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2. Ketolysis drives CD8+ T cell effector function through effects on histone acetylation

6. DNA methylation dynamics and dysregulation delineated by high-throughput profiling in the mouse

8. 13 C metabolite tracing reveals glutamine and acetate as critical in vivo fuels for CD8 T cells

9. Methionine Metabolism Shapes T Helper Cell Responses through Regulation of Epigenetic Reprogramming

13. Serine Is an Essential Metabolite for Effector T Cell Expansion

15. 13C metabolite tracing reveals glutamine and acetate as critical in vivo fuels for CD8+T cells

16. The histone lysine demethylase KDM5C fine-tunes gene expression to regulate dendritic cell heterogeneity and function

17. LKB1 controls inflammatory potential through CRTC2-dependent epigenetic remodeling

18. Inhibition of the mitochondrial pyruvate carrier simultaneously mitigates hyperinflammation and hyperglycemia in COVID-19

20. Inhibiting the MNK1/2-eIF4E axis impairs melanoma phenotype switching and potentiates antitumor immune responses

21. Human alveolar macrophage metabolism is compromised during Mycobacterium tuberculosis infection

22. Evolutionary Landscape of SOX Genes to Inform Genotype-to-Phenotype Relationships

24. Control of Effector CD8⁺ T Cell Function by the Transcription Factor Eomesodermin

27. Ketolysis is a metabolic driver of CD8+ T cell effector function through histone acetylation

32. DNA Methylation Dynamics and Dysregulation Delineated by High-Throughput Profiling in the Mouse

35. Th2 cell hyporesponsiveness during chronic murine schistosomiasis is cell intrinsic and linked to GRAIL expression

37. CD45 is a JAK phosphatase and negatively regulates cytokine receptor signalling

39. MicroRNA-9 Fine-Tunes Dendritic Cell Function by Suppressing Negative Regulators in a Cell-Type-Specific Manner

40. Negative regulation of lymphocyte activation and autoimmunity by the molecular adaptor Cbl-b

45. ACLY and ACSS2 link nutrient-dependent chromatin accessibility to CD8 T cell effector responses

46. Metabolic Profiling Using Stable Isotope Tracing Reveals Distinct Patterns of Glucose Utilization by Physiologically Activated CD8+ T Cells

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