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Lewis L. Lanier

Researcher at University of California, San Francisco

Publications -  576
Citations -  93495

Lewis L. Lanier is an academic researcher from University of California, San Francisco. The author has contributed to research in topics: Interleukin 21 & Natural killer cell. The author has an hindex of 159, co-authored 554 publications receiving 86677 citations. Previous affiliations of Lewis L. Lanier include University of Rome Tor Vergata & Cancer Research Institute.

Papers
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Journal ArticleDOI

Activating Receptors for Self-MHC Class I Enhance Effector Functions and Memory Differentiation of NK Cells during Mouse Cytomegalovirus Infection.

TL;DR: Comparison of the activation and differentiation of Ly49D-bearing NK cells in mice lacking or expressing H-2D(d), the cognate MHC class I ligand of Ly 49D shows that activating receptors for self-MHCclass I modulate the differentiation of MCMV-specific NK cells and are beneficial for host defense against MCVV infection.
Patent

Differentiation of natural killer cell subpopulations of cells

TL;DR: In this article, a method for distinguishing multiple subpopulations of a cell sample was proposed, whereby human natural killer cells sub-populations can be monitored by using two monoclonal antibodies identified as anti-Leu-7 and anti-leu-11.
Patent

Method for monitoring activated cell subpopulations

TL;DR: In this paper, a method of distinguishing multiple subpopulations of a cell sample was proposed, whereby resting and activated human natural killer cells sub-populations can be monitored using two monoclonal antibodies identified as antiLeu 11 and anti-DR (or anti-Leu 10 or anti-transferrin receptor).
Journal ArticleDOI

CD28/CTLA-4 ligands: the gene encoding CD86 (B70/B7.2) maps to the same region as CD80 (B7/B7.1) gene in human chromosome 3q13-q23.

TL;DR: The assignment of the CD86 gene to human chromosome 3 is reported here using Southern blot analysis on a panel of hamster × human somatic cell hybrid genomic DNA and fluorescence hybridization in situ on metaphase chromosomes coupled with GTG banding confirmed this assignment and localized it to 3q13‐q23 region.