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1 complementary information in attenuation and phase contrast.
2 ill be measured accurately, obtaining strong phase contrast.
3 ith BF at rest and validated using real-time phase-contrast.
4 nally introduced with visible light, Zernike phase contrast(1) is a well-established technique in ful
5     It is intrinsically trimodal, delivering phase contrast, absorption contrast, and scattering ("da
6 ing a time-resolved three-dimensional radial phase-contrast acquisition.
7                                       The 4D phase-contrast acquisitions were performed, on average,
8 ortic velocity curves created on three axial phase-contrast acquisitions.
9 rtual noncontrast (VNC) images from a single-phase contrast agent-enhanced examination, potentially r
10 ) with routine nonenhanced and portal venous phase contrast agent-enhanced liver CT imaging with thic
11 ct volumetric cardiac and respiratory motion phases, contrast-agent dynamics, and blood flow velocity
12  classical physicochemical characterization, phase contrast and confocal laser scaning microscopy, an
13 elated with optical microscopy (differential phase contrast and confocal microscopy of mutant strains
14                                 Here, we use phase contrast and fluorescence microscopy to observe gi
15 imuli were confirmed with alamar blue assay, phase contrast and fluorescence microscopy.
16      Quantitative values for attenuation and phase contrast and image noise were determined.
17 contributions increase at a higher rate than phase contrast and inelastic scattering.
18      These confounds are now overcome, using phase contrast and time-lapse videography to reveal the
19   This protocol describes a method combining phase-contrast and fluorescence microscopy, Raman spectr
20                 Using these substrates, both phase-contrast and NIMS images of phospholipids from a s
21 -beat BF time history derived from real-time phase-contrast and VMHD was highly correlated using a Sp
22 covery platforms, for example, bright-field, phase contrast, and fluorescence microscopies, are unabl
23  we demonstrate that absorption, dark-field, phase contrast, and two orthogonal differential phase co
24 erebral oxygen delivery was calculated using phase contrast angiography and pre-ductal pulse oximetry
25 aphic techniques, such as time of flight and phase contrast, are considered and their advantages and
26         Ultrahigh-field MRI and, especially, phase contrast, are highly sensitive to tissue changes i
27 y, many attempts have been made to image the phase contrast based on a concept of the beam being defl
28                    Using near-field spectral phase contrast based on the Amide I resonance of the pro
29    This technique is successfully applied to phase contrast, bright field, fluorescence microscopy an
30 ude-based contrast mechanisms), we show that phase contrast can actually disappear with extreme tissu
31 or in oximetry-derived flow parameters using phase-contrast cardiac MRI (CMR) as a reference.
32 vious studies demonstrated the usefulness of phase-contrast cardiovascular magnetic resonance (PC-CMR
33                   Each participant underwent phase-contrast cardiovascular magnetic resonance measure
34 the first time, time-lapse synchrotron X-ray phase contrast computed tomography (CT) has been used to
35 rt a method for three-dimensional (3D) X-ray phase contrast computed tomography (CT) which gives quan
36  and small intestine) were imaged with x-ray phase contrast computed tomography (PC-CT).
37                        Synchrotron radiation phase-contrast computed nanotomography (nano-CT) and two
38                                Grating-based phase-contrast computed tomography (PCCT) is a promising
39 We used cryo-electron tomography and Zernike phase contrast cryo-electron tomography to visualize pop
40                                Grating-based phase-contrast CT allows differentiation of simulated si
41  results of this study indicate that ex vivo phase-contrast CT can help identify and quantify atheros
42 nd sensitivity, specificity, and accuracy of phase-contrast CT for plaque detection and the potential
43                     Applying these criteria, phase-contrast CT had a good sensitivity for the detecti
44         Although not yet applicable in vivo, phase-contrast CT may become a valuable tool to monitor
45 s scanned with an experimental grating-based phase-contrast CT setup consisting of a Talbot-Lau inter
46                                     Finally, phase-contrast CT uses x-ray refraction properties to im
47 resolution (UHR) CT, photon-counting CT, and phase-contrast CT.
48 ng injury, using high-resolution synchrotron phase-contrast CT.
49     Under these conditions, we show that the phase contrast derives primarily from a unique energy fl
50 ans prefer intrinsic contrast in the form of phase-contrast, differential-interference contrast, or H
51  thin-film samples by combining differential phase contrast (DPC) magnetic imaging with in situ heati
52  its host cell, Synechococcus, using Zernike phase contrast electron cryo-tomography (cryoET).
53  have used the emerging technique of Zernike phase-contrast electron cryomicroscopy to enhance the im
54                LSN scores from portal venous phase contrast-enhanced thick-section CT images had sign
55                      Using synchrotron X-ray phase contrast-enhanced tomography we show exemplar data
56 e compared during the pancreatic parenchymal phase: contrast enhancement for the aorta, the pancreas,
57 4D flow was in better agreement with 2D cine phase-contrast flow (95% limits of agreement: -8.8 and 9
58  of growth and parasite-host interactions by phase contrast, fluorescence in situ hybridization, and
59                                              Phase contrast, fluorescence, and atomic force microscop
60  However, absorption often is negligible and phase contrast has not been easily available.
61 n provide comparable contributions to tissue phase contrast; however, the sign of iron and lipid cont
62 s obtained include (1) the brightness of the phase contrast image of an individual dormant spore is p
63 90% detection efficiency for brightfield and phase contrast images and provides a new open-source pla
64 , the training data sets of the differential phase contrast images at a pair of sample positions, one
65 se contrast, and two orthogonal differential phase contrast images can simultaneously be generated by
66 terative algorithms to recover amplitude and phase contrast images from diffraction intensity data.
67 chmark our software capability in processing phase contrast images from other laboratories against ot
68 ween the sharpness and spatial resolution in phase contrast images of this eutectic alloy obtained vi
69 ndividual bacterial and mammalian cells from phase contrast images without the need for a fluorescent
70 ne capable of reliable detection of cells in phase contrast images.
71  pairwise comparison of the attenuation- and phase-contrast images and both images simultaneously.
72           Contrary to the common assumption, phase-contrast images in liquids using soft microcantile
73              Using this source, high quality phase-contrast images of biological specimens with a 5-m
74 we precisely quantify these properties using phase-contrast images of hESC colonies of different size
75                            Three-dimensional phase-contrast images of the live mouse retina were crea
76          Cartesian two-dimensional (2D) cine phase-contrast images were also acquired in the portal v
77                    Standard attenuation- and phase-contrast images were reconstructed from the raw pr
78 cal tweezers; (iii) simultaneously measuring phase-contrast images, Raman spectra and fluorescence im
79 age 29 virions in buffer solutions using the phase-contrast images.
80 ed by a specimen, the so-called differential phase contrast imaging (DPC).
81 ities of synchrotron Propagation-based X-Ray Phase Contrast Imaging (PB-X-PCI) to study a wide range
82                                        X-ray phase contrast imaging (XPCI) is an innovative imaging t
83                                        X-ray phase contrast imaging (XPCI) is more sensitive to densi
84                                  Concomitant phase contrast imaging allowed us to extract a linear de
85                        Non-destructive X-ray phase contrast imaging and tomography of heterogeneous m
86             This method relies on the use of phase contrast imaging at high defocus to improve inform
87 es of this eutectic alloy obtained via X-ray phase contrast imaging at the Swiss Light Source (SLS) s
88                                        X-ray phase contrast imaging has overcome the limitations of X
89                                        X-ray phase contrast imaging offers a way to visualize the int
90 With tunicamycin or mutant SFTPC expression, phase contrast imaging revealed a change to a fibroblast
91                   Grating-based differential phase contrast imaging techniques are compatible with co
92                Here we use synchrotron X-ray phase contrast imaging to study cold hardiness-related c
93 ficient for phase recovery than conventional phase contrast imaging.
94 ed quantitatively whilst in flow using x-ray phase contrast imaging.
95 in pulmonary artery (PA) was quantified with phase contrast imaging.
96 were also observed by Live-Dead staining and phase contrast imaging.
97 he development of a phase plate for in-focus phase contrast imaging.
98                                        X-ray phase-contrast imaging (XPCI) can dramatically improve s
99                 After histologic processing, phase-contrast imaging and histopathologic data were mat
100 tive measurements of FC, NC, and CAs between phase-contrast imaging and histopathologic findings (R >
101 were used to determine the agreement between phase-contrast imaging and histopathologic findings for
102                                              Phase-contrast imaging at a range of energies provided h
103                                   Hard X-ray phase-contrast imaging characterizes the electron densit
104                                        X-ray phase-contrast imaging has recently led to a revolution
105 VCG-derived BF was performed using real-time phase-contrast imaging in 7 healthy subjects (n=7) durin
106 TEM has not been regarded as optimal for the phase-contrast imaging necessary for efficient imaging o
107                                  In previous phase-contrast imaging studies with betatron sources, si
108 ical dipole trap created using a generalized phase-contrast imaging technique.
109     In this study, we used synchrotron x-ray phase-contrast imaging to visualize the tracheal system
110                                              Phase-contrast imaging using X-ray sources with high spa
111                     High-temporal-resolution phase-contrast imaging was performed in the main and rig
112                                              Phase-contrast imaging was performed to quantify the deg
113                                   Values for phase-contrast imaging were substantially distinguishabl
114 a way for the application of high resolution phase-contrast imaging with stable betatron sources usin
115 n asymmetric mask concept that enables X-ray phase-contrast imaging without requiring any movement in
116                   Here, with ultrafast X-ray phase-contrast imaging, we show that the formation of vo
117 the optical pump pulse using magnified x-ray phase-contrast imaging.
118 , and swim at speeds detectable by real-time phase-contrast imaging.
119 wide range of liquids, using ultrafast X-ray phase-contrast imaging.
120 ved in the epidermis of Smed-TTBK-d(RNAi) by phase contrast, immunofluorescence, and transmission ele
121             We study the physical origins of phase contrast in dynamic atomic force microscopy (dAFM)
122                        We also show that the phase contrast in multiple sclerosis lesions could be al
123        Moreover, we predict that the sign of phase contrast in multiple sclerosis lesions indicates t
124          Contrary to an expectation that the phase contrast in multiple sclerosis lesions should alwa
125 we demonstrate the implementation of Zernike phase contrast in scanning X-ray microscopy, revealing s
126 ng, we have evaluated the x-ray differential phase contrast in view of the projected electron density
127 hy underwent CMR to measure planimetric AVA, phase-contrast indexed stroke volume, LV mass, and focal
128 accumulation of dark material observed using phase contrast light microscopy (indicative of a change
129                  Simultaneous acquisition of phase-contrast light microscopy and fluorescently labele
130 ional hemodynamic effects were quantified by phase contrast magnetic resonance angiography at baselin
131  embolization on blood flow as quantified by phase contrast magnetic resonance imaging and hypothesiz
132 atients underwent SPC flow quantification by phase contrast magnetic resonance imaging, including qua
133 imaged vascular structure, leveraging modern phase contrast magnetic resonance imaging, the virtual w
134 idate the capability of navigator-echo-gated phase-contrast magnetic resonance (MR) imaging for measu
135            Aortic arch PWV was measured with phase-contrast magnetic resonance (MR) imaging in a popu
136  thoracoabdominal, and neck vessels by using phase-contrast magnetic resonance (MR) imaging in childr
137 idate caval subtraction two-dimensional (2D) phase-contrast magnetic resonance (MR) imaging measureme
138 ients and control subjects who had undergone phase-contrast magnetic resonance (MR) imaging were incl
139            Quantitative flow was measured by phase-contrast magnetic resonance angiography of the cer
140 has expended due to numerous applications of phase-contrast magnetic resonance imaging (PC-MRI) in CS
141                                         Cine phase-contrast magnetic resonance imaging can be used to
142                                         Cine phase-contrast magnetic resonance imaging examinations w
143 easured cerebral blood flow by 2-dimensional phase-contrast magnetic resonance imaging in participant
144                                         Cine phase-contrast magnetic resonance imaging may be a valua
145                                         Cine phase-contrast magnetic resonance imaging measurement of
146 atio to assess kidney function and performed phase-contrast magnetic resonance imaging of basilar and
147 patients with acute kidney injury using cine phase-contrast magnetic resonance imaging.
148 ham-operated rats, were examined by cine and phase-contrast magnetic resonance imaging.
149 d calibrated versus aortic BF measured using phase-contrast magnetic resonance in 10 subjects (n=10)
150                            Baseline arterial phase contrast material-enhanced (CE) MR imaging was use
151          Purpose To determine whether single-phase contrast material-enhanced dual-energy material at
152 oracic junction is achieved with a quadruple-phase contrast media injection protocol.
153                                              Phase-contrast micro-CT achieved cellular resolution of
154 nerated by either CLT or DMM, we showed that phase-contrast micro-CT distinguished control and OA car
155 sion This work demonstrated the use of x-ray phase-contrast micro-CT for detailed volumetric anatomic
156 ord and column by comparing quality of x-ray phase-contrast micro-CT images of nondissected Thiel-emb
157 nd then employ monochromatic and propagation phase-contrast micro-CT imaging to enable the imaging of
158                                    The x-ray phase-contrast micro-CT of formalin-fixed boneless cords
159                            Results The x-ray phase-contrast micro-CT of Thiel-embalmed samples result
160 o evaluate the viability of postmortem x-ray phase-contrast micro-CT to provide tissue-conserving, hi
161                      Propagation-based x-ray phase-contrast micro-CT was used with monochromatic 60-k
162 ould also be observed in images generated by phase-contrast micro-CT.
163                                              Phase contrast microCT of chemically fixed yet unstained
164 phology of isolated MLECs were observed with phase contrast microscope.
165 sent a new approach for retrieving halo-free phase contrast microscopy (hfPC) images by upgrading the
166 ic acid and Ca(2+) (CaDPA) were monitored by phase contrast microscopy and Raman spectroscopy, respec
167                                              Phase contrast microscopy assesses changes in refractili
168                             Fluorescence and phase contrast microscopy revealed characteristic apopto
169 ology that combines fluorescence microscopy, phase contrast microscopy, and laser tweezers Raman spec
170 opy with simultaneous patch-clamp recording, phase contrast microscopy, and traction force microscopy
171 wth factor-beta1 (TGF-beta1) was analyzed by phase contrast microscopy, immunofluorescence, quantitat
172 d of the rapid drop in spore refractility by phase contrast microscopy, precisely corresponds to the
173 present a methodology that combines external phase contrast microscopy, Raman spectroscopy, and optic
174 ation and vegetative outgrowth by time lapse phase contrast microscopy, transmission electron microsc
175 ifferential interference contrast (DIC), and phase contrast microscopy, we tracked the movement of MT
176  imaging techniques such as fluorescence and phase contrast microscopy.
177 terns were linked in real-time to high power phase contrast microscopy.
178 erior vitreous detachment were examined with phase-contrast microscopy and confocal microscopy after
179 e periods on the order of weeks by utilizing phase-contrast microscopy and show that these cells acqu
180 ellar motion, visualizing the cell bodies by phase-contrast microscopy and the flagellar filaments by
181                                              Phase-contrast microscopy and Wright staining showed mor
182 rulent NAP1 strain using optical density and phase-contrast microscopy assays.
183                                              Phase-contrast microscopy consistently identified a crea
184  specimens were processed as flat mounts for phase-contrast microscopy followed by immunolabeling for
185 at combines the automated image analysis for phase-contrast microscopy movies with an easy-to-use int
186 pted to use multi-trap Raman spectroscopy or phase-contrast microscopy of spores adhered on a cover s
187 nveloping membranous structure identified on phase-contrast microscopy to show positive stain results
188          The experiments were videorecorded (phase-contrast microscopy), and PMN adhesion/migration w
189 pseudoholes (14 eyes) using interference and phase-contrast microscopy, immunocytochemistry, and tran
190 py and the motion of the underlying cells by phase-contrast microscopy.
191  NK cells and FLS were studied by time-lapse phase-contrast microscopy.
192 ten requires the use of transmitted light or phase-contrast microscopy.
193 ect diatoms on two-channel (fluorescence and phase-contrast) microscopy images by predicting bounding
194                            Here we present a phase-contrast microtomogram of a biological sample usin
195 ii by means of propagation X-Ray Synchrotron phase contrast microtomography using both holotomography
196                                        X-ray phase-contrast microtomography (XPCmuT) is a label-free,
197  measured in infants with CHD (n = 49) using phase contrast MR imaging and the relationship between C
198                                          The phase-contrast MR images obtained in five of the eight p
199 red with caval subtraction and direct inflow phase-contrast MR imaging (mean difference, -1.3 mL/min/
200 ty-encoded MR imaging and that measured with phase-contrast MR imaging (mean ICC, 0.96 +/- 0.03 vs 0.
201 ty-encoded MR imaging and that measured with phase-contrast MR imaging (mean ICC, 0.97 +/- 0.02 vs 0.
202 ificantly larger than that with conventional phase-contrast MR imaging (mean, 0.75 +/- 0.23 vs 0.65 +
203 hose obtained from two separate conventional phase-contrast MR imaging acquisitions, one optimized fo
204 pulmonary artery that is determined by using phase-contrast MR imaging allows accurate estimation of
205 good agreement between PV flow measured with phase-contrast MR imaging and that measured with transit
206 hom went on to undergo ETV, were imaged with phase-contrast MR imaging at 1.5 T to determine rates of
207                                              Phase-contrast MR imaging can be combined with navigator
208 spective study, healthy volunteers underwent phase-contrast MR imaging in a fasting state and again a
209 al, and neck vessels were estimated by using phase-contrast MR imaging in healthy volunteers to allow
210                Aortic arch PWV measured with phase-contrast MR imaging is a highly significant indepe
211                 Conclusion Caval subtraction phase-contrast MR imaging is a simple and clinically via
212 nge, as required for conventional sequential phase-contrast MR imaging measurements.
213  catheterization (RHC) and three-directional phase-contrast MR imaging of the main pulmonary artery.
214     Fifteen Sprague-Dawley rats underwent 2D phase-contrast MR imaging of the portal vein (PV) and in
215 8.3 years +/- 1.4) against directly measured phase-contrast MR imaging PV and proper hepatic arterial
216 Thereafter, consistency of caval subtraction phase-contrast MR imaging-derived TLBF and hepatic arter
217 es in a phantom and to prospectively use the phase-contrast MR sequence to measure three-directional
218 40 late-gestation normal human fetuses using phase-contrast MRI (mean gestational age, 37 [SD=1.1] we
219 ary hypertension by high temporal resolution phase-contrast MRI (PC-MRI) and to correlate the results
220 at the age of 9 years using velocity-encoded phase-contrast MRI and related to maternal oily fish con
221    Strain was measured using high-resolution phase-contrast MRI in 9 adult male rats with myocardial
222                                              Phase-contrast MRI with metric-optimized gating is a pro
223                                              Phase-contrast MRI, in combination with measurement of p
224 ploiting technical advances toward real-time phase-contrast MRI, the current work analyzed directions
225  combining X-ray fluorescence tomography and phase contrast nanotomography on the same cell with sub-
226                                              Phase-contrast OCT enables three-dimensional visualizati
227 of information about a 3D structure from the phase contrast of a single hologram acquired using a con
228 ion micro-computed tomography (micro-CT) and phase-contrast optics followed by quantitative analyses.
229 An electron microscope equipped with Zernike phase-contrast optics produces images with markedly incr
230 etting of optimal illumination necessary for phase contrast or the use of high magnification upright
231 t-tissue visibility with grating-based X-ray phase contrast (PC), we have developed a first preclinic
232 echnique yields attenuation, scattering, and phase-contrast (PC) images from a single exposure.
233                                              Phase-contrast (PC) MR imaging was performed as the refe
234                  In addition to differential phase contrast projection images, the method allows the
235  resulting shear waves are imaged by using a phase-contrast pulse sequence with motion-encoding gradi
236                          Utilising multi-MHz phase contrast radiography, extended sequences of the co
237 -phase atomic force microscopy with enhanced phase contrast revealed that the misfolding and folding
238 RI sequence and the conventional single-echo phase-contrast (SEPC) MRI sequence, E, E (m), and E/E (m
239 , the compressed-sensing parallel-imaging 4D phase-contrast sequence can augment conventional cardiac
240 hom a compressed-sensing parallel-imaging 4D phase-contrast sequence was performed as part of routine
241                                              Phase contrast sequences in the aorta and pulmonary arte
242 ed simulator that can accurately capture the phase-contrast signal from a human-scaled numerical phan
243 ll as a dark-field signal in addition to the phase-contrast signal.
244 ssessment of their distinct attenuation- and phase-contrast signal.
245 he data presented here, each cross-sectional phase-contrast slice resulted from five images of 100 or
246   Two radiologists independently reviewed 4D phase-contrast studies for each of 34 patients (mean age
247               Among 123 valves seen in 34 4D phase-contrast studies, 29 regurgitant valves were ident
248 cope for simultaneous amplitude-contrast and phase-contrast surface plasmon resonance imaging (SPRi).
249 utively imaged at 1.5-minute intervals using phase-contrast synchrotron imaging, at positive end-expi
250                            Using propagation phase-contrast synchrotron microtomography (PPC-SRmuCT)
251                                      We used phase-contrast synchrotron X-ray imaging and transmissio
252  greatly facilitate the translation of X-ray phase contrast techniques into mainstream applications.
253 ed tissue can be enhanced using staining and phase contrast techniques.
254                                              Phase-contrast techniques, such as differential interfer
255 iews, with over an order-of-magnitude higher phase contrast than current near-field grating interfero
256 independently assessed vessel conspicuity on phase-contrast three-dimensional angiograms.
257 n) enable quantitative automated analysis of phase-contrast time-lapse images of cultured neural stem
258                We have used high-resolution, phase-contrast time-lapse microscopy and developed sophi
259 or; (iii) monitoring the division process by phase-contrast time-lapse microscopy; and (iv) processin
260                                 The power of phase contrast to resolve subtle changes, such as those
261                                   We combine phase contrast tomographic microscopy (down to 3.3 mum v
262 gated tissue, we exploited synchrotron X-ray phase contrast tomography (XPCT), providing virtual slic
263 idated against independent measurements from phase contrast tomography and electron backscatter diffr
264                      Edge illumination x-ray phase contrast tomography is a recently developed imagin
265                            High energy X-ray phase contrast tomography is tremendously beneficial to
266 low electron doses comparable to traditional phase-contrast transmission electron microscopy.
267              As a proof-of-concept, an X-ray phase contrast under bending conditions was constructed
268 R imaging was performed by using a 4D radial phase-contrast vastly undersampled isotropic projection
269                            Respiratory-gated phase-contrast vastly undersampled isotropic projection
270 viation]) were imaged with respiratory-gated phase-contrast vastly undersampled isotropic projection
271               CMR RVol(AR) was calculated by phase-contrast velocity mapping at the aortic sinuses an
272  using regurgitant fraction (RF) measured by phase-contrast velocity mapping CMR at a median of 40 da
273  and performs well on live-cell, time-lapse, phase contrast video microscopy of hundreds of cells in
274                                              Phase-contrast video microscopy demonstrated that in the
275                                              Phase-contrast video microscopy was used to record the m
276 ays using mouse lung slices and confocal and phase-contrast video microscopy.
277 he unenhanced MR angiographic technique with phase-contrast VIPR allows for accurate noninvasive asse
278 es, and overall image quality scores between phase-contrast VIPR and contrast-enhanced MR angiographi
279 tative assessment included evaluation of the phase-contrast VIPR and contrast-enhanced MR angiographi
280 etween the noninvasive TSPG measurement with phase-contrast VIPR and invasive TSPG measurement for me
281                                              Phase-contrast VIPR images were successfully acquired in
282 the segmental renal arteries were higher for phase-contrast VIPR than for contrast-enhanced MR angiog
283   Although the noise scores were higher with phase-contrast VIPR than with contrast-enhanced MR angio
284                     The imaging duration for phase-contrast VIPR was 10 minutes and provided magnitud
285           The vessel diameters measured with phase-contrast VIPR were slightly greater than those mea
286                     Velocities measured with phase-contrast VIPR were used to calculate TSPGs by usin
287                                          The phase-contrast VIPR-derived TSPG measures were slightly
288 tenosis was too small to determine TSPG with phase-contrast VIPR.
289 ing reports, which were generated without 4D phase-contrast visualization.
290 emonstrates the feasibility of grating-based phase contrast with a rotating gantry for the first time
291 nsit (MCT) measurement that uses synchrotron phase contrast X-ray imaging (PCXI) to non-invasively me
292                                 By combining phase contrast X-ray imaging with an image reconstructio
293 een demonstrated as a valuable capability of phase contrast x-ray imaging.
294   Here we report a high-resolution, low-dose phase contrast X-ray tomographic method for 3D diagnosis
295 oof-of-concept study, we propose multi-scale phase contrast x-ray tomography as a tool to unravel the
296 logy and histopathology based on multi-scale phase contrast x-ray tomography, and use this to investi
297 sition time by ~74% relative to conventional phase contrast X-ray tomography, while maintaining high
298 we have developed theory for absorption- and phase-contrast X-ray imaging.
299 stem tetrapod Ichthyostega using propagation phase-contrast X-ray synchrotron microtomography.
300  when hRSV viruses were imaged using Zernike phase contrast (ZPC) cryo-electron tomography.

 
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