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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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Journal ArticleDOI

Shariant platform: Enabling evidence sharing across Australian clinical genetic-testing laboratories to support variant interpretation.

TL;DR: Shariant as mentioned in this paper is a platform for sharing genomic variant interpretations across laboratories to promote consistency in variant assertions and improve inter-laboratory concordance and enable opportunities to standardize interpretation practices.
Patent

Method and system for robust and sensitive analysis of bead-based assays

TL;DR: In this article, computer-implemented methods and systems for the analysis of multiplex fluorescent-dyed microsphere assays are provided for determination of differences in analyte quantities.
Journal ArticleDOI

Visualizing T cell recognition

TL;DR: Experimental "Autoimmune" versus "Allergic" Encephalomyelitis IL Dal Canto, G. Costa, L. Steinman, Stanford University, Stanford, USA, M. Fathman, and M. Dubois-Dalcq.
Posted ContentDOI

Single-cell sequencing unveils distinct immune microenvironment with CCR6-CCL20 crosstalk in human chronic pancreatitis

TL;DR: In this article, the authors performed single-cell level cellular indexing of transcriptomes and epitopes by sequencing (CITE-Seq) and T cell receptor sequencing of pancreatic immune cells isolated from organ donors, hereditary, and idiopathic CP patients who underwent total pancreatectomy.
Journal Article

An immunoglobulin heavy chain variable region gene is generated from three segments of DNA: VH, D and JH. 1980.

TL;DR: A model for variable region gene rearrangement mediated by proteins which recognize the same conserved sequences adjacent to both light and heavy chain immunoglobulin gene segments is proposed.