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  • 1965-1969  (4)
  • 1967  (4)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 159 (1967), S. 249-253 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Five-day-old mouse blastocysts were transferred into the oviducts of recipients on the second day of pregnancy. S35 methionine was then injected into the recipients and the blastocysts and native 2-celled eggs were recovered six hours later. Radioautographs reveal that the blastocysts incorporate S35 methionine while exposed to the tubal environment to the same degree that they would in the uterus. However, the 2-celled eggs in the same oviducal environment incorporate little or no methionine. It is therefore concluded that the difference in the incorporation of S35 methionine is due to maturational changes in the blastocyst rather than to a deficiency of the labelled amino acid in the tubal lumen.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 2
    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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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    American Journal of Anatomy 121 (1967), S. 249-258 
    ISSN: 0002-9106
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Pregnant hamsters consistently ovulated when injected with 20 IU of human chorionic gonadotropin (HCG). The induced ovulation rate from days 4-8 of pregnancy was comparable to that observed during the estrous cycle; however, starting at day 10, a marked increase occurred, culminating in a peak of 35 ova at day 12. Animals injected with HCG on day 16, the day before delivery, ovulated an average of 14.5 ova, although spontaneous postpartum ovulation does not occur in the hamster. The number of ovulations induced by HCG correlated with the varying number of antral follicles present during different stages of pregnancy.Unilaterally ovariectomized pregnant hamsters did not show a compensatory increase in induced ovulation rate in the remaining ovary.The induction of ovulation on days 4 or 10 of pregnancy did not interfere with embryonic development nor influence the time of parturition. Following parturition, the primary and induced corpora lutea regressed synchronously.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effects of pH on the polarization of fluorescence of dyes dissolved in media of high viscosity or conjugated to polypeptides that undergo no structural transitions indicate that DNS is useful for studying pH-dependent molecular transition over the range pH 2.5-14, whereas fluorescein is useful only over the range pH 6-8. Heating and cooling in aqueous solutions cause no change in the polarization of fluorescein or of DNS; therefore, the dyes themselves do not introduce artifacts into heating studies of the dye conjugates. The interaction between fluorescein or DNS and the molecule to which it is conjugated varies and thus may affect the measurements made with the conjugates: the rotational relaxation times of polylysine, of a copolymer of glutamic acid and lysine, and of lysozyme are approximately twice as long when measured with DNS-conjugates as when measured with fluorescein-conjugates. The explanation for this observation is postulated to lie in the tighter binding between fluorescein and the molecule to which it is conjugated, presumably around the point of its covalent attachment, which makes it a better indicator of the behavior of the rotational kinetic unit of the polypeptide chain. The stronger binding of fluorescein is inferred from two lines of evidence: (1) the fluorescent intensity and ultraviolet spectra of a fluorescein-polylysine conjugate are less susceptible to changes in solvent than those of the DNS conjugate, and (2) the net charge of the polypeptide affects the ionization of fluorescein much less than it affects the ionization of DNS. Additional evidence from previous studies corroborates this conclusion. Thus, it is important to establish the relationship between the fluorescent dye and the molecule to which it is conjugated before using the fluorescence data to calculate rotational relaxation times and other molecular parameters.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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