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  1. AU="Setter, Peter"
  2. AU=Shikata Chihiro
  3. AU="Jordan P. Metcalf"
  4. AU=Peri?i? Nanut Milica AU=Peri?i? Nanut Milica
  5. AU="Pramod, Ganapathiraju"
  6. AU="Fu, Chu-Jun"
  7. AU="Nejad, Harry G."
  8. AU="Zhang, Q E"
  9. AU="Oppenheim, Madeline"

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  1. Artikel ; Online: Top 10 research priorities for irritable bowel syndrome: results of a James Lind Alliance priority setting partnership.

    Black, Christopher J / McKenzie, Yvonne A / Scofield-Marlowe, Morgan / Setter, Peter / Tarpey, Maryrose / Ford, Alexander C

    The lancet. Gastroenterology & hepatology

    2023  Band 8, Heft 6, Seite(n) 499–501

    Mesh-Begriff(e) Humans ; Irritable Bowel Syndrome/therapy ; Biomedical Research
    Sprache Englisch
    Erscheinungsdatum 2023-03-27
    Erscheinungsland Netherlands
    Dokumenttyp Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 2468-1253
    ISSN (online) 2468-1253
    DOI 10.1016/S2468-1253(23)00072-9
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel: Studies on the immune response and preparation of antibodies against a large panel of conjugated neurotransmitters and biogenic amines: specific polyclonal antibody response and tolerance

    Huisman, Han / Wynveen, Paul / Setter, Peter W

    Journal of neurochemistry. 2010 Feb., v. 112, no. 3

    2010  

    Abstract: J. Neurochem. (2010) 112, 840-852. We described the production and characterization of antibodies against three important groups of neuro-active haptens, e.g., neurotransmitters and biogenic amines. First, from the tryptophane metabolic pathway: ... ...

    Abstract J. Neurochem. (2010) 112, 840-852. We described the production and characterization of antibodies against three important groups of neuro-active haptens, e.g., neurotransmitters and biogenic amines. First, from the tryptophane metabolic pathway: tryptamine, serotonin, 5-hydroxy-indole acetic acid, and melatonin. Secondly, the tyrosine metabolic pathway: tyramine, dopamine, dihydroxyphenyl acetic acid, and norepinephrine. Thirdly, antibodies against excitatory and inhibitory neurotransmitters: glycine, glutamate, glutamine, and GABA. Immunogenic conjugates were prepared after linking haptens to carrier proteins. Most antibodies displayed high specificity against corresponding neuro-active haptens conjugated in vitro and in situ in biological specimens, but not to closely related conjugated metabolites, precursors, pharmaceuticals, agonists, antagonists, or free neuro-active haptens. Conjugated norepinephrine was highly tolerant in different animal species and produced incidentally a short specific antibody response.
    Schlagwörter biogenic amines ; neurotransmitters ; polyclonal antibodies
    Sprache Englisch
    Erscheinungsverlauf 2010-02
    Umfang p. 829-841.
    Verlag Blackwell Publishing Ltd
    Erscheinungsort Oxford, UK
    Dokumenttyp Artikel
    ZDB-ID 80158-6
    ISSN 1471-4159 ; 0022-3042 ; 1474-1644
    ISSN (online) 1471-4159
    ISSN 0022-3042 ; 1474-1644
    DOI 10.1111/j.1471-4159.2009.06492.x
    Datenquelle NAL Katalog (AGRICOLA)

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  3. Artikel ; Online: Studies on the immune response and preparation of antibodies against a large panel of conjugated neurotransmitters and biogenic amines: specific polyclonal antibody response and tolerance.

    Huisman, Han / Wynveen, Paul / Setter, Peter W

    Journal of neurochemistry

    2010  Band 112, Heft 3, Seite(n) 829–841

    Abstract: We described the production and characterization of antibodies against three important groups of neuro-active haptens, e.g., neurotransmitters and biogenic amines. First, from the tryptophane metabolic pathway: tryptamine, serotonin, 5-hydroxy-indole ... ...

    Abstract We described the production and characterization of antibodies against three important groups of neuro-active haptens, e.g., neurotransmitters and biogenic amines. First, from the tryptophane metabolic pathway: tryptamine, serotonin, 5-hydroxy-indole acetic acid, and melatonin. Secondly, the tyrosine metabolic pathway: tyramine, dopamine, dihydroxyphenyl acetic acid, and norepinephrine. Thirdly, antibodies against excitatory and inhibitory neurotransmitters: glycine, glutamate, glutamine, and GABA. Immunogenic conjugates were prepared after linking haptens to carrier proteins. Most antibodies displayed high specificity against corresponding neuro-active haptens conjugated in vitro and in situ in biological specimens, but not to closely related conjugated metabolites, precursors, pharmaceuticals, agonists, antagonists, or free neuro-active haptens. Conjugated norepinephrine was highly tolerant in different animal species and produced incidentally a short specific antibody response.
    Mesh-Begriff(e) Animals ; Antibodies/immunology ; Antibodies/metabolism ; Antibody Formation/physiology ; Antibody Specificity/immunology ; Biogenic Amines/immunology ; Biogenic Amines/metabolism ; Cross Reactions/immunology ; Enzyme-Linked Immunosorbent Assay/methods ; Haptens/immunology ; Immunization/methods ; Neurotransmitter Agents/immunology ; Neurotransmitter Agents/metabolism ; Rabbits
    Chemische Substanzen Antibodies ; Biogenic Amines ; Haptens ; Neurotransmitter Agents
    Sprache Englisch
    Erscheinungsdatum 2010-02
    Erscheinungsland England
    Dokumenttyp Journal Article
    ZDB-ID 80158-6
    ISSN 1471-4159 ; 0022-3042 ; 1474-1644
    ISSN (online) 1471-4159
    ISSN 0022-3042 ; 1474-1644
    DOI 10.1111/j.1471-4159.2009.06492.x
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  4. Artikel: Tektin interactions and a model for molecular functions.

    Setter, Peter W / Malvey-Dorn, Erika / Steffen, Walter / Stephens, Raymond E / Linck, Richard W

    Experimental cell research

    2006  Band 312, Heft 15, Seite(n) 2880–2896

    Abstract: Tektins from echinoderm flagella were analyzed for microheterogeneity, self-associations and association with tubulin, resulting in a general model of tektin filament structure and function applicable to most eukaryotic cilia and flagella. Using a new ... ...

    Abstract Tektins from echinoderm flagella were analyzed for microheterogeneity, self-associations and association with tubulin, resulting in a general model of tektin filament structure and function applicable to most eukaryotic cilia and flagella. Using a new antibody to tektin consensus peptide RPNVELCRD, well-characterized chain-specific antibodies and quantitative gel densitometry, tektins A, B and C were found to be present in equimolar amounts in Sarkosyl-urea-stable filaments. In addition, two isoforms of tektin A are present in half-molar ratios to tektins B and C. Cross-linking of AB filaments indicates in situ nearest neighbor associations of tektin A1B and A2B heterodimers, -trimers, -tetramers and higher oligomers. Soluble purified tektin C is cross-linked as homodimers, trimers and tetramers, but not higher oligomers. Tektin filaments associate with both loosely bound and tightly bound tubulin, and with the latter in a 1:1 molar ratio, implying a specific, periodic association of tightly bound tubulin along the tektin axis. Similarly, in tektin-containing Sarkosyl-stable protofilament ribbons, two polypeptides ( approximately 67/73 kDa, homologues of rib72, efhc1 and efhc2) are present in equimolar ratios to each other and to individual tektins, co-fractionating with loosely bound tubulin. These results suggest a super-coiled arrangement of tektin filaments, the organization of which has important implications for the evolution, assembly and functions of cilia and flagella.
    Mesh-Begriff(e) Animals ; Cilia/metabolism ; Evolution, Molecular ; Male ; Microtubule Proteins/chemistry ; Microtubule Proteins/metabolism ; Microtubules/ultrastructure ; Models, Biological ; Polymers/metabolism ; Sarcosine/analogs & derivatives ; Sarcosine/metabolism ; Sea Urchins/cytology ; Sea Urchins/metabolism ; Sperm Tail/chemistry ; Sperm Tail/metabolism ; Sperm Tail/ultrastructure ; Tubulin/metabolism ; Urea/metabolism
    Chemische Substanzen Microtubule Proteins ; Polymers ; Tubulin ; tektins ; sarkosyl (632GS99618) ; Urea (8W8T17847W) ; Sarcosine (Z711V88R5F)
    Sprache Englisch
    Erscheinungsdatum 2006-09-10
    Erscheinungsland United States
    Dokumenttyp Journal Article ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 1493-x
    ISSN 1090-2422 ; 0014-4827
    ISSN (online) 1090-2422
    ISSN 0014-4827
    DOI 10.1016/j.yexcr.2006.05.014
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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