1 Here we show that 20E-triggered oviposition in these mos
2 Here, we show that 3D head-orienting movements (HOMs) mo
3 Here, we show that 4 bp of core-enclosing helix is requi
4 Here, we show that 80S ribosomes translate the 5'-proxim
5 Here we show that a male's presence by itself leads to l
6 Here we show that a plant virus, barley yellow dwarf vir
7 Here we show that a previously uncharacterized gene, ENL
8 Here we show that a sequence of increasingly complex rid
9 Here we show that a subpopulation of archetypal hPSC enr
10 Here, we show that a core component of the fork protecti
11 Here, we show that a designer protein-deprived diet enri
12 Here, we show that a large music festival held adjacent
13 Here, we show that a second-generation amino-acyl tRNA s
14 Here, we show that a single amino acid residue in CD28 d
15 Here, we show that a single dose of UV-4B (the hydrochlo
16 Here, we show that a structurally novel form of the hete
17 Here, we show that a virus without an intact vpr gene is
18 Here, we showed that a green fluorescence protein (GFP)
19 Here, we showed that a small, persistent increase in the
20 Here, we show that ablation of HNF-1beta in mIMCD3 renal
21 Here we show that about half of the recorded VTA DA neur
22 Here we showed that ACE2, but not TMPRSS2 or Furin, has
23 Here we show that acentrosomal spindle assembly followin
24 Here we show that acidic fibroblast growth factor (FGF1)
25 Here we show that activated AKT in human hepatocellular
26 Here we show that activation of the non-canonical NF-kap
27 Here, we show that acute administration of cocaine trigg
28 Here, we show that adrenergic stimulation of BAT activat
29 Here, we show that adult animals respond to ascarosides
30 Here we show that aerobic exercise training up-regulates
31 Here, we show that affinity can be significantly improve
32 Here, we show that Agd3 deacetylates GAG in a metal-depe
33 Here, we show that AhR is activated in cells infected wi
34 Here we show that Akt3 depletion in primary endothelial
35 Here, we show that although structurally clustered mutat
36 Here we show that,
although the N-terminal region of RNF
37 Here, we show that an AT-hook motif-containing nuclear l
38 Here, we show that analogues with an N-terminal polyethy
39 Here, we show that AND-gate optical imaging probes that
40 Here, we show that APMs and sympathetic nerves form a du
41 Here, we show that Arrdc3 is differentially regulated by
42 Here, we show that ASOs act upon nascent transcripts and
43 Here, we show that at 1 month postinfection, B cell defi
44 Here we show that Aurora B expression is elevated in bas
45 Here, we show that autophagy is specifically induced in
46 Here we show that BAF60a, a subunit of the SWI/SNF chrom
47 Here, we show that BAP1 is dependent on the ASXL protein
48 Here we show that BCL11A is regulated at the level of me
49 Here we show that beta-cells express abundant Kindlin-2
50 Here we show that beta4*nAChRs also are involved in non-
51 Here we show that binding of uPA to uPAR induces not onl
52 Here, we show that BioCer implants provide osteoinductiv
53 Here, we show that blocking GABA transporters (GATs) in
54 Here we show that both low blue light and a low-red to f
55 Here, we show that both IFN-gamma stimulation and murine
56 Here we show that branched actin filament networks, the
57 Here, we show that breast cancer cells maintained in hyp
58 Here we show that C(2+) n-alkane gases (ethane, propane,
59 Here, we show that Can GPC aggregates in the ER of infec
60 Here, we show that cancer cells can be selectively depri
61 Here we show that canonical Wnt signaling in mesoderm is
62 Here, we show that catalytic amounts of an appropriate e
63 Here we show that cationic proto-peptides (depsipeptides
64 Here, we show that cDC2s are abundant in the MZ of neona
65 Here, we show that cells survive retroviral replication,
66 Here, we show that chromosomal contacts of a DSB site ar
67 Here we show that chronic neuronal hyperexcitability, in
68 Here, we show that CLas movement through phloem pores of
69 Here, we show that clinically relevant antagonists used
70 Here, we show that competing energy scales present in th
71 Here, we show that conditional loss of a Mediator comple
72 Here, we show that constrained 31-residue-peptides ('msR
73 Here, we show that consuming necrotic cell debris via ma
74 Here, we show that contextual fear memory engrams in the
75 Here, we show that CSF1R inhibition by PLX5622 indeed af
76 Here, we show that cytotoxic chemotherapies induce dynam
77 Here, we show that D-mannose suppresses LPS-induced macr
78 Here we show that defects in both cell division and cell
79 However,
here we show that deletion of CTK complex components in
80 Here we show that depletion of transforming growth facto
81 Here we show that,
despite sequence homology and coexpre
82 Here we show that dopamine neurons in the VTA that proje
83 Here, we show that down-regulating PLCbeta1 or reducing
84 Here, we show that Drosophila HLBs form through phase se
85 Here, we show that Drosophila mutants in the homolog of
86 Here we show that during obesity MAIT cells promote infl
87 Here we show that dynamically growing somatosensory neur
88 Here we show that Dysf(-/-) mice develop adverse LV remo
89 Using the eye as a model CNS tissue,
here we show that ectopic expression of Oct4 (also known
90 Here, we show that efficiency of these processes is enha
91 Here, we show that ensilication stabilizes tetanus toxin
92 Here we show that entry into mouse torpor, a fasting-ind
93 Here we show that Escherichia coli DeltabipA cells grown
94 Here, we show that exposed phosphatidylserine (PS) repre
95 Here we show that exposure of the skin to the experiment
96 Here we show that expression of m(6)A demethylase ALKBH5
97 Here, we show that expression of a fusion protein combin
98 Here we show that eye movements are also inhibited befor
99 Here, we show that FAM111A, a PCNA-interacting protein,
100 Here we show that FERONIA controls several functionally
101 Here, we show that fibroblasts counteract the cytotoxic
102 Here, we show that FLD tightly associates with LUMINIDEP
103 Here, we show that,
for a range of solid tumours, a cycl
104 Here, we show that GAGA factor (GAF), a Drosophila pione
105 Here, we show that GBM-initiating cells induce mTOR sign
106 Here, we show that gene amplification is an additional e
107 Here, we show that genetic deficiency of Folliculin, a t
108 Here, we show that genotoxic agent-activated Wnt/beta-ca
109 Here we show that glutamate receptor interacting protein
110 Here we show that greater subsurface warming induced by
111 Here, we show that healthy human individuals exert more
112 Here we show that heterotypic multicomponent interaction
113 Here, we show that histone acetyltransferase MOF plays a
114 Here, we show that histone H4 lysine 16 acetylation (H4K
115 Here, we show that human and mouse fetal MCs phenotypica
116 Here, we show that human METTL2 forms a complex with DAL
117 Here we show that IL33 is upregulated in metastases-asso
118 Here we show that immediately before and during the erup
119 Here we show that impact angle and direction can be diag
120 Here we show that in mouse embryonic stem cells, EloA lo
121 Here we show that in neurons with no history of activity
122 Here we show that in vivo treatments modifying apoplasti
123 Here, we show that in Drosophila the small ubiquitin-lik
124 Here we show that,
in addition to chromosomally encoded
125 Here we show that,
in PDAC, MHC-I molecules are selectiv
126 Here we show that,
in the metabolically versatile photoh
127 Here, we show that,
in addition, mecA provides a broad s
128 Here we show that inappropriate, learning-resistant fear
129 Here, we show that interleukin (IL)-22, induced by colon
130 Here we show that interspersing coordination sites for d
131 Here, we show that intestinal epithelial cells expressin
132 Here, we show that it has another important benefit: in
133 Here, we show that JMJD1C is a specific histone demethyl
134 Here we show that keratin intermediate filaments directl
135 Here, we show that keratinocytes lacking hemidesmosomal
136 Here, we show that KP372-1 sensitizes NQO1-expressing pa
137 Here, we show that LDs induced by the yeast triacylglyce
138 Here, we show that liver X receptors (LXRs)-a class of n
139 Here, we show that loss of clustered gamma protocadherin
140 Here, we show that loss of Xinbeta, a newly-identified c
141 Here, we show that low SASH1 mRNA expression is associat
142 Here, we show that lung-specific loss of Kmt2d promotes
143 Here we show that macrophages take up HSV-1 via endocyto
144 Here, we show that macrophages not only fail to efficien
145 Here we show that male mice, pigs, goats, and cattle har
146 Here, we show that mass photometry (MP) can accurately c
147 Here we show that MeCP2 is a dynamic component of hetero
148 Here we show that MEKK1 contains a previously unidentifi
149 Here, we show that melanoma cells can adapt to targeted
150 Here we show that mice bearing human ALS-associated TBK1
151 Here we show that mice with inducible conditional knockd
152 Here, we show that mice in which alpha2-Na/K ATPase is c
153 Here we show that miR-17-92 forms a regulatory loop with
154 Here we show that modulations of surprise and uncertaint
155 omplex bound to ICL DNA-which we also report
here-we show that monoubiquitination triggers a complete
156 Here we show that mRNA-1273 induces potent neutralizing
157 Here, we show that multiple linked but recombining loci
158 Here, we show that mutant huntingtin (mHtt) aggregates a
159 Here, we show that mutation in TARANI/UBIQUITIN-SPECIFIC
160 Here, we show that mutation of the PTIP interaction site
161 Here, we show that MYCN-amplified neuroblastomas are cha
162 Here we show that N(6)-mA has a key role in changing the
163 Here we show that N(6)-methyladenosine (m(6)A) modificat
164 Here we show that naturalization likelihood is 18 times
165 Here, we show that NDP expression is enriched in neurolo
166 Here, we show that nearly all AD-associated-genes are ev
167 Here we show that neither memory nor perception are appr
168 Here, we show that newly introduced nitrogen atoms into
169 Here we show that Nf1 gene inactivation in adult oligode
170 Here we show that North America warmed at the rate of 0.
171 Here, we show that NP-Ct is necessary for IB formation w
172 Here, we show that Nr4a1 and Nr4a3 play partially redund
173 Here, we show that NSUN-1 is writing the second known 26
174 Here, we show that NUCKS1 physically and functionally in
175 Here, we show that nutritional omega-6 PUFA-derived endo
176 Here we show that obstruction of vascular invasion durin
177 Here we show that OCA-B, a B cell-specific coactivator e
178 Here, we show that olaparib combines synergistically wit
179 Here, we show that on top of meteorological influences,
180 Here we show that oncogenic KRAS alters the expression o
181 Here, we show that oncogenic ERG repressed PI3K signalin
182 Here, we show that ongoing warming has strong, increasin
183 Here we show that only females and not males show a high
184 Here, we show that opioid peptide receptors, GPCRs that
185 Here we show that pairs of neutrophils arriving closely
186 Here, we show that Pavarotti also functions during wound
187 Here, we show that persistent antigenic stimulation impa
188 Here, we show that phosphatidylethanolamine (PE) synergi
189 Here, we show that photoreceptors (PRs) of diseased indi
190 Here we show that PINCH-1 is highly expressed in lung ad
191 Here we show that polysynaptic inhibition between ChINs
192 Here we show that primary mouse and human T cells engage
193 Here we show that pull-push mechanisms can be recruited
194 Here, we show that pyruvate dehydrogenase kinase (PDK)-2
195 Here we show that R-loops form at many PREs in Drosophil
196 Here we show that Rad9 promotes stable annealing between
197 Here, we show that reactive oxygen species (ROS) functio
198 Here, we show that remdesivir (RDV) and IFNb have superi
199 Here we show that repair of the inactivated C16L/B22R ge
200 Here we show that RepoMan abundance is regulated by the
201 Here we show that resistance to 5FC in Cryptococcus deut
202 Here, we show that resistance to glyphosate in the studi
203 Here we show that RNA is evicted from prophase chromosom
204 Here, we show that RNA decay mechanisms involving upstre
205 Here, we show that RU.521 is capable of potently and sel
206 Here we show that RUNX1 functions as a bona fide repress
207 Here we show that S47 and P47 cells exhibit distinct met
208 Here we show that SARS-CoV-2 causes a respiratory diseas
209 Here we show that seafloor alteration of serpentinites i
210 Here, we show that SEG/GRP neurons express oxytocin rece
211 Here, we show that serotonergic input has separable supp
212 Here we show that short (3.4 s) tVNS pulses in naive hea
213 Here, we show that silencing netrin-1 in the adult subst
214 Here we show that similar transcriptional signatures cor
215 Here, we show that,
similar to primary phloem formation
216 isms can affect RNA secondary structure, and
here we show that single nucleotide polymorphisms can af
217 Here, we show that SOX11 confers distinct features to ER
218 Here, we show that starved bacteria encountering new res
219 Here we show that STAT5 is the earliest factor binding a
220 Here, we show that Stattic exerts many STAT3-independent
221 Here, we show that stress increases basolateral amygdala
222 Here we show that such eye movements can play an importa
223 Here, we show that such losses may be eliminated through
224 Here we show that synonymous codon substitutions encodin
225 Here, we show that synthetic [Fe(4)S(4)]-alkyl clusters
226 Here, we show that Syrian hamsters, in contrast to mice,
227 Here we show that T cell-specific Notch deficiency in mi
228 Here, we show that TA transcript levels can increase sub
229 Here we show that tacrolimus induces loss of human beta-
230 Here, we show that TDP2 co-purifies with K63 and K27 pol
231 Here, we show that TFL1 is recruited to thousands of loc
232 Here, we show that TGFbeta promotes protein translation
233 Here we show that that the lPBN is required for escape b
234 Here we show that the Arabidopsis quadruple mutant (min7
235 Here we show that the average degree of GDGT cyclization
236 Here we show that the commonly used TWSDI approach often
237 Here we show that the excitatory and inhibitory intracor
238 Here we show that the function of C. elegans Slo2 (SLO-2
239 Here we show that the key determinant of Grx function is
240 Here we show that the larval zebrafish retina extracts a
241 Here we show that the levels of Bim, a BH3-only protein,
242 Here we show that the limitations imposed by fluid insta
243 Here we show that the major subtropical WBC of the South
244 Here we show that the N170, a classic electrophysiologic
245 Here we show that the observed part of Phaethon does not
246 Here we show that the PAH composition of soot can be exa
247 Here we show that the plasmons in real quasi-2D metals a
248 Here we show that the trigeminal ganglion, which provide
249 Here, we show that the age-dependent downregulation of l
250 Here, we show that the AHR pathway is selectively active
251 Here, we show that the alternative sigma factor sigma(I)
252 Here, we show that the C terminus of RRS1-R but not RRS1
253 Here, we show that the chemical potentials of chalcogeni
254 Here, we show that the chiral crystal palladium gallium
255 Here, we show that the color changeability of biological
256 Here, we show that the direct link between the two phase
257 Here, we show that the FemA/FemB homologues FmhA and Fmh
258 Here, we show that the human cysteine protease legumain
259 Here, we show that the MA region is required for nuclear
260 Here, we show that the microcephalin 1/BRCT-repeats inhi
261 Here, we show that the N protein of SARS-CoV-2, together
262 Here, we show that the Parkinson's disease (PD)-related
263 Here, we show that the PAS domain regulates both kinase
264 Here, we show that the properties of the ground-state wa
265 Here, we show that the proportion of both asymptomatic a
266 Here, we show that the sushi domain protein SRPX2 is a n
267 Here, we show that the three major classes of LCCBs acti
268 Here we show that these speed variations are due to the
269 Here, we showed that these four CEKs have distinct subst
270 Here we show that this growth was driven by long-term en
271 Here we show that this is possible using a surface plasm
272 Here we show that this problem can be circumvented by as
273 Here we show that this system exhibits physiology-depend
274 Here, we show that this differentiation becomes possible
275 f intravacuolar pathogens such as Salmonella
Here, we show that this mechanism requires aconitate dec
276 Here, we show that this pattern arises almost entirely f
277 ional species with cryo-electron tomography,
here, we show that this subcomplex persists after flagel
278 Here, we show that this toughness design approach can be
279 Here we show that throughout a ~1000-km transect in Scot
280 Here, we show that TMC1/2 cannot form mechanotransductio
281 Here we show that topoisomerase 1-DNA covalent cleavage
282 Here we show that transcription factor EB (TFEB), a mast
283 Here, we show that tree mortality concomitant with droug
284 Here, we show that TRYPTOPHAN AMINOTRANSFERASE OF ARABID
285 Here, we show that two genes implicated in CHDs, Megf8 a
286 Here, we show that two members of the extended synaptota
287 Here, we show that Ulva meridionalis has the highest gro
288 Here, we show that upon cell stress, JNK directly phosph
289 Here we show that using prior knowledge to facilitate le
290 Here we show that vascular injury in rodent carotid arte
291 Using Sindbis virus (SINV) in Drosophila,
here we show that viral infections affect TE transcript
292 Here, we show that volumetric compression regulates the
293 Here, we show that Vpr mitigates the antiviral effects o
294 Here we show that Wdp modulates the Hedgehog (Hh) pathwa
295 Here, we show that we can decode natural sounds from act
296 Here we show that when magnetic pumping is extended to a
297 Here we show that,
when challenged with wild-type temper
298 Here we show that,
when making decisions between more th
299 Here we show that without forming an atomically structur
300 Here, we show that zebrafish embryonic tissue explants,