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1 d to induce approximately 50 dB elevation in auditory thresholds.
2 te to maintain binaural function with raised auditory thresholds after AT.
3 e sole study to assess relationships between auditory thresholds and central MS-related lesions, stro
4 ent, and because the VLFs were below or near auditory thresholds (and a subsequent experiment suggest
5 lyses of adult mice show a 10-15 dB shift in auditory threshold, and distortion product otoacoustic e
6           CRFR1(-/-) mice exhibited elevated auditory thresholds at all frequencies tested, indicatin
7                  The infant showed sensitive auditory thresholds beginning at 3 months.
8 cks and tone pips revealed no differences in auditory threshold between the 2 strains.
9 er perch can detect up to 4 kHz, with lowest auditory thresholds between 600 Hz and 1 kHz.
10     There were no significant differences in auditory thresholds between DKO mice and wild-type litte
11 alysis of Sef mutant mice, which have normal auditory thresholds but abnormal auditory brainstem resp
12      Animals and humans with HHL have normal auditory thresholds but defective cochlear neurotransmis
13 n hearing loss (HHL) characterized by normal auditory thresholds but reduced amplitude of sound-evoke
14 ics of auditory neuropathy, namely, elevated auditory thresholds combined with normal outer hair cell
15 zygous mutant mice have significantly raised auditory thresholds due to a conductive deafness arising
16  aural communication that persist long after auditory thresholds have returned to normal, reflecting
17 rstand speech in background noise, even when auditory thresholds in quiet are normal.
18 1PR2 gene were significantly associated with auditory thresholds in the 1958 British Birth Cohort (n
19               Thra(tm2/tm2) mice have normal auditory thresholds indicating that TR alpha 2 is dispen
20                      Late instar nymphs have auditory thresholds of 70-80 dB sound pressure level (SP
21                     Our results suggest that auditory thresholds of the last common ancestor of Homo
22 nging wire, footprint pathway, visual cliff, auditory threshold, pain threshold, and olfactory acuity
23 e rats (Heterocephalus glaber) have elevated auditory thresholds, poor frequency selectivity, and lim
24 tentials and a corresponding decrease in the auditory thresholds recorded from the saccule.
25 mmunication deficits that persist long after auditory thresholds return to normal.
26 nly control group showed frequency-dependent auditory threshold shifts (measured by auditory brainste
27                                              Auditory threshold shifts (measured by auditory brainste
28 xposure at 94 dB sound pressure level caused auditory threshold shifts that fully recovered in 2 week
29                             Despite elevated auditory thresholds, the Tecta mutant mice all exhibit a
30 ter earplug removal and the return of normal auditory thresholds, we trained and tested animals on an
31                                              Auditory thresholds were elevated in mutants, and correl
32         This sound transfer function affects auditory thresholds, which relate to speech reception th