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106 results on '"ANR-10-IAHU-0001,Imagine,Institut Hospitalo-Universitaire Imagine(2010)"'

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1. JAK inhibition in Aicardi-Goutières syndrome: a monocentric multidisciplinary real-world approach study

2. Type I interferons and SARS-CoV-2: from cells to organisms

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

4. Human type I IFN deficiency does not impair B cell response to SARS-CoV-2 mRNA vaccination

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

6. Defective activation and regulation of type I interferon immunity is associated with increasing COVID-19 severity

7. Type I interferon response and vascular alteration in chilblain‐like lesions during the COVID‐19 outbreak*

8. Defective type I interferon immunity is associated with increasing COVID-19 severity

9. Juvenile Neuropsychiatric Systemic Lupus Erythematosus: Identification of Novel Central Neuroinflammation Biomarkers

10. A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes

11. In silico model reveals the key role of GABA in KCNT1 ‐epilepsy in infancy with migrating focal seizures

12. Inherited IFNAR1 Deficiency in a Child with Both Critical COVID-19 Pneumonia and Multisystem Inflammatory Syndrome

13. Biallelic variants in TAMM41 are associated with low muscle cardiolipin levels, leading to neonatal mitochondrial disease

14. 2D and 3D Human Induced Pluripotent Stem Cell-Based Models to Dissect Primary Cilium Involvement during Neocortical Development

15. A partial form of inherited human USP18 deficiency underlies infection and inflammation

16. Three Copies of Four Interferon Receptor Genes Underlie a Mild Type I Interferonopathy in Down Syndrome

17. Severe COVID-19 is associated with hyperactivation of the alternative complement pathway

18. A global effort to dissect the human genetic basis of resistance to SARS-CoV-2 infection

19. Long-term safety and efficacy of lentiviral hematopoietic stem/progenitor cell gene therapy for Wiskott-Aldrich syndrome

20. 3D cell morphology detection by association for embryo heart morphogenesis

21. Genome sequencing for genetics diagnosis of patients with intellectual disability: the DEFIDIAG study

22. Mining electronic health records for drugs associated with 28-days mortality in COVID-19: a pharmacopoeia wide association study (PharmWAS)

23. Exploiting natural antiviral immunity for the control of pandemics: Lessons from Covid-19

24. Pseudodynamic analysis of heart tube formation in the mouse reveals strong regional variability and early left–right asymmetry

25. Platelet activation in critically ill COVID-19 patients

26. Inborn errors of TLR3- or MDA5-dependent type I IFN immunity in children with enterovirus rhombencephalitis

27. Monoclonal antibody-mediated neutralization of SARS-CoV-2 in an IRF9-deficient child

28. Early nasal type I IFN immunity against SARS-CoV-2 is compromised in patients with autoantibodies against type I IFNs

29. Recent Progress in Genome Editing for Gene Therapy Applications: The French Perspective

30. Autoantibodies Neutralizing Type I Interferons in 20% of COVID-19 Deaths in a French Hospital

31. Heart Development and Congenital Structural Heart Defects

32. Mitochondrial Nucleic Acid as a Driver of Pathogenic Type I Interferon Induction in Mendelian Disease

33. Immune checkpoint inhibitors increase T cell immunity during SARS-CoV-2 infection

34. Enhanced cGAS-STING–dependent interferon signaling associated with mutations in ATAD3A

35. Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes

36. SARS-CoV-2-related MIS-C:A key to the viral and genetic causes of Kawasaki disease?

37. Bi-allelic variants in IPO8 cause a connective tissue disorder associated with cardiovascular defects, skeletal abnormalities, and immune dysregulation

38. A monocyte/dendritic cell molecular signature of SARS-CoV2-related multisystem inflammatory syndrome in children (MIS-C) with severe myocarditis

39. Viral infections in humans and mice with genetic deficiencies of the type I IFN response pathway

40. Human ancient DNA analyses reveal the high burden of tuberculosis in Europeans over the last 2,000 years

41. Overview of STING-Associated Vasculopathy with Onset in Infancy (SAVI) Among 21 Patients

42. Differential Expression of Interferon-Alpha Protein Provides Clues to Tissue Specificity Across Type I Interferonopathies

43. Negative selection on human genes underlying inborn errors depends on disease outcome and both the mode and mechanism of inheritance

44. TLR3 controls constitutive IFN-β antiviral immunity in human fibroblasts and cortical neurons

45. Herpes simplex encephalitis in a patient with a distinctive form of inherited IFNAR1 deficiency

46. Pre-existing Autoantibodies Neutralizing High Concentrations of Type I Interferons in Almost 10% of COVID-19 Patients Admitted to Intensive Care in Barcelona

47. Human T-bet Governs Innate and Innate-like Adaptive IFN-γ Immunity against Mycobacteria

48. A common TMPRSS2 variant has a protective effect against severe COVID-19

49. Shaping the mouse heart tube from the second heart field epithelium

50. Transient Nodal Signaling in Left Precursors Coordinates Opposed Asymmetries Shaping the Heart Loop

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