Dysregulated RasGRP1 Responds to Cytokine Receptor Input in T Cell Leukemogenesis-Reference-Cited by-同舟云学术

Dysregulated RasGRP1 Responds to Cytokine Receptor Input in T Cell Leukemogenesis

Published:2013-03-26 Issue:268 Volume:6 Page:
ISSN:1945-0877
Container-title:Science Signaling
language:en
Short-container-title:Sci. Signal.

Author:

Hartzell Catherine¹,Ksionda Olga¹,Lemmens Ed¹,Coakley Kristen¹,Yang Ming²,Dail Monique³,Harvey Richard C.⁴,Govern Christopher²,Bakker Jeroen¹,Lenstra Tineke L.¹,Ammon Kristin³,Boeter Anne¹,Winter Stuart S.⁵,Loh Mignon³,Shannon Kevin³,Chakraborty Arup K.²⁶⁷⁸⁹,Wabl Matthias¹⁰,Roose Jeroen P.¹

Affiliation:

1. Department of Anatomy, University of California, San Francisco, San Francisco, CA 94143, USA.

2. Department of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, MA 02139, USA.

3. Department of Pediatrics, University of California, San Francisco, San Francisco, CA 94143, USA.

4. Department of Pathology, University of New Mexico School of Medicine, MSC 10 5590, Albuquerque, NM 87131, USA.

5. Department of Pediatrics, University of New Mexico School of Medicine, MSC 10 5590, Albuquerque, NM 87131, USA.

6. Department of Chemistry, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

7. Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

8. Department of Physics, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

9. Institute for Medical Engineering and Science, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

10. Department of Immunology, University of California, San Francisco, San Francisco, CA 94143, USA.

Abstract

Understanding the signaling mechanisms that can lead to T cell leukemia may enable personalized therapies.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference77 articles.

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2. Treatment of Acute Lymphoblastic Leukemia

3. Low incidence of second neoplasms among children diagnosed with acute lymphoblastic leukemia after 1983

4. Cytogenetics and molecular genetics of T-cell acute lymphoblastic leukemia: from thymocyte to lymphoblast

5. Molecular Genetics of Acute Lymphoblastic Leukemia

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