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1 ation of structures close in architecture to biological tissue.
2 s significantly reducing photo damage to the biological tissue.
3  a 3D rendered image of stained and embedded biological tissue.
4  processes and the spatial organization of a biological tissue.
5 ption, autofluorescence, and scattering from biological tissue.
6 lied when the laser light propagates through biological tissue.
7 in a sample that is placed behind a slice of biological tissue.
8  imaging 14C-labelled tracers in sections of biological tissue.
9 of two-photon excited fluorescence (TPEF) in biological tissue.
10 s, amides, triazine, imidazole, protein, and biological tissue.
11 ue three-dimensional image reconstruction of biological tissue.
12 ies observed from amino groups but none from biological tissue.
13 ey role in characterizing soft media such as biological tissue.
14 th diffusion, convection and reaction in the biological tissue.
15 ivery device and the subsequent transport in biological tissue.
16 ly improves quantitative imaging accuracy in biological tissue.
17 load for self-healing hydrogels or repair of biological tissue.
18 formal wrapping around 3D objects, including biological tissue.
19 h while retaining high spatial resolution in biological tissue.
20  be used to quantify important properties of biological tissue.
21 use the NIR light penetrated effectively the biological tissue.
22 ds (GNRs) that are weakly constrained by the biological tissue.
23 dy of the distribution of small molecules on biological tissues.
24 ailed assessment of structural morphology in biological tissues.
25 terials, from complex formulated products to biological tissues.
26 ed cell phone radiation in aqueous media and biological tissues.
27 ly applied to oligosaccharide pools in other biological tissues.
28  fluorescent probes in the context of living biological tissues.
29 ce and second-harmonic generation imaging of biological tissues.
30 ng electron microscopy (FIB/SEM)' applied to biological tissues.
31 ous in porous media, composite materials and biological tissues.
32 nanoparticles in the extracellular matrix of biological tissues.
33  suited for biofluid analysis and imaging of biological tissues.
34 ations concerning their effects and fates in biological tissues.
35  drug and metabolite detection directly from biological tissues.
36 k-fabricated for applying shearing forces to biological tissues.
37  optical absorption contrast in subcutaneous biological tissues.
38  blue wavelengths are strongly attenuated in biological tissues.
39  arises in complex or turbid samples such as biological tissues.
40 lar signals secreted from a large variety of biological tissues.
41  the absorption and scattering properties of biological tissues.
42 and sensitive tool for the mapping of PLs in biological tissues.
43 sting membrane potential and excitability of biological tissues.
44 ents the random bending of light that clouds biological tissues.
45 uman oesophagus resemble those of other soft biological tissues.
46 nation of acrolein metabolically produced in biological tissues.
47 iled resolution imaging of highly scattering biological tissues.
48 n used extensively to study and characterize biological tissues.
49  in unraveling the bioinorganic chemistry of biological tissues.
50 nal (3D) spatial mapping of free radicals in biological tissues.
51 plied successfully to microscale analysis of biological tissues.
52 of endothelial function and vascular tone in biological tissues.
53 with high spatial and temporal resolution in biological tissues.
54 predicting the scattering properties of many biological tissues.
55 of multiply charged lipids and proteins from biological tissues.
56 monstrated for the analysis of collagen-rich biological tissues.
57 ms, and absorb light that penetrates through biological tissues.
58 tial for characterization of a wide range of biological tissues.
59 trometry (DESI-MS) with a stable dication on biological tissues.
60 embedded in opaque scattering layers such as biological tissues.
61 hibits excellent light-guiding efficiency in biological tissues.
62 ced scattering of photons traversing through biological tissues.
63 tion is fundamentally incompatible with soft biological tissues.
64  sophisticated thermal modeling with complex biological tissues.
65 aterials and probing their interactions with biological tissues.
66 eds of microns beneath the surfaces of large biological tissues.
67 -signal and low-background labeling of thick biological tissues.
68 nd point objects, which often occurs in many biological tissues.
69 for in-situ extracellular ATP measurement in biological tissues.
70  of porous media [8, 9], and the invasion of biological tissues [10-12].
71 trate the ability of the approach to analyze biological tissue, a monolayer of onion epidermis was im
72 tials (APs) pass largely unperturbed through biological tissue, allowing magnetic measurements of AP
73 n by forward-peaked scattering media such as biological tissue and cells.
74 hree-dimensional tomographic imaging of soft biological tissue and other specimens whose details exhi
75 rals yields localized inorganic adhesion for biological tissue and reversible focal encapsulation for
76 ging because of the high scatter of light in biological tissue and the ill-posed nature of the recons
77                  The molecular complexity of biological tissue and the spatial and temporal variation
78 e sensitive and accurate analysis of complex biological tissue and tumor samples by comparison of lig
79 ry supplements, pharmaceutical formulations, biological tissues and body fluid.
80 nge of length scales: from nanometers, as in biological tissues and bundles of carbon nanotubes, to m
81 ge of the high native optical contrast among biological tissues and can treat microvessels without ca
82  enabled the in situ and in vivo analysis of biological tissues and cells.
83  the inherent light-scattering properties of biological tissues and cells.
84  second harmonic generation (SHG) imaging of biological tissues and demonstrate its utility for monit
85 mple, and rapid analyses from highly complex biological tissues and fluids.
86 networked materials that are similar to soft biological tissues and have highly variable mechanical p
87 maging and depth profiling of metabolites in biological tissues and live organisms.
88 -sensor pairs laminated on a variety of soft biological tissues and organ systems in animal models pr
89                Mechanical assessment of soft biological tissues and organs has broad relevance in cli
90 al domain, of probing bulk media, to imaging biological tissues and single cells at the micro scale,
91 s for structure-function characterization of biological tissues and their cellular inhabitants, seaml
92 dict the local mechanical environment within biological tissues and to investigate the relationship b
93  that is compatible with the transparency of biological tissues and with the emission of low-cost sem
94 demonstrate in-vivo feasibility using simple biological tissue) and human heads (to demonstrate feasi
95            Cellular structures also occur in biological tissue, and in magnetic, ferroelectric and co
96   A reflecting metal plate was placed within biological tissue, and the point spread function (PSF) w
97 se combinations are, however, commonplace in biological tissues, and are therefore needed for applica
98   Synthetic materials lack the complexity of biological tissues, and man-made materials that respond
99 composition, and classification accuracy for biological tissues are considered.
100 ions of high-frequency radio waves (RF) with biological tissues are currently being investigated as a
101                       The characteristics of biological tissues are determined by the interactions of
102            The mechanical properties of soft biological tissues are essential to their physiological
103                                              Biological tissues are rarely transparent, presenting ma
104 nmental matrices (water, soil, sediment, and biological tissues) are needed to address concerns about
105  derivative viscoelasticity observed in some biological tissue arises as a mechanical consequence of
106 to low concentrations in the environment and biological tissues as well as the complexity of the samp
107 ssues at an unprecedented depth of 2.5 mm in biological tissues at a lateral resolution of 36 mumx52
108 acquiring high-quality HR-MAS NMR spectra of biological tissues at low spinning rates (down to a few
109 ld be the most dominant HBCD diastereomer in biological tissues because it was metabolized to the low
110 electrophysiological studies of a variety of biological tissues both in vitro and ex vivo.
111 h degree of scattering of optical photons in biological tissue by making use of the photoacoustic eff
112 thods can facilitate deep optical imaging in biological tissue by reducing light scattering and this
113 -resolution fluorescence imaging deep inside biological tissues by digitally time-reversing ultrasoun
114 accurate determination of energy transfer in biological tissues by lifetime measurements of sensitize
115                         Volumetric images of biological tissues can be formed by two-dimensional rast
116 ficial imaging depth as random scattering in biological tissues causes exponential attenuation of the
117                                              Biological tissues contain variable amounts of unlabeled
118 trated as is the ability to obtain ions from biological tissue, currency, and other objects placed in
119     These include synthetic replacements for biological tissues, designing materials for specific med
120               Conventional analyses of these biological tissues employ liquid chromatography (LC) wit
121  firmly yet gently attach to an inorganic or biological tissue enabling enclosure of, for example, ne
122 e constituting the cytoskeleton of a cell or biological tissue, exhibit a nonlinear strain-stiffening
123  associated with the physiological status of biological tissue, existing high-resolution optical imag
124 cal models used for studying the response of biological tissues exposed to electric fields.
125 ation (LAESI), the native water molecules in biological tissues facilitate sampling by a focused mid-
126 which the dictation forms a stable bond with biological tissue fatty acids and lipids.
127 sity) may be most specifically adapted among biological tissues for high rate and complexity of infor
128 ze metallic ENPs in environmentally relevant biological tissues for the first time.
129  mapping of metabolites directly onto intact biological tissues, giving a spatial context to metaboli
130                  Metabolic fingerprinting of biological tissues has become an important area of resea
131              Consequently, their analysis in biological tissues has received increased attention.
132                                              Biological tissues have the remarkable ability to remode
133 nsor to measure extracellular ATP content in biological tissues (i.e., porcine intervertebral disc).
134 r electromagnetic radiation in reacting with biological tissues, (ii) nanostructured metamaterial (Au
135 s detection, natural products discovery, and biological tissue imaging, among other applications.
136  food water activity by the immersion of the biological tissue in hypertonic solutions.
137 d laser (PIRL) is capable of cutting through biological tissues in the absence of significant thermal
138 ly targeting, imaging, and treating specific biological tissues in vivo.
139        Articular cartilage is one of several biological tissues in which swelling effects are importa
140 tection of trace amounts of nanoparticles in biological tissues, in which MRI provides volume detecti
141 lices, is the primary building block of many biological tissues including bone, tendon, cartilage, an
142 method for chemical transformation of intact biological tissues into a hydrogel-tissue hybrid, which
143  isodesmosine as biomarkers in many types of biological tissues involving elastin degradation.
144 l transmission through complex media such as biological tissue is fundamentally limited by multiple l
145                        The growth of several biological tissues is known to be controlled in part by
146    Visualizing structures deep inside opaque biological tissues is one of the central challenges in b
147                       Delta(199)Hg in marine biological tissues is thought to reflect marine Hg photo
148 esion to wet and dynamic surfaces, including biological tissues, is important in many fields but has
149 surements of NO and CO generated from living biological tissue (mouse, c57, kidney) surfaces, for the
150 corresponded to a limit of quantification in biological tissue of 10 pmol/g for all analytes except 2
151 ation with the soft, curvilinear surfaces of biological tissues offer important opportunities for dia
152 se of ICP-MS to measure metal ion content in biological tissues offers a highly sensitive means to st
153                     Compound extraction from biological tissue often presents a challenge for the bio
154 ategory of soft glassy substances, including biological tissue, often exhibit a mechanical complex mo
155 lambdaem = 804 nm), which are much above the biological tissue opaque window (400-700 nm) ensuring be
156 trastructure in the mechanical response of a biological tissue or manufactured material to be studied
157 ronments, such as porous media, wet soil, or biological tissue, or act as a selection pressure in evo
158      How the collective motion of cells in a biological tissue originates in the behavior of a collec
159 f materials with high water content, such as biological tissues, over large volumes whereas designs w
160 cal analysis of SmicroXRD measurements using biological tissue paves the way for further structural i
161 offers superior optical sectioning deep into biological tissues, permitting analysis of large, hetero
162 ractions of acoustic cavitation bubbles with biological tissues play an important role in biomedical
163 g, the dominant light interaction process in biological tissues, prevents tissues from being transpar
164  Current advances in staining and imaging of biological tissues provide a wealth of data, but there a
165 n can help circumvent complex extractions of biological tissues, provide more accurate information on
166                  Imaging of nanomaterials in biological tissues provides vital information for the de
167 ogical abnormalities in epithelial and other biological tissues, raising novel predictions for future
168 s and quantitation of their concentration in biological tissue remain challenging tasks in microscopy
169     In this work, DESI DM-MSI experiments on biological tissue samples such as sea algae and mouse br
170 at allows for the study of the complexity of biological tissue samples to overcome the limitations of
171  (e.g., polycyclic aromatic hydrocarbons) in biological tissue samples.
172 to investigate the molecular distribution of biological tissue samples.
173 o image metabolites, lipids, and proteins in biological tissue samples.
174 kDa) from various materials including urine, biological tissue sections, paper, and plant material on
175  have been unmasked and imaged directly from biological tissue sections.
176 ues allow mapping of various analytes within biological tissue sections.
177 istributions of lipids and drug molecules in biological tissue sections.
178 mpare the effectiveness of a laser-activated biological tissue solder with that of standard sutures f
179 er to achieve a comprehensive description of biological tissue, spectral information about proteins,
180 , we use hydrogel-based substrata matched to biological tissue stiffness to investigate the effects o
181 holds great promise for the in vivo study of biological tissue structure with substantially improved
182 ber directions in structurally heterogeneous biological tissue substantially contributes to an unders
183  absorption coefficients of many homogeneous biological tissues such as muscle, skin, white matter in
184 llows clear imaging through extremely turbid biological tissue, such as the skull, over an extended c
185 ly modulate friction with soft materials and biological tissues, such as human fingertips.
186 o control the behavior of in vitro excitable biological tissue, suggesting their potential for clinic
187 hnique enables the study of microrheology of biological tissues that produce or detect sound.
188                                   Within the biological tissue, the model can account for nonlinear s
189 rtioned among four human groups in a natural biological tissue, the placenta.
190                        In the case of living biological tissue, the spatiotemporal patterns formed by
191 port-proteins and cell-cell heterogeneity in biological tissues, these findings generalize across mos
192          In development, cells organize into biological tissues through cell growth, migration, and d
193 ased structures can now be built from within biological tissue to allow subsequent removal of lipids
194                The thermodynamic response of biological tissue to pulsed infrared laser irradiation w
195 irectly monitor the distribution of drugs in biological tissues, to evaluate the distribution of TAA
196 l processing of porous samples such as fixed biological tissues typically relies on molecular diffusi
197      This investigation into the behavior of biological tissue under high C60(+) fluxes not only allo
198 y techniques for deep subsurface analysis of biological tissues unlocks new prospects for medical dia
199 he quantitative analysis of lipid species in biological tissues using internal standards for each lip
200             Intra- and interday precision in biological tissue was routinely approximately 20% or low
201 the complex refractive index distribution of biological tissue, which scrambles the incident light an
202  which enabled imaging both fixed and living biological tissue with 3D precision, high-resolution flu
203                        We present imaging of biological tissue with a proton microscope.
204 eover, we present a first tomography scan of biological tissue with complementary information in atte
205  structural and functional imaging of living biological tissue with label-free, optical absorption co
206 thermal damage generated during treatment of biological tissue with lasers and other sources of heat.
207 nsive mapping of chemical species throughout biological tissues with typical spatial resolution in th
208 cisely to match the non-linear properties of biological tissues, with application opportunities that
209 ze a variety of semisolid systems, including biological tissues, with virtually no sample preparation
210  tool for purifying metabolites from complex biological tissues would be of obvious utility to the fi
211 ivity, an elastic compliance similar to soft biological tissue (Young's modulus < 100 kPa), and the c

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