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Tumor and Stem Cell Biology

The Chemokine Receptor CXCR7 Is Highly Expressed in Human Glioma Cells and Mediates Antiapoptotic Effects

Kirsten Hattermann, Janka Held-Feindt, Ralph Lucius, Susanne Sebens Müerköster, Mark E.T. Penfold, Thomas J. Schall and Rolf Mentlein
Kirsten Hattermann
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Janka Held-Feindt
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DOI: 10.1158/0008-5472.CAN-09-3642 Published April 2010
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Volume 70, Issue 8, pp. 3299-3308

DOI 
https://doi.org/10.1158/0008-5472.CAN-09-3642
PubMed 
20388803

Published By 
American Association for Cancer Research
Print ISSN 
0008-5472
Online ISSN 
1538-7445
History 
  • Published first April 13, 2010.

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  • Previous version (April 13, 2010 - 10:35).
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©2010 American Association for Cancer Research.

Author Information

  1. Kirsten Hattermann1,
  2. Janka Held-Feindt2,
  3. Ralph Lucius1,
  4. Susanne Sebens Müerköster3,
  5. Mark E.T. Penfold4,
  6. Thomas J. Schall4, and
  7. Rolf Mentlein1
  1. Authors' Affiliations: 1Department of Anatomy, University of Kiel, Departments of 2Neurosurgery and 3Internal Medicine, University of Schleswig-Holstein Medical Center, Kiel, Germany; and 4ChemoCentryx, Mountain View, California
  1. Corresponding Author:
    Rolf Mentlein, Department of Anatomy, University of Kiel, Olshausenstraße 40, 24098 Kiel, Germany. Phone: 49-431-2460; Fax: 49-431-1557; E-mail: rment{at}anat.uni-kiel.de.
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Cancer Research: 70 (8)
April 2010
Volume 70, Issue 8
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The Chemokine Receptor CXCR7 Is Highly Expressed in Human Glioma Cells and Mediates Antiapoptotic Effects
Kirsten Hattermann, Janka Held-Feindt, Ralph Lucius, Susanne Sebens Müerköster, Mark E.T. Penfold, Thomas J. Schall and Rolf Mentlein
Cancer Res April 15 2010 (70) (8) 3299-3308; DOI: 10.1158/0008-5472.CAN-09-3642

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The Chemokine Receptor CXCR7 Is Highly Expressed in Human Glioma Cells and Mediates Antiapoptotic Effects
Kirsten Hattermann, Janka Held-Feindt, Ralph Lucius, Susanne Sebens Müerköster, Mark E.T. Penfold, Thomas J. Schall and Rolf Mentlein
Cancer Res April 15 2010 (70) (8) 3299-3308; DOI: 10.1158/0008-5472.CAN-09-3642
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Cancer Research Online ISSN: 1538-7445
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