Genetic model

Jobe, PC, Mishra, PK, Ludwig, N and Dailey, JW (1991) Scope and contribution of genetic models to an understanding of the epilepsies. Crit. Rev. Neurobiol. 6 183-215. [Pg.350]

FEARON E R and VOGELSTEIN B (1990) A genetic model for colorectal tumorigenesis . Cell, 16, 759-67. [Pg.40]

Keffer J, Probert L, Cazlaris H, et al. Transgenic mice expressing human tumour necrosis factor a predictive genetic model of arthritis. EMBO J I99l 10(13) 4025 t031. [Pg.188]

McGuffin P (1991). Genetic models of madness. In P McGuffin and RM Murray (eds), The New Genetics of Mental Health (pp. 27-43). Butterworth-Heinemann, Oxford, UK. [Pg.274]

Opperman, C.H. and Bird, D.M. (1998) The soybean cyst nematode, Heterodera glycines a genetic model system for the study of plant-parasitic nematodes. Current Opinion in Plant Biology 1,342—346. [Pg.172]

Smith, C. B. and Kang, J. Cerebral protein synthesis in a genetic model of phenylketonuria. Proc. Natl Acad. Sci. U.S.A. 97 11014-11019, 2000. [Pg.682]

SELECTED GENETIC MODELS OF RELEVANCE TO AMYOTROPHIC LATERAL SCLEROSIS 735... [Pg.731]

More information about fitting genetic models can be found in Neale and Cardon (1992) and Neale (1995) and references cited therein. Let s now turn to some actual psychological traits and representative findings. [Pg.123]

Gerlai, R., Lahav, M., Guo, S., and Rosenthal, A., Drinks like a fish Zebra fish (Danio rerio) as a behaviour genetic model to study alcohol effects, Pharmacol. Biochem. Behav., 67, 773-792,2000. [Pg.288]

Gerlai, R., Zebra fish an unchartered behaviour genetic model, Behav. Genet., 33,461-468,2003. [Pg.288]

E. R. Fearon and B. Vogelstein, A genetic model for colorectal tumouri-genesis, Cell, 1990, 61, 759. [Pg.94]

Kontak, D.J. Smith, P.K. 1989. Sulphur isotopic composition of sulphides from the Beaver Dam and other Meguma Group-hosted gold deposits, Nova Scotia implioations for genetic models. Canadian Journal of Earth Sciences, 26, 1617-1629. [Pg.246]

Abstract strong commodity prices in the last few years have led to a remarkable renaissance of uranium exploration in Labrador, focused in a complex and geologically diverse region known as the Central Mineral Belt (CMB). Potentially economic epigenetic U deposits are mostly hosted by supracrustal rocks of Paleoproterozoic and Mesoproterozoic age, and are difficult to place in the traditional pantheon of uranium deposit types. Recent exploration work implies that structural controls are important in some examples, but the relationships between mineralization and deformation remain far from clear. Geochronological data imply at least three periods of uranium mineralization between 1900 and 1650 Ma. It seems likely that the Labrador CMB represents a region in which U (and other lithophile elements) were repeatedly and sequentially concentrated by hydrothermal processes. The current exploration boom lends impetus for systematic research studies that may ultimately lead to refined genetic models that may be applicable elsewhere. [Pg.481]

Uranium mineralization in the CMB is characterized by a diversity of style and host rocks, and it is naive to suppose that a single genetic model can explain all its variations. Like many metallogenic provinces in which incompatible (or lithophile ) elements are important, the CMB of Labrador seems to represent an area in which U has been repeatedly and perhaps sequentially concentrated, and... [Pg.484]

Traditional exploration for sandstone-type uranium deposits has centered on genetic models and radiometric methods (Morse 1969 Harshman 1970 Rubin 1970). However, these methods have become prohibitive for sandstone-type uranium deposits hidden at a depth of hundreds of metres (Riese et al. 1978). Radioactivity detectors are ineffective in regions where there is a relatively thin inactive overburden (Bowie etal. 1970). [Pg.489]

Seredkin, M.V., Zotov, I.A., Karchevskii, P.I. 2004. Geological and genetic model for the formation of the Kovdor massif and the accompanying apatite-magnetite deposit. Petrology, 12, 519-539 (Transl. from Rus.)... [Pg.500]

The genesis of the Nash Creek deposit has been problematic as it does not fit easily into any one genetic model. The salient points to consider when formulating a model for this deposit are ... [Pg.514]

In an attempt to establish the fluid and metal sources and to help constrain a genetic model, stable isotope studies (O, Pb, S) were conducted on selected occurrences. Oxygen isotope analysis of quartz vein material from eight separate occurrences yielded values of 10.9-16.0%o. Assuming equilibrium between quartz and the hydrothermal fluid, the values calculated for the mineralizing fluids, at temperatures between 300-400°C, range between 4.0 and 11.9%o. This overlaps accepted values for both magmatic and metamorphic fluids. [Pg.553]

IRRINKI, R.R. 1992. Key Anacon sulfide deposit, Gloucester County, New Brunswick. Exploration Mining Geoiogy, 1, 121-129. Large, R.R. 1992. Australian volcanic-hosted massive sulfide deposits features, styles and genetic models. Economic Geoiogy, 87, 471-SI 0. [Pg.562]

Toth M (2003) 5-HT(lA) receptor knockout mouse as a genetic model of anxiety. Eur J Pharmacol 463 177-184... [Pg.111]

Stenzel-Poore MP, Heinrichs SC, Rivest S, Koob GF, Vale WW (1994) Overproduction of corticotropin-releasing factor in transgenic mice a genetic model of anxiogenic behavior. J Neurosci 14 2579-2584... [Pg.140]

Camadro, E. L., Masuelli, R. W. (1995). A genetic model for the endosperm balance number (EBN) in the wild potato Solanum acaule Bitt. and two related diploid species. Sex Plant Reproduction, 8,283-288. [Pg.52]

Jansky, S. H., Davis, G. L., Peloquin, S. J. (2004). A genetic model for tuberization in potato haploid-wild species hybrids grown under long-day conditions. American Journal of Potato Research, 81, 335-339. [Pg.56]

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