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  • Sprache: Englisch

    Verlag: Humana Press, 2008

    1588299481 / 9781588299482

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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    Zustand: New. pp. xi + 393 1st Edition.

  • Sprache: Englisch

    Verlag: Humana Press, 2008

    1588299481 / 9781588299482

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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    Zustand: New. pp. xi + 393 Illus.

  • Sprache: Englisch

    Verlag: Humana Press, 2008

    1588299481 / 9781588299482

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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    Zustand: New. pp. xi + 393.

  • Sprache: Englisch

    Verlag: Humana, 2008

    1588299481 / 9781588299482

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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  • Sprache: Englisch

    Verlag: Humana, 2008

    1588299481 / 9781588299482

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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    Zustand: Brand New. New. US edition. Expediting shipping for all USA and Europe orders excluding PO Box. Excellent Customer Service.

  • Sprache: Englisch

    Verlag: Humana, 2008

    1588299481 / 9781588299482

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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  • Sprache: Englisch

    Verlag: SP SPRINGER, 2008

    1588299481 / 9781588299482

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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    Zustand: New. Brand New ! Fast Delivery This is an International Edition and ship within 24-48 hours. Deliver by FedEx and Dhl, & Aramex, UPS, & USPS and we do accept APO and PO BOX Addresses. Order can be delivered worldwide within 6-10 days and we do have flat rate for up to 2LB. Extra shipping charges will be requested if the Book weight is more than 5 LB. This Item May be shipped from India, United states & United Kingdom. Depending on your location and availability.…

  • Sprache: Englisch

    Verlag: Humana, 2008

    1588299481 / 9781588299482

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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  • Sprache: Englisch

    Verlag: Humana, 2008

    1588299481 / 9781588299482

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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    Zustand: Brand New. New. US edition. Expediting shipping for all USA and Europe orders excluding PO Box. Excellent Customer Service.

  • Sprache: Englisch

    Verlag: Humana Pr Inc, 2008

    1588299481 / 9781588299482

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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    Brossura. Zustand: fine. 2008; br., pp. 393, cm 26x18. Libro.

  • Sprache: Englisch

    Verlag: Humana, 2008

    1588299481 / 9781588299482

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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  • Sprache: Englisch

    Verlag: Humana, 2011

    1617378534 / 9781617378539

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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    Taschenbuch. Zustand: Neu. EGFR Signaling Networks in Cancer Therapy | John D. Haley (u. a.) | Taschenbuch | Cancer Drug Discovery and Development | xi | Englisch | 2011 | Humana | EAN 9781617378539 | Verantwortliche Person für die EU: Humana Press in Springer Science + Business Media, Heidelberger Platz 3, 14197 Berlin, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu.…

  • Sprache: Englisch

    Verlag: Humana Press, 2011

    1617378534 / 9781617378539

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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    Paperback. Zustand: Brand New. 404 pages. 10.24x7.60x0.96 inches. In Stock.

  • Sprache: Englisch

    Verlag: Humana Press, 2011

    1617378534 / 9781617378539

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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    Zustand: New. pp. xi + 393.

  • Sprache: Englisch

    Verlag: Humana, 2011

    1617378534 / 9781617378539

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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    Zustand: new. Questo è un articolo print on demand.

  • Sprache: Englisch

    Verlag: Humana Press, 2008

    1588299481 / 9781588299482

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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    Zustand: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Probes the molecular pathways and the intersection of signaling networks which are frequently deregulated in human cancersDescribes EGF receptor in a tumor tissue specific context Illustrates the many ways in which EGF receptors contribute .…

  • Sprache: Englisch

    Verlag: Humana Press Sep 2008, 2008

    1588299481 / 9781588299482

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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    Anbieter: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, DeutschlandBuchWeltWeit Ludwig Meier e.K.

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    Buch. Zustand: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -The epidermal gro wth factor (EGF ) receptor and its downstream signal transduction networks have been implicated in the ontology and maintenance of tumor tissues, which has motivated the discovery and development of molecularly targeted anti-EGF receptor therapies. Over decades of study, the EGF receptor structure, its ligand binding domains, the physical biochemistry underlying its intrinsic tyrosine kinase catalytic function and the modular interactions with SH2, PTB, and SH3 domain containing signaling adaptor p- teins required for signal transduction, have been extensively dissected. Not only is the EGF receptor the nexus of many streams of information, but it also forms one part of a calcul- ing device by forming dimers and oligomers with the other three receptors in its family in response to at least eleven ligands (some of which are expressed in multiple forms with overlapping or quite distinct functions). This phenomenon, while recruiting to the inner surface of the cell membrane and activating multiple second messenger proteins, also allows the possibility of cross talk between these systems, permitting a further layer of information to be exchanged. Less well described are the cross re gulation of the EGF receptor and other anti-apoptotic, mitogenic and metabolic signaling systems. The study of these systems has yielded new surprises. One hurdle in these efforts has been that signal transduction pathways have frequently been defined in the generic absence of their tissue-specific or cell-interaction specific context. 408 pp. Englisch.…

  • Sprache: Englisch

    Verlag: Humana Press, 2011

    1617378534 / 9781617378539

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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    Kartoniert / Broschiert. Zustand: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Probes the molecular pathways and the intersection of signaling networks which are frequently deregulated in human cancersDescribes EGF receptor in a tumor tissue specific context Illustrates the many ways in which EGF receptors contribute .…

  • Sprache: Englisch

    Verlag: Humana, 2008

    1588299481 / 9781588299482

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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    Buch. Zustand: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - The epidermal gro wth factor (EGF ) receptor and its downstream signal transduction networks have been implicated in the ontology and maintenance of tumor tissues, which has motivated the discovery and development of molecularly targeted anti-EGF receptor therapies. Over decades of study, the EGF receptor structure, its ligand binding domains, the physical biochemistry underlying its intrinsic tyrosine kinase catalytic function and the modular interactions with SH2, PTB, and SH3 domain containing signaling adaptor p- teins required for signal transduction, have been extensively dissected. Not only is the EGF receptor the nexus of many streams of information, but it also forms one part of a calcul- ing device by forming dimers and oligomers with the other three receptors in its family in response to at least eleven ligands (some of which are expressed in multiple forms with overlapping or quite distinct functions). This phenomenon, while recruiting to the inner surface of the cell membrane and activating multiple second messenger proteins, also allows the possibility of cross talk between these systems, permitting a further layer of information to be exchanged. Less well described are the cross re gulation of the EGF receptor and other anti-apoptotic, mitogenic and metabolic signaling systems. The study of these systems has yielded new surprises. One hurdle in these efforts has been that signal transduction pathways have frequently been defined in the generic absence of their tissue-specific or cell-interaction specific context.…

  • Sprache: Englisch

    Verlag: Humana Press Jan 2011, 2011

    1617378534 / 9781617378539

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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    Taschenbuch. Zustand: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -The epidermal gro wth factor (EGF ) receptor and its downstream signal transduction networks have been implicated in the ontology and maintenance of tumor tissues, which has motivated the discovery and development of molecularly targeted anti-EGF receptor therapies. Over decades of study, the EGF receptor structure, its ligand binding domains, the physical biochemistry underlying its intrinsic tyrosine kinase catalytic function and the modular interactions with SH2, PTB, and SH3 domain containing signaling adaptor p- teins required for signal transduction, have been extensively dissected. Not only is the EGF receptor the nexus of many streams of information, but it also forms one part of a calcul- ing device by forming dimers and oligomers with the other three receptors in its family in response to at least eleven ligands (some of which are expressed in multiple forms with overlapping or quite distinct functions). This phenomenon, while recruiting to the inner surface of the cell membrane and activating multiple second messenger proteins, also allows the possibility of cross talk between these systems, permitting a further layer of information to be exchanged. Less well described are the cross re gulation of the EGF receptor and other anti-apoptotic, mitogenic and metabolic signaling systems. The study of these systems has yielded new surprises. One hurdle in these efforts has been that signal transduction pathways have frequently been defined in the generic absence of their tissue-specific or cell-interaction specific context. 408 pp. Englisch.…

  • Sprache: Englisch

    Verlag: Humana Press, Humana Sep 2008, 2008

    1588299481 / 9781588299482

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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    Buch. Zustand: Neu. This item is printed on demand - Print on Demand Titel. Neuware -The epidermal gro wth factor (EGF ) receptor and its downstream signal transduction networks have been implicated in the ontology and maintenance of tumor tissues, which has motivated the discovery and development of molecularly targeted anti-EGF receptor therapies. Over decades of study, the EGF receptor structure, its ligand binding domains, the physical biochemistry underlying its intrinsic tyrosine kinase catalytic function and the modular interactions with SH2, PTB, and SH3 domain containing signaling adaptor p- teins required for signal transduction, have been extensively dissected. Not only is the EGF receptor the nexus of many streams of information, but it also forms one part of a calcul- ing device by forming dimers and oligomers with the other three receptors in its family in response to at least eleven ligands (some of which are expressed in multiple forms with overlapping or quite distinct functions). This phenomenon, while recruiting to the inner surface of the cell membrane and activating multiple second messenger proteins, also allows the possibility of cross talk between these systems, permitting a further layer of information to be exchanged. Less well described are the cross re gulation of the EGF receptor and other anti-apoptotic, mitogenic and metabolic signaling systems. The study of these systems has yielded new surprises. One hurdle in these efforts has been that signal transduction pathways have frequently been defined in the generic absence of their tissue-specific or cell-interaction specific context.Springer-Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg 408 pp. Englisch.…

  • Sprache: Englisch

    Verlag: Humana, 2011

    1617378534 / 9781617378539

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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    Taschenbuch. Zustand: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - The epidermal gro wth factor (EGF ) receptor and its downstream signal transduction networks have been implicated in the ontology and maintenance of tumor tissues, which has motivated the discovery and development of molecularly targeted anti-EGF receptor therapies. Over decades of study, the EGF receptor structure, its ligand binding domains, the physical biochemistry underlying its intrinsic tyrosine kinase catalytic function and the modular interactions with SH2, PTB, and SH3 domain containing signaling adaptor p- teins required for signal transduction, have been extensively dissected. Not only is the EGF receptor the nexus of many streams of information, but it also forms one part of a calcul- ing device by forming dimers and oligomers with the other three receptors in its family in response to at least eleven ligands (some of which are expressed in multiple forms with overlapping or quite distinct functions). This phenomenon, while recruiting to the inner surface of the cell membrane and activating multiple second messenger proteins, also allows the possibility of cross talk between these systems, permitting a further layer of information to be exchanged. Less well described are the cross re gulation of the EGF receptor and other anti-apoptotic, mitogenic and metabolic signaling systems. The study of these systems has yielded new surprises. One hurdle in these efforts has been that signal transduction pathways have frequently been defined in the generic absence of their tissue-specific or cell-interaction specific context.…

  • Sprache: Englisch

    Verlag: Humana Press, Humana Press Jan 2011, 2011

    1617378534 / 9781617378539

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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    Taschenbuch. Zustand: Neu. This item is printed on demand - Print on Demand Titel. Neuware -The epidermal gro wth factor (EGF ) receptor and its downstream signal transduction networks have been implicated in the ontology and maintenance of tumor tissues, which has motivated the discovery and development of molecularly targeted anti-EGF receptor therapies. Over decades of study, the EGF receptor structure, its ligand binding domains, the physical biochemistry underlying its intrinsic tyrosine kinase catalytic function and the modular interactions with SH2, PTB, and SH3 domain containing signaling adaptor p- teins required for signal transduction, have been extensively dissected. Not only is the EGF receptor the nexus of many streams of information, but it also forms one part of a calcul- ing device by forming dimers and oligomers with the other three receptors in its family in response to at least eleven ligands (some of which are expressed in multiple forms with overlapping or quite distinct functions). This phenomenon, while recruiting to the inner surface of the cell membrane and activating multiple second messenger proteins, also allows the possibility of cross talk between these systems, permitting a further layer of information to be exchanged. Less well described are the cross re gulation of the EGF receptor and other anti-apoptotic, mitogenic and metabolic signaling systems. The study of these systems has yielded new surprises. One hurdle in these efforts has been that signal transduction pathways have frequently been defined in the generic absence of their tissue-specific or cell-interaction specific context.Humana Press in Springer Science + Business Media, Heidelberger Platz 3, 14197 Berlin 408 pp. Englisch.…

  • Sprache: Englisch

    Verlag: Humana Press, 2011

    1617378534 / 9781617378539

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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    Zustand: New. Print on Demand pp. xi + 393.

  • Sprache: Englisch

    Verlag: Humana Press, 2011

    1617378534 / 9781617378539

    Serie: Buch 56 von 96 - Cancer Drug Discovery and Development

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    Zustand: New. PRINT ON DEMAND pp. xi + 393.