Lista de obras - Yue Huang - Dominio Público Uruguay

Abnormal global functional network connectivity and its relationship to medial temporal atrophy in patients with amnestic mild cognitive impairment

artículo científico publicado en 2017

Alpha B-crystallin is a major component of glial cytoplasmic inclusions in multiple system atrophy.

artículo científico publicado en 2005

Anticipation of onset age in familial Parkinson's disease without SCA gene mutations

article

Aspects of innate immunity and Parkinson's disease

artículo científico publicado en 2012

Association study of clusterin polymorphism rs11136000 with late onset Alzheimer's disease in Chinese Han population

artículo científico publicado en 2011

Can we clinically diagnose dementia with Lewy bodies yet?

artículo científico publicado en 2013

Changes in the solubility and phosphorylation of α-synuclein over the course of Parkinson's disease

artículo científico publicado en 2011

Clinical and imaging features of a Chinese-speaking man with semantic dementia

scientific article published on 31 January 2008

Clinical correlates of similar pathologies in parkinsonian syndromes

artículo científico publicado en 2011

Clinical phenotypes in autopsy-confirmed Pick disease

scientific article published on 01 January 2011

DNA extraction from fresh-frozen and formalin-fixed, paraffin-embedded human brain tissue

artículo científico publicado en 2013

DNA methylation of the MAPT gene in Parkinson's disease cohorts and modulation by vitamin E in vitro

artículo científico publicado en 2013

Diffusion tensor imaging measures of normal appearing white matter in patients who are aging, or have amnestic mild cognitive impairment, or Alzheimer's disease

artículo científico publicado en 2013

Dissection of prodromal Alzheimer's disease

artículo científico publicado en 2018

Genetic contributions to Parkinson's disease

artículo científico publicado en 2004

Genetic polymorphisms in sigma-1 receptor and apolipoprotein E interact to influence the severity of Alzheimer's disease

artículo científico publicado en 2011

Genetics of Parkinson's Disease

scholarly article published 2007

Genetics of hereditary neurological disorders in children

artículo científico publicado en 2014

How does white matter microstructure differ between the vascular and amnestic mild cognitive impairment?

artículo científico publicado en 2017

Immunohistochemical evidence for macroautophagy in neurones and endothelial cells in Alzheimer's disease

artículo científico publicado en 2010

Interaction between α-synuclein and tau genotypes and the progression of Parkinson's disease

artículo científico publicado en 2011

LRRK2 and parkin immunoreactivity in multiple system atrophy inclusions

artículo científico publicado en 2008

LRRK2 interactions with α-synuclein in Parkinson's disease brains and in cell models

artículo científico publicado en 2013

Long noncoding RNAs in TDP-43 and FUS/TLS-related frontotemporal lobar degeneration (FTLD).

artículo científico

Macroautophagy in sporadic and the genetic form of Parkinson's disease with the A53T α-synuclein mutation

artículo científico publicado en 2012

Metabolomics: a novel approach to identify potential diagnostic biomarkers and pathogenesis in Alzheimer's disease

artículo científico publicado en 2012

MicroRNA-146a represses LRP2 translation and leads to cell apoptosis in Alzheimer's disease

artículo científico publicado en 2016

MicroRNA-146a suppresses ROCK1 allowing hyperphosphorylation of tau in Alzheimer's disease

artículo científico publicado en 2016

P25alpha immunoreactive but alpha-synuclein immunonegative neuronal inclusions in multiple system atrophy

artículo científico publicado en 2006

Pallidal stimulation reduces treatment-induced dyskinesias in "minimal-change" multiple system atrophy

artículo científico publicado en 2005

Parkin Co-Regulated Gene (PACRG) is regulated by the ubiquitin-proteasomal system and is present in the pathological features of Parkinsonian diseases

artículo científico publicado en 2007

Parkinson's disease-implicated kinases in the brain; insights into disease pathogenesis

artículo científico publicado en 2014

Predicting Development of Amyotrophic Lateral Sclerosis in Frontotemporal Dementia.

artículo científico publicado en 2017

Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's disease

artículo científico publicado en 2007

Quantitative protein profiling of hippocampus during human aging

artículo científico publicado en 2015

ROCK1 Is Associated with Alzheimer's Disease-Specific Plaques, as well as Enhances Autophagosome Formation But not Autophagic Aβ Clearance

artículo científico publicado en 2016

Reader response: Diagnosis and management of dementia with Lewy bodies: Fourth consensus report of the DLB Consortium.

artículo científico publicado en 2018

Retiring the term FTDP-17 as MAPT mutations are genetic forms of sporadic frontotemporal tauopathies.

artículo científico publicado en 2017

SNCA Gene, but Not MAPT, Influences Onset Age of Parkinson's Disease in Chinese and Australians

artículo científico publicado en 2015

SS31 ameliorates age-related activation of NF-κB signaling in senile mice model, SAMP8

artículo científico publicado en 2016

SUMO-1 marks the nuclear inclusions in familial neuronal intranuclear inclusion disease

artículo científico publicado en 2003

Standardized Operational Protocol for Human Brain Banking in China

article

Tenuigenin attenuates α-synuclein-induced cytotoxicity by down-regulating polo-like kinase 3.

artículo científico publicado en 2013

Utility and limitations of Addenbrooke's Cognitive Examination-Revised for detecting mild cognitive impairment in Parkinson's disease

artículo científico publicado en 2011

VISA--a pass to innate immunity

artículo científico publicado en 2006

Validation of the Chinese version of Addenbrooke's cognitive examination-revised for screening mild Alzheimer's disease and mild cognitive impairment

artículo científico publicado en 2013

Variants in the SNCA gene associate with motor progression while variants in the MAPT gene associate with the severity of Parkinson's disease

artículo científico publicado en 2015

p25alpha relocalizes in oligodendroglia from myelin to cytoplasmic inclusions in multiple system atrophy

artículo científico publicado en 2007

Lista de obras de Yue Huang

Abnormal global functional network connectivity and its relationship to medial temporal atrophy in patients with amnestic mild cognitive impairment

Alpha B-crystallin is a major component of glial cytoplasmic inclusions in multiple system atrophy.

Anticipation of onset age in familial Parkinson's disease without SCA gene mutations

Aspects of innate immunity and Parkinson's disease

Association study of clusterin polymorphism rs11136000 with late onset Alzheimer's disease in Chinese Han population

Can we clinically diagnose dementia with Lewy bodies yet?

Changes in the solubility and phosphorylation of α-synuclein over the course of Parkinson's disease

Clinical and imaging features of a Chinese-speaking man with semantic dementia

Clinical correlates of similar pathologies in parkinsonian syndromes

Clinical phenotypes in autopsy-confirmed Pick disease

DNA extraction from fresh-frozen and formalin-fixed, paraffin-embedded human brain tissue

DNA methylation of the MAPT gene in Parkinson's disease cohorts and modulation by vitamin E in vitro

Diffusion tensor imaging measures of normal appearing white matter in patients who are aging, or have amnestic mild cognitive impairment, or Alzheimer's disease

Dissection of prodromal Alzheimer's disease

Genetic contributions to Parkinson's disease

Genetic polymorphisms in sigma-1 receptor and apolipoprotein E interact to influence the severity of Alzheimer's disease

Genetics of Parkinson's Disease

Genetics of hereditary neurological disorders in children

How does white matter microstructure differ between the vascular and amnestic mild cognitive impairment?

Immunohistochemical evidence for macroautophagy in neurones and endothelial cells in Alzheimer's disease

Interaction between α-synuclein and tau genotypes and the progression of Parkinson's disease

LRRK2 and parkin immunoreactivity in multiple system atrophy inclusions

LRRK2 interactions with α-synuclein in Parkinson's disease brains and in cell models

Long noncoding RNAs in TDP-43 and FUS/TLS-related frontotemporal lobar degeneration (FTLD).

Macroautophagy in sporadic and the genetic form of Parkinson's disease with the A53T α-synuclein mutation

Metabolomics: a novel approach to identify potential diagnostic biomarkers and pathogenesis in Alzheimer's disease

MicroRNA-146a represses LRP2 translation and leads to cell apoptosis in Alzheimer's disease

MicroRNA-146a suppresses ROCK1 allowing hyperphosphorylation of tau in Alzheimer's disease

P25alpha immunoreactive but alpha-synuclein immunonegative neuronal inclusions in multiple system atrophy

Pallidal stimulation reduces treatment-induced dyskinesias in "minimal-change" multiple system atrophy

Parkin Co-Regulated Gene (PACRG) is regulated by the ubiquitin-proteasomal system and is present in the pathological features of Parkinsonian diseases

Parkinson's disease-implicated kinases in the brain; insights into disease pathogenesis

Predicting Development of Amyotrophic Lateral Sclerosis in Frontotemporal Dementia.

Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's disease

Quantitative protein profiling of hippocampus during human aging

ROCK1 Is Associated with Alzheimer's Disease-Specific Plaques, as well as Enhances Autophagosome Formation But not Autophagic Aβ Clearance

Reader response: Diagnosis and management of dementia with Lewy bodies: Fourth consensus report of the DLB Consortium.

Retiring the term FTDP-17 as MAPT mutations are genetic forms of sporadic frontotemporal tauopathies.

SNCA Gene, but Not MAPT, Influences Onset Age of Parkinson's Disease in Chinese and Australians

SS31 ameliorates age-related activation of NF-κB signaling in senile mice model, SAMP8

SUMO-1 marks the nuclear inclusions in familial neuronal intranuclear inclusion disease

Standardized Operational Protocol for Human Brain Banking in China

Tenuigenin attenuates α-synuclein-induced cytotoxicity by down-regulating polo-like kinase 3.

Utility and limitations of Addenbrooke's Cognitive Examination-Revised for detecting mild cognitive impairment in Parkinson's disease

VISA--a pass to innate immunity

Validation of the Chinese version of Addenbrooke's cognitive examination-revised for screening mild Alzheimer's disease and mild cognitive impairment

Variants in the SNCA gene associate with motor progression while variants in the MAPT gene associate with the severity of Parkinson's disease

p25alpha relocalizes in oligodendroglia from myelin to cytoplasmic inclusions in multiple system atrophy