2015 - Fellow of the American Academy of Arts and Sciences
2015 - Member of the National Academy of Medicine (NAM)
2012 - Member of the National Academy of Sciences
1999 - AAI-BD Biosciences Investigator Award, American Association of Immunologists
His main research concerns FOXP3, Cell biology, Immunology, Regulatory T cell and Cellular differentiation. FOXP3 is a primary field of his research addressed under Immune system. His Immune system study incorporates themes from Transforming growth factor beta and Cell type.
His Cell biology study combines topics from a wide range of disciplines, such as T cell, IL-2 receptor, Major histocompatibility complex, MHC class II and Receptor. His Cellular differentiation research is multidisciplinary, incorporating elements of Innate lymphoid cell, Cell growth and Cell fate determination. His Forkhead Transcription Factors study in the realm of Transcription factor interacts with subjects such as Dicer.
Alexander Y. Rudensky focuses on Cell biology, Immunology, FOXP3, Immune system and T cell. His studies deal with areas such as Regulatory T cell, IL-2 receptor, Antigen, MHC class II and Antigen presentation as well as Cell biology. The Immunology study combines topics in areas such as Cytotoxic T cell and CD40.
He combines subjects such as Cellular differentiation, Transcription factor, Immune tolerance, Regulation of gene expression and Autoimmunity with his study of FOXP3. His Immune system research is multidisciplinary, incorporating elements of Cancer research and Effector. His T cell research includes elements of Cell and CD8.
His primary areas of investigation include Cell biology, Immune system, Transcription factor, Effector and T cell. The study incorporates disciplines such as Cell, Regulation of gene expression, Autoimmunity and FOXP3 in addition to Cell biology. He has included themes like Regulatory T cell, Transgene, Immune tolerance and Function in his FOXP3 study.
His work carried out in the field of Immune system brings together such families of science as Cancer and Antigen. His Antigen study is concerned with the larger field of Immunology. His studies deal with areas such as Cytotoxic T cell, IL-2 receptor, Phenotype, Chromatin and Epigenetics as well as Transcription factor.
His primary areas of study are Cell biology, Immune system, FOXP3, Transcription factor and Cell. His Cell biology research incorporates themes from Regulation of gene expression, Autoimmunity and Gene expression. His Regulation of gene expression research integrates issues from Regulatory T cell and Cell culture.
His Regulatory T cell research is within the category of IL-2 receptor. The concepts of his FOXP3 study are interwoven with issues in Cytokine, Farnesoid X receptor, Bile acid and Antigen. His study in the field of GATA3 is also linked to topics like Chromatin immunoprecipitation.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Foxp3 programs the development and function of CD4 + CD25 + regulatory T cells
Jason D. Fontenot;Marc A. Gavin;Alexander Y. Rudensky.
Nature Immunology (2003)
Regulatory T Cell Lineage Specification by the Forkhead Transcription Factor Foxp3
Jason D. Fontenot;Jeffrey P. Rasmussen;Luke M. Williams;James L. Dooley.
Immunity (2005)
Regulatory T Cells: Mechanisms of Differentiation and Function
Steven Z. Josefowicz;Li-Fan Lu;Alexander Y. Rudensky.
Annual Review of Immunology (2012)
Metabolites produced by commensal bacteria promote peripheral regulatory T-cell generation
Nicholas Arpaia;Clarissa Campbell;Xiying Fan;Stanislav Dikiy.
Nature (2013)
A function for interleukin 2 in Foxp3-expressing regulatory T cells
Jason D Fontenot;Jason D Fontenot;Jeffrey P Rasmussen;Marc A Gavin;Alexander Y Rudensky.
Nature Immunology (2005)
TGF-β-induced Foxp3 inhibits T H 17 cell differentiation by antagonizing RORγt function
Liang Zhou;Jared E. Lopes;Jared E. Lopes;Mark M. W. Chong;Ivaylo I. Ivanov.
Nature (2008)
Regulatory T cells prevent catastrophic autoimmunity throughout the lifespan of mice.
Jeong M Kim;Jeffrey P Rasmussen;Alexander Y Rudensky.
Nature Immunology (2007)
TGF-β-induced Foxp3 inhibits TH17 cell differentiation by antagonizing RORγt function
Liang Zhou;Jared E. Lopes;Mark M. W. Chong;Ivaylo I. Ivanov.
Nature (2008)
TGF-beta-induced Foxp3 inhibits T(H)17 cell differentiation by antagonizing RORgammat function.
Liang Zhou;Jared E Lopes;Mark M W Chong;Ivaylo I Ivanov.
Nature (2008)
A well adapted regulatory contrivance: regulatory T cell development and the forkhead family transcription factor Foxp3.
Jason D Fontenot;Alexander Y Rudensky.
Nature Immunology (2005)
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