Supported Lipid Bilayer Technology for the Study of Cellular Interfaces-Reference-Cited by-同舟云学术

Supported Lipid Bilayer Technology for the Study of Cellular Interfaces

Published:2015-09 Issue:1 Volume:68 Page:
ISSN:1934-2500
Container-title:Current Protocols in Cell Biology
language:en
Short-container-title:Current Protocols in Cell Biology

Author:

Crites Travis J.¹²,Maddox Michael¹²,Padhan Kartika¹,Muller James¹³,Eigsti Calvin⁴,Varma Rajat¹

Affiliation:

1. Laboratory of Systems Biology, National Institute of Allergy and Infectious Diseases, National Institutes of Health Bethesda Maryland

2. These authors contributed equally to this work

3. Molecular Pathogenesis Program, Skirball Institute of Biomolecular Medicine, Department of Pathology, New York University School of Medicine New York New York

4. Flow Cytometry Section, Research Technologies Branch, National Institute of Allergy and Infectious Diseases, National Institutes of Health Bethesda Maryland

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/0471143030.cb2405s68

Reference69 articles.

1. Integration of the movement of signaling microclusters with cellular motility in immunological synapses

2. Cytoplasmic tail deletion of T cell receptor (TCR) beta‐chain results in its surface expression as glycosylphosphatidylinositol‐anchored polypeptide on mature T cells in the absence of TCR‐alpha;Bell L.M.;J. Biol. Chem.,1994

3. Actin and agonist MHC–peptide complex–dependent T cell receptor microclusters as scaffolds for signaling

4. LFA-1/ICAM-1 Interaction Lowers the Threshold of B Cell Activation by Facilitating B Cell Adhesion and Synapse Formation

5. Polarized release of T-cell-receptor-enriched microvesicles at the immunological synapse

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