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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 41 (1985), S. 609-611 
    ISSN: 1420-9071
    Keywords: Mouse ; ovarian follicle ; potential difference ; ovulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary A small potential difference (antrum positive) has been measured with fine-tipped glass microelectrodes across the epithelial cell layers of the mouse ovarian follicle wall. As ovulation approached the potential in the antrum became more positive compared to the outside. Metabolic inhibitors and locally active hormones also altered the potential difference. The ionic basis and the significance of the potential difference are unknown.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 41 (1985), S. 492-494 
    ISSN: 1420-9071
    Keywords: Mouse ; female offspring ; androstenedione treatment ; corticosterone treatment ; pregnancy ; estrous cycle
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Female offspring from mice injected with androstenedione during late pregnancy showed lengthened vaginal cycles, persistent estrus and decreased incidence of pro-estrus and dïestrus, whilst offspring from mice injected with corticosterone showed increased incidence of dïestrus. These observations give qualified support to the hypothesis that stress during pregnancy alters the female offspring reproductive system through the action of adrenal steroids.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Cellular and molecular life sciences 41 (1985), S. 925-928 
    ISSN: 1420-9071
    Keywords: Mouse ; endoradiotherapy ; α-particle track autoradiography ; 6-[211At]-astato-2-methyl-1,4-naphthoquinol bis (diphosphate salt)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The microscopic distribution of the potential endoradiotherapeutic drug, 6-[211At]-astato-2-methyl-1,4-naphthoquinol bis (diphosphate salt) in normal tissues of the mouse has been studied by α-particle track autoradiography. The uptake into critical radiosensitive tissues, especially bone marrow, colon and lung, was low.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 150 (1974), S. 323-329 
    ISSN: 1432-0878
    Keywords: Spermiogenesis ; Mouse ; Multinucleate spermatids ; Electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Electron microscope studies of the testes of five inbred and three outbred mouse strains show that the usual frequency of multinucleate spermatids is between one and two percent. In C57 BL/6J and A/Gr however it is higher (4–5%). The frequency of the shared acrosome condition, which would lead to the formation of an abnormal sperm, is 1.3 per thousand.
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  • 5
    ISSN: 1432-0878
    Keywords: Gastrin cell ; Pyloric mucosa ; Ontogenesis ; Immunohistochemistry ; Mouse
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Ontogenesis of gastrin cells was studied in the pyloroduodenal mucosa of the mouse using anti-human G17 serum, R-1301, and anti-human G34(1–15) serum, R-2703. R-1301-immunostained cells first appeared in the pyloric mucosa of 14-day-old fetuses. Cells stained with both R-1301 and R-2703 appeared immediately after birth, and gradually increased in number to the adult level. Most R-1301-reactive cells were also reactive to R-2703, whereas some cells that reacted with R-1301 exhibited very weak or no reaction with R-2703. The discrepancy between these two immunoreactivities is discussed. In the duodenum, a considerable number of R-1301-reactive cells were present from the perinatal stage and through out adult development. A few R-2703-reactive cells were seen in the duodenum of young mice but not of the adult.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 239 (1985), S. 567-574 
    ISSN: 1432-0878
    Keywords: Teeth ; Ameloblasts ; Vascular perfusion ; Colchicine ; Mouse ; Light- and electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary In order to revalue the effects of colchicine on incisor secretory ameloblasts, entire mice were perfused with Krebs solution supplemented with a buffer and amino acids, through the right common carotid artery. The normal ultrastructure of the cells was maintained for 2 h with the perfusate alone. When colchicine (0.3–3.0 μg/ml) was added to the perfusate, it induced ultrastructural changes, such as the loss of cytoplasmic microtubules, the loss of secretory granules in Tomes' process, the abnormal accumulation and secretion of secretory granules, disarranged Golgi apparatus and the fragmentation of rough endoplasmic reticulum. Vesicles (150–400 nm in diameter) resembling immature secretory granules also accumulated, the degree of accumulation depending on the duration of colchicine treatment. The accumulation of secretory granules and these vesicles suggests that the intracellular transport system was affected by colchicine but that the production of secretory granules was continuous throughout the experimental period. The present perfusion system has enabled us to treat ameloblasts with an agent that is a useful experimental tool for elucidating cell functions, despite being lethal to animals in vivo.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 239 (1985), S. 537-545 
    ISSN: 1432-0878
    Keywords: Mouse ; Pancreas, endocrine ; Insulin ; Acid phosphatase ; Lysosomes ; Crinophagy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary The relation between qualitative and quantitative glucose-dependent alterations of lysosomes in pancreatic islets and the function of the islets was studied. Isolated islets of the mouse were maintained in tissue culture for one week in either 28, 5.5 or 3.3 mmol/l glucose. Insulin biosynthesis, insulin secretion and insulin content of the cultured islets were determined. After culture, the islets were subjected to acid phosphatase cytochemistry and examined by electron microscopy and ultrastructural morphometry. Islets cultured in 28 mmol/l glucose both produced and secreted insulin rapidly. Such islets seemed, however, unable to maintain more than small amounts of granule-stored insulin. Islets cultured at the lower concentrations of glucose displayed a reduced insulin secretion, which apparently resulted in considerable amounts of intracellularly stored insulin. In all cultured islets different types of lysosomes, identified by their acid phosphatase reactivity, could be seen. Dense bodies, i.e., lysosomes characterized by a homogeneous, very fine, particulate content of high density, seemed to predominate at all concentrations of glucose. It is suggested that, in the islets, the dense bodies correspond morphologically to primary lysosomes. Other types of lysosomes with inclusions of various kinds, which were frequent at the two lower concentrations of glucose, may correspond to secondary lysosomes. Morphometry revealed differences between the size distributions of lysosomes in the three experimental groups. Thus, the average lysosomal size was inversely proportional to the concentration of glucose in the culture medium. However, the numerical density of lysosomes was greatest at the highest glucose concentration. The observation of secondary lysosomes, containing material resembling secretory granules, suggests that the increased size and lowered number of lysosomes in islets cultured at low glucose concentrations may depend on a crinophagic process. Such a process, together with insulin biosynthesis and insulin secretion, may be of physiological importance for control of the secretory granule content within the pancreatic B-cell.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 154 (1974), S. 321-327 
    ISSN: 1432-0878
    Keywords: Pituitary ; Mouse ; Pars intermedia ; Adrenoglomerulotropin ; Morphometric cytology
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Ultrastructural changes in the pars intermedia of the mouse pituitary caused by dietary sodium deprivation were investigated quantitatively. Of the six classes of organelles and inclusions selected for analysis in the pars intermedia cells, only the mitochondria showed no significant changes, while all of the remaining classes showed statistically significant changes. The most conspicuous changes were an abrupt decrease in the number of secretory granules and the appearance of parallel arrays of rough endoplasmic reticulum. The Golgi apparatus also showed hypertrophy accompanied by newly formed granules. The number of vesicles increased temporarily and then decreased. These findings indicate that dietary sodium depletion, a stimulus to greater aldosterone secretion, causes significant changes in the pars intermedia cells within 3 days, and these signs of hyperfunction last up to 5 days. The present study suggests a possible new role of the pars intermedia in the regulation of aldosterone secretion in response to dietary sodium deprivation in the mouse.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 239 (1985), S. 271-278 
    ISSN: 1432-0878
    Keywords: Brain macrophage ; Fetus ; Histogenesis ; Immunohistochemistry ; Monoclonal antibody ; Mouse
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary A study on the localization of fetal and neonatal brain macrophages of mice from embryonic day 10 (E10) to postnatal day 21 (P21) was carried out immunohistochemically using a monoclonal antibody against a macrophage differentiation antigen (Mac-1) and the labeled avidin-biotin technique. In the central nervous system, the macrophages recognized first were mainly located in the choroid plexuses of the fourth and lateral ventricles at E14. Their number increased at E17–P3 and gradually decreased thereafter. In the cerebral parenchyma, a few macrophages appeared at E14 in the matrix cell layer. They were also detected in the migrating zone at E15, E17 and in the cortical plate at E19. Mapping of positive cells at the stage of neuroblast formation (E15, E17, E19) disclosed the precise distribution of cerebral macrophages. The macrophages that appeared first in the choroid plexuses at E15 may be derived from the subarachnoid vessels, which extend into the stroma of the choroid plexuses when the matrix cell layer invaginates into the lateral ventricle to form the choroid plexuses. Almost all of the macrophages recognized in the cerebral parenchyma disappeared at P9 when the cytoarchitecture seemed to be completed. In the cerebellum, which develops later than the cerebrum, macrophages appeared after birth and were located mainly in the internal granular layer. The brain macrophages always appeared in the regions where cell proliferation and brain remodeling are most active at each stage. These findings suggest that fetal and neonatal brain macrophages may play an important role in scavenging degenerated cells and cell debris during histogenesis of the central nervous system.
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 148 (1974), S. 381-396 
    ISSN: 1432-0878
    Keywords: Placenta ; Mouse ; Syncytium ; Morphogenesis ; Ultrastructure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Description / Table of Contents: Résumé L'origine embryologique des constituants cytologiques de la barrière placentaire chez la Souris a été mise en évidence du 8ème au 11éme jour de la gestation et la séquence des phénomènes favorisant la formation d'un syncytium trophoblastique, précisée. La barrière placentaire trilaminaire a une double origine: la couche interne provient du trophoblaste chorionique, la couche médiane syncytiale comme la couche externe dérivent du trophoblaste ectoplacentaire. Le stimulus initial de la différenciation semble résulter au 9ème jour du contact entre le trophoblaste chorionique et le mésoderme allantoïdien. Quelques heures après, on observe la réaction des cellules chorioniques, caractérisée par une augmentation importante des nucléoprotéines cytoplasmiques, puis l'apparition de globules lipidiques et enfin des propriétés de motilité. Ces cellules établissent des jonctions complexes avec le trophoblaste ectoplacentaire indifférencié qu'elles côtoient. En même temps, le métabolisme nucléaire de ces cellules ectoplacentaires semble modifié. Ultérieurement, au 10éme jour de la gestation, la disparition des membranes plasmiques latérales de ces cellules, conduit à la formation d'un syncytium par fusion de cellules au même stade d'évolution.
    Notes: Summary The morphogenesis of the different layers forming the mouse placental barrier is described during the 8th to 11th day of gestation. The timing and events leading to the formation of the syncytiotrophoblast are analyzed. Two different processes lead to the formation of the hemotrichorial placental membrane: the internal layer is formed by the chorionic trophoblast, both the intermediate syncytial layer and the external cytotrophoblast layer are derived from the ectoplacental trophoblast. The differentiation of the placental barrier begins on the 9th day of gestation by the establishment of contact between the chorionic trophoblast and the allantoic mesoderm. A few hours later, the chorionic cells show a considerable increase in cytoplasmic nucleoproteins and lipids and become ameboid. Complex cell-junctions differentiate between these chorionic cells and the adjacent ectoplacental trophoblast. On the 10th day of gestation the lateral cytoplasmic membranes disappear leading to the formation of a syncytium.
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