1 Our findings
support a model by which CaM binds to Akt to facilitate
2 Combined with computer simulations, our data
support a model by which Nlgn1 tyrosine phosphorylation
3 Together, our results
support a model by which Tip60 protects against neurolog
4 icted subsequent TMS effects across subjects
supporting a model by which theta oscillations are excit
5 This
supports a model by which Cav1 is a central regulatory h
6 ion of SosV-RBP with other classical HN RBPs
supports a model by which pararubulaviruses only recentl
7 Our data
support a model demonstrating that heat shock factor 1 (
8 Collectively, these data
support a model for ALS pathogenesis whereby aberrant in
9 These structural snapshots
support a model for biogenesis of the F transfer system
10 Together, these observations
support a model for Cas9 specificity wherein gRNA-DNA mi
11 Our findings
support a model for functional conservation of lncRNAs i
12 Our findings
support a model for GAS skin tropism in which GAS genera
13 Our data
support a model for GCs to stabilize HIF through activat
14 The results
support a model for multiple myeloma progression with cl
15 These observations
support a model for native HIV-1 assembly wherein HIV-1
16 Our findings
support a model for negative selection in which the deat
17 -PTP with ESCRT-0, ESCRT-I and ESCRT-III and
support a model for regulation of ESCRT function by disp
18 Our findings
support a model for SIRT2's tumor-suppressive function i
19 Together, our results
support a model for the cellular function of ADAP1, wher
20 Collectively, our data
support a model for translational regulation primarily d
21 genes and is required for their expression,
supporting a model for transcriptional switch between Ml
22 This
supports a model for influenza virus entry where cells r
23 t-chain lipids in activating the transporter
supports a model for regulation within the highly dynami
24 The results
support a model in which a locus first duplicates, resul
25 These data
support a model in which a single neuronal stem cell can
26 Our presented data
support a model in which a two-authentication system mob
27 Our results
support a model in which a uORF coding sequence impacts
28 Our findings
support a model in which Abeta-independent sensitizing i
29 Findings
support a model in which abnormal frontoinsular dynamics
30 Together, our results
support a model in which acute inflammation after injury
31 with later development of CD; these findings
support a model in which altered intestinal barrier func
32 Our data
support a model in which ANKRD26 initiates a centriole-d
33 result in insertions or deletions, our data
support a model in which APOBEC3 enzymes use multiple me
34 her order assemblies on the nuclear envelope
support a model in which arachidonic acid is generated b
35 The data collectively
support a model in which asymptomatic mothers can harbor
36 epressing the master regulator, ler Our data
support a model in which Aurodox acts upstream of ler an
37 Taken together, these data
support a model in which autophagosomes were directed to
38 Our results
support a model in which Bdl mediates specific axo-dendr
39 Our findings
support a model in which binding of the PSL to the WD40
40 Our results
support a model in which biological outcomes of caspase
41 Our results
support a model in which both subunits of an Ube2D~Ub cl
42 The results of these studies
support a model in which bound PNAG is weakly associated
43 atic experimental and computational analyses
support a model in which C-signaling activates FruA at l
44 Our analyses
support a model in which cell-cell mechanical communicat
45 These results
support a model in which centriole amplification occurs
46 These data
support a model in which cholesterol passes through the
47 Our findings
support a model in which clustered vesicles are held tog
48 Our data
support a model in which confined diffusion of open Lck
49 Finally, single-molecule experiments
support a model in which conformational sampling between
50 These in vitro targeting experiments
support a model in which Cpn60 captures and then release
51 Our findings
support a model in which cues that emanate from intermed
52 Our results
support a model in which cyclin C binding stimulates the
53 Together, our data
support a model in which DACH1 stimulates coronary arter
54 These results
support a model in which DDR genes are uniquely suscepti
55 These results
support a model in which differences in pilus electrosta
56 Together, these studies
support a model in which differential association with c
57 get for amphetamines in dopamine neurons and
support a model in which distinct pools of TAAR1 mediate
58 evisiae initiators in origin recognition and
support a model in which DNA geometry and bendability co
59 Gene expression and mutant analyses
support a model in which DnaA and Rok cooperate to repre
60 Our study and those of others
support a model in which each kinetochore must undergo c
61 The data
support a model in which EAP deficits lead to poor funct
62 The findings in these index cases
support a model in which early development of occult hip
63 Our data
support a model in which early-acting spatial factors li
64 Together, these data
support a model in which EFTUD2 haploinsufficiency leads
65 Our results
support a model in which features of the ITS itself, suc
66 Taken together, these data
support a model in which FGFs, possibly from axons, acti
67 Our data
support a model in which flotillins are required for dir
68 These findings
support a model in which focal amplifications arise due
69 Together, these results
support a model in which FtsZ dynamics and associations
70 Our results
support a model in which full-length HIV-1 Env trimers a
71 These results
support a model in which FUS LC forms dynamic, multivale
72 Together, our findings
support a model in which GCNA provides genome maintenanc
73 graphy of hematopoietic differentiation, and
support a model in which genome-wide methylation changes
74 These quantitative results
support a model in which hCP exists in its heterodimeric
75 interaction mode between TBK1 and STING and
support a model in which high-order oligomerization of S
76 Our data
support a model in which HPr transfers a phosphate to an
77 These results
support a model in which increased level of kaempferol i
78 Our findings
support a model in which initial inhomogeneities in inpu
79 These results
support a model in which integrins are an upstream compo
80 Our results
support a model in which inter-chromosomal microtubules
81 These findings
support a model in which iRhom2 and ADAM17 are obligate
82 Altogether, our results
support a model in which L6CTs modulate first- and highe
83 Our results
support a model in which LetB establishes a physical lin
84 These data
support a model in which LGMDD1 mutations in DNAJB6 are
85 for Ldb1, a nonproto-oncogene, in T-ALL and
support a model in which Lmo2-induced T-ALL results from
86 These results
support a model in which localized synthesis of RBOHC an
87 These data
support a model in which LRRK2 associates with and disso
88 Our results
support a model in which LTP generates synaptic slots, w
89 Our findings
support a model in which LuxR/HapR bind proximally to RN
90 Altogether, these cell-based data
support a model in which MA-RNA binding ensures PM-speci
91 Our results
support a model in which many sensilla can respond to od
92 Our results
support a model in which mature pneumococcal peptidoglyc
93 Our findings
support a model in which Mcp1 and Vps13 work as function
94 These data
support a model in which mGluR5-mediated reduction in Gl
95 These results
support a model in which miR167-mediated anther growth a
96 Taken together, these data
support a model in which missense PMEL variants represen
97 Overall, our results
support a model in which MltG functions as a terminase f
98 Our results
support a model in which MRX-Sae2 catalyzes 5'-DNA end d
99 These findings
support a model in which MUC1-C activates the NuRD compl
100 The results
support a model in which multiple grooves on the ACD int
101 Collectively, our data
support a model in which multiple RNA polymerases initia
102 Our results
support a model in which MW deteriorates performance in
103 Taken together, our findings
support a model in which neighboring binding sites inter
104 Together, these data
support a model in which NEK6- and NEK7-dependent phosph
105 Our results
support a model in which NMC is dependent on ectopic NUT
106 These data
support a model in which non-rhythmic Treg cells are dri
107 Our data
support a model in which nuclear PHLPP1 dephosphorylates
108 The data
support a model in which only one RNA-binding mode is cr
109 Together, these data
support a model in which parallel OFF channels generated
110 These data
support a model in which pathogen effector transcription
111 The results
support a model in which perceptual filling-in is aided
112 These results
support a model in which phytochromes control PhAPG expr
113 In summary, our findings
support a model in which PI16 promotes neuropathic pain
114 Together, these data
support a model in which Pol delta promotes Alt-NHEJ in
115 Taken together, these results
support a model in which PPP2R5 degradation and global c
116 Our data
support a model in which PQM-1 controls a trade-off betw
117 These data
support a model in which pre-mRNA evicts PRC2 during gen
118 Our results
support a model in which presynaptic Ca(v) channels serv
119 some footprinting, and X-ray crystallography
support a model in which propylamycin functions by inter
120 Our results
support a model in which R-DPRs interfere with cargo loa
121 Altogether, our data
support a model in which Rab18 regulates kinectin-1 tran
122 Combined with previous work, these data
support a model in which RDN1 arabinosylates MtCLE12, an
123 Our findings
support a model in which repression of activin signaling
124 Our findings
support a model in which RPN13 recruitment to the protea
125 Our studies
support a model in which SF2312 acts as an analog of a h
126 The results
support a model in which signal-independent binding of S
127 Our data
support a model in which simultaneous interactions betwe
128 Our data
support a model in which skin plasma cells supply natura
129 Altogether, our data
support a model in which small neutral hydrophobic resid
130 Taken together, these data
support a model in which SNAP23 plays a crucial function
131 Our findings
support a model in which snoRNA-guided Nm modifications
132 Together, our findings
support a model in which splicing recruits transcription
133 Our data
support a model in which SpoIIIE is anchored at the edge
134 These results
support a model in which Src-family kinase binding induc
135 Together, our results
support a model in which stimulus-evoked exocytosis in r
136 Our data
support a model in which STR length in eukaryotic genome
137 Overall, these results
support a model in which structured RNA negatively regul
138 Our experimental data
support a model in which SurA binds uOMPs in a groove fo
139 that alter oxygen consumption or redox state
support a model in which surfactin-mediated membrane dep
140 These results
support a model in which synonymous codon substitutions
141 Our findings
support a model in which target-specific cortical subnet
142 ent only in response to biotic elicitors and
support a model in which TARK1 regulates stomatal openin
143 NMR and biochemical experiments
support a model in which the 5'UTR can transition betwee
144 These results
support a model in which the AE3 Cl(-)/HCO3(-) exchanger
145 Our studies
support a model in which the alignment of mitotic chromo
146 Our results
support a model in which the E. coli clamp loader active
147 Together, our results
support a model in which the E2 D-loop promotes the form
148 Our results
support a model in which the effect of GFI1's regulation
149 Our findings
support a model in which the folate receptor interacts w
150 Our data
support a model in which the hydration of the uppermost
151 Our data
support a model in which the identified pathogenic varia
152 Our results
support a model in which the interior wall of BamA acts
153 Our results
support a model in which the isoform-specific N-terminal
154 Our data
support a model in which the levels of newly synthetized
155 These findings
support a model in which the malate-aspartate shuttle, m
156 These data
support a model in which the MBD2/3 methylation-dependen
157 These data
support a model in which the modulation of PP-InsPs infl
158 Together, our data
support a model in which the nucleoplasmic HAL-2/HAL-3 p
159 cal, genetic and biochemical approaches that
support a model in which the PTS proteins HPr and Enzyme
160 Taken together, our findings
support a model in which the PVT1-214/Lin28/let-7 axis s
161 These findings
support a model in which the relative binding sites of R
162 tes cullins in vivo Combined, these findings
support a model in which the SCCRO, substrate, and subst
163 -EM structures of ClpXP bound to substrates,
support a model in which the ssrA degron initially binds
164 Our solution structural data
support a model in which the substrate is directly trans
165 Overall, our data
support a model in which the Zip2:Zip4:Spo16 complex bin
166 ights into B1/VRK signaling coregulation and
support a model in which these enzymes modulate B12 in a
167 Extensive data from studies in rodents
support a model in which theta oscillations fulfill this
168 Taken together, these results
support a model in which this IDR of Med13 plays a key r
169 These data
support a model in which this new regulator of iron home
170 Our findings
support a model in which tightly-intertwined biological
171 Our results
support a model in which TOPBP1(Dpb11) plays a conserved
172 Our findings
support a model in which topoisomerases participate in P
173 These findings
support a model in which utrophin-derived therapies migh
174 Taken together, these data
support a model in which VtlR indirectly regulates hundr
175 Together, these results
support a model in which WDR-48 binds and stabilizes USP
176 The data
support a model in which within-cell chromosome cooperat
177 riptome and at the metabolite analysis level
support a model in which WRKY1 enables plants to activat
178 Our results
support a model in which yeast cells mobilize, and perha
179 including catalase and GSH peroxidases, have
supported a model in which beta-cells are ill-equipped t
180 scussed in relation to O-O cleavage in HCOs,
supporting a model in which a peroxo intermediate serves
181 was 35-fold higher than the low-ROS pollen,
supporting a model in which a significant fraction of a
182 usly to require replication fork regression,
supporting a model in which fork regression depends on a
183 Here we present data
supporting a model in which NPA associates with PINs in
184 y combinatorial, distinct, and nonredundant,
supporting a model in which the +1 nucleosome is positio
185 Zip2:Spo16 severely compromise DNA binding,
supporting a model in which the complex's central and Hh
186 nit properties associated with each hotspot,
supporting a model in which the hotspots apply nonlinear
187 ar progression through these subpopulations,
supporting a model in which these three states correspon
188 ivity correlated with visual responsiveness,
supporting a model in which visual speech enhances the e
189 Our data
supports a model in which a single C-terminal tail tethe
190 Our work
supports a model in which AdamTS-A anchors cells in plac
191 Site-directed mutagenesis
supports a model in which adenosine 5'-triphosphate (ATP
192 Finally, mechanistic analysis
supports a model in which AKR1B10 serves to limit the to
193 Together, this work
supports a model in which an extrinsic signal triggers a
194 Recent evidence also
supports a model in which certain aspects of the wall it
195 The study
supports a model in which circulating fetal ILC1-like NK
196 This
supports a model in which dormant, balanced NEO1(-) Hoxb
197 Analysis of DNA replication intermediates
supports a model in which dysregulated Rad5 causes aberr
198 This novel work
supports a model in which protein S-nitrosylation may be
199 Our work
supports a model in which regulation of CO position earl
200 ant alkane synthesis enzymatic component and
supports a model in which several alkane-forming complex
201 cluding the meiotic clade relative Vps4, and
supports a model in which spastin utilizes a hand-over-h
202 This strongly
supports a model in which the CTD acts as a key bridging
203 two Meissner afferents within the corpuscle
supports a model in which the extent of lamellar cell wr
204 Such a transition state
supports a model in which the rate-limiting step of the
205 in XPF-deficient Caenorhabditis elegans and
supports a model in which translesion synthesis polymera
206 very of a second major protective TI epitope
supports a model in which uncleaved HA trimers exist on
207 These findings
support a model linking increased hippocampal activation
208 These findings
support a model mechanism wherein the NTD mediates allos
209 Our findings
support a model of a minimal integrase with an internal
210 y labeled as "high" or "low." These findings
support a model of aesthetic appreciation whereby domain
211 Results
support a model of aging where nutrient signaling pathwa
212 cial canals shouldn't be used to exclusively
support a model of aquatic foraging in theropods and arg
213 Our results
support a model of color pattern evolution in Heliconius
214 Our results
support a model of convergent evolution of proteins and
215 nt paths in different Magicicada species and
support a model of genomic degradation that is stochasti
216 The results
support a model of HCV infection influencing the binding
217 These analyses
support a model of human OFC in which epithelial cells a
218 trance and evidence of genetic heterogeneity
support a model of PAH as a Mendelian disorder with comp
219 These results
support a model of solvent-slaved protein dynamics.
220 Our results
support a model of tissue ILC differentiation ("ILC-poie
221 Our data
support a model of voltage-induced death, and separates
222 Analysis of variant allele frequencies
supported a model of tumor growth involving slow-cycling
223 We present several lines of evidence
supporting a model of antagonistic pleiotropy in the DNA
224 it texture and flavor, and provide evidences
supporting a model of apple fruit size evolution compris
225 also produced increased or novel responses,
supporting a model of Gr-Gr inhibitory interactions.
226 transcripts splicing HIV to STAT3 sequences
supports a model of LTR-driven STAT3 overexpression as a
227 Protein modelling
supports a model of reduced ability of regular autoinhib
228 These data
support a model that includes changes in brain bioenerge
229 These data
support a model that virulent X. nematophila have a sele
230 The results
support a model to test diets that favorably alter the m
231 These collective results
support a model where a FlaG filament capped by a FlaG-F
232 The results from our study
support a model where altered protein interactions with
233 Our data
support a model where Bcd influences chromatin structure
234 The data
support a model where CHK2 sequesters the AR through dir
235 harmacological and molecular biology results
support a model where ETR1 and ETR2 are indirectly affec
236 Collectively, results presented here
support a model where GSK3beta regulates signaling by co
237 Our data
support a model where H2A.Z in gene bodies has a strong
238 Collectively, these observations
support a model where larynx SCC are characterized by sl
239 These findings
support a model where loss of either component of the co
240 Our findings
support a model where MN-intrinsic transcriptional progr
241 Our data
support a model where nutrition is a key environmental f
242 Taken together these data
support a model where PDHK4 regulates KRAS signalling an
243 Collectively, our data
support a model where proproliferative activities of LMP
244 These results
support a model where RIN and ET, via ERFs, are required
245 idence from in vitro and in vivo experiments
support a model where RNAs produced during early steps i
246 Our findings
support a model where sites of glycosylation for many OG
247 on of DIAPH1 in vivo Collectively these data
support a model where the combined action of RhoA and an
248 Findings reported here
support a model where the developmental timing of estrog
249 Altogether, these results
support a model where the eVP30-eNP interaction plays a
250 These data
support a model where the genomic integrity of human gam
251 These findings
support a model where UK-5099 inhibits the MPC complex b
252 o subviral regions of a budding Gag lattice,
supporting a model where direct interactions and/or ster
253 l = 0.005) in genetic values among partners,
supporting a model where partners assort for risk factor
254 or Hts-M function in motor neurons or muscle
supports a model where presynaptic miR-34 inhibits Nrx-I
255 These data
support a model whereby Banf1 is crucial to reset oxidat
256 These results
support a model whereby CDK-catalyzed phosphorylation of
257 Our data
support a model whereby CTXphi and TCP bind in a tip-to-
258 Our findings
support a model whereby genetic determinants of smoking
259 Taken together, our results
support a model whereby hAgo2:miR-122 complexes alter th
260 These observations
support a model whereby lack of a cognate charged tRNA e
261 Our results
support a model whereby LIG1 fidelity is governed by a h
262 Our data
support a model whereby nascent NepR(IDR)-PhyR interacti
263 Our data
support a model whereby purine motifs towards the 3' end
264 Our data
support a model whereby Rab13 can mediate its effects on
265 These findings
support a model whereby repeat expansions elicit cellula
266 The results
support a model whereby SNX3-retromer is a minimally con
267 In all, these data
support a model whereby T-BET serves to promote appropri
268 Our data
support a model whereby tau, facilitated by Abeta, trans
269 Taken together, our results
support a model whereby the amphipathic helix in SM N100
270 Our data
support a model whereby the disulfide bond and PAS domai
271 These results
support a model whereby the flippase activity of ALA4 an
272 d paramyxovirus F-nAb structures, these data
support a model whereby the membrane-distal region of th
273 Our data
support a model whereby the PilY1/minor pilin complex fu
274 Our combined data
support a model whereby the risk variant augments the BC
275 These data
support a model whereby TRIM14 acts as a scaffold betwee
276 Our data
support a model whereby ubiquitinated Rsp5 adaptors are
277 Combined, our data
support a model whereby WNV infection of human DCs compr
278 hly proliferative "transit-amplifying" cells
supports a model whereby alpha-cells expand by self-rene
279 This work
supports a model whereby expression of a viral protein s
280 equirement for gsk-3 and cdk-2 This analysis
supports a model whereby MPK-1/ERK, GSK-3/GSK3 and CDK-2
281 In conclusion, our data
support a model wherein a pre-TfH wave of IL-4 secreted
282 nic amyloid precursor protein processing and
support a model wherein Abeta production is amplified by
283 Our data
support a model wherein conformational changes in SF3b1
284 These findings
support a model wherein diabetes-induced O-GlcNAcylation
285 These findings
support a model wherein E93 expression functions as an i
286 Our results
support a model wherein efficient electron propagation c
287 The findings
support a model wherein hyperglycemia-induced REDD1 blun
288 Our data
support a model wherein IFNs local to the maternal-fetal
289 These findings
support a model wherein interoceptive processing in the
290 damental aspects of the H3K27M inhibitor and
support a model wherein PRC2 becomes trapped at H3K27M-H
291 These results
support a model wherein Pumilio utilizes CNOT deadenylas
292 The results
support a model wherein slow-moving replication forks ca
293 Data presented
support a model wherein SrrAB-dependent biofilm formatio
294 Thus, our findings
support a model wherein substrate discrimination via the
295 Our findings
support a model wherein the degron is exposed when SMN i
296 Together our data
support a model wherein the production of type I interfe
297 Together, these data
support a model wherein TNK2, WASL, and NCK1 comprise a
298 sion, usually occur as individual complexes,
supporting a model wherein sister cohesion is mediated l
299 and middle domains, which has been taken to
support a model with 34 copies, is also supported.
300 Altogether, these data
support a model with the Rsb system responding different