about
Prolonged antigen presentation is required for optimal CD8+ T cell responses against malaria liver stage parasitesRegional CNS responses to IFN-gamma determine lesion localization patterns during EAE pathogenesisGeneration, persistence and plasticity of CD4 T-cell memories.Immunobiology of transplantation: impact on targets for large and small molecules.Myeloid derived suppressor cells in transplantation.Interferon gamma in autoimmunity: A complicated player on a complex stage.Pre-existing central nervous system lesions negate cytokine requirements for regional experimental autoimmune encephalomyelitis development.Encephalitogenic T-cells increase numbers of CNS T-cells regardless of antigen specificity by both increasing T-cell entry and preventing egress.T-cell trafficking competence is required for CNS invasion.IL-1R signaling within the central nervous system regulates CXCL12 expression at the blood-brain barrier and disease severity during experimental autoimmune encephalomyelitis.Odorants specifically modulate chemotaxis and tissue retention of CD4+ T cells via cyclic adenosine monophosphate inductionA little stress is good: IFN-gamma, demyelination, and multiple sclerosis.Platelet-mediated modulation of adaptive immunity. A communication link between innate and adaptive immune compartments.Deletion is neither sufficient nor necessary for the induction of peripheral tolerance in mature CD8+ T cells.T-cell recognition of a prostate specific antigen is not sufficient to induce prostate tissue destructionEndogenous expansion of regulatory T cells leads to long-term islet graft survival in diabetic NOD miceEngineered MBP-specific human Tregs ameliorate MOG-induced EAE through IL-2-triggered inhibition of effector T cells
P50
Q27314913-EEE113FB-8565-4C4A-9B32-AE1CF191136CQ36946579-4F33E585-DC50-496B-85B2-6055D813D1A3Q37750904-8703E2C5-EE21-44B6-A24E-0984A4B21EEAQ37895906-AA0168E2-6B28-4810-B28B-A8A0B6A8214AQ37908629-82013460-5D3F-475F-BF4D-B5CAF450E9E1Q38281276-DCDD3305-55E6-4BE5-8261-1BD079D7EC6DQ39250432-FB1E0634-6700-451A-B8D3-96F8E4C308BAQ39737745-42D54D51-1D9A-47AD-998E-709F776EB35FQ40258680-07C2CBD6-71AC-46C1-8B59-C9C4B4102953Q41480082-AA7E8B87-CE2F-465B-9DEF-FBC5994CA32EQ41649263-24AE8EEE-FCE5-412A-A26E-6999A36B4E40Q42062694-9C86F8C0-ED53-47F5-9A52-DAE70F2E7F77Q47749276-1F10C458-36C7-4720-BA2F-681C324809A5Q54621906-68D05B96-8D83-4772-ABAF-9FB51A226AE0Q56797380-550FE6CD-569B-45F6-93F6-1E194055FB8AQ83386553-A03AEF01-1901-4CEA-8B54-BD5C5CC704F4Q88953756-29141E21-2137-4AD0-A7BB-8DA6CF2D542F
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Jason R. Lees
@ast
Jason R. Lees
@en
Jason R. Lees
@es
Jason R. Lees
@sl
type
label
Jason R. Lees
@ast
Jason R. Lees
@en
Jason R. Lees
@es
Jason R. Lees
@sl
prefLabel
Jason R. Lees
@ast
Jason R. Lees
@en
Jason R. Lees
@es
Jason R. Lees
@sl
P106
P1153
7201847794
P21
P31
P496
0000-0002-9965-1414