Frontotemporal dementia and its subtypes: a genome-wide association study. - Wikidata - wikimedia - TriplyDB

Frontotemporal dementia and its subtypes: a genome-wide association study.

Frontotemporal dementia and its subtypes: a genome-wide association study.

http://www.wikidata.org/entity/Q33955007

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Understanding Neuropsychiatric Diseases, Analyzing the Peptide Sharing between Infectious Agents and the Language-Associated NMDA 2A Protein Therapeutic and diagnostic challenges for frontotemporal dementia Pathogenesis of FUS-associated ALS and FTD: insights from rodent models Essential role for autophagy in life span extension C9orf72 binds SMCR8, localizes to lysosomes, and regulates mTORC1 signaling.Genome-wide estimate of the heritability of Multiple System Atrophy Neuroinflammation - using big data to inform clinical practice.Systems biology approach to late-onset Alzheimer's disease genome-wide association study identifies novel candidate genes validated using brain expression data and Caenorhabditis elegans experiments.A multiancestral genome-wide exome array study of Alzheimer disease, frontotemporal dementia, and progressive supranuclear palsy Brain distribution of dipeptide repeat proteins in frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72 Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia.Reassessment of risk genotypes (GRN, TMEM106B, and ABCC9 variants) associated with hippocampal sclerosis of aging pathology Frontotemporal lobar degeneration: defining phenotypic diversity through personalized medicine.Epigenetic mechanisms underlying the pathogenesis of neurogenetic diseases A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia The NINDS Parkinson's disease biomarkers program.The executive prominent/memory prominent spectrum in Alzheimer's disease is highly heritable Novel diagnostic cerebrospinal fluid biomarkers for pathologic subtypes of frontotemporal dementia identified by proteomics.Defective recognition of LC3B by mutant SQSTM1/p62 implicates impairment of autophagy as a pathogenic mechanism in ALS-FTLD.Neuropsychiatric genomics in precision medicine: diagnostics, gene discovery, and translation.Increased prevalence of autoimmune disease within C9 and FTD/MND cohorts: Completing the picture.No association between gluten sensitivity and amyotrophic lateral sclerosis.Distinct Pattern of Microgliosis in the Olfactory Bulb of Neurodegenerative Proteinopathies.Microarray gene and miRNA expression studies: looking for new therapeutic targets for frontotemporal lobar degeneration.Genetics and underlying pathology of dementia.Atypical Parkinsonian syndromes: a general neurologist's perspective.FTD and ALS--translating mouse studies into clinical trials.Comparative Microarray Analysis Identifies Commonalities in Neuronal Injury: Evidence for Oxidative Stress, Dysfunction of Calcium Signalling, and Inhibition of Autophagy-Lysosomal Pathway.Iron and Neurodegeneration: Is Ferritinophagy the Link?Frontotemporal dementia: insights into the biological underpinnings of disease through gene co-expression network analysis Frontotemporal Lobar Degeneration: Mechanisms and Therapeutic Strategies.Walking the tightrope: proteostasis and neurodegenerative disease.Recent advances in the molecular genetics of frontotemporal lobar degeneration.Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia.Genetics of FTLD: overview and what else we can expect from genetic studies.Updated meta-analysis of the role of APOE ε2/ε3/ε4 alleles in frontotemporal lobar degeneration.Monoaminergic neuropathology in Alzheimer's disease.Molecular Genetics of Neurodegenerative Dementias.Weighted Protein Interaction Network Analysis of Frontotemporal Dementia.

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P2860

Frontotemporal dementia and its subtypes: a genome-wide association study.

http://www.wikidata.org/entity/Q33955007

description

2014 nî lūn-bûn

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2014 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2014 թվականի հուլիսին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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name

Frontotemporal dementia and its subtypes: a genome-wide association study.

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Frontotemporal dementia and its subtypes: a genome-wide association study.

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Frontotemporal dementia and its subtypes: a genome-wide association study.

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Frontotemporal dementia and its subtypes: a genome-wide association study.

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Frontotemporal dementia and its subtypes: a genome-wide association study.

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Frontotemporal dementia and its subtypes: a genome-wide association study.

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Lancet Neurology

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Frontotemporal dementia and its subtypes: a genome-wide association study.

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Adeline Rollin

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Adrian Danek

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Agustín Ruiz

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Alberto Lleó

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Alessandro Padovani

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Alexander Kurz

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Alfredo Postiglione

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Amalia C Bruni

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Anna M Karydas

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P2860

A two-stage meta-analysis identifies several new loci for Parkinson's disease

Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain

An integrated map of genetic variation from 1,092 human genomes

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

Serological cloning of a melanocyte rab guanosine 5'-triphosphate-binding protein and a chromosome condensation protein from a melanoma complementary DNA library

BLOC-2, AP-3, and AP-1 proteins function in concert with Rab38 and Rab32 proteins to mediate protein trafficking to lysosome-related organelles

Rab GTPases regulating phagosome maturation are differentially recruited to mycobacterial phagosomes

Classification of primary progressive aphasia and its variants

Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

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Philip Scheltens

Christine Van Broeckhoven

Pietro Pietrini

Rosa Rademakers

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Ekaterina Rogaeva

Jordan Henry Grafman

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