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1. Variants and vaccines impact nasal immunity over three waves of SARS-CoV-2

2. Regulation of Paneth cell-specific genes in COVID-19 patients and SARS-CoV-2-infected mice by quantification of mRNA from exfoliated cells in stool samples

3. Factors Associated with Delays in Initiating Biologic Therapy in Patients with Inflammatory Bowel Disease

4. Mast cell activation syndrome: Current understanding and research needs

6. Genetically defined individual reference ranges for tryptase limit unnecessary procedures and unmask myeloid neoplasms

7. Activity of Various Cathepsin Proteases and Enrichment of Klotho Protein in the Urine and Urinary Extracellular Vesicles After SARS-CoV-2 Infection.

11. Impaired local intrinsic immunity to SARS-CoV-2 infection in severe COVID-19

12. Small intestinal immunopathology and GI-associated antibody formation in hereditary alpha-tryptasemia

13. An enhanced IL17 and muted type I interferon nasal epithelial cell state characterizes severe COVID-19 with fungal coinfection

14. Elevated basal serum tryptase identifies a multisystem disorder associated with increased TPSAB1 copy number

19. Enhanced production of eicosanoids in plasma and activation of DNA damage pathways in PBMCs are correlated with the severity of ancestral COVID-19 infection

24. Interleukin 1β Mediates Intestinal Inflammation in Mice and Patients With Interleukin 10 Receptor Deficiency

30. Severe COVID-19 is associated with fungal colonization of the nasopharynx and potent induction of IL-17 responses in the nasal epithelium

31. Enhanced TH17 Responses in Patients with IL10 Receptor Deficiency and Infantile-onset IBD

32. The Current State of Care for Black and Hispanic Inflammatory Bowel Disease Patients

34. Genetically determining individualized clinical reference ranges for the biomarker tryptase can limit unnecessary procedures and unmask myeloid neoplasms

35. Meta-genomic detection of Candida spp. in the nasopharynx and upper airway of patients with severe COVID-19

39. 653: PATIENTS WITH INFLAMMATORY BOWEL DISEASE HAVE IMPAIRED HUMORAL BUT PRESERVED CELLULAR RESPONSES TO SARS-COV-2 MRNA VACCINATION

40. 656: POST-VACCINATION SYMPTOMS AFTER A THIRD DOSE OF SARS-COV-2 MRNA VACCINATION IN PATIENTS WITH INFLAMMATORY BOWEL DISEASE

42. Urinary manifestations in African American and Caucasian inflammatory bowel disease patients: a retrospective cohort study

45. S717 Lower Therapeutic Response to Anti-TNF Agents in African Americans with Inflammatory Bowel Disease

49. Response to Cheng et al.

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