Analysis of lipid pathway genes indicates association of sequence variation near SREBF1/TOM1L2/ATPAF2 with dementia risk - Wikidata - awgldk - TriplyDB

Analysis of lipid pathway genes indicates association of sequence variation near SREBF1/TOM1L2/ATPAF2 with dementia risk

Analysis of lipid pathway genes indicates association of sequence variation near SREBF1/TOM1L2/ATPAF2 with dementia risk

http://www.wikidata.org/entity/Q24631195

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Statistical assessment of crosstalk enrichment between gene groups in biological networks A Genetic Variant of the Sortilin 1 Gene is Associated with Reduced Risk of Alzheimer's Disease Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease PCSK9 Promotes oxLDL-Induced PC12 Cell Apoptosis Through the Bcl-2/Bax-Caspase 9/3 Signaling Pathway.Multivariate analysis reveals genetic associations of the resting default mode network in psychotic bipolar disorder and schizophrenia.Comparative interactomics with Funcoup 2.0.Association of the GALNT2 gene polymorphisms and several environmental factors with serum lipid levels in the Mulao and Han populations Genetic association of sequence variants near AGER/NOTCH4 and dementia.Association between the DOCK7, PCSK9 and GALNT2 Gene Polymorphisms and Serum Lipid levels Comprehensive analysis of the genome transcriptome and proteome landscapes of three tumor cell lines The dual behavior of PCSK9 in the regulation of apoptosis is crucial in Alzheimer's disease progression (Review).The multiscale backbone of the human phenotype network based on biological pathways PCSK9: an emerging target for treatment of hypercholesterolemia.Open chromatin profiling of human postmortem brain infers functional roles for non-coding schizophrenia loci.Design and rationale of the EBBINGHAUS trial: A phase 3, double-blind, placebo-controlled, multicenter study to assess the effect of evolocumab on cognitive function in patients with clinically evident cardiovascular disease and receiving statin bac Trafficking in Alzheimer's Disease: Modulation of APP Transport and Processing by the Transmembrane Proteins LRP1, SorLA, SorCS1c, Sortilin, and Calsyntenin.Increased PCSK9 Cerebrospinal Fluid Concentrations in Alzheimer's Disease.

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Analysis of lipid pathway genes indicates association of sequence variation near SREBF1/TOM1L2/ATPAF2 with dementia risk

http://www.wikidata.org/entity/Q24631195

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2010 nî lūn-bûn

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2010 թուականի Մայիսին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի մայիսին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Analysis of lipid pathway gene ...... M1L2/ATPAF2 with dementia risk

@ast

Analysis of lipid pathway gene ...... M1L2/ATPAF2 with dementia risk

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Analysis of lipid pathway gene ...... M1L2/ATPAF2 with dementia risk

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type

label

Analysis of lipid pathway gene ...... M1L2/ATPAF2 with dementia risk

@ast

Analysis of lipid pathway gene ...... M1L2/ATPAF2 with dementia risk

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Analysis of lipid pathway gene ...... M1L2/ATPAF2 with dementia risk

@nl

prefLabel

Analysis of lipid pathway gene ...... M1L2/ATPAF2 with dementia risk

@ast

Analysis of lipid pathway gene ...... M1L2/ATPAF2 with dementia risk

@en

Analysis of lipid pathway gene ...... M1L2/ATPAF2 with dementia risk

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Human Molecular Genetics

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Analysis of lipid pathway gene ...... M1L2/ATPAF2 with dementia risk

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Bo Malmberg

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Chandra A Reynolds

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Fredrik Wiklund

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Jonathan A Prince

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Mun-Gwan Hong

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Nancy L Pedersen

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Stig Berg

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Ulrika K Eriksson

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Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease

Recruitment of clathrin onto endosomes by the Tom1-Tollip complex

Isoform-specific interactions of apolipoprotein E with microtubule-associated protein tau: implications for Alzheimer disease

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

Common variants at 30 loci contribute to polygenic dyslipidemia

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

Variations in DNA elucidate molecular networks that cause disease

Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans

GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers

STRING 8--a global view on proteins and their functional interactions in 630 organisms

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10.1093/HMG/DDQ079

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10

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19

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Henrik Grönberg

Andrey Alexeyenko

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2010-05-15T00:00:00Z

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41486232

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20167577

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