A subtracted cDNA library from the Zebrafish (Danio rerio) embryonic inner ear

Genome Research

Volumn 12, Issue 6, 2002, Pages 1007-1011

  Coimbra, Roney S ^a   Weil, Dominique ^a   Brottier, Phillipe ^b   Blanchard, Stéphane ^a   Levi, Michael ^b   Hardelin, Jean Pierre ^a   Weissenbach, Jean ^b   Petit, Christine ^a  

^a CNRS   (France)

^b CENTRE NATIONAL DE SÉQUENÇAGE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; COMPLEMENTARY DNA; CONTIG; PROTEIN;

AMINO ACID SEQUENCE; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CELL DIFFERENTIATION; CONTIG MAPPING; CONTROLLED STUDY; DNA ISOLATION; DNA LIBRARY; EMBRYO; EMBRYO CELL; EMBRYO DEVELOPMENT; EPITHELIUM; EXPRESSED SEQUENCE TAG; FERTILIZATION; FISH GENETICS; GENE EXPRESSION; GENETIC CODE; HAIR CELL; INNER EAR; INNERVATION; LIVER; NEUROBLAST; NONHUMAN; NUCLEOTIDE SEQUENCE; OUTCOMES RESEARCH; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SEQUENCE DATABASE; SEQUENCE HOMOLOGY; SPECIES DIFFERENCE; UNINDEXED SEQUENCE; VALIDATION PROCESS; ZEBRA FISH;

ANIMALIA; DANIO; DANIO RERIO; VERTEBRATA;

EID: 0036075442     PISSN: 10889051     EISSN: None     Source Type: Journal    
DOI: 10.1101/gr.227502     Document Type: Article

References (49)

1. Human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family
2. A large-scale insertional mutagenesis screen in zebrafish
3. Otogelin: A glycoprotein specific to the acellular membranes of the inner ear
4. Hair cell regeneration: The identities of progenitor cells, potential triggers and instructive cues
5. Inherited diseases of the inner ear in man in the light of studies on the mouse
6. The relationship between abnormalities of pigmentation and of the inner ear
7. Genetic malformations of the inner ear in the mouse and man
8. Overexpression of a zebrafish homologue of the Drosophila neurogenic gene Delta perturbs differentiation of primary neurons and somite development
9. Regional expression of three homeobox transcripts in the inner ear of zebrafish embryos
10. Mariner is defective in myosin VIIA: A zebrafish model for human hereditary deafness
11. A genetic linkage map for zebrafish: Comparative analysis of genes and expressed sequences
12. A radiation hybrid map of the zebrafish genome
13. A type VII myosin encoded by the mouse deafness gene Shaker-1
14. Early ear development in the embryo of the zebrafish, Danio rerio
15. Delta-Notch signalling and the patterning of sensory cell differentiation in the zebrafish ear: Evidence from the mind bomb mutant
16. The identification of genes with unique and essential functions in the development of the zebrafish, Danio rerio
17. Molecular markers for cell types of the inner ear and candidate genes for hearing disorders
18. Table of gene expression in the developing ear
19. Radiation hybrid mapping of the zebrafish genome
20. Eya1 expression in the developing ear and kidney: Towards the understanding of the pathogenesis of branchio-oto-renal (BOR) syndrome
21. A microsatellite genetic linkage map for zebrafish (Danio rerio)
22. Rules for the production of sensory cells. Regeneration of vertebrate sensory cell
23. Essential role of BETA2/NeuroD1 in development of the vestibular and auditory systems
24. Mutations affecting development of the zebrafish ear
25. Retinoic acid rescues inner ear defects in Hoxa1 deficient mice
26. Zebrafish inner ear sensory surfaces are similar to those in goldfish
27. Sound detection and processing by fish: Critical review and major research questions
28. Vertebrate genome evolution and the zebrafish gene map
29. Effects of retinoid and thyroid receptors during development of the inner ear
30. Retinoic acid modulation of the early development of the inner ear is associated with control of c-fos expression
31. Regionalized expression of Nkx5-1, Nkx5-2, Pax2 and sek genes during mouse inner ear development
32. Isolation of novel and known genes from a human fetal cochlear cDNA library using subtractive hybridization and differential screening
33. Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunction
34. Differential and overlapping expression domains of Dlx-2 and Dlx-3 suggest distinct roles for Distal-less homeobox genes in craniofacial development
35. The zebrafish eya1 gene and its expression pattern during embryogenesis
36. Zebrafish genetic map with 2000 microsatellite markers
37. Targeted disruption of Otog results in deafness and severe imbalance
38. Inherited hearing defects in mice
39. Attainment of minimal biological variability and measurements of genotoxicity: Production of homozygous diploid zebra fish
40. Segregation analyses and gene-centromere distances in zebrafish
41. Production of clones of homozygous diploid zebra fish (Brachydanio rerio)
42. The development of the vertebrate inner ear
43. A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C
44. Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus
45. Epithelial fusion during early semicircular canal formation in the embryonic zebrafish, Brachydanio rerio
46. Defective; myosin VIIA gene responsible for Usher syndrome type 1B
47. Mutations affecting development of the zebrafish inner ear and lateral line
48. A mutation in OTOF, encoding otoferlin, a FER-1 like protein, causes DFNB9, a nonsyndromic form of deafness
49. A mutation in the Lunatic fringe gene suppresses the effects of a Jagged2 mutation on inner hair cell development in the cochlea