Failure of fluid absorption in the endolymphatic sac initiates cochlear enlargement that leads to deafness in mice lacking Pendrin expression

PLoS ONE

Volumn 5, Issue 11, 2010, Pages

  Kim, Hyoung Mi ^a   Wangemann, Philine ^a  

^a KANSAS STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PENDRIN; SEROTONIN TRANSPORTER; ANION TRANSPORT PROTEIN; SLC26A4 PROTEIN, MOUSE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; COCHLEAR ENLARGEMENT; CONTROLLED STUDY; DEVELOPMENTAL STAGE; EMBRYO; ENDOLYMPH; ENDOLYMPHATIC SAC; EX VIVO STUDY; FEMALE; FLUID TRANSPORT; HEARING IMPAIRMENT; INNER EAR DISEASE; MOUSE; NEWBORN; NONHUMAN; ONSET AGE; ORGAN CULTURE; PATHOGENESIS; PROTEIN EXPRESSION; 129 MOUSE; ABSORPTION; ANIMAL; ANIMAL EMBRYO; COCHLEA; CONFOCAL MICROSCOPY; CONGENITAL MALFORMATION; GENETICS; GROWTH, DEVELOPMENT AND AGING; HUMAN; IMMUNOHISTOCHEMISTRY; MALE; METABOLISM; MOUSE MUTANT; PRENATAL DEVELOPMENT; SECRETION; TIME;

MUS;

ABSORPTION; ANIMALS; ANIMALS, NEWBORN; ANION TRANSPORT PROTEINS; COCHLEA; DEAFNESS; EMBRYO, MAMMALIAN; ENDOLYMPH; ENDOLYMPHATIC SAC; FEMALE; HUMANS; IMMUNOHISTOCHEMISTRY; MALE; MICE; MICE, 129 STRAIN; MICE, KNOCKOUT; MICROSCOPY, CONFOCAL; TIME FACTORS;

EID: 78649511437     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0014041     Document Type: Article

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