Matthew E. Call, Ph.D.

Affiliations: 
2007 Harvard University, Cambridge, MA, United States 
Area:
T Cell Biology and Cancer Immunology
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"Matthew Call"
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Kai W. Wucherpfennig grad student 2007 Harvard
 (Intramembrane organization of T cell receptor-CD3 complex assembly.)
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Publications

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Ramesh S, Park S, Im W, et al. (2022) T cell and B cell antigen receptors share a conserved core transmembrane structure. Proceedings of the National Academy of Sciences of the United States of America. 119: e2208058119
Elazar A, Chandler NJ, Davey AS, et al. (2022) De novo-designed transmembrane domains tune engineered receptor functions. Elife. 11
Trenker R, Wu X, Nguyen JV, et al. (2021) Human and viral membrane-associated E3 ubiquitin ligases MARCH1 and MIR2 recognize different features of CD86 to downregulate surface expression. The Journal of Biological Chemistry. 100900
Davey AS, Call ME, Call MJ. (2020) The Influence of Chimeric Antigen Receptor Structural Domains on Clinical Outcomes and Associated Toxicities. Cancers. 13
Chandler NJ, Call MJ, Call ME. (2020) T Cell Activation Machinery: Form and Function in Natural and Engineered Immune Receptors. International Journal of Molecular Sciences. 21
Ramesh S, Park S, Call MJ, et al. (2020) Experimentally Guided Computational Methods Yield Highly Accurate Insights into Transmembrane Interactions within the T Cell Receptor Complex. The Journal of Physical Chemistry. B
Bridgford JL, Lee SM, Lee CMM, et al. (2019) Novel Drivers and Modifiers of MPL-dependent Oncogenic Transformation Identified by Deep Mutational Scanning. Blood
van 't Hag L, de Campo L, Tran N, et al. (2019) A Protein-Eye View of the In Meso Crystallization Mechanism. Langmuir : the Acs Journal of Surfaces and Colloids
Brooks A, Campos L, Lee C, et al. (2019) THE MECHANISM OF ONCOGENIC MUTATIONS IN THE JUXTAMEMBRANE AND TRANSMEMBRANE REGION OF IL7RA AND TPOR/MPL Experimental Hematology. 76: S59
Tan C, Byrne EFX, Ah-Cann C, et al. (2018) A serine in the first transmembrane domain of the human E3 ubiquitin ligase MARCH9 is critical for down-regulation of its protein substrates. The Journal of Biological Chemistry
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