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106 results on '"Yanick J. Crow"'

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

2. Type I interferonopathy due to a homozygous loss-of-inhibitory-function mutation in STAT2

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

4. STING-Mediated Lung Inflammation and Beyond

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

6. The 2021 Eurpean Alliance of Associations for Rheumatology/American College of Rheumatology points to consider for diagnosis and management of autoinflammatory type i interferonopathies: CANDLE/PRAAS, SAVI and AGS

7. Autosomal Dominant ADAR c.3019G>A (p.(G1007R)) Variant is an Important Mimic of Hereditary Spastic Paraplegia and Cerebral Palsy

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

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

10. Opsoclonus-myoclonus in Aicardi-Goutières syndrome

11. Use of ruxolitinib in COPA syndrome manifesting as life-threatening alveolar haemorrhage

12. DDX58 and Classic Singleton-Merten Syndrome

13. DNASE1L3 deficiency, new phenotypes, and evidence for a transient type I IFN signaling

14. 05 How interferonopathies inform SLE pathogenesis

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

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

17. Elevated antiviral, myeloid and endothelial inflammatory markers in severe COVID-19

18. Adult-Onset ANCA-Associated Vasculitis in SAVI: Extension of the Phenotypic Spectrum, Case Report and Review of the Literature

19. Mutations in COPA lead to abnormal trafficking of STING to the Golgi and interferon signaling

20. LACC1 deficiency links juvenile arthritis with autophagy and metabolism in macrophages

21. Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohorts

22. Severe type I interferonopathy and unrestrained interferon signaling due to a homozygous germline mutation in STAT2

23. PSMB10, the last immunoproteasome gene missing for PRAAS

24. A Brief Historical Perspective on the Pathological Consequences of Excessive Type I Interferon Exposure In vivo

25. International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity

26. Brief Report: Blockade of TANK-Binding Kinase 1/IKKɛ Inhibits Mutant Stimulator of Interferon Genes (STING)-Mediated Inflammatory Responses in Human Peripheral Blood Mononuclear Cells

27. Detection of interferon alpha protein reveals differential levels and cellular sources in disease

28. Tartrate‐Resistant Acid Phosphatase Deficiency in the Predisposition to Systemic Lupus Erythematosus

29. JAK 1/2 Blockade in MDA5 Gain-of-Function

30. Circulating interferon‐α measured with a highly sensitive assay as a biomarker for juvenile inflammatory myositis activity: Comment on the Article by Mathian et al

31. Self-Awareness: Nucleic Acid–Driven Inflammation and the Type I Interferonopathies

32. COPA syndrome as a cause of lupus nephritis

34. Efficacy of JAK1/2 inhibition in the treatment of chilblain lupus due to TREX1 deficiency

35. Bloom syndrome protein restrains innate immune sensing of micronuclei by cGAS

36. THU0009 Towards precision medicine in connective tissue diseases: genomic and transcriptomic studies

37. Comment on: ‘Aberrant tRNA processing causes an autoinflammatory syndrome responsive to TNF inhibitors’ by Giannelou et al : mutations in TRNT1 result in a constitutive activation of type I interferon signalling

38. Life-threatening influenza pneumonitis in a child with inherited IRF9 deficiency

39. Type I interferon-mediated autoinflammation due to DNase II deficiency

40. Interféronopathies de type I

41. Unusual cutaneous features associated with a heterozygous gain-of-function mutation inIFIH1: overlap between Aicardi-Goutières and Singleton-Merten syndromes

42. Mosaic Tetrasomy 9p: A Mendelian Condition Associated With Pediatric-Onset Overlap Myositis

43. Type I interferonopathies: Mendelian type I interferon up-regulation

44. Severe combined immunodeficiency in stimulator of interferon genes (STING) V154M/wild-type mice

45. Modeling of TREX1-Dependent Autoimmune Disease using Human Stem Cells Highlights L1 Accumulation as a Source of Neuroinflammation

46. The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies

47. Polymorphisms in IFIH1: the good and the bad

48. MDA5-associated neuroinflammation and the Singleton-Merten syndrome:two faces of the same type I interferonopathy spectrum

49. 320. TYPE 1 INTERFERON EXPRESSION IS ASSOCIATED WITH AUTOANTIBODIES ACROSS SYSTEMIC AUTOIMMUNE DISEASES: RESULTS FROM THE LUPUS EXTENDED AUTOIMMUNE PHENOTYPE STUDY

50. Assessment of Type I Interferon Signaling in Pediatric Inflammatory Disease

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