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29 results on '"Pelham, Simon J."'

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1. Tuberculosis in otherwise healthy adults with inherited TNF deficiency

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

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

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

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

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

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

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

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

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

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

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

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

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

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

18. Multibatch Cytometry Data Integration for Optimal Immunophenotyping

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

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

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

27. Multibatch Cytometry Data Integration for Optimal Immunophenotyping.

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

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

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