Hearing loss in the RBF/DnJ mouse, a proposed animal model of Usher syndrome type IIa
Tài liệu tham khảo
Bascom, 1992, Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGM, Am. J. Hum. Genet., 51, 1028
Bonhomme, 1989, The wild house mouse and its relatives, 649
Chang, 1993, New mouse primary retinal degeneration (rd-3), Genomics, 16, 45, 10.1006/geno.1993.1138
Copeland, 1991, Development and applications of a molecular genetic linage map of the mouse genome, Trend. Genet., 7, 113, 10.1016/0168-9525(91)90085-5
Copeland, 1993, A genetic linkage map of the mouse, Science, 262, 57, 10.1126/science.8211130
DeBry, 1996, Human/mouse orthology, Genomics, 33, 337, 10.1006/geno.1996.0209
Dietrich, 1994, Nature Genet., 7, 220, 10.1038/ng0694supp-220
Dryja, 1995, Molecular genetics of retinitis pigmentosa, Hum. Mol. Genet., 4, 1739, 10.1093/hmg/4.suppl_1.1739
Festing, 1989, Inbred strains of mice, 636
Fletcher, 1986, Genetic expression of cyclic GMP phosphodiesterase activity defines abnormal photoreceptor differentiation in neurological mutant of inherited retinal degeneration, J. Neurochem., 46, 1240, 10.1111/j.1471-4159.1986.tb00644.x
Gibson, 1995, A type VII myosin encoded by the mouse deafness gene shaker-1, Nature, 374, 62, 10.1038/374062a0
Green, 1991
Heckenlively, 1993, Variable expressivity of rd3 retinal degeneration dependent on background strain, 273
Heckenlively, 1989, Screening for mouse retinal degenerations, Doc. Ophthalmol., 71, 229, 10.1007/BF00170972
Henry, 1992, The mouse as a model for human audition, Audiology, 31, 181, 10.3109/00206099209081653
Kajiwara, 1994, Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci, Science, 264, 1604, 10.1126/science.8202715
Kimberling, 1995, Clinical and molecular genetics of Usher syndrome, J. Am. Acad. Audiol., 6, 63
Kimberling, 1995, Gene mapping of Usher syndrome type IIa: Localization of the gene to a 2.1 centimorgan segment on chromosome 1q41, Am. J. Hum. Genet., 56, 216
1996
Nadeau, 1989, Maps of linkage and synteny homologies between mouse and man, Trends Genet., 5, 82, 10.1016/0168-9525(89)90031-0
Nadeau, 1991, Comparative gene mapping, genome duplication and the genetics of hearing, Ann. NY Acad. Sci., 630, 49, 10.1111/j.1749-6632.1991.tb19575.x
Naash, 1996, Polygenic disease and retinitis pigmentosa: albinism exacerbates photoreceptor degeneration induced by the expression of a mutant opsin in transgenic mice, J. Neurosci., 16, 7853, 10.1523/JNEUROSCI.16-24-07853.1996
Roderick, 1994
Steel, 1995, Inherited hearing defects in mice, Annu. Rev. Genet., 29, 675, 10.1146/annurev.ge.29.120195.003331
Sumegi, 1996, The construction of a yeast artificial chromosome (YAC) contig in the vicinity of the Usher syndrome type IIa (USH2A) gene in 1q41, Genomics, 35, 79, 10.1006/geno.1996.0325
Takumida, 1989, The endolymphatic sac and inner ear homeostasis, Hear. Res., 40, 17, 10.1016/0378-5955(89)90095-6
Weil, 1995, Defective myosin VIIA gene responsible for Usher syndrome type 1B, Nature, 374, 60, 10.1038/374060a0
Weil, 1996, Human myosin VIIa responsible for the Usher IB syndrome, 93, 3232
1983