G
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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Functional cloning of SPIN-2, a nuclear anti-apoptotic protein with roles in cell cycle progression
TL;DR: It is suggested that SPIN-2 is a novel nuclear protein that functions to regulate cell cycle progression and this activity is related to the inhibition of apoptosis following the removal of essential growth factors.
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Unipotent Megakaryopoietic Pathway Bridging Hematopoietic Stem Cells and Mature Megakaryocytes
Hidekazu Nishikii,Yosuke Kanazawa,Terumasa Umemoto,Yury Goltsev,Yu Matsuzaki,Kenji Matsushita,Masayuki Yamato,Garry P. Nolan,Robert S. Negrin,Shigeru Chiba,Shigeru Chiba +10 more
TL;DR: The results suggest that the CD41+CD42b+LSK are straightforward progenies of megakaryocytes/platelet‐biased stem/repopulating cells, but not progenying of biEMP.
Patent
Rapid, stable high-titre production of recombing retrovirus
Garry P. Nolan,Todd Kinsella +1 more
TL;DR: In this article, a high titre helper-free recombinant retrovirus is produced by growing a transfected host cell, produced by transfecting a eukaryotic host cell with a recombinant vector capable of stable episomal maintenance in the host cell.
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Proliferation tracing with single-cell mass cytometry optimizes generation of stem cell memory-like T cells.
Zinaida Good,Luciene Borges,Nora Vivanco Gonzalez,Bita Sahaf,Nikolay Samusik,Robert Tibshirani,Garry P. Nolan,Sean C. Bendall +7 more
TL;DR: A dye dilution assay for tracking cell proliferative history through mass cytometry and uncouple division, time and regulatory protein expression in single naive human T cells during their activation and expansion in a complex ex vivo milieu can be broadly applied for directing cellular differentiation.
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Electron microscopy localization and characterization of functionalized composite organic-inorganic SERS nanoparticles on leukemia cells
TL;DR: The use of electron microscopy is demonstrated as a powerful characterization tool to identify and locate antibody-conjugated composite organic-inorganic nanoparticle (COINs) surface enhanced Raman scattering (SERS) nanoparticles on cells.