1 Our findings
support a model by which CaM binds to Akt to facilitate
2 Our results
support a model by which drug-evoked synaptic plasticity
3 Thus, these findings
support a model by which the selective stabilization of
4 Our data
support a model demonstrating that heat shock factor 1 (
5 Together, these results
support a model for allostery in PheH in which phenylala
6 Together, these observations
support a model for Cas9 specificity wherein gRNA-DNA mi
7 Together our data
support a model for contact guidance in which the ECM en
8 Our data
support a model for GCs to stabilize HIF through activat
9 Our results
support a model for induction of contact activation in w
10 The results
support a model for multiple myeloma progression with cl
11 These observations
support a model for native HIV-1 assembly wherein HIV-1
12 Taken together, these data
support a model for native infection wherein structural
13 These results
support a model for precipitation of proteins by proanth
14 These measurements
support a model for PROPPIN-membrane binding, where the
15 -PTP with ESCRT-0, ESCRT-I and ESCRT-III and
support a model for regulation of ESCRT function by disp
16 Our data
support a model for sHSP function wherein cell stress tr
17 Our findings
support a model for SIRT2's tumor-suppressive function i
18 Our findings
support a model for taste coding in larvae, in which dis
19 genes and is required for their expression,
supporting a model for transcriptional switch between Ml
20 anta and heterologous expression in bacteria
supports a model for a beta-diketone biosynthesis pathwa
21 t-chain lipids in activating the transporter
supports a model for regulation within the highly dynami
22 Our results
support a model in which 5-hmC regulates differentiation
23 Our data
support a model in which a heritable 5' noncoding mRNA e
24 These data
support a model in which a single neuronal stem cell can
25 Together, our results
support a model in which acute inflammation after injury
26 These findings
support a model in which an AGO2 phosphorylation cycle s
27 Together, the data
support a model in which AP-1 family members contribute
28 Taken together, these data
support a model in which autophagosomes were directed to
29 These data
support a model in which B1 and VRK2 share additional su
30 Our results
support a model in which biological outcomes of caspase
31 The results
support a model in which bitter Grs interact, exhibiting
32 Our data
support a model in which BRD4-NUT-stimulated histone hyp
33 These data
support a model in which cancer cell invasion into local
34 These data
support a model in which CD8(+) T cells upon activation
35 Our results
support a model in which Cdk-counteracting phosphatases
36 Furthermore, our data
support a model in which Cdk5 activators play nonoverlap
37 Our data
support a model in which central command circuits recrui
38 Together, our data
support a model in which clusters of GBSs observed with
39 Rather, our measurements
support a model in which collision with a trailing ribos
40 Finally, single-molecule experiments
support a model in which conformational sampling between
41 Taken together, our results
support a model in which correct peptidyl-proline hydrox
42 ns of cytokinin with auxin and ethylene, and
support a model in which cytokinin regulates shootward a
43 Together, our data
support a model in which DACH1 stimulates coronary arter
44 Our data
support a model in which dephosphorylation of Cdk sites
45 Taken together, our data
support a model in which DiRas1 expression inhibits mali
46 The data
support a model in which Dlx recruitment of Sp7 to osteo
47 Gene expression and mutant analyses
support a model in which DnaA and Rok cooperate to repre
48 Our results
support a model in which Dok1 phosphorylation normally s
49 Together, our results
support a model in which dorsally expressed gdf6a limits
50 ich domain of Nip100/p150(glued) Our results
support a model in which dynein destabilizes its microtu
51 Overall our findings
support a model in which each SAMP repeat plays a mechan
52 The data
support a model in which EAP deficits lead to poor funct
53 The findings in these index cases
support a model in which early development of occult hip
54 These data strongly
support a model in which EBNA3A is tethered to DNA throu
55 predominant source of BMP6 in the liver and
support a model in which EC BMP6 has paracrine actions o
56 Our results
support a model in which elevating astrocytic alphaBc co
57 These findings
support a model in which Ent5 clathrin binding performs
58 These data
support a model in which expansion of Ag-specific B cell
59 Our data
support a model in which FAK Y397 autophosphorylation is
60 Our data
support a model in which FAT4 in the stroma binds to DCH
61 Taken together, these data
support a model in which FGFs, possibly from axons, acti
62 Our results do not
support a model in which fluorogenicity arises from the
63 Together, these data
support a model in which FoxQ2 initiates an anterior pat
64 Our results
support a model in which FtsL, along with its partners F
65 These results
support a model in which GpsB negatively regulates perip
66 Our data
support a model in which H2S exerts its cytoprotective e
67 Thus, our data
support a model in which HD5 prevents furin from accessi
68 In total, our results
support a model in which HopG1 induces changes in the or
69 These data
support a model in which HSCs are titrated against a per
70 Their data
support a model in which IL-34 production by Tregs promo
71 These findings
support a model in which information flow from SL to SP
72 Our findings
support a model in which initial inhomogeneities in inpu
73 Our results
support a model in which inter-chromosomal microtubules
74 The results
support a model in which intracellular iron promotes inf
75 Taken together, these results
support a model in which IRS2, MTOR, and cyclin D2, but
76 Together, these data
support a model in which Ist1-Did2 interactions during E
77 Our data
support a model in which KAE609 exerts its antimalarial
78 Coupled with previous studies, these data
support a model in which L. donovani amastigotes readily
79 Our findings
support a model in which Ldo proteins modulate the activ
80 Our data
support a model in which LDs provide a lipid buffering s
81 These results
support a model in which leaving the stem cell niche and
82 Instead, our results
support a model in which long, active regions of transcr
83 Together, the findings
support a model in which low early-life n-6/n-3 ratios r
84 Our results
support a model in which LsERF1 acts through the promoti
85 Thus, our data
support a model in which Ltc1 is a sterol-dependent regu
86 mage response, and our findings collectively
support a model in which m(6)A RNA serves as a beacon fo
87 Our results do not
support a model in which Mad2 catalytically generates a
88 Our findings
support a model in which Mcp1 and Vps13 work as function
89 These data
support a model in which metavinculin tunes the actin bu
90 These findings
support a model in which mouse MX1 interacts with the in
91 Our results
support a model in which MOV10L1 RNA helicase activity p
92 ilaments are important for shape control and
support a model in which MreB organizes the cell wall gr
93 These results
support a model in which MUC1-C-induced TAK1short right
94 Our results
support a model in which MW deteriorates performance in
95 Taken together, our findings
support a model in which neighboring binding sites inter
96 Together these data
support a model in which neogenin acts as a scaffold to
97 Our results
support a model in which NMC is dependent on ectopic NUT
98 Our results
support a model in which NMDAR signaling, independent of
99 These experiments
support a model in which NPC1 protein functions to trans
100 Our findings
support a model in which nuclear EGFR acts as a transcri
101 Taken together, these results
support a model in which OGT modifies HIRA to regulate H
102 Taken together, our results
support a model in which oxy-Mb is a novel regulator of
103 The results
support a model in which perceptual filling-in is aided
104 Our data
support a model in which phosphorylation and dephosphory
105 Together, these data
support a model in which physiological levels of Ca(2+)
106 These data
support a model in which PlrS senses conditions present
107 Together, these results
support a model in which podocytes sense the disruption
108 the bypass phenotype on the PBP1b structure
support a model in which polymerization activation proce
109 Our data
support a model in which polyQ peptides containing stron
110 Our data
support a model in which PRC1 and PRC2 reinforce each ot
111 Together, our findings
support a model in which PrgU proteins represent a novel
112 These findings
support a model in which Ptch1/2 mediate secretion of a
113 Together, our findings
support a model in which R-loop accumulation and subsequ
114 Our findings
support a model in which R. equi virulence is conferred
115 Our data
support a model in which RA on the dorsal side of the em
116 These results
support a model in which RAD54L and RAD54B counteract ge
117 These data
support a model in which RAN translation at CGG repeats
118 Combined with previous work, these data
support a model in which RDN1 arabinosylates MtCLE12, an
119 Our results
support a model in which ReAsH fluorescence depends on t
120 Our findings
support a model in which repression of activin signaling
121 Our data
support a model in which RNA editing is executed via mul
122 Our findings
support a model in which sensory neurons express overlap
123 These data
support a model in which SHH signaling plays both positi
124 Our data
support a model in which signals in the tumor microenvir
125 Our data
support a model in which simultaneous interactions betwe
126 Collectively, our results
support a model in which SirA targets DnaA Domain I to i
127 Together, our findings
support a model in which sliding helicase-loading interm
128 Altogether, our data
support a model in which small neutral hydrophobic resid
129 These data
support a model in which SMC complexes function by proce
130 Moreover, 3D dSTORM data
support a model in which some but not all ERC vesicles a
131 Taken together, our results
support a model in which Spt16 has a role in maintaining
132 In summary, our results
support a model in which Src and cortactin regulate grow
133 These results
support a model in which Src-family kinase binding induc
134 These observations
support a model in which ssDNA plays a central role in t
135 Combined observations
support a model in which stalled ribosomes are reactivat
136 Collectively, our analyses
support a model in which stereocilia actin cores are sta
137 Together, our results
support a model in which stimulus-evoked exocytosis in r
138 These data
support a model in which stressed mitochondria generate
139 These results
support a model in which stromules aid in the amplificat
140 Overall, these results
support a model in which structured RNA negatively regul
141 Together, our data
support a model in which suppression of alternative macr
142 These findings
support a model in which syllabic and temporal features
143 Our data
support a model in which T-bet is a universal controller
144 Our findings
support a model in which TFAM first recruits POLRMT to t
145 These data
support a model in which the ability of TRIP13(PCH-2) to
146 These data
support a model in which the activation of certain pathw
147 In conclusion, our data
support a model in which the adoption of T-lineage fate
148 These results
support a model in which the AE3 Cl(-)/HCO3(-) exchanger
149 Our data
support a model in which the balanced activities of Pdi1
150 The results
support a model in which the conductive pili permeate th
151 Our data
support a model in which the daughter centriole promotes
152 Our results
support a model in which the E. coli clamp loader active
153 Taken together, our findings
support a model in which the evolution of the bipolar ma
154 vitro, in organello, and in vivo approaches
support a model in which the FGLK domains mediate intera
155 Our findings
support a model in which the folate receptor interacts w
156 gether with the structural data, our results
support a model in which the gate loop, acting in concer
157 These results
support a model in which the interaction of RyR with CaM
158 A variety of data
support a model in which the loss of K(+) ions from the
159 These data
support a model in which the MBD2/3 methylation-dependen
160 The data
support a model in which the negative affective state fo
161 Genetic and biochemical data
support a model in which the pupylation machinery is res
162 These data
support a model in which the quasi-envelope is degraded
163 tes cullins in vivo Combined, these findings
support a model in which the SCCRO, substrate, and subst
164 These data
support a model in which the sequential actions of two d
165 Together, our experiments
support a model in which the transition from sedentary t
166 tations for different chemical states of CcO
support a model in which the volume and hydration level
167 Taken together, these results
support a model in which this IDR of Med13 plays a key r
168 These results
support a model in which Tie1 directly interacts with Ti
169 Our results
support a model in which TOPBP1(Dpb11) plays a conserved
170 Together, these data
support a model in which TUG acetylation modulates its i
171 Previous results
support a model in which TUG traps GLUT4 in intracellula
172 n controlling promoter occupancy by Gcn4 and
support a model in which ubiquitylation of activators-no
173 Together, these results
support a model in which UPF1 mutations downregulate NMD
174 Our results
support a model in which UPF3A serves as a molecular rhe
175 Our findings
support a model in which voluntary persistence emerges f
176 Together, our results
support a model in which YY1 acts as an architectural pr
177 Collectively, our findings
support a model in which zinc plays a dual role in activ
178 Our results instead
support a model in which, despite the apoptotic machiner
179 obtained using small-angle X-ray scattering
supported a model in which CacyBP/SIP occupies an anti-p
180 scussed in relation to O-O cleavage in HCOs,
supporting a model in which a peroxo intermediate serves
181 collaborate with HslV in their degradation,
supporting a model in which ATP hydrolysis and linked me
182 uced downstream of Draper in AD model flies,
supporting a model in which glia engulf and destroy Abet
183 airpins and/or distal U-tract interruptions,
supporting a model in which NusA is directly involved in
184 We provide evidence
supporting a model in which the linkage between genomic
185 ar progression through these subpopulations,
supporting a model in which these three states correspon
186 Our work
supports a model in which a polyubiquitin chain associat
187 Our work
supports a model in which AdamTS-A anchors cells in plac
188 Together, this work
supports a model in which an extrinsic signal triggers a
189 of architectural proteins for enhancers and
supports a model in which animal genomes use the nuclear
190 Analysis of the antibody-antigen interaction
supports a model in which antibodies that can interfere
191 The structure
supports a model in which association of RelA with the r
192 Our work
supports a model in which context-specific modulation of
193 Accumulating evidence
supports a model in which CpG islands recruit Polycomb g
194 The preponderance of evidence
supports a model in which DNA polymerase epsilon (Pol ep
195 This study
supports a model in which leptin exerts concerted traffi
196 Our work
supports a model in which multiple surfaces of Ska1 inte
197 an farmers and the inhabitants of Ganj Dareh
supports a model in which Neolithic societies in these a
198 The present evidence
supports a model in which the natural statistics of temp
199 Such a transition state
supports a model in which the rate-limiting step of the
200 in XPF-deficient Caenorhabditis elegans and
supports a model in which translesion synthesis polymera
201 The structure
supports a model in which two substrate radicals bind to
202 These findings
support a model linking increased hippocampal activation
203 These results
support a model of "empathic blame", whereby the perceiv
204 These data
support a model of an unexplored mode of locomotion--"bo
205 cial canals shouldn't be used to exclusively
support a model of aquatic foraging in theropods and arg
206 Our data
support a model of chromatin architecture in intact inte
207 variation seen across eukaryotes, as well as
support a model of CTD expansion and contraction to main
208 nt paths in different Magicicada species and
support a model of genomic degradation that is stochasti
209 The results
support a model of HCV infection influencing the binding
210 Our findings
support a model of independent assembly and evolution in
211 Archaeobotanical data may
support a model of indirect Austronesian colonization of
212 These
support a model of initial erosion of the Dover Strait b
213 navirus entry, provide a structural basis to
support a model of membrane fusion mediated by progressi
214 These results
support a model of pneumococcal CCR in which HPr-Ser app
215 Together, these data
support a model of rapid gene innovation by fusion of in
216 nlinearly transform odor representations and
support a model of selective and nonrandom inhibition am
217 These results
support a model of solvent-slaved protein dynamics.
218 pattern of sequence diversity here does not
support a model of strong selective constraint on MC1R i
219 These results
support a model of the hygiene hypothesis in which certa
220 Our results
support a model of tissue ILC differentiation ("ILC-poie
221 These data
support a model of tumorigenesis whereby PDTCs and ATCs
222 it texture and flavor, and provide evidences
supporting a model of apple fruit size evolution compris
223 ed compared with the phosphorylation of AKT,
supporting a model of negative feedback downstream of PR
224 with RIP2 CARD but not RhoGDI binding sites,
supporting a model of receptor activation triggered by s
225 able at all points assayed across 6.5 years,
supporting a model of serological memory based upon intr
226 The closed state
supports a model of catalysis in which the substrate is
227 s of serotonin neuron firing and release and
supports a model of impaired serotonin signaling in suic
228 ants overexpressing miRNA396a-resistant GRF1
support a model proposing that distinct associations of
229 ipid MA:membrane binding models, and instead
support a model put forward from coarse-grained simulati
230 The data
support a model suggesting that the unique architectural
231 Our results
support a model that both corneal epithelial homeostasis
232 These data
support a model that includes changes in brain bioenerge
233 The data also
support a model that LC translocation proceeds from the
234 avior and visual neural signals consistently
supported a model that assumes a mixing of prediction er
235 Our data
support a model where adding AMPA receptors is sufficien
236 Our in vitro and in vivo data
support a model where an oxidized dNTPs pool together wi
237 These data
support a model where Arabidopsis CRKs are synthesized u
238 These data
support a model where Asna1 ensures retrograde transport
239 Our data
support a model where Bcd influences chromatin structure
240 Our data
support a model where both an increased expression of Ga
241 Our data
support a model where clonal epigenetic reprogramming to
242 Collectively, our results
support a model where ERalpha signals activate MeA neuro
243 harmacological and molecular biology results
support a model where ETR1 and ETR2 are indirectly affec
244 eregulation contributes to FXS pathology and
support a model where FMRP, by controlling the translati
245 Collectively, results presented here
support a model where GSK3beta regulates signaling by co
246 Our data
support a model where H2A.Z in gene bodies has a strong
247 Taken together, our data
support a model where IcsA and N-WASP form a tight compl
248 Our findings
support a model where low-dose IL-2 selectively activate
249 Our data
support a model where nutrition is a key environmental f
250 Taken together these data
support a model where PDHK4 regulates KRAS signalling an
251 These results
support a model where Pil1-Lsp1 heterodimers are the min
252 The results
support a model where Pol iota occasionally accesses the
253 Our results
support a model where residues in these positions determ
254 Our observations
support a model where specificity is generated through c
255 Together, these findings
support a model where spontaneous control of HCV such as
256 Our data
support a model where the balance of activating and inhi
257 Our data
support a model where the density of shared RNA binding
258 Altogether, these results
support a model where the eVP30-eNP interaction plays a
259 The results
support a model where the pseudokinase domain regulates
260 A thermodynamic analysis
supports a model where the N terminus is folded around t
261 Our data
support a model whereby a hot L1 source element on Chrom
262 The data
support a model whereby a hydrophobic patch on the ProTx
263 Together, these results
support a model whereby afadin determines lumen placemen
264 Our results
support a model whereby emergent metabolites signal a be
265 Our results
support a model whereby Gpd1 may be imported as a monome
266 Together, our results
support a model whereby increased tooth number and an ac
267 Therefore, the present data
support a model whereby MCL-1 depletion increases 53BP1
268 Together with previous studies, our data
support a model whereby Munc18-1 acts as a template for
269 Our data
support a model whereby nascent NepR(IDR)-PhyR interacti
270 Our data
support a model whereby postnatal loss of hair forming a
271 These findings
support a model whereby repeat expansions elicit cellula
272 These results
support a model whereby RPA, best known for its role in
273 Altogether, the data
support a model whereby stereocilia actin cores are larg
274 These data
support a model whereby STIM1 is critical to deactivate
275 Taken together, our results
support a model whereby the amphipathic helix in SM N100
276 Our data
support a model whereby the degree of apoptosis inductio
277 Our combined data
support a model whereby the risk variant augments the BC
278 These findings
support a model whereby the selective removal of Nup FG
279 These data
support a model whereby these two functionally distinct
280 Our genetic and biochemical studies
support a model whereby Top1p recruits Sir2p to the rDNA
281 Overall, our results
support a model whereby TRPV4 differentially regulates c
282 nd markedly removed from the Rac1 interface,
supporting a model whereby P-Rex1 binding to PIP3 and/or
283 This study
supports a model whereby SMN deficiency impedes transpor
284 In conclusion, our data
support a model wherein a pre-TfH wave of IL-4 secreted
285 nic amyloid precursor protein processing and
support a model wherein Abeta production is amplified by
286 Our data
support a model wherein conformational changes in SF3b1
287 The results
support a model wherein dNTP elevation is needed to faci
288 Our results
support a model wherein efficient electron propagation c
289 These findings
support a model wherein interactions between transcripti
290 These findings
support a model wherein interoceptive processing in the
291 Together, these data
support a model wherein KLK5-mediated PAR-2 activation r
292 Our combined data
support a model wherein modest alterations in B cell-int
293 Data presented
support a model wherein SrrAB-dependent biofilm formatio
294 Our findings
support a model wherein the degron is exposed when SMN i
295 Collectively, our data
support a model wherein the in vivo role of VitD3 during
296 Together our data
support a model wherein the production of type I interfe
297 les of PABPs in miRNA-mediated silencing and
support a model wherein they enable miRNA-binding sites
298 Thus, the data
support a model wherein tumor Treg cells sustain and amp
299 and middle domains, which has been taken to
support a model with 34 copies, is also supported.
300 These findings
support a model with two mechanisms: a dual-rate adaptat