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100%: Sous la direction de: H.J. Muller-Eberhard, Sous la direction de: P.A. Miescher: Complement (Paperback) (ISBN: 9783540150756) 1985, in Deutsch, Taschenbuch.
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100%: H.J. Muller-Eberhard, Editor: P.A. Miescher: Complement (Springer Seminars in Immunopathology, Vol 6, No 2/3 & R, Vol 7, No 2/3) (ISBN: 9780387150758) 1985, Springer-Verlag New York, LLC, Erstausgabe, in Englisch, Bände: 6, 7.
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Complement (Springer Seminars in Immunopathology, Vol 6, No 2/3 & R, Vol 7, No 2/3) (1985)
EN PB NW FE
ISBN: 9780387150758 bzw. 0387150757, Bände: 6, 7, in Englisch, 474 Seiten, Springer-Verlag, Taschenbuch, neu, Erstausgabe.
Lieferung aus: Vereinigte Staaten von Amerika, Usually ships in 1 to 3 months.
Von Händler/Antiquariat, Amazon.com.
Activation of the complement system gives rise to a number of molecular species which can interact with host-derived cells and regulate their function. This interaction is mediated through distinct cell surface complement receptors, and receptor engagement produces biologic responses which can either modulate host defense reactions or enhance inflammation. Although the first complement receptor was recognized more than 30 years ago [80J, detailed biochemical information concerning the receptors has only recently become available. Currently, eight distinct complement receptors are recognized. Five receptors (CRl, CR2, CR3, C3a receptor, and C3e receptor) react with various regions on C3 while the other receptors display specificity for Clq, C5a, or Factor H. This chapter focusses on the chemistry of the various ligands and receptors and discusses the biologic activities which arise as a result of receptor-ligand interaction. II. CIQ Receptor A. The Ligand Clq is the recognition molecule of the classical complement pathway [reviewed in 20, 130]. In serum, it is part of a calcium-dependent penta molecular complex containing one molecule ofClq and two molecules each of the pro enzymes Clr and CIs. During classical pathway activation, the macromolecular complex becomes associated with the activator through the Clq subcomponent. Bound Clq undergoes a conformational change and induces the proteolytic autoactivation of Clr which in turn effects the proteolytic activation of CIs. This process is controlled by the Cl inhibitor (ClINH) which binds irreversibly to activated Clr and CIs, and inhibits their enzymatic activities. Paperback, Ausgabe: 1, Label: Springer-Verlag, Springer-Verlag, Produktgruppe: Book, Publiziert: 1985-05, Studio: Springer-Verlag.
Von Händler/Antiquariat, Amazon.com.
Activation of the complement system gives rise to a number of molecular species which can interact with host-derived cells and regulate their function. This interaction is mediated through distinct cell surface complement receptors, and receptor engagement produces biologic responses which can either modulate host defense reactions or enhance inflammation. Although the first complement receptor was recognized more than 30 years ago [80J, detailed biochemical information concerning the receptors has only recently become available. Currently, eight distinct complement receptors are recognized. Five receptors (CRl, CR2, CR3, C3a receptor, and C3e receptor) react with various regions on C3 while the other receptors display specificity for Clq, C5a, or Factor H. This chapter focusses on the chemistry of the various ligands and receptors and discusses the biologic activities which arise as a result of receptor-ligand interaction. II. CIQ Receptor A. The Ligand Clq is the recognition molecule of the classical complement pathway [reviewed in 20, 130]. In serum, it is part of a calcium-dependent penta molecular complex containing one molecule ofClq and two molecules each of the pro enzymes Clr and CIs. During classical pathway activation, the macromolecular complex becomes associated with the activator through the Clq subcomponent. Bound Clq undergoes a conformational change and induces the proteolytic autoactivation of Clr which in turn effects the proteolytic activation of CIs. This process is controlled by the Cl inhibitor (ClINH) which binds irreversibly to activated Clr and CIs, and inhibits their enzymatic activities. Paperback, Ausgabe: 1, Label: Springer-Verlag, Springer-Verlag, Produktgruppe: Book, Publiziert: 1985-05, Studio: Springer-Verlag.
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Complement
DE US
ISBN: 9783540150756 bzw. 3540150757, in Deutsch, Springer Berlin Heidelberg, Springer Berlin Heidelberg, Springer Berlin Heidelberg, gebraucht.
Lieferung aus: Vereinigte Staaten von Amerika, zzgl. Versandkosten, Free Shipping on eligible orders over $25, in-stock.
H.J. Muller-Eberhard (Editor), P.A. Miescher (Editor),Paperback, Edition: 1, English-language edition, Pub by Springer Berlin Heidelberg.
H.J. Muller-Eberhard (Editor), P.A. Miescher (Editor),Paperback, Edition: 1, English-language edition, Pub by Springer Berlin Heidelberg.
3
Complement
DE PB NW
ISBN: 9783540150756 bzw. 3540150757, in Deutsch, Springer, Berlin, Taschenbuch, neu.
Lieferung aus: Deutschland, Versandkostenfrei.
buecher.de GmbH & Co. KG, [1].
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buecher.de GmbH & Co. KG, [1].
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4
Complement
DE PB NW
ISBN: 9783540150756 bzw. 3540150757, in Deutsch, Springer, Berlin, Taschenbuch, neu.
Lieferung aus: Deutschland, Versandkostenfrei.
buecher.de GmbH & Co. KG, [1].
Die Beschreibung dieses Angebotes ist von geringer Qualität oder in einer Fremdsprache. Trotzdem anzeigen
buecher.de GmbH & Co. KG, [1].
Die Beschreibung dieses Angebotes ist von geringer Qualität oder in einer Fremdsprache. Trotzdem anzeigen
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Complement (1985)
DE PB NW RP
ISBN: 9783540150756 bzw. 3540150757, in Deutsch, Springer Apr 1985, Taschenbuch, neu, Nachdruck.
Von Händler/Antiquariat, AHA-BUCH GmbH [51283250], Einbeck, Germany.
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