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1  The deep tendon reflexes were symmetrically hypoactive.
2  lacking rostral brainstem acetylcholine are hypoactive.
3 afish larvae, whereas nmu mutant animals are hypoactive.
4           Most cases of delirium were of the hypoactive (46%) and mixed (45%) subtypes; only 8% of de
5 of highly edited mRNA variants (which encode hypoactive 5-HT2CR receptors) in the brains of suicide v
6 y suggest that midbrain dopamine neurons are hypoactive after prolonged cocaine exposure, a state tha
7 ctive aggression in youths with CU traits to hypoactive amygdala responses to emotional distress cues
8 oxylase (TH) in dopaminergic neurons, become hypoactive and aphagic and die by 4 weeks of age.
9 wever, these mice developed seizures, became hypoactive and approximately 30% of them died by 1 year
10                            These mice become hypoactive and hypophagic and die of starvation by 4 wee
11 eurons, are born normal but gradually become hypoactive and hypophagic, and die at 3 weeks of age.
12       The mutant animals do not feed and are hypoactive and markedly hypotonic.
13 , motoric subtypes of delirium (hyperactive, hypoactive), and the association of delirium with dement
14 ive and, interestingly, the S147P protein is hypoactive as compared to the DUSP5 WT protein in two di
15                                     Abnormal hypoactive behavior was manifested by 4.5-mo-old Naglu-/
16 bladder afferent pathways, thereby improving hypoactive bladder function in diabetes.
17                               Survivors of a hypoactive delirium subtype performed significantly bett
18 mixed, 10 (11.5%) hyperactive and 26 (29.9%) hypoactive delirium subtypes.
19  26-52%, with a significant percentage being hypoactive delirium.
20                                        Other hypoactive DeltaVD mutants formed stable and characteris
21                   The brain is assumed to be hypoactive during cardiac arrest.
22 onically hyperactive in mutants, but becomes hypoactive during social behaviour.
23                          The pivotal role of hypoactive endogenous fibrinolysis in the occurrence of
24                                         This hypoactive form of ANTP, but not the alanine-substituted
25   Delirium is a common event, especially the hypoactive forms in the elderly.
26  the agitated (hyperactive) and nonagitated (hypoactive) forms of delirium are harbingers of impendin
27 t (i) A3B expressed in human cells exists in hypoactive high-molecular-weight (HMW) complexes, which
28     Mice without CB1 receptors are extremely hypoactive in a test for exploratory behavior (open-fiel
29 ge-sensitive superior temporal cortices were hypoactive in ASD toddlers with poor language outcome.
30 nt findings that the default mode network is hypoactive in autism, our data raise the possibility tha
31 egulates fear memories and is reported to be hypoactive in PTSD.
32 he cardiac surgery ICU and was predominately hypoactive in subtype.
33                   Depletion of OLA1 caused a hypoactive ISR and greater survival in stressed cells.
34        The mice with the small deletion were hypoactive like the large deletion mice and they also sh
35                                Specifically, hypoactive medial OFC and hyperactive right hippocampus
36 % of patients near the end of life develop a hypoactive, nonagitated delirium.
37 e engineered deletion or the duplication are hypoactive or hyperactive, respectively.
38 dentified 21% with delirium, 88% of whom had hypoactive or normal psychomotor features.
39                                    A similar hypoactive pattern was found during early conditioning (
40                     Both the hyperactive and hypoactive phases of motor dysfunction preceded the dete
41                        These DCs exhibited a hypoactive phenotype with low CD40, MHC II, CD80/CD86 ex
42 he combination of a hyperactive amygdala and hypoactive prefrontal regions is associated with diminis
43                Furthermore, compensating for hypoactive prelimbic cortex neurons with in vivo optogen
44 ntaneous locomotor activity were found to be hypoactive relative to young animals.
45 tosensory and auditory cortex shifted from a hypoactive state in P45 to hyperactivity in P120.
46 ulated by phosphorylation in both hyper- and hypoactive striatal DA neurons; in the latter case, acti
47               Nearly all (92%) exhibited the hypoactive subtype of delirium.
48 ereas SLC10A4 null mutant mice were slightly hypoactive, they displayed hypersensitivity to administr
49         Delirium symptoms were nearly always hypoactive, were detected mean 6 days after intracerebra

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