Immunology, Cellular differentiation, Interleukin 4, Transcription factor and Cell biology are his primary areas of study. As a part of the same scientific family, Jinfang Zhu mostly works in the field of Cellular differentiation, focusing on Lymphokine and, on occasion, T helper cell and Cell activation. He has included themes like T-helper cell differentiation, Molecular biology, Immunoglobulin E and Immunity in his Interleukin 4 study.
He focuses mostly in the field of Transcription factor, narrowing it down to topics relating to Receptor and, in certain cases, Lymphocyte subsets and Epigenesis. His studies deal with areas such as Genetics, Cytokine and IL-2 receptor as well as Cell biology. His biological study spans a wide range of topics, including Interleukin 12, CD40 and Antigen-presenting cell.
His scientific interests lie mostly in Cell biology, Transcription factor, Immunology, Cellular differentiation and Molecular biology. Jinfang Zhu interconnects IL-2 receptor, Cytokine, Interleukin 4, GATA3 and Innate lymphoid cell in the investigation of issues within Cell biology. His work deals with themes such as Growth factor, Regulation of gene expression and Transcription, which intersect with Transcription factor.
His study in Immunology is interdisciplinary in nature, drawing from both Cell and Cytotoxic T cell. His Cellular differentiation research includes themes of T cell, Cancer research and Interferon gamma. His Molecular biology study integrates concerns from other disciplines, such as Interleukin 2, Chromatin, Signal transduction and Phosphorylation.
Jinfang Zhu spends much of his time researching Cell biology, Innate lymphoid cell, Transcription factor, Immune system and Immunology. His studies in Cell biology integrate themes in fields like Phenotype, Cell and Cytokine. His study focuses on the intersection of Innate lymphoid cell and fields such as Lymphatic system with connections in the field of Cell–cell interaction.
The concepts of his Transcription factor study are interwoven with issues in Progenitor cell, Germinal center and Cellular differentiation. His study on Cellular differentiation is mostly dedicated to connecting different topics, such as GATA3. His Immune system research also works with subjects such as
Jinfang Zhu mostly deals with Cell biology, Transcription factor, Immune system, Germinal center and Cell fate determination. His Cell biology research incorporates themes from Sphingosine, Chemotaxis, Innate lymphoid cell, Immunity and Lymphatic system. His Innate lymphoid cell study results in a more complete grasp of Acquired immune system.
His Transcription factor study incorporates themes from Progenitor cell, T cell, Cytokine and Cellular differentiation. His research integrates issues of Cell, Inflammation, Tumor-infiltrating lymphocytes, Antigen and FOXP3 in his study of Cellular differentiation. His research in Germinal center intersects with topics in Humoral immunity, Molecular biology and Memory B cell.
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Differentiation of Effector CD4 T Cell Populations
Jinfang Zhu;Hidehiro Yamane;William E. Paul.
Annual Review of Immunology (2010)
CD4 T cells: fates, functions, and faults
Jinfang Zhu;William E. Paul.
Blood (2008)
Global Mapping of H3K4me3 and H3K27me3 Reveals Specificity and Plasticity in Lineage Fate Determination of Differentiating CD4+ T Cells
Gang Wei;Lai Wei;Jinfang Zhu;Chongzhi Zang.
Immunity (2009)
How are T H 2-type immune responses initiated and amplified?
William E. Paul;Jinfang Zhu.
Nature Reviews Immunology (2010)
A Molecular Roadmap of Reprogramming Somatic Cells into iPS Cells
Jose M. Polo;Endre Anderssen;Endre Anderssen;Ryan M. Walsh;Benjamin A. Schwarz.
Cell (2012)
Conditional deletion of Gata3 shows its essential function in T(H)1-T(H)2 responses.
Jinfang Zhu;Booki Min;Jane Hu-Li;Cynthia J Watson.
Nature Immunology (2004)
Heterogeneity and plasticity of T helper cells.
Jinfang Zhu;William E Paul.
Cell Research (2010)
Peripheral CD4+ T‐cell differentiation regulated by networks of cytokines and transcription factors
Jinfang Zhu;William E. Paul.
Immunological Reviews (2010)
Opposing regulation of the locus encoding IL-17 through direct, reciprocal actions of STAT3 and STAT5.
Xiang Ping Yang;Kamran Ghoreschi;Scott M. Steward-Tharp;Jaime Rodriguez-Canales.
Nature Immunology (2011)
GATA-3 promotes Th2 responses through three different mechanisms: induction of Th2 cytokine production, selective growth of Th2 cells and inhibition of Th1 cell-specific factors
Jinfang Zhu;Hidehiro Yamane;Javier Cote-Sierra;Liying Guo.
Cell Research (2006)
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