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1. Incontinentia pigmenti underlies thymic dysplasia, autoantibodies to type I IFNs, and viral diseases.

2. Tuberculosis in otherwise healthy adults with inherited TNF deficiency

3. Neutralizing IFN-γ autoantibodies are rare and pathogenic in HLA-DRB1*15:02 or 16:02 individuals.

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

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

7. Recombinant IFN-γ1b Treatment in a Patient with Inherited IFN-γ Deficiency

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

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

12. New Dominant-Negative IL6ST Variants Expand the Immunological and Clinical Spectrum of GP130-Dependent Hyper-IgE Syndrome

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

16. Neutralizing IFN-[gamma] autoantibodies are rare and pathogenic in HLA-DRB1*15:02 or 16:02 individuals

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

20. Human inherited CCR2 deficiency underlies progressive polycystic lung disease

21. Mendelian Susceptibility to Mycobacterial Disease (MSMD): Clinical, Immunological, and Genetic Features of 22 Patients from 15 Moroccan Kindreds

23. Human MCTS1-dependent translation of JAK2 is essential for IFN-γ immunity to mycobacteria

24. Anti-GM-CSF Neutralizing Autoantibodies in Colombian Patients with Disseminated Cryptococcosis

25. Mendelian Susceptibility to Mycobacterial Disease: Retrospective Clinical and Genetic Study in Mexico

26. Lymphoma as an Exclusion Criteria for CVID Diagnosis Revisited

28. List Of Contributors

30. Human IRF1 governs macrophagic IFN-γ immunity to mycobacteria

32. Correction to: New Dominant‑Negative IL6ST Variants Expand the Immunological and Clinical Spectrum of GP130‑Dependent Hyper‑IgE Syndrome

34. SCID and Other Inborn Errors of Immunity with Low TRECs — the Brazilian Experience

35. Pulmonary Alveolar Proteinosis and Multiple Infectious Diseases in a Child with Autosomal Recessive Complete IRF8 Deficiency

37. Inherited deficiency of stress granule ZNFX1 in patients with monocytosis and mycobacterial disease

38. Human CFTR deficient iPSC-macrophages reveal impaired functional and transcriptomic response upon Pseudomonas aeruginosa infection.

39. Case report: A novel JAK3 homozygous variant in a patient with severe combined immunodeficiency and persistent COVID-19.

40. A sensitive assay for measuring whole-blood responses to type I IFNs.

46. Multifocal tuberculosis: a phenotype of Mendelian susceptibility to mycobacterial disease

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

48. Hematologically important mutations: The autosomal forms of chronic granulomatous disease (third update)

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