180 results on '"Comegna, Marika"'
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2. Matrix metalloproteinases (MMP) 3 and 9 as biomarkers of severity in COVID-19 patients
3. Lumacaftor/ivacaftor improves liver cholesterol metabolism but does not influence hypocholesterolemia in patients with cystic fibrosis
4. The relevance of prothrombotic genetic variants in women who experienced pregnancy loss or embryo implantation failure: A retrospective analysis of 1922 cases
5. Assisting PNA transport through cystic fibrosis human airway epithelia with biodegradable hybrid lipid-polymer nanoparticles
6. The relevance of prothrombotic genetic variants in women who experienced pregnancy loss or embryo implantation failure: A retrospective analysis of 1922 cases.
7. TAS2R38 is a novel modifier gene in patients with cystic fibrosis
8. Proteomic analysis reveals novel common genes modulated in both replicative and stress-induced senescence
9. Inducible Nitric Oxide Synthase (iNOS): Why a Different Production in COVID-19 Patients of the Two Waves?
10. Corrigendum: Age-Related Differences in the Expression of Most Relevant Mediators of SARS-CoV-2 Infection in Human Respiratory and Gastrointestinal Tract
11. Further Findings Concerning Endothelial Damage in COVID-19 Patients
12. A Transient Increase in the Serum ANCAs in Patients with SARS-CoV-2 Infection: A Signal of Subclinical Vasculitis or an Epiphenomenon with No Clinical Manifestations? A Pilot Study
13. Effectiveness of Elexacaftor/Tezacaftor/Ivacaftor Therapy in Three Subjects with the Cystic Fibrosis Genotype Phe508del/Unknown and Advanced Lung Disease
14. Age-Related Differences in the Expression of Most Relevant Mediators of SARS-CoV-2 Infection in Human Respiratory and Gastrointestinal Tract
15. Molecular Analysis of Prothrombotic Gene Variants in Patients with Acute Ischemic Stroke and with Transient Ischemic Attack
16. Elexacaftor–Tezacaftor–Ivacaftor Therapy for Cystic Fibrosis Patients with The F508del/Unknown Genotype
17. Long-chain polyphosphates impair SARS-CoV-2 infection and replication
18. Abstracts from the 23rd Italian congress of Cystic Fibrosis and the 13th National congress of Cystic Fibrosis Italian Society
19. SARS-CoV-2 Subgenomic N (sgN) Transcripts in Oro-Nasopharyngeal Swabs Correlate with the Highest Viral Load, as Evaluated by Five Different Molecular Methods
20. NGS Gene Panel Analysis Revealed Novel Mutations in Patients with Rare Congenital Diarrheal Disorders
21. Lung Microbiome in Cystic Fibrosis
22. Assisting PNA Transport Through Cystic Fibrosis Human Airway Epithelia With Biodegradable Hybrid Lipid-Polymer Nanoparticles
23. Extensive CFTR Gene Analysis Revealed a Higher Occurrence of Cystic Fibrosis Transmembrane Regulator-Related Disorders (CFTR-RD) among CF Carriers
24. Long-chain polyphosphates impair SARS-CoV-2 infection and replication: a route for therapy in man
25. Impaired Ratio of Unsaturated to Saturated Non-Esterified Fatty Acids in Saliva from Patients with Cystic Fibrosis
26. Prothrombotic gene variants in acute myocardial infarction at a young age (yAMI). Rationale for tailored prevention strategies in specific risk-group subjects for acute coronary disease?
27. Salivary Cytokines and Airways Disease Severity in Patients with Cystic Fibrosis
28. Molecular Analysis of Prothrombotic Gene Variants in Venous Thrombosis: A Potential Role for Sex and Thrombotic Localization
29. Influence of pancreatic status on circulating plasma sterols in patients with cystic fibrosis
30. Comparative Evaluation of Nasal and Small Intestine Expression of ACE2, TMPRSS2 and ACE1 and in Children and in Adults
31. Prenatal Diagnosis of Cystic Fibrosis and Hemophilia: Incidental Findings and Weak Points
32. Molecular analysis of prothrombotic gene variants in venous thrombotic diseases. Different risk factors in different sex and clinical forms.
33. Adiponectin Expression Is Modulated by Long-Term Physical Activity in Adult Patients Affected by Cystic Fibrosis
34. Cystic Fibrosis: The Sense of Smell
35. Corrigendum: Gut Microbiota Features in Young Children With Autism Spectrum Disorders
36. Two CFTR mutations within codon 970 differently impact on the chloride channel functionality
37. Gut Microbiota Features in Young Children With Autism Spectrum Disorders
38. Clinical implication of cellular senescence on CFTR expression
39. Cystic Fibrosis: The Sense of Smell.
40. Two cases of microvillous inclusion disease caused by novel mutations inMYO5Bgene
41. S737F is a new CFTR mutation typical of patients originally from the Tuscany region in Italy
42. microRNA-494 promotes cellular senescence in human diploid fibroblasts by targeting several genes
43. Proteomics unveils novel targets of mir-494 involved in senescence
44. Twelve Novel Mutations in the SLC26A3 Gene in 17 Sporadic Cases of Congenital Chloride Diarrhea
45. Letter to the Editor: Is there an Indication for Testing the Methylenetetrahydrofolate reductase A1298C Variant in Routine Clinical Settings?
46. microRNA expression during the induction of cellular senescence
47. Genotype–phenotype correlation and functional studies in patients with cystic fibrosis bearing CFTR complex alleles
48. Genotype-phenotype correlation and functional studies in patients.
49. Comparative Analysis of Gene Expression Data Reveals Novel Targets of Senescence-Associated microRNAs
50. Identification of miR‐494 direct targets involved in senescence of human diploid fibroblasts
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