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1 be crucial for medical applications of stem cell technology.
2 mutation at the DMa locus via embryonic stem cell technology.
3 m the endogenous genome using embryonic stem cell technology.
4 r1) gene were generated using embryonic stem cell technology.
5 icient for both genes through embryonic stem cell technology.
6 mutation at the DMa locus via embryonic stem cell technology.
7 -deficient mice through mouse embryonic stem cell technology.
8 deficient in Smad5 using embryonic stem (ES) cell technology.
9 nalyze Smad2 mutant embryos created using ES cell technology.
10 eficient in FKBP12 using embryonic stem (ES) cell technology.
11 H beta subunit and therefore in FSH using ES cell technology.
12 homologous recombination and embryonic stem cell technology.
13 cin have been generated using embryonic stem cell technology.
14 e region were generated using embryonic stem cell technology.
15 essed with LT-alpha using baculovirus/insect cell technology.
16 ity of iPS cells is an important goal in iPS cell technology.
17 R) are at the heart of key green-energy fuel cell technology.
18 such as artificial photosynthesis and solar cell technology.
19 he I(-)/I3(-) couple in dye-sensitized solar cell technology.
20 overall efficiency and marketability of fuel cell technology.
21 commercial viability of direct methanol fuel cell technology.
22 basis for the market-leading thin-film solar-cell technology.
23 herapeutic approaches using pluripotent stem cell technology.
24 pening the door for a truly recyclable solar cell technology.
25 n be applied to any multi-dimensional single-cell technology.
26 novel mouse strains via embryonic stem (ES) cell technology.
27 rovide an alternative to hydrogen-based fuel-cell technologies.
28 s low-cost competitor to silicon based solar cell technologies.
29 heterogeneity is a major advantage of single-cell technologies.
30 e tissues profiled using a variety of single-cell technologies.
31 terogeneous data obtained using these single-cell technologies.
32 d disease models that have incorporated stem cell technologies.
33 iciencies comparable to other emerging solar cell technologies.
34 ranslational ramifications for cortical stem cell technologies.
35 ctive AAEMs could significantly advance fuel cell technologies.
36 nered increasing support for the use of fuel-cell technology, a prime example being the solid-oxide f
38 which can be harnessed using microbial fuel-cell technology, allowing both wastewater treatment and
40 der the key challenges posed by various stem cell technologies and liver pathologies for developing c
41 human PSC clinical trials by Geron, Advanced Cell Technology and the Kobe Center for Developmental Bi
42 ranslational step in the development of stem cell technology and the subject of a report in this issu
43 fluorescent-tags are desirable in basic stem cell technology and therapeutic applications of cells.
44 ssible links between ES-cell and neural stem-cell technologies, and the strategies used to isolate an
45 spinal cord injury, there is no agreement on cell technology, and claims of beneficial results lack i
47 se oxidation is of great interest in biofuel cell technology because the enzyme are unaffected by the
48 were generated by traditional embryonic stem cell technology, but these animals contain a biased T ce
49 ion of the development of innovation in stem cell technologies by network analysis of stem cell paten
53 aches for reducing the Dmin, e.g., collision cell technology (CCT) and analyte isotope selection, are
54 ning public because of the promise that stem cell technology could deliver tissue regeneration for in
56 er intravitreal implantation of encapsulated cell technology (ECT) devices releasing ciliary neurotro
58 The DARC (Detection of Apoptosing Retinal Cells) technology enables in vivo real-time non-invasive
64 the development of induced pluripotent stem cell technology for the use of patient-specific iPSCs to
65 ed a combination of induced pluripotent stem cell technology, genomics, and molecular biology in this
69 Recent breakthroughs in pluripotent stem cell technologies have enabled a new class of in vitro s
70 Advances in flow cytometry and other single-cell technologies have enabled high-dimensional, high-th
80 , fetal intervention, and hematopoietic stem cell technology have removed many of the practical, tech
83 reater challenges, but rapidly emerging stem cell technologies hold the promise of autologous grafts
84 recent development of progenitor and/or stem cell technologies holds promise for the treatment of cur
86 , tissue engineering, aided by emerging stem cell technology, holds immense potential for the treatme
87 gest that CNTF delivered by the encapsulated cell technology implant appears to slow the progression
89 l received CNTF delivered by an encapsulated cell technology implant in one eye and sham surgery in t
91 Review, we describe the current state of iPS cell technology, including approaches by which they are
92 The introduction of liquid microjet and flow cell technologies into XAS experiments has enabled the g
94 dvent of high-throughput/high-content single cell technologies is leading to an explosion in the numb
97 n be incorporated by means of embryonic stem cell technology, little progress has been made toward in
101 vances in cell-sorting techniques and single-cell technologies now make this possible, with the ident
104 otype, termed induced pluripotent stem (iPS) cell technology, presents an exciting potential venue to
106 , but recent integration of genomic and stem cell technologies promises a route through this impasse.
108 gy strategies have rapidly entered mammalian cell technology providing novel therapeutic solutions.
113 s of state-of-the-art and forthcoming single-cell technologies, such as multidimensional mass cytomet
116 measurements and explore advances in single-cell technologies that overcome these problems by expand
117 reater understanding of the capacity of stem cell technologies, there is growing public hope that ste
118 t al. (2015) combine gene targeting and stem cell technologies to identify a significant cellular eff
119 nally, we highlight opportunities for single cell technologies to shed light on the causes and conseq
121 the seasonal deficits by using automated red cell technology to collect double red blood cell units;
122 ated Ucn-deficient mice using embryonic stem cell technology to determine its role in stress-induced
123 combination of transgenic and embryonic stem cell technology to generate a mouse line in which the mu
124 n metabolism in vivo, we used embryonic stem cell technology to generate GGT-deficient (GGTm1/GGTm1)
125 d tissue injury in humans include using stem cell technology to generate human cells for screening fo
127 Consortium has used induced pluripotent stem cell technology to study the effects of common genetic v
128 ategies supporting the rapid advance of stem cell technology to the clinic, the philosophies behind t
130 derlying principles and compromises of CAR T-cell technology using the CD19-targeted CAR as a paradig
133 ular components, and the advent of human iPS cell technology when combined with recent advances in th
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