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1 ressed in CHO cells using the mammalian cell transfection method.
2 ilar to that from traditional triple-plasmid transfection method.
3 etter performance compared with conventional transfection methods.
4 rs obtained by conventional multiple plasmid transfection methods.
5 XAS using in vitro transcription and in vivo transfection methods.
6 rovided by biological, biochemical, and gene transfection methods.
7 e low efficiency of current transduction and transfection methods.
8                           Our acoustothermal transfection method addresses a key bottleneck in balanc
9                  The commonly used transient-transfection method, although versatile and free of aden
10 t reporters allowed us to evaluate different transfection methods and revealed that schizont-stage tr
11                    Although various nonviral transfection methods are available, cell toxicity, low t
12 ious transgenic approaches or virus-mediated transfection methods are available, they are time consum
13 c cell function and differentiation, classic transfection methods are limited by their poor efficienc
14                           We present a 'poly-transfection' method as a simple yet high-throughput alt
15  To enforce miR expression, we employed both transfection methods, as well as a retroviral construct
16 ate effectiveness of the electrochemical DNA transfection method developed and could be applied for o
17                             Current nonviral transfection methods, empirically designed to maximize D
18 of the cell line used for expression and the transfection method employed.
19                         In order to select a transfection method for any particular experiment, the s
20 n this report, we describe a simple 293 cell transfection method for efficient intracellular producti
21  pigment epithelium (RPE), by using nonviral transfection methods for gene transfer and the integrase
22        However, in vivo transient and stable transfection method has not been established for Babesia
23                        Electroporation-based transfection methods have allowed the study of gene func
24                          Recently, transient transfection methods have been developed for the human f
25                           The Ca2+-phosphate transfection method is widely used in transfecting neuro
26 bly low efficiency using either contemporary transfection methods or retroviral transduction.
27                               In situ T cell transfection methods overcome the complexity and high co
28 ells within a larger population, since other transfection methods, such as viral transfection and lip
29                          We have developed a transfection method that enables us to transfect randoml
30        This study presents an acoustothermal transfection method that leverages acoustic and thermal
31           We have optimized a liposome-based transfection method that mediated highly efficient stabl
32 studies in cell culture used oligonucleotide transfection methods that cannot be safely translated in
33  use of HEK293T or COS-7 cells and transient transfection methods that CHIP overexpression causes a d
34                We used a novel plasmid-based transfection method to cell-autonomously suppress CLIC4
35                        Additionally, using a transfection method to express HCV antigen within the li
36 ap genes were able to function in the triple transfection method to generate recombinant AAV.
37    Furthermore, it can be used as an in vivo transfection method to study biochemical cross talks amo
38 particle-mediated gene transfer (biolistics) transfection methods to identify critical DNA sequences
39                  Here, using a novel protein transfection method, we demonstrate that AvrRpt2 and Avr
40                      To develop an efficient transfection method, we formulated a simple nanocomplex
41                  Using the calcium phosphate transfection method, we show that the introduction of DN
42                                         Four transfection methods were examined for their ability to
43                                         This transfection method, which produces synchronized pulses
44 l describes a high-efficiency Ca2+-phosphate transfection method with low cell toxicity.