2022 - Research.com Immunology in Ireland Leader Award
2014 - Member of the Royal Irish Academy
Padraic G. Fallon mostly deals with Immunology, Innate lymphoid cell, Interleukin 13, Immune system and Cytokine. His Immunology research focuses on Interleukin, Inflammation, Atopic dermatitis, Interleukin 33 and Schistosoma mansoni. His Innate lymphoid cell study integrates concerns from other disciplines, such as Cell and Cellular differentiation.
He usually deals with Interleukin 13 and limits it to topics linked to Nippostrongylus brasiliensis and Immunoglobulin E, Antigen presentation, Interleukin 2 and Cell signaling. In general Immune system, his work in Acquired immune system, Interleukin 10, Regulatory B cells and IL-2 receptor is often linked to Population linking many areas of study. His research in Cytokine intersects with topics in Proinflammatory cytokine and Molecular biology.
Padraic G. Fallon spends much of his time researching Immunology, Immune system, Cell biology, Inflammation and Cytokine. His works in Schistosoma mansoni, Innate lymphoid cell, Atopic dermatitis, Antigen and Filaggrin are all subjects of inquiry into Immunology. His Innate lymphoid cell research incorporates themes from Cell and Interleukin 13.
His research in the fields of Immunity, Nippostrongylus brasiliensis, Regulatory B cells and Interleukin 10 overlaps with other disciplines such as Population. The various areas that Padraic G. Fallon examines in his Cell biology study include Receptor, Transcription factor and Cellular differentiation. His Inflammation research incorporates elements of Interleukin 33, Colitis and Psoriasis.
Immunology, Inflammation, Immune system, Atopic dermatitis and Innate lymphoid cell are his primary areas of study. His Immunology study frequently involves adjacent topics like Disease. His studies in Inflammation integrate themes in fields like Psoriasis, Stromal cell, Lung and Pathogenesis.
His work carried out in the field of Immune system brings together such families of science as Interleukin, Cytokine, Schistosoma mansoni and Cell biology. The concepts of his Atopic dermatitis study are interwoven with issues in Microbiome and Immunoglobulin E. His Innate lymphoid cell research is multidisciplinary, relying on both Interleukin 33, Cell, Interleukin 13 and Nippostrongylus brasiliensis.
His primary areas of investigation include Immunology, Inflammation, Innate lymphoid cell, Atopic dermatitis and Filaggrin. His Immunology study incorporates themes from Cell, Cancer research and Transcription factor. His studies deal with areas such as Psoriasis, House dust mite, Pathogenesis, Immune system and Receptor as well as Inflammation.
His study in Immune system is interdisciplinary in nature, drawing from both Antibody, Schistosoma mansoni and Microbiology. His work deals with themes such as Nippostrongylus brasiliensis, Interleukin 33, Interleukin 13 and Cytokine, which intersect with Innate lymphoid cell. His Atopic dermatitis study combines topics from a wide range of disciplines, such as Corneocyte and Cornified envelope.
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Nuocytes represent a new innate effector leukocyte that mediates type-2 immunity
Daniel R. Neill;See Heng Wong;Agustin Bellosi;Robin J. Flynn.
Nature (2010)
Identification of an interleukin (IL)-25–dependent cell population that provides IL-4, IL-5, and IL-13 at the onset of helminth expulsion
Padraic G. Fallon;Sarah J. Ballantyne;Niamh E. Mangan;Jillian L. Barlow.
Journal of Experimental Medicine (2006)
A role for IL-25 and IL-33-driven type-2 innate lymphoid cells in atopic dermatitis.
Maryam Salimi;Jillian L. Barlow;Sean P. Saunders;Luzheng Xue.
Journal of Experimental Medicine (2013)
The alarmin IL-33 promotes regulatory T-cell function in the intestine
Chris Schiering;Thomas Krausgruber;Agnieszka Chomka;Anja Fröhlich.
Nature (2014)
Transcription factor ROR alpha is critical for nuocyte development
See Heng Wong;See Heng Wong;Jennifer A Walker;Helen E Jolin;Lesley F Drynan.
Nature Immunology (2012)
T1/St2-Deficient Mice Demonstrate the Importance of T1/St2 in Developing Primary T Helper Cell Type 2 Responses
Michael J. Townsend;Padraic G. Fallon;David J. Matthews;Helen E. Jolin.
Journal of Experimental Medicine (2000)
Drug-resistant schistosomiasis: resistance to praziquantel and oxamniquine induced in Schistosoma mansoni in mice is drug specific.
Padraic G. Fallon;Michael J. Doenhoff.
American Journal of Tropical Medicine and Hygiene (1994)
Schistosome Infection of Transgenic Mice Defines Distinct and Contrasting Pathogenic Roles for IL-4 and IL-13: IL-13 Is a Profibrotic Agent
Padraic G. Fallon;Emma J. Richardson;Grahame J. McKenzie;Andrew N. J. McKenzie.
Journal of Immunology (2000)
MHCII-Mediated Dialog between Group 2 Innate Lymphoid Cells and CD4+ T Cells Potentiates Type 2 Immunity and Promotes Parasitic Helminth Expulsion
Christopher J. Oliphant;You Yi Hwang;Jennifer A. Walker;Maryam Salimi.
Immunity (2014)
A homozygous frameshift mutation in the mouse Flg gene facilitates enhanced percutaneous allergen priming
Padraic G Fallon;Takashi Sasaki;Aileen Sandilands;Linda E Campbell.
Nature Genetics (2009)
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