Hayglass Kent | Department Of Paediatrics And Child Health Mmunology Basic Medical Sciences Building
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概要
- HAYGLASS Kent T.の詳細を見る
- 同名の論文著者
- Department Of Paediatrics And Child Health Mmunology Basic Medical Sciences Buildingの論文著者
関連著者
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Hayglass Kent
Department Of Paediatrics And Child Health Mmunology Basic Medical Sciences Building
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HAYGLASS Kent
Department of Immunology, University of Manitoba
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Hayglass Kent
Departments Of Lmmunology University Of Manitoba
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Simons F.
Department Of Immunology University Of Manitoba
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SIMONS F.
Departments of Pediatrics University of Manitoba
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JAY Francis
Departments Medical Microbiology University of Manitoba
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Li Yan
Department Of Applied Physics Graduate School Of Engineering Osaka University
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Hayglass K
Basic Medical Sci. Building Manitoba Can
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REMPEL Julia
Department of Neuropharmacology
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WANG Mingdong
Department of Immunology, University of Manitoba
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Wang Mingdong
Department Of Immunology University Of Manitoba
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IMADA Mie
Department of Immunology, University of Manitoba
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Li Yan
Departments Of Lmmunology University Of Manitoba
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Simons F.
Department Of Paediatrics And Child Health Mmunology Basic Medical Sciences Building
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CAMPBELL J.
Department of Paediatrics and Child Health, mmunology, Basic Medical Sciences Building
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STINSON Monique
Department of Paediatrics and Child Health, mmunology, Basic Medical Sciences Building
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Stinson Monique
Department Of Paediatrics And Child Health Mmunology Basic Medical Sciences Building
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Imada Mie
Health Sciences Clinical Research Centre Department Of Immunology Faculty Of Medicine University Of
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Li Yan
Department Of Applied Chemistry Graduate School Of Engineering Kyushu University
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Campbell J.
Department Of Paediatrics And Child Health Mmunology Basic Medical Sciences Building
著作論文
- Failure of γIL-12 administration to inhibit established lgE responses in vivo is associated with enhanced IL-4 synthesisby non-B/non-T cells
- Allergen-driven limiting dilution analysis of human IL-4 and IFN-γ production in allergic rhinitis and clinically tolerant individuals
- Antigen mediated and polyclonal stimulation of human cytokine production elicit qualitatively different patterns of cytokine gene expression
- Systemic chemokine and chemokine receptor responses are divergent in allergic versus non-allergic humans