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1 nforcement learning-based chemical graph-set designer.
2 in which some action is chosen by the study designer.
3 ; and attract a diverse community of product designers.
4 nd of factors outside the control of program designers.
14 s story as it is the ability to generate the designer azadipyrromethene that opens the door to exciti
15 In this study, flubromazepam, a recognized designer benzodiazepine since 2012, was targeted for syn
18 their promise for the future development of designer biocatalysis for the selective late-stage modif
21 heir knowledge system can help institutional designers build more efficient and effective institution
22 ience to generate precise disease models and designer cell samples for personalized therapeutics will
23 The unorthodox use of aerobic enzymes in designer cellulosome machinery effects simultaneous degr
26 quences and the introduction of thousands of designer changes may affect genome organization and pote
27 rane pores opens the door to the creation of designer channels and pores for a wide variety of applic
28 gues use a laminin polymerization-competent, designer chimeric BM protein in vivo to restore function
33 graphs generated by RAG Sampler, and (c) RAG Designer: designs sequences that fold onto novel RNA mot
36 The ability to rapidly and robustly generate designer DNA molecules in an autonomous manner should ha
40 y designer receptor exclusively activated by designer drug (DREADD) chemogenetic technology, we found
41 designer receptors exclusively activated by designer drug (DREADD) in the hypoglossal motorneurons.
42 esigner receptors exclusively activated by a designer drug (DREADD), promotes anxiety-like behavior.
43 Designer receptors exclusively activated by designer drug (DREADDs) are a novel tool with the potent
44 designer receptors exclusively activated by designer drug (DREADDs) as a means of bidirectionally mo
46 designer receptor exclusively activated by a designer drug (Gq-DREADD) in all inhibitory interneuron
47 d designer receptor exclusively activated by designer drug also led to the elevation of AMPAR functio
48 d designer receptor exclusively activated by designer drug augmented CD8(+) T(EM) bone marrow accumul
49 designer receptor exclusively activated by a designer drug in PVT neurons, we show that the PVT is ce
50 , designer receptor exclusively activated by designer drug technology to specifically manipulate CA1
51 graft-derived interneurons was silenced by a designer drug while using donor hiPSC-MGE cells expressi
53 designer receptor exclusively activated by a designer drug) in dACC neurons, and examined the effects
54 (designer receptor exclusively activated by designer drug) injected into the rostral ventrolateral m
55 Designer Receptor Exclusively Activated by a Designer Drug) knock-in mouse line to manipulate intrace
56 (designer receptor exclusively activated by designer drug) receptor hM4Di in sensorimotor cortex and
59 r designer receptor exclusively activated by designer drug-directed specific increases in CA1 excitat
60 y designer receptor exclusively activated by designer drugs (DREADD) hM3Dq was used to induce PFC act
61 designer receptors exclusively activated by designer drugs (DREADD) technology to specifically activ
62 designer receptors exclusively activated by designer drugs (DREADD) viruses into the hypothalamus of
63 'designer receptors exclusively activated by designer drugs (DREADD)' approach, and ChAT-IRES-Cre mic
64 Designer Receptors Exclusively Activated by Designer Drugs (DREADD)-based chemogenetic tools are now
66 designer receptors exclusively activated by designer drugs (DREADDs) afford remotely reversible cont
67 Designer Receptors Exclusively Activated by Designer Drugs (DREADDs) are a popular chemogenetic tech
68 ry Designer Receptors Exclusive Activated by Designer Drugs (DREADDs) before cisplatin treatment.
69 designer receptors exclusively activated by designer drugs (DREADDs) confirmed that G(i) differentia
70 y designer receptor exclusively activated by designer drugs (DREADDs) constructs expressed in GABAerg
71 designer receptors exclusively activated by designer drugs (DREADDs) has made it possible to dissect
72 designer receptors exclusively activated by designer drugs (DREADDs) induced A1R-mediated synaptic d
73 designer receptors exclusively activated by designer drugs (DREADDs) or by the treatment with glutam
74 designer receptors exclusively activated by designer drugs (DREADDs) specifically in the adrenal cor
75 designer receptors exclusively activated by designer drugs (DREADDs) technology, we found that stimu
76 designer receptors exclusively activated by designer drugs (DREADDs) to determine the anatomic and f
77 Designer Receptors Exclusively Activated by Designer Drugs (DREADDs) to GABA neurons in the VTA of w
78 designer receptors exclusively activated by designer drugs (DREADDs) to selectively activate or inhi
79 designer receptors exclusively activated by designer drugs (DREADDs) were delivered after 4-weeks of
80 designer receptors exclusively activated by designer drugs (DREADDs) were infused and subsequently a
81 Designer Receptors Exclusively Activated by Designer Drugs (DREADDs)) provides a reliable and robust
82 designer receptors exclusively activated by designer drugs (DREADDs), behavioral pharmacology, elect
83 designer receptors exclusively activated by designer drugs (DREADDs), exposure to a novel environmen
84 designer receptors exclusively activated by designer drugs (DREADDs), through virtual lesioning of a
85 designer receptors exclusively activated by designer drugs (DREADDs), uses a non-endogenous actuator
86 designer receptors exclusively activated by designer drugs (DREADDs), we show in two AD-like mouse m
88 designer receptors exclusively activated by designer drugs (DREADDs)-based manipulation of neuronal
89 designer receptors exclusively activated by designer drugs (DREADDs)-mediated synaptic silencing abl
93 q-coupled receptors exclusively activated by designer drugs (Gq-DREADD) during fear extinction had no
94 (designer receptors exclusively activated by designer drugs [DREADD]) inhibition of tachykininergic n
95 e presented, including the identification of designer drugs and chemical derivatives not present in t
97 designer receptors exclusively activated by designer drugs in female rats throughout repeated restra
100 Designer receptors exclusively activated by designer drugs were used to inhibit orexin activation th
101 (designer receptors exclusively activated by designer drugs) (Gi) to amplify and reduce transmission,
102 (designer receptors exclusively activated by designer drugs) during a variety of cocaine-seeking beha
103 (designer receptors exclusively activated by designer drugs) is widely used for remote manipulation o
104 (designer receptors exclusively activated by designer drugs) mimicked the antidepressant-like respons
105 (designer receptors exclusively activated by designer drugs) resulted in reduced PPI further demonstr
106 (designer receptors exclusively activated by designer drugs) selectively in mPFC neurons projecting t
107 (designer receptor exclusively activated by designer drugs) strategy to manipulate vHPC-NAc excitabi
108 (designer receptors exclusively activated by designer drugs) system in which a mutated muscarinic G p
109 (designer receptors exclusively activated by designer drugs) technology by creating ROSA26-based knoc
110 (designer receptor exclusively activated by designer drugs) was used to inhibit glutamatergic projec
111 (designer receptor exclusively activated by designer drugs)-based inhibition of the mPFC-AcbSh pathw
112 (designer receptor exclusively activated by designer drugs)-mediated causal approach to test the hyp
113 (designer receptor exclusively activated by designer drugs)-mediated chemogenic activation/inhibitio
117 apidly reacting to emerging threats, such as designer drugs, biological therapeutic agents, and techn
118 he specific detection of a family of illicit designer drugs, the synthetic cathinones, with customize
120 re metallic substrates strongly screen their designer electronic properties and limit further applica
123 copic observations of recombinantly produced designer FADGDH confirmed the intramolecular electron tr
124 An enzyme electrode with the immobilized designer FADGDH showed an increase in current immediatel
129 illustration of theoretical predictions that designer flows can offer multiple ecological and societa
131 rrangement and remodelling of liposomes with designer geometry: all of which are exquisitely controll
132 ith transgenic mice expressing a G(q)-linked designer GPCR selectively in SKM cells demonstrated that
137 ther sectors, such as social welfare, policy designers have purposefully adjusted the costs of progra
140 al control of inversion-symmetry breaking in designer heterostructures of oxides and other material c
145 nsive approach for creating robust, elastic, designer Lunar and Martian regolith simulant (LRS and MR
147 al user interfaces (GUIs) generated with App Designer, making it an easy-to-use application for quick
149 y opens new avenues for facile syntheses of "designer materials" where chemical components from discr
150 for encoding highly complex information into designer metasurfaces, thus having the potential to driv
152 Here we demonstrate that vitamin E-derived designer micelles, originally developed for use in synth
155 otential of a nonhypotensive pGC-A activator/designer natriuretic peptide, CRRL269, in a short-term,
156 We demonstrate that dsRNA can be loaded on designer, non-toxic, degradable, layered double hydroxid
157 Here we demonstrate the use of multiple designer nucleases and variant-aware library design to i
163 d destruction of the mitochondrial genome by designer nucleases(9,10).Here we describe an interbacter
169 an essential first step in the creation of a designer organelle.Designer organelles could allow the i
170 step in the creation of a designer organelle.Designer organelles could allow the isolation of synthet
173 the engineering of multicompartment-spanning designer pathways that can be utilized to control downst
175 d or otherwise, and typically results in the designer performing electromagnetic simulations of a lar
180 HPAs holds great potential for production of designer platelets for diagnostic, investigative, and, u
181 s a set, allow a wide range of stakeholders (designers, policy-makers, and vehicle manufacturers and
182 bility of engineered biocatalysts to produce designer products at high carbon and energy efficiency w
183 orporate particles with the well-established designer properties of MOFs and, therefore, increase the
184 discovery of sequence defined polymers with designer properties, such as oligonucleotide binding.
191 s of these compounds, indicating promise for designer quantum systems synthesized from the bottom-up.
192 tic approach expressing the inhibitory hM4Di designer receptor exclusively activated by a designer dr
193 e virally expressed inhibitory hM4Di DREADD (designer receptor exclusively activated by a designer dr
196 eteroreceptor signaling using a G(i)-coupled designer receptor exclusively activated by designer drug
197 chain reaction, calcium imaging, and DREADD (designer receptor exclusively activated by designer drug
198 e basolateral amygdala (BLA) using a DREADD (designer receptor exclusively activated by designer drug
199 olution approaches combining mouse genetics, designer receptor exclusively activated by designer drug
200 idal neurons with a CaMKII-driven Gq-coupled designer receptor exclusively activated by designer drug
201 ive deficits that could be rescued by either designer receptor exclusively activated by designer drug
202 nally, we used an intersecting viral DREADD (designer receptor exclusively activated by designer drug
204 virus (AAV)-expressing Cre-dependent DREADD (designer receptor exclusively activated by designer drug
205 sconnected these regions using hM4Di-DREADD (designer receptor exclusively activated by designer drug
206 ifferent experimental approaches, especially designer receptor exclusively activated by designer drug
207 sympathetic outflow using Gi-coupled DREADD (designer receptor exclusively activated by designer drug
209 l ganglion activity by activating Gq-coupled designer receptor exclusively activated by designer drug
210 a projection-specific Cre-dependent DREADD (designer receptor exclusively activated by designer drug
211 bition using either excitatory or inhibitory designer receptor exclusively activated by designer drug
213 o this end, we expressed the Galphai-coupled designer receptor hM4D in adult striatopallidal neurons
214 RP neurons, and activation of the inhibitory designer receptor hM4Di on AgRP neurons did not affect s
215 of GABA release from PV neurons through the designer receptor hM4Di selectively expressed in PV-cont
218 We used viral-mediated gene transfer of designer receptors (DREADDs) to activate vmPFC neurons a
219 in combination with Cre-dependent inhibitory Designer Receptors Exclusive Activated by Designer Drugs
220 ons using hM3Dq, but neither hM4Di nor rM3Ds designer receptors exclusively activated by a designer d
221 in mice with C-FOS immunohistochemistry and designer receptors exclusively activated by designer dru
223 while using donor hiPSC-MGE cells expressing designer receptors exclusively activated by designer dru
224 ine neuron G-protein signaling with DREADDs (designer receptors exclusively activated by designer dru
227 common chemogenetic neuromodulatory system, designer receptors exclusively activated by designer dru
229 al activity with distinct stimuli, including designer receptors exclusively activated by designer dru
232 chemogenetic locus coeruleus activation via designer receptors exclusively activated by designer dru
233 ection strategies, pharmacologic rescue, and designer receptors exclusively activated by designer dru
234 ved using chemogenetic approach by deploying designer receptors exclusively activated by designer dru
235 The development of designer GPCRs known as designer receptors exclusively activated by designer dru
236 glutamatergic vCA1 to mPFC projections using designer receptors exclusively activated by designer dru
238 an M3 muscarinic receptor (hM3Dq), a type of designer receptors exclusively activated by designer dru
239 In this issue of the JCI, Gaykema et al. use designer receptors exclusively activated by designer dru
240 s in vivo, we harnessed the power of DREADD (designer receptors exclusively activated by designer dru
241 modulation of neuroanatomical circuits using designer receptors exclusively activated by designer dru
242 nstrated that our chemogenetic approach (eg, Designer Receptors Exclusively Activated by Designer Dru
243 nt with this, astrocyte activation with G(q) designer receptors exclusively activated by designer dru
244 netic method in mice and rats is the DREADD (designer receptors exclusively activated by designer dru
245 ent and reacquisition of alcohol seeking via designer receptors exclusively activated by designer dru
247 elevant Ca(2+) influx by the introduction of designer receptors exclusively activated by designer dru
248 eneration of transgenic mice with Gq-coupled designer receptors exclusively activated by designer dru
249 ion of the vHipp-mPFC pathway using DREADDs (designer receptors exclusively activated by designer dru
250 d this region using CaMKII-driven Gs-coupled designer receptors exclusively activated by designer dru
251 um using the pharmacogenetic technique, the 'designer receptors exclusively activated by designer dru
253 ed from hPSCs engineered to express DREADDs (designer receptors exclusively activated by designer dru
256 approach to express G(i/o)-coupled DREADDs (designer receptors exclusively activated by designer dru
258 ng stimulatory (hM3Dq) or inhibitory (hM4Di) designer receptors exclusively activated by designer dru
259 stabilized step function opsin) and DREADDs (designer receptors exclusively activated by designer dru
260 expression of hM3Dq, the excitatory DREADDs (designer receptors exclusively activated by designer dru
262 viral vector approach to restrict activating Designer Receptors Exclusively Activated by Designer Dru
263 To determine this, we injected Cre-dependent designer receptors exclusively activated by designer dru
264 rgic neurons in the medial septum by DREADD (designer receptors exclusively activated by designer dru
265 er, chemogenetic control of G(i) and G(q) by designer receptors exclusively activated by designer dru
267 transgene strategy to express and stimulate designer receptors that mimicked mGluR5 signaling throug
269 ngineered ribosome may have on the cell, the designer ribosome needs to be functionally isolated from
270 revious study in Arabidopsis that employed a designer RNA-binding protein as a psbA RNA affinity tag.
271 in vitro directed evolution of proteins with designer single-molecule conformational phenotypes of in
274 ngineered receptors exclusively activated by designer small molecules enable manipulation of specific
275 pramolecular self-assembly enables access to designer soft materials that typically exhibit high-symm
277 e promising for applications as inexpensive "designer" solvents exhibiting a host of tunable physicoc
278 ogy is adopted to prepare a bio-conduit with designer structures for peripheral nerve regeneration.
283 ient temperatures using small amounts of the designer surfactant TPGS-750-M, thereby eliminating the
284 studies have shown that aqueous solutions of designer surfactants enable a wide variety of valuable t
287 tput, and open up the possibilities of using designer-tailored pulses for controlling molecular dynam
288 atible strains or by engineering a synthetic designer TAL effector to boost SWEET gene expression.
291 gnatures characteristic to different genetic designers, termed 'genetic engineering attribution', wou
292 open source interactive microfluidic system designer that readily supports state of the art design a
295 of detail is a step forward that now allows designers to inspect and refine their designs with base-
296 gs show that gold mesoflowers may serve as a designer toolkit for engineering colloidal interaction a
297 duced a kinetically sensitive dual-frequency designer waveform into the Fourier-transformed large-amp
298 in the use of de novo metabolic pathways and designer whole-cells for small molecule synthesis, the i
299 Cyclic peptides have long tantalized drug designers with their potential ability to combine the be
300 erially and in parallel through the workflow designer, with multiple, customizable reference database