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30 results on '"Pelham, Simon J"'

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1. Tuberculosis in otherwise healthy adults with inherited TNF deficiency

2. Impaired development of memory B cells and antibody responses in humans and mice deficient in PD-1 signaling

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

4. STAT5B restrains human B-cell differentiation to maintain humoral immune homeostasis

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

7. Activating mutations in PIK3CD disrupt the differentiation and function of human and murine CD4+ T cells

8. Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficiencies

9. Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis

10. X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

11. X-linked recessive TLR7 deficiency in similar to 1% of men under 60 years old with life-threatening COVID-19

12. Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency

13. Biallelic TRAF3IP2 variants causing chronic mucocutaneous candidiasis in a child harboring a STAT1 variant

15. HumanSTAT3variants underlie autosomal dominant hyper-IgE syndrome by negative dominance

16. X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

17. X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19.

18. X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

19. Multibatch Cytometry Data Integration for Optimal Immunophenotyping

20. Activating mutations in PIK3CD and murine CD4(+) T cells

22. A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity

27. Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis

28. Multibatch Cytometry Data Integration for Optimal Immunophenotyping.

29. A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity

30. X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19.

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