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1 est in this target as potential treatment of cocaine addiction.
2 shows promise as a treatment for people with cocaine addiction.
3 d inform the development of therapeutics for cocaine addiction.
4 t to the pathophysiologic characteristics of cocaine addiction.
5 e tendencies and relationships may pre-exist cocaine addiction.
6 a period of heightened propensity to develop cocaine addiction.
7 date could facilitate control of behavior in cocaine addiction.
8 ere are no FDA-approved medications to treat cocaine addiction.
9 ovel therapeutic target for the treatment of cocaine addiction.
10 g, making it a promising pharmacotherapy for cocaine addiction.
11 agonism as a viable therapeutic strategy for cocaine addiction.
12 Administration-approved pharmacotherapy for cocaine addiction.
13 ortant target for cue-exposure therapies for cocaine addiction.
14 es to diverse types of plasticity, including cocaine addiction.
15 ern of maladaptive behaviors associated with cocaine addiction.
16 receptors that are involved in the action of cocaine addiction.
17 stitute a risk factor for the development of cocaine addiction.
18 cluding heroin and prescription opioids, and cocaine addiction.
19 promoting long-term resistance to relapse to cocaine addiction.
20 er impair executive function and learning in cocaine addiction.
21 th cue exposure therapy for the treatment of cocaine addiction.
22 gene silencing, is involved in regulation of cocaine addiction.
23 tial treatment for both cocaine overdose and cocaine addiction.
24 tion-related behaviors in an animal model of cocaine addiction.
25 al morphology and behavior that may underlie cocaine addiction.
26 provide evidence for a key role of miRNAs in cocaine addiction.
27 be important in regulating vulnerability to cocaine addiction.
28 ls, MPH did not improve treatment outcome in cocaine addiction.
29 of miRNAs that are likely to play a role in cocaine addiction.
30 ich may provide a new rationale for treating cocaine addiction.
31 t individuals with combined heroin and crack cocaine addiction.
32 lasticity associated with the development of cocaine addiction.
33 g GLT1 as a potential therapeutic target for cocaine addiction.
34 long-term behavioral changes associated with cocaine addiction.
35 herapeutic option in the treatment of severe cocaine addiction.
36 et for drug development for the treatment of cocaine addiction.
37 eceptors, within brain regions implicated in cocaine addiction.
38 e likely to be therapeutically beneficial in cocaine addiction.
39 tial inroads for therapeutic intervention in cocaine addiction.
40 s potential medications for the treatment of cocaine addiction.
41 ting changes in neuronal function underlying cocaine addiction.
42 ontal cortex (mPFC) plays a critical role in cocaine addiction.
43 target for the development of treatments for cocaine addiction.
44 g-term depression, associative learning, and cocaine addiction.
45 dentify clusters of genes that contribute to cocaine addiction.
46 havioral and molecular mechanisms underlying cocaine addiction.
47 vide tools for the study of the mechanism of cocaine addiction.
48 sses for regulating at least some aspects of cocaine addiction.
49 ral associations, including vulnerability to cocaine addiction.
50 relapse to drug use is a primary symptom of cocaine addiction.
51 and has been hypothesized to play a role in cocaine addiction.
52 target for prospective pharmacotherapies for cocaine addiction.
53 a range of neurological disorders including cocaine addiction.
54 rget for pharmacotherapies designed to treat cocaine addiction.
55 to adaptive changes in the brain related to cocaine addiction.
56 in long-lasting relapse risk associated with cocaine addiction.
57 ons in patients with Parkinson's disease and cocaine addiction.
58 f early childhood stress in vulnerability to cocaine addiction.
59 sporter plays a key role in the mechanism of cocaine addiction.
60 ity to cocaine and may thereby contribute to cocaine addiction.
61 produce substantial adverse consequences for cocaine addiction.
62 paper describes an immunological approach to cocaine addiction.
63 apeutic cocaine vaccine for the treatment of cocaine addiction.
64 r agonists as a possible pharmacotherapy for cocaine addiction.
65 e their potential pathophysiological role in cocaine addiction.
66 may be useful pharmacotherapeutic agents for cocaine addiction.
67 lso offer a route towards gene therapies for cocaine addiction.
68 e social-emotional functional alterations in cocaine addiction.
69 g to study transcription factors involved in cocaine addiction.
70 g preclinical evidence for its impairment in cocaine addiction.
71 implicated noradrenergic (NA) dysfunction in cocaine addiction.
72 have therapeutic value for the treatment of cocaine addiction.
73 rstanding of molecular mechanisms underlying cocaine addiction.
74 ay have translational potential for treating cocaine addiction.
75 d maladaptive drug-related attention bias in cocaine addiction.
76 ntibody research to aid in the fight against cocaine addiction.
77 he understanding of the role of microglia in cocaine addiction.
78 f opiate and nicotine addiction, but not for cocaine addiction.
79 support a personalized treatment approach to cocaine addiction.
80 for the development of relapse treatment of cocaine addiction.
81 tment of disrupting mitochondrial fission in cocaine addiction.
82 complexes may be efficacious treatments for cocaine addiction.
83 ntial as an agonist therapy for treatment of cocaine addiction.
84 ovel therapeutic target for the treatment of cocaine addiction.
85 a promising drug target for the treatment of cocaine addiction.
86 , may render individuals more susceptible to cocaine addiction.
87 norectic and a candidate pharmacotherapy for cocaine addiction.
88 icant barrier to the successful treatment of cocaine addiction.
89 n may be valuable tools for the treatment of cocaine addiction.
90 tagonizing 5-HT1A autoreceptors for treating cocaine addiction.
91 harmacological strategy for the treatment of cocaine addiction.
92 of addiction endophenotypes, especially for cocaine addiction.
93 tify and develop novel pharmacotherapies for cocaine addiction.
94 ers including depression, visceral pain, and cocaine addiction.
95 mphetamine addictions, but not for heroin or cocaine addiction.
96 be a therapeutic target for the treatment of cocaine addiction.
97 idates for the development of treatments for cocaine addiction.
98 zheimer's disease, Huntington's disease, and cocaine addiction.
99 tionale supporting sleep-based therapies for cocaine addiction.
100 have therapeutic utility in the treatment of cocaine addiction.
101 te sleep-based therapeutic opportunities for cocaine addiction.
102 including stroke, motor neuron disease, and cocaine addiction.
103 ription of specific genes that contribute to cocaine addiction.
104 ent a novel drug target for the treatment of cocaine addiction.
105 ression is a potential therapeutic target in cocaine addiction.
106 mor growth and invasion, viral infection and cocaine addiction.
107 te alterations in the glutamate signaling in cocaine addiction.
108 havior and may be useful in the treatment of cocaine addiction.
109 provide novel therapeutic opportunities for cocaine addiction.
110 against cocaine be a viable prophylaxis for cocaine addiction?
112 rticipation of thalamic dopamine pathways in cocaine addiction, a possibility that merits further inv
113 subjective effects is a cardinal symptom of cocaine addiction and a DSM-V criterion for substance ab
115 e a novel role for G9a in promoting comorbid cocaine addiction and anxiety and suggest that increased
118 ld be considered for their potential role in cocaine addiction and hippocampal-mediated relapse after
119 icroRNA let-7d, which has been implicated in cocaine addiction and other neurological disorders, targ
122 a critical step in developing treatment for cocaine addiction and preventing cardiac complications.
124 ecture and molecular neuropathology of human cocaine addiction and provides a framework for translati
127 ing efforts to find effective treatments for cocaine addiction and suggest the application of this pr
128 on resting-state functional connectivity in cocaine addiction and tested whether resting-state funct
130 be advantageous in immunopharmacotherapy for cocaine addiction, and for emergency cases of drug overd
132 tially generalizable to other subgroups with cocaine addiction, and to additional substance use disor
133 eurons modulate numerous distinct aspects of cocaine addiction- and relapse-related behaviors, and po
134 al, predict choice to view cocaine images in cocaine addiction; and (ii) whether such behaviour predi
137 Whether these two prominent features of cocaine addiction are related to each other and are medi
138 ussed with respect to the role of the BLA in cocaine addiction as well as previous studies characteri
139 cleus accumbens (NAc) has been implicated in cocaine addiction because (1) cocaine reinforcement is m
140 ent a novel pharmacotherapeutic approach for cocaine addiction because it may simultaneously function
142 be exploited to develop novel therapies for cocaine addiction, but a molecular target has not yet be
143 l-molecule therapeutic is available to treat cocaine addiction, but enzyme-based therapy to accelerat
144 terventions have been explored to counteract cocaine addiction, but to date no market-approved medica
145 g cocaine self-administration contributes to cocaine addiction by acting to facilitate subsequent coc
146 eking behavior, a defining characteristic of cocaine addiction, can be precipitated by contextual cue
149 Abnormal function in reward circuitry in cocaine addiction could predate drug use as a risk facto
150 to control participants, people with chronic cocaine addiction demonstrate reduced utility PEs in the
153 Methylphenidate has been used to mediate cocaine addiction due to its lower pharmacokinetics, whi
154 There is evidence for sex differences in cocaine addiction from both clinical and preclinical stu
155 armacotherapeutic actions of amphetamine for cocaine addiction go beyond that of replacement therapy.
158 isastrous medical and social consequences of cocaine addiction have made the development of an antico
159 armacological approaches to the treatment of cocaine addiction have thus far been disappointing, and
165 1.6 million people who meet the criteria for cocaine addiction in the United States, and there are cu
167 mechanisms that lead to comorbid anxiety and cocaine addiction, irrespective of which comes first, is
177 sequences on behavior.SIGNIFICANCE STATEMENT Cocaine addiction is a neuropsychiatric disorder that is
179 etically tractable model system for studying cocaine addiction is already providing new clues that ma
190 he relationship between anxiety symptoms and cocaine addiction is complicated; anxiety can be both a
192 ted learning.SIGNIFICANCE STATEMENT Although cocaine addiction is driven in part by the formation of
193 ferences in drug abuse, and a key feature of cocaine addiction is pathologically high motivation for
199 Relapse, a major problem in the treatment of cocaine addiction, is proposed to result in part from ne
201 bits is not necessary for the development of cocaine addiction-like behavior in rats.SIGNIFICANCE STA
203 e amygdala of outbred rats with high and low cocaine addiction-like behaviors following prolonged abs
207 ining CM with bupropion for the treatment of cocaine addiction may significantly improve outcomes rel
211 f acupuncture as a stand-alone treatment for cocaine addiction or in contexts in which patients recei
213 no market-approved medications for treating cocaine addiction or relapse exist, and effective interv
214 nsisted of all adults with a heroin or crack cocaine addiction, or both, who started pharmacological
215 D3/D4 receptors as potential treatments for cocaine addiction, particularly in combination with enri
221 al responses to cocaine in all phases of the cocaine addiction process (induction, maintenance, and r
222 genetic and neurobiological contributions to cocaine addiction, provides a rapid approach for generat
224 In addition to serving as a therapy for cocaine addiction-related diseases, enhanced bioscavengi
230 logical basis of sex-specific differences in cocaine addiction resides in the disparate regulation of
231 and, an induced plasticity evoked by chronic cocaine addiction resulted in progressive transcriptiona
232 oimaging studies have shown that people with cocaine addiction retain some degree of control over dru
233 s a key role in determining vulnerability to cocaine addiction, reveal new molecular regulators that
234 sing therapeutic target for the treatment of cocaine addiction, schizophrenia, Parkinson's disease, a
235 ossibility that the behaviors characterizing cocaine addiction, such as craving-induced relapse, may
236 gene and protein expression associated with cocaine addiction suggest the existence of a mechanism t
237 h rate of comorbidity between depression and cocaine addiction suggests shared molecular mechanisms a
240 lying the vulnerability of impulsive rats to cocaine addiction that localize to the OFC, infralimbic
241 network interactions have been identified in cocaine addiction, the association between these brain n
242 asingly more at risk for the consequences of cocaine addiction, the need to establish better-tailored
243 an established role in preclinical models of cocaine addiction, the translational significance of the
245 ver, the actual therapeutic use of a CocH in cocaine addiction treatment is limited by its short biol
246 l drug repurposing candidates for opioid and cocaine addiction treatment, bridging the gap between tr
249 ed at these complexes may have potential for cocaine addiction treatment.SIGNIFICANCE STATEMENT Toler
252 patients with schizophrenia, depression, or cocaine addiction, using functional magnetic resonance i
254 evel effects of methylphenidate; severity of cocaine addiction was assessed by interview and question
256 ocaine-induced increases in actin cycling in cocaine addiction was examined using the reinstatement o
257 velop a pharmacotherapy for the treatment of cocaine addiction, we embarked on synthesizing novel mol
258 ne oxidase inhibitor selegiline for treating cocaine addiction, we required a method for measuring ur