Author

Douglas F. Nixon

Division of Experimental Medicine Department of Medicine University of California San Francisco San Francisco USAPrimary ORCID profile (0000-0002-2801-1786 · 7 papers)Unclaimed ORCID profile · follow to get notified of new preprints

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Same name, identified by ORCID

Douglas F. NixoniD7 papers · Cornell University

Biology Disciplines

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Immunology· 2

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Assay:flow cytometry· 1

Frequent Co-Authors

Danielle Friberg· 1 shared Devi SenGupta· 1 shared Fabio Eudes Leal· 1 shared Inga E. Rødahl· 1 shared Jakob Michaëlsson· 1 shared Jeff E. Mold· 1 shared Jenny MjösbergiD· 1 shared Johan Van WeyenberghiD· 1 shared

Activity by Year

2018-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperImmunology

Danielle Friberg

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2 papers

Recent·Most cited

Distinct tissue-dependent composition and gene expression of human fetal innate lymphoid cells

Inga E. Rødahl, Martin A. Ivarsson, Liyen Loh, Jeff E. Mold, Magnus Westgren, Danielle Friberg, Jenny Mjösberg, Niklas K. Björkström, Nicole Marquardt, Douglas F. Nixon, Jakob Michaëlsson

This study examines fetal innate lymphoid cells (ILCs) across human tissues, revealing distinct distribution, developmental kinetics, and gene expression profiles, with a novel ILC progenitor identified in the fetal intestine.

bioRxiv · Mar 12, 2024Immunology

Age but not disease progression defines CD4+ and CD8+ T stem cell memory levels in human retroviral infections: contrasting effects of HTLV-1 and HIV-1

Soraya Maria Menezes, Fabio Eudes Leal, Susan Pereira Ribeiro, Tim Dierckx, Mario Roederer, Devi SenGupta, Douglas F. Nixon, Johan Van Weyenbergh

This study compares CD4+ and CD8+ TSCM levels in HTLV-1 and HIV-1 infections, finding age-driven accumulation in HTLV-1 and age-related loss in HIV-1 after treatment.

bioRxiv · Nov 19, 2018 · PreprintImmunology