Dynamic interaction networks in a hierarchically organized tissue-Reference-Cited by-同舟云学术

Dynamic interaction networks in a hierarchically organized tissue

Published:2010-01 Issue:1 Volume:6 Page:417
ISSN:1744-4292
Container-title:Molecular Systems Biology
language:en
Short-container-title:Mol Syst Biol

Author:

Kirouac Daniel C¹,Ito Caryn¹,Csaszar Elizabeth¹²,Roch Aline³,Yu Mei¹,Sykes Edward A¹,Bader Gary D⁴⁵⁶⁷⁸,Zandstra Peter W¹²⁴⁹¹⁰

Affiliation:

1. Institute for Biomaterials and Biomedical Engineering, University of Toronto Toronto Ontario Canada

2. Department of Chemical Engineering and Applied Chemistry, University of Toronto Toronto Ontario Canada

3. Ecole Polytechnique Fédérale de Lausanne Lausanne Switzerland

4. Terrence Donnelly Centre for Cellular and Biomolecular Research, University of Toronto Toronto Ontario Canada

5. Banting and Best Department of Medical Research, University of Toronto Toronto Ontario Canada

6. Department of Medical Genetics, University of Toronto Toronto Ontario Canada

7. Department of Computer Science, University of Toronto Toronto Ontario Canada

8. Samuel Luenfeld Research Institute, Joseph and Wolf Lebovic Health Complex, Mount Sinai Hospital Toronto Ontario Canada

9. Heart and Stroke/Richard Lewar Centre of Excellence, University of Toronto Toronto Ontario Canada

10. McEwen Centre for Regenerative Medicine, University Health Network, Toronto Medical Discovery Tower Toronto Ontario Canada

Publisher

EMBO

Subject

Applied Mathematics,Computational Theory and Mathematics,General Agricultural and Biological Sciences,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Information Systems

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1038/msb.2010.71

Reference39 articles.

1. Assessment of Chemical Coverage of Kinome Space and Its Implications for Kinase Drug Discovery

2. Online Predicted Human Interaction Database

3. Regulation of hematopoiesis in a sea of chemokine family members with a plethora of redundant activities

4. Self-Renewal of Multipotent Long-Term Repopulating Hematopoietic Stem Cells Is Negatively Regulated by FAS and Tumor Necrosis Factor Receptor Activation

5. Mechanisms that regulate the cell cycle status of very primitive hematopoietic cells in long-term human marrow cultures. I. Stimulatory role of a variety of mesenchymal cell activators and inhibitory role of TGF-beta

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