Auditory function in the Tc1 mouse model of down syndrome suggests a limited region of human chromosome 21 involved in otitis media

PLoS ONE

Volumn 7, Issue 2, 2012, Pages

  Kuhn, Stephanie ^a   Ingham, Neil ^b   Pearson, Selina ^b   Gribble, Susan M ^b   Clayton, Stephen ^b   Steel, Karen P ^b   Marcotti, Walter ^a  

^a UNIVERSITY OF SHEFFIELD   (United Kingdom)

^b WELLCOME TRUST SANGER INSTITUTE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

LARGE CONDUCTANCE CALCIUM ACTIVATED POTASSIUM CHANNEL; C8ORF4 PROTEIN, MOUSE; TUMOR PROTEIN;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUDITORY THRESHOLD; BRAIN STEM RESPONSE; CHROMOSOME 21; COCHLEA; CONTROLLED STUDY; DISEASE PREDISPOSITION; DOWN SYNDROME; FEMALE; FUNCTIONAL ASSESSMENT; GENETIC ASSOCIATION; GENOTYPE; HAIR CELL; HEARING; HOMOZYGOSITY; HYPERPOLARIZATION; INNER EAR; MALE; MEMBRANE STEADY POTENTIAL; MIDDLE EAR; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; OTITIS MEDIA; SIGNAL TRANSDUCTION; ANIMAL; DISEASE MODEL; EVOKED BRAIN STEM AUDITORY RESPONSE; GENETICS; HUMAN; PATHOPHYSIOLOGY; PHYSIOLOGY; TRANSGENIC MOUSE;

MUS;

ANIMALS; CHROMOSOMES, HUMAN, PAIR 21; COCHLEA; DISEASE MODELS, ANIMAL; DOWN SYNDROME; EVOKED POTENTIALS, AUDITORY, BRAIN STEM; HAIR CELLS, AUDITORY; HEARING; HUMANS; MICE; MICE, TRANSGENIC; NEOPLASM PROTEINS; OTITIS MEDIA;

EID: 84856935541     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0031433     Document Type: Article

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