TREM2 is associated with the risk of Alzheimer's disease in Spanish population - Wikidata - awgldk - TriplyDB

TREM2 is associated with the risk of Alzheimer's disease in Spanish population

TREM2 is associated with the risk of Alzheimer's disease in Spanish population

http://www.wikidata.org/entity/Q36681136

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Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease Modeling Alzheimer's Disease with Induced Pluripotent Stem Cells: Current Challenges and Future Concerns TREM2 in CNS homeostasis and neurodegenerative disease R47H Variant of TREM2 Associated With Alzheimer Disease in a Large Late-Onset Family: Clinical, Genetic, and Neuropathological Study A rare mutation in UNC5C predisposes to late-onset Alzheimer's disease and increases neuronal cell death.Neuroimaging and genetic risk for Alzheimer's disease and addiction-related degenerative brain disorders.Family-based genome scan for age at onset of late-onset Alzheimer's disease in whole exome sequencing data The PSEN1, p.E318G variant increases the risk of Alzheimer's disease in APOE-ε4 carriers TREM2 and neurodegenerative disease.TREM2 variant p.R47H as a risk factor for sporadic amyotrophic lateral sclerosis.The rare TREM2 R47H variant exerts only a modest effect on Alzheimer disease risk.Coding variants in TREM2 increase risk for Alzheimer's disease Identification of rare variants in Alzheimer's disease.Frontobasal gray matter loss is associated with the TREM2 p.R47H variant Genomics in neurological disorders.TREM2 is associated with increased risk for Alzheimer's disease in African Americans.Lack of genetic association between TREM2 and Alzheimer's disease in East Asian population: a systematic review and meta-analysis.A TREM1 variant alters the accumulation of Alzheimer-related amyloid pathology.The triggering receptor expressed on myeloid cells 2 (TREM2) is associated with enhanced inflammation, neuropathological lesions and increased risk for Alzheimer's dementia More evidence for association of a rare TREM2 mutation (R47H) with Alzheimer's disease risk.DAP12 Stabilizes the C-terminal Fragment of the Triggering Receptor Expressed on Myeloid Cells-2 (TREM2) and Protects against LPS-induced Pro-inflammatory Response.R47H TREM2 variant increases risk of typical early-onset Alzheimer's disease but not of prion or frontotemporal dementia The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease.Apolipoprotein E Is a Ligand for Triggering Receptor Expressed on Myeloid Cells 2 (TREM2).Fine-mapping of the human leukocyte antigen locus as a risk factor for Alzheimer disease: A case-control study.Role of ABCA7 loss-of-function variant in Alzheimer's disease: a replication study in European-Americans Association study of TREM2 polymorphism rs75932628 with leucoaraiosis or Parkinson's disease in the Han Chinese population Resequencing analysis of five Mendelian genes and the top genes from genome-wide association studies in Parkinson's Disease.Cerebrospinal fluid soluble TREM2 is higher in Alzheimer disease and associated with mutation status.Investigation of triggering receptor expressed on myeloid cells 2 variant in the Wisconsin Registry for Alzheimer's Prevention.Missense variant in TREML2 protects against Alzheimer's disease.Genetic discoveries in AD using CSF amyloid and tau.Preparation, crystallization, and preliminary crystallographic analysis of wild-type and mutant human TREM-2 ectodomains linked to neurodegenerative and inflammatory diseases Alzheimer's disease risk alleles in TREM2 illuminate innate immunity in Alzheimer's disease.Next generation transcriptomics and genomics elucidate biological complexity of microglia in health and disease.TREM2 in Neurodegenerative Diseases.Genome-wide association study identifies four novel loci associated with Alzheimer's endophenotypes and disease modifiers.The clinical spectrum of sporadic and familial forms of frontotemporal dementia.Estrogens, Neuroinflammation, and Neurodegeneration.Genome research in pre-dementia stages of Alzheimer's disease.

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TREM2 is associated with the risk of Alzheimer's disease in Spanish population

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2013 nî lūn-bûn

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TREM2 is associated with the risk of Alzheimer's disease in Spanish population

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TREM2 is associated with the risk of Alzheimer's disease in Spanish population

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TREM2 is associated with the risk of Alzheimer's disease in Spanish population

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TREM2 is associated with the risk of Alzheimer's disease in Spanish population

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J.NEUROBIOLAGING.2012.12.018

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Neurobiology of Aging

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TREM2 is associated with the risk of Alzheimer's disease in Spanish population

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Breanna Cooper

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Elena Lorenzo

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Sebastian Cervantes

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Sheng-Chih Jin

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P2860

Exome-sequencing confirms DNAJC5 mutations as cause of adult neuronal ceroid-lipofuscinosis

TREM2 Variants in Alzheimer's Disease

Variant of TREM2 Associated with the Risk of Alzheimer's Disease

An Italian family affected by Nasu-Hakola disease with a novel genetic mutation in the TREM2 gene

DAP12/TREM2 deficiency results in impaired osteoclast differentiation and osteoporotic features

Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease

Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvement

Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families

The genetic causes of basal ganglia calcification, dementia, and bone cysts: DAP12 and TREM2.

Pooled-DNA sequencing identifies novel causative variants in PSEN1, GRN and MAPT in a clinical early-onset and familial Alzheimer's disease Ibero-American cohort.

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Bruno A Benitez

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Alzheimer's disease

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