S. Gaffen

Immunology · 2007–2019

A researcher in the Science corpus: 7 papers; trusts 17 researchers and is trusted by 7 researchers here, as inferred from the citation graph.

Subfields

Whom S. Gaffen trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

  1. I. McInnes
  2. Georg Schett
  3. D. Cua
  4. M. McGeachy
  5. L. Harrington
  6. Xuexian O. Yang
  7. Yi Chen
  8. L. Steinman
  9. Paul R. Mangan
  10. E. Bettelli

Who trusts S. Gaffen overall

  1. D. Cua
  2. Nilesh Amatya
  3. Adriana Rendon
  4. M. McGeachy
  5. K. Futosi
  6. C. Rosales
  7. A. Garg

Papers from S. Gaffen's perspective

Ordered by how strongly the researchers S. Gaffen trusts endorse each paper. Same corpus, a different order for every researcher.

  1. Novel p19 protein engages IL-12p40 to form a cytokine, IL-23, with biological activities similar as well as distinct from IL-12.
  2. New IL-17 Family Members Promote Th1 or Th2 Responses in the Lung: In Vivo Function of the Novel Cytokine IL-251 (Journal of Immunology)
  3. Interleukin-23 Promotes a Distinct CD4 T Cell Activation State Characterized by the Production of Interleukin-17*
  4. Requirement of Interleukin 17 Receptor Signaling for Lung Cxc Chemokine and Granulocyte Colony-Stimulating Factor Expression, Neutrophil Recruitment, and Host Defense (Journal of Experimental Medicine)
  5. Divergent Pro- and Antiinflammatory Roles for IL-23 and IL-12 in Joint Autoimmune Inflammation (Journal of Experimental Medicine)
  6. Interleukin 27 limits autoimmune encephalomyelitis by suppressing the development of interleukin 17–producing T cells (Nature Immunology)
  7. Interleukin 17–producing CD4+ effector T cells develop via a lineage distinct from the T helper type 1 and 2 lineages (Nature Immunology)
  8. Induction of intestinal Th17 cells by segmented filamentous bacteria (Cell)
  9. IL-23 drives a pathogenic T cell population that induces autoimmune inflammation
  10. Interleukin 27 negatively regulates the development of interleukin 17–producing T helper cells during chronic inflammation of the central nervous system (Nature Immunology)

Their papers