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1                                              C(4) photosynthesis evolved multiple times independently
2                                              C-C chemokine receptor type 2 (CCR2) is expressed on mon
3                                              C-type inactivation is attributed to a nonconductive con
4                                              C. abbreviata abundance had strong, negative relationshi
5 ll counts (15.8 vs 7 x 10(3) /uL, P = .019), C-reactive protein (198 vs. 107 mg/L, P = .010) and D-di
6 he N and C termini, and deletion of up to 11 C-terminal residues had little impact on the agonist-ind
7         We used simultaneously acquired (11) C-PBR28 positron emission tomography/magnetic resonance
8                                         [(11)C]UCB-J V(T) was significantly lower in the frontal and
9                  The correlation between (11)C-choline PET/CT positivity and initial treatment, Gleas
10 labeled with the short half-life isotope (11)C.
11 eptor (KOR) by naltrexone measured with [(11)C]-LY2795050 positron emission tomography (PET) as a pre
12 rsity of Florida breeding line #394-1-27-12 (C. moschata) is conferred by three independent dominant
13  kinetic studies involving H/D and (13)C/(12)C exchange, coupled with operando infrared spectroscopy
14 lationship in a C(4) plant between delta(13) C(leaf) and WUE(plant) under well watered and water-limi
15 following injection of hyperpolarized [1-(13)C]pyruvate.
16  were characterized by means of (1)H and (13)C NMR spectrometry as well as single-crystal X-ray diffr
17  using (14)C-radiolabeled ((14)C-AA) and (13)C-labeled ((13)C(3)-AA) materials.
18 nsient kinetic studies involving H/D and (13)C/(12)C exchange, coupled with operando infrared spectro
19 d Tanzania, using compound-specific delta(13)C and Delta(13)C values of the major fatty acids, provid
20            Stable isotope analyses (delta(13)C and delta(15)N) indicated that the elephants were not
21                                     delta(13)C signatures of pure-phase CFCs and hydrochlorofluorocar
22 ng compound-specific delta(13)C and Delta(13)C values of the major fatty acids, provides chemical evi
23                                  Dynamic (13)C MRSI was performed following injection of hyperpolariz
24 oncentrations in the membrane, the (19)F-(13)C distance data indicate three cholesterol molecules bou
25 od that assesses HBP flux as UDP-GlcNAc ((13)C)-molar percent enrichment (MPE) and concentration and
26 ctate dehydrogenase using hyperpolarized (13)C magnetic resonance, a technique which can be used for
27 phytol, all show increasing depletion in (13)C over the transect from the control site towards the se
28                     Large intramolecular (13)C kinetic isotope effects (KIEs) for the di-pai-methane
29 diolabeled ((14)C-AA) and (13)C-labeled ((13)C(3)-AA) materials.
30  we accept the more disputed evidence of (13)C-depleted zircon deposits.
31                  We observed substantial (13)C enrichment in SMCs that were adjacent to [(13)C]choles
32 nrichment in SMCs that were adjacent to [(13)C]cholesterol-loaded macrophages-including in cytosolic
33 on was studied using (14)C-radiolabeled ((14)C-AA) and (13)C-labeled ((13)C(3)-AA) materials.
34 brewed-like extraction was studied using (14)C-radiolabeled ((14)C-AA) and (13)C-labeled ((13)C(3)-AA
35 oid Ga(Nacnac) (Nacnac=HC[C(Me)N(2,6-i-Pr(2) C(6) H(3) )](2) ).
36 d)][(Me) LZn(S)] (2) ((Me) L={(2,6-(i) Pr(2) C(6) H(3) )NC(Me)}(2) CH), was isolated via reaction of
37 nd carboxamide oxygens within Mn-mu-S-CH(2) -C-O, 5-membered rings.
38 iled to fully explain the means by which s(2)C(32) restricts I(34) wobbling.
39  spark plasma sintered Fe(48)Cr(15)Mo(14)Y(2)C(15)B(6) metallic glass is established by analyzing the
40 ruption and pore formation in HeLa and BE(2)-C cells and inhibition and eradication of C. albicans bi
41 complexes, made by the reaction of Rh(eta(2)-C(2)H(4))(2)(acetylacetonate) with the support and ancho
42 )H(6)/C(2)H(4) and ternary C(2)H(4)/C(2)H(2)/C(2)H(6) mixture.
43 vailable annotated reference sequences of 22 C. albicans strains, thus offering a higher coverage and
44         Herein, a 2D titanium carbide (Ti(3) C(2) ) MXene film with transparent conducting electrode
45 s compared to previously reported pure Ti(3) C(2) T(x) films.
46                Here, it is reported on Ti(3) C(2) T(x) MXene microstrip transmission lines with low-e
47 forward method for the formation of C(sp(3))-C(sp(2)) bonds.
48 nscriptome-wide quantitative mapping of ac(4)C at single-nucleotide resolution.
49                          Here we report ac(4)C-seq, a chemical genomic method for the transcriptome-w
50 ed through the isolated (N, O)(Ph, C(6)H(4), C) oxaphosphetanes (Channel A), whereas MoBA compounds d
51 inary C(2)H(6)/C(2)H(4) and ternary C(2)H(4)/C(2)H(2)/C(2)H(6) mixture.
52                        While individual m(5) C-methyltransferases have been studied, the impact of th
53                         [(64)Cu]Cu-c[R(4)W(5)C] demonstrated significantly reduced uptake in the brai
54  with the acid-mediated [(64)Cu]Cu-c[E(4)W(5)C] tracer.
55 eparation of C(2)H(4) from a binary C(2)H(6)/C(2)H(4) and ternary C(2)H(4)/C(2)H(2)/C(2)H(6) mixture.
56 hour (normal range, 0-30 mm per hour), and a C-reactive protein level of 203.8 mg/L (1940.9 nmol/L) (
57 of an N-terminal effector domain (NTD) and a C-terminal regulatory domain (CTD); a carotenoid spans t
58 parameter value attains a maximum value at a C/Zr ~ 0.83.
59 el including the screening test result had a C-statistic of 0.860, c-slope of 0.997, and R(2) of 0.59
60 mine if there is a genetic relationship in a C(4) plant between delta(13) C(leaf) and WUE(plant) unde
61 on the ribosome revealed the disruption of a C(32-)A(38) cross-loop interaction but failed to fully e
62         Here, we determined the ability of a C. trachomatis recombinant major outer membrane protein
63 86 +/- 0.35 mum diameter cell) compared to a C. elegans embryo (5.78 +/- 0.18 mum(2) in a 55.83 +/- 1
64                             New pS22-Lamin A/C binding was accompanied by increased histone acetylati
65                     Mutations in the lamin A/C gene (LMNA) are identified in patients with various ty
66                       In particular, lamin A/C, an intermediate filament protein critical for the int
67 thesis that human immunoglobulins may affect C. neoformans virulence in vivo warrants further investi
68 about how reactive Fe and Al minerals affect C cycling in restored wetlands.
69              Our data show human IgM affects C. neoformans morphology in vitro and suggest that the h
70 required for PIV-mediated protection against C. burnetii infection.
71                       These strategies allow C-C bond formations in a regioselective manner to synthe
72  multiple times independently from ancestral C(3) photosynthesis in a broad range of flowering land p
73 LC stage 0 (9.4%), A (59.5%), B (16.2%), and C (14.9%).
74 vely), while CC genotype (3.8% vs. 4.4%) and C allele (20.4% vs. 23.9%) carriers were the lowest.
75 cochemical sensitive dyes, Di-4-ANEPPDHQ and C-laurdan, we demonstrated that AdipoRon decreased the r
76 f Barcelona Clinic Liver Cancer (BCLC) B and C, and the presence of cirrhosis, respectively.
77  and their analogues with modified A, B, and C rings, as well as hybrid compounds derived from colchi
78  tropomyosin receptor kinase (TRK) A, B, and C, which has been shown to have anti-tumour activity aga
79 ss caused by Corynebacterium diphtheriae and C. ulcerans, and use of diphtheria anti-toxin in the Uni
80 e analogs along with the natural A, T, G and C bases during DNA synthesis, which allows for labeling
81 tions cluster within the conserved N-Lip and C-Lip regions that are separated by 500-residues in huma
82 clusters of polar residues at both the N and C termini, and deletion of up to 11 C-terminal residues
83 e disordered region that connects the N- and C-terminal halves in many eukaryotic ABC transporters, a
84 bstrate; an interfacial site between TMD and C-terminal domain (CTD) that modulates the Zn(2+) transp
85    Anaphase promoting complex/cyclosome (APC/C) is reported to play an important role in metaphase-to
86 ntal material is available for this article.(C) RSNA, 2020.
87 ntal material is available for this article.(C) RSNA, 2020.
88 ntal material is available for this article.(C) RSNA, 2020.
89 d greater microbial respiration of available C, greater overwinter CO(2) efflux and greater nutrient
90 tients were categorized into 4 groups (A, B, C, and D) corresponding to the manufacturer from which t
91 E4 family comprises four subtypes, PDE4A, B, C, and D.
92 ty using legacy models (e.g. Brooks-Corey (B-C), van Genuchten, etc.) that were developed for convent
93                 Older age (OR-1.07), grade B/C pancreatic fistula (OR-3.84), and epidural use (OR-3.1
94  under UF cell culture conditions or in Balb/C mice and led to an over 2-fold increase in CTC attachm
95 ld increase in CTC attachment to ECs or Balb/C mouse lungs, respectively, compared to untreated condi
96  and stereoselective distal allylic/benzylic C-H functionalization of allyl and benzyl silyl ethers w
97 ficient separation of C(2)H(4) from a binary C(2)H(6)/C(2)H(4) and ternary C(2)H(4)/C(2)H(2)/C(2)H(6)
98                                      In both C. elegans and human cancer cells, ether-lipid synthesis
99 egradation pathway known to be stimulated by C(12) accumulation, was increased in Sirt5KO liver.
100 lants may be symmetrically linked to carbon (C) transfer from plant to fungus or governed by sink-sou
101 use of F(+) oxidants permits the challenging C(sp(3))-OC(sp(3)) bond formation at a high-valent nicke
102 class B1 NDM-1 and VIM-2 MBLs, and the class C P. aeruginosa AmpC.
103 he CLIF consortium organ failure score (CLIF-C OFs).
104 , hampering long-term predictions of climate C-feedbacks.
105 oups of isomers, named open (O-) and closed (C-), based on the ring conformations in the vicinity of
106  pair of recurrent cortico-thalamo-cortical (C-T-C) loops.
107 ns of eGFR (based on creatinine and cystatin C) and ACR with cancer risk using Cox regression models
108 h America warmed at the rate of 0.02 degrees C/y.
109          Multiyear stanzas above 2.1 degrees C become commonplace in projections from ~2030 onward, w
110  presentation he was febrile at 40.1 degrees C but hemodynamically stable.
111 uration of 6.10 +/- 0.08 days per 1- degrees C increase in global mean surface air temperature.
112  adapted populations, whereas the 10 degrees C adapted strains were rapidly inactivated at higher tem
113 acyl analogues (RX, NaHCO(3)/DMF/100 degrees C) in high overall yields.
114                In 100 degrees to 120 degrees C sediments, isotopic evidence and increased cell concen
115 erature used, as random (Co, Cd, 120 degrees C), short duplicates (Co, Cd, 85 degrees C), long duplic
116 at samples stored at 4 degrees C, 15 degrees C and 25 degrees C using our proposed technique was foun
117 rmation from CO(2)/H(2) feeds at 170 degrees C and 1-8 bar pressure.
118 onse rate increased to 2.54 km m(-2) degrees C(-1) Soil moisture was negatively correlated with fine-
119         When E681 was cultured at 20 degrees C or lower, it exhibited no variation for 7 days and sti
120  see text] surfaces operating at 200 degrees C for an hour in a vacuum oven.
121 kness fringes for films grown at 200 degrees C under 15 mTorr Ar, indicating excellent crystallinity
122 cterised after 96 h at 95% RH and 22 degrees C.
123 ture critical temperatures up to 242 degrees C and a 7500-oersted room-temperature coercivity.
124  at 4 degrees C, 15 degrees C and 25 degrees C using our proposed technique was found to be 105 h, 48
125 L) under two temperatures (25 and 28 degrees C) with/without predator cues from climbing perch (Anaba
126 tic resistance from residents than 3 degrees C of climate warming.
127  increased thermotolerance of the 30 degrees C adapted populations, whereas the 10 degrees C adapted
128 lly triggered crystallization at -30 degrees C for the first time.
129 , three temperatures (20, 25, and 30 degrees C) and four concentrations of glacial acetic acid (0.5%,
130 hway (Acheson process) at about 3000 degrees C.
131 und that anterograde transport at 32 degrees C, permissive conditions, through the Golgi apparatus wa
132 s C (in situ cooling [ISC]) or 33-36 degrees C (normothermic regional perfusion [NRP]).
133 tissue cultures were incubated at 37 degrees C in a 5% CO(2) environment and at days 7 and 14, the sp
134 rfusion can be performed at either 4 degrees C (in situ cooling [ISC]) or 33-36 degrees C (normotherm
135 canned on sturgeon samples kept at 4 degrees C up to 12 days.
136  of chicken meat samples stored at 4 degrees C, 15 degrees C and 25 degrees C using our proposed tech
137 wavelength IR region, performed at 4 degrees C, lead to marked sensitivity improvements over conventi
138 on (0-20 Gy), and hyperthermia at 47 degrees C (0-780 CEM(43)) has been evaluated.
139 rming scenarios: +1.5, +2, +3 and +5 degrees C.
140  increasing the temperature up to 50 degrees C.
141                             Above 55 degrees C, protein surface hydrophobicity and particle size incr
142 over an aluminum plate can achieve 6 degrees C (7 degrees C on a scale-model building) below the ambi
143 num plate can achieve 6 degrees C (7 degrees C on a scale-model building) below the ambient temperatu
144 ing procedure and (2) prebake at 700 degrees C in 20 mTorr O(2) is shown by atomic force microscopy t
145 e presence of 2.2.2-cryptand, at -78 degrees C.
146 rees C), long duplicates (Co, Pb, 85 degrees C), and insertions (Co, Mn, 85 degrees C).
147 ees C), short duplicates (Co, Cd, 85 degrees C), long duplicates (Co, Pb, 85 degrees C), and insertio
148 grees C), and insertions (Co, Mn, 85 degrees C).
149 racted by room temperature water, 90 degrees C-water, CDTA and Na(2)CO(3).
150 Our data showed that Ca37 was able to detect C. albicans cells, and it bound to Adh1 in yeast and Adh
151 of runtimes and performance of the different C++ highly reusable coalescence mergers (binary, multipl
152 ,beta-dehydro-amino acid intermediate during C(alpha)-thioether bridge LC-MS/MS fragmentation.
153                     However, total ecosystem C storage that includes soil organic C (SOC) must be con
154  coli (E. coli), and Caenorhabditis elegans (C. elegan) datasets.
155 robable association with older age; elevated C-reactive protein (CRP), D-dimer, and fibrinogen levels
156                             Enantioselective C(sp(3))-H aminations allow an efficient access to nonra
157  survivin levels was also detected following C. trachomatis infection, which was reversed by blocking
158 are presented that reveal two mechanisms for C-H borylation, (i) electrophilic aromatic substitution
159 rogenic acid and quercetin in the fruit from C.IZC were associated with molybdenum and nickel found i
160 mposite material by coupling DMASnBr(3) to g-C(3) N(4) , taking advantage from the combination of the
161  (66.1%) as Grade B, and 65 (22.2%) as Grade C.
162 lesion has normal characteristics; and Group C (control) in which the area is healthy.
163 in group A and 6.3 months (6.2-7.0) in group C (stratified hazard ratio [HR] 0.82, 95% CI 0.70-0.96;
164 ant in FAF1 in the validation cohort (c.254G>C; p.Arg85Pro).
165  suggest that the two carbon atoms of the L->C(2) complex both have carbene character.
166    The tris- and tetra-adducts of M(3)N@I(h)-C(80) metallofullerenes were synthesized and characteriz
167 eaction from rhodium to carbon to form the H-C bond.
168                         An additional Rh-H...C stabilization in some intermediates or transition stat
169  the gallium carbenoid Ga(Nacnac) (Nacnac=HC[C(Me)N(2,6-i-Pr(2) C(6) H(3) )](2) ).
170 n triglycerides level, 240 mg/dL; median HDL-C level, 36 mg/dL; and median high-sensitivity C-reactiv
171                            Compared with HDL-C, HDL-P was consistently associated with MI and ischemi
172                                    Hepatitis C virus SVR decreased monocyte interferon genes MX1, IFI
173 ition (aOR, 2.2; 95% CI, 1.3-3.9), hepatitis C infection (aOR, 1.9; 95% CI, 1.1-3.4), black race (aOR
174  model specific virus types (e.g., hepatitis C) and add additional cellular mechanisms (tissue recove
175 o eIF3 recognizing motifs found in hepatitis C virus (HCV)-like IRESs, suggesting mechanistic similar
176                       Clearance of hepatitis C virus (HCV) results in rapid changes in metabolic para
177                                           Hi-C was performed on ROs, and differential expression of r
178 solution chromosome conformation capture (Hi-C) analysis revealed multiplex, activated enhancer-promo
179          Chromosome conformation capture (Hi-C)(1,2) analysis has revealed a complex genomic landscap
180 ysis of a combination of RNA-seq, Capture Hi-C, and patient survival data suggests that CALCOCO1 and
181 tin compartmental domains in single cells Hi-C matrices.
182 o form the loops of typical sizes seen in Hi-C experiments using these low-effective-diffusion consta
183 nse and repair on 3D genome folding using Hi-C experiments on wild type cells and ataxia telangiectas
184 rmation of a genome can be profiled using Hi-C, a technique that combines chromatin conformation capt
185 wide chromatin interaction mapping, using Hi-C, reveals condensin-mediated chromatin interactions in
186     We find that nanopore sequencing with Hi-C scaffolding produces highly contiguous, chromosome-len
187 in Listeria (similar to SauCas9) and Type II-C Cas9s, likely due to Cas9 HNH domain conservation.
188 ns, redox disproportionation forms [Cu(III)](C=CAr)(R) species that reductively eliminate R-C=CAr pro
189 Here we report transcriptional adaptation in C. elegans, and find that this process requires factors
190 RO function and carboxylesterase homologs in C. elegans and other animals may reveal additional new c
191 WC(ON), a well-described olfactory neuron in C. elegans, here we derive a general and broadly useful
192 e changes under DI, RNA-seq was performed in C-76 and Val-C.
193 imate change mitigation results in increased C storage.
194 rmation (up to 20 transgenes) for increasing C and N flows with the purpose of increasing tomato frui
195 ion strategy enabling assaying of individual C-subtypes and impurities for ototoxicity and antimicrob
196  sMMO-Q necessary to attack the highly inert C-H bonds of methane.
197                               Intermolecular C-C bond-forming reactions are underdeveloped transforma
198 nstrate that introducing N and Mo atoms into C and Ru lattices, respectively, triggers electron accum
199  compounds decomposed faster via the isomer (C(6)H(4), O)(C, N, Ph) formed by P-stereomutation involv
200 tention through a mechanism dependent on its C-terminal lysine residue; its deletion led to modest re
201 pore-forming alpha1 subunit and, through its C-terminal region, scaffolds the beta subunit of VGCC an
202 nsense mutations that partially truncate its C-terminal cytoplasmic regulatory domain impair NHE6 act
203 training, and personal factors, and lastly, (C) cognitive architecture and human nature that impacts
204 ian follow-up of 3.1 years, the achieved LDL-C concentrations were 64 mg/dL (1.64 mmol/L) in the lowe
205  and identify poor performance in real life.(C) RSNA, 2020Keywords: Breast, ScreeningSee also the com
206                                     An N-Lip C-Lip fusion of mouse lipin-2 is catalytically active, w
207 h as FLOWERING LOCUS T (FT), FLOWERING LOCUS C (FLC), AGAMOUS (AG) and APETALA 3 (AP3).
208 rd automated PET/CT assessment for lymphoma.(C) RSNA, 2020.
209                                       Median C-reactive protein [138 mg/L (IQR: 83-179) vs 73 mg/L (I
210 abilizes C-MYC by antagonizing FBW7-mediated C-MYC ubiquitination and degradation.
211 the similarities and differences between MIS-C and Kawasaki disease, focusing on their epidemiology,
212 ystem inflammatory syndrome in children (MIS-C) emerged.
213 ystem inflammatory syndrome in children (MIS-C) is associated with coronavirus disease 2019.
214 ening multisystem inflammatory syndrome (MIS-C)(3-5).
215 recognition and quality control of misfolded C-Pro domains is mediated by recognizing stalled assembl
216 s indicate the GoM open (- 0.06 +/- 0.45 mol C m(-2) year(-1)) and coastal (- 0.03 +/- 1.83 mol C m(-
217 ) year(-1)) and coastal (- 0.03 +/- 1.83 mol C m(-2) year(-1)) ocean are approximately neutral in ter
218 on with increasing N/C and is regulated by N/C.
219 lines in tight association with increasing N/C and is regulated by N/C.
220  the distinct motor programs of the nematode C. elegans are coupled together across behavioral states
221 composed faster via the isomer (C(6)H(4), O)(C, N, Ph) formed by P-stereomutation involving a M(B2) p
222 2)-C cells and inhibition and eradication of C. albicans biofilms.
223  straightforward method for the formation of C(sp(3))-C(sp(2)) bonds.
224 nate, a crucial metabolite for the growth of C. difficile, and therefore prevented the growth of C. d
225 icile, and therefore prevented the growth of C. difficile.
226   CPM-733-dps is stable and shows no loss of C(2) H(2) adsorption capacity following multiple adsorpt
227 ntly alter the structure and organization of C. elegans sarcomeres.
228                            Overexpression of C/EBPbeta in human wild-type alpha-Syn transgenic mice f
229                               At the peak of C. rodentium infection, increased arginine concentration
230                                 Promotion of C-C bonds is one of the key fundamental questions in the
231 ated with higher antibiotic use and rates of C. difficile infection.
232                              The reaction of C(60) with pregnen-20-carboxaldehyde, a biologically act
233 rmophilum demonstrates that the H2 region of C. thermophilum IC has a low helical propensity and esta
234                      The regioselectivity of C-H activation is dominated by steric considerations and
235 imary metabolism and metabolic regulation of C. acetobutylicum.
236 ructure comprising two intercalated rings of C-type lectin-like domains, where the N-terminal cystein
237 In vivo testing confirmed the selectivity of C(3)-ZIF(MCF) to accumulate in MCF-7 tumor cells.
238 ork (MOF) for highly efficient separation of C(2)H(4) from a binary C(2)H(6)/C(2)H(4) and ternary C(2
239 evelopmental polyadenylated transcriptome of C. elegans Taking advantage of long reads spanning the f
240                                  Focusing on C-MYC, a well-known oncoprotein overexpressed in most hu
241 , which may be exerting top-down pressure on C. abbreviata populations.
242 osystem C storage that includes soil organic C (SOC) must be considered to determine whether planting
243                   Phosphonate-directed ortho C-H borylation of aromatic phosphonates is reported.
244  like H-bonding, solvent bonding, S-H...pai, C-H...pai, pai-pai stacking, charge-transfer complexatio
245 w a unique interaction of between pathogenic C difficile and F nucleatum in the intestinal mucus laye
246 s olefinated through the isolated (N, O)(Ph, C(6)H(4), C) oxaphosphetanes (Channel A), whereas MoBA c
247 ->AlPorF(5)-Ph-C(60), BTMPA-Im->AlPorF(3)-Ph-C(60), and BTMPA-Im->AlPor-Ph-C(60), respectively.
248 0, 740, and 56 ns for BTMPA-Im->AlPorF(5)-Ph-C(60), BTMPA-Im->AlPorF(3)-Ph-C(60), and BTMPA-Im->AlPor
249 ->AlPorF(3)-Ph-C(60), and BTMPA-Im->AlPor-Ph-C(60), respectively.
250 e lifetime of the BTMPA(*+)-Im->AlPorF(n)-Ph-C(60)(*-) radical pair was found to be very different in
251 05), but were less likely to have a previous C-section, gestational diabetes, preeclampsia/eclampsia
252 eveloping on the C-O carbon atom progressing C-H abstraction.
253 Septic Shock) and $30,911 (Activated Protein C and Corticosteroids for Human Septic Shock) per patien
254 ent domain containing myosin binding protein-C, the "C-zone." Myosin motors in domains further from t
255 erforming those assembled with commercial Pt/C+RuO(2) catalyst.
256 CAr)(R) species that reductively eliminate R-C=CAr products.
257 etween the carbon to zirconium atomic ratio (C/Zr) and the lattice parameter, in contrast with a more
258 on-metal-catalyzed, template-directed remote C-H activation reactions of alcohols, carboxylic acids,
259 l the crucial role of the initial reversible C-C single bond formation for the synthesis of crystalli
260  disrupt the coding sequence of a S. rosetta C-type lectin gene, rosetteless, and thereby demonstrate
261  catalyst system to promote a para-selective C-H functionalization reaction from benzylic electrophil
262 The assay allowed a rapid and high-sensitive C. acutatum detection mean, being able to detect the inf
263 h rising baseline levels of high-sensitivity C-reactive protein (hsCRP), and both hsCRP and IL-6 decr
264 level, 36 mg/dL; and median high-sensitivity C-reactive protein level, 2.1 mg/L), 12 633 (96.6%) comp
265                          Substrate sequences C-terminal to the dephosphorylation site make intimate c
266 s have been proposed as a means to sequester C for climate change mitigation, yet little is known abo
267 r, the mechanisms underlying changes in soil C storage are not well understood, hampering long-term p
268 nts comprehensive estimates of seagrass soil C(org) erosion following eutrophication-driven seagrass
269 uman cancers, we show that FBXL16 stabilizes C-MYC by antagonizing FBW7-mediated C-MYC ubiquitination
270  achieving highly regio- and stereoselective C-H functionalization reactions using a newly developed
271 r of recurrent cortico-thalamo-cortical (C-T-C) loops.
272  from a binary C(2)H(6)/C(2)H(4) and ternary C(2)H(4)/C(2)H(2)/C(2)H(6) mixture.
273                              We propose that C-C bond coupling in Y-DeAlBEA proceeds via the reaction
274                                          The C-CNN also achieved an average root-mean-square deviatio
275                                          The C-terminal BON domain binds anionic phospholipids throug
276 the N-terminal myristoylation signal and the C-terminal FXXF motif in PKAc regulate its thermal stabi
277 t stem cells, we show that a mutation at the C terminus of eIF2gamma impairs CDC123 promotion of eIF2
278 ed line (RIL) population created between the C(4) grasses Setaria viridis and S. italica.
279  Y102E are similar in that neither binds the C terminus of Brd4, but in all other aspects the mutant
280 ubstrates in the PHDs are conserved, but the C-terminal helix of the PHDs is strikingly absent.
281    In contrast, we found two residues in the C-terminal domain, tyrosine 351 and glutamate 355, that
282 tablished receptors, an extended loop in the C-terminal receptor-binding domain (HC) of BoNT/B (HC/B)
283 d not result in a consistent decrease in the C. difficile life cycle in vivo, it was able to attenuat
284                                       In the C. papaya chloroplast genome, there are 46 RNA editing l
285 n high-risk neuroblastoma, we integrated the C-circle assay [a marker for alternative lengthening of
286 e data also suggest the participation of the C terminus in membrane localization, which is generally
287 lical domains or by direct engagement of the C-Pro itself.
288 is partial positive charge developing on the C-O carbon atom progressing C-H abstraction.
289 me3 to H3K27ac at the promoter, recruits the C/EBPbeta (CREB-binding protein) and CBP transcription f
290  SpxA2 but remained stable when fused to the C-terminal acidic tail of SpxA1.
291 ing oligomerization involving binding to the C-terminal region.
292 in containing myosin binding protein-C, the "C-zone." Myosin motors in domains further from the filam
293  and the subsequent adsorption of thiophene (C(4)H(4)S) depends strongly on the location on the edge
294 -positive viral test with a cycle threshold (C(T) ) of <35 or seroconverted during the follow-up peri
295 nvironments as a water-saving alternative to C(3) photosynthesis.
296  that these organelles could be connected to C. neoformans melanin synthesis.
297  were tested for non-toxigenic and toxigenic C. difficile (TCD).
298  mechanism allows access to both traditional C-N adducts at room temperature as well as a large range
299 er DI, RNA-seq was performed in C-76 and Val-C.
300 tivity are governed by various types of weak C-H hydrogen bonds.
301 s and 2% died; 3 deaths were associated with C. difficile and 1 with norovirus.

 
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