1 PDF analysis reveals strong local structural distortion
2 PDF data for nanocrystalline platinum (n-Pt) were collec
3 PDF measurements reveal that on the length scale of the
4 PDF neuron rescue induced high amplitude rhythms in the
5 PDF-expressing neurons consist of two neuronal clusters:
6 PDFs of n-Pt and nano Au (n-Au) under quasi-hydrostatic
7 , the American Diabetes Association (ADA1-
17-
PDF-138) (Y.H.), the US Department of Agriculture (USDA)
8 ross a range of microsites, which leads to
a PDF of heterotrophic respiration and O(2) consumption am
9 the same rate and particles surviving the
A-
PDF had an even higher oxidative potential on a per PM m
10 between the interdivision-time and cell-
age PDFs.
11 tify a novel role of DH31, in which DH31
and PDF hierarchically regulate free-running rhythmicity thr
12 01) double mutants, suggesting that DH31
and PDF may act on DN1ps to regulate free-running rhythmicit
13 X-ray absorption fine structure (EXAFS)
and PDF analyses show that Y is retained by basaluminite, fo
14 chniques, including Raman, XANES, EXAFS,
and PDF, reveal 6 to have similarities with related compound
15 The error has been corrected in the HTML
and PDF version of the article.
16 e errors have been corrected in the HTML
and PDF version of the article.
17 his error has been corrected in the HTML
and PDF versions of the article.
18 has now been corrected in both the html
and PDF versions of the article.
19 The error has been corrected in the HTML
and PDF versions of the article.
20 has now been corrected in both the HTML
and PDF versions of the Article.
21 e errors have been corrected in the HTML
and PDF versions of the article.
22 The error has been corrected in the HTML
and PDF versions of the article.
23 legends have been corrected in the HTML
and PDF versions of the article.
24 e errors have been corrected in the HTML
and PDF versions of the article.An amendment to this paper h
25 rors have now been corrected in the HTML
and PDF versions of the manuscript.
26 competing interests section of the HTML
and PDF versions of the manuscript.
27 The error has been corrected in the HTML
and PDF versions of the paper.
28 The error has been corrected in the HTML
and PDF versions of the paper.
29 This has now been corrected in the HTML
and PDF versions of the paper.
30 dded to the Acknowledgements in the HTML
and PDF versions of the paper.
31 his error has been corrected in the HTML
and PDF versions of the paper.
32 e errors have been corrected in the HTML
and PDF versions of the protocol.
33 The HTML
and PDF versions of this Article have been corrected.
34 The HTML
and PDF versions of this Article were updated after publicat
35 This has now been corrected in the HTML
and PDF versions of this Article.
36 The error has been corrected in the HTML
and PDF versions of this article.
37 The error has been corrected in the HTML
and PDF versions of this article.
38 competing interests section of the HTML
and PDF versions of this manuscript originally did not inclu
39 en published and is linked from the HTML
and PDF versions of this paper.
40 blished and is appended to both the HTML
and PDF versions of this paper.
41 en published and is linked from the HTML
and PDF versions of this paper.
42 The combination of XRD, IR, ICP,
and PDF experiments was essential in confirming the integrit
43 Immunoreactivity for both InvD1L
and PDF (type II acini exclusively) revealed positive axons
44 X-ray total scattering
and PDF analysis indicate that the majority phase for both t
45 modes, and it outputs data files in text
and PDF formats.
46 action intermediates from techniques such
as PDF can be a valuable asset in the development of system
47 Additionally, cell-
autonomous PDF signaling reversed the circadian behavioral effects
48 ions from collagen were observed in
biogenic PDFs when compared to synthetic PDFs (namely r < 15 angs
49 Both PDF and sNPF suppress basal Ca(2+) levels in target pace
50 utoreceptors, diurnal PDF release keeps
both PDF-dependent clock circuits in antiphase.
51 PDF) neuropeptide into the dorsal brain,
but PDF expression persists in their cell bodies and remaini
52 ction eliminates sLNvdorsal projections,
but PDF expression persists in sLNvand large ventral lateral
53 e circuit also features negative feedback
by PDF to truncate the s-LNv Ca(2+) wave and terminate PDF
54 and Engineering Research Council of
Canada (
PDF-532926-2019), National Institute of Allergy and Infe
55 erlapped with PDFLAs that mostly
colocalized PDF, FMRFamide, and 5-HT immunoreactivities, and with te
56 that diuretic hormone 31 (DH31)
complements PDF function in regulating free-running rhythmicity usin
57 Both
d-
PDF and EXAFS results indicated that the bidentate binuc
58 s differential pair distribution function (
d-
PDF) analysis and extended X-ray absorption fine structu
59 by 2 essential enzymes, peptide
deformylase (
PDF) and methionine aminopeptidase (MAP).
60 CRISPR/Cas9 assay, we show that lLNv-
derived PDF directly interacts with neurons important for E acti
61 Combining this data with
differential PDF and XAS allowed us to conclude that As adsorption oc
62 and EDX mapping with the bulk (
differential)
PDF and extended X-ray absorption fine structure (EXAFS)
63 PDFMEs inhibitory PDF autoreceptors,
diurnal PDF release keeps both PDF-dependent clock circuits in a
64 who were randomly assigned to receive
either PDF or TF from term age until 6-mo CA.A total of 79 of 1
65 ut can also diminish, depending on the
event PDF.
66 a I and Ga II, based on fitting
experimental PDF to known crystal structure, with a controversy.
67 rt that Ap and Chi in the neurons
expressing PDF, a neuropeptide, play important roles in proper slee
68 the neuropeptide pigment-dispersing
factor (
PDF) amplifies the molecular rhythms via time-of-day- an
69 levels within the pigment dispersing
factor (
PDF) cell-pacemaker neurons; only mir-92a peaks during t
70 Pigment-dispersing
factor (
PDF) denotes a conserved family of homologous neuropepti
71 PERIOD (PER) and pigment-dispersing
factor (
PDF) expression show similar but distinct circuit organi
72 he recruitment of pigment dispersing
factor (
PDF) filled dense core vesicles (DCVs) to the terminals
73 and neuropeptide pigment dispersing
factor (
PDF) from morning cells (s-LNv) together delay the phase
74 Pigment-dispersing
factor (
PDF) is critical to the circadian rhythms in Drosophila
75 rons that release pigment-dispersing
factor (
PDF) neuropeptide into the dorsal brain, but PDF express
76 ires signaling by Pigment-dispersing
factor (
PDF), a neuromodulatory signaling peptide produced only
77 _R), neuropeptide pigment dispersing
factor (
PDF), and the invertebrate-specific D1-like dopamine rec
78 the neuropeptide pigment-dispersing
factor (
PDF), released by the well-characterized central pacemak
79 the neuropeptide pigment-dispersing
factor (
PDF), which mediates pacemaker neuron synchrony and outp
80 the neuropeptide pigment-dispersing
factor (
PDF).
81 is antagonized by pigment-dispersing
factor (
PDF).
82 coupling peptide pigment-dispersing
factor (
PDF).
83 The clock within the
famous PDF-expressing s-LNv neurons however was strongly depend
84 health variables when comparing children
fed PDF with those fed TF.
85 changes in local structure were observed
for PDFs of synthetic hydroxyapatites with differing carbona
86 and mineral-enriched postdischarge
formula (
PDF) from term age to 6-mo corrected age (CA) gained mor
87 long records, probability density
function (
PDF) analyses of the 95% percentile exceedance of total
88 ters (GPFs), a probability density
function (
PDF) based heterogeneous multiscale filtration (HMF) mod
89 is based on a probability density
function (
PDF) description of the pore size distribution and class
90 ynamics of the probability density
function (
PDF) of barrier elevation at a point.
91 widths and the probability density
function (
PDF) of their widths resembles the statistical distribut
92 ynchrotron X-ray pair distribution
function (
PDF) (100-503 K) and inelastic neutron scattering (INS)
93 Pair distribution
function (
PDF) analyses and ab initio molecular dynamics density f
94 In situ pair distribution
function (
PDF) analyses and density functional theory (DFT) comput
95 Operando pair distribution
function (
PDF) analysis and ex situ (23)Na magic-angle spinning so
96 ering and atomic pair distribution
function (
PDF) analysis are used to show that precursors that firs
97 Diffraction and Pair Distribution
Function (
PDF) analysis in amorphous solid dispersions of lapatini
98 diffraction, and pair distribution
function (
PDF) analysis of X-ray total scattering from standard an
99 Pair distribution
function (
PDF) analysis was applied to hydroxyapatites in the 1970
100 otal scattering, pair distribution
function (
PDF) analysis, and As K-edge X-ray absorption spectrosco
101 In addition, Pair Distribution
Function (
PDF) data were collected on the POM@MOF composite and pr
102 eam suitable for pair distribution
function (
PDF) measurements at high pressure using a diamond anvil
103 action and X-ray pair distribution
function (
PDF) measurements characterize bulk perovskite CsPbI(3)
104 igh energy X-ray pair distribution
function (
PDF) measurements, microtomography and reverse Monte Car
105 by Rietveld and pair distribution
function (
PDF) methods.
106 using the atomic pair-distribution
function (
PDF) obtained from electron diffraction.
107 og-normal probability distribution
function (
PDF) of carbon and water content across a range of micro
108 The probability distribution
function (
PDF) of CTT for dust-mixed clouds shifted to the warmer
109 ork, we combined Pair Distribution
Function (
PDF) technique with Raman spectroscopy and electrical re
110 attering (SAXS), pair distribution
function (
PDF), and electrospray ionization mass spectrometry (ESI
111 attering (SAXS), pair distribution
function (
PDF), and X-ray powder diffraction (XRPD) techniques, is
112 around the dawn hours to promote
functional PDF signaling.
113 of the joint probability density
functions (
PDFs) between second and third invariants of the velocit
114 ) MEMLET fits probability density
functions (
PDFs) for many common distributions (exponential, multie
115 division-time probability density
functions (
PDFs) have been extensively investigated since the 1940s
116 senting event probability density
functions (
PDFs) in each of three sensory modalities.
117 nd fat-tailed probability density
functions (
PDFs).
118 employs atomic pair distribution
functions (
PDFs), determined from X-ray total scattering that depen
119 r-Planck equation with strongly non-
Gaussian PDFs in much higher dimensions even with orders in the m
120 h the transient and equilibrium non-
Gaussian PDFs requires only [Formula: see text] samples!
121 Thus, RalA activity confers
high PDF responsiveness, providing a daily gate around the da
122 evening (LNd) group by approximately 12
hr;
PDF alone delays the phase of the DN3 group by approxima
123 This error has been corrected for the
HTML,
PDF and print versions of the article.
124 ct pigment-dispersing factor-
immunoreactive (
PDF-ir) circadian pacemaker neurons with somata in the l
125 st, in constant darkness, knockdown of Ap
in PDF-expressing neurons did not promote arousal, indicati
126 n of dominant-negative forms of Ap or Chi
in PDF-expressing neurons or l-LNvs promoted arousal.
127 al, indicating that a reduced Ap function
in PDF-expressing neurons promotes light-driven arousal.
128 sample results and supporting information
in PDF format.
129 PRL-1 knockdown
in PDF clock neurons dramatically lengthens circadian perio
130 -LNvs, particularly the circadian rhythms
in PDF accumulation and axonal arbor remodeling.
131 utputs an overview of genome-wide synteny
in PDF.
132 be important for activity rhythms,
including PDF accumulation and arborization rhythms in the small v
133 citatory and contralateral PDFMEs
inhibitory PDF autoreceptors, diurnal PDF release keeps both PDF-de
134 The classical teardrop shape of the
joint PDF between Q and R has been observed away from active w
135 r (e.g. [Formula: see text]) where the
joint PDF exhibits a shape mirrored at the vertical Q-axis.
136 In contrast to flies that
lack PDF, flies that lackLaranticipate lights-on and lights-o
137 nticipatory activity seen in flies that
lack PDF,LarRNAi knockdown flies anticipate the lights-on and
138 ness and does not require endogenous
ligand (
PDF) signaling or rhythmic receptor gene transcription.
139 ME via lamina organ photoreceptors
maintains PDF release orchestrating phases of sleep-wake cycles.
140 r sharing workshop content is through
making PDF, PowerPoint and Word documents available online.
141 al mir-92a target and that mir-92a
modulates PDF neuronal excitability via suppressing SIRT2 levels i
142 Loss of the receptor for the
neuropeptide PDF promoted synchrony of Ca(2+) waves.
143 The
neuropeptide PDF promotes the normal sequencing of circadian behavior
144 h of the asynchrony caused by the absence
of PDF.
145 are valence-specific pathways downstream
of PDF that regulate memory formation.
146 In vivo calcium monitoring, dynamics
of PDF projections, ArcLight, GCaMP6 imaging and sleep assa
147 The effect
of PDF on clock gene transcription and the known role of PD
148 strates an acute direct excitatory effect
of PDF on target neurons to control neuronal output.
149 ren, we showed that the favorable effects
of PDF at 6-mo CA either were not maintained or could not b
150 Immunolocalization
of PDF-like peptides in six onychophoran species, by using
151 The lack
of PDF-like-immunoreactive somata associated with the onych
152 memory in male and female Drosophila Loss
of PDF signaling significantly decreases the ability to for
153 the mechanistic understanding of the role
of PDF in controlling the synchrony of the pacemaker neuron
154 ock gene transcription and the known role
of PDF in enhancing PER/TIM stability occur via independent
155 nsiveness also cycles, in phase with that
of PDF, in the same pacemakers, but does not cycle in large
156 incipal component analysis and comparison
of PDFs.
157 error has not been corrected in the HTML
or PDF of the original Article.
158 The error has not been fixed in the
original PDF and HTML versions of the Article.
159 The
original PDF version of this Article contained an error in the Ad
160 The
original PDF version of this Article contained errors in two equa
161 The
original PDF version of this Article inadvertently highlighted th
162 In the
original PDF version of this Article, which was published on 16 O
163 In the
original PDF version of this Article, which was published on 16 O
164 graphical output plus an in-depth multi-
page PDF report including error profile, quality and yield da
165 The errors have been corrected in the
print,
PDF and HTML versions of the article.
166 The error has been corrected in the
print,
PDF and HTML versions of the article.
167 ese errors have been corrected in the
print,
PDF and HTML versions of the article.
168 " The error has been corrected in the
print,
PDF and HTML versions of this article.
169 idl." The error has been fixed in the
print,
PDF and HTML versions of this article.
170 The label is now correct in the
print,
PDF, and HTML versions of the paper.
171 Here, synchrotron X-
ray PDF analysis is compared to techniques commonly used to
172 w that perceptual systems use the
reciprocal PDF and not the HR to model event probability density.
173 e stable computation than HR: the
reciprocal PDF of events in time.
174 a broadly reactive antibody that
recognizes PDF/PDH peptides in numerous species, revealed an elabor
175 e activity of RalA GTPase in s-LNv
regulates PDF responsiveness and behavioral locomotor rhythms.
176 normally, which suggests that the
remaining PDF expression mediates activity during light/dark cycle
177 Interestingly, aversive STM
requires PDF but not PDFR, suggesting that there are valence-spec
178 One stands for the age-at-
rupture PDF and is experimentally observable, whereas the other
179 While
several PDF parsing tools that extract information from such doc
180 r < 15 angstrom), consistent with
simulated PDFs of collagen structures.
181 , Gaussian, etc.), as well as user-
specified PDFs without the need for binning.
182 The
supplemental PDF serves as a practical guide, with complete and repro
183 in biogenic PDFs when compared to
synthetic PDFs (namely r < 15 angstrom), consistent with simulated
184 truncate the s-LNv Ca(2+) wave and
terminate PDF release.
185 The expression of
tethered-
PDF or tethered-DH31 in clock cells, posterior dorsal ne
186 Document input format can be plain
text,
PDF or BioC (uploaded locally or automatically retrieved
187 The results indicate
that PDF contributes to clock neuron synchrony by increasing
188 RNAi and rescue experiments show
that PDF from these cells is necessary and sufficient for del
189 rsal projection development and suggest
that PDF expression in LNvcell bodies and their remaining pro
190 The PDF and HTML versions of the Article have been modified
191 The PDF and HTML versions of the paper have been modified ac
192 The PDF and HTML versions of the paper have been modified ac
193 The PDF for relatively pristine cloud only show one peak at
194 The PDF indicates that the Zr-Zr distances in this glass are
195 The PDF is sensitive to local ionic displacements and their
196 The PDF results show that the structure of SiOC alloys are n
197 The PDF version of the article was correct at the time of pu
198 The PDF version was correct from the time of publication.
199 attempt to identify images by analyzing
the PDF encoding and structure and the complex graphical obj
200 cted in the HTML version of the Article;
the PDF version was correct at the time of publication.
201 ted. This has now been corrected in both
the PDF and HTML versions of the Article.
202 s work.' This has been corrected in both
the PDF and HTML versions of the Article.
203 e errors have now been corrected in both
the PDF and HTML versions of the Article.
204 21)."This has now been corrected in both
the PDF and HTML versions of the Article.
205 ia.' This has now been corrected in both
the PDF and HTML versions of the Article.
206 This error has now corrected in both
the PDF and HTML versions of the Article.
207 ina.'This has now been corrected in both
the PDF and HTML versions of the Article.
208 The errors have been corrected in both
the PDF and HTML versions of the Article.
209 This has now been corrected in both
the PDF and HTML versions of the article.
210 ia.' This has now been corrected in both
the PDF and HTML versions of the Article.
211 hina.This has now been corrected in both
the PDF and HTML versions of the Article.
212 000'.This has now been corrected in both
the PDF and HTML versions of the Article.
213 s error. This has been corrected in both
the PDF and HTML versions of the article.
214 This has now been corrected in both
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215 These errors have been corrected in both
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216 This has been corrected in both
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217 e errors have now been corrected in both
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218 his error has now been corrected in both
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219 e errors have all been corrected in both
the PDF and HTML versions of the Article.
220 These errors have been corrected in both
the PDF and HTML versions of the Article.
221 an.' This has now been corrected in both
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222 This error has been corrected in both
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223 SA.' This has now been corrected in both
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224 67.' This has now been corrected in both
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225 hina.This has now been corrected in both
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226 rs.' This has now been corrected in both
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227 This has been corrected in both
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228 , they have now been re-numbered in both
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229 These have been corrected in both
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230 This has now been corrected in both
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231 This has now been corrected in both
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232 This has been corrected in both
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233 This error has been corrected in both
the PDF and HTML versions of the paper.
234 e errors have now been corrected in both
the PDF and the HTML versions of the Article.
235 of this, changes have been made to both
the PDF and the HTML versions of the Article.
236 number of changes have been made to both
the PDF and the HTML versions of the Article.
237 This has been corrected in both
the PDF and the HTML versions of the Article.
238 trations of O(2) , which then determines
the PDF of microsites that produce or consume CH(4) and N(2)
239 this Bench to Bedisde, open or download
the PDF.
240 this Bench to Bedside, open or download
the PDF.
241 To view this SnapShot, open or download
the PDF.
242 To view this Timeline, open or download
the PDF.
243 This has been removed from
the PDF version of the Article.
244 These corrections have been made in
the PDF and HTML versions of the article, as well as in any
245 ist, and the error has been corrected in
the PDF and HTML versions of the article.
246 These errors have now been corrected in
the PDF and HTML versions of the article.
247 This has been corrected in
the PDF and HTML versions of the Article.
248 LUE." The omission has been corrected in
the PDF and HTML versions of the article.
249 7,21,47-53).' This has been corrected in
the PDF and HTML versions of the Article.
250 This has now been corrected in
the PDF and HTML versions of the Article.
251 -76, and the error has been corrected in
the PDF and HTML versions of the article.
252 These errors have now been corrected in
the PDF and HTML versions of the Article.
253 This error has now been corrected in
the PDF and HTML versions of the Article.
254 This error has been corrected in
the PDF and HTML versions of the article.
255 -0.09." This error has been corrected in
the PDF and HTML versions of the article.
256 The error has been corrected in
the PDF and HTML versions of the manuscript.
257 The figures have been updated in
the PDF and HTML versions of the paper, and the revised Supp
258 These errors have been corrected in
the PDF and HTML versions of the paper.
259 This error has been corrected in
the PDF and HTML versions of the paper.
260 The error has been corrected in
the PDF and HTML versions of the paper.
261 ll." These errors have been corrected in
the PDF and HTML versions of the protocol.
262 These changes are reflected in
the PDF and HTML versions of the protocol.
263 These changes have been made in
the PDF and HTML versions of the protocol.
264 This has now been corrected in
the PDF and online.
265 structures is the only motif apparent in
the PDF of either precursor.
266 This has not been fixed in
the PDF or HTML versions of the Article but can be seen in t
267 graded.' The error has not been fixed in
the PDF or HTML versions of the Article.
268 These have now been corrected in
the PDF version of the Article.
269 The errors have been corrected in
the PDF version of the article.
270 This has now been corrected in
the PDF version of the article.
271 These errors have been corrected in
the PDF version of the Article; the HTML version was correct
272 In
the PDF version of this article, Eq.
273 of this article initially published, in
the PDF, equations (2) and (4) erroneously displayed a curly
274 fat body clock require clock function in
the PDF-positive cells of the fly brain.
275 This has now been corrected in
the PDF; the HTML version of the paper was correct from the
276 Thandavarayan Ramamurthy were inverted (
the PDF and print versions of the Letter were correct); the
277 Subtraction of
the PDF of crystalline NaxSb phases from the total PDF, an a
278 r via independent pathways downstream of
the PDF receptor, the former through a cAMP-independent mech
279 mposition and its correlates" (page 3 of
the PDF).
280 rected in the HTML version of the paper,
the PDF was correct at the time of publication.
281 se projections in the heart suggest that
the PDF neuropeptides functioned as both circulating hormone
282 t nanocrystals form the IJS according to
the PDF-4 simulation.
283 e composed by nanocrystals, according to
the PDF-4+2019 software.
284 nanoscale structural changes observed in
the PDFs are dominated by piezoelectric lattice strain and i
285 The proper modification of
the PDFs occurs automatically in the program and greatly inc
286 e substitution from peak position within
the PDFs.
287 , two definitions for the interdivision-
time PDF have been proposed.
288 ining to the unobservable interdivision-
time PDF, Painter and Marr derived an inequality that is true
289 ween the cell-age and the interdivision-
time PDFs are derived in this work from an age-structured mod
290 This contrasts
to PDF that derives from the small ventral-lateral neurons
291 eport daily rhythmicity in responsiveness
to PDF in critical pacemakers called small LNvs.
292 .e., instrument "dead time") when fitting
to PDFs.
293 ermolecular drug interactions from the
total PDF x-ray pattern was successfully applied allowing the
294 F of crystalline NaxSb phases from the
total PDF, an approach constrained by chemical phase informati
295 fortunately, the confusion between these
two PDFs persists.
296 The original
version (
PDF) is appended to this article as a Supplement.
297 (PKA) and a molecular target (TIM) by
which PDF resets and synchronizes clocks and demonstrates an a
298 Consistent
with PDF analysis, Raman spectroscopy data suggest that the l
299 In addition, mir-92a levels
within PDF cells respond to light pulses and also affect the ph
300 In situ
XRD-
PDF, XAFS and AP-XPS structural studies reveal that the