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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Neuroscience and behavioral physiology 10 (1980), S. 393-400 
    ISSN: 1573-899X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Conclusions 1. Ability to extrapolate was studied in mice with Robertsonian translocations Rb(8,17)1IEM; Rb(9,14)6Bnr; Rb(16,17)7Bnr; Rb(5,19)1Wh; and Rb(6,15)1ALD in their karyotype. 2. Among mice with the Rb(8,17)1IEM translocation the number of correct solutions to the extrapolation problem was significantly higher than the 50% random level; this evidently points to an influence of this chromosomal aberration on the level of elementary reasoning activity. 3. Ability to extrapolate was studied in mice of two sublines selected for large (subline L) and small (subline S) brain weight, and differing significantly (P〈0.001) for this feature. 4. In mice of the S subline the proportion of correct solutions during both first and repeated presentations was significantly above the 50% random level. In generations F3-F10 the proportion of correct solutions achieved by mice of the S subline was significantly (P 〈 0.001) higher than that achieved by mice of the L subline. No significant differences were found in generation F11-F13. No absolute correction is evidently present between brain weight and the level of elementary reasoning activity within the limits of one species. 5. In populations of laboratory mice, unable on the whole to solve this logical problem, there are groups of individuals which possess this ability to a significant degree. 6. Ability to solve an extrapolation problem as a manifestation of elementary reasoning activity in mice is largely hereditarily determined. 7. Selective lines of mice and mice with chromosomal aberrations are a convenient model with which to study the physiological and genetic basis of elementary reasoning activity.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Bulletin of experimental biology and medicine 124 (1997), S. 1214-1216 
    ISSN: 1573-8221
    Keywords: Morris' test ; training ; memory ; 101/H and CBA mice
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract The rate of formation of the habit of search for submerged platform was studied by the modified Morris' test in 101/H and CBA mice. The former strain was trained slower than the latter; in addition, 101/H mice of different sexes differed by the time of latent periods of searching for the platform. The results are interpreted as a manifestation of genetically determined disorders of training and/or memory in 101/H mice.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-8221
    Keywords: ACTH 4–10 ; monoamines ; early influences ; brain development ; strain mice
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract ACTH4–10 increases the concentration of monoaminergic neurotransmitters and the number of their metabolites in the brain of CBA and 101/HY mice. Different reactions to the peptide were revealed in both strains: the alterations were found either in brain stem (CBA strain) or in the hippocamp (101/HY strain).
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Behavior genetics 23 (1993), S. 467-475 
    ISSN: 1573-3297
    Keywords: Rodents ; foxes ; animal cognition ; domestication ; extrapolation ; Robertsonian translocation ; brain weight
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Psychology
    Notes: Abstract This paper reviews the investigations of Prof. L. V. Krushinsky and his colleagues into the genetics of complex behaviors in mammals. The ability of animals to extrapolate the direction of a food stimulus movement was investigated in wild and domesticated foxes (including different fur-color mutants), wild brown rats, and laboratory rats and mice. Wild animals (raised in the laboratory) were shown to be superior to their respective domesticated forms on performance of the extrapolation task, especially in their scores for the first presentation, in which no previous experience could be used. Laboratory rats and mice demonstrated a low level of extrapolation performance. This means that only a few laboratory animals were capable of solving the task, i.e., the percentage of correct solutions was equivalent to chance. The brain weight selection program resulted in two mice strains with a 20% (90-mg) difference in brain weight. Ability to solve the extrapolation task was present in low-brain weight mice in generations 7–11 but declined with further selection. Investigation of extrapolation ability in mice with different chromosomal anomalies demonstrated that animals with Robertsonian translocations Rb(8,17) 1lem and Rb(8,17) 6Sic were capable of solving this task in a statistically significant majority of cases, while mice with fusion of other chromosomes, as well as CBA normal karyotype mice, performed no better than expected by chance. Mice with two types of partial trisomies and animals homo- and heterozygous for translocations were also tested. Although mice with T6 trisomy performed no better than expected by chance, animals with trisomy for a chromosome 17 fragment solved the task successfully. Thus, a genetic component underlying the ability to solve the extrapolation task was demonstrated in three animal species. The extrapolation task in animals is considered to reveal a general capacity for elementary reasoning. The genetic basis of this capacity is very complex.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1608-3369
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Studies of behavior, neurophysiological reactions, neuromediator synthesis and brain structure of mice of the 101/HY strain (including those of the authors) are reviewed. This mouse strain is characterized by a chromosomal instability because of a recessive mutation mutator-1(mut-1) and the defective DNA excision repair. Experimental studies revealed a number of behavioral and neurological deviations in the 101/HY as compared to the CBA and the C3H mouse strains. These are abnormalities in spatial orientation, altered fear and anxiety reactions, anomalous locomotion, seizure developing in response to agents of various nature, and disturbances of the central nervous system, both structural and biochemical. Genome instability results in a number of neurological mutations, that may lead to the phenotypical effects observed in the 101/HY mice. Since the 101/HY mice partially display signs of severe human hereditary diseases caused by chromosomal instability and defective DNA repair, they can serve as a promising genetic model for these and other diseases related to impairment of the central nervous system.
    Type of Medium: Electronic Resource
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