Library

X
feed icon rss

Your email was sent successfully. Check your inbox.

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

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Nerval-Neuroendokrine Komplexe in Magenschleimhaut bei Zollinger-Ellison-Syndrom (1995)
    Springer
    Der Pathologe 16 (1995), S. 404-407 
    Details
    ISSN: 1432-1963
    Keywords: Schlüsselwörter Nerval-neuroendokriner Komplex ; Zollinger-Ellison-Syndrom ; Magenschleimhaut ; Elektronenmikroskopie ; Key words Nerve fibre-neuroendocrine cell complex ; Stomach ; Zollinger-Ellison-Syndrom ; Electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary Nerve fibre-neuroendocrine cell complexes (NF-NEC-C's) are neuroendocrine cells located in the lamina propria of the gastrointestinal tract directly connected with nerve fibres of Meissner's plexus. We report on a patient with sporadic Zollinger-Ellison syndrome (ZES) with electron microscopically demonstrated multiple NF-NEC-C's in non-antral gastric mucosa. It is suspected that in ZES the hypergastrinaemia may represent a trophic stimulus for the proliferation of NF-NEC-C's in the gastric mucosa.
    Notes: Zusammenfassung Unter nerval-neuroendokrinen Komplexen (N-NE-K) versteht man in der Lamina propria mucosae des Magen-Darm-Traktes gelegene Nester neuroendokriner Zellen, die in direktem Kontakt zu Nervenfasern des Meissner-Plexus stehen. Es wird über einen Patienten mit sporadischem Zollinger-Ellison-Syndrom (ZES) berichtet, bei dem sich elektronenmikroskopisch in nonantraler Magenschleimhaut multiple N-NE-K fanden. Möglicherweise stellt die Hypergastrinämie bei ZES einen trophischen Stimulus für die Proliferation von N-NE-K in der Magenschleimhaut dar.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/s002920050121
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 2
    Electronic Resource
    Electronic Resource
    Immunologische und elektronenmikroskopische Befunde eines ungewöhnlichen Falles von M. Whipple (1985)
    Springer
    Journal of molecular medicine 63 (1985), S. 176-183 
    Details
    ISSN: 1432-1440
    Keywords: Whipple's disease ; Electron microscopy ; Disturbed cellular immunology
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Whipple's disease is a curious disorder with the involvement of many organ systems, primarily gut, synovium and the central nervous system, characterized by the presence of numerous proliferating bacteria in tissue macrophages and other cell types. While clinically this disease entity has previously been defined by the classical triad of diarrhoea, malabsorption and weight loss, some patients do not show these features. In this report, a clinically unusual case of Whipple's disease is described presenting with high persistent fever, severe arthralgias and headaches, but without malabsorption, diarrhoea or weight loss. Nevertheless, the histological and electron microscopical pictures demonstrated the typical findings of intracellular micro-organisms along with the presence of bacteria in Schwann nerve cells, which has only once been described previously. Immunological findings before treatment demonstrated a decrease of T cells with the helper/inducer phenotype, and a concomitant rise in cells with the suppressor/cytotoxic phenotype, an elevation of “activated” Ia positive T cells and a significant reduction of T cell mitogenic responsiveness. Of special interest, after a successful treatment these immunological abnormalities shifted to normal with the exception of a still elevated number of Ia+ T cells. The discussion of this unusual case of Whipple's disease includes — besides possible cellular immunological abnormalities — genetic factors, especially since this patient was HLA-B-27-positive as was his son who is suffering from ankylosing spondylitis.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01732172
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 3
    Electronic Resource
    Electronic Resource
    On the ultrastructure of the gastric “borderline lesion” (1983)
    Springer
    Journal of cancer research and clinical oncology 105 (1983), S. 285-291 
    Details
    ISSN: 1432-1335
    Keywords: Borderline lesion ; Severe dysplasia ; Gastric precancerosis ; Electron microscopy ; Morphometric analysis ; Bleb formation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The “borderline lesion” of the stomach (severe dysplasia of the protruded type) is nowadays considered to be a true precancerous lesion. Histologically, this lesion is characterized by a proliferation in the area of the glandular neck, combined with severe cellular atypia. Investigation by means of transmission electron microscopy reveals the structure of these cells to be very similar to the structure of cells of an intestinal-cell-type carcinoma of the stomach. In addition to signs for a loss of differentiation of the cells, such as the absence of rough-surfaced endoplasmatic reticulum, mucin granules, and of the polarity of the cells, remarkably frequently luminal bulges and “blebs” developed to various extents can be detected. Morphometric analysis is delineating the tendency of structural features of the borderline lesion to develop toward the gastric cancer cell. These irregularities might be expressions of the beginning of expansive growth and signs pointing to differentiation into malignant neoplasia.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00395760
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 4
    Electronic Resource
    Electronic Resource
    ESR-Untersuchungen an bestrahlten PhosphatgläsernProfessor Günther Rienäcker zum 70. Geburtstage am 13. Mai 1974 gewidmet. (1974)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 405 (1974), S. 286-298 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: ESR Studies of Radiation Processes in Phosphate GlassesRadiation processes in phosphate glasses are investigated by ESR and optical measurements. ESR shows a hole-centre in the systems K2O/P2O5 and K2O/MGO/P2O5 which depends on manner and concentration of the cations. Its nature is explained in somewhat a different way than given by BEEKENKAMP or by MIURA and HASEGAWA. Another hole-centre which is independent of cations is discussed in agreement with optical investigations. The electrons set free by radiation react with O2 solved in the glass or with cations. The particels Ag0, Ag2+, Ag+2 have been found and Agn+4 may be present too in the system K2O/MgO/Ag2O/P2O5. The system K2O/MgO/Tl2O/P2O5 shows analogous reactions, but full explanation of the lines could not yet be given.
    Notes: Durch ESR-Untersuchungen und Vergleiche mit optischen Messungen werden Aussagen über die durch Bestrahlung in Phosphatgläsern ablaufenden Vorgänge gemacht. In den Systemen K2O/P2O5 und K2O/MgO/P2O5 wird durch ESR-Messungen ein kationenabhängiges Lochzentrum gefunden, dessen Natur in Abweichung von den Modellen nach BEEKENKAMP und nach MIURA u. HASEGAWA erklärt wird. Ein weiteres kationenunabhängiges Lochzentrum wird in Übereinstimmung mit optischen Untersuchungen gedeutet. Die durch Bestrahlung freigesetzten Elektronen lagern sich an im Glas gelösten Sauerstoff (O2) an oder reagieren mit den Kationen. Im System K2O/MgO/Ag2O/P2O5 werden die Teilchen Ag0, Ag2+, Ag+2 gefunden und Agn+4 wahrscheinlich gemacht. Für das System K2O/MgO/Tl2O/P2O5 gelten analoge Verhältnisse. Eine ausführliche Zuordnung konnte aber dabei noch nicht vorgenommen werden.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19744050309
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 5
    Electronic Resource
    Electronic Resource
    Über die Cycloaddition von Dithiocyan und Trithiocyan mit Hexafluoraceton und Folgeprodukte aus der Spaltung der Schwefel-Schwefel-Bindung mit elementarem Chlor im Dithiocyan-Hexafluoraceton-AdduktProfessor Gerhard Gattow zum 60. Geburtstage am 6. Februar 1986 gewidmet (1986)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 532 (1986), S. 131-136 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Cycloaddition of Dithiocyanogen and Trithiocyanogen with Hexafluoroacetone and Products of the Cleavage of the Sulfur-Sulfur Bond in Dithiocyan-Hexafluoroacetone Adduct by Elemental ChlorineThe reaction of dithiocyanogen and trithiocyanogen with hexafluoroacetone (HFA) leads to the cycloaddition products (SCN)2 · 4 HFA 1 and S(SCN)2 · 4 HFA 2. These are the first reactions of (SCN)2 and S(SCN)2 without cleavage of the S - S bonds. Elemental chlorine cleaves in 1 the S—S bond and 3 is formed. In 3 the chlorine atom can be replaced by the rests  - CN 4, (C6H11)2N -  5, and n-C4H9- 6. 6 eliminates one molecule of HFA by warming up and the four-membered ring 7 is formed. The compounds were characterized on the basis of mass and nmr spectra.
    Notes: Die Reaktion von Dithiocyan und Trithiocyan mit Hexafluoraceton (HFA) führt zu den Cycloadditionsprodukten (SCN)2 · 4 HFA 1 und S(SCN)2 · 4 HFA 2. Es sind die ersten Reaktionen des (SCN)2 und S(SCN)2, die nicht unter Spaltung der S—S-Bindungen verlaufen. Durch elementares Chlor wird 1 an der S—S-Bindung gespalten und es entsteht 3. In 3 kann das Chloratom durch die Reste  - CN 4, (C6H11)2N -  5 und n-C4H9- 6 ersetzt werden. Beim Erwärmen verliert 6 ein Molekül HFA und es entsteht der viergliedrige Ring 7. Die Verbindungen wurden anhand ihrer Massen- und NMR-Spektren eindeutig charakterisiert.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19865320118
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 6
    Electronic Resource
    Electronic Resource
    Ylidenmalonitrilphosphine (NC)2C=C(X)PRR′Professor Gerhard Fritz zum 60. Geburtstage gewidmet (1979)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 459 (1979), S. 131-139 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Ylidenmalonitrilphosphines (NC)2C=C(X)PRR′Ylidenmalonitrilphosphines of the general formula (NC)2C=C(X)PRR′ (X = Alkyl, Cl, NH2, PRR′; R = Ph, R′ = Ph, H) are prepared under different conditions from (NC)2C=C(X)Cl (X = Alkyl, Cl, NH2) and prim. or sek. phosphines and their monosubstituted alkali or trimethylsilyl derivatives respectively. The synthesis as well as the behaviour of (NC)2C=C(X)PRR′ are compared with the corresponding oxygen analogues of the type O=C(X)PRR′. The structure of the title compounds are elucidated by investigation of their mass, i.r., and n.m.r. spectra.
    Notes: Ylidenmalonitrilphosphine der allgemeinen Formel (NC)2C=C(X)PRR′ (X = Alkyl, Cl, NH2, PRR′; R = Ph, R′ = H, Ph) lassen sich unter verschiedenen Reaktionsbedingungen aus (NC)2C=CXCl (X = Alkyl, Cl, NH2) und prim. oder sek. Phosphinen bzw. deren monosubstituierten Alkali- sowie Trimethylsilylderivate herstellen. Sowohl Synthese als auch Eigenschaften der Ylidenmalonitrilphosphine werden mit den Sauerstoffanaloga des Typs O=C(X)PRR′ verglichen und IR-, NMR- sowie massenspektroskopisch charakterisiert.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19794590114
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 7
    Electronic Resource
    Electronic Resource
    2,4,6-Tris(tert.butyl)phenyl-substituierte Phosphine (1982)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 488 (1982), S. 75-79 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 2,4,6-Tris(tert.butyl)phenyl Substituted PhosphinesTris(tert.butyl)phenyl-lithium reacts with PCl3 to give 2,4,6-tris(tert.butyl)phenyldihalogenophosphine which is reduced by LiAlH4 yielding 2,4,6-tris(tert.butyl)phenylphosphine. The same reaction by using (CH3)3Si—CH2—PCl2 leads to 2,4,6-tris(tert.butyl)phenyl-trimethylsilylmethylhalogenophosphine. Thermal treatment of this compound results under elimination of HCl and (CH3)3SiCl in the formation of . The nmr data of the compounds synthesized are discussed.
    Notes: Tris(tert.butyl)phenyl-lithium reagiert mit PCl3 oder (CH3)3Si—CH2—PCl2 zum 2,4,6-Tris(tert.butyl)phenyl-dihalogenphosphin bzw. entsprechenden -trimethylsilylmethylhalogenphosphin. Während sich ersteres mit LiAlH4 in das 2,4,6-Tris(tert.butyl)phenylphosphin überführen läßt, liefert letzteres durch thermische Beanspruchung nach Abspalten von HCl bzw. (CH3)3SiCl die Phosphine mit zweifach koordiniertem Phosphor. Die 1H- sowie 31P-NMR-Daten der dargestellten Verbindungen werden diskutiert.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19824880109
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 8
    Electronic Resource
    Electronic Resource
    Reaktion des aktivierten 1,2-Diphosphinobenzens mit Diphenylcarbodiimid (1985)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 529 (1985), S. 216-221 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reaction of Activated 1,2-Diphosphinobenzene with Diphenylcarbodiimide.The reaction behaviour of 1,2-(Ptms2)2C6H4 and 1,2-(PHLi)2C6H4 towards Ph—N=C=N—Ph leads to phosphaguanidino derivatives of 1,2-diphosphinobenzene and 2-(phenyltrimethylsilylamino)-3-trimethylsilyl-1,3-benzodiphosphole. The structure of the compounds are discussed on the basis of their n.m.r. spectra.
    Notes: Die Umsetzungen von Tetrakis(trimethylsilyl)-1,2-diphosphinobenzen sowie von 1,2-Di(lithiophosphino)benzen mit Diphenylcarbodiimid führen zu Phosphaguanidino-derivaten des 1,2-Diphosphinobenzens sowie zum 2-(Phenyl-trimethylsilylamino)-3-trimethylsilyl-1,3-Benzodiphosphol. Die Strukturen der dargestellten Verbindungen werden anhand der NMR-Daten diskutiert.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19855291027
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 9
    Electronic Resource
    Electronic Resource
    Über Oberflächenverbindungen von Übergangsmetallen. V. Oligomere Reaktionsprodukte bei der Polyäthylen- Synthese mit Chrom-Oberflächenverbindungen (1972)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 392 (1972), S. 258-270 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On surface compounds of transition metals. V. Oligomeric reaction products by the polymerization of ethylene with chromium surface compoundsShort time polymerization of ethylene with Cr(II) and Cr(VI) surface species on oxide carriers produces oligomeric reaction products, when followed by protonolysis, that originate, at least in part, from the decomposition of a soluble organochromium complex. Different homologous series result according to the type of heterogeneous catalyst employed: with Cr(II) contact α-olefines are obtained (in presence of O2 the corresponding n-aldehydes are formed), Cr(VI) contacts give straightchain methylketones. Whereas the aldehyde formation occurs in secondary reactions the CH3CO endgroup is produced evidently through the primary oxidation of C2H4 with surface Cr(VI). A polymerization sequence is then discussed in terms of protonolysis products wherein the alkene and acetyl endgroups are attached at that chain end which is not bound to chromium.
    Notes: Nach kurzzeitiger Polymerisation von Äthylen an Cr(II)- bzw. Cr(VI)-Oberflächenverbindungen auf oxydischen Trägern und anschließender Protolyse lassen sich oligomere Reaktionsprodukte fassen, die zumindest teilweise durch Zersetzung eines löslichen Chrom-organischen Komplexes entstanden sind. Je nach Katalysatortyp entstehen dabei verschiedene homologe Reihen: mit Cr(II)-Kontakten erhält man α-Olefine (bei Ablösung nach O2-Zutritt die entsprechenden n-Aldehyde), mit Cr(VI)-Kontakten die geradkettigen Methylketone. Während die Aldehyd-Bildung durch eine Sekundär-Reaktion erfolgt, entsteht die CH3CO-Endgruppe offenbar durch primäre Oxydation des C2H4 durch O'fl.Cr(VI).  -  Auf Grund der Protolyseprodukte läßt sich ein Polymerisationsverlauf diskutieren, bei dem die Alken- bzw. Acetyl-Endgruppen an den nicht an Cr gebundenen Kettenenden eingebaut werden.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19723920310
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 10
    Electronic Resource
    Electronic Resource
    Carbosilylierte Phospha-alkeneProfessor Rolf Appel zum 60. Geburtstage am 25. Februar 1981 gewidmet (1981)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 473 (1981), S. 85-90 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Carbosilylated phospha-alkenesLithium-tris-trimethylsilylmethanide, (Me3Si)3C-Li, reacts with various organodichlorophosphines to give tris-(trimethylsilyl)-methyl-organochlorophosphines, the termal treatment of which under elimination of trimethylchlorosilane results in formation of the title compounds of the general formula B.NMR-data as well as the synthesis of compounds A and B will be discussed.
    Notes: Lithium-tris-trimethylsilylmethanid, (Me3Si)3C-Li, reagiert mit verschieden substituierten Organyldichlorphosphinen zur Tris-Trimethylsilylmethyl-organylchlorphosphinen A, deren thermische Beanspruchung unter Abspaltung von Trimethylchlorsilan zu den Titelverbindungen der allgemeinen Formel B führt.Die NMR-spektroskopischen Daten der Verbindungen des Typs A und B sowie deren Synthese wer-den diskntiert.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19814730209
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...