Lista de obras - Paola Piscopo - Dominio Público Uruguay

A novel PSEN2 mutation associated with a peculiar phenotype

artículo científico publicado en 2008

A novel mutation in the predicted TMIII domain of the PSEN2 gene in an Italian pedigree with atypical Alzheimer's disease

artículo científico publicado en 2010

Altered expression of cyclooxygenase-2, presenilins and oxygen radical scavenging enzymes in a rat model of global perinatal asphyxia

artículo científico publicado en 2007

Altered oxidative stress profile in the cortex of mice fed an enriched branched-chain amino acids diet: Possible link with amyotrophic lateral sclerosis?

artículo científico publicado en 2011

Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentation

artículo científico publicado en 2013

Binge eating and fast cognitive worsening in an early-onset bvFTD patient carrying C9ORF72 expansion

artículo científico publicado en 2014

Changes in cholesterol metabolism are associated with PS1 and PS2 gene regulation in SK-N-BE.

artículo científico publicado en 2006

Circulating miRNAs as biomarkers for neurodegenerative disorders.

artículo científico

Circulating microRNAs in Neurodegenerative Diseases.

artículo científico publicado en 2015

Cognitive and neurological deficits induced by early and prolonged basal forebrain cholinergic hypofunction in rats

artículo científico publicado en 2004

Familial Alzheimer's disease sustained by presenilin 2 mutations: systematic review of literature and genotype-phenotype correlation

artículo científico

Frontotemporal Lobar Degeneration and MicroRNAs

artículo científico publicado en 2016

Gender differences in Parkinson's disease: focus on plasma α-synuclein

artículo científico

Gender effects on plasma PGRN levels in patients with Alzheimer's disease: a preliminary study

artículo científico publicado en 2013

Gene expression profiles of APP and BACE1 in Tg SOD1G93A cortical cells

artículo científico publicado en 2009

Genetic study of Sardinian patients with Alzheimer's disease

artículo científico publicado en 2006

Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family

artículo científico publicado en 2015

Hypoxia induces up-regulation of progranulin in neuroblastoma cell lines

artículo científico publicado en 2010

Increased levels of acute-phase inflammatory proteins in plasma of patients with sporadic CJD.

artículo científico publicado en 2012

Neuropsychological predictors of rapidly progressive Alzheimer's disease

artículo científico publicado en 2015

Nicastrin gene in familial and sporadic Alzheimer's disease

artículo científico publicado en 2003

PEN-2 gene mutation in a familial Alzheimer's disease case.

artículo científico publicado en 2005

PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population.

artículo científico publicado en 2016

Presenilin 2 mutation R71W in an Italian early-onset sporadic Alzheimer's disease case.

artículo científico publicado en 2011

Proteic marker of hypoxic-ischemic damage

artículo científico publicado en 2001

Rat nicastrin gene: cDNA isolation, mRNA variants and expression pattern analysis

artículo científico publicado en 2005

Reduced miR-659-3p Levels Correlate with Progranulin Increase in Hypoxic Conditions: Implications for Frontotemporal Dementia

artículo científico publicado en 2016

Rosuvastatin and thapsigargin modulate γ-secretase gene expression and APP processing in a human neuroglioma model

artículo científico publicado en 2010

SORL1 Gene is Associated with the Conversion from Mild Cognitive Impairment to Alzheimer's Disease

artículo científico publicado en 2015

T lymphocytes from patients with systemic lupus erythematosus are resistant to induction of autophagy

artículo científico publicado en 2012

Thapsigargin affects presenilin-2 but not presenilin-1 regulation in SK-N-BE cells.

artículo científico publicado en 2013

The London APP mutation (Val717Ile) associated with early shifting abilities and behavioral changes in two Italian families with early-onset Alzheimer's disease

artículo científico publicado en 2010

gamma-Secretase is differentially modulated by alterations of homocysteine cycle in neuroblastoma and glioblastoma cells.

artículo científico publicado en 2007

Lista de obras de Paola Piscopo

A novel PSEN2 mutation associated with a peculiar phenotype

A novel mutation in the predicted TMIII domain of the PSEN2 gene in an Italian pedigree with atypical Alzheimer's disease

Altered expression of cyclooxygenase-2, presenilins and oxygen radical scavenging enzymes in a rat model of global perinatal asphyxia

Altered oxidative stress profile in the cortex of mice fed an enriched branched-chain amino acids diet: Possible link with amyotrophic lateral sclerosis?

Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentation

Binge eating and fast cognitive worsening in an early-onset bvFTD patient carrying C9ORF72 expansion

Changes in cholesterol metabolism are associated with PS1 and PS2 gene regulation in SK-N-BE.

Circulating miRNAs as biomarkers for neurodegenerative disorders.

Circulating microRNAs in Neurodegenerative Diseases.

Cognitive and neurological deficits induced by early and prolonged basal forebrain cholinergic hypofunction in rats

Familial Alzheimer's disease sustained by presenilin 2 mutations: systematic review of literature and genotype-phenotype correlation

Frontotemporal Lobar Degeneration and MicroRNAs

Gender differences in Parkinson's disease: focus on plasma α-synuclein

Gender effects on plasma PGRN levels in patients with Alzheimer's disease: a preliminary study

Gene expression profiles of APP and BACE1 in Tg SOD1G93A cortical cells

Genetic study of Sardinian patients with Alzheimer's disease

Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family

Hypoxia induces up-regulation of progranulin in neuroblastoma cell lines

Increased levels of acute-phase inflammatory proteins in plasma of patients with sporadic CJD.

Neuropsychological predictors of rapidly progressive Alzheimer's disease

Nicastrin gene in familial and sporadic Alzheimer's disease

PEN-2 gene mutation in a familial Alzheimer's disease case.

PRNP P39L Variant is a Rare Cause of Frontotemporal Dementia in Italian Population.

Presenilin 2 mutation R71W in an Italian early-onset sporadic Alzheimer's disease case.

Proteic marker of hypoxic-ischemic damage

Rat nicastrin gene: cDNA isolation, mRNA variants and expression pattern analysis

Reduced miR-659-3p Levels Correlate with Progranulin Increase in Hypoxic Conditions: Implications for Frontotemporal Dementia

Rosuvastatin and thapsigargin modulate γ-secretase gene expression and APP processing in a human neuroglioma model

SORL1 Gene is Associated with the Conversion from Mild Cognitive Impairment to Alzheimer's Disease

T lymphocytes from patients with systemic lupus erythematosus are resistant to induction of autophagy

Thapsigargin affects presenilin-2 but not presenilin-1 regulation in SK-N-BE cells.

The London APP mutation (Val717Ile) associated with early shifting abilities and behavioral changes in two Italian families with early-onset Alzheimer's disease

gamma-Secretase is differentially modulated by alterations of homocysteine cycle in neuroblastoma and glioblastoma cells.