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   1 high titers of anti-MPO antibodies are often drug-associated.                                        
  
  
  
  
  
     7 ions, such as nonsteroidal anti-inflammatory drug-associated angioedema and serum sickness-like react
  
  
  
    11 drug-seeking behavior that was maintained by drug-associated conditioned reinforcers and assessed usi
  
    13 mote cocaine-seeking behavior in response to drug-associated conditioned stimuli (CS) and share dense
  
    15 a significant increase in preference for the drug-associated context, with a linear trend for increas
    16 re-activation of these neuronal ensembles by drug-associated contexts during abstinence provoked drug
  
    18 s examining the potential reconsolidation of drug-associated contextual memories, rats were given a s
    19 a renewal procedure, the authors report that drug-associated contextual stimuli play a critical role 
  
  
    22 dependent increase in their response for the drug-associated cue as compared to mice that self-admini
  
    24  VTA dopamine neurons blocked the ability of drug-associated cues (but not a cocaine prime) to reinst
    25 mental drug-seeking behavior that depends on drug-associated cues acting as conditioned reinforcers. 
  
    27 tablished as associations are formed between drug-associated cues and the conditioned responses they 
  
  
  
    31 ning addictive behaviors, as presentation of drug-associated cues can elicit drug seeking and relapse
    32 g abuse; however, it remains unclear whether drug-associated cues can elicit the emotional withdrawal
  
  
  
    36 ed that the PL-NAcC pathway was recruited by drug-associated cues in a dopamine-dependent manner to d
    37 uggest that LTCC blockade during exposure to drug-associated cues may cause unlearning of the increas
    38 ty to addiction involves robust memories for drug-associated cues that are difficult to extinguish.  
  
    40  prefrontal cortex that are thought to allow drug-associated cues to drive compulsive drug seeking an
    41 t aspect of drug addiction is the ability of drug-associated cues to elicit craving and facilitate re
  
    43  powerful and sometimes surprising ways, and drug-associated cues trigger relapse to drug seeking in 
  
    45 evealing a bottleneck in brain processing of drug-associated cues where therapeutic interventions cou
  
    47 g seeking becomes habitual and controlled by drug-associated cues, and the neural locus of control ov
    48 oms including enhanced incentive salience of drug-associated cues, but also a negative affective stat
    49 hat in the absence of conscious awareness of drug-associated cues, cocaine and alcohol activate only 
    50  Drug use is provoked by the presentation of drug-associated cues, even following long periods of abs
  
  
    53 to drug seeking can be caused by exposure to drug-associated cues, provoking drug craving even after 
  
    55 aviour that depends upon the presentation of drug-associated cues, without having any intrinsic, prim
  
  
  
  
  
  
    62 l immune-related adverse events and consider drug-associated dermatomyositis in the differential diag
  
    64 he prior history of morphine exposure in the drug-associated environment, since alterations of AMPAR 
  
    66 nisms that mediate the effects of real-world drug-associated environments on drug taking behavior und
    67  with high titers of anti-MPO antibodies are drug-associated, especially following exposure to hydral
  
  
    70 rse interaction drugs, drug primary targets, drug-associated genes, and proteins directly interacting
  
    72  of malate dehydrogenase displayed prominent drug-associated increases in expression compared with un
  
  
  
  
  
  
    79 anol experience may promote the formation of drug-associated memories by enhancing synaptic plasticit
  
  
    82 enetic mechanism, nucleosome remodelling, in drug-associated memories remains largely unexplored.    
  
    84 g to the formation and persistence of strong drug-associated memories that lead to craving and relaps
  
    86 evention therapies attempt to interfere with drug-associated memories, but are often hindered by unin
    87 ucleus accumbens (NAc) is essential to these drug-associated memories, but underlying mechanisms are 
  
  
    90  a memory reactivation session disrupted the drug-associated memory and abolished subsequent instrume
    91 neural circuitry that mediates expression of drug-associated memory is therefore of crucial importanc
  
    93  blockade could induce long-term deficits in drug-associated memory retrieval by reducing neuronal ex
  
  
  
    97 ias as isoimmune, autoimmune (including some drug-associated neutropenias), and idiopathic (cases pos
    98 ed receptor models that require formation of drug-associated nonconducting states with high affinity 
    99  and habitual drug seeking, the influence of drug-associated Pavlovian-conditioned stimuli on drug se
  
  
  
   103 ring the development of addiction in humans, drug-associated stimuli acquire increasingly stronger in
  
   105 locus in mediating the effects of previously drug-associated stimuli on subsequent drug-seeking behav
   106 , combined with enhanced excitatory drive by drug-associated stimuli, contributes to the two cardinal
   107 ein signaling in the PFC focuses behavior on drug-associated stimuli, while dysregulated PFC-accumben
  
  
  
  
   112 ed conditioned reinforcing properties of the drug-associated stimulus and thus its impact on the lear
   113 gical and behavioral treatments that disrupt drug-associated stimulus memories could be beneficial in
   114 s suggesting that rats avoided intake of the drug-associated taste cue because the value of the taste
   115  liver disease/nonalcoholic steatohepatitis, drug-associated toxicities, and other metabolic/genetic 
   116 patients (12.5%) were removed from study for drug-associated toxicity (five thromboembolic events, on
  
   118 anagement of chronic infection by decreasing drug-associated toxicity and improving quality of life w
  
   120 t of the most and the most recent reports of drug-associated TTP-HUS are discussed: mitomycin C, cycl
  
  
   123 in antimetastatic activity without producing drug-associated weight loss as observed with systemic ad
   124 id (TA) is a non-steroidal anti-inflammatory drug associated with anti-tumorigenic and pro-apoptotic 
   125 ated the metabolic footprint of metformin, a drug associated with improved post-MI LV function in exp
  
   127 of the interactions, as well as diseases and drugs associated with a single nucleotide polymorphism o
   128 ug Administration (FDA)-approved peptidergic drugs associated with allergic-type injection-site react
  
  
  
  
  
   134 al corticosteroids alone, are oral antiviral drugs associated with improved outcomes when combined wi
   135 ve affective biases following treatment with drugs associated with inducing negative affective states
  
  
   138 d MRGPRX2 are targets of many small-molecule drugs associated with systemic pseudo-allergic, or anaph
   139 rt the notion that many of the antipsychotic drugs associated with the development of movement disord
   140 t Reporting System database was searched for drugs associated with thrombocytopenia by use of data mi
   141 arrhythmic drugs, especially amiodarone, and drugs associated with torsade de pointes may have contri
   142 idine and clopidogrel, are the 2 most common drugs associated with TTP in databases maintained by the
  
  
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