Results 161 to 170 of about 4,824,676 (233)

Toward HRTF personalization: an auditory-perceptual evaluation of simulated and measured HRTFs

open access: yes, 2008
Presented at the 14th International Conference on Auditory Display (ICAD2008) on June 24-27, 2008 in Paris, France.Presented at the 14th International Conference on Auditory Display (ICAD2008) on June 24-27, 2008 in Paris, France.Sound localization tests
Mokhtari, Parham   +2 more
core  

Auditory assistive devices for the blind

open access: yes, 2003
Proceedings of the 9th International Conference on Auditory Display (ICAD), Boston, MA, July 7-9, 2003.Presented at the 9th International Conference on Auditory Display (ICAD), Boston, MA, July 7-9, 2003.Most auditory assistive devices for the Blind ...
Massof, Robert W.
core  

IGF‐1/SLC25A33 Maintains Blood‐Labyrinth Barrier Integrity by Suppressing TGF‐β/Smad2‐Mediated Pericyte Activation in Age‐Related Hearing Loss

open access: yesAging Cell, Volume 25, Issue 10, October 2026.
IGF‐1/SLC25A33–TGF‐β/Smad2 axis can regulate pericyte activation and BLB integrity, which may be a potential therapeutic target for preserving hearing in ARHL. ABSTRACT Age‐related hearing loss (ARHL) is a prevalent sensory disorder in the elderly, yet the molecular mechanisms underlying cochlear aging remain incompletely understood. While insulin‐like
Rui Xu   +9 more
wiley   +1 more source

Congruency effects with dynamic auditory stimuli: design implications

open access: yes, 1997
Presented at the 4th International Conference on Auditory Display (ICAD), Palo Alto, California, November 2-5, 1997.Presented at the 4th International Conference on Auditory Display (ICAD), Palo Alto, California, November 2-5, 1997.Since pitch is a ...
Ehrenstein, Addie, Walker, Bruce N.
core  

Cousin Syndrome Due to TBX15 Gene Variants: Three Novel Cases and Review of the Literature

open access: yesClinical Genetics, Volume 110, Issue 4, Page 480-486, October 2026.
Cousin syndrome (MIM#260660) is a rare recognizable genetic disorder characterized by short stature, pelvi‐scapular dysplasia, and craniofacial dysmorphism due to biallelic pathogenic variants in the TBX15 gene. ABSTRACT Cousin syndrome (MIM#260660) is a rare genetic disorder characterized by short stature, pelvi‐scapular dysplasia and craniofacial ...
Wafaa Alharbi   +6 more
wiley   +1 more source

New aspects of comparative peripheral auditory physiology [PDF]

open access: yes, 1988
Kaiser, Alexander   +11 more
core   +1 more source

Auditory displays on the depth of hypertext

open access: yes, 2003
Proceedings of the 9th International Conference on Auditory Display (ICAD), Boston, MA, July 7-9, 2003.Presented at the 9th International Conference on Auditory Display (ICAD), Boston, MA, July 7-9, 2003.This study presents an overview of work on the ...
Lee, Ju-Hwan   +2 more
core  

Chronic Pre‐Trauma Corticosterone Attenuates Trauma Memory Formation and Alters Gene Expression in Glucocorticoid Signalling Pathways

open access: yesGenes, Brain and Behavior, Volume 25, Issue 5, October 2026.
The graphical abstract outlines the experimental workflow and key findings, showing how chronic or acute corticosterone elevations alter FC‐induced molecular and behavioural changes during trauma memory formation, consolidation, and recall. Abbreviations: Cort.—Corticosterone; FC—Fear Conditioning; PRPs—Plasticity‐Related Proteins.
Gia Kutelia   +6 more
wiley   +1 more source

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