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  • 1
    ISSN: 1432-0568
    Keywords: Human placenta ; Smooth muscle-like cells ; Perivascular contractile sheath ; Nitric oxide synthase type I ; Dipeptidyl peptidase IV
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract In the human placenta, besides the fetal blood vessel system a second extravascular contractile system exists. It is localized in the chorionic plate and runs in a longitudinal direction and adjacent to fetal blood vessels into the stem villi, where it forms perivascular contractile sheaths. Characteristically, cells of the extravascular contractile system are extremely long and spindle-shaped and give rise to fine cell processes, by which they obviously contact each other or insert into the basement membrane of the trophoblast. They show immunoreactivity with desmin, vimentin, α-actin, myosin, nitric oxide synthase type I (brain form) and dipeptidyl peptidase IV. The ultrastructure suggests that cells of the extravascular contractile system are related to smooth muscle cells, including subpopulations with myofibroblastic features. In stem villi a few cells are nitric oxide synthase type I immunoreactive. These cells are thought to be specialized smooth-muscle-like cells of the extravascular contractile system or cells of the extravascular contractile system related to paraneurons that generate nitric oxide, which, in turn, may modulate the tone of perivascular contractile sheaths. The high dipeptidyl peptidase IV activity suggests that modulation of the extravascular contractile system may also occur by substance P.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Archives of gynecology and obstetrics 183 (1953), S. 321-321 
    ISSN: 1432-0711
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    [S.l.] : International Union of Crystallography (IUCr)
    Acta crystallographica 39 (1983), S. 679-682 
    ISSN: 1600-5724
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The fundamental equations for dynamical magnetic neutron diffraction including an external magnetic field are given. The reflecting power is calculated for some special cases for asymmetrical Laue geometry. Some Pendellösung effects are discussed. Analytical and numerical results for the integrated reflecting power are presented
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    [S.l.] : International Union of Crystallography (IUCr)
    Acta crystallographica 39 (1983), S. 682-685 
    ISSN: 1600-5724
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The integrated reflecting powers of two nuclear and one magnetic reflexions of a DyFeO3 crystal have been measured. The results indicate that dynamical magnetic diffraction occurs. In addition, the integrated reflecting power of the magnetic reflexion was measured as a function of the magnetic field applied to the crystal, The results are discussed.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1365-2036
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Background : Mutations within the NOD2/CARD15 gene have recently been shown to be associated with Crohn's disease.Aims : To investigate the clinical impact of the three common NOD2/CARD15 mutations in patients with Crohn's disease.Methods : We investigated the prevalence of the three common NOD2/CARD15 mutations (Arg702Trp, Gly908Arg, 3020insC) in 180 patients with Crohn's disease, 70 patients with ulcerative colitis and 97 controls. In patients with Crohn's disease, prevalence of NOD2/CARD15 mutations were correlated to clinical and demographical parameters.Results : In Crohn's disease patients, 35.6% carried at least one mutant allele of NOD2/CARD15 mutations compared with 14.3% of patients with ulcerative colitis (P = 0.006) and to 15.5% of controls (P = 0.0001). Genotype phenotype analyses revealed that NOD2/CARD15 mutations determined younger age at disease diagnosis (P = 0.03), ileal disease location (P = 0.01) and ileocecal resections (P = 0.0002). Interestingly, reoperation with resection of the anastomosis was significantly more frequent in patients with NOD2/CARD15 mutations (P = 0.01).Conclusions : Our investigations support the current hypothesis that NOD2/CARD15 mutations are associated with a phenotype of Crohn's disease with younger age at diagnosis, ileal involvement, ileocecal resections and a high risk of postoperative relapse and reoperation. NOD2/CARD15 mutations might therefore be used to identify high risk patients for relapse prevention strategies.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1432-2307
    Keywords: Key words BCR-ABL ; Amplification ; CML ; Blast crisis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  Although chronic phase myelogenous leukaemia (CML) is characterised by the Philadelphia (Ph) chromosome leading to a fusion of the BCR and ABL genes, additional genetic alterations involved in blast crisis are poorly understood. We report an at least 15-fold amplification of the ABL oncogene in a 29-year-old male patient with a variant Ph-positive t(19;22)(p13;q11.2) CML who presented in lymphoid blast crisis. Our finding suggests that an amplification of the ABL oncogene might play a part in the appearance of an aggressive phenotype in some cases of CML.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Der Internist 38 (1997), S. 406-410 
    ISSN: 1432-1289
    Keywords: Schlüsselwörter NO-Synthase ; Peroxiynitrit ; Sauerstoffradikale ; Reperfusion ; Entzündung ; cGMP ; Proteinkinasen ; Arteriosklerose
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Zum Thema Stickstoffmonoxid (NO) ist ein sehr ungewöhnlicher, gasförmiger, kurzlebiger interzellulärer Botenstoff. In Blutgefäßen wird NO vor allem im Endothel gebildet (Donorzelle). Es wirkt auf verschiedene Targetzellen und zwar sowohl akut, über eine Erhöhung des intrazellulären zyklischen GMP-Gehalts, vasodilatatorisch und antithrombotisch, als auch über Langzeitmechanismen als wichtiges lokales vasoprotektives Gewebehormon. Bei vielen Gefäßerkrankungen, z.B. endothelialer Dysfunktion, Ischämie/Reperfusion und Entzündung, liegen klinisch relevante Fehlregulationen der Bildung oder Wirkung von NO vor. Die Ursachen hierfür sind vielfältig; das gleichzeitige Auftreten von NO und reaktiven Sauerstoffspezies scheint jedoch von herausragender Bedeutung zu sein.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Der Internist 40 (1999), S. 493-501 
    ISSN: 1432-1289
    Keywords: Schlüsselwörter Amyloidose ; hereditäre ; Transthyretin ; Familiäre Amyloid Polyneuropathie ; Polyneuropathie ; Amyloidose
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Zum Thema Amyloidosen sind durch extrazelluläre, unlösliche Proteinablagerungen in Form von Fibrillen in Faltblattstruktur und mit kristallinen Eigenschaften charakterisiert. Ätiologisch werden hereditäre und die weitaus häufigeren sekundären Formen unterschieden, die z.B. durch das dialyseassoziierte β2-Mikroglobulin hervorgerufen werden. An dieser Stelle wird über die hereditären Formen der Amyloidose mit meist autosomal dominantem Vererbungsmodus referiert. Die Inzidenz der häufigsten Transthyretin-(TTR)-Mutationen variiert extrem nach geographischer Lage, sie wird für die USA mit 1:100.000 und für Nordschweden mit 1:170 geschätzt. Das Protein TTR hat Transportfunktion für Thyroxin (T4) und Retinol. Pathogenetisch verursachen TTR-Mutationen Veränderungen der Oberflächenstruktur des Moleküls, die zu Aggregationen von Molekülen und zu anschließender Ablagerung von Proteinfibrillen führen. Im Detail ist dieser Vorgang, der allerdings nicht für alle Mutationen zutreffen dürfte, noch nicht geklärt. Patienten mit hereditärer Amyloidose erkranken zwischen dem 30. und 70. Lebensjahr und versterben ca. 5–15 Jahre später. In der vorliegenden Arbeit wird über Ätiologie, Pathogenese, Diagnostik und die derzeitig einzige Therapieoption, die Lebertransplantation, referiert.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 358 (1998), S. 111-112 
    ISSN: 1432-1912
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    The European physical journal 313 (1983), S. 325-337 
    ISSN: 1434-601X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The nucleus24Na has been investigated by studying the gamma-rays emitted following thermal neutron capture in23Na, with curved crystal and Ge(Li) spectrometers. Of the 277 transitions assigned to24Na, 216 were placed in the24Na level scheme containing 45 levels, of which six (1,961, 1,977, 3,866, 5,810, 5,918, and 6,222 keV) are reported for the first time. An average gamma-ray multiplicity of 3.3 gammas per neutron capture was observed. The neutron binding energy was determined to be 6,959.73 (14) keV. The resulting level scheme is compared to shell and rotational model predictions.
    Type of Medium: Electronic Resource
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