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  • 1965-1969  (12)
  • 1960-1964  (7)
  • 1925-1929  (1)
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 68 (1964), S. 1601-1602 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 69 (1965), S. 3089-3091 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 64 (1960), S. 825-826 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 90 (1968), S. 6571-6572 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 87 (1965), S. 4188-4189 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
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    Unknown
    New York : Periodicals Archive Online (PAO)
    Foreign Affairs. 4:1/4 (1925/1926) 1 
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  • 7
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Additional Material: 4 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 149 (1964), S. 411-433 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The distribution and origin of interstitial tissue has been studied in various mammalian ovaries with histochemcal techniques for lipids. The interstitial tissue contains sudanophilic droplets of different sizes consisting of phospholipids, triglycerides and cholesterol and its esters; the lipids are comparatively unsaturated.The granulosa of normal follicles contains heterogeneous lipid bodies of various sizes composed of unsaturated phospholipids. With the start of atresia these lipid bodies also develop neutral fats (triglycerides). Besides the heterogeneous lipid bodies, another type of sudanophilic lipid droplets of atresia, consisting of triglycerides, cholesterol and its ester and little phospholopids, are formed in the granulosa cells. When the number of these lipid droplets is sufficiently increased, the heterogeneous lipid bodies disappear from the atretic follicles. The theca of such atretic follicles hypertrophies and persists to form the interstitial tissue whereas the granulosa cells, along with the lipid droplets, regress and disappear.In the rat ovary, the interstitial tissue occurs as scattered patches of various sizes that are derived from the theca of atretic preantral and antral follicles. Most of the lipid droplets of the interstitial tissue are mobilized from the preovulatory rat ovary. All of the bat ovary is occupied by interstitial tissue except for the cortex; the tissue is formed in the same way as in the rat. In the cat ovary, the interstitial tissue is sparsely scattered between the follicles and originates from the theca and adjacent stromal cells of normal and atretic follicles. In the dog ovary the interstitial tissue has a similar origin and also arises from invaginations of germinal epithelium. In the opossum ovary the interstitial tissue is present in the form of sparsely scattered patches of cells which arise from the theca of large preantral follicles. A few lipid bodies, consisting of unsaturated phospholipids, appear in the interstitial tissue.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 157 (1967), S. 163-172 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: The effect of exogenous estrogen on tubal transport of ova was determined in the guinea pig, hamster, mouse, rabbit and rat. The animals were given a single injection of estradiol cyclopentylpropionate (ECP) shortly after mating. The dose of ECP required to interrupt pregnancy in 80% or more of the animals was as follows: guinea pig (10 μg); hamster (25 μg); mouse (1 μg); rabbit (50 μg); rat (10 μg). Acceleration of egg transport through the oviduct occurred after the following doses of ECP: guinea pig (50-100 μg); hamster (100 μg); mouse (1 μg and above); rabbit (25 μg); rat (10 μg and above). Hence, the amount of estrogen which accelerates egg transport in the guinea pig and hamster is considerably higher than the dose which interrupts pregnancy.Retentionof ova for longer than the normal period of tubal passage (tube-locking) resulted from the following doses of ECP: guinea pig (250 μg); hamster (250 μg); mouse (1 μg); rabbit (100 μg); rat (no dose). In the species in which ova were tubelocked, the majority of eggs were located at the ampullary-isthmic junction rather than the utero-tubal region of the oviduct.Tube-locking of ova was never observed in the rat; ECP always caused premature entry of eggs into the uterus and eventual expulsion per vaginam. For example, eggs passed through the cervix by 12 hours after the administration of 250 μg ECP at day 1 of pregnancy.
    Additional Material: 13 Tab.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 163 (1969), S. 373-387 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Pregnant mice were hypophysectomized on day 6 and injected subcutaneously with various hormones from days 6 to 9 to establish the minimal requirements for the maintenance of functional corpora lutea. Luteal activity was assessed by the maintenance of pregnancy, weight of embryonic swellings, mean diameter and morphology of corpora lutea, and vaginal histology.Treatment with 2 mg progesterone maintained pregnancy but not corpora lutea in three of five animals. However, the embryonic swellings were significantly (P 〈 0.0005) smaller than those of pregnant control animals. Pregnancy was maintained in all animals when progesterone was combined with 1 μg of estrone. The weights of embryonic swellings and the degree of vaginal mucification in the combined steroid group were similar to those of intact control animals.Treatment with either ovine prolactin, bovine LH, ovine FSH or estrone failed to maintain corpora lutea or pregnancy. Combined injection of prolactin with LH or estrone did not maintain pregnancy or corpora lutea. On the other hand, treatment with 500 μg of prolactin and 200 μg of FSH maintained pregnancy in 12 of 14 animals. All of the aforementioned parameters of luteal activity were comparable to values in intact, control animals.The data indicate that luteal function in the mouse during the early post-implantation period requires a luteotropic complex rather than a single hormone. Prolactin and FSH constitute the minimal luteotropic complex in the pregnant mouse. The luteotropic activity of FSH was not due to its contamination with LH and the effect of FSH was apparently not mediated through estrogen secretion, since pregnancy was not maintained by prolactin and estrone.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
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