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1. A prospective study of risk factors associated with seroprevalence of SARS-CoV-2 antibodies in healthcare workers at a large UK teaching hospital

2. SARS-CoV-2 spike N-terminal domain modulates TMPRSS2-dependent viral entry and fusogenicity

3. Coagulation factor V is a T-cell inhibitor expressed by leukocytes in COVID-19

4. Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome

5. Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations

6. Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders

7. Germline mutations in the transcription factor IKZF5 cause thrombocytopenia

8. Human Semaphorin 3 Variants Link Melanocortin Circuit Development and Energy Balance

9. Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

10. Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes

11. Characterisation of dstpk61 in Drosophila development and the role of extramacrochaetae in Drosophila oogenesis

12. Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease

13. A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss

14. A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders

15. Phenotypic Characterization of EIF2AK4 Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension

16. SARS-CoV-2 spike N-terminal domain modulates TMPRSS2-dependent viral entry and fusogenicity

17. SARS-CoV-2 B.1.617.2 Delta variant replication and immune evasion

18. Whole-genome sequencing of patients with rare diseases in a national health system

19. Age-related immune response heterogeneity to SARS-CoV-2 vaccine BNT162b2

20. Single-cell multi-omics analysis of the immune response in COVID-19

21. Germline mutations in the transcription factor IKZF5 cause thrombocytopenia

22. Combined Point-of-Care Nucleic Acid and Antibody Testing for SARS-CoV-2 following Emergence of D614G Spike Variant

23. Publisher Correction:Whole-genome sequencing of a sporadic primary immunodeficiency cohort (Nature, (2020), 583, 7814, (90-95), 10.1038/s41586-020-2265-1)

24. Screening of healthcare workers for SARS-CoV-2 highlights the role of asymptomatic carriage in COVID-19 transmission

25. SARS-CoV-2 B.1.617.2 Delta variant replication and immune evasion

26. The Dichotomy of NMDA Receptor Signaling

27. Depression, anxiety and PTSD symptoms before and during the COVID-19 pandemic in the UK

28. Bayesian Inference Associates Rare KDR Variants With Specific Phenotypes in Pulmonary Arterial Hypertension

29. Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

30. Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations

31. Combined Point-of-Care Nucleic Acid and Antibody Testing for SARS-CoV-2 following Emergence of D614G Spike Variant

33. Phenotypic Characterization of EIF2AK4 Mutation Carriers in a Large Cohort of Patients Diagnosed Clinically With Pulmonary Arterial Hypertension

35. Whole-genome sequencing of a sporadic primary immunodeficiency cohort

36. A thermostable, closed SARS-CoV-2 spike protein trimer

38. Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis

39. Combined point of care nucleic acid and antibody testing for SARS-CoV-2 following emergence of D614G Spike Variant

40. Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome

42. De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures

43. Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity

44. A Prospective Study of Risk Factors Associated with Seroprevalence of SARS-CoV-2 Antibodies in Healthcare Workers at a Large UK Teaching Hospital

45. Telomerecat: A ploidy-agnostic method for estimating telomere length from whole genome sequencing data (vol 8, 1300, 2018)

46. Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

47. Expanded repertoire of RASGRP2 variants responsible for platelet dysfunction and severe bleeding

48. Cellular Notch responsiveness is defined by phosphoinositide 3-kinase-dependent signals

49. Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration

50. Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopenia

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