Double gene deletion reveals lack of cooperation between claudin 11 and claudin 14 tight junction proteins

Cell and Tissue Research

Volumn 333, Issue 3, 2008, Pages 427-438

  Elkouby Naor, Liron ^a   Abassi, Zaid ^a   Lagziel, Ayala ^b   Gow, Alexander ^c   Ben Yosef, Tamar ^a  

^a TECHNION ISRAEL INSTITUTE OF TECHNOLOGY   (Israel)

^b NATIONAL INSTITUTE ON DEAFNESS AND OTHER COMMUNICATION DISORDERS   (United States)

^c WAYNE STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Claudin 11; Claudin 14; Knockout mouse; Tight junction

Indexed keywords

CALCIUM ION; CLAUDIN; CLAUDIN 11; CLAUDIN 14; MAGNESIUM ION; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; EVOKED BRAIN STEM AUDITORY RESPONSE; FEMALE; GENE DELETION; HEARING IMPAIRMENT; HENLE LOOP; KIDNEY DISTAL TUBULE; KIDNEY FUNCTION; KIDNEY PROXIMAL TUBULE; MALE; MALE STERILITY; MOUSE; NEUROLOGIC DISEASE; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; PROTEIN PROTEIN INTERACTION; TIGHT JUNCTION; URINARY EXCRETION; WILD TYPE;

ANIMALS; COCHLEA; GENE DELETION; HEARING LOSS; KIDNEY; KIDNEY FUNCTION TESTS; MEMBRANE PROTEINS; MICE; MICE, KNOCKOUT; NERVE TISSUE PROTEINS; PHENOTYPE; TIGHT JUNCTIONS;

ANIMALIA; MUS;

EID: 49749124586     PISSN: 0302766X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00441-008-0621-9     Document Type: Article

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