Human myosin VIIA responsible for the Usher 1B syndrome: A predicted membrane-associated motor protein expressed in developing sensory epithelia

Proceedings of the National Academy of Sciences of the United States of America

Volumn 93, Issue 8, 1996, Pages 3232-3237

  Weil, Dominique ^a   Lévy, Gallia ^a   Sahly, Iman ^b   Lévi Acobas, Fabienne ^a   Blanchard, Stéphane ^a   El Amraoui, Aziz ^a   Crozet, Fabien ^a   Philippe, Hervé ^c   Abitbol, Marc ^b   Petit, Christine ^a  

^a CNRS   (France)

^b UNIVERSITÉ PARIS DESCARTES   (France)

^c UNIVERSITÉ PARIS SACLAY   (France)

Author keywords

alternative mRNA splicing; band 4.1 family; deafness; retinitis pigmentosa; unconventional myosins

Indexed keywords

MYOSIN;

ALTERNATIVE RNA SPLICING; ANIMAL TISSUE; ARTICLE; CARBOXY TERMINAL SEQUENCE; DIMERIZATION; EMBRYO; FETUS; HUMAN; HUMAN TISSUE; IN SITU HYBRIDIZATION; MORPHOGENESIS; MOUSE; NEUROEPITHELIUM; NONHUMAN; PERCEPTION DEAFNESS; PHOTORECEPTOR; PIGMENT EPITHELIUM; PRIORITY JOURNAL; PROTEIN STRUCTURE; RETINITIS PIGMENTOSA; SEQUENCE HOMOLOGY; STEREOCILIUM; USHER SYNDROME; VESTIBULAR DISORDER;

ALTERNATIVE SPLICING; AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; BINDING SITES; DEAFNESS; DNA PROBES; DNA, COMPLEMENTARY; DYNEIN ATPASE; EPITHELIUM; FETUS; GENE EXPRESSION; HUMANS; IN SITU HYBRIDIZATION; MICE; MOLECULAR SEQUENCE DATA; MYOSINS; NERVOUS SYSTEM; RETINITIS PIGMENTOSA; SEQUENCE HOMOLOGY, AMINO ACID; SYNDROME; VESTIBULAR DISEASES;

EID: 9244233852     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.93.8.3232     Document Type: Article

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