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COCH gene
Known as:
COCH
, COCH-5B2
, COCH5B2
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National Institutes of Health
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Related topics
Related topics
1 relation
COCH protein, human
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Novel COCH mutation in a family with autosomal dominant late onset sensorineural hearing impairment and tinnitus.
Emily Gallant
,
L. Francey
,
+5 authors
I. Krantz
American Journal of Otolaryngology
2013
Corpus ID: 22862465
2013
2013
Clinical characterization of a novel COCH mutation G87V in a Chinese DFNA9 family.
Dong-ye Chen
,
Y. Chai
,
T. Yang
,
Hao Wu
International Journal of Pediatric…
2013
Corpus ID: 2569132
2013
2013
The LIF receptor antagonist PEGLA is effectively delivered to the uterine endometrium and blocks LIF activity in cynomolgus monkeys.
Lindsey C Aschenbach
,
Kim E. Hester
,
Nicole C McCann
,
Jian‐guo Zhang
,
E. Dimitriadis
,
D. Duffy
Contraception
2013
Corpus ID: 2490156
2010
2010
A novel mutation in COCH—implications for genotype‐phenotype correlations in DFNA9 hearing loss
M. Hildebrand
,
Luke C. Gandolfo
,
+7 authors
M. Bahlo
The Laryngoscope
2010
Corpus ID: 21300569
To determine the cause of autosomal dominant hearing loss segregating in an American family.
2009
2009
Cochlin Expression in Anterior Segment Organ Culture Models after TGF 2 Treatment
S. Bhattacharya
,
B. Gabelt
,
J. Ruiz
,
R. Picciani
,
P. Kaufman
2009
Corpus ID: 166420
RESULTS. TGF 2 infusion produced elevated IOP in MOCAS (usually after 5 days), that was approximately 45% greater than baseline…
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2007
2007
Phenotype Description of a Novel DFNA9/COCH Mutation, I109T
R. Pauw
,
P. Huygen
,
+4 authors
W. Cremers
Annals of Otology, Rhinology and Laryngology
2007
Corpus ID: 26531200
Objectives: This is a report of the audiological and vestibular characteristics of a Dutch DFNA9 family with a novel mutation…
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2006
2006
Identification of a novel COCH mutation, G87W, causing autosomal dominant hearing impairment (DFNA9)
R. Collin
,
R. Pauw
,
+4 authors
H. Kremer
American Journal of Medical Genetics. Part A
2006
Corpus ID: 43399742
Non-syndromic hearing impairment (NSHI) is a very heterogeneous disorder, both clinically and genetically, and can be inherited…
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2005
2005
Novel soluble molecule, Akhirin, is expressed in the embryonic chick eyes and exhibits heterophilic cell‐adhesion activity
M. Ahsan
,
K. Ohta
,
S. Kuriyama
,
Hideaki Tanaka
Developmental Dynamics
2005
Corpus ID: 25833217
Akhirin, a novel secreted protein of 90 kDa, has been identified using signal sequence trap cDNA screening of an embryonic day 6…
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2001
2001
Hereditary Otovestibular Dysfunction and Ménière's Disease in a Large Belgian Family Is Caused by a Missense Mutation in the COCH Gene
M. Verstreken
,
F. Declau
,
+9 authors
P. V. D. Heyning
Otology and Neurotology
2001
Corpus ID: 45918026
Objective To report the clinical, auditory, and vestibular characteristics of a nonsyndromic otovestibular dysfunction in a large…
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2001
2001
Speech recognition scores related to age and degree of hearing impairment in DFNA2/KCNQ4 and DFNA9/COCH.
S. Bom
,
E. De Leenheer
,
+10 authors
C. Cremers
Archives of Otolaryngology - Head and Neck…
2001
Corpus ID: 15625683
OBJECTIVE To analyze the relationship between pure-tone hearing threshold and speech recognition performance in DFNA2/KCNQ4 and…
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