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 lyses of adult mice show a 10-15 dB shift in auditory threshold, and distortion product otoacoustic e

5           CRFR1(-/-) mice exhibited elevated auditory thresholds at all frequencies tested, indicatin

6 cks and tone pips revealed no differences in auditory threshold between the 2 strains.

7 er perch can detect up to 4 kHz, with lowest auditory thresholds between 600 Hz and 1 kHz.

8 alysis of Sef mutant mice, which have normal auditory thresholds but abnormal auditory brainstem resp

9      Animals and humans with HHL have normal auditory thresholds but defective cochlear neurotransmis

10 ics of auditory neuropathy, namely, elevated auditory thresholds combined with normal outer hair cell

11 zygous mutant mice have significantly raised auditory thresholds due to a conductive deafness arising

12 1PR2 gene were significantly associated with auditory thresholds in the 1958 British Birth Cohort (n

13               Thra(tm2/tm2) mice have normal auditory thresholds indicating that TR alpha 2 is dispen

14                      Late instar nymphs have auditory thresholds of 70-80 dB sound pressure level (SP

15 nging wire, footprint pathway, visual cliff, auditory threshold, pain threshold, and olfactory acuity

16 tentials and a corresponding decrease in the auditory thresholds recorded from the saccule.

17 nly control group showed frequency-dependent auditory threshold shifts (measured by auditory brainste

18                                              Auditory threshold shifts (measured by auditory brainste

19                             Despite elevated auditory thresholds, the Tecta mutant mice all exhibit a