1 Here we showed that (
1) Glycine significantly promoted a
2 Here we show that 100 microM of ascorbate induced apopto
3 Here we show that 5-hydroxyindoles exhibit remarkably hi
4 Here we show that a chemically defined maturation medium
5 Here we show that a decline in the autophagy-lysosome sy
6 Here we show that a microfluidic system supports murine
7 Here we show that a population of the model diatom Phaeo
8 Here we show that a significant variation in the rate of
9 Here we show that a subset of SLC25A46 interacts with mi
10 Here, we show that a dual role for Hippo effectors TAZ a
11 Here, we show that a dynamic competition for DNA binding
12 Here, we show that a highly selective TLR7 agonist, GS-9
13 Here, we show that a missense mutation, p.Arg918Gln (c.2
14 Here, we show that absolute seed size and the rate of ch
15 ther AChE functions in this capacity in vivo
Here, we show that AChE plays an essential non-classical
16 Here, we show that activated Ca(2+)/calmodulin-dependent
17 Here, we show that activated Notch1 receptors (N1ICD) ar
18 Here, we show that adeno-associated virus-driven express
19 Here we show that adiposity significantly amplifies the
20 Here we show that adult drug-naive male offspring of coc
21 Here we show that,
although the MKP DUSP5 both inactivat
22 Here we show that,
among hotspots suggested to overlie m
23 Here we show that an HD-Zip transcription factor homolog
24 Here, we show that an acupoint is one form of neurogenic
25 Here, we show that anaerobic microsites are important re
26 Here, we show that angiosperm xylem contains abundant hy
27 Here we show that apoptotic cell extrusion is provoked b
28 Here we show that approximating the solution of the opti
29 Here we show that ASL pH in children with CF is similar
30 Here we show that assumption ii is not valid, due to str
31 Here we show that ATM is hyperactive when the catalytic
32 Here we show that auxin response and ARF activity cell-a
33 Here we show that aza-glycine substitution enhances the
34 Here we show that BCAT1 is the predominant BCAT isoform
35 Here, we show that BDV infection induces expression of k
36 Here we show that,
besides these local subcellular mecha
37 Here, we show that beta-TrCP, the substrate recognition
38 Here, we show that binocular matching is completely bloc
39 Here, we show that BMP signaling plays a critical role i
40 Here, we show that both 2009 pandemic H1N1 influenza A (
41 Here, we show that Bvg- phase genes are involved in the
42 For hybrid organic-inorganic nanomaterials,
here we show that by using 1,3,5 silyl benzene precursor
43 Here, we show that by using specific intracellular immun
44 Here, we show that Ca(2+) regulates TRPA1 through calmod
45 Here, we show that CAFs exposed to chemotherapy have an
46 Here we show that caspase-3 cleaves the GSDMD-related pr
47 Here, we showed that CC using polyethylene glycol (PEG)
48 Here, we show that cell senescence is an intrinsic part
49 Here, we show that Cet1's N-terminal domain (NTD) promot
50 Here, we show that CIB1 negatively regulates degeneratio
51 Here we show that clinically ill transgenic mice overexp
52 Here, we show that codelivery of insulin with otherwise
53 Here, we show that constitutive NIK expression that is r
54 Here we show that contrary to general belief, exsolved p
55 Here, we show that copper is essential for spore germina
56 r precisely controlling retinal stimulation,
here we show that covert attention flexibly improves and
57 Here we show that Csm6 proteins are activated through a
58 Here we show that damage-induced fork reversal in mammal
59 Here we show that dbetah promoter-mediated expression of
60 Here we show that deficiency of Wiskott-Aldrich syndrome
61 Here we show that deletion of the cohesin-loading factor
62 Here, we show that depletion of the nuclear export adapt
63 Here we show that despite these negative trends, there i
64 Here we show that developmental origins influence fine-s
65 Here, we show that differentiation of new taste bud cell
66 Here we show that DIM-2 can also mediate repeat-induced
67 Here, we show that dominant-negative mutants of ATL1 in
68 Here we show that drugs that inhibit important kinases i
69 Here we show that during bacterial infection, lysozyme i
70 Here, we show that during evolution N-glycosylation trig
71 Here, we showed that during mouse development, the histo
72 Here, we show that electrical coupling between RGCs and
73 Here we show that ephrin type-B receptor 1 (EphB1) is up
74 Here we show that ER-localized THBS1 is cytoprotective t
75 Here, we show that ER Ca(2+)-store depletion rapidly ind
76 Here, we show that ERG, through its physical interaction
77 Here, we show that exhaustion of the metabolic inputs th
78 Here we show that expression of MPP1, a PDZ-domain-conta
79 Here, we show that Ezrin links CFTR and TLR4 signaling,
80 Here we show that FGF19 triggers a previously unsuspecte
81 Here, we show that Fgfr2 regulates both the formation an
82 Here, we show that FOSL1 is the main immediate early AP-
83 Here we show that Foxo3 is required for auditory functio
84 Here, we show that FXR activation triggers a rapid postt
85 Here we show that genetic deletion of alpha2delta-1, the
86 Here we show that genetic knockout of Gsto1 alters the r
87 Here we show that glutamate-releasing ARC neurons expres
88 In contrast to fixed genomic alterations,
here we show that GR-mediated antiandrogen resistance is
89 Here we show that GSCs can reversibly transition to a sl
90 role in HHV-8 pathogenesis and KS.IMPORTANCE
Here we show that HHV-8, a DNA tumor virus that causes K
91 Here we show that high salt intake affects the gut micro
92 Here we show that HSUR2 also base-pairs with mRNAs in in
93 Here we show that human cord plasma treatment revitalize
94 Here we show that human peripheral blood IFN-gamma(+)IL-
95 Here we show that human RNase H2 is unable to process an
96 Here, we show that human electrophysiology can be used t
97 Here, we show that hundreds of springs currently distrib
98 Here we show that hydrolase levels between human ALF fro
99 Here we show that IL-4 or IL-13 alone was not sufficient
100 Here, we show that ILC2 are present in para-aortic adipo
101 Here we show that in a cell culture model of colorectal
102 ted in the initiation of senescence in vitro
Here we show that in a mouse model of prostate cancer, S
103 Here we show that in Fgfr3;Fgfr4 (Fgfr3;4) global mutant
104 Here we show that in hypercaloric diet-induced obese mic
105 Here we show that in mice DND1 binds a UU(A/U) trinucleo
106 Here we show that in patients with ischemic stroke and i
107 Here we show that in primary human erythroblasts, lncRNA
108 Here we show that in rats on a high-cholesterol diet, ch
109 Here we show that in rats, genetic silencing of the larg
110 Here, we show that in addition to dramatic increases in
111 Here, we show that in developing T cells, the Bcl11b enh
112 Here, we show that in Drosophila melanogaster Cdk5 regul
113 Here, we show that,
in a mouse model for the polyglutami
114 Here, we show that,
in contrast to dopamine neurons in t
115 Here, we show that,
in mice, liver mass, hepatocyte size
116 Here we show that inactivated rabies virus particles con
117 Here we show that inactivation of the beta-arrestin-2 ge
118 Here we show that,
indeed, while stoichiometric Ga2FeO4
119 Here, we show that individuals with anatomically incompl
120 Here, we show that inducible expression of OCT4 (iOCT4)
121 Here, we show that infection-derived lipids 1-palmitoyl-
122 Here, we show that Int3 activates NF-kappaB in HC11 cell
123 Here, we show that intercellular Celsr1 complexes that c
124 Here we show that intestinal Th2 responses against Trich
125 Here, we show that intracortical administration of NR bu
126 Here we show that intrahippocampal injection of ASC spec
127 Here we show that intrinsic doping surges in methylammon
128 Here we show that intrinsic sequence patterns between in
129 Here, we show that IRF8 is required for Th9 differentiat
130 Here we show that iron forms chemical bonds of similar s
131 Here we show that it was caused by a single strain with
132 's pedal ganglion during fictive locomotion,
here we show that its population-wide activity arises fr
133 Here, we show that knockdown of Hop in the germ line nur
134 Here, we show that lamin A/C expressing cells can form a
135 Here we show that localized states of a disordered optic
136 Here we show that locoregional and systemic delivery of
137 Here, we show that loss of PGANT4 disrupts the mucosal b
138 Here we show that lower quality, or more dilute, nectars
139 Here, we show that LRE is expressed in the synergid, egg
140 Here we show that macrocyclic cinnamate dimers combine t
141 Here, we show that male rhesus macaques can learn catego
142 tumor-infiltrating lymphocytes to the tumor,
here we show that MEK inhibition adversely affects early
143 Here, we show that "
memory" of anomeric configuration is
144 Here we show that MG-specific overexpression of Ascl1, t
145 Here we show that mice with an adipose-tissue-specific k
146 Here we show that microRNA-34a provides homoeostatic con
147 Here, we show that miR-29 promotes pathologic hypertroph
148 Here, we show that mitochondrial fission is triggered by
149 Here, we show that mixing between water masses is suffic
150 Here, we show that modeling of neural sound representati
151 Here we show that models of measured fish sound producti
152 bark tissues in young American elm saplings,
here we show that most disease-responsive genes exhibite
153 c18c is known to regulate Stx4 activity, and
here we show that Munc18c is required for Stx4-mediated
154 Here, we show that mutagenic damage accounts for the maj
155 Here we show that mutant strains of S. praecaptivus that
156 Here, we show that mutation of the ciaR gene, encoding t
157 Here, we show that mutation of the mouse orthologue of G
158 Here we show that myomixer expression during zebrafish e
159 Here, we show that natural C. elegans isolates differ in
160 Here we show that NETs are induced by mitogens and accom
161 Here, we show that NKT-specific deletion of Hdac3 result
162 Here we show that nutrient pulses from decomposing Atlan
163 Here we show that oncogenic miR-182 is a strong regulato
164 Here, we show that oncogenic RAS and BRAF induce perinuc
165 Here we show that optogenetic inhibition of the BLA has
166 Here we show that,
over the twenty first century, temper
167 Here, we show that overexpression of a dominant-negative
168 ck-in (KI) or ApoE knockout (KO) background,
here we show that P301S/E4 mice have significantly highe
169 Here, we show that p38alpha kinase promotes EZH2 degrada
170 Here, we show that palmitate-stimulated CD11b(+)F4/80(lo
171 Here we show that parasites trap host autophagic factors
172 Here we show that pharmacological inhibition or gene abl
173 Here we show that phosphorylation of GSK3beta on Ser(389
174 Here, we show that phyllotaxis regularity depends on the
175 Here we show that piRNAs and piRNA biogenesis components
176 Here, we show that platelet-derived growth factor recept
177 Here, we show that PlrS is required for BvgAS to become
178 Here, we show that point chirality of a ligand decisivel
179 Here we show that Pol III limits lifespan downstream of
180 Here we show that Polycomb-repressive complex 1 (PRC1) d
181 Here, we show that pregnancy analgesia can produce a com
182 Here we show that primary cells from the rat central ner
183 Here we show that Protein Kinase B-mechanistic Target of
184 Here, we show that PTEN deletion in HCT116 and DLD1 colo
185 Here we show that purified transposase binds specificall
186 Here we show that PYK10, the most abundant beta-glucosid
187 Here we show that R-loops accumulate preferentially in b
188 Here, we show that reactivation-based consolidation proc
189 Here we show that replacing the peripheral macrophage po
190 Here we show that restricting dietary yeast during Droso
191 Here, we show that retbindin ablation in mice causes a r
192 Here we show that Rga1 transiently localizes to the imme
193 Here we show that ripple bursts in CA1 and medial entorh
194 Here we show that RSPO3 antagonism synergizes with pacli
195 Here, we show that S. aureus inhibits wound closure and
196 Here, we show that Salmonella Typhimurium infection was
197 Here, we show that selection on photosynthetic traits wi
198 Here we show that semaphorin 2b (Sema2b) is a target-der
199 Here we show that single crystals of thiolate-protected
200 Here we show that single crystals of uranium dioxide sub
201 Here we show that sirtuin 1 deacetylase (Sirt1) deacetyl
202 Here we show that sleep is also present in Cnidaria [6-8
203 Here we show that SOCS3-dependent cytokine expression re
204 Here we show that soluble klotho binds membrane lipid ra
205 Here, we show that Sonic hedgehog (Shh), which encodes a
206 Here, we show that specific deletion of CB1R in the rena
207 I in humans and a simulation of London (UK),
here we show that,
specifically when new streets are ent
208 Here we show that stabilizer-free polydispersed inorgani
209 Here, we show that stimulants like cocaine and methamphe
210 Here, we show that substitution of APP C-terminal lysine
211 Here, we show that suppression of PAX7 target genes is a
212 Here we show that tardigrade-specific intrinsically diso
213 Here we show that targeting glioma stem cell (GSC)-deriv
214 Here, we show that TFR cells are highly permissive to HI
215 Here, we show that TGFbeta induces robust TAZ but not YA
216 Here we show that Th17 cells are a source of tumour-indu
217 Here we show that the accurate measurement of solvent pa
218 Here we show that the brain-enriched miRNAs miR-9/9( *)
219 Here we show that the budding yeast mismatch repair rela
220 Here we show that the calcification to carbon fixation r
221 Here we show that the concerted action of two enzymes co
222 Here we show that the DGC component dystroglycan 1 (Dag1
223 Using the Xenopus nuclear extract system,
here we show that the Dna2 nuclease directly initiates t
224 Here we show that the dynamics of an anthrax-causing age
225 Here we show that the Escherichia coli UbiD enzyme, whic
226 Here we show that the expression of Secreted frizzled-re
227 Here we show that the gut bacterium Bacteroides thetaiot
228 Here we show that the high reactivity at these sites is
229 Here we show that the induction of a myokine, irisin, im
230 Here we show that the INO80 chromatin remodeling complex
231 Here we show that the mere feeling of lower socioeconomi
232 Here we show that the pan-BET inhibitor (+)-JQ1 protects
233 Here we show that the panda receptor, when purified and
234 Here we show that the presence of SOS1/EPS8/ABI1 complex
235 Here we show that the PYD-only protein POP2 inhibits inf
236 and EM, together with biochemical evidences,
here we show that the three domains of SepCysE each bind
237 Here we show that the transcriptional response in neuron
238 Here we show that the transmission of metabolic informat
239 Here we show that the Voronoi entropy of the cluster ten
240 Here we show that the Xist locus is coated with a broad
241 Here we show that the XPC DNA repair complex is a potent
242 Here, we show that the absence of CobB in a DeltacobB mu
243 Here, we show that the absence of two DUF300 domain-cont
244 Here, we show that the adenosine A2a receptor (ADORA2A)
245 Here, we show that the Arabidopsis (Arabidopsis thaliana
246 Here, we show that the behavioral state alters the basel
247 Here, we show that the C-type lectin receptor CD69 contr
248 Here, we show that the capacity of presynaptic cholinerg
249 Here, we show that the cell cycle regulator, cyclin-depe
250 Here, we show that the cytokine activin-A instructs the
251 Here, we show that the demographic collapse induced by c
252 Here, we show that the dorsal column (DC) somatosensory
253 Here, we show that the H15 HA has a high preference for
254 Here, we show that the human hippocampal-entorhinal syst
255 Here, we show that the inactive X chromosome (Xi) of pri
256 Here, we show that the interference effects associated w
257 Here, we show that the interruption of long nights by sh
258 Here, we show that the introduction of a single lipid-fa
259 Here, we show that the lack of regeneration of these pop
260 Here, we show that the mammalian kinesin-4 KIF21B is a p
261 Here, we show that the microbiome of reef corals is diff
262 Here, we show that the mRNAs and proteins of these four
263 Here, we show that the new parameters enable quantitativ
264 Here, we show that the optical 2D photon echo spectra of
265 Here, we show that the output of triboelectric nanogener
266 Here, we show that the phosphoinositide signaling modula
267 Here, we show that the phosphorylation status of NBS1 de
268 Here, we show that the regulatory N-terminal residues an
269 Here, we show that the retrograde signal decreases ACh r
270 Here, we show that the topography of the environment sig
271 Here, we show that the valuation process in human subjec
272 Here, we show that the VAPB-PTPIP51 tethers regulate aut
273 Here, we showed that the expression of RGC32 was signifi
274 Here we show that these two activities are carried out b
275 er a delay, these areas show "reactivation."
Here, we show that these areas are also activated and re
276 Here we show that this measure of neural engagement pred
277 plexes found frequently in guanine-rich DNA,
here we show that this structural motif can be exploited
278 Here we show that this variability is largely explained
279 Here, we show that this can actually occur through a for
280 Here, we show that this PKA-induced retrograde trafficki
281 Here, we show that this updating process critically depe
282 Here we show that tight regulation of buffered intracell
283 Here, we show that TIGIT bound to the immunoglobulin dom
284 Here, we show that Tomt/Comt2, the murine ortholog of LR
285 Here, we show that trace fear memory undergoes a protein
286 Here, we show that transient expression of the transcrip
287 Here, we show that translation of VEGFA mRNA in human my
288 Here we show that transplanting the pore domain of TRPV1
289 Here we show that two structurally different phycobilipr
290 Here, we show that two Arabidopsis thaliana transcriptio
291 Here, we show that under steady state, jagged-2 is diffe
292 Here we show that,
unlike other remodellers, INO80 trans
293 Here, we show that upon HIV-1 infection, a free pool of
294 Here, we show that variations in the mathematical functi
295 Here we show that very diverse communities could persist
296 Here we show that when MDM2-ALT1 is ubiquitously express
297 Here we show that,
when TnBVank1 was stably expressed in
298 Here, we show that wild-living bonobos are endemically P
299 Here, we showed that XPO1 is robustly expressed in prima
300 Here we show that ZIKV infects the subventricular zone i