Genetic localization and phenotypic expression of X-linked cataract (Xcat) in Mus musculus

Genetical Research

Volumn 56, Issue 2-3, 1990, Pages 157-162

  Favor, Jack ^a   Pretsch, Walter ^a  

^a INSTITUTE OF EPIDEMIOLOGY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CATARACT; FEMALE; GENE ACTIVITY; GENE LOCATION; GENETIC DISORDER; HUMAN; LENS EPITHELIUM; MOUSE; MUTATION; NONHUMAN; TOOTH DISEASE; X CHROMOSOME LINKAGE;

ANIMAL; CATARACT; CHROMOSOME MAPPING; FEMALE; GENE EXPRESSION; GENES; HUMAN; LINKAGE (GENETICS); MALE; MICE; MUTATION; PHENOTYPE; SEQUENCE HOMOLOGY, NUCLEIC ACID; SUPPORT, NON-U.S. GOV'T; X CHROMOSOME;

ANIMALIA; MUS MUSCULUS; MUSCULUS;

EID: 0025201544     PISSN: 00166723     EISSN: 14695073     Source Type: Journal    
DOI: 10.1017/S0016672300035242     Document Type: Article

References (20)

1. Charles D. J. & Pretsch W. (1987). Linear dose-response relationship of erythrocyte enzyme-activity mutations in offspring of ethylnitrosourea-treated mice. Mutation Research 176, 81–91.
2. Davisson M. T. & Roderick T. H. (1989). Linkage Map. In Genetic Variants and Strains of the Laboratory Mouse (ed. Lyon M.F. and Searle A.G.), 2nd Ed., pp. 413–427. Oxford, New York and Tokyo: Oxford University Press.
3. Ehling U. H. (1985). Induction and manifestation of hereditary cataracts. In Assessment of Risk from Low-Level Exposure to Radiation and Chemicals, (ed. Woodhead A.D., Shellabarger C. J., Pond V. and Hollaender A.), pp. 345–368. New York: Plenum Publishing Corp.
4. Ehling U. H., Favor J., Kratochvilova J. & Neuhäuser-Klaus A. (1982). Dominant cataract mutations and specific-locus mutations in mice induced by radiation or ethylnitrosourea, Mutation Research 92, 181–192.
5. Favor J. (1983). A comparison of the dominant cataract and recessive specific-locus mutation rates induced by treatment of male mice with ethylnitrosourea, Mutation Research 110, 367–382.
6. Favor J. (1986). The frequency of dominant cataract and recessive specific-locus mutations in mice derived from 80 or 160mg ethylnitrosourea per kg body weight treated spermatogonia, Mutation Research 162, 69–80.
7. Favor J. & Pretsch W. (1987). Position of Xcat, a new X-linked cataract mutation, Mouse News Letters 77, 139.
8. Favor J., Neuhäuser-Klaus A. & Ehling U. H. (1987). Radiation-induced forward and reverse specific locus mutations and dominant cataract mutations in treated strain BALB/c and DBA/2 male mice, Mutation Research 177, 161–169.
9. Favor J., Neuhäuser-Klaus A. & Ehling U. H. (1988). The effect of dose fractionation on the frequency of ethylnitrosourea-induced dominant cataract and recessive specific locus mutations in germ cells of the mouse. Mutation Research 198, 269–275.
10. Favor J., Neuhäuser-Klaus A. & Ehling U. H. (1990). The frequency of dominant cataract and recessive specificlocus mutations and mutation mosaics in F1 mice derived from post-spermatogonial treatment with ethylnitrosourea, Mutation Research 229, 105–114.
11. Graw J., Favor J., Neuhäuser-Klaus A. & Ehling U. H. (1986). Dominant cataract and recessive specific locus mutations in offspring of X-irradiated male mice, Mutation Research 159, 47–54.
12. Green M. C. (1989). Catalog of mutant genes and polymorphic loci. In Genetic Variants and Strains of the Laboratory Mouse (ed. Lyon M.F. and Searle A.G.) 2nd ed., pp. 12–403. Oxford, New York and Tokyo: Oxford University Press
13. Kratochvilova J. (1981). Dominant cataract mutations detected in offspring of gamma-irradiated male mice, Journal of Heredity 72, 302–307.
14. Kratochvilova J. & Ehling U. H. (1979). Dominant cataract mutations induced by Υ-irradiation of male mice, Mutation Research 63, 221–223.
15. Kratochvilova J. & Favor J. (1988). Phenotypic characterization and genetic analysis of twenty dominant cataract mutations detected in offspring of irradiated male mice, Genetical Research 52, 125–134.
16. Kratochvilova J., Favor J. & Neuhäuser-Klaus A. (1988). Dominant cataract and recessive specific-locus mutations detected in offspring of procarbazine-treated male mice, Mutation Research 198, 295–301.
17. McKusick V. A. (1989). Mendelian Inheritance in Man. 8th Ed., Baltimore and London: The Johns Hopkins University Press.
18. Peters J., Ball S. T., Charles D. J., Pretsch W., Bulfield G., Miller D. & Chapman V. M. (1988). The localization of G6pd, glucose-6-phosphate dehydrogenase, and max, muscular dystrophy in the mouse X chromosome, Genetical Research 52, 195–201.
19. Pretsch W., Charles D. J. & Merkle S. (1988). X-linked glucose-6-phosphate dehydrogenase deficiency in Mus musculus, Biochemical Genetics 26, 89–103.
20. West J. D. (1978). Clonal growth versus cell mingling. In Genetic Mosaics and Chimeras in Mammals (ed. Russell L.B.), pp. 361–377. New York and London: Plenum Publishing Corp.