List of works - Raffaela Rametta

A novel alpha1-antitrypsin null variant (PiQ0Milano ).

scientific article published on August 2013

A randomized trial of iron depletion in patients with nonalcoholic fatty liver disease and hyperferritinemia.

scientific article published on March 2014

A tetra-primer amplification refractory mutation system polymerase chain reaction for the evaluation of rs12979860 IL28B genotype.

scientific article published on 26 July 2010

Beta-globin mutations are associated with parenchymal siderosis and fibrosis in patients with non-alcoholic fatty liver disease

scientific article

Characterization and sub-cellular localization of SS1R, SS2R, and SS5R in human late-stage prostate cancer cells: effect of mono- and bi-specific somatostatin analogs on cell growth.

scientific article published on 5 November 2013

Dietary iron overload induces visceral adipose tissue insulin resistance.

scientific article published on 8 April 2013

Dysmetabolic hyperferritinemia and dysmetabolic iron overload syndrome (DIOS): two related conditions or different entities?

scientific article published on 30 January 2020

Effect of the A736V TMPRSS6 polymorphism on the penetrance and clinical expression of hereditary hemochromatosis.

scientific article

GNPAT p.D519G variant and iron metabolism during oral iron tolerance test.

scientific article published on 2 August 2016

GNPAT rs11558492 is not a Major Modifier of Iron Status: Study of Italian Hemochromatosis Patients and Blood Donors

scientific article published on May 2017

Genetic and Epigenetic Modifiers of Alcoholic Liver Disease

scientific article published in 2018

HFE Gene Mutations and Oxidative Stress Influence Serum Ferritin, Associated with Vascular Damage, in Hemodialysis Patients

article

HFE Genotype Influences Erythropoiesis Support Requirement in Hemodialysis Patients: A Prospective Study

scientific article published on 16 November 2007

HFE mutations modulate the effect of iron on serum hepcidin-25 in chronic hemodialysis patients

scientific article published on 18 June 2009

Hepatic notch signaling correlates with insulin resistance and nonalcoholic fatty liver disease.

scientific article published on 29 August 2013

Hepatic steatosis and PNPLA3 I148M variant are associated with serum Fetuin-A independently of insulin resistance.

scientific article

Hepcidin resistance in dysmetabolic iron overload.

scientific article published on 6 April 2016

High fat diet subverts hepatocellular iron uptake determining dysmetabolic iron overload

scientific article

Homozygosity for the patatin-like phospholipase-3/adiponutrin I148M polymorphism influences liver fibrosis in patients with nonalcoholic fatty liver disease.

scientific article published in April 2010

Impact of natural neuromedin-B receptor variants on iron metabolism

scientific article published on 16 December 2019

Increased Expression and Activity of the Transcription Factor FOXO1 in Nonalcoholic Steatohepatitis

scientific article published on 03 March 2008

Increased circulating adiponectin in males with chronic HCV hepatitis.

scientific article published on 17 August 2015

Increased insulin receptor substrate 2 expression is associated with steatohepatitis and altered lipid metabolism in obese subjects.

scientific article

Insulin resistance promotes Lysyl Oxidase Like 2 induction and fibrosis accumulation in non-alcoholic fatty liver disease

scientific article published on 3 May 2017

Juvenile hemochromatosis associated with heterozygosity for novel hemojuvelin mutations and with unknown cofactors

scientific article published in September 2014

LPIN1 rs13412852 Polymorphism in Pediatric Nonalcoholic Fatty Liver Disease

scientific article published on 01 May 2012

Liver transplantation for hepatocellular carcinoma in a patient with a novel telomerase mutation and steatosis

scientific article published on 19 September 2012

MERTK rs4374383 polymorphism affects the severity of fibrosis in non-alcoholic fatty liver disease.

scientific article published on 24 October 2015

PNPLA3 I148M Variant Influences Circulating Retinol in Adults with Nonalcoholic Fatty Liver Disease or Obesity

scientific article published in July 2015

PNPLA3 I148M polymorphism, clinical presentation, and survival in patients with hepatocellular carcinoma

scientific article

PNPLA3 has retinyl-palmitate lipase activity in human hepatic stellate cells

scientific article

Paradoxical dissociation between hepatic fat content and de novo lipogenesis due to PNPLA3 sequence variant.

scientific article

Patatin-Like phospholipase domain-containing 3 I148M polymorphism, steatosis, and liver damage in chronic hepatitis C

scientific article published on 11 February 2011

Patatin-like phospholipase domain containing-3 gene I148M polymorphism, steatosis, and liver damage in hereditary hemochromatosis.

scientific article

Proprotein convertase 7 rs236918 associated with liver fibrosis in Italian patients with HFE-related hemochromatosis.

scientific article

Protective effect of TAT-delivered alpha-synuclein: relevance of the C-terminal domain and involvement of HSP70.

scientific article published on 2 September 2004

Retracted: DJ-1 Modulates α-Synuclein Aggregation State in a Cellular Model of Oxidative Stress: Relevance for Parkinson's Disease and Involvement of HSP70

retracted article

Serum Hepcidin and Macrophage Iron Correlate With MCP-1 Release and Vascular Damage in Patients With Metabolic Syndrome Alterations

scientific article published on 23 December 2010

Serum ferritin levels are associated with vascular damage in patients with nonalcoholic fatty liver disease.

scientific article published on 13 April 2010

Statin use and non-alcoholic steatohepatitis in at risk individuals.

scientific article

The A736V TMPRSS6 polymorphism influences hepatic iron overload in nonalcoholic fatty liver disease

scientific article

The A736V TMPRSS6 polymorphism influences hepcidin and iron metabolism in chronic hemodialysis patients: TMPRSS6 and hepcidin in hemodialysis.

scientific article

The APOC3 T-455C and C-482T promoter region polymorphisms are not associated with the severity of liver damage independently of PNPLA3 I148M genotype in patients with nonalcoholic fatty liver

scientific article published on 21 July 2011

The MBOAT7-TMC4 Variant rs641738 Increases Risk of Nonalcoholic Fatty Liver Disease in Individuals of European Descent

scientific article published on 2 February 2016

The UCP2 -866 G>A promoter region polymorphism is associated with nonalcoholic steatohepatitis.

scientific article published on 20 November 2014

The role of insulin resistance in nonalcoholic steatohepatitis and liver disease development--a potential therapeutic target?

scientific article

The rs2294918 E434K variant modulates patatin-like phospholipase domain-containing 3 expression and liver damage.

scientific article published on 14 January 2016

Transmembrane 6 superfamily member 2 gene variant disentangles nonalcoholic steatohepatitis from cardiovascular disease

scientific article published in February 2015

List of works by Raffaela Rametta

A novel alpha1-antitrypsin null variant (PiQ0Milano ).

A randomized trial of iron depletion in patients with nonalcoholic fatty liver disease and hyperferritinemia.

A tetra-primer amplification refractory mutation system polymerase chain reaction for the evaluation of rs12979860 IL28B genotype.

Beta-globin mutations are associated with parenchymal siderosis and fibrosis in patients with non-alcoholic fatty liver disease

Characterization and sub-cellular localization of SS1R, SS2R, and SS5R in human late-stage prostate cancer cells: effect of mono- and bi-specific somatostatin analogs on cell growth.

Dietary iron overload induces visceral adipose tissue insulin resistance.

Dysmetabolic hyperferritinemia and dysmetabolic iron overload syndrome (DIOS): two related conditions or different entities?

Effect of the A736V TMPRSS6 polymorphism on the penetrance and clinical expression of hereditary hemochromatosis.

GNPAT p.D519G variant and iron metabolism during oral iron tolerance test.

GNPAT rs11558492 is not a Major Modifier of Iron Status: Study of Italian Hemochromatosis Patients and Blood Donors

Genetic and Epigenetic Modifiers of Alcoholic Liver Disease

HFE Gene Mutations and Oxidative Stress Influence Serum Ferritin, Associated with Vascular Damage, in Hemodialysis Patients

HFE Genotype Influences Erythropoiesis Support Requirement in Hemodialysis Patients: A Prospective Study

HFE mutations modulate the effect of iron on serum hepcidin-25 in chronic hemodialysis patients

Hepatic notch signaling correlates with insulin resistance and nonalcoholic fatty liver disease.

Hepatic steatosis and PNPLA3 I148M variant are associated with serum Fetuin-A independently of insulin resistance.

Hepcidin resistance in dysmetabolic iron overload.

High fat diet subverts hepatocellular iron uptake determining dysmetabolic iron overload

Homozygosity for the patatin-like phospholipase-3/adiponutrin I148M polymorphism influences liver fibrosis in patients with nonalcoholic fatty liver disease.

Impact of natural neuromedin-B receptor variants on iron metabolism

Increased Expression and Activity of the Transcription Factor FOXO1 in Nonalcoholic Steatohepatitis

Increased circulating adiponectin in males with chronic HCV hepatitis.

Increased insulin receptor substrate 2 expression is associated with steatohepatitis and altered lipid metabolism in obese subjects.

Insulin resistance promotes Lysyl Oxidase Like 2 induction and fibrosis accumulation in non-alcoholic fatty liver disease

Juvenile hemochromatosis associated with heterozygosity for novel hemojuvelin mutations and with unknown cofactors

LPIN1 rs13412852 Polymorphism in Pediatric Nonalcoholic Fatty Liver Disease

Liver transplantation for hepatocellular carcinoma in a patient with a novel telomerase mutation and steatosis

MERTK rs4374383 polymorphism affects the severity of fibrosis in non-alcoholic fatty liver disease.

PNPLA3 I148M Variant Influences Circulating Retinol in Adults with Nonalcoholic Fatty Liver Disease or Obesity

PNPLA3 I148M polymorphism, clinical presentation, and survival in patients with hepatocellular carcinoma

PNPLA3 has retinyl-palmitate lipase activity in human hepatic stellate cells

Paradoxical dissociation between hepatic fat content and de novo lipogenesis due to PNPLA3 sequence variant.

Patatin-Like phospholipase domain-containing 3 I148M polymorphism, steatosis, and liver damage in chronic hepatitis C

Patatin-like phospholipase domain containing-3 gene I148M polymorphism, steatosis, and liver damage in hereditary hemochromatosis.

Proprotein convertase 7 rs236918 associated with liver fibrosis in Italian patients with HFE-related hemochromatosis.

Protective effect of TAT-delivered alpha-synuclein: relevance of the C-terminal domain and involvement of HSP70.

Retracted: DJ-1 Modulates α-Synuclein Aggregation State in a Cellular Model of Oxidative Stress: Relevance for Parkinson's Disease and Involvement of HSP70

Serum Hepcidin and Macrophage Iron Correlate With MCP-1 Release and Vascular Damage in Patients With Metabolic Syndrome Alterations

Serum ferritin levels are associated with vascular damage in patients with nonalcoholic fatty liver disease.

Statin use and non-alcoholic steatohepatitis in at risk individuals.

The A736V TMPRSS6 polymorphism influences hepatic iron overload in nonalcoholic fatty liver disease

The A736V TMPRSS6 polymorphism influences hepcidin and iron metabolism in chronic hemodialysis patients: TMPRSS6 and hepcidin in hemodialysis.

The APOC3 T-455C and C-482T promoter region polymorphisms are not associated with the severity of liver damage independently of PNPLA3 I148M genotype in patients with nonalcoholic fatty liver

The MBOAT7-TMC4 Variant rs641738 Increases Risk of Nonalcoholic Fatty Liver Disease in Individuals of European Descent

The UCP2 -866 G>A promoter region polymorphism is associated with nonalcoholic steatohepatitis.

The role of insulin resistance in nonalcoholic steatohepatitis and liver disease development--a potential therapeutic target?

The rs2294918 E434K variant modulates patatin-like phospholipase domain-containing 3 expression and liver damage.

Transmembrane 6 superfamily member 2 gene variant disentangles nonalcoholic steatohepatitis from cardiovascular disease