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

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

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

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

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

8. Genetic adaptation to pathogens and increased risk of inflammatory disorders in post-Neolithic Europe

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

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

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

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

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

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

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

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

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

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

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

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

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

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