Lista de obras - L Sacchetti - Dominio Público Uruguay

A paraoxonase gene polymorphism, PON 1 (55), as an independent risk factor for increased carotid intima-media thickness in middle-aged women

artículo científico publicado en 2003

Adaptations of striatal endocannabinoid system during stress.

artículo científico publicado en 2009

Age-Related Reference Intervals of the Main Biochemical and Hematological Parameters in C57BL/6J, 129SV/EV and C3H/HeJ Mouse Strains

artículo científico publicado en 2008

An altered gut microbiome profile in a child affected by Crohn's disease normalized after nutritional therapy

artículo científico publicado en 2013

Association of impaired glucose homeostasis with preclinical carotid atherosclerosis in women: Impact of the new American Diabetes Association criteria.

artículo científico publicado en 2002

Association of obesity and central fat distribution with carotid artery wall thickening in middle-aged women

artículo científico publicado en 2002

Brain-derived neurotrophic factor controls cannabinoid CB1 receptor function in the striatum.

artículo científico publicado en 2010

Changes in the MicroRNA Profile Observed in the Subcutaneous Adipose Tissue of Obese Patients after Laparoscopic Adjustable Gastric Banding.

artículo científico publicado en 2017

Characterization of the Duodenal Mucosal Microbiome in Obese Adult Subjects by 16S rRNA Sequencing

scientific article published on 29 March 2020

Comparison of seven serum assays on four automatic analysers

artículo científico publicado en 1989

Comparison of the TaqMan and LightCycler systems in pharmacogenetic testing: evaluation of CYP2C92/3 polymorphisms.

artículo científico publicado en 2006

Corrigendum to "Sequence Analysis of the UCP1 Gene in a Severe Obese Population from Southern Italy"

artículo científico publicado en 2018

Diagnostic efficiency in discriminating liver malignancies from cirrhosis by serum gamma-glutamyltransferase isoforms

artículo científico publicado en 1988

Duodenal Metatranscriptomics to Define Human and Microbial Functional Alterations Associated with Severe Obesity: A Pilot Study

artículo científico publicado en 2020

Effects of caffeine on striatal neurotransmission: focus on cannabinoid CB1 receptors

artículo científico publicado en 2010

Electrophoretic behavior and partial characterization of disease-associated serum forms of gamma-glutamyltransferase.

artículo científico publicado en 1989

Evaluation of pancreatic amylase immunoassay in acute pancreatitis

artículo científico publicado en 1989

Functional analysis of melanocortin-4-receptor mutants identified in severely obese subjects living in Southern Italy.

artículo científico publicado en 2010

Glucokinase (GCK) mutations and their characterization in MODY2 children of southern Italy

artículo científico publicado en 2012

Glucokinase gene mutations: structural and genotype-phenotype analyses in MODY children from South Italy

artículo científico publicado en 2008

HLA related genetic risk for coeliac disease.

artículo científico publicado en 2007

Haplogroup T is an obesity risk factor: mitochondrial DNA haplotyping in a morbid obese population from southern Italy

artículo científico publicado en 2013

High Frequency of Haplotype HLA-DQ7 in Celiac Disease Patients from South Italy: Retrospective Evaluation of 5,535 Subjects at Risk of Celiac Disease.

artículo científico publicado en 2015

High aminopeptidase N/CD13 levels characterize human amniotic mesenchymal stem cells and drive their increased adipogenic potential in obese women.

artículo científico publicado en 2013

High leptin/adiponectin ratio and serum triglycerides are associated with an "at-risk" phenotype in young severely obese patients.

artículo científico publicado en 2010

Homocysteine levels and sustained virological response to pegylated-interferon alpha2b plus ribavirin therapy for chronic hepatitis C: a prospective study

artículo científico publicado en 2008

Identification of candidate children for maturity-onset diabetes of the young type 2 (MODY2) gene testing: a seven-item clinical flowchart (7-iF).

artículo científico publicado en 2013

Immune-metabolic profiling of anorexic patients reveals an anti-oxidant and anti-inflammatory phenotype

artículo científico publicado en 2014

Improving the estimation of celiac disease sibling risk by non-HLA genes

artículo científico publicado en 2011

Laparoscopic Adjustable Gastric Banding Reduces Subcutaneous Adipose Tissue and Blood Inflammation in Nondiabetic Morbidly Obese Individuals

scientific article published on 01 December 2014

Loss of striatal cannabinoid CB1 receptor function in attention-deficit / hyperactivity disorder mice with point-mutation of the dopamine transporter

artículo científico publicado en 2011

Metabolic syndrome: analogies with subtypes of protein energy malnutrition

artículo científico publicado en 2006

Metagenomics Reveals Dysbiosis and a Potentially Pathogenic N. flavescens Strain in Duodenum of Adult Celiac Patients

artículo científico publicado en 2016

MicroRNA-449a overexpression, reduced NOTCH1 signals and scarce goblet cells characterize the small intestine of celiac patients

artículo científico publicado en 2011

Mitochondrial diabetes in children: seek and you will find it

artículo científico publicado en 2012

Multiple sclerosis and hepatitis C virus infection are associated with single nucleotide polymorphisms in interferon pathway genes

artículo científico publicado en 2008

Multivariate discriminant analysis of biochemical parameters for the differentiation of clinically confounding liver diseases.

artículo científico publicado en 1997

Nonsynonimous mutation of catechol-O-methyl-transferase (COMT) gene in a patient with temporomandibular disorder.

artículo científico publicado en 2010

Orexin-A represses satiety-inducing POMC neurons and contributes to obesity via stimulation of endocannabinoid signaling

artículo científico publicado en 2016

Prenatal diagnosis of cystic fibrosis: an experience of 181 cases

artículo científico publicado en 2013

Preservation of striatal cannabinoid CB1 receptor function correlates with the antianxiety effects of fatty acid amide hydrolase inhibition

artículo científico publicado en 2010

Problems and perspectives of clinical biochemistry training, and the example of Italy.

artículo científico publicado en 1996

Proteome analysis of human amniotic mesenchymal stem cells (hA-MSCs) reveals impaired antioxidant ability, cytoskeleton and metabolic functionality in maternal obesity.

artículo científico publicado en 2016

Radical-trapping activity, blood pressure, and carotid enlargement in women

artículo científico publicado en 2003

Sequence Analysis of the UCP1 Gene in a Severe Obese Population from Southern Italy

artículo científico publicado en 2011

Serum Mn-superoxide dismutase in acute myocardial infarction

artículo científico publicado en 1997

Serum type-2 macro-creatine kinase isoenzyme is not a useful marker of severe liver diseases or neoplasia

artículo científico publicado en 1990

Six novel mutations in the proopiomelanocortin and melanocortin receptor 4 genes in severely obese adults living in southern Italy

artículo científico publicado en 2005

The Cause of Death of a Child in the 18th Century Solved by Bone Microbiome Typing Using Laser Microdissection and Next Generation Sequencing

artículo científico publicado en 2017

The FTO gene polymorphism (rs9939609) is associated with metabolic syndrome in morbidly obese subjects from southern Italy

artículo científico publicado en 2014

The mtDNA 15497 G/A polymorphism in cytochrome b in severe obese subjects from Southern Italy

artículo científico publicado en 2005

Voluntary exercise and sucrose consumption enhance cannabinoid CB1 receptor sensitivity in the striatum

artículo científico publicado en 2010

Warfarin anticoagulant therapy: a Southern Italy pharmacogenetics-based dosing model

artículo científico publicado en 2013

Y-chromosome short tandem repeat (STR) haplotypes in a Campania population sample

artículo científico publicado en 2005

miR-138/miR-222 Overexpression Characterizes the miRNome of Amniotic Mesenchymal Stem Cells in Obesity

artículo científico publicado en 2016

miR-519d overexpression is associated with human obesity.

artículo científico publicado en 2010

Lista de obras de L Sacchetti

A paraoxonase gene polymorphism, PON 1 (55), as an independent risk factor for increased carotid intima-media thickness in middle-aged women

Adaptations of striatal endocannabinoid system during stress.

Age-Related Reference Intervals of the Main Biochemical and Hematological Parameters in C57BL/6J, 129SV/EV and C3H/HeJ Mouse Strains

An altered gut microbiome profile in a child affected by Crohn's disease normalized after nutritional therapy

Association of impaired glucose homeostasis with preclinical carotid atherosclerosis in women: Impact of the new American Diabetes Association criteria.

Association of obesity and central fat distribution with carotid artery wall thickening in middle-aged women

Brain-derived neurotrophic factor controls cannabinoid CB1 receptor function in the striatum.

Changes in the MicroRNA Profile Observed in the Subcutaneous Adipose Tissue of Obese Patients after Laparoscopic Adjustable Gastric Banding.

Characterization of the Duodenal Mucosal Microbiome in Obese Adult Subjects by 16S rRNA Sequencing

Comparison of seven serum assays on four automatic analysers

Comparison of the TaqMan and LightCycler systems in pharmacogenetic testing: evaluation of CYP2C9*2/*3 polymorphisms.

Corrigendum to "Sequence Analysis of the UCP1 Gene in a Severe Obese Population from Southern Italy"

Diagnostic efficiency in discriminating liver malignancies from cirrhosis by serum gamma-glutamyltransferase isoforms

Duodenal Metatranscriptomics to Define Human and Microbial Functional Alterations Associated with Severe Obesity: A Pilot Study

Effects of caffeine on striatal neurotransmission: focus on cannabinoid CB1 receptors

Electrophoretic behavior and partial characterization of disease-associated serum forms of gamma-glutamyltransferase.

Evaluation of pancreatic amylase immunoassay in acute pancreatitis

Functional analysis of melanocortin-4-receptor mutants identified in severely obese subjects living in Southern Italy.

Glucokinase (GCK) mutations and their characterization in MODY2 children of southern Italy

Glucokinase gene mutations: structural and genotype-phenotype analyses in MODY children from South Italy

HLA related genetic risk for coeliac disease.

Haplogroup T is an obesity risk factor: mitochondrial DNA haplotyping in a morbid obese population from southern Italy

High Frequency of Haplotype HLA-DQ7 in Celiac Disease Patients from South Italy: Retrospective Evaluation of 5,535 Subjects at Risk of Celiac Disease.

High aminopeptidase N/CD13 levels characterize human amniotic mesenchymal stem cells and drive their increased adipogenic potential in obese women.

High leptin/adiponectin ratio and serum triglycerides are associated with an "at-risk" phenotype in young severely obese patients.

Homocysteine levels and sustained virological response to pegylated-interferon alpha2b plus ribavirin therapy for chronic hepatitis C: a prospective study

Identification of candidate children for maturity-onset diabetes of the young type 2 (MODY2) gene testing: a seven-item clinical flowchart (7-iF).

Immune-metabolic profiling of anorexic patients reveals an anti-oxidant and anti-inflammatory phenotype

Improving the estimation of celiac disease sibling risk by non-HLA genes

Laparoscopic Adjustable Gastric Banding Reduces Subcutaneous Adipose Tissue and Blood Inflammation in Nondiabetic Morbidly Obese Individuals

Loss of striatal cannabinoid CB1 receptor function in attention-deficit / hyperactivity disorder mice with point-mutation of the dopamine transporter

Metabolic syndrome: analogies with subtypes of protein energy malnutrition

Metagenomics Reveals Dysbiosis and a Potentially Pathogenic N. flavescens Strain in Duodenum of Adult Celiac Patients

MicroRNA-449a overexpression, reduced NOTCH1 signals and scarce goblet cells characterize the small intestine of celiac patients

Mitochondrial diabetes in children: seek and you will find it

Multiple sclerosis and hepatitis C virus infection are associated with single nucleotide polymorphisms in interferon pathway genes

Multivariate discriminant analysis of biochemical parameters for the differentiation of clinically confounding liver diseases.

Nonsynonimous mutation of catechol-O-methyl-transferase (COMT) gene in a patient with temporomandibular disorder.

Orexin-A represses satiety-inducing POMC neurons and contributes to obesity via stimulation of endocannabinoid signaling

Prenatal diagnosis of cystic fibrosis: an experience of 181 cases

Preservation of striatal cannabinoid CB1 receptor function correlates with the antianxiety effects of fatty acid amide hydrolase inhibition

Problems and perspectives of clinical biochemistry training, and the example of Italy.

Proteome analysis of human amniotic mesenchymal stem cells (hA-MSCs) reveals impaired antioxidant ability, cytoskeleton and metabolic functionality in maternal obesity.

Radical-trapping activity, blood pressure, and carotid enlargement in women

Sequence Analysis of the UCP1 Gene in a Severe Obese Population from Southern Italy

Serum Mn-superoxide dismutase in acute myocardial infarction

Serum type-2 macro-creatine kinase isoenzyme is not a useful marker of severe liver diseases or neoplasia

Six novel mutations in the proopiomelanocortin and melanocortin receptor 4 genes in severely obese adults living in southern Italy

The Cause of Death of a Child in the 18th Century Solved by Bone Microbiome Typing Using Laser Microdissection and Next Generation Sequencing

The FTO gene polymorphism (rs9939609) is associated with metabolic syndrome in morbidly obese subjects from southern Italy

The mtDNA 15497 G/A polymorphism in cytochrome b in severe obese subjects from Southern Italy

Voluntary exercise and sucrose consumption enhance cannabinoid CB1 receptor sensitivity in the striatum

Warfarin anticoagulant therapy: a Southern Italy pharmacogenetics-based dosing model

Y-chromosome short tandem repeat (STR) haplotypes in a Campania population sample

miR-138/miR-222 Overexpression Characterizes the miRNome of Amniotic Mesenchymal Stem Cells in Obesity

miR-519d overexpression is associated with human obesity.

Comparison of the TaqMan and LightCycler systems in pharmacogenetic testing: evaluation of CYP2C92/3 polymorphisms.