276 results on '"Bonfiglio, Ferdinando"'
Search Results
2. Best practices for germline variant and DNA methylation analysis of second- and third-generation sequencing data
3. Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders
4. Rome III Criteria Capture Higher Irritable Bowel Syndrome SNP-Heritability and Highlight a Novel Genetic Link With Cardiovascular Traits
5. Functional Variation in Human CAZyme Genes in Relation to the Efficacy of a Carbohydrate-Restricted Diet in IBS Patients
6. Inherited rare variants in homologous recombination and neurodevelopmental genes are associated with increased risk of neuroblastoma
7. Germline rare variants of lectin pathway genes predispose to asymptomatic SARS-CoV-2 infection in elderly individuals
8. Genetic and phenotypic attributes of splenic marginal zone lymphoma
9. Increased Prevalence of Rare Sucrase-isomaltase Pathogenic Variants in Irritable Bowel Syndrome Patients
10. Female-Specific Association Between Variants on Chromosome 9 and Self-Reported Diagnosis of Irritable Bowel Syndrome
11. Single-cell transcriptomics of neuroblastoma identifies chemoresistance-associated genes and pathways
12. Exploring the role of HLA variants in neuroblastoma susceptibility through whole exome sequencing
13. Circulating tumor DNA for comprehensive noninvasive monitoring of lymphoma treated with ibrutinib plus nivolumab
14. Systemic Inflammation in Preclinical Ulcerative Colitis
15. Rare Hypomorphic Sucrase Isomaltase Variants in Relation to Irritable Bowel Syndrome Risk in UK Biobank
16. Dynamics of the human gut microbiome in inflammatory bowel disease.
17. Common variants at 21q22.3 locus influence MX1 and TMPRSS2 gene expression and susceptibility to severe COVID-19
18. A rationally designed oral vaccine induces immunoglobulin A in the murine gut that directs the evolution of attenuated Salmonella variants
19. Collagenous Colitis Is Associated With HLA Signature and Shares Genetic Risks With Other Immune-Mediated Diseases
20. Noncoding Regulatory Mutations as a Driving Event for the Oncogenic Core Regulatory Circuitries of Neuroblastoma
21. Functional variation in human Carbohydrate-Active enZYmes (hCAZymes) in relation to the efficacy of a FODMAP-reducing diet in IBS patients
22. Human CAZyme genes polymorphism and risk of IBS: a population-based study
23. Crohn’s Disease Is Associated With Activation of Circulating Innate Lymphoid Cells
24. P1225: CYLD, A NOVEL REGULATOR OF SPLENIC MARGINAL ZONE LYMPHOMA PATHOGENESIS
25. Human Leukocyte Antigen Signatures as Pathophysiological Discriminants of Microscopic Colitis Subtypes.
26. Clinical exome-based panel testing for medically actionable secondary findings in a cohort of 383 Italian participants
27. Human Leukocyte Antigen Signatures as Pathophysiological Discriminants of Microscopic Colitis Subtypes
28. Sucrase-isomaltase genotype and response to a starch-reduced and sucrose-reduced diet in IBS-D patients
29. Targeted Analysis of Serum Proteins Encoded at Known Inflammatory Bowel Disease Risk Loci
30. Sucrase-isomaltase genotype and response to a starch-reduced and sucrose-reduced diet in IBS-D patients.
31. Functional variants in the sucrase–isomaltase gene associate with increased risk of irritable bowel syndrome
32. Mitochondrial dysfunction in down syndrome: molecular mechanisms and therapeutic targets
33. TRPM8 polymorphisms associated with increased risk of IBS-C and IBS-M
34. Metformin restores the mitochondrial network and reverses mitochondrial dysfunction in Down syndrome cells
35. Stool frequency is associated with gut microbiota composition
36. Dense genotyping of immune-related loci identifies HLA variants associated with increased risk of collagenous colitis
37. Overexpression of the Hsa21 Transcription Factor RUNX1 Modulates the Extracellular Matrix in Trisomy 21 Cells
38. GWAS of stool frequency provides insights into gastrointestinal motility and irritable bowel syndrome
39. Functional annotation and investigation of the 10q24.33 melanoma risk locus identifies a common variant that influences transcriptional regulation ofOBFC1
40. Interferon-λ Enhances the Differentiation of Naive B Cells into Plasmablasts via the mTORC1 Pathway
41. NRIP1/RIP140 siRNA-mediated attenuation counteracts mitochondrial dysfunction in Down syndrome
42. Noncoding Regulatory Mutations as a Driving Event for the Oncogenic Core Regulatory Circuitries of Neuroblastoma †.
43. Human Trisomic iPSCs from Down Syndrome Fibroblasts Manifest Mitochondrial Alterations Early during Neuronal Differentiation
44. Tailored intestinal IgA responses can set an evolutionary trap for Salmonella Typhimurium
45. Systemic Inflammation in Preclinical Ulcerative Colitis
46. Crohn's Disease Is Associated With Activation of Circulating Innate Lymphoid Cells
47. 669 GASTROINTESTINAL DISEASE-RELATED SINGLE-NUCLEOTIDE VARIANTS (SNVS) COLOCALIZE WITH CIS-REGULATORY ELEMENTS (CRES) OF THE ELECTRICAL SLOW WAVE (SW)-ASSOCIATED GENE SLC4A4 IN A HUMAN MODEL OF PACEMAKER INTERSTITIAL CELLS OF CAJAL (ICC)
48. Chronic pro-oxidative state and mitochondrial dysfunctions are more pronounced in fibroblasts from Down syndrome foeti with congenital heart defects
49. Common Variants at 21q22.3 Locus Influence MX1 Gene Expression and Susceptibility to Severe COVID-19
50. Common variants at 21q22.3 locus influenceMX1gene expression and susceptibility to severe COVID-19
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.