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

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

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

http://www.wikidata.org/entity/Q33999208

about

Progranulin in frontotemporal lobar degeneration and neuroinflammation The genetics and neuropathology of frontotemporal lobar degeneration Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadics Word-finding difficulty: a clinical analysis of the progressive aphasias.Understanding Neuropsychiatric Diseases, Analyzing the Peptide Sharing between Infectious Agents and the Language-Associated NMDA 2A Protein Molecular Pathways Bridging Frontotemporal Lobar Degeneration and Psychiatric Disorders Phenotypic Heterogeneity of Monogenic Frontotemporal Dementia The epidemiology of frontotemporal dementia Mechanisms of granulin deficiency: lessons from cellular and animal models Mouse models of frontotemporal dementia Parkinsonian syndrome in familial frontotemporal dementia Therapeutic and diagnostic challenges for frontotemporal dementia Hyperphosphorylation as a defense mechanism to reduce TDP-43 aggregation Characterization of Movement Disorder Phenomenology in Genetically Proven, Familial Frontotemporal Lobar Degeneration: A Systematic Review and Meta-Analysis.Frontotemporal dementia: a bridge between dementia and neuromuscular disease Clinicopathological correlations in corticobasal degeneration Progranulin: normal function and role in neurodegeneration Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis Targeted manipulation of the sortilin-progranulin axis rescues progranulin haploinsufficiency Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families TARDBP 3'-UTR variant in autopsy-confirmed frontotemporal lobar degeneration with TDP-43 proteinopathy Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions.Mapping the progression of progranulin-associated frontotemporal lobar degeneration Creation of an open-access, mutation-defined fibroblast resource for neurological disease research.The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegeneration Progranulin modulates zebrafish motoneuron development in vivo and rescues truncation defects associated with knockdown of Survival motor neuron 1.A neurodegenerative disease mutation that accelerates the clearance of apoptotic cells Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration Clinicopathologic variability of the GRN A9D mutation, including amyotrophic lateral sclerosis Progranulin protects against amyloid β deposition and toxicity in Alzheimer's disease mouse models.Progranulin gene variability and plasma levels in bipolar disorder and schizophrenia.Variation at GRN 3'-UTR rs5848 is not associated with a risk of frontotemporal lobar degeneration in Dutch population.ALS and FTLD: two faces of TDP-43 proteinopathy.A thorough assessment of benign genetic variability in GRN and MAPT.The genetics of dementia.Protein Quality Control and the Amyotrophic Lateral Sclerosis/Frontotemporal Dementia Continuum Accumulation of multiple neurodegenerative disease-related proteins in familial frontotemporal lobar degeneration associated with granulin mutation.Mitochondrial DNA haplogroups in early-onset Alzheimer's disease and frontotemporal lobar degeneration Rs5848 variant influences GRN mRNA levels in brain and peripheral mononuclear cells in patients with Alzheimer's disease.Common variant in GRN is a genetic risk factor for hippocampal sclerosis in the elderly.

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P2860

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

http://www.wikidata.org/entity/Q33999208

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2006 nî lūn-bûn

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2006 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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Mutations in progranulin are a ...... totemporal lobar degeneration.

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Mutations in progranulin are a ...... totemporal lobar degeneration.

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Mutations in progranulin are a ...... totemporal lobar degeneration.

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Mutations in progranulin are a ...... totemporal lobar degeneration.

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Mutations in progranulin are a ...... totemporal lobar degeneration.

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Mutations in progranulin are a ...... totemporal lobar degeneration.

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Human Molecular Genetics

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Mutations in progranulin are a ...... totemporal lobar degeneration.

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P2093

Ashley Cannon

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Bradley Boeve

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Bryan Woodruff

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Dave Knopman

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Eileen Bigio

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Ging-Yuek Hsiung

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Ian R Mackenzie

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Jennifer Adamson

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Jennifer Gass

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John Gonzalez

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10.1093/HMG/DDL241

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20

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15

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Rosa Rademakers

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