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  • 1
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract HSRs (homogeneously staining regions) are the cytological correlates of DNA amplification. In the house mouse, Mus musculus, many populations are polymorphic for the presence or absence of HSRs on chromosome 1. In the semispecies M. m. domesticus the amplified DNA is present within one HSR, whereas in M. m. musculus chromosomes 1 with two HSRs are found. Hybridization of HSR-specific probes to Southern blots of HSR-carrying genomic DNAs from different localities and semispecies revealed similar complex band patterns. the remaining variation is restricted to sequences with a low degree of amplification. Variation is higher between semispecies than within one semispecies. It is assumed that HSRs are derived from one original amplification event and that unequal recombination is the mechanism underlying the length variation of HSRs present today in both semispecies. Evidence from G-banding and in situ hybridization shows that the two HSRs of M. m. musculus originated from a single HSR by means of a paracentric inversion, where one break-point was located within the single HSR and the second outside the HSR. As a consequence of the paracentric inversion the two HSRs of M. m. musculus are permanently linked together. Since exchange of genes between the two semispecies is restricted to a narrow hybrid zone the amplification that gave rise to the HSR most probably occurred prior to the divergence into the semispecies M. m. domesticus and M. m. musculus about 1 million years ago.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Experimental Cell Research 22 (1961), S. 146-150 
    ISSN: 0014-4827
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Experimental Cell Research 36 (1964), S. 696-699 
    ISSN: 0014-4827
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Medicine
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 442 (1985), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Notes: It appears that the chance of an in vitro fertilization (IVF) embryo to produce a pregnancy carried to term is about 10%.1 Consequently, one of the most important factors in increasing the pregnancy rate after in vitro fertilization and embryo transfer is replacement of multiple embryos.2 When we consider that the estimated human fecundity rate is about 25%,3 it seems likely that the quality of the embryo is one determining factor for a successful pregnancy rate. Different types of defects of gametes and embryos might contribute to the explanation of why the vast majority of IVF embryos do not give rise to any sign of pregnancy after replacement.It is well documented that chromosomal abnormalities among first trimester spontaneous abortions occur at a rate of about 60%, indicating that chromosomal abnormalities might be common in human gametes and early development stages.4 Abnormal karyotypes found were aneuploidy (i.e., complements with one extra or one missing chromosome) and polyploidy.Recently, a new technique allowing direct analysis of the chromosomal constitution of human spermatozoa has been reported.5 This technique utilizes the ability of capacitated human spermatozoa to penetrate zona-free hamster oocytes. Five to 10% of penetrating human spermatozoa have shown chromosomal abnormalities. Various degrees of hyperploidy and hypoploidy ranging from three extra to three missing chromosomes were found in a series of 1000 human spermatozoal chromosome constitutions.6 It is interesting to note that among spontaneous first trimester abortions such serious numerical abnormalities have not been found.4
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Human genetics 〈Berlin〉 58 (1981), S. 98-104 
    ISSN: 1432-1203
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The wood lemming, Myopus schisticolor, possesses a unique sex determining system comprising both XX and XY females. Normal female development in the presence of XY is guaranteed by a mutation on the X, apparently associated with a structural rearrangement in Xp. This mutation inactivates the testis-inducing and male-determining factor on the Y and distinguishes X* from X, and X*Y females from XY males. Normal fertility of X*Y females is ensured by a mitotic (double) nondisjunction mechanism which, at an early fetal stage, eliminates the Y from the germ line and replaces it by a copy of the X*. Numerical sex chromosome aberrations are not infrequent and the trisomics XXY and X*XY are relatively common. XXY individuals are sterile males with severe suppression of spermatogenesis. Among X*XY animals, both males and females, as well as a true lateral hermaphrodite have been observed. Primary deficiency of germ cells, impairment of spermatogenesis and sterility are characteristic traits of the X*XY males, whereas X*XY females have normal oogenesis and are fertile. Both these extremes (except female fertility) coexist in the true hermaphrodite described in the present study. These apparently contradictory observations are explainable under the assumption that X* and X in X*XY individuals are inactivated non-randomly or that the cells are distributed unequally. Inactivation of the X or X* determines whether or not the H-Y antigen will be expressed. When comparing conditions in Myopus and in man, an additional assumption has to be made in relation to the gene(s) involved in sex determination, located in Xp:In Myopus they do not escape inactivation, whereas in man they have been claimed to remain active.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Genetica 74 (1987), S. 143-147 
    ISSN: 1573-6857
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The karyotype of the osprey consists of 74 chromosomes. There are no large macrochromosomes and no typical microchromosomes. Autosome No. 2 has a prominent secondary constriction in the long arm. The Z chromosome is similar in size and shape to the largest autosome, the W is a small metacentric. Among the Falconiformes, the osprey karyotype mainly resembles the karyotypes of some accipitrid species. However, certain characteristic features of the karyotype, a unique secondary constriction chromosome and absence of microchromosomes, speak in favour of maintaining the osprey in a family of its own, Pandionidae.
    Type of Medium: Electronic Resource
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