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James N. Ihle

Researcher at St. Jude Children's Research Hospital

Publications -  284
Citations -  49163

James N. Ihle is an academic researcher from St. Jude Children's Research Hospital. The author has contributed to research in topics: Signal transduction & Interleukin 3. The author has an hindex of 110, co-authored 284 publications receiving 48182 citations. Previous affiliations of James N. Ihle include Columbia University & Ben-Gurion University of the Negev.

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STATs: signal transducers and activators of transcription.

TL;DR: Regarding biological functions, it can be anticipated that in the very near future the phenotypes of mice deficient in the remaining STATs will be described and will thus eliminate further speculation, and it would seem less likely as time goes on that additional family members will emerge.
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Lack of IL-4-induced Th2 response and IgE class switching in mice with disrupted Stat6 gene.

TL;DR: Stat6-l- mice were deficient in IL-4-mediated functions including Th2 helper T-cell differentiation, expression of cell surface markers, and immunoglobulin class switching to IgE, indicating the lack of a non-redundant function in normal development.
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Stat5a and Stat5b Proteins Have Essential and Nonessential, or Redundant, Roles in Cytokine Responses

TL;DR: The phenotypes of the mice demonstrate an essential, and often redundant, role for the two Stat5 proteins in a spectrum of physiological responses associated with growth hormone and prolactin.
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Cytokine receptor signalling

TL;DR: Many cell functions are regulated by members of the cytokine receptor superfamily, a family of transcription factors that contribute to the diversity of cytokine responses.
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Requirement for Stat4 in interleukin-12-mediated responses of natural killer and T cells

TL;DR: All IL-12 functions tested were disrupted, including the induction of IFN-γ, mitogenesis, enhancement of natural killer cytolytic function and Thl differentiation.