Environmental chemical mutagens and genetic risks: Lessons from radiation genetics

Environmental and Molecular Mutagenesis

Volumn 28, Issue 2, 1996, Pages 65-70

  Sankaranarayanan, K ^a  

^a LEIDEN UNIVERSITY   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ENVIRONMENTAL CHEMICAL; MUTAGENIC AGENT;

ANIMAL MODEL; BIOMETRY; GENETIC RISK; HUMAN; IN VITRO STUDY; IONIZING RADIATION; MOLECULAR BIOLOGY; MUTATION; NONHUMAN; RADIATION DOSE; RISK ASSESSMENT; SHORT SURVEY; STATISTICAL ANALYSIS; TECHNIQUE;

ANIMALS; ENVIRONMENTAL POLLUTANTS; GENETIC DISEASES, INBORN; HUMANS; MODELS, GENETIC; MOLECULAR BIOLOGY; MUTAGENESIS; MUTAGENS; MUTATION; POPULATION; RISK FACTORS; TRINUCLEOTIDE REPEATS;

ANIMALIA;

EID: 0029861805     PISSN: 08936692     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-2280(1996)28:2<65::AID-EM1>3.0.CO;2-D     Document Type: Short Survey

References (24)

1. Bates G, Lehrach H (1994): Trinucleotide repeat expansions and human genetic disease. BioEssays 16:277-284.
2. Campuzano V, Moniermini L, Moltò MD, Pianese L, Cessée M, Cavalcanti F, Monros E, Rodius F, Duclos F, Montincelli A, Zara F, Canizares J, Koutnikova H, Bidichandani SI, Gellera C, Brice A, Trouillas P, De Michele G, Filla A, De Frutos R, Palau F, Patel PI, Di Donato S, Mandel JL, Cocozza S, Koenig M, Pandolfo M (1996): Friedreich's ataxia: Autosomal recessive disease caused by an intronic GAA triplet repeat expansion. Science 271:1423-1427.
3. Carrano AV (1994): Human genome project and mutation research: A mating that needs to happen. Environ Mol Mutagen 23: (Suppl. 24):39-43.
4. Cattanach BM, Burtenshaw MD, Raspberry C, Evans EP (1993): Large deletions and other gross forms of chromosome imbalance compatible with viability and fertility in the mouse. Nature Genet 3:56-61.
5. Cattanach BM, Evans EP, Raspberry C, Burtenshaw MD (1996): Incidence and distribution of radiation-induced large deletions in the mouse. In: Proceedings 10th International Congress of Radiation Research (Aug 27-Sept 1, 1995, Würzburg, Germany), in press.
6. Cooper DN, Krawczak M (1993): "Human Gene Mutation." Oxford: Bios Scientific Publishers.
7. Johnson DK, Stubbs LJ, Culiat CT, Montgomery CS, Russell LB, Rinchik EM (1995): Molecular analysis of 36 mutations at the mouse pink-eyed dilution (p) locus of the mouse. Genetics 141:1563-1571.
8. Koide R, Ikeuchi T, Onodera O, Tanaka H, Igarashi S, Endo K, Takahashi H, Kondo R, Ishikawa A, Hayashi T, Saito M, Tomoda A, Miike T, Naito H, Ikuta F, Tsuji S (1994): Unstable expansion of CAG repeat in hereditary dentatorubral pallidoluysian atrophy (DRPLA). Nature Genet 6:9-13.
9. Maruyama H, Nakamura S, Matsuyama Z, Sakai T, Doyu M, Sobue G, Seto M, Tsujihata M, Oh-i T, Nishio T, Sunohara N, Takahashi R, Hayashi M, Nishino I, Ohtake T, Oda T, Nishimura M, Saida T, Matsumoto H, Baba M, Kawaguchi Y, Kakizuka A, Kawakami H (1994): Molecular features of the CAG repeals and clinical manifestation of Machado-Joseph disease. Hum Mol Genet 4:807-812.
10. McKusick VA (1994): "Mendelian Inheritance in Man." 11th ed. Vols. 1 and 2. Baltimore, Johns Hopkins.
11. Muenke M, Schell U (1995): Fibroblast growth factor receptor mutations in human skeletal disorders. Trends Genet 11:308-313.
12. Neel JV, Schull WJ, Awa AA, Satoh C, Kato H, Otake M, Yoshimoto Y (1990): The children of parents exposed to atomic bombs: Estimates of the gametic doubling dose of radiation for humans. Am J Hum Genet 46:1053-1072.
13. Rinchik EM, Russell LB (1990): Germ-line deletion mutations in the mouse: Tools for intensive functional and physical mapping of regions of mammalian genome. In: Davies KE, Tilghman SM (eds): "Genome Analysis: Vol 1, Genetic and Physical Mapping." Cold Spring Harbor, New York: Cold Spring Harbor Laboratory Press, pp 121-158.
14. Russell LB, Montgomery CS, Cacheiro NLA, Johnson DK (1995): Complementation analysis for 45 mutations encompassing the pink-eyed dilution (p) locus of the mouse. Genetics 141:1547-1562.
15. Sankaranarayanan K (1991a): Ionizing radiation and genetic risks: I. Epidemiological population genetic, biochemical and molecular aspects of Mendelian diseases. Mutat Res 258:3-49.
16. Sankaranarayanan K (1991b): Ionizing radiation and genetic risks: II. Nature of radiation-induced mutations in experimental mammalian in vivo systems. Mutat Res 258:51-73.
17. Sankaranarayanan K (1991c): Ionizing radiation and genetic risks: III. Nature of spontaneous and radiation-induced mutations in mammalian in vitro systems and mechanisms of induction of mutations by radiation. Mutat Res 258:75-97.
18. Sankaranarayanan K (1991d): Ionizing radiation and genetic risks: IV. Current methods, estimates of risk of Mendelian disease, human data and lessons from biochemical and molecular studies of mutations. Mutat Res 258:99-122.
19. Sankaranarayanan K (1993): Ionising radiation, genetic risk estimation and molecular biology: Impact and inferences. Trends Genet 9:79-84.
20. Sankaranarayanan K (1994): Estimation of genetic risks of exposure to chemical mutagens: Relevance of data on spontaneous mutations and of experience with ionizing radiation. Mutat Res 304:139-158.
21. Sankaranarayanan K (1996): The impact of advances in human molecular biology on radiation genetic risk estimation in man. In: Sood DD, Jain HC, Reddy AVR, Ramakumar KL, Kulkarni SG (eds): "100 Years of X-Rays and Radioactivity." Mumbai (India): Bhabha Atomic Res. Centre, pp 317-330.
22. Schinzel A, McKusick VA, Pearson PL (1994): Report of the committee for clinical disorders and chromosome aberrations. In: Cuticcchia AL, Pearson PL (eds): Human Gene Mapping. Baltimore: Johns Hopkins, pp 735-772.
23. United Nations (1993): "Sources and Effects of Ionizing Radiation." UNSCEAR 1993 Report to the General Assembly with Scientific Annexes. New York: United Nations.
24. US National Research Council - National Academy of Sciences (1994): "Science and Judgment in Risk Assessment." Washington, DC: National Academy Press.