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1 ergy surfaces by a water-assisted variant of microcontact printing.
2 aphy or via selective growth with the aid of microcontact printing.
3 n of cross-linked polymer thin-films through microcontact printing.
4 ently attaching and patterning a dye through microcontact printing.
5 ly onto self-assembled monolayer (SAM) using microcontact printing.
6 chlorosilane (OTS) monolayer patterned using microcontact printing.
7 zed on azide-modified glass substrates using microcontact printing and a strain-promoted azide-alkyne
8 in chain organization between SAMs formed by microcontact printing and by solution deposition are als
9 rminated monolayers on gold surfaces and use microcontact printing and Dip-Pen Nanolithography (DPN)
10                                 Here, we use microcontact printing and microfabricated arrays of elas
11 d based on experimentally simple techniques--microcontact printing and micromolding in capillaries--t
12                       In this study, we used microcontact printing and micropost arrays to control ce
13               Using samples prepared by DPN, microcontact printing, and adsorption on macroscopic sub
14 lectric-field alignment and crystallization, microcontact printing, and selective metallization.
15                               In traditional microcontact printing, diffusion limits resolution of pa
16 microelectrodes, microlenses, and stamps for microcontact printing, following methods described previ
17 ly larger compared to the currently-employed microcontact printing for PEMs.
18 , including methods for (i) rubber stamping (microcontact printing) high-resolution ( approximately 1
19 printing with microfluidic patterning, where microcontact printing is employed for silanization using
20 EMs were created by ionic interactions using microcontact printing (microCP) technique.
21 face, we use techniques of soft lithography (microcontact printing, microfluidics, and patterning thr
22 ing micro- and nanodeposition tools, such as microcontact printing (muCP) and dip-pen nanolithography
23 e involves repeated surface patterning using microcontact printing (muCP) of initiator-terminated thi
24 tudy was conducted to investigate the use of microcontact printing (muCP) to direct cultured or expla
25 variety of experimental techniques including microcontact printing (muCP), surface plasmon resonance
26 monly used soft lithographic techniques: (i) microcontact printing of alkanethiols and proteins on go
27               Microarrays were fabricated by microcontact printing of BSA-PBA in line patterns (10 x
28                                           By microcontact printing of culture surfaces, we forced the
29 te pretreatment, and stamp contact times--on microcontact printing of m-dPEG acid molecules onto PEM
30 ts by geometrically inducing defects through microcontact printing of patterned monolayers.
31 M-1, created by combining multiple rounds of microcontact printing on a single surface.
32             Alkane thiols were patterned via microcontact printing on gold, and their effects on the
33 d onto the substrate by optical lithography, microcontact printing or vapour deposition.
34                                              Microcontact printing provides an alternative to previou
35                                        Using microcontact printing, small (200-microm diameter) hydro
36 most of the patterning techniques, including microcontact printing (soft lithography), photolithograp
37 lica substrates through the combination of a microcontact printing technique and fusion of lipid vesi
38 near ECM islands, which were created using a microcontact printing technique and were 1 microm wide a
39                          In conjunction with microcontact printing, this biomimetically catalyzed enc
40                                        Using microcontact printing to achieve spatial control of DNA-
41 um from sheep valve endothelial cells, using microcontact printing to mimic the regions of isotropy a
42                                       We use microcontact printing to pattern pentafluorobenzyl phosp
43 tionalized with extracellular matrix through microcontact printing to promote cell adhesion.
44                                              Microcontact printing was employed to pattern rHIgM12 an
45                                              Microcontact printing was used to functionalize portions
46           Using these features together with microcontact printing, we demonstrate straightforward pa
47                                Using protein microcontact printing, we show that platelets spread bey
48           This approach consists of coupling microcontact printing with microfluidic patterning, wher
49 obilized catalyst, the lateral resolution of microcontact printing would depend only on the length an

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