Three deaf mice: Mouse models for TECTA-based human hereditary deafness reveal domain-specific structural phenotypes in the tectorial membrane

Human Molecular Genetics

Volumn 23, Issue 10, 2014, Pages 2551-2568

  Legan, P Kevin ^a   Goodyear, Richard J ^a   Morín, Matías ^b,c   Mencia, Angeles ^b,c   Pollard, Hilary ^a   Olavarrieta, Leticia ^a,b,c   Korchagina, Julia ^a   Modamio Hoybjor, Silvia ^b,c   Mayo, Fernando ^b,c   Moreno, Felipe ^b,c   Moreno Pelayo, Miguel Angel ^b,c   Richardson, Guy P ^a  

^a UNIVERSITY OF SUSSEX   (United Kingdom)

^b INSTITUTO RAMÓN Y CAJAL DE INVESTIGACIÓN SANITARIA IRYCIS   (Spain)

^c CENTRO DE INVESTIGACIÓN BIOMÉDICA EN RED DE ENFERMEDADES RARAS CIBERER   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOSYLPHOSPHATIDYLINOSITOL ANCHORED PROTEIN; MOLECULAR MOTOR; PRES PROTEIN, MOUSE; SCLEROPROTEIN; TECTA PROTEIN, HUMAN;

129 MOUSE; ANIMAL; AUDITORY STIMULATION; COCHLEA DUCT; CORTI ORGAN; DISEASE MODEL; FEMALE; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; GENETICS; HAIR CELL; HEARING IMPAIRMENT; HOMOZYGOTE; HUMAN; MALE; METABOLISM; MISSENSE MUTATION; PATHOLOGY; PATHOPHYSIOLOGY; PHENOTYPE; REFLEX EPILEPSY; TRANSGENIC MOUSE;

ACOUSTIC STIMULATION; ANIMALS; DEAFNESS; DISEASE MODELS, ANIMAL; EPILEPSY, REFLEX; EXTRACELLULAR MATRIX PROTEINS; FEMALE; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GPI-LINKED PROTEINS; HAIR CELLS, AUDITORY, INNER; HOMOZYGOTE; HUMANS; MALE; MICE, 129 STRAIN; MICE, TRANSGENIC; MOLECULAR MOTOR PROTEINS; MUTATION, MISSENSE; ORGAN OF CORTI; PHENOTYPE; TECTORIAL MEMBRANE;

EID: 84898793240     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddt646     Document Type: Article

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