User:Mpalmer

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[[Image:MPalmer_Profile_Pic.jpg|thumb|right|Megan J Palmer]]
[[Image:MPalmer_Profile_Pic.jpg|thumb|right|Megan J Palmer]]
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==Personal==
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==Bio==
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===Bio===
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I am a Postdoctoral Scholar in the [http://bioengineering.stanford.edu/ Department of Bioengineering] at [http://www.stanford.edu/ Stanford University] in the the labs of [[Endy_Lab | Drew Endy]] and [[Smolke | Christina Smolke]] and am serving as the Deputy Director of [http://synberc.org/practices Practices] for the [http://synberc.org/ Synthetic Biology Engineering Research Center (SynBERC)].
I am a Postdoctoral Scholar in the [http://bioengineering.stanford.edu/ Department of Bioengineering] at [http://www.stanford.edu/ Stanford University] in the the labs of [[Endy_Lab | Drew Endy]] and [[Smolke | Christina Smolke]] and am serving as the Deputy Director of [http://synberc.org/practices Practices] for the [http://synberc.org/ Synthetic Biology Engineering Research Center (SynBERC)].
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==Contact Info==
==Contact Info==
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Megan J Palmer, PhD
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Megan J. Palmer, Ph.D.
Stanford University
Stanford University
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473 Via Ortega, B07 Bioengineering
473 Via Ortega, B07 Bioengineering
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Stanford, California, USA
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Stanford, California, 94306
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USA
mjpalmer 'AT' stanford.edu
mjpalmer 'AT' stanford.edu
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2004 B.Sc.E. Engineering Chemistry, Queen's University, Kingston, ON, Canada
2004 B.Sc.E. Engineering Chemistry, Queen's University, Kingston, ON, Canada
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==Postdoctoral Research==
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'''Synthetic Biology Engineering Research Center (SynBERC)''', Deputy Director of Practices
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* Advisor: Drew Endy
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* Co-direct efforts within a multi-university engineering research center to explore how scientists and engineers can consider and respond to societal ramifications of developments in synthetic biology.
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'''Smolke Lab''', Stanford University, Department of Bioengineering
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* Advisor: Christina D. Smolke
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* Development of RNA devices to control cytokine responsiveness of T cells for immunotherapy applications
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==Graduate Research==
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'''Lauffenburger Lab''', Massachusetts Institute of Technology, Deptartment of Biological Engineering
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* Advisors: Douglas A. Lauffenburger, Darrell J. Irvine
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* ''Thesis Title: Cytokine Signaling Control of Naïve CD8+ T Cell Homeostasis''
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* Identified and characterized novel heterogeneities within CD8+ T cell populations in terms of their responsiveness to interleukin (IL) family cytokines supporting homeostatic survival and proliferation.
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* Performed experimental and mathematical modeling analysis of IL‐7 ligand/receptor binding dynamics and signaling, revealing receptor expression as the dominant controller of T cell responsiveness to IL‐7.
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* Translated in vitro results to in vivo murine models, demonstrating that modulation of IL‐7 levels in vivo alters the clonal composition of the T cell repertoire and revealing IL‐7 levels supporting homeostatic diversity.
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==Publications==
==Publications==
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Palmer MJ, Mahajan VS, Trajman LC, Irvine DJ, Lauffenburger DA, Chen J. (2008). Interleukin 7 Receptor Signaling Network: An Integrated Systems Perspective. Cellular and Molecular Immunology. 5(2): 79‐89.
Palmer MJ, Mahajan VS, Trajman LC, Irvine DJ, Lauffenburger DA, Chen J. (2008). Interleukin 7 Receptor Signaling Network: An Integrated Systems Perspective. Cellular and Molecular Immunology. 5(2): 79‐89.
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==Other==
==Other==

Revision as of 13:15, 25 June 2011

Back to Lab Members

Megan J Palmer
Megan J Palmer

Contents

Bio

I am a Postdoctoral Scholar in the Department of Bioengineering at Stanford University in the the labs of Drew Endy and Christina Smolke and am serving as the Deputy Director of Practices for the Synthetic Biology Engineering Research Center (SynBERC).


Contact Info

Megan J. Palmer, Ph.D.

Stanford University

Y2E2 Building

473 Via Ortega, B07 Bioengineering

Stanford, California, 94306

USA

mjpalmer 'AT' stanford.edu


Education

2010 Ph.D. Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA

2004 B.Sc.E. Engineering Chemistry, Queen's University, Kingston, ON, Canada


Postdoctoral Research

Synthetic Biology Engineering Research Center (SynBERC), Deputy Director of Practices

  • Advisor: Drew Endy
  • Co-direct efforts within a multi-university engineering research center to explore how scientists and engineers can consider and respond to societal ramifications of developments in synthetic biology.

Smolke Lab, Stanford University, Department of Bioengineering

  • Advisor: Christina D. Smolke
  • Development of RNA devices to control cytokine responsiveness of T cells for immunotherapy applications


Graduate Research

Lauffenburger Lab, Massachusetts Institute of Technology, Deptartment of Biological Engineering

  • Advisors: Douglas A. Lauffenburger, Darrell J. Irvine
  • Thesis Title: Cytokine Signaling Control of Naïve CD8+ T Cell Homeostasis
  • Identified and characterized novel heterogeneities within CD8+ T cell populations in terms of their responsiveness to interleukin (IL) family cytokines supporting homeostatic survival and proliferation.
  • Performed experimental and mathematical modeling analysis of IL‐7 ligand/receptor binding dynamics and signaling, revealing receptor expression as the dominant controller of T cell responsiveness to IL‐7.
  • Translated in vitro results to in vivo murine models, demonstrating that modulation of IL‐7 levels in vivo alters the clonal composition of the T cell repertoire and revealing IL‐7 levels supporting homeostatic diversity.


Publications

Palmer MJ*, Mahajan VS*, Chen J, Irvine DJ, Lauffenburger DA. (2011). Signaling Thresholds Govern Heterogeneity in IL‐7 Receptor‐Mediated Responses of Naïve CD8+ T Cells. "In Press". (*authors contributed equally)

Palmer MJ, Mahajan VS, Trajman LC, Irvine DJ, Lauffenburger DA, Chen J. (2008). Interleukin 7 Receptor Signaling Network: An Integrated Systems Perspective. Cellular and Molecular Immunology. 5(2): 79‐89.


Other

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