Expression of Pcdh15 in the inner ear, nervous system and various epithelia of the developing embryo

Mechanisms of Development

Volumn 105, Issue 1-2, 2001, Pages 163-166

  Murcia, Crystal L ^a   Woychik, Richard P ^b,c  

^a CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b CASE WESTERN RESERVE UNIVERSITY   (United States)

^c ILLUMINA INC   (United States)

Author keywords

Ames waltzer; Cadherin; Cell adhesion molecule; Deafness; Pcdh15; Protocadherin

Indexed keywords

CADHERIN; PROTOCADHERIN 15; UNCLASSIFIED DRUG;

ARTICLE; EMBRYO; EMBRYO DEVELOPMENT; EPITHELIUM; GENE EXPRESSION; IN SITU HYBRIDIZATION; INNER EAR; MOUSE; MUTATION; NERVOUS SYSTEM; NONHUMAN; PRIORITY JOURNAL; PROTEIN FAMILY;

ANIMALS; CADHERINS; CENTRAL NERVOUS SYSTEM; EAR; EPITHELIUM; IN SITU HYBRIDIZATION; KIDNEY; MUTATION; NERVOUS SYSTEM; PROTEIN PRECURSORS; RNA, MESSENGER; TIME FACTORS; ZEBRAFISH;

EID: 0034955437     PISSN: 09254773     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0925-4773(01)00388-4     Document Type: Article

References (7)

1. Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer
2. The mouse Ames Waltzer hearing-loss mutant is caused by mutation of Pcdh15, a new protocadherin gene
3. Planar polarization of Drosophila and vertebrate epithelia
4. The ETS domain factor Pet-1 is an early and precise marker of central serotonin neurons and interacts with a conserved element in serotonergic genes
5. Expression of a novel protocadherin, OL-protocadherin, in a subset of functional systems in the developing mouse brain
6. Protocadherins: a large family of cadherin-related molecules in central nervous system
7. Characterization of two novel protocadherins (PCDH8 and PCDH9) localized on human chromosome 13 and mouse chromosome 14