Association of progranulin polymorphism rs5848 with neurodegenerative diseases: a meta-analysis. - sprookjes - yvandenbroek - TriplyDB

Association of progranulin polymorphism rs5848 with neurodegenerative diseases: a meta-analysis.

Association of progranulin polymorphism rs5848 with neurodegenerative diseases: a meta-analysis.

http://www.wikidata.org/entity/Q41595939

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Recent advances in amyotrophic lateral sclerosis Phenotypic Heterogeneity of Monogenic Frontotemporal Dementia Copy number variability in Parkinson's disease: assembling the puzzle through a systems biology approach Trehalose upregulates progranulin expression in human and mouse models of GRN haploinsufficiency: a novel therapeutic lead to treat frontotemporal dementia.Advances in understanding genomic markers and pharmacogenetics of Parkinson's disease.Progranulin: A key player in autoimmune diseases.Meta-analysis of the association between variants in MAPT and neurodegenerative diseases.Association analysis of the GRN rs5848 and MAPT rs242557 polymorphisms in Parkinson's disease and multiple system atrophy: a large-scale population-based study and meta-analysis.Intracellular Proteolysis of Progranulin Generates Stable, Lysosomal Granulins that Are Haploinsufficient in Patients with Frontotemporal Dementia Caused by GRN Mutations.PGRN Is Associated with Late-Onset Alzheimer's Disease: a Case-Control Replication Study and Meta-analysis.Loss of Neuroprotective Factors in Neurodegenerative Dementias: The End or the Starting Point?Intranasal administration of recombinant progranulin inhibits bronchial smooth muscle hyperresponsiveness in mouse allergic asthma.

P2860

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P2860

Association of progranulin polymorphism rs5848 with neurodegenerative diseases: a meta-analysis.

http://www.wikidata.org/entity/Q41595939

description

2015 nî lūn-bûn

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name

Association of progranulin pol ...... ive diseases: a meta-analysis.

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Association of progranulin pol ...... ive diseases: a meta-analysis.

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Association of progranulin pol ...... ive diseases: a meta-analysis.

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P1433

Journal of Neurology

P1476

Association of progranulin pol ...... ive diseases: a meta-analysis.

@en

P2093

Guangdi Chen

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Jinghao Sheng

http://www.w3.org/2001/XMLSchema#string

Liling Su

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Siqi Li

http://www.w3.org/2001/XMLSchema#string

Wen Lv

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Yongdui Chen

http://www.w3.org/2001/XMLSchema#string

Zhengping Xu

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P2860

Neurodegenerative diseases: an overview of environmental risk factors

Potential mechanisms of progranulin-deficient FTLD

Operating characteristics of a rank correlation test for publication bias

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

Clinicopathologic variability of the GRN A9D mutation, including amyotrophic lateral sclerosis

Progranulin expression correlates with dense-core amyloid plaque burden in Alzheimer disease mouse models.

Variation at GRN 3'-UTR rs5848 is not associated with a risk of frontotemporal lobar degeneration in Dutch population.

Common variant in GRN is a genetic risk factor for hippocampal sclerosis in the elderly.

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration.

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4

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neurodegeneration