Behavioral characterization of the cochlear amplifier lesion due to loss of function of stereocilin (STRC) in human subjects
出版年份 2023 全文链接
标题
Behavioral characterization of the cochlear amplifier lesion due to loss of function of stereocilin (STRC) in human subjects
作者
关键词
-
出版物
HEARING RESEARCH
Volume 439, Issue -, Pages 108898
出版商
Elsevier BV
发表日期
2023-10-20
DOI
10.1016/j.heares.2023.108898
参考文献
相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。- Association of Genetic Diagnoses of Childhood-Onset Hearing Loss With Cochlear Implant Outcomes
- (2023) Ryan J. Carlson et al. JAMA Otolaryngology-Head & Neck Surgery
- Frequency of the STRC-CATSPER2 deletion in STRC-associated hearing loss patients
- (2022) Shin-ya Nishio et al. Scientific Reports
- Audiologic Phenotype and Progression in Pediatric STRC‐Related Autosomal Recessive Hearing Loss
- (2021) Andrea Simi et al. LARYNGOSCOPE
- Prevalence and Characteristics of STRC Gene Mutations (DFNB16): A Systematic Review and Meta-Analysis
- (2021) Shuang Han et al. Frontiers in Genetics
- Effect of the number of amplitude-compression channels and compression speed on speech recognition by listeners with mild to moderate sensorineural hearing loss
- (2020) Marina Salorio-Corbetto et al. JOURNAL OF THE ACOUSTICAL SOCIETY OF AMERICA
- Effects of hearing loss and age on the binaural processing of temporal envelope and temporal fine structure information
- (2020) Brian C.J. Moore HEARING RESEARCH
- The TECTA mutation R1890C is identified as one of the causes of genetic hearing loss: a case report
- (2019) Gi-Sung Nam et al. BMC Medical Genetics
- The Prevalence and Clinical Characteristics of TECTA-Associated Autosomal Dominant Hearing Loss
- (2019) Rika Yasukawa et al. Genes
- AzBio Speech Understanding Performance in Quiet and Noise in High Performing Cochlear Implant Users
- (2018) Jason A. Brant et al. OTOLOGY & NEUROTOLOGY
- Auditory sensitivity to spectral modulation phase reversal as a function of modulation depth
- (2018) Emily Buss et al. PLoS One
- Phenotypic Characterization of DFNB16-associated Hearing Loss
- (2018) Daniela Back et al. OTOLOGY & NEUROTOLOGY
- Effects of age and hearing mechanism on spectral resolution in normal hearing and cochlear-implanted listeners
- (2017) David L. Horn et al. JOURNAL OF THE ACOUSTICAL SOCIETY OF AMERICA
- STRC Deletion is a Frequent Cause of Slight to Moderate Congenital Hearing Impairment in the Czech Republic
- (2017) Pavlina Plevova et al. OTOLOGY & NEUROTOLOGY
- Identification of a nonsense mutation in the STRC gene in a Korean family with moderate hearing loss
- (2016) Borum Sagong et al. INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY
- Speech Understanding in Children With Normal Hearing
- (2016) Jourdan T. Holder et al. OTOLOGY & NEUROTOLOGY
- Individual differences in selective attention predict speech identification at a cocktail party
- (2016) Daniel Oberfeld et al. eLife
- Acoustic Temporal Modulation Detection in Normal-Hearing and Cochlear Implanted Listeners: Effects of Hearing Mechanism and Development
- (2015) Min-Hyun Park et al. JARO-JOURNAL OF THE ASSOCIATION FOR RESEARCH IN OTOLARYNGOLOGY
- Comparing auditory filter bandwidths, spectral ripple modulation detection, spectral ripple discrimination, and speech recognition: Normal and impaired hearing
- (2015) Evelyn Davies-Venn et al. JOURNAL OF THE ACOUSTICAL SOCIETY OF AMERICA
- Development and Validation of the Pediatric AzBio Sentence Lists
- (2014) Anthony J. Spahr et al. EAR AND HEARING
- DFNB16 is a frequent cause of congenital hearing impairment: implementation ofSTRCmutation analysis in routine diagnostics
- (2013) B. Vona et al. CLINICAL GENETICS
- Children's Identification of Consonants in a Speech-Shaped Noise or a Two-Talker Masker
- (2013) Lori J. Leibold et al. JOURNAL OF SPEECH LANGUAGE AND HEARING RESEARCH
- Psychoacoustic Performance and Music and Speech Perception in Prelingually Deafened Children with Cochlear Implants
- (2012) Kyu Hwan Jung et al. AUDIOLOGY AND NEURO-OTOLOGY
- Assessing the role of spectral and intensity cues in spectral ripple detection and discrimination in cochlear-implant users
- (2012) Elizabeth S. Anderson et al. JOURNAL OF THE ACOUSTICAL SOCIETY OF AMERICA
- Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment
- (2011) Lauren J. Francey et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Acoustic temporal modulation detection and speech perception in cochlear implant listeners
- (2011) Jong Ho Won et al. JOURNAL OF THE ACOUSTICAL SOCIETY OF AMERICA
- Spatial Selective Auditory Attention in the Presence of Reverberant Energy: Individual Differences in Normal-Hearing Listeners
- (2010) Dorea Ruggles et al. JARO-JOURNAL OF THE ASSOCIATION FOR RESEARCH IN OTOLARYNGOLOGY
- Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane
- (2010) Elisabeth Verpy et al. JOURNAL OF COMPARATIVE NEUROLOGY
- Spectral modulation detection and vowel and consonant identifications in cochlear implant listeners
- (2009) Aniket A. Saoji et al. JOURNAL OF THE ACOUSTICAL SOCIETY OF AMERICA
- Characterization of a Spontaneous, Recessive, Missense Mutation Arising in the Tecta Gene
- (2008) Miguel Ángel Moreno-Pelayo et al. JARO-JOURNAL OF THE ASSOCIATION FOR RESEARCH IN OTOLARYNGOLOGY
- Stereocilin-deficient mice reveal the origin of cochlear waveform distortions
- (2008) Elisabeth Verpy et al. NATURE
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started