ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

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
  • Chemistry  (8)
  • Adrenal medulla  (1)
  • Alimentary tract  (1)
  • 1
    ISSN: 1432-0878
    Keywords: 1,25-dihydroxyvitamin D3 ; Adrenal medulla ; Ontogenetic development ; Phenylethanolamine-N-methyltransferase ; Vitamin D-dependent calcium-binding protein ; Mouse, rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Target cells for 1,25-dihydroxyvitamin D3 were demonstrated in the adrenal medulla by frozen-section autoradiography. The appearance of these target cells was age-dependent in neonatal mice. Immunocytochemical staining for phenylethanolamine-N-methyltransferase revealed that both epinephrine and non-epinephrine cells concentrate 1,25-dihydroxyvitamin D3 in their nuclei. In contrast, immunocytochemical staining for “vitamin D-dependent calcium-binding protein” (D-CaBP) demonstrated that D-CaBP immunoreactivity is localized in only a small percentage of adrenomedullary cells, in mice and rats. Comparison of PNMT and D-CaBP immunoreactivities in sequential sections showed that epinephrine-producing cells do not contain D-CaBP. These results indicate that adrenal medullary cells have receptors for 1,25-dihydroxyvitamin D3 and that 1,25-dihydroxyvitamin D3 may directly affect certain functions of these endocrine cells.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 276 (1994), S. 333-345 
    ISSN: 1432-0878
    Keywords: Vitamin D receptor ; Brain, vertebrate ; Immune system ; Heart ; Alimentary tract ; Pancreas ; Uropygial gland ; Taeniopygia guttata (Aves, Passeriformes)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract In this study, we describe the distribution of high affinity binding sites for 1,25(OH)2-vitamin D3 (1,25-D3) in the zebra finch (Taeniopygia guttata). Four hours following the injection of tritiated 1,25-D3, binding of the steroid hormone was found primarily in the cell nuclei of a variety of differnt organs. Neurons in numerous discrete regions of the forebrain were labeled. These forebrain regions included the nucleus accumbens, nucleus dorsomedialis posterior thalami, lobus parolfactorius, nucleus septalis lateralis and medialis, nucleus septalis, lamina medullaris dorsalis, nucleus striae terminalis, palaeostriatum augmentatum, and stratum griseum. The choroid plexuses, however, remained clear. Labeled cells were seen in several organs of the alimentary canal, in both the exocrine and the endocrine pancreas, in the proximal tubules of the kidney, in the spleen, in the bursa of Fabricius, and in the heart. The basal cells of the uropygial gland were also labeled. No specific retention was evident in the gonads of either sex. Vitamin D is thus bound by cells in systems with widely different functions. Since several of the labeled tissues are not primarily involved in calcium homeostasis, the data support the concept that vitamin D-soltriol is a steroid hormone that acts as a seasonal neuroendocrine-endocrine regulator and somatotrophic modulator.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 61 (1949), S. 400-405 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Druckhydrierung wäßrig-alkalischer Sulfitablaugen bei 350° und hohem Wasserstoffdruck wird durch die Autoklavenwand katalysiert (Nickel, Chrom und entspr. Stähle). Bei einem NaOH-Lignin-Verhältnis von etwa 4:5 aufwärts entstehen Neutralstoffe, Phenole und Säuren nebeneinander. Weniger als 10% NaOH gibt besondere Neutralstoffe, über 10% NaOH in niedrig legierten Autoklaven als Hauptprodukt Säuren. Etwa 2/3 des Lignins werden in destillierbare, flüssige Produkte verwandelt.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 681 (1965), S. 30-32 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cyclododecanon wird durch H2O2 bei Zusatz von SeO2 unter Ringverengung in Cycloundecancarbonsäure übergeführt, deren Konstitution durch Abbau des Säureamides zum Cycloundecylamin bewiesen wird.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 687 (1965), S. 136-149 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Das Gemisch der Monoepoxide 2a, b von cis,trans,trans-Cyclododecatrien-(1.5.9) (1a) wird in das Ketongemisch (3a-c) umgelagert und über die Semicarbazone in ein Gemisch von 92% cis,trans- und 8% trans,trans-Cyclododecadien-(1.5) (4a bzw. 4b) übergeführt. Diese werden entsprechend über 6a-d in ein Gemisch von 78% cis- und 22% trans-Cyclododecen (7a bzw. 7b) umgewandelt. Bei der Epoxidierung von 1a mit Peressigsäure reagieren die trans-Doppelbindungen 6.6 mal so schnell wie die cis-Doppelbindung. Entsprechend wird die trans-Doppelbindung von 4a 5.7 mal so schnell wie die cis-Doppelbindung angegriffen.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 681 (1965), S. 28-30 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Durch Oxydation von Cyclododecanon mit Peressigsäure wird Dodecanolid in einer Ausbeute von 50% erhalten.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 681 (1965), S. 35-38 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aus C12-Ring-Ketonen wurden nach der Bucherer-Berg-Synthese die entsprechenden Hydantoine und hieraus durch Hydrolyse α-Aminocarbonsäuren hergestellt.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 681 (1965), S. 32-35 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cyclododecanoncyanhydrin wird in präparativem Maßstab in hoher Ausbeute hergestellt. Die Wasserabspaltung führt zu 1-Cyan-cyclododecen, Verseifung der Nitrilgruppe zu Cyclododecen-(1)-carbonsäure und deren Hydrierung zu Cyclododecancarbonsäure. Bei der Hydrierung des Cyanhydrins wird 1-Aminomethyl-cyclododecanol erhalten, das sich zu Cyclotridecanon umlagern läßt.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 687 (1965), S. 124-135 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Durch Umsetzung von C12-Cycloolefinen mit Maleinsäureanhydrid sowie Estern der Maleinsäure und der Fumarsäure werden die 1:1-Addukte 1-3 erhalten. Ihre Ausbeute beträgt in Gegenwart von Inhibitoren (besonders Thionin, Phenthiazin) über 80% d. Th. Durch Ozonspaltung wurde die Konstitution der Addukte wie folgt aufgeklärt: 1 ist cis,trans,trans-bzw. trans,trans,trans-Cyclododecatrien-(2.5.9)-yl-bernsteinsäureanhydrid;2 erweist sich als cis,trans- bzw. trans,trans-Cyclododecadien-(2.9)-yl-bernsteinsäureanhydrid (neben ca. 15% des 2.5-Isomeren) und 3 als cis- bzw. trans-Cyclododecen-(2)-yl-bernsteinsäureanhydrid.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...