Lista de obras - Giuliana Fortunato - Dominio Público Uruguay

A case of discordance between genotype and phenotype in a malignant hyperthermia family

artículo científico publicado en 1999

A method for the assay of phosphatidylinositol-specific phospholipase D activity in serum

scientific article published on 01 June 1993

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

Allele frequency distributions at several variable number of tandem repeat (VNTR) and short tandem repeat (STR) loci in a restricted Caucasian population from south Italy and their evaluation for paternity and forensic use.

artículo científico publicado en 1996

Altered expression of inflammation-related genes in human carotid atherosclerotic plaques

article

An improved method on stimulated T-lymphocytes to functionally characterize novel and known LDLR mutations.

artículo científico publicado en 2011

Association of USF1 and APOA5 polymorphisms with familial combined hyperlipidemia in an Italian population

article

C-reactive protein levels are associated with paraoxonase polymorphism L55M in patients undergoing cardiac SPECT imaging

artículo científico publicado en 2011

Cardiac troponin T and amino-terminal pro-natriuretic peptide concentrations in fetuses in the second trimester and in healthy neonates

artículo científico publicado en 2006

Carotid artery remodeling in middle-aged women with the metabolic syndrome (from the "Progetto ATENA" study).

artículo científico publicado en 2005

Comparative characteristics of mesenchymal stem cells from human bone marrow and placenta: CD10, CD49d, and CD56 make a difference.

artículo científico publicado en 2008

Decreased paraoxonase-2 expression in human carotids during the progression of atherosclerosis

artículo científico publicado en 2008

Divergent expression of CD133 in different studies on HCT-116 cell line

artículo científico publicado en 2011

Functional characterization of mutant genes associated with autosomal dominant familial hypercholesterolemia: integration and evolution of genetic diagnosis.

artículo científico

Genetic typing of Corallium rubrum

artículo científico publicado en 2004

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 and functional characterization of LDLR mutations in familial hypercholesterolemia patients from Southern Italy

artículo científico publicado en 2009

Identification and functional characterization of malignant hyperthermia mutation T1354S in the outer pore of the Cavalpha1S-subunit

artículo científico publicado en 2010

Identification of a novel mutation in the ryanodine receptor gene (RYR1) in a malignant hyperthermia Italian family

artículo científico publicado en 2000

Macro-creatine kinase and macro-lactate dehydrogenase in a girl with ulcerative colitis

artículo científico publicado en 2007

Measurement of spleen volume by ultrasound scanning in patients with thrombocytosis: a prospective study

artículo científico publicado en 2002

Miniaturized flow cytometry-based BCR-ABL immunoassay in detecting leptomeningeal disease.

artículo científico publicado en 2011

Mollicutes contamination: a new strategy for an effective rescue of cancer cell lines.

artículo científico publicado en 2011

Nanon effects on mammalian cell long-term cultures: a caveat for experimental hematologists dealing with in vitro long-term culture assays

artículo científico publicado en 2009

Paraoxonase and superoxide dismutase gene polymorphisms and noise-induced hearing loss

artículo científico publicado en 2004

Polychromatic flow cytometry analysis of CD34+ hematopoietic stem cells in cryopreserved early preterm human cord blood samples

artículo científico publicado en 2011

Polymorphisms and the expression of genes encoding enzymes involved in cardiovascular diseases.

artículo científico publicado en 2007

Prenatal diagnosis of inherited diseases: 20 years' experience of an Italian Regional Reference Centre.

artículo científico publicado en 2013

Prevalence and long-term course of macro-aspartate aminotransferase in children

artículo científico publicado en 2008

RAS and MTHFR gene polymorphisms in a healthy exercise-trained population: association with the MTHFR (TT) genotype and a lower hemoglobin level.

artículo científico publicado en 2006

Recent advances in the diagnosis of malignant hyperthermia susceptibility: how confident can we be of genetic testing?

artículo científico publicado en 2003

Refinement of variant selection for the LDL cholesterol genetic risk score in the diagnosis of the polygenic form of clinical familial hypercholesterolemia and replication in samples from 6 countries

artículo científico publicado en 2014

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 pseudouridine in the diagnosis of acute leukaemias and as a novel prognostic indicator in acute lymphoblastic leukaemia

scientific article published on 01 December 1993

The novel variant p.Ser465Leu in the PCSK9 gene does not account for the decreased LDLR activity in members of a FH family

article

The percentage of CD133+ cells in human colorectal cancer cell lines is influenced by Mycoplasma hyorhinis infection

artículo científico publicado en 2010

Lista de obras de Giuliana Fortunato

A case of discordance between genotype and phenotype in a malignant hyperthermia family

A method for the assay of phosphatidylinositol-specific phospholipase D activity in serum

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

Allele frequency distributions at several variable number of tandem repeat (VNTR) and short tandem repeat (STR) loci in a restricted Caucasian population from south Italy and their evaluation for paternity and forensic use.

Altered expression of inflammation-related genes in human carotid atherosclerotic plaques

An improved method on stimulated T-lymphocytes to functionally characterize novel and known LDLR mutations.

Association of USF1 and APOA5 polymorphisms with familial combined hyperlipidemia in an Italian population

C-reactive protein levels are associated with paraoxonase polymorphism L55M in patients undergoing cardiac SPECT imaging

Cardiac troponin T and amino-terminal pro-natriuretic peptide concentrations in fetuses in the second trimester and in healthy neonates

Carotid artery remodeling in middle-aged women with the metabolic syndrome (from the "Progetto ATENA" study).

Comparative characteristics of mesenchymal stem cells from human bone marrow and placenta: CD10, CD49d, and CD56 make a difference.

Decreased paraoxonase-2 expression in human carotids during the progression of atherosclerosis

Divergent expression of CD133 in different studies on HCT-116 cell line

Functional characterization of mutant genes associated with autosomal dominant familial hypercholesterolemia: integration and evolution of genetic diagnosis.

Genetic typing of Corallium rubrum

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

Identification and functional characterization of LDLR mutations in familial hypercholesterolemia patients from Southern Italy

Identification and functional characterization of malignant hyperthermia mutation T1354S in the outer pore of the Cavalpha1S-subunit

Identification of a novel mutation in the ryanodine receptor gene (RYR1) in a malignant hyperthermia Italian family

Macro-creatine kinase and macro-lactate dehydrogenase in a girl with ulcerative colitis

Measurement of spleen volume by ultrasound scanning in patients with thrombocytosis: a prospective study

Miniaturized flow cytometry-based BCR-ABL immunoassay in detecting leptomeningeal disease.

Mollicutes contamination: a new strategy for an effective rescue of cancer cell lines.

Nanon effects on mammalian cell long-term cultures: a caveat for experimental hematologists dealing with in vitro long-term culture assays

Paraoxonase and superoxide dismutase gene polymorphisms and noise-induced hearing loss

Polychromatic flow cytometry analysis of CD34+ hematopoietic stem cells in cryopreserved early preterm human cord blood samples

Polymorphisms and the expression of genes encoding enzymes involved in cardiovascular diseases.

Prenatal diagnosis of inherited diseases: 20 years' experience of an Italian Regional Reference Centre.

Prevalence and long-term course of macro-aspartate aminotransferase in children

RAS and MTHFR gene polymorphisms in a healthy exercise-trained population: association with the MTHFR (TT) genotype and a lower hemoglobin level.

Recent advances in the diagnosis of malignant hyperthermia susceptibility: how confident can we be of genetic testing?

Refinement of variant selection for the LDL cholesterol genetic risk score in the diagnosis of the polygenic form of clinical familial hypercholesterolemia and replication in samples from 6 countries

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

Serum Mn-superoxide dismutase in acute myocardial infarction

Serum pseudouridine in the diagnosis of acute leukaemias and as a novel prognostic indicator in acute lymphoblastic leukaemia

The novel variant p.Ser465Leu in the PCSK9 gene does not account for the decreased LDLR activity in members of a FH family

The percentage of CD133+ cells in human colorectal cancer cell lines is influenced by Mycoplasma hyorhinis infection