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1 lex biomolecules has become a cornerstone of chemical biology.
2 binatorial chemistry, organic synthesis, and chemical biology.
3 cks for medicinal chemistry and as tools for chemical biology.
4 ellular functions is commonly referred to as chemical biology.
5 creasingly important topic in structural and chemical biology.
6 ufficiently validated, compounds employed in chemical biology.
7 on should find applications in many areas of chemical biology.
8 those of the azido group for applications in chemical biology.
9 rged as important bioorthogonal reactions in chemical biology.
10 pects on the possible further development of chemical biology.
11 nt roles as drug candidates and as tools for chemical biology.
12 drug discovery, proteomics, metabolomics and chemical biology.
13 s a classical model system for environmental chemical biology.
14 s powerfully enabling for drug discovery and chemical biology.
15 on in organic synthesis, drug discovery, and chemical biology.
16 e a stabilized diazo group as a reporter for chemical biology.
17 computational drug discovery and systems and chemical biology.
18 ing workflows relevant to drug discovery and chemical biology.
19 l for developing therapeutics and probes for chemical biology.
20 ndly affect the future of drug discovery and chemical biology.
21  synthetic chemistry, materials science, and chemical biology.
22  a significant challenge at the forefront of chemical biology.
23 s to address a wide range of applications in chemical biology.
24  biotechnology, transplantation medicine and chemical biology.
25 tant role of protein-protein interactions in chemical biology.
26 macological agents is a longstanding goal in chemical biology.
27 nic chemistry but have untapped potential in chemical biology.
28 reactivity could have substantial utility in chemical biology.
29 nt and improvement of intein-based tools for chemical biology.
30 many outstanding questions in biophysics and chemical biology.
31 ic cellular proteins are essential tools for chemical biology.
32 enetic alphabet has been a long-time goal of chemical biology.
33 ew lead identification in drug discovery and chemical biology.
34 the future use of carrier protein fusions in chemical biology.
35 ule interfaces represents a powerful tool of chemical biology.
36 catalysts remains a formidable challenge for chemical biology.
37  common to model self-replication systems in chemical biology.
38  for further advances in total synthesis and chemical biology.
39 lular organic synthesis with applications in chemical biology.
40 tructural biology, cloning, glycobiology and chemical biology.
41  to the key area of clinical diagnostics and chemical biology.
42  FRB, a system relevant in both medicine and chemical biology.
43  uncaging reactions offer versatile tools in chemical biology.
44 l issue in the fields of pharmaceuticals and chemical biology.
45 bitors are widely used in drug discovery and chemical biology.
46  well as their applications as probes and in chemical biology.
47 subcellular compartments is an unmet need in chemical biology.
48 ting applications in medicinal chemistry and chemical biology.
49 here has important implications for cell and chemical biology.
50 t this method could find new applications in chemical biology.
51 ter of what, 30 years later, would be called chemical biology.
52  organic synthesis, medicinal chemistry, and chemical biology.
53  become one of the great frontiers of modern chemical biology.
54 emerging field of RNA splicing chemistry and chemical biology.
55 g drug discovery, ecology, biosynthesis, and chemical biology, among others.
56 ression in living cells is a central goal of chemical biology and antisense therapeutic development.
57 ation of proteins plays an important role in chemical biology and biomaterials science.
58 menon has found a variety of applications in chemical biology and biotechnology, precious little is k
59 FRET can be generalized with applications in chemical biology and biotechnology, such as target engag
60 by split inteins has found widespread use in chemical biology and biotechnology.
61 ly split inteins has found widespread use in chemical biology and biotechnology.
62                             In recent years, chemical biology and chemical genomics have been increas
63 ill find significant utility in the areas of chemical biology and chemically enabled/enhanced biother
64 earned about targeted protein degradation in chemical biology and drug discovery and systematically r
65 inescent reporter enzyme, is broadly used in chemical biology and drug discovery assays.
66 is outlined and will be of value to both the chemical biology and drug discovery fields.
67 oteases, the undisputed potential of GTs for chemical biology and drug discovery has remained largely
68 e importance of alpha-helix-mediated PPIs to chemical biology and drug discovery with a focus on desi
69 icine, and its research is a top priority in chemical biology and drug discovery.
70 tions (PPIs) represents a major challenge in chemical biology and drug discovery.
71 ical activities is an important step in both chemical biology and drug discovery.
72 velopment of new caging groups/catalysts for chemical biology and drug-delivery applications.
73 r quality and utility across a wide range of chemical biology and drug-discovery research problems.
74                            Rapid advances in chemical biology and functional genomics have facilitate
75 netics and drug discovery, but the fields of chemical biology and genetics have evolved to a point wh
76 h dipolarophiles, and recent applications in chemical biology and heterocycle synthesis.
77 hat would be of interest for applications in chemical biology and in a therapeutic setting.
78  be used to identify innovative compounds in chemical biology and in the early stages of drug discove
79    Chirality is a major field of research of chemical biology and is essential in pharmacology.
80 otoclick reactions and their applications in chemical biology and materials science.
81 a "click" reaction with many applications in chemical biology and materials science.
82 ural products is of particular relevance for chemical biology and medicinal chemistry.
83        Key to establishing a new paradigm in chemical biology and medicine is the development of meth
84                   A fundamental challenge in chemical biology and medicine is to understand and expan
85 tissues, providing an innovative platform in chemical biology and molecular medicine.
86 e nanoscale scaffolds that have relevance in chemical biology and nanotechnology, with diverse areas
87 noparticles, with widespread applications in chemical biology and nanotechnology.
88 s for further investigation of this strain's chemical biology and potential for interaction with its
89 emporary translational science tools such as chemical biology and real-time imaging.
90  AURKA inhibitors, with implications for the chemical biology and selective therapeutic targeting of
91 s an important technique for drug discovery, chemical biology and structural biology.
92 eral fields: materials science, nanoscience, chemical biology and supramolecular chemistry.
93                           Recent advances in chemical biology and the advantages presented by in vivo
94 n of new lead scaffolds for targeting DNA in chemical biology and therapeutic applications.
95 ctivating contexts, and can be exploited for chemical biology and therapeutic applications.
96 case the potential of organic synthesis for (chemical) biology and immunology.
97 ysis are of interest in biomedical research, chemical biology, and biomimetic materials science.
98  We have used a combination of cell biology, chemical biology, and enzymology approaches to analyze t
99 sition in synthetic and medicinal chemistry, chemical biology, and materials science.
100 n in organic synthesis, medicinal chemistry, chemical biology, and materials science.
101       We combined yeast genetic engineering, chemical biology, and multiwavelength fluorescence micro
102 ations driven by advances in bioinformatics, chemical biology, and synthetic biology in concert with
103 en inhibitor candidates for therapeutics and chemical biology, and to unravel the diverse signaling c
104                                              Chemical-biology- and live cell-imaging techniques revea
105  useful photophysical properties for further chemical biology applications.
106 oaches to bioconjugation chemistry and other chemical biology applications.
107 e as scaffolds for the display of ligands in chemical-biology applications and as spacers and constru
108                                         This chemical biology approach allows to interrogate phenotyp
109      Here, utilizing both a gain-of-function chemical biology approach and loss-of-function genetic a
110                                          The chemical biology approach described here can be used to
111                               We undertook a chemical biology approach for investigating mechanisms o
112                                            A chemical biology approach identifies a beta 2 adrenergic
113 ese phenotypes were recapitulated by using a chemical biology approach in which pyrazolopyrimidine-de
114          Transcription unlocked: A synthetic chemical biology approach involving unlocked nucleic aci
115                               This synthetic chemical biology approach may be extended to understand
116 sults demonstrate that CHAMP is a successful chemical biology approach that can provide specific tool
117            Accordingly, we describe herein a chemical biology approach that enabled the reconstitutio
118                            Here, by taking a chemical biology approach that integrates results from i
119                                         This chemical biology approach to defining drug-enzyme intera
120                              Here, we used a chemical biology approach to demonstrate that binding an
121                           Here, we develop a chemical biology approach to determine mammalian nucleos
122                Here, we report an integrated chemical biology approach to explore protein myristoylat
123                                Here we use a chemical biology approach to map the binding interface o
124  colleagues address this shortcoming using a chemical biology approach to monitor ubiquitination with
125                               Here we used a chemical biology approach to perturb the cellular ubiqui
126                              Here, we take a chemical biology approach to probe cell:cell cooperation
127 As such, we provide proof of concept of this chemical biology approach to screen for inhibitors of li
128                           We describe here a chemical biology approach to structural analysis of Abet
129                           Here we employed a chemical biology approach using selective small molecule
130                                      Using a chemical biology approach, it was determined that compou
131 c investigation of the WaaL function using a chemical biology approach, providing a system that could
132                        Using a complementary chemical biology approach, we developed a new class of s
133                            Using an unbiased chemical biology approach, we identified a novel role fo
134                           Through a targeted chemical biology approach, we identify ROD as the Spindl
135                                      Using a chemical biology approach, we purified the sigma2 recept
136                                      Using a chemical biology approach, we show that ORC-Cdc6-Cdt1-de
137 rlying the mammalian circadian clock using a chemical biology approach.
138               Therefore, by using a rational chemical-biology approach, we derived antiapoptotic comp
139                   We highlight some of these chemical biology approaches across three areas.
140                                      We used chemical biology approaches and live-cell microscopy to
141  biosynthesis and function are emerging, and chemical biology approaches are accelerating the pace of
142                  Conventional structural and chemical biology approaches are applied to macromolecule
143 foundation for further exploration utilizing chemical biology approaches focusing on validating this
144      Herein, we review the key chemistry and chemical biology approaches that have furthered our stud
145 l properties, H2S is an appealing target for chemical biology approaches to elucidate its production,
146 ion of high quality chemical tools and other chemical biology approaches to target validation in canc
147 molecular chemistry and the state-of-the-art chemical biology approaches to unravel the formation and
148 hosphorylation have been obtained with these chemical biology approaches, but continuing opportunitie
149 he recent development of biotherapeutics and chemical biology approaches.
150  an array of spectroscopic, theoretical, and chemical biology approaches.
151 , and (3) the impact of the ethynyl group on chemical biology approaches.
152  a valuable probe for further structural and chemical biology approaches.
153  strategy in the field of drug discovery and chemical biology are provided.
154 and practical significance in structural and chemical biology as well as in nanobiotechnology.
155 ument its current status with an emphasis on chemical biology aspects of modulating its activity to g
156 sumption by combining laser microsurgery and chemical biology assays in cultured mammalian cells.
157                              Using different chemical biology-based protein unfolding systems, we rev
158 sion that this tool may find applications in chemical biology, bioengineering and medicine.
159 mulated interest for various applications in chemical biology, bioseparations, drug delivery, and sen
160 ights will advance the utility of inteins in chemical biology, biotechnology, and medicine.
161 nes has found widespread use in the field of chemical biology, but the mechanism of the transformatio
162             The combination of stem cell and chemical biology can provide novel approaches to investi
163 s of research involving medicinal chemistry, chemical biology, cancer biology, and molecular imaging.
164                       Recently, the power of chemical biology, combined with model systems like zebra
165 nding field of chimeric molecules leveraging chemical biology concepts.
166         PubChem also collaborates with other chemical biology database stakeholders with data exchang
167                                       Recent chemical biology developments are beginning to demonstra
168 y split inteins have found widespread use in chemical biology due to their ability to drive the ligat
169 tional group has assumed a prominent role in chemical biology efforts in recent years.
170                                      Through chemical biology efforts involving the design and synthe
171 een used to impact actual drug discovery and chemical biology efforts.
172 ul in organic synthesis, drug discovery, and chemical biology endeavors.
173        A particularly challenging problem in chemical biology entails developing systems for modulati
174 advances in terpenoid cyclase structural and chemical biology, focusing mainly on terpenoid cyclases
175 e past years, it has been used especially in chemical biology for peptide/protein synthesis, posttran
176 rterial-venous identity and the potential of chemical biology for providing new insights into this fi
177 induced dimerization is an important tool in chemical biology for the analysis of protein function in
178                           Recent advances in chemical biology have produced light-sensitive compounds
179 inned by many disciplines, but chemistry and chemical biology have undoubtedly played a significant r
180  evidence for their formation in cells using chemical biology, imaging and genomic technologies.
181 gulon in P. aeruginosa by using genetics and chemical biology in combination with transcriptomics and
182 lockworks and highlight the effectiveness of chemical biology in exploring unidentified mechanisms of
183 ontext of the role of structural biology and chemical biology in innovative drug discovery.
184 upramolecular chemistry, in nanosciences, in chemical-biology, in polymers and materials science.
185 l to other protein-tagging methods in modern chemical biology including activity-based protein profil
186  catalytic X-H insertion towards problems in chemical biology indicate that this field has ample room
187                                We describe a chemical biology-informed framework for studying cellula
188 fluorescent dyes, and highlight the relevant chemical biology innovations that can be instrumental fo
189                                              Chemical biology-inspired design of tunable chemical too
190 me one of the main driving forces in current chemical biology, inspiring the search for novel biocomp
191 ulators of 14-3-3 are much needed agents for chemical biology investigations and therapeutic developm
192 the complementary approaches of genetics and chemical biology, involving a variety of model organisms
193                              We propose that chemical biology is a promising approach for studying th
194                                              Chemical biology is an emerging field that enables the s
195                                Increasingly, chemical biology is being used in the context of bacteri
196                                              Chemical biology is efficient to dissect molecular mecha
197  One of the grand challenges in contemporary chemical biology is the generation of a probe for every
198  the complementary strengths of genetics and chemical biology, it is hoped that novel therapeutic app
199 pportunities between synthetic chemistry and chemical biology labs interested in creating first-in-cl
200                With the rapid development of chemical biology, many diagnostic fluorophore-based tool
201                                 We introduce chemical biology methods to investigate the heterogeneit
202                              Bioengineering, chemical biology, molecular biology, and computer scienc
203 ility, and is moving towards applications in chemical biology, nanotechnology and material science.
204 a foundation for studying the structural and chemical biology of arginase I in the immune response, a
205 this work sets a foundation for studying the chemical biology of autophagy through the structure-base
206 e literature also implies that the mammalian chemical biology of CS2 has broader implications from in
207  disclose our complete studies regarding the chemical biology of diazonamide A and its structural con
208                                 However, the chemical biology of HSNO remains poorly understood.
209 been hampered by a poor understanding of the chemical biology of inflammation, the lack of sensitive
210       Here, we review recent advances in the chemical biology of lysine-targeted covalent inhibitors
211  solution and is a viable participant in the chemical biology of nitric oxide and derivatives.
212                                 However, the chemical biology of NO- remains largely unknown.
213                                 We cover the chemical biology of persulfides and the chemical probes
214 r chaperones and assess the potential of the chemical biology of proteostasis.
215 cial to a comprehensive understanding of the chemical biology of psymberin and related compounds that
216                     This article surveys the chemical biology of quadruplexes.
217               In this review, we explore the chemical biology of the cyclooxygenases through the lens
218 vides an additional tool for deciphering the chemical biology of the gut microbiome and might advance
219  as playing important roles in the mammalian chemical biology of the ubiquitous bioregulator nitric o
220  Aspects of the pharmacokinetic behavior and chemical biology of these drug candidates are also descr
221 his Review highlights both the chemistry and chemical biology of this fascinating natural product, an
222 et GAG-binding protein(s), which may lead to chemical biology or drug discovery tools.
223 y plays a fundamental and underlying role in chemical biology, pharmacology, and medicine to discover
224 d discoveries stemming from these innovative chemical biology platforms.
225    It seeks to critically re-evaluate recent chemical biology practice, such as the presence of PAINs
226 ne functionality is frequently introduced in chemical biology probes as a click handle to identify mo
227 research is important for the development of chemical biology probes.
228 eveloped through a collaboration between the Chemical Biology Program and Platform at the Broad Insti
229      The results provide a novel integrative chemical biology proof in support of the neuroinflammati
230 splicing has found extensive applications in chemical biology, protein chemistry, and biotechnology.
231  is a host of methodological approaches from chemical biology, proteomics, genomics, cell biology, an
232 erdisciplinary and promises to revolutionize chemical biology, radiochemistry and materials science.
233  Modern high-throughput discovery efforts in chemical biology rely heavily upon this principle.
234 ng experiments, medicinal chemistry studies, chemical biology research and drug discovery programs.
235 uest for novel bioactive small molecules for chemical biology research and drug discovery.
236           As an information resource for the chemical biology research community, it routinely receiv
237 ation resource supporting drug discovery and chemical biology research.
238 d tools that leverage this carefully curated chemical biology resource.
239                               We conducted a chemical biology screen and identified a subset of neuro
240                            Here, we report a chemical biology screen that identifies small molecules
241      In this work, we used a high-throughput chemical biology screen to identify a small-molecule pro
242   A recent elegant study published in Nature Chemical Biology sheds light on a new resistance mechani
243        Advances in somatic cell genetics and chemical biology should facilitate the development of a
244 lucidated through a combination of genetics, chemical biology, solution biochemistry, and crystallogr
245                                 Finally, new chemical biology strategies are being used to probe the
246   We argue that complementary biological and chemical biology strategies are essential for robust tar
247                                              Chemical biology strategies for directly perturbing prot
248 nding and, provides a suitable complement to chemical biology strategies for the discovery of novel S
249 ate the effects of AEE788 on T. brucei using chemical biology strategies.
250  synthetic antagonists, thus demonstrating a chemical biology strategy of using chemically engineered
251                     In this study, we used a chemical biology strategy to experimentally characterize
252  engineered KAT enzymes, provide a versatile chemical biology strategy to label and profile cellular
253         The bump-hole approach is a powerful chemical biology strategy to specifically probe the func
254                 Here we apply a multilayered chemical biology strategy to unravel the mode of action
255  activity and helps EV71 replicate through a chemical biology strategy.
256 , and this capability is being leveraged for chemical biology studies and clinical pathology, enabled
257                                              Chemical biology studies employing photoaffinity probes
258 gest the method could be a valuable tool for chemical biology studies of proteins.
259 tion of Shp2 as a therapeutic target and for chemical biology studies of Shp2 function.
260 tational analysis, cell-free, cell-based and chemical biology studies that have sought to elucidate t
261 d cellular assays, as a negative control for chemical biology studies.
262 outine preparation of protein conjugates for chemical biology studies.
263 zido-group labeling in organic synthesis and chemical biology studies.
264      Our findings demonstrate the utility of chemical biology techniques in analysis of infection pro
265                       Herein, we examine the chemical biology that confers NDRG1 responsiveness at th
266 e findings thus define a G-CSF effect on MPO chemical biology that endows unsuspected functional vers
267 combinant fragments-is a burgeoning field of chemical biology that has impacted many areas in the lif
268 al review focuses on an important example of chemical biology-the melding of old and new chemical kno
269  for use in fundamental biophysical studies, chemical biology, therapeutic protein development, and b
270        We used a combination of genetics and chemical biology to characterize the mechanism of depupy
271  research areas ranging from bioanalysis and chemical biology to drug discovery and probing of cell-m
272 rged as a major opportunity in synthetic and chemical biology to generate novel biological insights a
273  for the application of chemical ecology and chemical biology to human health.
274   Here, we combine molecular, structural and chemical biology to identify a determinant for PLK1 subs
275 stry, synthetic chemistry, biochemistry, and chemical biology to identify the substrates of peptidase
276                                   We applied chemical biology to screen small molecules that regulate
277                                Using a novel chemical biology tool that allows rapidly tunable manipu
278                        We further apply this chemical biology tool to cell-based studies on the role
279  FabI inhibitor, AFN-1252, was deployed as a chemical biology tool to determine whether Neisseria can
280 zyl-2-pyridyl)quinazoline (BPQ), providing a chemical-biology tool which has been exploited in two li
281      These selective compounds are useful as chemical biology tools and for future drug discovery eff
282 rescent inhibitors that we show to be useful chemical biology tools especially in determination of di
283 it SPase, suggesting that they may be useful chemical biology tools for characterizing the secretome.
284 it SPase, suggesting that they may be useful chemical biology tools for characterizing the secretome.
285 s are amenable for bioconjugation, providing chemical biology tools for thaumatin:taste receptor inte
286 gest that the arylomycins should be valuable chemical biology tools for the study of protein secretio
287  5'-diphosphate ribose (cADPR) analogues are chemical biology tools that can probe the Ca(2+) release
288            Thus, we advance first generation chemical biology tools to aid in the identification of k
289 h inhibitors find use as mechanistic probes, chemical biology tools, and therapeutics.
290                         By using genetic and chemical biology tools, we show that EYA contributes to
291 h inhibitors have the potential to be useful chemical biology tools.
292 of new transition-state analogues for use as chemical biology tools.
293 ties to study challenging targets or provide chemical biology tools.
294 n DUB structural studies, assay formats, and chemical biology tools.
295 ceptualizing the powerful proximity-enhanced chemical biology toolsets into two paradigms: "multifunc
296                Specifically, the concepts of chemical biology were used to develop synthetically and
297 lded in the areas of systems, synthetic, and chemical biology, where the need for comprehensive, hypo
298                In the future, the utility of chemical biology will grow as technologies for rapid ide
299  provide researchers new to the field of H2S chemical biology with practical considerations, pitfalls
300        The final products are of interest to chemical biology, with a platform for Zn-aminopeptidase

 
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