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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 513 (1987), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 513 (1987), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 513 (1987), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract. The lateral elements (LEs) of synaptonemal complexes (SCs) of the rat contain major components with relative electrophoretic mobilities (M r s) of 30000–33000, which are the products of a single gene. After one-dimensional separation of SC proteins on polyacrylamide-SDS gels, these components show up as two major bands, whereas upon two-dimensional electrophoresis they are resolved in at least 24 spots, which focus at pH 6.5 to 9.5. In this paper we show that these spots represent phosphorylation variants. For the analysis of the phosphorylation of the 30000- to 33000-M r SC components during progression through meiotic prophase, we developed a procedure for isolation of fractions of testicular cells of the rat that are enriched in separate stages of meiotic prophase. Analysis of the 30000- to 33000-M r SC components in these fractions by two-dimensional electrophoresis and immunoblotting showed that phosphorylated variants of the 30000- to 33000-M r SC proteins occur throughout meiotic prophase. However, the extent of phosphorylation changes between early and mid-pachytene, when one phosphate group is probably added to each of the variants.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 187 (1977), S. 113-123 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: In this article a description of the process of spermatogenesis in the Chinese hamster is given.Spermiogenesis could be divided into 16 steps. The cycle of the seminiferous epithelium was divided into 12 stages, coinciding with the first 12 steps of spermiogenesis. The relative and absolute duration of the stages was determined. The duration of the cycle of the seminiferous epithelium was found to be 17.0 days.The morphology of the spermatogonia was studied in seminiferous tubules mounted “in toto.” Four classes of spermatogonia could be discerned: undifferentiated A spermatogonia (Ais, Apr, Aal), differentiated A spermatogonia (A1, A2, A3). In spermatogonia and B spermatogonia (B1, B2). It is interesting to note that the last generation of spermatogonia (B2) arises at the beginning of stage 7 and divides to give rise to primary spermatocytes in the second half of this stage; in most other species the last generation of spermatogonia arises in stage 4, giving rise to primary spermatocytes in stage 6.The undifferentiated A spermatogonia were counted in six stages of the cycle, together with the differentiated A, In or B spermatogonia present in the same stages. The results of these cell counts are discussed in detail. One of the conclusions that could be drawn about the behaviour of the Ais and Apr spermatogonia during the cycle of the epithelium was that there is mitotic activity in these cells in several stages of the cycle. It is suggested that this mitotic activity serves to generate the Aal spermatogonia, which after one or more divisions transform into A1 spermatogonia between stages 2 and 8.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 203 (1982), S. 83-99 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The population of undifferentiated spermatogonia was studied in whole mounted seminiferous tubules of the Chinese hamster and the ram. The morphology of the differentiating spermatogonia in the ram is also described.The nuclear morphology of the undifferentiated spermatogonia was found to vary considerably. 3H-thymidine labeling studies in the Chinese hamster revealed that this variability is associated with the phases of the cell cycle. In both animals the undifferentiated spermatogonia were found to lie isolated (As), paired (Apr), or in groups of four, eight, or sixteen cells (Aal). We described how the varying morphology can be used to identify the composing clones of a cluster of undifferentiated spermatogonia.Cell counts performed throughout the whole cycle of the seminiferous epithelium revealed a very similar pattern of proliferation in the Chinese hamster and the ram. The number of As + Apr spermatogonia remained constant throughout the epithelial cycle. However, the occurrence of labeled and mitotic cells showed that As, Apr as well as Aal spermatogonia do proliferate. In both animals the mitotic activity of the undifferentiated spermatogonia is very low during the lifespan of A2 spermatogonia but increases considerably among A3, staying high among Intermediate spermatogonia. Thereafter, mitotic activity subsides to a lower level until the cycle repeats itself. Clones of 16 Aal in the Chinese hamster only exceptionally divide further.The results in the ram are incompatible with a scheme of stem cell renewal in which the A1 spermatogonia derive from A2 spermatogonia (Hochereau-de Reviers et al., 1976). It is proposed that in the ram, like in rodents, the As spermatogonia are the spermatogonial stem cells and that the A1 spermatogonia derive quantitatively from the undifferentiated spermatogonia at each epithelial cycle.It could be calculated from the number of newly formed clones that both in the Chinese hamster and the ram, on the average, each As spermatogonium will have to divide several times during one epithelial cycle.Unlike in rodents, in the ram differentiation into A1 spermatogonia brings about a distinct morphologic change enabling us to observe that some Apr and rarely As spermatogonia transform into A1 spermatogonia. Thus, all undifferentiated spermatogonia are able to differentiate into A1 but the chance for this to occur increases strongly with the clonal size.
    Additional Material: 28 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 217 (1987), S. 124-130 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The topographical arrangement of the clones of Asingle, Apaired, and Aaligned (As, Apr, and Aal) spermatogonia on the basement membrane of seminiferous tubules of the Chinese hamster was studied. It was found that at least some of these clones are not distributed at random as clones of similar cell number were often seen in clusters. Areas were found with few or many As spermatogonia. Also, clusters of Apr spermatogonia were found, indicating that in such an area many As spermatogonia more or less synchronously formed Apr spermatogonia. Since clusters of clones of 16 Aal spermatogonia were observed, it can be concluded that these clusters of Apr spermatogonia may proliferate in at least a roughly synchronous way.It was found that over large areas the densities of undifferentiated spermatogonia may be very low or high in comparison to the mean density in the animal. Whether the ratio of self-renewal and differentiation of the stem cells changed locally in response to the high or low density of undifferentiated spermatogonia in particular areas was investigated. No indications for a regulatory mechanism to keep the density of stem cells and/or the density of undifferentiated spermatogonial clones at a certain level could be detected in the normal Chinese hamster. This lack of regulation was at least partly responsible for the widely different numbers of A1 spermatogonia that were formed in the various areas studied in stage IX.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 217 (1987), S. 131-136 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: In this study the yield of the proliferation of the differentiating spermatogonia into spermatocytes was determined in five Chinese hamsters. Large differences of up to a factor 2 were found between the numbers of A1 spermatogonia in the various animals. However, the numbers of leptotene spermatocytes varied only by up to a factor 1.2 between animals. It is concluded that more spermatogonial degeneration takes place in animals with a relatively large number of A1 spermatogonia than in those with a small number of these cells. In such a way in all animals ultimately about the same number of spermatocytes is formed.An experiment was done in which the number of A1 spermatogonia was lowered with the S-phase killer cytosine arabinoside (Ara-C). It was found that this greatly increased the yield of the spermatogonial proliferation, showing a direct relationship between the number of A1 spermatogonia in an animal and the extent of the spermatogonial degeneration.In addition to the variation in the number of A1 spermatogonia found between various animals, an even larger variation of up to a factor 3.7 was found between the numbers of A1 spermatogonia in different areas of seminiferous tubules within each animal. Nevertheless the variation in the number of leptotene spermatocytes in different areas within each animal was not larger than a factor 1.3. It is concluded that in the normal animal the phenomenon of spermatogonial degeneration depends on the local density of these spermatogonia. Apparently, when too many spermatogonia are present the surplus of cells degenerates.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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