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Wenhao Chen

Researcher at Houston Methodist Hospital

Publications -  91
Citations -  2784

Wenhao Chen is an academic researcher from Houston Methodist Hospital. The author has contributed to research in topics: T cell & Transplantation. The author has an hindex of 24, co-authored 78 publications receiving 2420 citations. Previous affiliations of Wenhao Chen include University Health Network & University of Toledo.

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Unloaded heart in vivo replicates fetal gene expression of cardiac hypertrophy

TL;DR: In this article, the authors compared the patterns of gene expression in unloaded rat heart with those in hypertrophied rat heart and found that both conditions induced a re-expression of growth factors and proto-oncogenes, and a downregulation of the adult isoforms, but not of the 'fetal' isoforms.
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Generation and regulation of human CD4+ IL-17-producing T cells in ovarian cancer

TL;DR: A set of key cytokines secreted by ovarian tumor cells and tumor-associated APCs that favor the generation and expansion of human Th17 cells are identified and should accelerate efforts to define the function of this important subset of CD4+ T cells in the human immune response to cancer.
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Characterization of Distinct Conventional and Plasmacytoid Dendritic Cell-Committed Precursors in Murine Bone Marrow

TL;DR: It is reported that murine CD11c+MHC II− bone marrow cells, which are immediate DC precursors of CD8 α+, CD8α−, and B220+ DC in vivo, can be separated into B 220+ and B 220− DC precursor subpopulations.
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In Situ Replication of Immediate Dendritic Cell (DC) Precursors Contributes to Conventional DC Homeostasis in Lymphoid Tissue

TL;DR: It is shown that mouse CD11c+ MHC class II−lineage− cells are immediate precursors of conventional DC and are widely distributed in both bone marrow and lymphoid tissues and highlight the importance of in situ replication of immediate DCp and DC in maintaining conventional DC populations.
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“Default” Generation of Neonatal Regulatory T Cells

TL;DR: In this paper, the induction of Treg cells from neonatal T cells with various TCR stimulatory conditions, because TCR stimulation is required for Treg cell generation, was studied.