Lista de obras -

A prolonged neonatal jaundice associated with a rare G6PD mutation.

artículo científico publicado en 2009

Abeta(31-35) and Abeta(25-35) fragments of amyloid beta-protein induce cellular death through apoptotic signals: Role of the redox state of methionine-35.

artículo científico publicado en 2005

Abeta(31-35) peptide induce apoptosis in PC 12 cells: contrast with Abeta(25-35) peptide and examination of underlying mechanisms.

artículo científico publicado en 2005

Acute haemolytic crisis due to concomitant presence of infection and possible altered acetaminophen catabolism in a Philipino child carrying the G6PD-Vanua Lava mutation.

artículo científico publicado en 2011

Advanced tools for BRCA1/2 mutational screening: comparison between two methods for large genomic rearrangements (LGRs) detection.

artículo científico publicado en 2014

Amyloid peptide inhibits ATP release from human erythrocytes.

artículo científico publicado en 2008

Amyloid-beta peptide affects the oxygen dependence of erythrocyte metabolism: A role for caspase 3

artículo científico publicado en 2006

Could G6PD-Buenos-Aires confirm the existence of the "structural NADP+ binding site" and its strategic role for the stability and/or activity enzyme?

artículo científico publicado en 2008

DNA from buccal swab is suitable for rapid genotyping of angiotensin-converting enzyme insertion/deletion (I/D) polymorphism.

artículo científico publicado en 2014

Description of a novel missense mutation of glucose-6-phosphate dehydrogenase gene associated with asymptomatic high enzyme deficiency

article

Doxorubicin-derived metabolites induce release of cytochrome C and inhibition of respiration on cardiac isolated mitochondria.

artículo científico publicado en 2003

Drug-eluting stents in a patient with favism: is the aspirin administration safe?

artículo científico publicado en 2008

Fibroblast apoptosis in a patient affected by lamellar ichthyosis.

artículo científico publicado en 2009

Fragment 31-35 of beta-amyloid peptide induces neurodegeneration in rat cerebellar granule cells via bax gene expression and caspase-3 activation. A crucial role for the redox state of methionine-35 residue.

artículo científico publicado en 2006

Functional analysis of two rare CYP21A2 mutations detected in Italian patients with a mildest form of congenital adrenal hyperplasia

article

G6PD Murcia, G6PD Ube and G6PD Orissa: report of three G6PD mutations unusual for Italian population.

artículo científico publicado en 2010

GSTT1 and GSTM1 allelic polymorphisms in head and neck cancer patients from Italian Lazio Region.

artículo científico publicado en 2006

Genes, pseudogenes and like genes: the case of 21-hydroxylase in Italian population.

artículo científico publicado en 2013

Glucose-6-phosphate dehydrogenase (G6PD) mutations database: review of the "old" and update of the new mutations.

artículo científico publicado en 2012

Glucose-6-phosphate dehydrogenase Buenos Aires: a novel de novo missense mutation associated with severe enzyme deficiency.

artículo científico publicado en 2007

Glucose-6-phosphate dehydrogenase laboratory assay: How, when, and why?

artículo científico publicado en 2009

Identification of RFLP G6PD mutations by using microcapillary electrophoretic chips (Experion).

artículo científico publicado en 2008

Identification of a novel mutation in UDP-glucuronosyltransferase (UGT1A1) gene in a child with neonatal unconjugated hyperbilirubinemia

scientific article published on 22 October 2012

Oxidation of methionine 35 reduces toxicity of the amyloid beta-peptide(1-42) in neuroblastoma cells (IMR-32) via enzyme methionine sulfoxide reductase A expression and function.

artículo científico publicado en 2010

Oxidative effects of gemfibrozil on anion influx and metabolism in normal and Beta-thalassemic erythrocytes: physiological implications.

artículo científico publicado en 2008

Phenotype heterogeneity of hyperbilirubinemia condition: the lesson by coinheritance of glucose-6-phosphate dehydrogenase deficiency and Crigler-Najjar syndrome type II in an Italian patient.

artículo científico publicado en 2012

Pilot phase IIA study for evaluation of the efficacy of folic acid in the treatment of laryngeal leucoplakia

scientific article published on 01 July 2006

Rapid and simple identification of the commonest glucose-6-phosphate dehydrogenase (G6PD) Italian mutations: from DNA extraction to genotyping.

artículo científico publicado en 2012

Role of methionine 35 in the intracellular Ca2+ homeostasis dysregulation and Ca2+-dependent apoptosis induced by amyloid beta-peptide in human neuroblastoma IMR32 cells

artículo científico publicado en 2008

Salivary glutathione and uric acid levels in patients with head and neck squamous cell carcinoma.

artículo científico publicado en 2007

Serum folate and homocysteine levels in head and neck squamous cell carcinoma.

artículo científico publicado en 2002

Serum levels of folate, homocysteine, and vitamin B12 in head and neck squamous cell carcinoma and in laryngeal leukoplakia.

artículo científico publicado en 2005

Worsening of the clinical-hematological picture in a patient with a rare PK-LR compound heterozygosis after mitral replacement.

artículo científico publicado en 2011

Lista de obras de

A prolonged neonatal jaundice associated with a rare G6PD mutation.

Abeta(31-35) and Abeta(25-35) fragments of amyloid beta-protein induce cellular death through apoptotic signals: Role of the redox state of methionine-35.

Abeta(31-35) peptide induce apoptosis in PC 12 cells: contrast with Abeta(25-35) peptide and examination of underlying mechanisms.

Acute haemolytic crisis due to concomitant presence of infection and possible altered acetaminophen catabolism in a Philipino child carrying the G6PD-Vanua Lava mutation.

Advanced tools for BRCA1/2 mutational screening: comparison between two methods for large genomic rearrangements (LGRs) detection.

Amyloid peptide inhibits ATP release from human erythrocytes.

Amyloid-beta peptide affects the oxygen dependence of erythrocyte metabolism: A role for caspase 3

Could G6PD-Buenos-Aires confirm the existence of the "structural NADP+ binding site" and its strategic role for the stability and/or activity enzyme?

DNA from buccal swab is suitable for rapid genotyping of angiotensin-converting enzyme insertion/deletion (I/D) polymorphism.

Description of a novel missense mutation of glucose-6-phosphate dehydrogenase gene associated with asymptomatic high enzyme deficiency

Doxorubicin-derived metabolites induce release of cytochrome C and inhibition of respiration on cardiac isolated mitochondria.

Drug-eluting stents in a patient with favism: is the aspirin administration safe?

Fibroblast apoptosis in a patient affected by lamellar ichthyosis.

Fragment 31-35 of beta-amyloid peptide induces neurodegeneration in rat cerebellar granule cells via bax gene expression and caspase-3 activation. A crucial role for the redox state of methionine-35 residue.

Functional analysis of two rare CYP21A2 mutations detected in Italian patients with a mildest form of congenital adrenal hyperplasia

G6PD Murcia, G6PD Ube and G6PD Orissa: report of three G6PD mutations unusual for Italian population.

GSTT1 and GSTM1 allelic polymorphisms in head and neck cancer patients from Italian Lazio Region.

Genes, pseudogenes and like genes: the case of 21-hydroxylase in Italian population.

Glucose-6-phosphate dehydrogenase (G6PD) mutations database: review of the "old" and update of the new mutations.

Glucose-6-phosphate dehydrogenase Buenos Aires: a novel de novo missense mutation associated with severe enzyme deficiency.

Glucose-6-phosphate dehydrogenase laboratory assay: How, when, and why?

Identification of RFLP G6PD mutations by using microcapillary electrophoretic chips (Experion).

Identification of a novel mutation in UDP-glucuronosyltransferase (UGT1A1) gene in a child with neonatal unconjugated hyperbilirubinemia

Oxidation of methionine 35 reduces toxicity of the amyloid beta-peptide(1-42) in neuroblastoma cells (IMR-32) via enzyme methionine sulfoxide reductase A expression and function.

Oxidative effects of gemfibrozil on anion influx and metabolism in normal and Beta-thalassemic erythrocytes: physiological implications.

Phenotype heterogeneity of hyperbilirubinemia condition: the lesson by coinheritance of glucose-6-phosphate dehydrogenase deficiency and Crigler-Najjar syndrome type II in an Italian patient.

Pilot phase IIA study for evaluation of the efficacy of folic acid in the treatment of laryngeal leucoplakia

Rapid and simple identification of the commonest glucose-6-phosphate dehydrogenase (G6PD) Italian mutations: from DNA extraction to genotyping.

Role of methionine 35 in the intracellular Ca2+ homeostasis dysregulation and Ca2+-dependent apoptosis induced by amyloid beta-peptide in human neuroblastoma IMR32 cells

Salivary glutathione and uric acid levels in patients with head and neck squamous cell carcinoma.

Serum folate and homocysteine levels in head and neck squamous cell carcinoma.

Serum levels of folate, homocysteine, and vitamin B12 in head and neck squamous cell carcinoma and in laryngeal leukoplakia.

Worsening of the clinical-hematological picture in a patient with a rare PK-LR compound heterozygosis after mitral replacement.