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Mouse Model of Devil Facial Tumour Disease Establishes That an Effective Immune Response Can be Generated Against the Cancer CellsThe Tasmanian devil transcriptome reveals Schwann cell origins of a clonally transmissible cancerTransmission of a fatal clonal tumor by biting occurs due to depleted MHC diversity in a threatened carnivorous marsupialFucoidan and cancer: a multifunctional molecule with anti-tumor potentialImmunology of a Transmissible Cancer Spreading among Tasmanian DevilsAcquisition of immune function during the development of the Langerhans cell network in neonatal miceReversible epigenetic down-regulation of MHC molecules by devil facial tumour disease illustrates immune escape by a contagious cancerA murine xenograft model for a transmissible cancer in Tasmanian devils.Genetic diversity and population structure of the endangered marsupial Sarcophilus harrisii (Tasmanian devil)Identification of dendritic cells, B cell and T cell subsets in Tasmanian devil lymphoid tissue; evidence for poor immune cell infiltration into devil facial tumors.Genome sequencing and analysis of the Tasmanian devil and its transmissible cancer.Natural killer cell mediated cytotoxic responses in the Tasmanian devilReduced effect of Tasmanian devil facial tumor disease at the disease front.A second transmissible cancer in Tasmanian devils.Demonstration of immune responses against devil facial tumour disease in wild Tasmanian devils.Fucoidan enhances the therapeutic potential of arsenic trioxide and all-trans retinoic acid in acute promyelocytic leukemia, in vitro and in vivo.The two faces of metallothionein in carcinogenesis: photoprotection against UVR-induced cancer and promotion of tumour survival.Ultraviolet radiation effects on the proteome of skin cells.Devil Facial Tumor Disease.Fucoidan Suppresses the Growth of Human Acute Promyelocytic Leukemia Cells In Vitro and In Vivo.Evidence for induction of humoral and cytotoxic immune responses against devil facial tumor disease cells in Tasmanian devils (Sarcophilus harrisii) immunized with killed cell preparations.Toll-like receptor signaling is functional in immune cells of the endangered Tasmanian devil.Comparative Analysis of Immune Checkpoint Molecules and Their Potential Role in the Transmissible Tasmanian Devil Facial Tumor Disease.Evidence that natural killer cells express mini P-glycoproteins but not classic 170 kDa P-glycoprotein.Mitochondrial cytochrome c release precedes transmembrane depolarisation and caspase-3 activation during ceramide-induced apoptosis of Jurkat T cells.DEC-205lo Langerinlo neonatal Langerhans' cells preferentially utilize a wortmannin-sensitive, fluid-phase pathway to internalize exogenous antigen.In vitro testing to diagnose venom allergy and monitor immunotherapy: a placebo-controlled, crossover trial.Vitamin D3 deficiency enhances contact hypersensitivity in male but not in female mice.Mitogen-activated Tasmanian devil blood mononuclear cells kill devil facial tumour disease cells.A histological and immunohistochemical analysis of lymphoid tissues of the Tasmanian devil.Discovery of Biomarkers for Tasmanian Devil Cancer (DFTD) by Metabolic Profiling of Serum.Dietary vitamin D alters the response of the skin to UVB-irradiation depending on the genetic background of the mice.The newly-arisen Devil facial tumour disease 2 (DFT2) reveals a mechanism for the emergence of a contagious cancerCarcinogen-modified dendritic cells induce immunosuppression by incomplete T-cell activation resulting from impaired antigen uptake and reduced CD86 expressionThe effect of season on cytokine expression in multiple sclerosis and healthy subjectsDecrease in Langerhans Cells and Increase in Lymph Node Dendritic Cells Following Chronic Exposure of Mice to Suberythemal Doses of Solar Simulated RadiationTumor-Specific Diagnostic Marker for Transmissible Facial Tumors of Tasmanian DevilsImpaired CD40-signalling in Langerhans' cells from murine neonatal draining lymph nodes: implications for neonatally induced cutaneous toleranceInduction of peripheral tolerance in neonatally thymectomized mice by immunization through chemical carcinogen-altered skinProteomics identifies enhanced expression of stefin A in neonatal murine skin compared with adults: functional implications
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P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Gregory M Woods
@ast
Gregory M Woods
@en
Gregory M Woods
@es
Gregory M Woods
@nl
type
label
Gregory M Woods
@ast
Gregory M Woods
@en
Gregory M Woods
@es
Gregory M Woods
@nl
altLabel
Greg Woods
@en
prefLabel
Gregory M Woods
@ast
Gregory M Woods
@en
Gregory M Woods
@es
Gregory M Woods
@nl
P1053
J-7533-2014
P106
P21
P31
P496
0000-0001-8421-7917