Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • 1970-1974  (2)
  • 1960-1964  (2)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    American Journal of Anatomy 111 (1962), S. 111-129 
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    American Journal of Anatomy 112 (1963), S. 35-51 
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    American Journal of Anatomy 128 (1970), S. 265-281 
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: In the normal adult rat testis, type A0 spermatogonia do not appear to participate to a significant extent in the production of spermatocytes, while type A1 spermatogonia periodically initiate a series of divisions resulting in the production of spermatocytes and new type A1 spermatogonia.The behavior of type A0 and A1 spermatogonia was investigated following administration of a single dose of x-rays (300 r) to the testis. Using whole mounts of seminiferous tubules, the type A0 and A1 cells were counted at various intervals after irradiation. At 8 and 13 days after irradiation, type A1 spermatogonia reached lowest values, i.e., 6% and 3% of non-irradiated control, while type A0 reached the lowest value, i.e., 62% of control at eight days. Thereafter the numbers of type A0 and A1 progressively increased to return to normal at 39 days. It was thus concluded that the type A0 were comparatively more resistant to x-irradiation than type A1 spermatogonia.To verify if the surviving type A0 proliferated in the irradiated testis, animals were injected with 3H-thymidine three hours before they were sacrificed at various times after x-irradiation. In irradiated testes the labeling indices of the surviving type A (A0, A1-A4) were the same as in the non-irradiated testes except in stages V-VI of the cycle of the seminiferous epithelium. While in the controls only 2% of type A cells were labeled at these two stages of the cycle, after irradiation the labeling index of type A reached a maximum of 31% at 13 days to return to control values by 39 days. Since at 13 days after irradiation type A0 spermatogonia were the predominant component of the spermatogonial population, it was concluded that these cells must have incorporated 3H-thymidine and thereby contributed to the reconstruction of the spermatogonial population partially destroyed by irradiation.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    American Journal of Anatomy 136 (1973), S. 153-165 
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Monkeys were sacrificed at three hours and at 12 days-3 hours after an intraperitoneal injection with 3H-thymidine. Radioautographs were prepared of periodic acid-Schiff-hematoxylin-stained sections of the testes. At three hours, the most evolved labeled germ cells were leptotene spermatocytes in stage VIII of the cycle; at 12 days-three hours the most evolved labeled cells were pachytene spermatocytes in stage IX of the succeeding cycle. Thus, over a 12-day interval, the most evolved labeled spermatocytes had advanced through slightly more than one complete cycle. A quantitative analysis of tubular cross sections containing labeled spermatocytes permitted the calculation of the duration of one cycle of the seminiferous epithelium which turned out to be 11.6 days. The whole process of spermatogenesis which begins with the first spermatogonial mitoses taking place in stage VIII and terminates with the release of spermatozoa taking place in stage VI of the cycle, extends over the duration of 3.8 consecutive cycles and therefore requires approximately 44 days.On the same histological material counts of resting and dividing spermatogonia were performed at various stages of the cycle to determine their mode of proliferation and renewal. Six mitotic peaks were disclosed and were located in stages VIII, X, XII, II, IV and VI of the cycle. Cell counts and labeling indices indicated that the pale type A spermatogonia were the cells dividing during the first two of these six peaks of mitoses while the type B spermatogonia divided during the remaining four peaks of mitoses. The dark type A spermatogonia were not seen to divide during the cycle and may be considered as “reserve stem cells.” Cell counts and cell ratios indicated further that the pale type A spermatogonia divided in stage VIII of the cycle (and some in stage IX) to yield about twice their number of pale type A spermatogonia: of several possible schemes the authors believe that half of these entered a long interphase and became stem cells for the spermatogonia to be formed during the next cycle; these may be referred to as “renewing stem cells”; we consider that the other half of the pale type A spermatogonia arising from stage VIII peak of mitoses divided in stage X to produce type B spermatogonia. The latter cells then could enter the series of four consecutive mitoses during which they doubled their number each time to yield a generation of primary spermatocytes.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...