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  1. Article: Effect of N(G)-nitro-L-arginine methyl ester on functionally characterized muscarinic receptors in anesthetized cats.

    Koss, M C

    European journal of pharmacology

    1997  Volume 335, Issue 2-3, Page(s) 199–204

    Abstract: This study was undertaken to determine if the nitric oxide (NO) synthase inhibitor, NG-nitro-L ... arginine methyl ester (L-NAME), is a competitive antagonist of muscarinic receptors in vivo. Cats were ... groups of animals were administered L-NAME (50 mg/kg, i.v.) to determine if this agent would alter ...

    Abstract This study was undertaken to determine if the nitric oxide (NO) synthase inhibitor, NG-nitro-L-arginine methyl ester (L-NAME), is a competitive antagonist of muscarinic receptors in vivo. Cats were anesthetized with pentobarbital (36 mg/kg, i.p.). Five peripheral muscarinic responses were characterized based on their sensitivity to intravenous administration of atropine (1-100 microg/kg), pirenzepine (1-100 microg/kg) or gallamine (30-3000 microg/kg) as follows: (1) muscarinic ganglionic transmission through the superior cervical ganglion to the nictitating membrane (M1), (2) electrically elicited vagal bradycardia (M2), (3) neurally evoked sudomotor responses (M3; non-endothelial), (4) basal pupil tone in sympathectomized cats (M3; non-endothelial) and (5) methacholine-induced depression of arterial blood pressure (M3; endothelial). Additional groups of animals were administered L-NAME (50 mg/kg, i.v.) to determine if this agent would alter activation of these muscarinic systems. L-NAME was devoid of effect on responses elicited by stimulation of muscarinic M1, M2 and M3 (non-endothelial) receptors. In contrast, L-NAME significantly reduced the depressor responses to i.v. methacholine (M3; endothelial), as did its non-alkyl ester congener, L-NA (NG-nitro-L-arginine; 25 mg/kg, i.v.). These results support the conclusion that although L-NAME inhibits synthesis of nitric oxide in vascular endothelial cells, it is not a generalized muscarinic receptor antagonist in vivo.
    MeSH term(s) Animals ; Atropine/pharmacology ; Cats ; Enzyme Inhibitors/pharmacology ; Gallamine Triethiodide/pharmacology ; Muscarinic Antagonists/pharmacology ; NG-Nitroarginine Methyl Ester/pharmacology ; Nitric Oxide Synthase/antagonists & inhibitors ; Nitroarginine/pharmacology ; Pirenzepine/pharmacology ; Receptor, Muscarinic M1 ; Receptor, Muscarinic M2 ; Receptor, Muscarinic M3 ; Receptors, Muscarinic/drug effects
    Chemical Substances Enzyme Inhibitors ; Muscarinic Antagonists ; Receptor, Muscarinic M1 ; Receptor, Muscarinic M2 ; Receptor, Muscarinic M3 ; Receptors, Muscarinic ; Nitroarginine (2149-70-4) ; Pirenzepine (3G0285N20N) ; Atropine (7C0697DR9I) ; Nitric Oxide Synthase (EC 1.14.13.39) ; Gallamine Triethiodide (Q3254X40X2) ; NG-Nitroarginine Methyl Ester (V55S2QJN2X)
    Language English
    Publishing date 1997-09-24
    Publishing country Netherlands
    Document type Comparative Study ; Journal Article ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 80121-5
    ISSN 1879-0712 ; 0014-2999
    ISSN (online) 1879-0712
    ISSN 0014-2999
    DOI 10.1016/s0014-2999(97)01236-3
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  2. Article ; Online: Bioprocess in-line monitoring using Raman spectroscopy and Indirect Hard Modeling (IHM): A simple calibration yields a robust model.

    Müller, David Heinrich / Flake, Carsten / Brands, Thorsten / Koß, Hans-Jürgen

    Biotechnology and bioengineering

    2023  Volume 120, Issue 7, Page(s) 1857–1868

    Abstract: ... Nevertheless, IHM's root mean square errors of prediction (RMSEPs) for glucose (3.68 g/L) and ethanol (1.69 g/L) were ...

    Abstract To increase the process productivity and product quality of bioprocesses, the in-line monitoring of critical process parameters is highly important. For monitoring substrate, metabolite, and product concentrations, Raman spectroscopy is a commonly used Process Analytical Technology (PAT) tool that can be applied in-situ and non-invasively. However, evaluating bioprocess Raman spectra with a robust state-of-the-art statistical model requires effortful model calibration. In the present study, we in-line monitored a glucose to ethanol fermentation by Saccharomyces cerevisiae (S. cerevisiae) using Raman spectroscopy in combination with the physics-based Indirect Hard Modeling (IHM) and showed successfully that IHM is an alternative to statistical models with significantly lower calibration effort. The IHM prediction model was developed and calibrated with only 16 Raman spectra in total, which did not include any process spectra. Nevertheless, IHM's root mean square errors of prediction (RMSEPs) for glucose (3.68 g/L) and ethanol (1.69 g/L) were comparable to the prediction quality of similar studies that used statistical models calibrated with several calibration batches. Despite our simple calibration, we succeeded in developing a robust model for evaluating bioprocess Raman spectra.
    MeSH term(s) Calibration ; Spectrum Analysis, Raman/methods ; Saccharomyces cerevisiae/metabolism ; Ethanol/metabolism ; Glucose/metabolism
    Chemical Substances Ethanol (3K9958V90M) ; Glucose (IY9XDZ35W2)
    Language English
    Publishing date 2023-05-11
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 280318-5
    ISSN 1097-0290 ; 0006-3592
    ISSN (online) 1097-0290
    ISSN 0006-3592
    DOI 10.1002/bit.28424
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  3. Article ; Online: Social integration buffers the impact of financial distress on coparenting.

    Stanford, William D / Futris, Ted G / Richardson, Evin W / Koss, Kalsea J / Brown, Geoffrey L

    Journal of family psychology : JFP : journal of the Division of Family Psychology of the American Psychological Association (Division 43)

    2022  Volume 36, Issue 6, Page(s) 919–931

    Abstract: ... coparenting support. The findings highlight the critical role of external support systems (e.g., friends and ...

    Abstract The authors of this study examined how families may pull upon their shared social networks to generate positive relationship dynamics in the midst of financial distress. Prior research regarding the relevance of social integration to the associations between financial distress and the coparenting relationship have produced mixed and limited results. This study explores how each partner's belief that the couple is integrated within a supportive social network interacts with the strain of financial hardship to influence the coparenting relationship. The authors test whether social integration constitutes a capability for bonadaptation. Data for the present study were collected from 247 couples referred to a community-based, relationship enrichment program who were parents (or pregnant) and had received supportive social services within the last year. The authors estimated an actor-partner interdependence model examining the association between financial distress and each participant's report of their partner's supportive coparenting, as well as the moderating effects of perceived social integration upon this association. The association between financial distress (from either partner) and maternal reports of paternal coparenting support were buffered by mothers' perception of couple social integration. Fathers' perceptions of social integration buffered the association between maternal financial distress and his perception of his partner's coparenting support. The findings highlight the critical role of external support systems (e.g., friends and family) in buffering the effects of financial distress on the coparenting relationship for a diverse, low-income population. (PsycInfo Database Record (c) 2022 APA, all rights reserved).
    MeSH term(s) Fathers/psychology ; Female ; Humans ; Male ; Mothers/psychology ; Parenting/psychology ; Parents/psychology ; Pregnancy ; Social Integration
    Language English
    Publishing date 2022-05-05
    Publishing country United States
    Document type Journal Article
    ZDB-ID 619328-6
    ISSN 1939-1293 ; 0893-3200
    ISSN (online) 1939-1293
    ISSN 0893-3200
    DOI 10.1037/fam0000995
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  4. Book: Diagnostic cytology and its histopathologic bases / 2

    Koss, Leopold G.

    1992  

    Author's details Leopold G. Koss
    Collection Diagnostic cytology and its histopathologic bases
    Keywords Cytodiagnostik
    Subject Zelldiagnostik ; Punktionszytologie ; Punktionscytologie ; Zytodiagnostik
    Language English
    Size XX S., S. 890 - 1657, 56 S. : zahlr. Ill., graph. Darst.
    Edition 4. ed.
    Publisher Lippincott
    Publishing place Philadelphia u.a.
    Publishing country United States
    Document type Book
    HBZ-ID HT004278614
    ISBN 0-397-51222-8 ; 0-397-51049-7 ; 978-0-397-51222-5 ; 978-0-397-51049-8
    Database Catalogue ZB MED Medicine, Health

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  5. Book: Diagnostic cytology and its histopathologic bases / 1

    Koss, Leopold G.

    1992  

    Author's details Leopold G. Koss
    Collection Diagnostic cytology and its histopathologic bases
    Keywords Cytodiagnostik
    Subject Zelldiagnostik ; Punktionszytologie ; Punktionscytologie ; Zytodiagnostik
    Language English
    Size XXVIII, 888, 56 S. : zahlr. Ill., graph. Darst.
    Edition 4. ed.
    Publisher Lippincott
    Publishing place Philadelphia u.a.
    Publishing country United States
    Document type Book
    HBZ-ID HT004278610
    ISBN 0-397-51223-6 ; 0-397-51049-7 ; 978-0-397-51223-2 ; 978-0-397-51049-8
    Database Catalogue ZB MED Medicine, Health

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  6. Article ; Online: Dimerization of Cadherin-11 involves multi-site coupled unfolding and strand swapping.

    Koss, Hans / Honig, Barry / Shapiro, Lawrence / Palmer, Arthur G

    Structure (London, England : 1993)

    2021  Volume 29, Issue 10, Page(s) 1105–1115.e6

    Abstract: Cadherin extracellular domain 1 (EC1) mediates homophilic dimerization in adherens junctions. Conserved Trp2 and Trp4 residues in type II cadherins anchor the EC1 A strand intermolecularly in strand-swapped dimers. Herein, NMR spectroscopy is used to ... ...

    Abstract Cadherin extracellular domain 1 (EC1) mediates homophilic dimerization in adherens junctions. Conserved Trp2 and Trp4 residues in type II cadherins anchor the EC1 A strand intermolecularly in strand-swapped dimers. Herein, NMR spectroscopy is used to elucidate the roles of Trp2 and Trp4 in Cadherin-11 dimerization. The monomeric state, with the A strand and Trp side chains packed intramolecularly, is in equilibrium with sparsely populated partially and fully A-strand-exposed states, in which Trp2 (and Trp4, respectively) side-chain packing is disrupted. Exchange kinetics between the major state and the partially (fully) A-strand-exposed state is slow-intermediate (intermediate-fast). A separate very fast process exchanges ordered and random-coil BC-loop conformations with populations dependent on A-strand exposure and dimerization status. In addition, very slow processes connect the folded A-strand-exposed conformation to partially unfolded states, which may represent additional domain-swapping intermediates. The dimerization mechanism of type II cadherins is revealed as coupled folding and strand swapping.
    MeSH term(s) Amino Acid Substitution ; Animals ; Cadherins/chemistry ; Cadherins/genetics ; Cadherins/metabolism ; Mice ; Protein Conformation, alpha-Helical ; Protein Domains ; Protein Folding ; Protein Multimerization
    Chemical Substances Cadherins ; osteoblast cadherin (156621-71-5)
    Language English
    Publishing date 2021-06-23
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 1213087-4
    ISSN 1878-4186 ; 0969-2126
    ISSN (online) 1878-4186
    ISSN 0969-2126
    DOI 10.1016/j.str.2021.06.006
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  7. Article: Harry m. Zimmerman, m.d. (1901-1995).

    Koss, L G

    The American journal of pathology

    2009  Volume 148, Issue 1, Page(s) 341

    Language English
    Publishing date 2009-12-07
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2943-9
    ISSN 1525-2191 ; 0002-9440
    ISSN (online) 1525-2191
    ISSN 0002-9440
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  8. Article ; Online: The mystery of chromosomal translocations in cancer.

    Koss, L G

    Cytogenetic and genome research

    2007  Volume 118, Issue 2-4, Page(s) 247–251

    Abstract: Chromosomal translocations in human cancer may result in products that can be suppressed by targeting drugs. An example is bcr-abl tyrosine kinase in chronic myelogenous leukemia that can be treated with imatinib mesylate. However, the mechanisms of ... ...

    Abstract Chromosomal translocations in human cancer may result in products that can be suppressed by targeting drugs. An example is bcr-abl tyrosine kinase in chronic myelogenous leukemia that can be treated with imatinib mesylate. However, the mechanisms of translocations or exchanges of chromosomal segments are virtually unknown. In this summary, chromosomal translocations in human cancer are compared with 'crossing over' of chromosomal segments occurring during the first meiotic division. Several proposed mechanisms of the exchange of DNA between and among chromosomes are discussed. The conditions that appear essential for these events to occur are listed. Among them are proximity of the involved DNA segments, mechanisms of excising the target DNA, its transport to the new location, and integration into the pre-existing chromosome. The conclusion based on extensive review of the literature is that practically nothing is known about the mechanism of 'crossing over' or translocation. Based on prior work on normal human cells, it is suggested that only one of the two autosomes participates in these events that may include loss of heterozygozity, another common abnormality in human cancer.
    MeSH term(s) Crossing Over, Genetic ; Humans ; Loss of Heterozygosity ; Meiosis/genetics ; Neoplasms/genetics ; Translocation, Genetic
    Language English
    Publishing date 2007
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2087824-2
    ISSN 1424-859X ; 1424-8581
    ISSN (online) 1424-859X
    ISSN 1424-8581
    DOI 10.1159/000108307
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  9. Book: Diagnostic cytology and its histopathologic bases / 1

    Koss, Leopold G.

    1979  

    Author's details Leopold G. Koss
    Collection Diagnostic cytology and its histopathologic bases
    Keywords Cytologie ; Histopathologie
    Subject Gewebepathologie ; Histologische Diagnose ; Histologische Pathologie ; Pathohistologie ; Pathologische Histologie ; Zellbiologie ; Zellenlehre ; Zellforschung ; Zellkunde ; Zelluologie ; Zytologie ; Zelle
    Language English
    Size XXXI, 533, 48 S. : zahlr. Ill., graph. Darst.
    Edition 3. ed.
    Publisher Lippincott
    Publishing place Philadelphia u.a.
    Publishing country United States
    Document type Book
    HBZ-ID HT004278596
    ISBN 0-397-50402-0 ; 978-0-397-50402-2
    Database Catalogue ZB MED Medicine, Health

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  10. Book ; Collection: Diagnostic cytology and its histopathologic bases

    Koss, Leopold G.

    1979  

    Author's details Leopold G. Koss
    Keywords Cytodiagnosis ; Neoplasms / diagnosis
    Language English
    Dates of publication 1979-9999
    Publisher Lippincott
    Publishing place Philadelphia u.a.
    Publishing country United States
    Document type Book ; Collection (display volumes)
    New title 5. Aufl. u.d.T. Koss' diagnostic cytology and its histopathologic bases
    HBZ-ID HT000224020
    Database Catalogue ZB MED Medicine, Health

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