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282 results on '"Cooper, Megan A."'

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1. Monoallelic expression can govern penetrance of inborn errors of immunity

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

5. Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome.

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

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

9. A Case of Severe Combined Immunodeficiency Missed by Newborn Screening

10. Immunodeficiency and bone marrow failure with mosaic and germline TLR8 gain of function

11. Heterozygous mutations in the C-terminal domain of COPA underlie a complex autoinflammatory syndrome

12. Multiplexed Functional Assessment of Genetic Variants in CARD11

13. Responsiveness of sphingosine phosphate lyase insufficiency syndrome to vitamin B6 cofactor supplementation.

14. Hematopoietic Cell Transplantation in Patients With Primary Immune Regulatory Disorders (PIRD): A Primary Immune Deficiency Treatment Consortium (PIDTC) Survey.

15. Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis

16. STAT3 gain-of-function mutations connect leukemia with autoimmune disease by pathological NKG2Dhi CD8+ T cell dysregulation and accumulation

17. Gain-of-function mutations in RPA1 cause a syndrome with short telomeres and somatic genetic rescue

18. A human STAT3 gain-of-function variant drives local Th17 dysregulation and skin inflammation in mice

19. Case report: Deep sequencing and long-read genome sequencing refine prior genetic analyses in families with apparent gonadal mosaicism in PIK3CD-related activated PI3K delta syndrome.

21. MicroRNA-142 Is Critical for the Homeostasis and Function of Type 1 Innate Lymphoid Cells

23. Somatic mutations and clonal hematopoiesis in congenital neutropenia

26. Clonal hematopoiesis in survivors of childhood cancer

28. Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia

29. Monogenic early-onset lymphoproliferation and autoimmunity: Natural history of STAT3 gain-of-function syndrome

32. Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutations

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

34. Additional file 1 of Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

37. A human STAT3 gain-of-function variant confers T cell dysregulation without predominant Treg dysfunction in mice

39. Autoantibodies against type I IFNs in patients with critical influenza pneumonia

41. Vaccine breakthrough hypoxemic COVID-19 pneumonia in patients with auto-Abs neutralizing type I IFNs

42. Mutations in sphingosine-1-phosphate lyase cause nephrosis with ichthyosis and adrenal insufficiency

45. Clinical care of pregnant and postpartum women with COVID‐19: Living recommendations from the National COVID‐19 Clinical Evidence Taskforce

47. Building Life-Cycle Enhancement Multifunctionality into Glass Fiber Reinforced Composite Laminates via Hierarchical Assemblies of Aligned Carbon Nanotubes

49. Studying severe long COVID to understand post-infectious disorders beyond COVID-19

50. The risk of COVID-19 death is much greater and age-dependent with type I IFN autoantibodies

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