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1. Correction: Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

2. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

3. Autoantibody discovery across monogenic, acquired, and COVID-19-associated autoimmunity with scalable PhIP-seq.

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

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

6. Perturbations of the T-cell receptor repertoire in response to SARS-CoV-2 in immunocompetent and immunocompromised individuals

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

8. Genetically corrected RAG2-SCID human hematopoietic stem cells restore V(D)J-recombinase and rescue lymphoid deficiency

9. Poor T-cell receptor β repertoire diversity early posttransplant for severe combined immunodeficiency predicts failure of immune reconstitution

10. Autoantibodies Against Proteins Previously Associated With Autoimmunity in Adult and Pediatric Patients With COVID-19 and Children With MIS-C

11. Inherited ARPC5 mutations cause an actinopathy impairing cell motility and disrupting cytokine signaling

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

13. Disease-associated AIOLOS variants lead to immune deficiency/dysregulation by haploinsufficiency and redefine AIOLOS functional domains

14. Autoimmunity and immunodeficiency associated with monoallelic LIG4 mutations via haploinsufficiency

15. Artificial thymic organoids represent a reliable tool to study T-cell differentiation in patients with severe T-cell lymphopenia

18. Clinical exome sequencing of 1000 families with complex immune phenotypes: Toward comprehensive genomic evaluations

19. Immunopathological signatures in multisystem inflammatory syndrome in children and pediatric COVID-19

20. Case report: Artificial thymic organoids facilitate clinical decisions for a patient with a TP63 variant and severe persistent T cell lymphopenia.

21. Antibody responses to the SARS-CoV-2 vaccine in individuals with various inborn errors of immunity

22. SASH3 variants cause a novel form of X-linked combined immunodeficiency with immune dysregulation

23. Humans with inherited T cell CD28 deficiency are susceptible to skin papillomaviruses but are otherwise healthy

24. Time-resolved systems immunology reveals a late juncture linked to fatal COVID-19

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

29. The immunopathological landscape of human pre-TCRα deficiency: From rare to common variants

36. Mulibrey nanism and immunological complications: a comprehensive case report and literature review

37. Perturbations of the T-cell receptor repertoire in response to SARS-CoV-2 in immunocompetent and immunocompromised individuals.

38. Characterization of the antispike IgG immune response to COVID-19 vaccines in people with a wide variety of immunodeficiencies

39. Patients with CD3G mutations reveal a role for human CD3γ in Treg diversity and suppressive function

40. Expanded microbiome niches of RAG-deficient patients

42. Correction to: Gene Editing Rescues in Vitro T Cell Development of RAG2-Deficient Induced Pluripotent Stem Cells in an Artificial Thymic Organoid System

44. Autoimmunity and immunodeficiency associated with monoallelic LIG4 mutations via haploinsufficiency

45. Additional file 1 of Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

47. Autoantibody discovery across monogenic, acquired, and COVID-19-associated autoimmunity with scalable PhIP-seq

48. ImmunoTyper-SR: A computational approach for genotyping immunoglobulin heavy chain variable genes using short-read data

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