Lista de obras - Andrew Robinson - Dominio Público Uruguay

Accumulation of dipeptide repeat proteins predates that of TDP-43 in frontotemporal lobar degeneration associated with hexanucleotide repeat expansions in C9ORF72 gene

artículo científico publicado en 2015

Accumulation of multiple neurodegenerative disease-related proteins in familial frontotemporal lobar degeneration associated with granulin mutation

artículo científico publicado en 2017

Analysis of the hexanucleotide repeat in C9ORF72 in Alzheimer's disease

artículo científico publicado en 2012

Biochemical classification of tauopathies by immunoblot, protein sequence and mass spectrometric analyses of sarkosyl-insoluble and trypsin-resistant tau

artículo científico publicado en 2015

Brain distribution of dipeptide repeat proteins in frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72

artículo científico publicado en 2014

Dipeptide repeat proteins are present in the p62 positive inclusions in patients with frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72.

artículo científico publicado en 2013

Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations

artículo científico publicado en 2012

Dysregulation of BDNF in Prefrontal Cortex in Alzheimer's Disease

artículo científico publicado en 2019

Dysregulation of C-X-C motif ligand 10 during aging and association with cognitive performance.

artículo científico publicado en 2017

Early changes in extracellular matrix in Alzheimer's disease.

artículo científico publicado en 2015

Effects of Alterations of Post-Mortem Delay and Other Tissue-Collection Variables on Metabolite Levels in Human and Rat Brain

artículo científico publicado en 2020

Expression of one important chaperone protein, heat shock protein 27, in neurodegenerative diseases

artículo científico publicado en 2014

Extended post-mortem delay times should not be viewed as a deterrent to the scientific investigation of human brain tissue: a study from the Brains for Dementia Research Network Neuropathology Study Group, UK.

artículo científico publicado en 2016

Granular expression of prolyl-peptidyl isomerase PIN1 is a constant and specific feature of Alzheimer's disease pathology and is independent of tau, Aβ and TDP-43 pathology

artículo científico publicado en 2011

Heterogeneous ribonuclear protein A3 (hnRNP A3) is present in dipeptide repeat protein containing inclusions in Frontotemporal Lobar Degeneration and Motor Neurone disease associated with expansions in C9orf72 gene

artículo científico publicado en 2017

Heterogeneous ribonuclear protein E2 (hnRNP E2) is associated with TDP-43-immunoreactive neurites in Semantic Dementia but not with other TDP-43 pathological subtypes of Frontotemporal Lobar Degeneration

artículo científico publicado en 2017

Histone deacetylase class II and acetylated core histone immunohistochemistry in human brains with Huntington's disease.

artículo científico publicado en 2013

Histone deacetylases (HDACs) in frontotemporal lobar degeneration

artículo científico publicado en 2015

Human tauopathy-derived tau strains determine the substrates recruited for templated amplification

scientific article published on 01 September 2021

Immunohistochemical detection of C9orf72 protein in frontotemporal lobar degeneration and motor neurone disease: patterns of immunostaining and an evaluation of commercial antibodies

artículo científico publicado en 2017

Inflammatory pathology markers (activated microglia and reactive astrocytes) in early and late onset Alzheimer disease: a post mortem study

artículo científico publicado en 2017

Influence of APOE genotype in primary age-related tauopathy

artículo científico publicado en 2020

Lysosomes, autophagosomes and Alzheimer pathology in dementia with Lewy body disease

scientific article published on 10 May 2018

Mid to late-life scores of depression in the cognitively healthy are associated with cognitive status and Alzheimer's disease pathology at death

artículo científico publicado en 2020

Neurodegeneration in frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9orf72 is linked to TDP-43 pathology and not associated with aggregated forms of dipeptide repeat proteins.

artículo científico publicado en 2015

Neuropathology of a case of fragile X-associated tremor ataxia syndrome without tremor

scientific article published on 23 August 2020

No association between head injury with loss of consciousness and Alzheimer disease pathology-Findings from the University of Manchester Longitudinal Study of Cognition in Normal Healthy Old Age

scientific article published on 10 May 2019

No interaction between tau and TDP-43 pathologies in either frontotemporal lobar degeneration or motor neurone disease

artículo científico publicado en 2014

Novel Metabolite Biomarkers of Huntington's Disease As Detected by High-Resolution Mass Spectrometry.

artículo científico publicado en 2016

Nuclear carrier and RNA-binding proteins in frontotemporal lobar degeneration associated with fused in sarcoma (FUS) pathological changes.

artículo científico publicado en 2013

Pathological Correlates of Cognitive Impairment in The University of Manchester Longitudinal Study of Cognition in Normal Healthy Old Age

artículo científico publicado en 2018

Pathological assessments for the presence of hexanucleotide repeat expansions in C9ORF72 in Alzheimer's disease

artículo científico publicado en 2013

Pathological tau deposition in Motor Neurone Disease and frontotemporal lobar degeneration associated with TDP-43 proteinopathy

artículo científico publicado en 2016

Patterns and severity of vascular amyloid in Alzheimer's disease associated with duplications and missense mutations in APP gene, Down syndrome and sporadic Alzheimer's disease

article

Patterns of Microglial Cell Activation in Alzheimer Disease and Frontotemporal Lobar Degeneration

artículo científico publicado en 2017

Patterns of microglial cell activation in frontotemporal lobar degeneration

artículo científico publicado en 2014

Plasma levels of progranulin and interleukin-6 in frontotemporal lobar degeneration

artículo científico publicado en 2014

Psychosis associated with expansions in the C9orf72 gene: the influence of a 10 base pair gene deletion

artículo científico publicado en 2015

Scores Obtained from a Simple Cognitive Test of Visuospatial Episodic Memory Performed Decades before Death Are Associated with the Ultimate Presence of Alzheimer Disease Pathology.

artículo científico publicado en 2018

Small deletion in C9orf72 hides a proportion of expansion carriers in FTLD.

artículo científico publicado en 2014

Structure-based classification of tauopathies

artículo científico publicado en 2021

TDP-43 pathological changes in early onset familial and sporadic Alzheimer's disease, late onset Alzheimer's disease and Down's syndrome: association with age, hippocampal sclerosis and clinical phenotype

artículo científico publicado en 2011

Targeted biochemical profiling of brain from Huntington's disease patients reveals novel metabolic pathways of interest

artículo científico publicado en 2018

Targeted deletion of the mitogen-activated protein kinase kinase 4 gene in the nervous system causes severe brain developmental defects and premature death

artículo científico publicado en 2007

The age of onset and evolution of Braak tangle stage and Thal amyloid pathology of Alzheimer's disease in individuals with Down syndrome.

artículo científico publicado en 2018

The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene

artículo científico

The regulation of Bax by c-Jun N-terminal protein kinase (JNK) is a prerequisite to the mitochondrial-induced apoptotic pathway

scientific journal article

The role of lysosomes and autophagosomes in frontotemporal lobar degeneration

artículo científico publicado en 2018

Lista de obras de Andrew Robinson

Accumulation of dipeptide repeat proteins predates that of TDP-43 in frontotemporal lobar degeneration associated with hexanucleotide repeat expansions in C9ORF72 gene

Accumulation of multiple neurodegenerative disease-related proteins in familial frontotemporal lobar degeneration associated with granulin mutation

Analysis of the hexanucleotide repeat in C9ORF72 in Alzheimer's disease

Biochemical classification of tauopathies by immunoblot, protein sequence and mass spectrometric analyses of sarkosyl-insoluble and trypsin-resistant tau

Brain distribution of dipeptide repeat proteins in frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72

Dipeptide repeat proteins are present in the p62 positive inclusions in patients with frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72.

Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations

Dysregulation of BDNF in Prefrontal Cortex in Alzheimer's Disease

Dysregulation of C-X-C motif ligand 10 during aging and association with cognitive performance.

Early changes in extracellular matrix in Alzheimer's disease.

Effects of Alterations of Post-Mortem Delay and Other Tissue-Collection Variables on Metabolite Levels in Human and Rat Brain

Expression of one important chaperone protein, heat shock protein 27, in neurodegenerative diseases

Extended post-mortem delay times should not be viewed as a deterrent to the scientific investigation of human brain tissue: a study from the Brains for Dementia Research Network Neuropathology Study Group, UK.

Granular expression of prolyl-peptidyl isomerase PIN1 is a constant and specific feature of Alzheimer's disease pathology and is independent of tau, Aβ and TDP-43 pathology

Heterogeneous ribonuclear protein A3 (hnRNP A3) is present in dipeptide repeat protein containing inclusions in Frontotemporal Lobar Degeneration and Motor Neurone disease associated with expansions in C9orf72 gene

Heterogeneous ribonuclear protein E2 (hnRNP E2) is associated with TDP-43-immunoreactive neurites in Semantic Dementia but not with other TDP-43 pathological subtypes of Frontotemporal Lobar Degeneration

Histone deacetylase class II and acetylated core histone immunohistochemistry in human brains with Huntington's disease.

Histone deacetylases (HDACs) in frontotemporal lobar degeneration

Human tauopathy-derived tau strains determine the substrates recruited for templated amplification

Immunohistochemical detection of C9orf72 protein in frontotemporal lobar degeneration and motor neurone disease: patterns of immunostaining and an evaluation of commercial antibodies

Inflammatory pathology markers (activated microglia and reactive astrocytes) in early and late onset Alzheimer disease: a post mortem study

Influence of APOE genotype in primary age-related tauopathy

Lysosomes, autophagosomes and Alzheimer pathology in dementia with Lewy body disease

Mid to late-life scores of depression in the cognitively healthy are associated with cognitive status and Alzheimer's disease pathology at death

Neurodegeneration in frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9orf72 is linked to TDP-43 pathology and not associated with aggregated forms of dipeptide repeat proteins.

Neuropathology of a case of fragile X-associated tremor ataxia syndrome without tremor

No association between head injury with loss of consciousness and Alzheimer disease pathology-Findings from the University of Manchester Longitudinal Study of Cognition in Normal Healthy Old Age

No interaction between tau and TDP-43 pathologies in either frontotemporal lobar degeneration or motor neurone disease

Novel Metabolite Biomarkers of Huntington's Disease As Detected by High-Resolution Mass Spectrometry.

Nuclear carrier and RNA-binding proteins in frontotemporal lobar degeneration associated with fused in sarcoma (FUS) pathological changes.

Pathological Correlates of Cognitive Impairment in The University of Manchester Longitudinal Study of Cognition in Normal Healthy Old Age

Pathological assessments for the presence of hexanucleotide repeat expansions in C9ORF72 in Alzheimer's disease

Pathological tau deposition in Motor Neurone Disease and frontotemporal lobar degeneration associated with TDP-43 proteinopathy

Patterns and severity of vascular amyloid in Alzheimer's disease associated with duplications and missense mutations in APP gene, Down syndrome and sporadic Alzheimer's disease

Patterns of Microglial Cell Activation in Alzheimer Disease and Frontotemporal Lobar Degeneration

Patterns of microglial cell activation in frontotemporal lobar degeneration

Plasma levels of progranulin and interleukin-6 in frontotemporal lobar degeneration

Psychosis associated with expansions in the C9orf72 gene: the influence of a 10 base pair gene deletion

Scores Obtained from a Simple Cognitive Test of Visuospatial Episodic Memory Performed Decades before Death Are Associated with the Ultimate Presence of Alzheimer Disease Pathology.

Small deletion in C9orf72 hides a proportion of expansion carriers in FTLD.

Structure-based classification of tauopathies

TDP-43 pathological changes in early onset familial and sporadic Alzheimer's disease, late onset Alzheimer's disease and Down's syndrome: association with age, hippocampal sclerosis and clinical phenotype

Targeted biochemical profiling of brain from Huntington's disease patients reveals novel metabolic pathways of interest

Targeted deletion of the mitogen-activated protein kinase kinase 4 gene in the nervous system causes severe brain developmental defects and premature death

The age of onset and evolution of Braak tangle stage and Thal amyloid pathology of Alzheimer's disease in individuals with Down syndrome.

The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene

The regulation of Bax by c-Jun N-terminal protein kinase (JNK) is a prerequisite to the mitochondrial-induced apoptotic pathway

The role of lysosomes and autophagosomes in frontotemporal lobar degeneration