Lista de obras -

5-HT2A T102C receptor polymorphism and neuropsychiatric symptoms in Alzheimer's disease

artículo científico publicado en 2004

A PIN1 polymorphism that prevents its suppression by AP4 associates with delayed onset of Alzheimer's disease

artículo científico publicado en 2010

A home-based exercise intervention for caregivers of persons with dementia: study protocol for a randomised controlled trial.

artículo científico publicado en 2016

Aberrant interhemispheric functional connectivity within default mode network and its relationships with neurocognitive features in cognitively normal APOE ε 4 elderly carriers.

artículo científico publicado en 2017

Apolipoprotein E epsilon4 allele is associated with vascular dementia.

artículo científico publicado en 2006

Apolipoprotein epsilon-4 allele and the two-year progression of cognitive function in Chinese subjects with late-onset Alzheimer's disease.

artículo científico publicado en 2006

Association between HLA-A alleles and Alzheimer's disease in a southern Chinese community.

artículo científico publicado en 2008

Association between tumor necrosis factor-alpha promoter polymorphism and Alzheimer's disease.

artículo científico publicado en 2004

Association of gene expression and methylation of UQCRC1 to the predisposition of Alzheimer's disease in a Chinese population.

artículo científico publicado en 2016

Association of prostaglandin-endoperoxide synthase 2 (PTGS2) polymorphisms and Alzheimer's disease in Chinese.

artículo científico publicado en 2007

Cholesterol 24-hydroxylase (CYP46A1) polymorphisms are associated with faster cognitive deterioration in Chinese older persons: a two-year follow up study

artículo científico publicado en 2009

Effect of CYP2D6 and CYP3A4 Genotypes on the Efficacy of Cholinesterase Inhibitors in Southern Chinese Patients With Alzheimer's Disease

scientific article published on 07 May 2019

Estrogen receptor α polymorphisms and the risk of cognitive decline: A 2-year follow-up study

artículo científico publicado en 2013

Evaluation of an algorithm of tagging SNPs selection by linkage disequilibrium.

artículo científico publicado en 2006

Functional interaction between SNPs and microsatellite in the transcriptional regulation of insulin-like growth factor 1.

artículo científico publicado en 2013

Gastrointestinal Problems in Chinese Children with Autism Spectrum Disorder

scientific article published on 24 July 2020

Genetic association study between mbl2 and asthma phenotypes in Chinese children

artículo científico publicado en 2006

Haplotype effect in the IGF1 promoter accounts for the association between microsatellite and serum IGF1 concentration

artículo científico publicado en 2011

Home-based exercise intervention for caregivers of persons with dementia: a randomised controlled trial: abridged secondary publication

scientific article published on 01 December 2020

Lack of association of the interleukin-1beta gene polymorphism with Alzheimer's disease in a Chinese population.

artículo científico publicado en 2003

Low-density lipoprotein receptor-related protein 8 (apolipoprotein E receptor 2) gene polymorphisms in Alzheimer's disease

artículo científico publicado en 2002

Melatonin receptor 1B (MTNR1B) gene polymorphism is associated with the occurrence of adolescent idiopathic scoliosis.

artículo científico publicado en 2007

Molecular evolution in the CREB1 signal pathway and a rare haplotype in CREB1 with genetic predisposition to schizophrenia

artículo científico publicado en 2014

MxA polymorphisms are associated with risk and age-at-onset in Alzheimer disease and accelerated cognitive decline in Chinese elders

artículo científico publicado en 2012

Novel mutations in type 2 Gaucher disease in Chinese and their functional characterization by heterologous expression.

artículo científico publicado en 2005

Panel of Genetic Variations as a Potential Non-invasive Biomarker for Early Diagnosis of Alzheimer's Disease.

artículo científico publicado en 2011

Polymorphisms of the cholesterol 24-hydroxylase (CYP46A1) gene and the risk of Alzheimer's disease in a Chinese population

artículo científico publicado en 2006

Polymorphisms of the estrogen receptor alpha (ESR1) gene and the risk of Alzheimer's disease in a southern Chinese community

artículo científico publicado en 2009

Prolyl isomerase Pin1 promotes amyloid precursor protein (APP) turnover by inhibiting glycogen synthase kinase-3β (GSK3β) activity: novel mechanism for Pin1 to protect against Alzheimer disease.

artículo científico publicado en 2011

Telomere length and cognitive function in southern Chinese community-dwelling male elders

artículo científico publicado en 2013

The association between promoter polymorphism of the interleukin-10 gene and Alzheimer's disease.

artículo científico publicado en 2004

The effects of apolipoprotein ε 4 on aging brain in cognitively normal Chinese elderly: a surface-based morphometry study.

artículo científico publicado en 2016

The mechanism of transactivation regulation due to polymorphic short tandem repeats (STRs) using IGF1 promoter as a model

artículo científico publicado en 2016

Lista de obras de

5-HT2A T102C receptor polymorphism and neuropsychiatric symptoms in Alzheimer's disease

A PIN1 polymorphism that prevents its suppression by AP4 associates with delayed onset of Alzheimer's disease

A home-based exercise intervention for caregivers of persons with dementia: study protocol for a randomised controlled trial.

Aberrant interhemispheric functional connectivity within default mode network and its relationships with neurocognitive features in cognitively normal APOE ε 4 elderly carriers.

Apolipoprotein E epsilon4 allele is associated with vascular dementia.

Apolipoprotein epsilon-4 allele and the two-year progression of cognitive function in Chinese subjects with late-onset Alzheimer's disease.

Association between HLA-A alleles and Alzheimer's disease in a southern Chinese community.

Association between tumor necrosis factor-alpha promoter polymorphism and Alzheimer's disease.

Association of gene expression and methylation of UQCRC1 to the predisposition of Alzheimer's disease in a Chinese population.

Association of prostaglandin-endoperoxide synthase 2 (PTGS2) polymorphisms and Alzheimer's disease in Chinese.

Cholesterol 24-hydroxylase (CYP46A1) polymorphisms are associated with faster cognitive deterioration in Chinese older persons: a two-year follow up study

Effect of CYP2D6 and CYP3A4 Genotypes on the Efficacy of Cholinesterase Inhibitors in Southern Chinese Patients With Alzheimer's Disease

Estrogen receptor α polymorphisms and the risk of cognitive decline: A 2-year follow-up study

Evaluation of an algorithm of tagging SNPs selection by linkage disequilibrium.

Functional interaction between SNPs and microsatellite in the transcriptional regulation of insulin-like growth factor 1.

Gastrointestinal Problems in Chinese Children with Autism Spectrum Disorder

Genetic association study between mbl2 and asthma phenotypes in Chinese children

Haplotype effect in the IGF1 promoter accounts for the association between microsatellite and serum IGF1 concentration

Home-based exercise intervention for caregivers of persons with dementia: a randomised controlled trial: abridged secondary publication

Lack of association of the interleukin-1beta gene polymorphism with Alzheimer's disease in a Chinese population.

Low-density lipoprotein receptor-related protein 8 (apolipoprotein E receptor 2) gene polymorphisms in Alzheimer's disease

Melatonin receptor 1B (MTNR1B) gene polymorphism is associated with the occurrence of adolescent idiopathic scoliosis.

Molecular evolution in the CREB1 signal pathway and a rare haplotype in CREB1 with genetic predisposition to schizophrenia

MxA polymorphisms are associated with risk and age-at-onset in Alzheimer disease and accelerated cognitive decline in Chinese elders

Novel mutations in type 2 Gaucher disease in Chinese and their functional characterization by heterologous expression.

Panel of Genetic Variations as a Potential Non-invasive Biomarker for Early Diagnosis of Alzheimer's Disease.

Polymorphisms of the cholesterol 24-hydroxylase (CYP46A1) gene and the risk of Alzheimer's disease in a Chinese population

Polymorphisms of the estrogen receptor alpha (ESR1) gene and the risk of Alzheimer's disease in a southern Chinese community

Prolyl isomerase Pin1 promotes amyloid precursor protein (APP) turnover by inhibiting glycogen synthase kinase-3β (GSK3β) activity: novel mechanism for Pin1 to protect against Alzheimer disease.

Telomere length and cognitive function in southern Chinese community-dwelling male elders

The association between promoter polymorphism of the interleukin-10 gene and Alzheimer's disease.

The effects of apolipoprotein ε 4 on aging brain in cognitively normal Chinese elderly: a surface-based morphometry study.

The mechanism of transactivation regulation due to polymorphic short tandem repeats (STRs) using IGF1 promoter as a model