123 results on '"Dongiovanni, Paola"'
Search Results
2. TOP-301 Impact of clonal hematopoiesis of indeterminate potential on hepatocellular carcinoma in steatotic liver disease
3. WED-218 Circulating mitochondrial bioenergetic profile reflects the hepatic one and represents a non-invasive biomarker of disease severity in MASLD genetically predisposed individuals
4. FRI-544 KLB depletion fosters stem-like properties and epithelialmesenchymal transition plasticity in HepG2 cells
5. Rare ATG7 genetic variants predispose patients to severe fatty liver disease
6. Corrigendum to “SIRT5 rs12216101 T>G variant is associated with liver damage and mitochondrial dysfunction in patients with non-alcoholic fatty liver disease” [J Hepatol 80 (2024) 10-19]
7. SIRT5 rs12216101 T>G variant is associated with liver damage and mitochondrial dysfunction in patients with non-alcoholic fatty liver disease
8. Metabolic associated fatty liver disease: different impact of the three defining criteria on the hepatic and cardiovascular complications
9. The PNPLA3 I148M variant aggravates inflammation through dysfunctional LXR and PPAR gamma signalling in macrophages
10. The PNPLA3 I148M variant initiates metabolic reprogramming in macrophages
11. Programmed cell death 1 genetic variant and liver damage in non-alcoholic fatty liver disease
12. Combined hepatic and adipose tissue transcriptomics highlights circulating NASH biomarkers
13. The overexpression of TM6SF2 and/or MBOAT7 wild-type genes restores the mitochondrial lifecycle and activity in an in vitro NAFLD model
14. b-Klotho deficiency in hepatic stellate cells (HSCs) prompts inflammation, oxidative stress and a pro-fibrotic phenotype
15. PNPLA3, MBOAT7 and TM6SF2 modify mitochondrial dynamics in NAFLD patients: dissecting the role of cell-free circulating mtDNA and copy number
16. A functional interaction between hepatic estrogen receptor-α and PNPLA3 p.I148M inherited variant drives fatty liver disease susceptibility in women
17. MERTK rs4374383 polymorphism affects the severity of fibrosis in non-alcoholic fatty liver disease
18. Statin use and non-alcoholic steatohepatitis in at risk individuals
19. Rare ATG7 genetic variants predispose patients to severe fatty liver disease
20. Comparison of hepatic and cardiovascular damage between HIV patients with steatosis and NAFLD: role of metabolic alterations and low visceral adiposity
21. The co-presence of PNPLA3, MBOAT7 and TM6SF2 loss-of-functions impairs mitochondrial morphology and number in severe NAFLD patients
22. Increased burden of inherited IRF3 rare genetic variants in Europeans with severe Non-alcoholic fatty liver diease
23. The I48M PNPLA3 variant mitigates Niacin beneficial effects: how the genetic screening in non-alcoholic fatty liver disease (NAFLD) patients gains value
24. SIRT5 rs12216101 T > G variant is associated with mitochondrial dysfunction and disease severity in patients with NAFLD
25. The overexpression of TM6SF2 and/or MBOAT7 wild-type genes re-establishes the mitochondrial dynamics in an in vitro NAFLD model.
26. The different modulation of KLB expression impacts on liver damage in NAFLD patients and in an in vitro model: a novel druggable target?
27. Ceruloplasmin gene variants are associated with hyperferritinemia and increased liver iron in patients with NAFLD
28. Non-invasive stratification of hepatocellular carcinoma risk in non-alcoholic fatty liver using polygenic risk scores
29. WED-549 - Programmed cell death 1 genetic variant and liver damage in non-alcoholic fatty liver disease
30. WED-459 - Combined hepatic and adipose tissue transcriptomics highlights circulating NASH biomarkers
31. WED-547 - The overexpression of TM6SF2 and/or MBOAT7 wild-type genes restores the mitochondrial lifecycle and activity in an in vitro NAFLD model
32. WED-507 - b-Klotho deficiency in hepatic stellate cells (HSCs) prompts inflammation, oxidative stress and a pro-fibrotic phenotype
33. WED-418 - The PNPLA3 I148M variant aggravates inflammation through dysfunctional LXR and PPAR gamma signalling in macrophages
34. WED-405 - The PNPLA3 I148M variant initiates metabolic reprogramming in macrophages
35. WED-413 - PNPLA3, MBOAT7 and TM6SF2 modify mitochondrial dynamics in NAFLD patients: dissecting the role of cell-free circulating mtDNA and copy number
36. WED-393 - A functional interaction between hepatic estrogen receptor-α and PNPLA3 p.I148M inherited variant drives fatty liver disease susceptibility in women
37. THU-461 - Metabolic associated fatty liver disease: different impact of the three defining criteria on the hepatic and cardiovascular complications
38. TM6SF2/PNPLA3/MBOAT7 loss-of function genetic variants impact on NAFLD development and progression both in patients and in in vitro models
39. The PSRC1 rs599839 A > G variant disentangles the risk of coronary artery disease and hepatocellular carcinoma in Italian NAFLD patients
40. A polygenic risk score for progressive non-alcoholic fatty liver disease risk stratification
41. Validation of interleukin-32 as a new circulating fatty liver biomarker
42. Variants in PCSK7, PNPLA3 and TM6SF2 are risk factors for the development of cirrhosis in people with hereditary haemochromatosis
43. β-Klotho gene variation is associated with liver damage in children with NAFLD
44. TNFα genotype affects TNFα release, insulin sensitivity and the severity of liver disease in HCV chronic hepatitis
45. FRI-320-TM6SF2 silencing impairs lipid metabolism and trafficking in HepG2 cells carrying the I148M PNPLA3 variant and MBOAT7 deletion
46. PS-005-Evaluation of neuromedin-B receptor variants effect on iron metabolism and liver disease
47. PS-006-MBOAT7 downregulation induces hepatic lipid accumulation
48. FRI-333-ATG7 genetic variant and defective autophagy: A novel risk factor for non-alcoholic fatty liver disease progression in patients with type 2 diabetes mellitus
49. SAT-275-Interleukin-32 as a novel NAFLD biomarker in PNPLA31148M variant carriers
50. THU-323-Impact of genetic polymorphisms associated with NAFLD on hepatic and vascular complications in diabetes
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