A class III myosin expressed in the retina is a potential candidate for Bardet-Biedl syndrome

Genomics

Volumn 79, Issue 5, 2002, Pages 621-624

  Dosé, Andréa C ^a   Burnside, Beth ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MYOSIN;

ARTICLE; BARDET BIEDL SYNDROME; CHROMOSOME 2Q; DROSOPHILA MELANOGASTER; GENE MAPPING; NONHUMAN; PHOTORECEPTOR; PRIORITY JOURNAL; PROTEIN EXPRESSION; RETINA; RETINA DEGENERATION;

DROSOPHILA MELANOGASTER; MELANOGASTER;

EID: 0036252649     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.2002.6749     Document Type: Article

References (20)

1. Cloning and chromosomal localization of a human class III myosin
2. Localization of the Usher syndrome type 1F (Ush1F) to chromosome 10
3. A fifth locus for Bardet-Biedl syndrome maps to chromosome 2q31
4. Myosin structure and function in cell motility
5. Regulation of the enzymatic and motor activities of myosin I
6. A myosin family tree
7. Class V myosins
8. Myosins: A diverse superfamily
9. The Drosophila NINAC kinase-myosin is a calmodulin-binding protein required for phototransduction and prevention of light-induced retinal degeneration
10. The Drosophila ninaC locus encodes two photoreceptor cell specific proteins with domains homologous to protein kinases and the myosin heavy chain head
11. A myosin III from Limulus eyes is a clock-regulated phosphoprotein
12. A potential vertebrate homologue of Drosophila NINAC
13. A vertebrate homologue of the Limulus class III myosin
14. A millenial myosin census
15. Gapped BLAST and PSI-BLAST: A new generation of protein database search programs
16. The cardinal manifestations of Bardet-Biedl syndrome, a form of Lawrence-Moon-Biedl syndrome
17. The importance of renal impairmant in the natural history of Bardet-Biedl syndrome
18. Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2)
19. Cloning of a novel C-terminal kinesin (KIFC3) that maps to human chromosome 16q13-q21 and thus is a candidate for Bardet-Biedl syndrome
20. The cloning and developmental expression of unconventional myosin IXA (Myo9A), a gene in the Bardet-Biedl syndrome (BBS4) region at chromosome 15q22-q23