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5. Melanoma to Vitiligo: The Melanocyte in Biology & Medicine–Joint Montagna Symposium on the Biology of Skin/PanAmerican Society for Pigment Cell Research Annual Meeting

6. Immune Assessment Today: Optimizing and Standardizing Efforts to Monitor Immune Responses in Cancer and Beyond

8. Increased Otoferlin Expression in B Cells Is Associated with Muscle Weakness in Untreated Juvenile Dermatomyositis: A Pilot Study

9. Melanocyte-keratinocyte cross-talk in vitiligo

11. Targeting ULK1 Decreases IFNγ-Mediated Resistance to Immune Checkpoint Inhibitors

13. Clinical and immunologic evaluation of three metastatic melanoma patients treated with autologous melanoma-reactive TCR-transduced T cells

14. Alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 can support immune responses toward tumors overexpressing ganglioside D3 in mice

17. Benign tumors in TSC are amenable to treatment by GD3 CAR T cells in mice

18. Correction to: Clinical and immunologic evaluation of three metastatic melanoma patients treated with autologous melanoma-reactive TCR-transduced T cells

19. Editorial: Immunology of Vitiligo

23. Antigen Specificity Enhances Disease Control by Tregs in Vitiligo

25. Adoptive T-Cell Transfer to Treat Lymphangioleiomyomatosis

33. Adoptive T-Cell Transfer to Treat Lymphangioleiomyomatosis.

35. Ccl22 Diverts T Regulatory Cells and Controls the Growth of Melanoma

36. Alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1 can support immune responses toward tumors overexpressing ganglioside D3 in mice

37. The transfer of genetically engineered lymphocytes in melanoma patients: a Phase I dose escalation study

39. HSP70I IS A CRITICAL COMPONENT OF THE IMMUNE RESPONSE LEADING TO VITILIGO

41. Melanoma-Associated Antigen Expression in Lymphangioleiomyomatosis Renders Tumor Cells Susceptible to Cytotoxic T Cells

48. ORIGINAL ARTICLE Autoimmune Aspects of Depigmentation in Vitiligo.

49. A Quantitative Increase in Regulatory T Cells Controls Development of Vitiligo.

50. Monobenzyl Ether of Hydroquinone and 4-Tertiary Butyl Phenol Activate Markedly Different Physiological Responses in Melanocytes: Relevance to Skin Depigmentation.

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