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Mark M. Davis

Researcher at Stanford University

Publications -  623
Citations -  84251

Mark M. Davis is an academic researcher from Stanford University. The author has contributed to research in topics: T cell & T-cell receptor. The author has an hindex of 144, co-authored 581 publications receiving 74358 citations. Previous affiliations of Mark M. Davis include Washington University in St. Louis & University of Chicago.

Papers
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Will Systems Biology Deliver Its Promise and Contribute to the Development of New or Improved Vaccines? Seeing the Forest Rather than a Few Trees

TL;DR: The level of success achieved as compared to the original promise of systems methodologies is discussed, and it is concluded that while inroads have been made into understanding the immune response to vaccines, there is still much to learn and gain from the more comprehensive approach of systems-level analysis.
Patent

Systems and methods for multiplexed measurements in single and ensemble cells

TL;DR: In this paper, systems and methods that can combine T cell receptor sequencing (TCRseq) and Assay for Transposase Accessible Chromatin using sequencing (ATAC-seq) are presented.
Journal Article

T-cell development in T cell receptor alphabeta transgenic mice.

TL;DR: Analysis of mice expressing transgenic T cell receptors specific for antigen plus MHC class I or class II molecules have demonstrated several important features of T cell development, including T cell maturation in the thymus is dependent on expression of an MHC molecule recognized by the T cell receptor.
Patent

Diagnostic markers of immunosenescence and methods of use thereof

TL;DR: In this paper, diagnostic markers of immunosenescence and methods of identifying individuals with impaired immune function based on a combination of such markers obtained from various analyses, primarily from blood, testing immune function including the analysis of immune cell subset frequencies, gene expression, cytokine and chemokine levels, and signaling responses to stimulation with cytokines (cytokine response).