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1. Severe Acute Flaccid Myelitis Associated With Enterovirus in Children: Two Phenotypes for Two Evolution Profiles?

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

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

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

5. SARS-CoV-2 activates the TLR4/MyD88 pathway in human macrophages: A possible correlation with strong pro-inflammatory responses in severe COVID-19

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

7. Single-Cell and Bulk RNA-Sequencing Reveal Differences in Monocyte Susceptibility to Influenza A Virus Infection Between Africans and Europeans

8. Toll-Like Receptor 3 Mediates Aortic Stenosis Through a Conserved Mechanism of Calcification

9. Inherited and acquired errors of type I interferon immunity govern susceptibility to COVID-19 and multisystem inflammatory syndrome in children

11. La panencéphalite sclérosante subaiguë de la rougeole

12. Encephalitis and poor neuronal death–mediated control of herpes simplex virus in human inherited RIPK3 deficiency

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

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

16. Measles Sclerosing Subacute PanEncephalitis (SSPE), an intriguing and ever-present disease: Data, assumptions and new perspectives

17. Neuron-intrinsic immunity to viruses in mice and humans

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

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

20. A computational approach for detecting physiological homogeneity in the midst of genetic heterogeneity

21. Author response: Autoantibody discovery across monogenic, acquired, and COVID-19-associated autoimmunity with scalable PhIP-seq

22. [Measles subacute sclerosing panencephalitis (SSPE): A still present and still mysterious fatal disease. History, Diagnosis and Assumptions]

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

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

26. Neuroinflammatory Disease following Severe Acute Respiratory Syndrome Coronavirus 2 Infection in Children

27. Genetic and immunologic evaluation of children with inborn errors of immunity and severe or critical COVID-19

28. Impaired IL-23-dependent induction of IFN-gamma underlies mycobacterial disease in patients with inherited TYK2 deficiency

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

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

31. Coronavirus Disease (COVID-19): Pathophysiology, Epidemiology, Clinical Management and Public Health Response

32. Herpes simplex virus encephalitis of childhood: inborn errors of central nervous system cell-intrinsic immunity

33. Inherited IFNAR1 deficiency in otherwise healthy patients with adverse reaction to measles and yellow fever live vaccines

34. A monocyte/dendritic cell molecular signature of SARS-CoV-2-related multisystem inflammatory syndrome in children with severe myocarditis

35. Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency

36. Autoantibodies neutralizing type I IFNs are present in

37. Insufficient type I IFN immunity underlies life-threatening COVID-19 pneumonia

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

39. Polyclonal expansion of TCR Vb 21.3 + CD4 + and CD8 + T cells is a hallmark of multisystem inflammatory syndrome in children

40. Polyclonal expansion of TCR Vbeta 21.3

41. Superantigenic TCR Vbeta 21.3 signature in Multisystem Inflammatory Syndrome in Children

42. SARS-CoV-2 induces human plasmacytoid predendritic cell diversification via UNC93B and IRAK4

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

47. A Monocyte/Dendritic Cell Molecular Signature of SARS-CoV-2 Related Multisystem Inflammatory Syndrome in Children (MIS-C) with Severe Myocarditis

49. Genome-wide detection of human variants that disrupt intronic branchpoints.

50. Heterogeneity of monocyte subsets and susceptibility to influenza virus contribute to inter-population variability of protective immunity

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