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ArticlesPeer ReviewedFull Text
Otoancorin, An Inner Ear Protein Restricted to the Interface between the Apical Surface of Sensory Epithelia and Their Overlying Acellular Gels, Is Defective in Autosomal Recessive Deafness DFNB22
Author / Creator:Zwaenepoel, Ingrid ; Mustapha, Mirna ; Leibovici, Michel ; Verpy, Elisabeth ; Goodyear, Richard ; Liu, Xue Zhong ; Nouaille, Sylvie ; Nance, Walter E. ; Kanaan, Moien ; Avraham, Karen B. ; Tekaia, Fredj ; Loiselet, Jacques ; Lathrop, Marc ; Richardson, Guy ; Petit, Christine
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2002-04, Vol.99 (9), p.6240-6245
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ArticlesPeer ReviewedFull Text
Mesothelin, Stereocilin, and Otoancorin are predicted to have superhelical structures with ARM-type repeats
Author / Creator:Sathyanarayana, Bangalore K ; Hahn, Yoonsoo ; Patankar, Manish S ; Pastan, Ira ; Lee, Byungkook
Publisher:England: BioMed Central Ltd
Journal title:BMC structural biology, 2009-01, Vol.9 (1), p.1-1, Article 1
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ArticlesPeer ReviewedFull Text
Increased Spontaneous Otoacoustic Emissions in Mice with a Detached Tectorial Membrane
Author / Creator:Cheatham, Mary Ann ; Ahmad, Aisha ; Zhou, Yingjie ; Goodyear, Richard J. ; Dallos, Peter ; Richardson, Guy P.
Publisher:New York: Springer US
Journal title:Journal of the Association for Research in Otolaryngology, 2016-04, Vol.17 (2), p.81-88
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ArticlesPeer ReviewedFull Text
Preliminary studies on differential expression of auditory functional genes in the brain after repeated blast exposures
Author / Creator:Valiyaveettil, Manojkumar ; Alamneh, Yonas ; Miller, Stacy-Ann ; Hammamieh, Rasha ; Wang, Ying ; Arun, Peethambaran ; Wei, Yanling ; Oguntayo, Samuel ; Nambiar, Madhusoodana P
Publisher:United States: Department of Veterans Affairs
Journal title:Journal of rehabilitation research and development, 2012-01, Vol.49 (7), p.1153-1162
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ArticlesPeer ReviewedFull Text
Genomic analysis of a heterogeneous Mendelian phenotype: multiple novel alleles for inherited hearing loss in the Palestinian population
Author / Creator:Walsh, Tom ; Abu Rayan, Amal ; Abu Sa'ed, Judeh ; Shahin, Hashem ; Shepshelovich, Jeanne ; Lee, Ming K ; Hirschberg, Koret ; Tekin, Mustafa ; Salhab, Wa'el ; Avraham, Karen B ; King, Mary-Claire ; Kanaan, Moien
Publisher:England: BioMed Central
Journal title:Human genomics, 2006-01, Vol.2 (4), p.203-211, Article 203
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ArticlesPeer ReviewedFull Text
mouse model for human deafness DFNB22 reveals that hearing impairment is due to a loss of inner hair cell stimulation
Author / Creator:Lukashkin, Andrei N ; Legan, P. Kevin ; Weddell, Thomas D ; Lukashkina, Victoria A ; Goodyear, Richard J ; Welstead, Lindsey J ; Petit, Christine ; Russell, Ian J ; Richardson, Guy P
Publisher:United States: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2012-11, Vol.109 (47), p.19351-19356
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ArticlesPeer ReviewedFull Text
Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss
Author / Creator:Haraksingh, Rajini R ; Jahanbani, Fereshteh ; Rodriguez-Paris, Juan ; Gelernter, Joel ; Nadeau, Kari C ; Oghalai, John S ; Schrijver, Iris ; Snyder, Michael P
Publisher:England: BioMed Central Ltd
Journal title:BMC genomics, 2014-12, Vol.15 (1), p.1155-1155, Article 1155
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ArticlesPeer ReviewedFull Text
Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families
Author / Creator:Shahin, Hashem ; Walsh, Tom ; Rayyan, Amal Abu ; Lee, Ming K ; Higgins, Jake ; Dickel, Diane ; Lewis, Kristen ; Thompson, James ; Baker, Carl ; Nord, Alex S ; Stray, Sunday ; Gurwitz, David ; Avraham, Karen B ; King, Mary-Claire ; Kanaan, Moien
Publisher:Cham: Springer International Publishing
Journal title:European journal of human genetics : EJHG, 2010-04, Vol.18 (4), p.407-413
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ArticlesPeer ReviewedFull Text
Otoacorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22
Author / Creator:Zwaenepoel, Ingrid ; Mustapha, Mirna ; Leibovici, Michel ; Verpy, Elisabeth
Publisher:Washington: National Academy of Sciences
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2002-04, Vol.99 (9), p.6240
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Newsletter articlesFull Text
Hearing Disorders; Stanford University School of Medicine Describes Findings in Hearing Loss (Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural...
Publisher:Atlanta: NewsRx
Journal title:Life Science Weekly, 2015, p.3284
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Newsletter articlesFull Text
Hearing Loss; Research on Hearing Loss Reported by Scientists at Bethlehem University
Publisher:Atlanta: NewsRx
Journal title:Obesity, Fitness & Wellness Week, 2011
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ArticlesPeer ReviewedFull Text
Compound Heterozygosity for OTOA Truncating Variant and Genomic Rearrangement Cause Autosomal Recessive Sensorineural Hearing Loss in an Italian Family
Author / Creator:Ortore, Rocco Pio ; Leone, Maria Pia ; Palumbo, Orazio ; Petracca, Antonio ; Trecca, Eleonora M. C. ; D’Ecclesia, Aurelio ; Vigliaroli, Ciro Lucio ; Micale, Lucia ; Longo, Francesco ; Melchionda, Salvatore ; Castori, Marco
Publisher:Basel: MDPI AG
Journal title:Audiology research (Pavia, Italy), 2021-09, Vol.11 (3), p.443-451
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Otoancorin, An Inner Ear Protein Restricted to the Interface between the Apical Surface of Sensory Epithelia and Their Overlying Acellular Gels, Is Defective in Autosomal Recessive Deafness DFNB22

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Mesothelin, Stereocilin, and Otoancorin are predicted to have superhelical structures with ARM-type repeats

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Increased Spontaneous Otoacoustic Emissions in Mice with a Detached Tectorial Membrane

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Preliminary studies on differential expression of auditory functional genes in the brain after repeated blast exposures

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Genomic analysis of a heterogeneous Mendelian phenotype: multiple novel alleles for inherited hearing loss in the Palestinian population

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mouse model for human deafness DFNB22 reveals that hearing impairment is due to a loss of inner hair cell stimulation

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Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss

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Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families

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Otoacorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22

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Hearing Disorders; Stanford University School of Medicine Describes Findings in Hearing Loss (Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural...

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Hearing Loss; Research on Hearing Loss Reported by Scientists at Bethlehem University

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Compound Heterozygosity for OTOA Truncating Variant and Genomic Rearrangement Cause Autosomal Recessive Sensorineural Hearing Loss in an Italian Family

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