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1. Tuberculosis in otherwise healthy adults with inherited TNF deficiency

2. Role of IL-27 in Epstein–Barr virus infection revealed by IL-27RA deficiency

4. Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency.

5. A Novel Case of IFNAR1 Deficiency Identified a Common Canonical Splice Site Variant in DOCK8 in Western Polynesia: The Importance of Validating Variants of Unknown Significance in Under-Represented Ancestries

6. A Novel Heterozygous Variant in AICDA Impairs Ig Class Switching and Somatic Hypermutation in Human B Cells and is Associated with Autosomal Dominant HIGM2 Syndrome

7. Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome.

9. Contributors

10. Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency

13. Human Inborn Errors of Immunity: 2022 Update on the Classification from the International Union of Immunological Societies Expert Committee.

14. Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection

15. FLT3L governs the development of partially overlapping hematopoietic lineages in humans and mice

16. Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths

17. Human STAT3 variants underlie autosomal dominant hyper-IgE syndrome by negative dominance

18. The Ever-Increasing Array of Novel Inborn Errors of Immunity: an Interim Update by the IUIS Committee

19. Coronavirus disease 2019 in patients with inborn errors of immunity: An international study

20. The 2022 Update of IUIS Phenotypical Classification for Human Inborn Errors of Immunity

22. Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome.

23. Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee.

24. Correction to: Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee

25. Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification

28. Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection

29. Helper T cell immunity in humans with inherited CD4 deficiency

30. STAT3 gain-of-function mutations connect leukemia with autoimmune disease by pathological NKG2Dhi CD8+ T cell dysregulation and accumulation

31. An essential role for the Zn2+ transporter ZIP7 in B cell development

34. Intrinsic Defects in B Cell Development and Differentiation, T Cell Exhaustion and Altered Unconventional T Cell Generation Characterize Human Adenosine Deaminase Type 2 Deficiency

35. International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity

36. The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies

37. Expanded T cell clones with lymphoma driver somatic mutations in refractory celiac disease

38. A Novel Heterozygous Variant in AICDA Impairs Ig Class Switching and Somatic Hypermutation in Human B Cells and is Associated with Autosomal Dominant HIGM2 Syndrome

41. Inherited PD-1 deficiency underlies tuberculosis and autoimmunity in a child

42. Genomic Spectrum and Phenotypic Heterogeneity of Human IL-21 Receptor Deficiency

43. Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency

45. Isolated Chronic Mucocutaneous Candidiasis due to a Novel Duplication Variant of IL17RC

47. A deep intronic splice mutation of STAT3 underlies hyper IgE syndrome by negative dominance

48. CD8+ T cell landscape in Indigenous and non-Indigenous people restricted by influenza mortality-associated HLA-A*24:02 allomorph

49. Three Copies of Four Interferon Receptor Genes Underlie a Mild Type I Interferonopathy in Down Syndrome

50. Everolimus-Induced Remission of Classic Kaposi’s Sarcoma Secondary to Cryptic Splicing Mediated CTLA4 Haploinsufficiency

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