戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (left1)

通し番号をクリックするとPubMedの該当ページを表示します
1                                              AFM and dSTORM particle size distributions showed cohere
2                                              AFM imaging and force spectroscopy at 20% relative humid
3                                              AFM imaging in air with controlled humidity preserves th
4                                              AFM measurements indicated that cellular adhesion force
5                                              AFM reveals that the large length (L) to width (W) ratio
6                                              AFM topography maps revealed amiodarone-treated cells wi
7                                              AFM-IR and TERS fundamentals will be reviewed in detail
8                                              AFM-IR combines the chemical sensitivity of infrared spe
9                                              AFM-IR distribution of eu- and heterochromatin was compa
10                                              AFM-IR revealed striking heterogeneity in chemical compo
11                              Aflatoxin M(1) (AFM(1)) in milk and milk products has been recognised as
12 s of aflatoxin B(1), aflatoxin M(1) (AFB(1), AFM(1)) in pure water was studied.
13                                 To date, all AFM studies of the PS film have relied on the model of L
14 ckout and wild-type mice, we have devised an AFM protocol that does not rely on the use of glue or ch
15 e excitation of the resonance spectrum of an AFM cantilever in contact with the sample.
16                                     Using an AFM cantilever tip, mechanically compliant acicular micr
17 mJ/cm(2) UV-A irradiation reduced AFB(1) and AFM(1) concentrations by 70 +/- 0.27 and 84 +/- 1.95%, r
18 ght may have caused photolysis of AFB(1) and AFM(1) molecules in water.
19              The concentration of AFB(1) and AFM(1) was determined by HPLC with fluorescence detectio
20 emi-quantify degraded products of AFB(1) and AFM(1).
21                Comparison of QPI-derived and AFM moduli shows good agreement between the two measures
22  of temperature-induced transition of FM and AFM IEC in the same sample suggests the possibility of d
23 ccessibility assay, DNase I footprinting and AFM experiments reveal perturbed histone-DNA interaction
24    The off-line hyphenation of nES GEMMA and AFM-IR is introduced to enable chemical imaging of singl
25 ng atomic force microscopy (AFM) imaging and AFM-based nanoindentation in a liquid environment.
26 zed by electrochemical techniques, FT-IR and AFM.
27  design of the sample preparation method and AFM parameters for faster scan with micrometer resolutio
28 fluorescence, time-lapse TIRF microscopy and AFM imaging we characterize this phenomenon and identify
29    We obtained spatially resolved O-PTIR and AFM-IR spectra confirming the presence of peaks related
30 mational changes of ectoIRR in both SAXS and AFM experiments, an observation that agreed well with pr
31                         In addition, SEM and AFM images illustrated a completely non-uniform surface
32 rication steps were carried out with SEM and AFM monitoring.
33              Based on C-K NEXAFS spectra and AFM images of the ~1.5 nm thick films, the diradical mol
34 evaluated using PSI, Raman spectroscopy, and AFM.
35 aracterized using electrochemistry, XPS, and AFM, and switching between open and closed forms using l
36 ng ferromagnetic (FM) and antiferromagnetic (AFM) exchange interactions for Eu- and S- terminated EuS
37 cal optical effects(8) in antiferromagnetic (AFM) bilayers.
38 e suppresses local-moment antiferromagnetic (AFM) order and induces superconductivity in a dome aroun
39      While the control of antiferromagnetic (AFM) orders has been realized by various means, applicab
40 intronic devices based on antiferromagnetic (AFM) materials hold the promise of fast switching speeds
41 ttering suggests that the antiferromagnetic (AFM) long-range order, which is believed to reconstruct
42 Fermi level emerge in the antiferromagnetic (AFM) phase.
43  5.08 eV, harboring both antiferromagnetism (AFM) and strong red photoluminescence (PL).
44                            Antiferromagnets (AFMs) possess great potential in spintronics because of
45 be a prototype dispersive optics-based array AFM capable of simultaneously monitoring multiple probe-
46 point analysis; widespread adoption of array AFMs for simultaneous multipoint study is challenging ow
47 rmal induced resonance (PTIR), also known as AFM-IR and tip-enhanced Raman spectroscopy (TERS).
48  discovered that the functionalized and bare AFM tips showed mitigated adhesion forces in calcium ion
49                   Force-distance curve-based AFM (FD-AFM) was utilized to directly probe and localize
50  EVs within the hour time scale, using basic AFM equipment and skills and only needing freely availab
51     The Pd/Au electrode was characterized by AFM and XPS as well as multiple electrochemical techniqu
52 f Lsbgal onto nanocomposite was confirmed by AFM, FE-SEM, FTIR, and CLSM.
53 ecific biomolecular interactions detected by AFM for single bonds and extend the discussion to multip
54 namic persistence length of DNA (measured by AFM and MT, respectively).
55 s, with the mean Young's modulus measured by AFM passing from 17 +/- 6 kPa to 56 +/- 18 kPa.
56 ded or extended conformations as observed by AFM.
57 fferent elastic moduli in tissue sections by AFM has remained elusive so far, due to the lack of corr
58 tate molecular junctions (MJs), in which a C-AFM tip is used as the top contact, were fabricated with
59                          In the static case (AFM), in which tension is not applied to the molecule, t
60 ilicon validates the robust capability of CL AFM-IR in routine mapping of nanoscale molecular informa
61 h various bias voltages applied to Pt-coated AFM tips, and the saturated density is almost 30 times h
62 lly, we highlight the potential of combining AFM with optical microscopy and spectroscopy to address
63                                   Conductive AFM experiments further support the feasibility of the p
64                     Treating milk containing AFM(1) is an alternative control measure, however, there
65 monstrate a piezoelectric, strain-controlled AFM memory that is fully operational in strong magnetic
66                                  Controlling AFM(1) in milk is important to protect human health and
67                                 Conventional AFMs only permit sequential single-point analysis; wides
68 controller design for responsivity-corrected AFM-IR imaging.
69                            Using time course AFM, we observe that chromatin condensation by H1.5 is d
70 s study reviews the strategies for degrading AFM(1) in milk including yeast, lactic acid bacteria, en
71 ntages and limitations in applying different AFM modes to chemically image, sense, and manipulate bio
72 trae and sieve plates using four-dimensional AFM (X, Y, Z, and t) on intact LSECs in vitro.
73 ure and quantify cellular deformation during AFM indentation using live cell stains and SDC, and sugg
74  characterized using UV-Vis, TEM, SAED, EDX, AFM, and electrochemical techniques including LSV and EI
75 nological improvements that have established AFM as an analytical tool to observe and quantify native
76                                           FD-AFM data are inconsistent with a two-state model but ins
77                                           FD-AFM was applied to rhodopsin, the light receptor and a p
78           Force-distance curve-based AFM (FD-AFM) was utilized to directly probe and localize the con
79                                      Both FD-AFM and computational studies on coarse-grained models o
80 is no single sensitive and specific test for AFM, and the diagnosis relies on identification of sever
81 immobilised on trisNTA-Ni(2+) functionalized AFM cantilevers and the OH and COOH SAM surfaces were pr
82  was given to the carboxylate-functionalized AFM tips because of their prominent ion-specific effects
83  the interactions between the functionalized AFM tips and the calcite surfaces were mainly through ca
84 pic chemical laboratories by functionalizing AFM tips and outline the advantages and limitations in a
85 ration, and recombination using SCLC, GIXRD, AFM, XPS, NEXAFS, R-SoXS, TEM, STEM, fs/ns TA spectrosco
86                           On the other hand, AFM-IR users should carefully consider the composition a
87                                           HS-AFM data reveal that the CNTPs undergo diffusive motion
88                                           HS-AFM experiments, supported by molecular dynamics simulat
89                                           HS-AFM was used to directly visualize the tropomyosin-tropo
90 ating transition of single CorA channels: HS-AFM movies during Mg(2+)-depletion experiments revealed
91  used high-speed atomic force microscopy (HS-AFM) and all-atom molecular dynamics (MD) simulations to
92  used high-speed atomic force microscopy (HS-AFM) and kinetic modeling which allowed us to determine
93       High-speed atomic force microscopy (HS-AFM) can be used to study dynamic processes with real-ti
94 using high-speed atomic force microscopy (HS-AFM) is reported.
95 e use high-speed atomic force microscopy (HS-AFM), fluorescence recovery after photobleaching (FRAP),
96 Using high-speed atomic force microscopy (HS-AFM), we explored the Mg(2+)-dependent gating transition
97 me by high-speed atomic force microscopy (HS-AFM).
98 ed atomic force microscopy line-scanning (HS-AFM-LS) combined with automated state assignment and tra
99    Motion trajectories extracted from the HS-AFM movies indicate that CNTPs exhibit diffusion coeffic
100                            More importantly, AFM imaging revealed striking differences in sEV nanosca
101    Hence, we employed the latest advances in AFM imaging on living LSECs.
102 high levels of CSF EV-specific antibodies in AFM compared with controls, providing further evidence f
103 y overlooked source of data and artifacts in AFM-IR analysis; reflection from the buried interface.
104 idence for a causal role of non-polio EVs in AFM.
105  are used to show that the overall signal in AFM-IR is affected by the wavelength-dependent reflectiv
106 tile, low-field control of spin transport in AFM systems.
107   Tissue stiffness increased with increasing AFM indentation depth.
108 ly discussed external magnetic-field-induced AFM long-range order in QOM explains the FS reconstructi
109                We show that chemically inert AFM tips terminated by an oxygen adatom provide excellen
110  including Atomic Force Microscopy Infrared (AFM-IR) and confocal Raman microscopy to discover new bi
111 oscopy and atomic force microscopy infrared (AFM-IR) spectroscopy to probe nanochemical domains of po
112            Atomic force microscopy-infrared (AFM-IR) spectroscopic imaging offers non-perturbative, m
113      Using atomic force microscopy-infrared (AFM-IR) spectroscopy, we were able to probe structural o
114 ental evidence that an easy-plane insulating AFM, an alpha-Fe(2)O(3) thin film, can efficiently trans
115                   The coupling of insulating AFMs to spin-orbit materials(3-7) enables spin transport
116 s of topological insulator: axion insulator, AFM topological crystalline insulator (TCI), and higher
117 Here, we showed the first, to our knowledge, AFM imaging of adsorbed PS films under physiologically r
118 netic conducting atomic force microscopy (mC-AFM), spin-dependent electrochemistry, and spin Hall dev
119 bly for different peptides, lipid-membranes, AFM tips (prepared under identical conditions), and retr
120  was analyzed using atomic force microscope (AFM) and scanning electron microscope (SEM) imaging tech
121                     Atomic force microscope (AFM) based single molecule force spectroscopy (SMFS) and
122 d with a commercial atomic force microscope (AFM) is such that a dynamic range of 80 dB -- achievable
123 when pulled with an atomic force microscope (AFM) tip.
124 also measured using atomic force microscope (AFM) to identify a possible mode of action of isoprene i
125  microscope with an atomic force microscope (AFM), providing simultaneous volumetric imaging with hig
126 n experiments using Atomic Force Microscope (AFM).
127 ryogenic transmission electron microscopies (AFM and cryo-TEM) tracked these transformations over ang
128 c force-scanning electrochemical microscopy (AFM-SECM) probes with electrochemically deposited PDA re
129                     Atomic force microscopy (AFM) allows nanoscale structure-function imaging in vari
130 ation of noncontact atomic force microscopy (AFM) and density functional theory (DFT) to resolve [For
131 spectroscopy (EDS), atomic force microscopy (AFM) and grazing incidence X-ray diffractometer (GIXRD).
132 e with contact-mode atomic force microscopy (AFM) and Kelvin force microscopy (KFM).
133     Here we combine atomic force microscopy (AFM) and optical tweezers (OT) experiments to show that
134 n Microscopy (SEM), Atomic Force Microscopy (AFM) and Raman Spectroscopy.
135 chniques, including atomic force microscopy (AFM) and the DNA tightrope assay.
136                     Atomic force microscopy (AFM) and transmission electron microscopy (TEM) were use
137 inous tissues using atomic force microscopy (AFM) and ultrasound elastography.
138 a deeper focus into atomic force microscopy (AFM) applications that can bridge diverse length and tim
139 uctures, we used an Atomic Force Microscopy (AFM) assay.
140 ined approach using atomic force microscopy (AFM) based single molecule force spectroscopy (SMFS) exp
141 we demonstrate that atomic force microscopy (AFM) can be used to reshape, resize and relocate single-
142        Among these, atomic force microscopy (AFM) combined with modeling has been widely used to char
143    Here, we utilize atomic force microscopy (AFM) coupled with other methods to reveal time- and conc
144 were examined using atomic force microscopy (AFM) force volume mapping.
145  Recent progress in atomic force microscopy (AFM) has allowed the study of live cells in three dimens
146 rbed PS films using atomic force microscopy (AFM) has been proven to be technically challenging.
147 PPC) bilayers using atomic force microscopy (AFM) imaging and AFM-based nanoindentation in a liquid e
148                     Atomic force microscopy (AFM) imaging of medin aggregates at different stages of
149     Here, we report atomic force microscopy (AFM) imaging of S. pombe Ctp1-DNA complexes revealing th
150  Here, we use rapid atomic force microscopy (AFM) imaging to show that MAC proteins oligomerize withi
151         Here, using atomic force microscopy (AFM) in conjunction with direct stochastic optical recon
152 improvements turned atomic force microscopy (AFM) into a nanoscopic laboratory to directly observe an
153 t results of direct atomic force microscopy (AFM) measurements of adhesion of two MXenes (Ti(3)C(2)T(
154 R) spectroscopy and atomic force microscopy (AFM) methods were utilized for all characterizations of
155  the fabrication of atomic force microscopy (AFM) probes for force spectroscopy using robust diamond-
156 vated locally using atomic force microscopy (AFM) probes to deliver mechanical stimulation.
157  Measurements using atomic force microscopy (AFM) reveal that these spots represent three-dimensional
158                     Atomic Force Microscopy (AFM) revealed that the liposomes were covalently attache
159 resolution, in situ atomic force microscopy (AFM) showed that altering one amino acid within the muri
160 anoscale imaging by atomic force microscopy (AFM) showed that the ring-like structure of the human Mr
161             In situ atomic force microscopy (AFM) shows that micelle assembly occurs in two steps, st
162 viously reported an atomic force microscopy (AFM) study on the calcium-mediated adhesion of nanomater
163 ditionally, dynamic atomic force microscopy (AFM) techniques are based on the analysis of the quasi-s
164 oscopy (dSTORM) and atomic force microscopy (AFM) to characterize the DNA origami nanostructures and
165        Here, we use atomic force microscopy (AFM) to determine the three-dimensional (3D) depth profi
166 used microtiter and atomic force microscopy (AFM) to investigate adhesion by variants of full-length
167 This study utilized atomic force microscopy (AFM) to quantify difference in elasticity between human
168      Here, we apply Atomic Force Microscopy (AFM) to quantitatively measure the change in biomechanic
169 cidocaldarius using atomic force microscopy (AFM) to understand how this macromolecular machinery orc
170 resistance, we used atomic force microscopy (AFM) with 10-um spherical tips to probe the stiffness of
171 w-temperature (5 K) atomic force microscopy (AFM) with CO-terminated tips assisted by density functio
172 g microscopy (STM), atomic force microscopy (AFM) with CO-tip, scanning tunneling spectroscopy (STS),
173  features imaged by atomic force microscopy (AFM) with the dynamics measured using ITIR-FCS.
174 on resonance (SPR), atomic force microscopy (AFM), and fluorescence microscopy.
175 nd IR spectroscopy, atomic force microscopy (AFM), and theoretical calculations, revealing that their
176 icroscopy (SEM) and atomic force microscopy (AFM), and Ti dissolution via light microscopy and Induct
177 Raman spectroscopy, atomic force microscopy (AFM), and transmission electron microscopy in production
178 n microscopy (SEM), atomic force microscopy (AFM), differential pulse (DPV), and cyclic voltammetry (
179  electron (SEM) and atomic force microscopy (AFM), electrochemical impedance spectroscopy (EIS) and c
180 c voltammetry (CV), atomic force microscopy (AFM), Field emission-scanning electron microscopy (FE-SE
181 esonance (SPR) with atomic force microscopy (AFM), here we studied two complement system proteins at
182                     Atomic force microscopy (AFM), High-resolution transmission electron microscope (
183 ectroscopy (RM) and atomic force microscopy (AFM), respectively.
184 igated by employing atomic force microscopy (AFM), scanning electron microscopy (SEM) and electrochem
185  magnetic tweezers, atomic force microscopy (AFM), single-molecule fluorescence resonance energy tran
186               Using atomic force microscopy (AFM), we demonstrate that mESCs lacking Cltc display hig
187 attering (SAXS) and atomic force microscopy (AFM), we investigated the overall conformation of the re
188 We have studied the atomic force microscopy (AFM), X-ray Bragg reflections, X-ray absorption spectra
189                     Atomic force microscopy (AFM)-based TERS is especially versatile, as it can be ap
190 attering (SAXS) and atomic force microscopy (AFM).
191 scosity measured by atomic force microscopy (AFM).
192 osits acquired from atomic force microscopy (AFM).
193 rface, studied with atomic force microscopy (AFM).
194 ere performed using atomic force microscopy (AFM).
195 etry (ToF-SIMS) and atomic force microscopy (AFM).
196 ned substrates with atomic force microscopy (AFM).
197  based on a modular atomic force microscopy (AFM).
198 rform TERS imaging using a transmission-mode AFM-TERS configuration on both biological and non-biolog
199 force of a positively polarized PDA-modified AFM-SECM probe was 6.2 +/- 2.2 nN, and it was about 50%
200 an appropriate potential to the PDA-modified AFM-SECM probe, thereby enabling adhesion measurements u
201                      Acute flaccid myelitis (AFM) is a disabling, polio-like illness mainly affecting
202 l spike in pediatric acute flaccid myelitis (AFM)(1-6).
203  recent outbreaks of acute flaccid myelitis (AFM), a poliomyelitis-like spinal cord syndrome that can
204 lastic coupling of the SOP is detected by nc-AFM and STM.
205  and non-contact atomic force microscopy (nc-AFM) combined with first-principle calculations, we repo
206 ) and noncontact atomic force microscopy (nc-AFM).
207 , and macroscopic levels by a combination of AFM-assisted force spectroscopy, peel and static shear a
208  family significantly enriched by the CSF of AFM cases relative to controls was Picornaviridae, with
209 ts further demonstrated the effectiveness of AFM-IR in differentiating the liposome containing ciprof
210                           The integration of AFM data with data of the molecular composition contribu
211 ~160% in a simple resistor structure made of AFM Sr(2)IrO(4) without auxiliary reference layer.
212 ratio images, or indeed the normalization of AFM-IR spectra, should be approached with caution in the
213                                 Outbreaks of AFM have occurred across multiple global regions since 2
214 , clinical features, course, and outcomes of AFM to help to guide diagnosis, management, and rehabili
215                 Following the acute phase of AFM, patients typically have substantial residual disabi
216          These data demonstrate the power of AFM nanoindentation to probe tissue mechanics, and delin
217                      Based on the results of AFM (atomic force microscopy) observations together with
218  the treatment of milk to reduce the risk of AFM(1) contamination.
219 iated functionalities on the readout side of AFM-based devices are urgently desired.
220 Our results thus demonstrated the utility of AFM-IR for characterization of nanosized phages present
221                                     Overall, AFM provides a highly sensitive technique to measure org
222  confinement while simultaneously performing AFM indentation.
223                                   Easy-plane AFMs with two orthogonal, linearly polarized magnon eige
224 ly be further validated by more quantitative AFM force spectroscopy.
225 M-IR overall signal, i.e., the integrated RE-AFM-IR signal amplitude versus AFM-derived cell thicknes
226 nhanced infrared atomic force microscopy (RE-AFM-IR) is a near-field photothermal vibrational nanopro
227  and unsupervised chemometric analysis of RE-AFM-IR nanospectra generated from the nuclear and perinu
228 eports a first application of synchrotron RE-AFM-IR to interrogate biological soft matter at the subc
229 not only the applicability of Synchrotron RE-AFM-IR to soft biological matters with subcellular spati
230 hole cell were analyzed by exploiting the RE-AFM-IR overall signal, i.e., the integrated RE-AFM-IR si
231                 We have used high resolution AFM based dynamic force spectroscopy to investigate pept
232                        Ultra-high-resolution AFM imaging of single molecules of kekulene and computat
233                           Spatially resolved AFM-IR spectra acquired from individual liposomes confir
234 sive as documented in single-molecule scale (AFM), bulk solution phase (FRAP), and ex vivo tissue exp
235                                    Fast-scan AFM videos (at 1-2 frames per second) of M/R complexes r
236 erized by means of dynamic light scattering, AFM and cryoSEM, revealing spherical particles of ~100 n
237 ilus, has been investigated by means of SEM, AFM and impedimetric measurements.
238                          Additionally, since AFM cannot be employed on live animals, we have also dev
239 synephrine analyte was examined with in situ AFM imaging.
240 sion over several micrometres occurs in some AFMs with easy-axis anisotropy(8,9).
241 omic force microscopy-infrared spectroscopy (AFM-IR) as an advanced spectroscopic system was employed
242 omic force microscopy infrared spectroscopy (AFM-IR) to assess the chemical composition of individual
243 omic force microscopy infrared spectroscopy (AFM-IR) to assess the presence of phages and investigate
244 omic force microscopy-infrared spectroscopy (AFM-IR) with first-principles calculations and phase-fie
245 omic force microscopy-infrared spectroscopy (AFM-IR), we were able to reveal the structure of alpha-s
246 orce-microscopy-based infrared spectroscopy (AFM-IR), which circumvents the Abbe diffraction limit, a
247       Finally, we demonstrate how high-speed AFM can visualize plasmid DNA dynamics, intermittent nuc
248  the human Mre11/Rad50 complex by high-speed AFM shows that the Rad50 coiled-coil arms are consistent
249 us postmortem human eyes, and 1-um spherical AFM tips to probe the region immediately below the tissu
250              Being implemented on a standard AFM, this method has the potential for a broad applicabi
251           The versatility of such switchable AFM-SECM probes is demonstrated for electrochemical forc
252 PS, XRD, Raman spectroscopy, FE-SEM, HR-TEM, AFM, UV-Vis and FL, revealed successful doping carbon na
253 suite of biophysical methods, including TEM, AFM, high-resolution cryo-EM, and SAXS/WAXS measurements
254                            Microscopic (TEM, AFM) and spectroscopic (steady-state UV-vis and fluoresc
255 ified and supported by a combination of TEM, AFM, and multiscale simulation techniques.
256 ntally demonstrated, such as low-temperature AFM tunnel junctions that operate as spin-valves(6), or
257 erate as spin-valves(6), or room-temperature AFM memory, for which either thermal heating in combinat
258                        Our results show that AFM-IR and TERS provide different but complementary info
259 structive nature of the method, suggest that AFM-IR can be used to investigate mechanisms of wax depo
260  Taken together, this evidence suggests that AFM sharp tip and TM emphasize properties of the actin-r
261                                          The AFM images showed array like formation of BioPE-DOTAP on
262        Specifically, this work describes the AFM-IR spectra of red blood cells under polyvinyl alcoho
263 vents was also investigated by employing the AFM for the first time.
264                                      For the AFM-IR measurements, spray-dried Staphylococcal phage Sa
265 ng with the absence of amyloid fibers in the AFM and transmission electron microscopy images, suggest
266 ields but that is still quite unknown in the AFM context: the wavelet analysis.
267 cs reveal the molecular-level details in the AFM experiments.
268 late-calcite interactions, thus lowering the AFM adhesion forces.
269 al conditions), and retraction speeds of the AFM cantilever, could not be described in terms of the s
270  parameters that perturb the dynamics of the AFM probe, such as the tip radius, Hamaker constant, sam
271 h(2)Si(2) indicate that the formation of the AFM state in YbRh(2)Si(2) is very likely also connected
272     Strong magnetic fields also suppress the AFM order at a field-induced QCP at B(c) ~ 50 T.
273 o pull a single FH molecule, anchored to the AFM probe, from its complex with surface-attached C3b.
274 om the photothermal expansion mixes with the AFM cantilever oscillation to provide the PiFM signal.
275 mpact oligomers, largely consistent with the AFM data, and larger protofibrillar structures.
276  differentiated to CMs and employed with the AFM/MEA platform for diseased CMs' drug response testing
277                                  Even though AFM-IR and TERS have developed independently and have in
278 in-rich shell of the cell, whereas round-tip AFM and OMTC emphasize those of the noncortical intracel
279 ed by TM and stiffness reported by sharp-tip AFM as compared to corresponding controls.
280                        We here developed tiv-AFM, combining time-lapse in vivo atomic force microscop
281 ese measurements are difficult to compare to AFM-derived measurements of Young's modulus.
282 frequency matches the difference between two AFM mechanical modes, leading to detectable PiFM signals
283           We show that it is feasible to use AFM-IR to chemically characterize this type of substrate
284  using QPI, as well as Young's modulus using AFM, across two breast cancer cell-line populations dose
285 m the level of the single infected RBC using AFM-IR and confocal Raman to the detection of the parasi
286 f polythiophenes (PTs) may be resolved using AFM under ambient conditions through the low-amplitude (
287 manipulation of the crystal waveguides using AFM is non-invasive, and after bending their emissive sp
288 al imaging approach developed here utilizing AFM force volume mapping, ToF-SIMS chemical mapping, and
289 integrated RE-AFM-IR signal amplitude versus AFM-derived cell thickness, also on lateral resolution a
290 it materials(3-7) enables spin transport via AFM magnons.
291                                 Force volume AFM can precisely capture the mechanical properties of b
292                   In this work, force volume AFM is used to identify collagen-enriched domains, natur
293        However, mechanical dissociation with AFM showed significantly increased tensile strength for
294 RRAS and UV-vis spectroscopy and imaged with AFM.
295 mbining Line Bessel light sheet imaging with AFM, we measured the forces exerted by a macrophage duri
296               From analyses carried out with AFM and XPS, the final samples exhibited a flat morpholo
297                        Sixteen patients with AFM had nerve transfers, with a male predominance (75%)
298 tive case analysis was made of patients with AFM treated with nerve transfer surgery between 2007 and
299 tion imaging of the membrane structures with AFM.
300          These observations agreed well with AFM experiments and provided new insights for the compet

 
Page Top