415 results on '"MacLeod, Annette"'
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2. γδ T cells control murine skin inflammation and subcutaneous adipose wasting during chronic Trypanosoma brucei infection
3. Phenome-wide analysis reveals epistatic associations between APOL1 variants and chronic kidney disease and multiple other disorders
4. An easy to use tool for the analysis of subcellular mRNA transcript colocalisation in smFISH data
5. Impact of environmental factors on Biomphalaria pfeifferi vector capacity leading to human infection by Schistosoma mansoni in two regions of western Côte d'Ivoire
6. Publisher Correction: IL-17 signalling is critical for controlling subcutaneous adipose tissue dynamics and parasite burden during chronic murine Trypanosoma brucei infection
7. Murine trypanosomiasis recapitulates transcriptomic features of acute kidney injury
8. Interleukin 21 is a marker of Human African Trypanosomiasis Infection and a contributor to pathology in mice
9. Single cell and spatial transcriptomic analyses reveal microglia-plasma cell crosstalk in the brain during Trypanosoma brucei infection
10. Prevalence of dermal trypanosomes in suspected and confirmed cases of gambiense human African trypanosomiasis in Guinea.
11. APOL1 variants G1, G2 and N264K affect APOL1 plasma protein concentration: a UK Biobank study
12. FLAgellum Member 8 modulates extravascular distribution of African trypanosomes
13. Integrated spatial and single cell transcriptomic analyses reveal a critical role for V6 T cells in the control of skin inflammation during infection
14. Transcriptome profiles of Trypanosoma brucei rhodesiense in Malawi reveal focus specific gene expression profiles associated with pathology.
15. The murine meninges acquire lymphoid tissue properties and harbour autoreactive B cells during chronic Trypanosoma brucei infection
16. Differences in gene expression profiles in early and late stage rhodesiense HAT individuals in Malawi.
17. Association between polymorphisms of IL4, IL13, IL10, STAT6 and IFNG genes, cytokines and immunoglobulin E levels with high burden of Schistosoma mansoni in children from schistosomiasis endemic areas of Cameroon
18. Do Cryptic Reservoirs Threaten Gambiense-Sleeping Sickness Elimination?
19. The murine meninges acquire lymphoid tissue properties and harbour autoreactive B cells during chronic Trypanosoma brucei infection
20. The Genome of the African Trypanosome Trypanosoma brucei
21. The murine meninges acquire lymphoid tissue properties and harbour autoreactive B cells during chronic Trypanosoma brucei infection
22. The murine meninges acquire lymphoid tissue properties and harbour autoreactive B cells during chronicTrypanosoma bruceiinfection
23. Spatially-resolved single cell transcriptomics reveal a critical role for γδ T cells in the control of skin inflammation and subcutaneous adipose wasting during chronic Trypanosoma brucei infection
24. Spatially-resolved single cell transcriptomics reveal a critical role for γδ T cells in the control of skin inflammation and subcutaneous adipose wasting during chronicTrypanosoma bruceiinfection
25. Genetic Analysis of Phenotype in Trypanosoma brucei: A Classical Approach to Potentially Complex Traits
26. The Population Genetics of Trypanosoma brucei and the Origin of Human Infectivity
27. Minisatellite Marker Analysis of Trypanosoma brucei: Reconciliation of Clonal, Panmictic, and Epidemic Population Genetic Structures
28. The murine meninges acquire lymphoid tissue properties and harbour autoreactive B cells during chronic Trypanosoma brucei infection:Functional characterisation of the murine meninges during chronic infections
29. Genetic analysis of Trypanosoma brucei
30. Phenome-wide analysis ofAPOL1risk variants reveals associations between one combination of haplotypes and multiple disease phenotypes in addition to chronic kidney disease
31. FLAgellum Member 8 modulates extravasation and extravascular distribution of African trypanosomes
32. Normal Human Serum Lysis of Non-human Trypanosomes and Resistance of T. b. rhodesiense and T. b. gambiense
33. Distinct Differences in Gene Expression Profiles in Early and Late Stage Rhodesiense HAT Individuals in Malawi
34. Preliminary population genetic analysis of Trypanosoma lewisi
35. Interleukin-17 drives sex-dependent weight loss and changes in feeding behaviour during Trypanosoma brucei infection
36. Persistently High Incidences of Trypanosoma brucei rhodesiense Sleeping Sickness With Contrasting Focus-Dependent Clinical Phenotypes in Malawi
37. SARS-CoV-2 seroprevalence at urban and rural sites in Kaduna State, Nigeria, during October/November 2021, immediately prior to detection of the Omicron variant
38. Single cell and spatial transcriptomic analyses reveal microglia-plasma cell crosstalk in the brain during Trypanosoma brucei infection
39. Integrative single cell and spatial transcriptomic analysis reveal reciprocal microglia-plasma cell crosstalk in the mouse brain during chronicTrypanosoma bruceiinfection
40. Trypanosome resistance to human innate immunity: targeting Achilles’ heel
41. SARS-CoV-2 seroprevalence in Kaduna State, Nigeria during October/November 2021, following three waves of infection and immediately prior to detection of the Omicron variant
42. Mechanism of Trypanosoma brucei gambiense (group 1) resistance to human trypanosome lytic factor
43. Trypanosome genetics: Populations, phenotypes and diversity
44. Spatially and Genetically Distinct African Trypanosome Virulence Variants Defined by Host Interferon-γ Response
45. Raman spectroscopic analysis of skin as a diagnostic tool for Human African Trypanosomiasis
46. Transcriptional differentiation of Trypanosoma brucei during in vitro acquisition of resistance to acoziborole
47. A combination of variant genotypes at two loci in the APOL1 gene is associated with adverse outcomes in SARS-CoV-2: a UK Biobank study.
48. Corrigendum: To the Skin and Beyond: The Immune Response to African Trypanosomes as They Enter and Exit the Vertebrate Host
49. Extravascular dermal trypanosomes in suspected and confirmed cases of gambiense Human African Trypanosomiasis
50. Exploiting Genetic Variation to Discover Genes Involved in Important Disease Phenotypes
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