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1. Tuberculosis in otherwise healthy adults with inherited TNF deficiency

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

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

6. Human inherited CCR2 deficiency underlies progressive polycystic lung disease

7. Preexisting autoantibodies to type I IFNs underlie critical COVID-19 pneumonia in patients with APS-1

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

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

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

15. Inherited GATA2 Deficiency Is Dominant by Haploinsufficiency and Displays Incomplete Clinical Penetrance

16. A novel pediatric polycystic lung disease caused by CCR2 deficiency

18. Inborn errors of OAS-RNase L in SARS-CoV-2-related multisystem inflammatory syndrome in children

19. OC 9 - HOMOZYGOUS CBL MUTATION IN B LYMPHOCYTES AFTER CBL-DRIVEN JMML IMPAIRS B CELL MATURATION, FUNCTION AND ANTIBACTERIAL IMMUNITY

20. Human IL-23 is essential for IFN-γ–dependent immunity to mycobacteria

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

22. Inborn errors of OAS–RNase L in SARS-CoV-2–related multisystem inflammatory syndrome in children

23. A New Patient with p40phox Deficiency and Chronic Immune Thrombocytopenia.

25. Fulminant Viral Hepatitis in Two Siblings with Inherited IL-10RB Deficiency

27. Human OTULIN haploinsufficiency impairs cell-intrinsic immunity to staphylococcal a-toxin

28. Human OTULIN haploinsufficiency impairs cell-intrinsic immunity to staphylococcal α-toxin

29. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

30. Human genetic and immunological determinants of critical COVID-19 pneumonia

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

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

33. Impaired respiratory burst contributes to infections in PKCδ-deficient patients

34. Genetic, Immunological, and Clinical Features of 32 Patients with Autosomal Recessive STAT1 Deficiency

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

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

37. Gap Junction Dependent Cell Communication Is Modulated During Transdifferentiation of Mesenchymal Stem/Stromal Cells Towards Neuron-Like Cells

38. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

39. Human Lentiviral Gene Therapy Restores the Cellular Phenotype of Autosomal Recessive Complete IFN-γR1 Deficiency

40. Patient iPSC-Derived Macrophages to Study Inborn Errors of the IFN-γ Responsive Pathway

41. Fatal Cytomegalovirus Infection in an Adult with Inherited NOS2 Deficiency

42. An immune cell spray (ICS) formulation allows for the delivery of functional monocyte/ macrophages

43. Protocol to develop human Alveolar Macrophage-Like (AML) cells from mononuclear cells or purified monocytes for use in respiratory biology research

44. Impaired IFNγ-Signaling and Mycobacterial Clearance in IFNγR1-Deficient Human iPSC-Derived Macrophages

47. Impaired respiratory burst contributes to infections in PKC delta-deficient patients

48. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

49. Impaired respiratory burst contributes to infections in PKC-deficient patients

50. Inborn errors of OAS-RNase L in SARS-CoV-2-related multisystem inflammatory syndrome in children.

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