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Garry P. Nolan

Researcher at Stanford University

Publications -  519
Citations -  54521

Garry P. Nolan is an academic researcher from Stanford University. The author has contributed to research in topics: Immune system & T cell. The author has an hindex of 104, co-authored 474 publications receiving 46025 citations. Previous affiliations of Garry P. Nolan include Massachusetts Institute of Technology & New York University.

Papers
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Journal ArticleDOI

Isotopically Encoded Nanotags for Multiplexed Ion Beam Imaging.

TL;DR: A nanobarcoding platform is developed for multiplexed ion beam imaging (MIBI) using secondary ion beam spectrometry that utilizes fabricated isotopically encoded nanotags that should boost the performance of mass imaging platforms, such as MIBI and other elemental‐based bioimaging approaches.
Journal ArticleDOI

A Profile of 648 Signaling Network Events Identifies Cell Subsets with Diverse, Abnormal Responses to Lymphocyte Stimuli within Follicular Lymphoma Tumors.

TL;DR: The patterns of abnormal signaling observed in tumor B cells and tumor infiltrating T cells suggest that measuring the activity of key signaling network nodes can identify targets for therapeutic attention in FL, and suggests that signaling can distinguish between tumor sub-clones and could be used to measure tumor heterogeneity.
Journal ArticleDOI

Identification of a Novel Splice Donor Mutation In the Thrombopoietin Gene In a Philippine Family with Hereditary Thrombocythemia

TL;DR: The analysis of a Philippine family with a novel THPO gene mutation which segregates with the thrombocytosis phenotype demonstrates that the serum TPO concentration of family members with the THPO mutation was significantly higher than those family members without the mutation.
Patent

Lanthanide mass dots: nanoparticle isotope tags

TL;DR: In this article, compositions and methods for the use of nanoparticles, referred to herein as mass dots, as mass tags for probes such as antibodies, aptamers, nucleic acids, etc.
Posted ContentDOI

Multimodal and spatially resolved profiling identifies distinct patterns of T-cell infiltration in nodal B-cell lymphoma entities

TL;DR: In this paper , the authors employed single-cell RNA and T-cell receptor sequencing alongside quantification of surface proteins, flow cytometry and multiplexed immunofluorescence on 101 lymph nodes from healthy controls, and patients with diffuse large B-cell, mantle cell, follicular, or marginal zone lymphoma.