)H, and (15)N/(14)N ratios of NDMA give rise to isotope fractionatio

17 l procedure is 0.6 per thousand for delta(15)N and 0.5 per thousand for delta(18)O.

18 relationship between NAO index and delta(15)N values in guano for the instrumental period, we recons

19 n redox chemistry with nitrogen isotope ((15)N/(14)N) values from approximately 2.31-billion-year-old

20 ryl)iminomethane (BIM) complex [Pt(kappa(2) -N,B-(Cy2) BIM)(CNAr(Dipp2) )] can effect the oxidative i

21 eter and temporalis muscle activities per 20-N bite-force (T20 N, microV), which defined thresholds.

22 ay incidence of postdischarge VTE was 0.29% (N = 269).

23 a BCVA above baseline with 18 of those (39% N = 46) maintaining a 10-letter gain throughout the 24 m

24 ables the synthesis of the squares [Pt4(en)4(N intersectionN)4][CF3SO3]8 (en= ethylenediamine, N inte

25 r cancers: adjusted IRR 2.2, 95% CI 0.9-5.4; N = 89 cases).

26 onths of treatment and monitoring, 27 (58.7% N = 46) kept a BCVA above baseline with 18 of those (39%

27 ype based on the Symptoms Checklist (SCL-90; N=3845) and a case-control sample with the categorical p

28 +, 33 HV+, and 11 FDG+HV+) and 37 were Abeta+N+ (17.7%; 22 FDG+, 26 HV+, and 11 FDG+HV+).

29 neration biomarkers; of these, 52 were Abeta-N+ (24.9%; 30 FDG+, 33 HV+, and 11 FDG+HV+) and 37 were

30 aratus, and has a preference for acetylating N termini of the transmembrane proteins.

31 The N(tz) ADP(+) /N(tz) ADPH cycle can be monitored in real time by fluore

32 ate regression showed that successful agers (N = 789) reported 3.79 (95% confidence interval (CI): 1.

33 Agmatine N-acetyltransferase (AgmNAT) catalyzes the formation of

34 vised by [4 + 1] heterocyclization of alpha-(N-hydroxy/aryl)imino-beta-oxodithioesters with in situ g

35 In addition, an N-linked sugar of the integrin attaches to the previousl

36 escence and excellent photostability, (b) an N-methyl group at each end of the squaraine core that en

37 We identified an N-TIMP2 mutant, with five mutations in its interface, th

38 ine, real-rTMS, sham-rTMS), all including an N-back task (3 task loads: N1, N2, N3; control condition

39 tein is a fusion of two distinct modules: an N-terminal sugar phosphate isomerase-like domain associa

40 he EISA precursor analogues consisting of an N-capped d-tetrapeptide, a phosphotyrosine residue, and

41 We show that an N-terminal fragment comprising the catalytic domain can

42 ing properties of 40 CBMs, in fusion with an N-terminal GFP domain, revealed that type A CBMs possess

43 found to be the main precursors of AGEs and N(epsilon)-(carboxymethyl)lysine (CML) found to be predo

44 H,2'H-3,3'-bipyrazole (4) by N-amination and N-azo coupling reactions is described.

45 alkali-metal-mediated metalation (AMMM) and N-heterocyclic carbene (NHC) chemistry, a novel C-N bond

46 (R)-2,3-Di-O-benzylglyceraldehyde and N-tosyl homoallylamine undergo aza-Prins cyclization to

47 nstream factors, including FBP17, Cdc42, and N-WASP.

48 er locations mass balance considerations and N contents of high pressure metamorphic rocks imply mass

49 ations, with significantly increased C:P and N:P ratios for evergreen broadleaf forest and highly wea

50 further influencing photosynthetic rates and N-use efficiency of these critically important forests.

51 ld, apparent N recovery efficiency (REN) and N balance when using urea applied with or without Limus

52 e performance of networks with N-stable and (N-1)-stable network-capacity allocations by triggering c

53 versed by its product lactate or antioxidant N-acetylcysteine, suggesting that Y10 phosphorylation-me

54 Grain yield, apparent N recovery efficiency (REN) and N balance when using ure

55 PAIB-SOs are N-dealkylated into cytotoxic phenyl 4-(2-oxo-3-imidazoli

56 Alumni athletes (N=33, aged 34-71 years) and an age-matched sample of com

57 We demonstrate here that the formation of B-N Lewis pairs at the periphery of anthracene leads to bu

58 t plus the implementation of knowledge-based N management practices.

59 pants who had suicidal ideation at baseline (N=167).

60 deposition both in vitro and in vivo Because N-terminally truncated pyroglutamate (pE)-modified Abeta

61 to OGA in O-GlcNAc regulation.O-linked beta-N-acetyl glucosamine (O-GlcNAc) is an important protein

62 tion of nucleocytoplasmic proteins with beta-N-acetylglucosamine (GlcNAc) and regulates numerous biol

63 al beta-GlcNAc moiety by treatment with beta-N-acetylglucosaminidase and selective extension of the o

64 lts provide evidence of interactions between N deposition and temperature sensitivity, which could in

65 This resulted from both N-domain twisting and rotation of the C domain (up to 30

66 most common and was predicted best when both N-methyl-D-aspartate receptor-IgG and aquaporin-4-IgG co

67 n of DNA, resulting in the formation of BPDE-N(2)-dG, an adduct formed between deoxyguanosine and a d

68 ,5'-tetranitro-2H,2'H-3,3'-bipyrazole (4) by N-amination and N-azo coupling reactions is described.

69 rane extraction and assembly, is followed by N-methylation of the mature (pseudo)pilin N terminus.

70 lglucosamine (GlcNAc), which is generated by N-acetylglucosaminyltransferase (GnT)-IV, is a good subs

71 ecent advancement in functionalizing gold by N-heterocyclic carbenes (NHCs), a promising alternative

72 the benzoxazinoid breakdown product MBOA by N-glycosylation.

73 , glycosylation site, and their occupancy by N-glycans are all detected and identified in a single ex

74 nto the molecular basis of MMP regulation by N-TIMP2 and identifies a promising MMP-14 inhibitor as a

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

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

77 y oxidative addition of an activated amide C-N bond to a Ni(0) catalyst and proceeds via alkene inser

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

79 through inter- and intramolecular C-C and C-N bond formation.

80 ation and the construction of both C-C and C-N bonds.

81 erocyclic carbene (NHC) chemistry, a novel C-N bond activation and ring-opening process is described

82 The temporal trends in soil C-N-P stoichiometry differed among vegetation, soil, paren

83 h the overall formation of one C-C and two C-N bonds, in moderate to excellent yields.

84 ion process that generates two C-C and two C-N bonds, with water as the only side product.

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

86 d more pronounced temporal changes in soil C:N, N:P, and C:P ratios at low elevations.

87 ter reaction pathway requires a C13=C14, C15=N double-isomerization of the retinal chromophore, where

88 for a better understanding of OST-catalyzed N-glycosylation.

89 rming feedback was modulated by the changing N and rainfall regimes.

90 e made as precursors with positively charged N-terminal anchors, whose cleavage via the prepilin pept

91 The reaction of chiral N-tert-butanesulfinyl aldimines with beta-keto acids und

92 its open Ca(2+)-activated C-lobe and closed N-lobe cooperate to recognize a mixed alpha/310 helix in

93 ation) "undocks" and repositions the cofilin N terminus away from the filament axis, which compromise

94 in the International Lung Cancer Consortium (N=60,586, meta-analysis P=0.0095, OR=1.05, and 95% CI=1.

95 ase and ATP or (tz) ATP to the corresponding N(tz) ADP(+) .

96 egrees -250 degrees E, 0 degrees -20 degrees N).

97 mination of N; (2) demonstration that deltaN/N for CP-AFM junctions is remarkably small (</=2%) and t

98 design included all persons born in Denmark (N = 1683385) between January 1, 1967, and December 31, 1

99 A5 after Asp270 to generate a necrotic DFNA5-N fragment that targets the plasma membrane to induce se

100 collection of urethral discharge to diagnose N. gonorrhoeae and Chlamydia trachomatis infection in ce

101 The detection limits for differing N-nitrosamines ranged between 0.07 muM (14 pmol injected

102 St. Lawn fertilizer and pet waste dominated N and P inputs, respectively, underscoring the importanc

103 his study, we explore the effect of low dose N-acetyl-L-cysteine therapy, delivered using a targeted,

104 Using the endocytic protein epsin1 N-terminal homology domain (ENTH), previously thought to

105 ed Lys-72 as an acetylation site in the ERK1 N terminus, adjacent to Lys-71, which binds to ATP, sugg

106 ersectionN)4][CF3SO3]8 (en= ethylenediamine, N intersectionN = 4,4'-bipyridine derivatives) from comm

107 in oPOM at a greater rate under experimental N deposition, relative to the ambient treatment.

108 in a consensus meeting attended by experts (N = 12) with representatives from each group.

109 ored C terminus, whereas the surface-exposed N terminus is highly variable, a feature used for identi

110 d reactivity against recombinantly expressed N-terminal LRP2 fragments on Western blots and immunopre

111 munoprecipitated the recombinantly expressed N-terminal region of LRP2.

112 urface of the beta1AR, but the extracellular N-terminus, which is a target for post-translational mod

113 a large variety of amines provided the final N-acylguanidines, with the overall formation of one C-C

114 els that estimate photosynthesis from foliar N would be improved only modestly by including additiona

115 stage was good/substantial (k=0.790) and for N stage was moderate (k=0.458) between MRI and histopath

116 ide concentrations-are increasing demand for N, the element limiting primary productivity in temperat

117 prove solubility, which led to a change from N-methylpyridone to a tetrahydropyranyl oxy-pyridine der

118 is of N-heterocycle-fused-beta-lactones from N-linked ketoacids is described.

119 In humans and FVB/N mice, loss of functional tetraspanin CD151 is associat

120 Male FVB/N-Tg(MMTVneu)202Mul/J (Her2) transgenic mice were bred t

121 N gene (pre-N) or between the N and P genes (N-P) of rHPIV1 bearing a stabilized attenuating mutation

122 renic motoneuron expression of glutamatergic N-methyl-D-aspartate (NMDA) receptors and decreased expr

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

124 Elemental compositions (C, H, N, O, S), Py-GC/FID, Py-GC/MS and SEM imaging reveal ext

125 -hexaazatriphenylene) by hydroquinone (H2Q), N-acetyl-tyrosine (N-Ac-Tyr) or guanosine-5'-monophospha

126 In HD8 (N = 1,064; median follow-up, 153 months), noninferiority

127 Here, we report that the hydrophilic N-terminal domain of Brassica napus DGAT1 (BnaDGAT11-113

128 state concentrations of endoxifen (4-hydroxy-N-desmethyltamoxifen), the most potent antiestrogenic me

129 The isotropic and nematic (I + N) coexistence for rod-like colloids is a signature of t

130 ed point mutation (RIP) of repetitive DNA in N. crassa.

131 nthetic capacity of TMFs, with variations in N allocation and Rubisco activation state further influe

132 ses, we dissected the function of individual N-glycan sites in beta3 integrin activation.

133 community-ascertained sample of individuals (N = 347, 18-59 years of age) completed a battery of beha

134 potential for abrupt increases in inorganic N sources to induce cascading effects on dissolved organ

135 e matrix domain (MA) of HIV-1 Gag protein is N-myristoylated and plays an important role in virus bud

136 y with the crystal structure of the isolated N-terminal extracellular domain of the GLP-1R in complex

137 OX20 stabilizes COX2 during insertion of its N-proximal transmembrane domain, and subsequently, COX18

138 ptor Toll-like receptor 4 (TLR4) through its N terminal and modulates STAT3 and TBK1 signaling, trigg

139 Nesprin-2G engaged actin through its N terminus and microtubules through a novel dynein inter

140 f laryngeal C neurons in the nodose/jugular (N/J) ganglia.

141 We show that ATZ induces activation of c-Jun N-terminal kinase (JNK) and c-Jun and that genetic ablat

142 c-Jun N-terminal kinase (JNK) plays a vital role in malignant

143 lator of both IkappaB kinase (IKK) and c-Jun N-terminal kinase (JNK), and an important mediator of au

144 essor function for KIND1, and identify c-Jun N-terminal kinase and NF-kappaB as potential therapeutic

145 anidine derivative (11)C-GMOM ((11)C-labeled N-(2-chloro-3-thiomethylphenyl)-N'-(3-methoxyphenyl)-N'-

146 of the permeation of the lethal factor (LF) N-terminal segment through the anthrax channel.

147 binary liposome mixture of cationic liposome N-[1-(2,3-Dioleoyloxy)propyl]-N,N,N-trimethylammonium pr

148 32 mL [517-768 mL]; P<0.0001), despite lower N-terminal pro-B-type natriuretic peptide levels.

149 d tau uptake in an epitope-dependent manner: N-terminal (Tau13) and middomain (6C5 and HT7) antibodie

150 eAN)2Cu(II)2(O2(2-))](2+) ((S)P(MeAN), MeAN: N-methyl-N,N-bis[3-(dimethylamino)propyl]amine) that fea

151 in conjunction with experimentally measured N K-edge absorption spectra, reveals the different natur

152 Failure score (48 versus 40), higher median N-terminal pro-B-type natriuretic peptide concentration

153 oro-3-thiomethylphenyl)-N'-(3-methoxyphenyl)-N'-methylguanidine) has been used successfully to quanti

154 I)2(O2(2-))](2+) ((S)P(MeAN), MeAN: N-methyl-N,N-bis[3-(dimethylamino)propyl]amine) that featured an

155 A novel DNA adenine modification, N(6)-methyladenine (6mA), has recently been found in mam

156 lead to both symmetric and unsymmetric N,N',N''-substituted derivatives.

157 ore pronounced temporal changes in soil C:N, N:P, and C:P ratios at low elevations.

158 c liposome N-[1-(2,3-Dioleoyloxy)propyl]-N,N,N-trimethylammonium propane (DOTAP) and the zwitterionic

159 sue consumed could be predicted based on Na, N or net primary productivity.

160 cotinine (COT-OH), N-nitrosoanabasine (NAB), N-nitrosoanatabine (NAT), N-nitrosonornicotine (NNN), 4-

161 gen species (ROS) in podocytes and that NAC (N-acetyl-cysteine), a potent antioxidant, significantly

162 soanabasine (NAB), N-nitrosoanatabine (NAT), N-nitrosonornicotine (NNN), 4-(methylnitrosamino)-1-(3-p

163 rodigious bite forces (8,526-34,522 newtons [N]) and tooth pressures (718-2,974 megapascals [MPa]) pr

164 inputs, outputs, and retention for nitrogen (N) and phosphorus (P) in seven subwatersheds of the Miss

165 al patterns and temporal trends of nitrogen (N) and phosphorus (P) deposition are important for quant

166 The level of nitrogen (N), phosphorus (P), zinc (Zn), iron (Fe), and copper (Cu

167 non-destructive diagnosis of rice nitrogen (N) status.

168 recycling of subducted sedimentary nitrogen (N) back to the atmosphere through arc volcanism has been

169 samino)-1-(3-pyridyl)-1-butanol (NNAL), NNAL-N-beta-glucuronide, and NNAL-O-beta-glucuronide.

170 NO3(-) leachate load from soybean fields (no N fertilizer applied).

171 reaction employing an internally oxidizing O-N bond as a directing group.

172 s studies have shown that the aggregation of N-terminal fragments (encoded by HTT exon 1) underlies t

173 t, in the presence of iron, large amounts of N-nitroso-tryptophan can be formed even at neutral pH, a

174 o accelerate the cleavage of the C-H bond of N-pentafluorophenylbenzamides, providing a new structura

175 understanding the causes and consequences of N limitation in coupled nutrient cycles, as well as mode

176 main results are (1) direct determination of N; (2) demonstration that deltaN/N for CP-AFM junctions

177 diately after the serendipitous discovery of N-confused porphyrins, remarkably diverse carbaporphyrin

178 some information on certain endosymbionts of N. cucumeris and T. putrescentiae exists, it is unclear

179 fferent enrichment methods for enrichment of N- and O-linked glycopeptides.

180 nsferase (AgmNAT) catalyzes the formation of N-acetylagmatine from acetyl-CoA and agmatine.

181 rectly identified on the polylactosamines of N-glycans of SKOV3, IGROV1, OV90, and OVCA433.

182 P and reducing equivalents, and recycling of N and possibly CO2 through refixation.

183 It was found that removal of N-glycans prior to enrichment of O-linked glycopeptides

184 strate the persistent ecosystem retention of N deposition even as it redistributes, without additiona

185 Understanding the biologic role of N(6)-methyladenosine (m(6)A) RNA modifications in mRNA r

186 diastereo- and enantioselective synthesis of N-heterocycle-fused-beta-lactones from N-linked ketoacid

187 However, our understanding of N deposition effects on microbial communities is far fro

188 A highly functionalized variety of N-substituted pyridine-fused chromeno and pyrano derivat

189 ne (COT), trans-3'-hydroxycotinine (COT-OH), N-nitrosoanabasine (NAB), N-nitrosoanatabine (NAT), N-ni

190 f high-dose spironolactone and usual care on N-terminal pro-B-type natriuretic peptide (NT-proBNP) le

191 diphosphine ligand with alkyl/aryl groups on N and P), have been developed for heterolytic cleavage o

192 es bearing 2,2-dialkoxyethyl substitution on N-1.

193 but not the C-6-oxo group, N-1-hydrogen, or N-7-nitrogen, of GDP for the cap formation.

194 , the main coupling site for STIM1, the Orai N terminus is indispensable for Orai channel gating.

195 ove benzyl O-protective groups from oxyarene N-heterocycles at positions capable for 2-/4-O-pyridine-

196 e-matched sample of comparison participants (N=18) were administered measures of cognitive function a

197 Human participants (N = 17) were scanned, over two sessions, while viewing 3

198 approaches, including use of either peptide:N-glycosidases F and A (PNGase F and A) or anhydrous hyd

199 n individuals with or without periodontitis (N = 88).

200 Here, we investigate the impact of the PHF1 N-terminal domain (NTD) on the Tudor domain interaction

201 by N-methylation of the mature (pseudo)pilin N terminus.

202 vior of microspheres in the presence of poly(N-isopropylacrylamide) (PNiPAm) microgels at the air/wat

203 ecules present in saliva by brushes of poly[(N-(2-hydroxypropyl) methacrylamide)-co-(carboxybetaine m

204 as inserted either preceding the N gene (pre-N) or between the N and P genes (N-P) of rHPIV1 bearing

205 ion class III/IV, RVESRI, and log NT-proBNP (N-Terminal Pro-B-Type Natriuretic Peptide) were retained

206 ionic liposome N-[1-(2,3-Dioleoyloxy)propyl]-N,N,N-trimethylammonium propane (DOTAP) and the zwitteri

207 dine) has been used successfully to quantify N-methyl-d-aspartate (NMDA) receptor binding in humans.

208 Reacting N-aryliminophosphoranes with 1-(het)aroyl-2-aryldiazenes

209 n temperate forests, which could be reducing N availability.

210 CML36 interacts directly with the regulative N terminus of the Arabidopsis plasma membrane Ca(2+)-ATP

211 Here, we show that Cet1's N-terminal domain (NTD) promotes the recruitment of FACT

212 rein, the preparation of the regioisomer (S)-N(1)-methyl-2-[2'-(3''-methoxy-4''-hydroxyphenyl)ethyl]-

213 We find low peptide-S/N concordance between arrays, demonstrating that differe

214 l characterization and that global peptide-S/N relationships are difficult to identify.

215 a, each of which may be formed from the same N-allyl precursor by stereodivergent alkene isomerizatio

216 finding in a larger dimensional ACQ sample (N=2547) and in independent samples with a dichotomous AG

217 sis of 102 hemispheres of in vivo MRI scans (N = 51 males, mean +/- SD 24.1 +/- 3.1 years of age) sho

218 imeric proteins to test whether DAT and SERT N and C termini contribute to transporter substrate and

219 ss spectrometry analysis showed that several N-terminally truncated amyloid-beta42 species, represent

220 red to a regular supply and increasing shoot N concentration more when lower water amounts were appli

221 esolution X-ray crystal structure of a sigma(N) fragment in complex with its cognate promoter DNA, re

222 lar details of promoter recognition by sigma(N) The structure allowed us to build and refine an impro

223 wed us to build and refine an improved sigma(N)-holoenzyme model based on previously published 3.8-A

224 ided empirical evidence supporting that soil N availability, under global warming scenarios, is expec

225 W was significantly correlated with T stage, N stage, TNM stage, and histological type of the disease

226 ic rocks imply massive addition of subducted N to the mantle and past the zones of arc magma generati

227 A series of 4-substituted N-alkoxypiperidines were prepared and studied by variabl

228 SNF may play a role in both by supplying N to leaf tissues for acclimation and by facilitating co

229 ful information for enhancing or suppressing N-glycosylation at a site of interest and valuable data

230 The iron-regulated metastasis suppressor N-myc downstream-regulated gene 1 (NDRG1) has been shown

231 dergoing major scheduled noncardiac surgery (N = 566; 24% delirium).

232 ld-induced metamagnetic phase transitions (T N = 58 K) and high spontaneous polarization ( 63.3 muC.

233 s muscle activities per 20-N bite-force (T20 N, microV), which defined thresholds.

234 We tested the hypothesis that N-cadherin is part of a novel mechanosensory mechanism i

235 the N-Srcs are unknown and it is likely that N-Src signalling events have been misattributed to C-Src

236 The N(tz) ADP(+) /N(tz) ADPH cycle can be monitored in real

237 The N-terminus of MerA is able to extract the bound Pb(VI) b

238 exchange in the stalk region abolishing the N-linked glycosylation site; and 2 variants represented

239 not nitrogen inversion or rotation about the N-O bond.

240 king that occurs between the toluene and the N-oxyl aromatic rings in the transition state structures

241 inds to both the closed conformation and the N-peptide of Syx4.

242 al state resistance often referred to as the N-shaped temperature dependence, is omnipresent in disor

243 The zf-MYND-like domain at the N terminus of rice CCR4 and the PXLXP motif of rice CAF1

244 ng of the antiviral drug, amantadine, at the N-terminal pore at low pH did not convert all histidines

245 vity of SWR, whereas an acidic region at the N-terminus is required for optimal SWR function.

246 t the C-terminus of aspartic acid and at the N-terminus of cysteine.

247 preceding the N gene (pre-N) or between the N and P genes (N-P) of rHPIV1 bearing a stabilized atten

248 ted versions of SS4 and a fusion between the N-terminal region of SS4 and GS in the Arabidopsis ss4 m

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

250 terference of HCA1 interaction with both the N-glycan and peptide-moiety of SV2.

251 s-the bacterial chemotaxis protein CheY, the N-terminal receiver domain of the nitrogen regulation pr

252 and A) or anhydrous hydrazine to cleave the N-glycans from glycopeptides.

253 After processing in the Golgi to cleave the N-terminal prodomain from the C-terminal growth factor (

254 NA isoforms were full length, containing the N-terminal nuclear localization signal.

255 interacts with a novel binding motif in the N-terminal domain of CaV1 LTCC alpha1 subunits that is n

256 xAC database, confirms that mutations in the N-terminal end of the kinase domain are more disruptive

257 beta contains a specific NLS sequence in the N-terminal lyase domain that promotes transport of the p

258 cated in the membrane-proximal region of the N terminus of chECL1, suggesting that the binding site o

259 We investigated the specific roles of the N- and C-terminal regions of SS4 by expressing truncated

260 The activation of the N-methyl D-aspartate receptor (NMDAR) is controlled by a

261 However, the exact functions of the N-Srcs are unknown and it is likely that N-Src signallin

262 onformational change unveils a region of the N-terminal cytosolic tail targeted by the Art1 alpha-arr

263 Here we solve the crystal structures of the N-terminal domains of PHF1 and MTF2 with bound CpG-conta

264 Manipulation of the N-terminal sequence affected the amount of Polbeta in th

265 The polarity of the N-tier ahead of the C-tier places the leading Pol epsilo

266 GP was inserted either preceding the N gene (pre-N) or between the N and P genes (N-P) of rHP

267 TFAM tethers the N-terminal region of mtRNAP to recruit the polymerase to

268 Here we demonstrate that the N terminus of E3 is necessary to inhibit an IFN-primed v

269 the presence of Ng13-49 by showing that the N-terminal acidic region of Ng peptide pries open the be

270 directly destabilize the complex through the N-terminal linker.

271 t prevents the specific interaction with the N-terminal domain of Hsp90 required for catalysis.

272 ls where it truncates core histones at their N-terminal ends.

273 These N-oxide compounds display promising performance properti

274 11)C-labeled N-(2-chloro-3-thiomethylphenyl)-N'-(3-methoxyphenyl)-N'-methylguanidine) has been used s

275 nt breast cancer cellular invasiveness, this N-TIMP2 mutant acted as a functional inhibitor.

276 Bacteria encoding L27 with this N-terminal extension also encode a sequence-specific cys

277 effects on the response of Rs, Rh, and Ra to N supply.

278 ing cascade and connecting PAK1 signaling to N-WASP-cortactin-mediated actin polymerization and GLUT4

279 he electron-rich HO-H bond via H transfer to N on the nickel surface, beneficial to the overall hydro

280 der mesic conditions, are most vulnerable to N loss via NO as interactions between pH, SOM, and droug

281 99.2%; kappa, 0.89), with the Lumipulse G TP-N having a shorter time to first and subsequent results.

282 nsaturated lipid species, and trimethylamine-N-oxide), thus in effect linking diverse exposures such

283 cal data, and discovered that trimethylamine-N-oxide (TMAO) crosses the blood-brain barrier.

284 he mechanisms and kinetic laws of tryptophan N-nitrosation were determined.

285 tions conducted for the reactions of the two N-oxyl radicals with toluene, which indicate that the HA

286 harides into structurally uniform human-type N-glycans.

287 e) by hydroquinone (H2Q), N-acetyl-tyrosine (N-Ac-Tyr) or guanosine-5'-monophosphate (GMP) was invest

288 ng blocks of HA, UDP-Glucuronic acid and UDP-N-Acetyl-Glucosamine, as well as hyaluronic acid synthas

289 was recently identified as an unconventional N-terminal acetyltransferase (NAT) because it localizes

290 Under N starvation, TCP20-NLP6&7 heterodimers accumulate in th

291 P6&7 also support root meristem growth under N starvation.

292 tructure of many mineral soils could undergo N-dependent changes as atmospheric CO2 concentrations ri

293 s for a number of substituted and unreactive N-allyl-2-furfurylamines under biomimetic conditions, wi

294 could lead to both symmetric and unsymmetric N,N',N''-substituted derivatives.

295 adamantanyl thioglycoside in the donor with N-iodosuccinimide and trifluoromethanesulfonic acid in d

296 mes using RNA-seq and amino acid levels with N treatment in tea (Camellia sinensis), the most popular

297 and compare the performance of networks with N-stable and (N-1)-stable network-capacity allocations b

298 nary glycan [A3(2,4,2) type] terminated with N-acetylglucosamine (GlcNAc), which is generated by N-ac

299 inamide mononucleotide and (tz) ATP to yield N(tz) AD(+) , which can be enzymatically phosphorylated

300 ucts from the corresponding starting E- or Z-N'-alkenyl urea, each of which may be formed from the sa