ライフサイエンスコーパス: CN

1 CN allowed the healing of NK in all patients as well as

2 CN dephosphorylates human and yeast NPC proteins and pro

3 CN(-) results in large conformational changes including

4 CN-Learn recovers twice as many CNVs compared to individ

5 CN-null fibroblasts had a greater migratory capacity, in

6 Er(1) /CN-NT is a highly efficient and robust photocatalyst tha

7 upported on carbon nitride nanotubes (Er(1) /CN-NT) with a tunable dispersion density of single atoms

8 Furthermore, Ir(1)/CN displays high tolerance to CO poisoning.

9 The iridium variant Ir(1)/CN electrocatalyses the formic acid oxidation reaction w

10 The activity of Ir(1)/CN is also 16 and 19 times greater than those of Pd/C an

11 theory reveals that the properties of Ir(1)/CN stem from the spatial isolation of iridium sites and

12 tom catalysts on nitrogen-doped carbon (M(1)/CN, M = Pt, Ir, Pd, Ru, Mo, Ga, Cu, Ni, Mn).

13 t the complexes Lambda/Delta-[Ru(TAP)(2) (11-CN-dppz)](2+) (TAP=1,4,5,8-tetraazaphenanthrene, dppz=di

14 ort the structure of Lambda-[Ru(phen)(2) (11-CN-dppz)](2+) bound to d(TCGGCGCCGA), a duplex-forming s

15 r for the generation of the monoanion [B(12)(CN)(11)](-), which indeed spontaneously binds Ar at 298

16 synthesized the percyano-dodecoborate [B(12)(CN)(12)](2-), the electronically most stable dianion eve

17 n with (13)CN-containing carrier affords (13)CN-labeled enzyme as verified by electron paramagnetic r

18 Maturation with (13)CN-containing carrier affords (13)CN-labeled enzyme as v

19 caffold with various acceptor groups at C-2 (CN, SO(2)R) and a primary amino group at C-7 for conjuga

20 yhydrido copper clusters [Cu(28) H(15) (S(2) CN(n) Bu(2) )(12) ](+) or [Cu(20) H(11) {S(2) P(O(i) Pr)

21 ((ket)guan)Co(N(3))(2)] ((ket)guan = [(tBu(2)CN)C(NDipp)(2)](-), Dipp = 2,6-diisopropylphenyl) (3a) i

22 Pt(II)(DMSO)Cl(2)](2) (1) and Fe(II)(bpy)(2)(CN)(2)-[Au(I)Cl](2), were synthesized, and corresponding

23 lic donor-acceptor ensembles, Fe(II)(bpy)(2)(CN)(2)-[Pt(II)(DMSO)Cl(2)](2) (1) and Fe(II)(bpy)(2)(CN)

24 placed by adding a synthetic [Fe(Cys)(CO)(2)(CN)] carrier in the maturation reaction.

25 ow that the HydG product [Fe(II)(Cys)(CO)(2)(CN)] synthon is the substrate of the radical SAM enzyme

26 bond, producing a mononuclear [Fe(I)(CO)(2)(CN)S] species that serves as the precursor to the dinucl

27 is the formation of RE carbodiimides (RE(2)(CN(2))(3)) along with Pt particles.

28 E)(3)][((Me(3)Si)(2)N)(2)U(mu-N)(mu-kappa(2):CN-CH(2)SiMe(2)NSiMe(3))U(N(SiMe(3))(2))(2)] (DME = 1,2-

29 (CN) without WMH (CN without SCeVD, n = 20), CN with SCeVD (n = 22), preclinical AD (pAD) + mild cogn

30 active-state structure of HTR2A bound to 25-CN-NBOH-a prototypical hallucinogen-in complex with an e

31 s in the entorhinal cortex (ERC; AD: n = 25; CN: n = 52) and hippocampus (AD: n = 29; CN: n = 56).

32 25; CN: n = 52) and hippocampus (AD: n = 29; CN: n = 56).

33 pared with those of cyano-vinylene-linked 2D-CN-PPQV1 (E(g) =2.4 eV) produced by the Knoevenagel reac

34 ive addition and transmetalation, and CCl(3) CN-induced reductive elimination.

35 yl-4-methoxypyridyl-2-methyl)amine) in CH(3) CN with 4 equiv CAN and 200 equiv HClO(4) at 20 degrees

36 es, [(H(3)dpat)(2)][(Nd(NO(3))(6))(2)].2CH(3)CN (1), and the related [(H(3)dpat)(2)][(Er(NO(3))(5))(3

37 ted [(H(3)dpat)(2)][(Er(NO(3))(5))(3)].3CH(3)CN.2H(2)O (2).

38 -propenones (mixture of Z,E-isomers) in CH(3)CN containing InCl(3) and In(OTf)(3) at 80 degrees C aff

39 The double helix forms in dilute CH(3)CN solution of the micromolar concentration level, e.g.,

40 lambda increased to values expected in CH(3)CN solution when the molecule was positioned at a distan

41 howed the ability to capture CO(2) from CH(3)CN solutions to form a zwitterionic alkylcarbonate adduc

42 edict that the oxidation potentials (in CH(3)CN) of various DAC-benzene derivatives will range from +

43 on of CO(2) to formate in acetonitrile (CH(3)CN).

44 trongly emissive ( (f) of up to 0.92 in CH(3)CN).

45 is work, we show that [Fe(II)(Me(3)NTB)(CH(3)CN)](CF(3)SO(3))(2) (Me(3)NTB = tris((1-methyl-1H-benzo[

46 Using CsF as the fluoride source in CH(3)CN, the N-H benzotriazoles are formed in high selectivit

47 Et(4)](2)Mn(II)(3)(CN)(8), [NEt(4)]Mn(II)(3)(CN)(7), and Mn(CN)(2) form stoichiometrically related A

48 ), NEtMe(3)) along with [NEt(4)](2)Mn(II)(3)(CN)(8), [NEt(4)]Mn(II)(3)(CN)(7), and Mn(CN)(2) form sto

49 e heteroleptic complexes, trans-[M(IV) F(4) (CN)(2) ](2-) (M=Re, Os), obtained from their homoleptic

50 in the magnetic anisotropy of trans-[ReF(4) (CN)(2) ](2-) as compared to [ReF(6) ](2-) , reflecting t

51 group at benzothiazole unit (Ar = 4-C(6)H(4)CN) exhibits a comparatively high fluorescence quantum y

52 no significant differences among SN (68.5%), CN (26.4%), and SASF (5.2%).

53 ) forms a hydrated material of A(3)Mn(II)(5)(CN)(13) composition.

54 A(3)Mn(II)(5)(CN)(13) forms a complex, 3-D extended structural motif w

55 A(3)Mn(5)(CN)(13) (A = NMe(4), NEtMe(3)) along with [NEt(4)](2)Mn(

56 s, including NOTCH1, which we establish as a CN substrate.

57 The optimized MOF-sensor had a CN(-) -detection limit of 0.05 mum, which is much lower

58 dinates to the active-site Zn(II) ions via a CN and that maximizes a pai-pai interaction with Trp(227

59 he reaction of Mn(II)(O(2)CCH(3))(2) and A(+)CN(-) (A = NMe(4), NEtMe(3)) forms a hydrated material o

60 clonal haematopoiesis with specific acquired CN-LOH mutations.

61 ation complexes, such as Au(CN)(2)(-) and Ag(CN)(2)(-) with linear geometries, while the K(+) ions fu

62 rossover framework, [Fe(II) (pdm)(H(2) O)[Ag(CN)(2) ](2) .H(2) O, under identical experimental condit

63 ctive for Au(CN)(2)(-) in the presence of Ag(CN)(2)(-), which has a lower binding affinity toward alp

64 In addition, AMY1 CN was not associated with anthropometric or glycemic ou

65 a-to-Bacteriodes ratio (P/B ratio), and AMY1 CN influence weight change.

66 e means +/- SDs of log10(P/B ratio) and AMY1 CN were -2.1 +/- 1.8 and 6.6 +/- 2.4, respectively.

67 baseline, a modest association between AMY1 CN and BMI (P = 0.04) was observed.

68 Interaction analyses between AMY1 CN and nutrient intake did not reveal any significant as

69 among subjects in both groups with high AMY1 CN [-0.17 kg/unit (95% CI: -1.01, 0.66; n = 24; P = 0.68

70 However, among subjects with low AMY1 CN (<6.5 copies), baseline P/B ratio predicted a 2.12-kg

71 The combined use of low AMY1 CN and pretreatment P/B ratio for weight loss prediction

72 aches the colon in individuals with low AMY1 CN, and that the fate of this starch depends on the gut

73 ween salivary amylase gene copy number (AMY1 CN) and weight management is likely modified by diet and

74 this study was to assess the impact of AMY1 CN on anthropometrics and glycemic outcomes in obese ind

75 ding biomarker [log10(P/B ratio) and/or AMY1 CN] diet-group interactions.

76 jectories or glycemic improvements, the AMY1 CN cannot be considered as an important biomarker for re

77 red with those on the ADD diet, whereas AMY1 CN was not found to predict weight loss differences betw

78 ecal samples were collected, from which AMY1 CN and P/B ratio, respectively, were determined.

79 n drove gut microbiome convergence, and AMY1-CN correlated with oral and gut microbiome composition a

80 High-AMY1-CN subjects had higher levels of salivary Porphyromonas;

81 The microbiomes of low-AMY1-CN subjects had enhanced capacity to break down complex

82 rovides a resource to investigate Ca(2+) and CN signaling and demonstrates synergy between experiment

83 0, 60:40 and 50:50), while WP aggregates and CN-WP aggregates were the primary constituents of whey p

84 in AKI patients with elevated bilirubin and CN might be the result of toxic effects of cholestasis a

85 ayer was predominantly covered by the CN and CN-WP aggregates in the presence of equal or greater amo

86 cute kidney injury in patients with LCCD and CN, and chronic glomerular disease in the other types, 3

87 hed MMR-D from copy number (CN)-low-like and CN-high-like ECs with an area under the receiver operati

88 sulfanyl (SBu- t), alkoxide (OEt, OMe), and CN.

89 types are seen when hindbrain patterning and CN V gross morphology is altered, but not when it is nor

90 he photo-induced electron transfer (PET) and CN isomerisation mechanisms.

91 d focal copy number (CN) events, and SNV and CN signatures.

92 ichiometry between alpha-cyclodextrin and Au(CN)(2)(-) is favored in the presence of ethanol.

93 for metal-coordination complexes, such as Au(CN)(2)(-) and Ag(CN)(2)(-) with linear geometries, while

94 A 1:1 binding stoichiometry between Au(CN)(2)(-) and alpha-cyclodextrin in aqueous solution, re

95 , this stripping process is selective for Au(CN)(2)(-) in the presence of Ag(CN)(2)(-), which has a l

96 e report the molecular recognition of the Au(CN)(2)(-) anion, a crucial intermediate in today's gold

97 m stoichiometrically related A (a)Mn(II) (b)(CN) (a+2 b) ( a = 0, b = 1; a = 2, b = 3; a = 1, b = 3;

98 Excitation of B-CN/N-NH(2) 1,4-azaborine would have a few effects: intra

99 tive, such as alpha(S1)-CN f(24-32) and beta-CN f(193-209).

100 beta-Lg and beta-CN were digested faster in yogurt than milk, which was m

101 Beta-casein (beta-CN) phenotypes in cow milk were determined using ultra-h

102 Five beta-CN phenotypes A1A1, A1A2, A1I, A2A2 and A2I were found w

103 The higher proportion of beta-CN phenotype A2A2 compared to other phenotypes was expec

104 tive of this study was to determine the beta-CN phenotypes in cow milk collected from HF and cross-br

105 The results showed that three beta-CN variants A1, A2 and I were detected and identified in

106 of synaptic transmission were shared between CN and PT.

107 es, and phospho-181T-tau were higher in both CN and pAD/MCI with SCeVD groups than in the correspondi

108 ered AP sites in mtDNA within 20 s, and BTBM-CN(2) presented a "turn-on" red fluorescence signal at 5

109 Then, about 100 s later, BTBM-CN(2) emitted a new green fluorescence signal at 480 nm,

110 ive AP site-specific fluorescent rotor (BTBM-CN(2)) was designed by the strategy of molecular conform

111 ntracellular experiments indicated that BTBM-CN(2) could detect AP sites in mtDNA in a rapid and quan

112 ECM generated by CN-null fibroblasts contained more collagen with greater

113 In fact, ~58% of all true CNVs recovered by CN-Learn were either singletons or calls that lacked sup

114 rter, suggesting conserved NPC regulation by CN.

115 ractions to direct the enantio-determining C-CN bond formation.

116 hieved by exploiting the lower barrier for C-CN oxidative addition and reductive elimination at benzy

117 idate the regulatory network of calcineurin (CN)/PP2B, the Ca(2+)-activated phosphatase that recogniz

118 ated by the Ser/Thr phosphatase calcineurin (CN).

119 riyl)tris(([1,1'-biphenyl]-3-carbonitrile)) (CN-T2T) (DeltaE(ST) = 30 meV) and BCzPh:bis-4,6-(3,5-di-

120 n solving the complex IEF pattern of casein (CN) mixtures observed when Italian and foreign WB milk a

121 ns varied depending on the ratio of caseins (CN) and whey proteins (WP) in the continuous phase.

122 u growing Prussian blue analogs (PBAs, Co[Co(CN)(6)], Fe[Fe(CN)(6)] and Co[Fe(CN)(6)]) on a natural l

123 orescent linker and a hemicyanine-containing CN(-) -responsive linker were sequentially installed int

124 he AD (n = 213), MCI (n = 322), and control (CN, n = 322) groups, we used structural MRI data and neu

125 17; Asymptomatic AD [ASY]: n = 13; Control [CN]: n = 13) (overall 37.2% female; mean age at death 86

126 Thus, the diatomic cyanide (-CN) and isocyanide (-NC) ligands are as capable of stabi

127 iron atom is co-coordinated by two cyanides (CN(-)) and one carbon monoxide (CO) ligand.

128 (m)CD-decorated CN stably produces stoichiometric oxygen and methanol fr

129 this preference is not key to this exquisite CN selectivity.

130 e redox DMPC liposome collisions with K(3)Fe(CN)(6)/K(4)Fe(CN)(6) as the encapsulated aqueous redox p

131 de is a Zn-insertion Prussian blue, Zn(3)[Fe(CN)(6)](2).

132 iposome collisions with K(3)Fe(CN)(6)/K(4)Fe(CN)(6) as the encapsulated aqueous redox probe.

133 dox couple ferri/ferro cyanide (K(3)/K(4)[Fe(CN)(6)]).

134 as investigated by EIS in a Fe(CN(6))(4-)/Fe(CN(6))(3-) red-ox system, being able to quantitatively d

135 effect and a redox couple [Fe(CN)(6) (4-)/Fe(CN)(6) (3-)] for thermogalvanic effect.

136 e of the DPV signal for the Fe(CN)(6)(4-)/Fe(CN)(6)(3-) redox probe with the increase of the p-syneph

137 A dissolution of [Fe(CN)(6)](4-)/[Fe(CN)(6)](3-) as a redox probe was used to study the elect

138 d CTV target was investigated by EIS in a Fe(CN(6))(4-)/Fe(CN(6))(3-) red-ox system, being able to qu

139 Enzymes and cofactors (NAD(+) and Fe(CN)(6)(3-)) were immobilized by modification of screen-p

140 PBAs, Co[Co(CN)(6)], Fe[Fe(CN)(6)] and Co[Fe(CN)(6)]) on a natural loofa (L) by a room-temperature we

141 hermodiffusion effect and a redox couple [Fe(CN)(6) (4-)/Fe(CN)(6) (3-)] for thermogalvanic effect.

142 ian blue analogs (PBAs, Co[Co(CN)(6)], Fe[Fe(CN)(6)] and Co[Fe(CN)(6)]) on a natural loofa (L) by a r

143 peaks with a DeltaE(p) value of 0.26 V in Fe(CN)(6)(3-/4-) bench mark solution.

144 oltammetry (CV) with the redox indicator [Fe(CN)(6)](3-/4-).

145 Both redox ions ([Fe(CN)(6)](3-/4-)) and redox organic compounds (dopamine) a

146 node and Prussian blue analog Na(1.88) Mn[Fe(CN)(6) ](0.97) .1.35H(2) O cathode can be coupled to con

147 scopy to visualize the thermal aspects of Fe(CN)(6)(3-/4-) redox, and compare the estimated cooling t

148 A dissolution of [Fe(CN)(6)](4-)/[Fe(CN)(6)](3-) as a redox probe was used to

149 high conformational entropy change of the Fe(CN)(6)(3-/4-) redox reaction can be used as the basis fo

150 at the decrease of the DPV signal for the Fe(CN)(6)(4-)/Fe(CN)(6)(3-) redox probe with the increase o

151 r resistance (DeltaR(ct)) relative to the Fe(CN)(6)(4-/3-) electrochemical probe after immunoassays i

152 l impedance spectroscopy (EIS) using the [Fe(CN)6](3-)/(4-) (1:1) as a hybridization index.

153 Liposomes (~200 nm diameter) loaded with Fe(CN)(6)(4-) are driven out of the nanopipette orifice whe

154 f possibly increased complications following CN in renal cell carcinoma patients, when TKI treatment

155 reases the postoperative morbidity following CN in renal cell carcinoma patients.

156 olution, SNVs and indels (both corrected for CN in aneuploid regions), loss of heterozygosity, megaba

157 ntributed most to the AD classification from CN.

158 Such (m)CD rapidly extracts holes from CN and prevents the surface adsorption of methanol, favo

159 haracterized by recurrent chromosomal gains, CN-LOH, DAXX mutations, and ALT-positivity.

160 1(+)CD4(+) T cells only within a granulocyte CN positively correlated with survival in a high-risk pa

161 cles bearing the electron-withdrawing groups CN, Cl, NO(2), and CF(3) are introduced.

162 copy number neutral loss of heterozygosity (CN-LOH) were identified by STR and SNP arrays.

163 ons and copy-neutral loss of heterozygosity (CN-LOH)) on all chromosomes(1,2,5,6,9), but the sources

164 e dynamics of frontier orbitals during the I-CN bond cleavage process.

165 form of [Fe(II)(CN)(5)(CO)](3-) and [Fe(II)(CN)(4)(CO)(2)](2-).

166 cyanide is primarily in the form of [Fe(II)(CN)(5)(CO)](3-) and [Fe(II)(CN)(4)(CO)(2)](2-).

167 e served as precursors to the unusual Fe(II)(CN)(CO) moieties that form the catalytic centers of hydr

168 l battery with a solid-state NaFe(II)Fe(III)(CN)(6) (Prussian Blue) cathode, showing approximately an

169 ical data to support the assumptions used in CN-TBMs, we put their global climate change predictions

170 ed genotypes to determine whether individual CN V motor and sensory axons wander, branch and sprout a

171 D on renal recovery of patients with initial CN not requiring dialysis.

172 and macrophage CNs, and disruption of inter-CN communication was associated with inferior outcomes.

173 KAu(CN)(2)C(alpha-cyclodextrin)(2), and KAg(CN)(2)C(alpha-cyclodextrin)(2)-demonstrate that the bind

174 n process between alpha-cyclodextrin and KAu(CN)(2) can be applied to the stripping of gold from the

175 tructures-KAu(CN)(2)Calpha-cyclodextrin, KAu(CN)(2)C(alpha-cyclodextrin)(2), and KAg(CN)(2)C(alpha-cy

176 The adduct formation of KAu(CN)(2)Calpha-cyclodextrin in aqueous solution is sustain

177 ree X-ray single-crystal superstructures-KAu(CN)(2)Calpha-cyclodextrin, KAu(CN)(2)C(alpha-cyclodextri

178 nces between the NND and ADD groups [0.05 kg/CN (95% CI: -0.40, 0.51; n = 54; P = 0.83)].

179 h the majority of these genes being at lower CN in the polar bear.

180 The primary interest in [M(CN)8]n--based networks was focused on their application

181 ial structural and electronic features of [M(CN)8]n- ions, which are purposefully explored to introdu

182 The [M(CN)8]n- ions comprise a series of complexes of heavy tra

183 which, when coupled with hexasulfide, [{(Me)CN(i-Pr)}(2)CH](+)(2)[S(6)](2-) (4), and N-heterocyclic

184 radical 2(*) with the imidazolium salt [{(Me)CN(i-Pr)}(2)CH](+)[Cl](-) (in a 1:1 molar ratio) gives t

185 very of the pioneering bimetallic {MnII4[MIV(CN)8]2} and {MnII9[MV(CN)8]6} (M = Mo, W) molecules in 2

186 (3)(CN)(8), [NEt(4)]Mn(II)(3)(CN)(7), and Mn(CN)(2) form stoichiometrically related A (a)Mn(II) (b)(C

187 f-assembly of the pentagonal bipyramidal [Mo(CN)(7) ](4-) anion and the Mn(II) unit with a tridentate

188 Most CN neurons are born between E10.5 and E13.5, with a peak

189 coupled with mesoporous carbon nitride (mpg-CN(x) ) as the photosensitizer.

190 mtDNA CN was measured in the ALIVE (AIDS Linked to the Intrave

191 Before 50 years of age, mtDNA CN is similar between HIV-infected individuals with well

192 ositivity assessed the relationship of mtDNA CN to HIV markers (CD4+ T-cell counts, viral load, antir

193 articipants, from age 50 years onward, mtDNA CN declined significantly faster among HIV-infected indi

194 ected persons, but from age 50 onward, mtDNA CN declines significantly faster among all infected indi

195 bimetallic {MnII4[MIV(CN)8]2} and {MnII9[MV(CN)8]6} (M = Mo, W) molecules in 2000, octacyanidometall

196 ea cycle disorders (UCDs) or Crigler-Najjar (CN) syndrome 6 months posttransplantation.

197 by long-lived electron accumulation in (NCN)CN(x) after hole extraction.

198 f photogenerated electrons and holes in (NCN)CN(x) can be well described by a random walk model.

199 nctionalized melon-type carbon nitride ((NCN)CN(x)) has been selected as an example of emerging carbo

200 es the extraction of electrons from the (NCN)CN(x) and increases the H(2) production efficiency under

201 LCDD [n = 154], LCDD with cast nephropathy (CN) [n = 58]), HCDD (n = 23), or LHCDD (n = 20).

202 ients with initial myeloma cast nephropathy (CN) and acute kidney injury (AKI) without need for dialy

203 erative localization of the cavernous nerve (CN) network for nerve-sparing radical prostatectomy usin

204 Divergent trigeminal nerve (CN V) differentiation and altered trigeminal ganglion (C

205 ted differentiation of the trigeminal nerve (CN V), a cranial nerve essential for suckling, feeding a

206 metal-organic framework (M'MOF), [Fe(pyz)Ni(CN)(4) ] (FeNi-M'MOF, pyz=pyrazine), with multiple funct

207 Biosynthesis of the NiFe(CN)(2)(CO) cofactor requires the activity of at least si

208 (abdominal length <1.5 cm), a Collis-Nissen (CN) or stomach around the stomach fundoplication (SASF)

209 lectron lifetime (t(50%)) of carbon nitride (CN) by six folds, favouring a six-electron product.

210 cipants were recruited; 35 cognitive normal (CN, age = 83.8 +/- 6.9), 34 MCI (age = 83.9 +/- 6.6), an

211 inc, copper, selenium in cognitively normal (CN) and AD subjects.

212 uld also be found in the cognitively normal (CN) participants.

213 cerebrovascular disease: cognitively normal (CN) without WMH (CN without SCeVD, n = 20), CN with SCeV

214 ication model of AD from cognitively normal (CN) yielded an average accuracy of 90.8% based on five-f

215 This study included 83 cognitively normal (CN), 160 mild cognitive impairment (MCI), and 73 AD subj

216 n independent discovery [cognitively normal (CN), 19; mild cognitive impairment (MCI) risk, 43; MCI,

217 ed (CNG) channels convert cyclic nucleotide (CN) binding and unbinding into electrical signals in sen

218 -3) mm(2)/s, p = 0.031) and caudate nucleus (CN) (1.319 vs. 1.394 x 10(-3) mm(2)/s, p = 0.04).

219 riatal areas (putamen (PT), caudate nucleus (CN) and accumbens nucleus (NAC)) from postmortem brain t

220 iome and specific alleles, gene copy number (CN) also varies.

221 other than loss of RB1 few gene-copy number (CN) alterations are associated with irreversible-resista

222 Copy number (CN) differences in genomic regions between closely relat

223 en, global, arm-level and focal copy number (CN) events, and SNV and CN signatures.

224 Low mitochondrial DNA (mtDNA) copy number (CN) is a predictor of adverse aging outcomes, and its st

225 lenge of delivering informative copy number (CN) profiles from formalin-fixed paraffin embedded (FFPE

226 DNA copy number (CN) profiling of ensembles of tumors allows a thermodyna

227 cation distinguished MMR-D from copy number (CN)-low-like and CN-high-like ECs with an area under the

228 enome characteristics in K562: copy numbers (CN) of aneuploid chromosome segments at high-resolution,

229 Olfactory receptors composed 47% of CN differentiated genes, with the majority of these gene

230 results suggest a chaperone-like activity of CN on beta-lg pressure-induced aggregation which needs f

231 This successful analysis of CN in FFPE material using NGS provides proof of principl

232 The selective binding of CN(-) to hemicyanine inhibited the energy transfer betwe

233 ied the effect of different concentration of CN on alpha-la purity and recovery.

234 stigate the frequency and clinical course of CN.

235 In vitro proteome-wide detection of CN-binding peptides, in vivo SLiM-dependent proximity la

236 Renal biopsy revealed the diagnosis of CN in 8 of 45 patients with AKI (17.8%), whereas none of

237 n as predictive factors for the diagnosis of CN.

238 erning and gross morphological disruption of CN V seen in LgDel+/-.

239 genes per individual that showed evidence of CN variation (CNV).

240 This disordered growth of CN V sensory and motor axons, whose appropriate targetin

241 For the much smaller number of CN-TBMs that explicitly model individual-based belowgrou

242 he entire CNgV transcriptome at the onset of CN V differentiation prefigure subsequent disruption of

243 with our initial hypothesis, the presence of CN decreased beta-lg pressure-induced aggregation and co

244 into the allosteric gating and regulation of CN-gated and nucleotide-modulated channels and CNG chann

245 In a subset of CN participants who progressed to mild cognitive impairm

246 ing were distributed into control offspring (CN-o) and periodontal disease offspring (PED-o) groups.

247 x 10(3) M(-1) was obtained when Q(+) was a p-CN-substituted benzylic trimethylammonium.

248 I) compound [(ADC(Ph))Ge](2) (4) (ADC(Ph) = {CN(Dipp)}(2)CPh, Dipp = 2,6-iPr(2)C(6)H(3)) containing a

249 vibration associated with the photogenerated CN fragment.

250 Here, we present CN-Learn, a machine-learning framework that integrates c

251 To sense As(V), S. putrefaciens CN-32 requires functional arsenate respiratory reductase

252 arsenate (As(V)) by Shewanella putrefaciens CN-32, a model dissimilatory metal-reducing bacterium (D

253 ridine-2,6-bis(N-cyanocarboxamidine) (PyBCam(CN)).

254 ition was associated with loss of ER and RB1 CN.

255 ent (MCI) risk, 43; MCI, 6] and replication (CN,73; MCI, 45; AD, 20) cohorts.

256 Interestingly, SA-Rh/CN exhibits greatly enhanced tolerance to CO poisoning,

257 ed carbon (SA-Rh/CN) and discover that SA-Rh/CN exhibits promising electrocatalytic properties for fo

258 rance to CO poisoning, and Rh atoms in SA-Rh/CN resist sintering after long-term testing, resulting i

259 ically dispersed Rh on N-doped carbon (SA-Rh/CN) and discover that SA-Rh/CN exhibits promising electr

260 he formate route is more favourable on SA-Rh/CN.

261 s recognized as bioactive, such as alpha(S1)-CN f(24-32) and beta-CN f(193-209).

262 comprising 15 sub-types, three LN and seven CN types were identified.

263 We combined rapid in vivo labeling of single CN V axons in LgDel+/- mouse embryos, a genomically accu

264 Nearly 200 genes displayed species-specific CN differences between polar bear and brown bear species

265 al ligands to an Fe-Fe binuclear subcluster: CN(-), CO, and an azadithiolate (adt) ligand that provid

266 Comparison with targeted CN assessment showed consistency with the Next Generatio

267 ADC values of thalami, CN, and CH were significantly lower in IUGR than control

268 In addition, we found that CN-LOH mutations across the genome tended to cause chrom

269 The analysis uncovers that CN states having a narrower distribution are energetical

270 The CN network assembled here provides a resource to investi

271 Here, we analyzed the CN profiles of 17 polar bears, 9 brown bears, and 2 blac

272 hallenging owing to its instability, but the CN(-) complex is both stable and an excellent mimic of t

273 acial layer was predominantly covered by the CN and CN-WP aggregates in the presence of equal or grea

274 ualizes membrane potential variations in the CN and its branches (CNB) in real time.

275 oup was significantly worse than that in the CN group.

276 ) were similarly significantly higher in the CN with SCeVD and pAD/MCI with SCeVD groups than their c

277 the pAD/MCI with SCeVD group but not in the CN with SCeVD group relative to controls without SCeVD.

278 , we performed trans-fascial staining of the CN by direct VSD administration.

279 in response to electrical stimulation of the CN, which was clearly differentiated from surrounding ti

280 id 1f was obtained through hydrolysis of the CN.

281 trafast dynamics of a vibrational probe (the CN stretch of phenyl selenocyanate) in poly(methyl metha

282 d from the matrix infrared spectra of their -CN and -NC chromophore ligand stretching modes, were con

283 ated phosphorus was higher in AD compared to CN subjects, while calcium, iron, zinc, copper and selen

284 )) and calcium (p = 0.025) in AD compared to CN subjects, with higher phosphorus/calcium (p = 2.55 x

285 We relate microbiome diversity to CN variation of the AMY1 locus, which encodes salivary a

286 The results point to CN changes that are more common in high-ploidy tumors an

287 On unadjusted analysis, TKI use prior to CN was associated with higher overall complication rate

288 centrations of metabolites in AD relative to CN samples, as well as associations with severity of bot

289 he synthesis of a nanosized complex, [Fe(Tp)(CN)(3)](8)[Fe(H(2)O)(DMSO)](6) (abbreviated as [Fe(14)],

290 05 mum, which is much lower than traditional CN(-) fluorescent sensors (about 0.2 mum).

291 In the presence of TSE, CN and SASF performed according to determined surgical p

292 f motif determinants uncovered unanticipated CN interactors, including NOTCH1, which we establish as

293 f consecutive patients with NK who underwent CN between November 2014 and October 2019.

294 Stage IV renal cell carcinoma who underwent CN from 2007-2010 utilizing the SEER-Medicare database.

295 Unexpectedly, CN shows SLiM-dependent proximity to centrosomal and nuc

296 ent the P450cam-Pdx structure complexed with CN(-).

297 of the patients with CKD was diagnosed with CN.

298 As data on patients with CN are obtained primarily from case reports or autopsy s

299 with a recovery of 88% for solution without CN.

300 isease: cognitively normal (CN) without WMH (CN without SCeVD, n = 20), CN with SCeVD (n = 22), precl

301 es (Ar = p-FC(6)H(4)) LPt(IV)F(py)(Ar)X (X = CN, Cl, 4-OC(6)H(4)NO(2)) and LPt(IV)F(2)(Ar)(HX) (X = N