Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains

Temporal lobe proteins implicated in synaptic failure exhibit differential expression and deamidation in vascular dementia

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Frontotemporal dementia: a bridge between dementia and neuromuscular disease

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Aberrant sumoylation signaling evoked by reactive oxygen species impairs protective function of Prdx6 by destabilization and repression of its transcription

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Single nucleotide polymorphism in the neuroplastin locus associates with cortical thickness and intellectual ability in adolescents

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Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy

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Pathological mechanisms underlying TDP-43 driven neurodegeneration in FTLD-ALS spectrum disorders

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Overexpression of ALS-Associated p.M337V Human TDP-43 in Mice Worsens Disease Features Compared to Wild-type Human TDP-43 Mice

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Metabolism of inflammation limited by AMPK and pseudo-starvation

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Textrous!: Extracting Semantic Textual Meaning from Gene Sets

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Loss of ALS-associated TDP-43 in zebrafish causes muscle degeneration, vascular dysfunction, and reduced motor neuron axon outgrowth

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Filamin C-related myopathies: pathology and mechanisms

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The molecular basis of the frontotemporal lobar degeneration–amyotrophic lateral sclerosis spectrum

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Filamins in Mechanosensing and Signaling

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Euglycemic Agent-mediated Hypothalamic Transcriptomic Manipulation in the N171–82Q Model of Huntington Disease Is Related to Their Physiological Efficacy

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

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TREM2 Variants in Alzheimer's Disease

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TDP-43: gumming up neurons through protein–protein and protein–RNA interactions

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Mutations in the N-terminal Actin-Binding Domain of Filamin C Cause a Distal Myopathy

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

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A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study

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Optimized filtering reduces the error rate in detecting genomic variants by short-read sequencing

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Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43

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Ataxin-2 polyQ expansions in FTLD-ALS spectrum disorders in Flanders-Belgian cohorts

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The filamins

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DNA sequencing errors in molecular diagnostics of filamin myopathy

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Chaperone-Assisted Selective Autophagy Is Essential for Muscle Maintenance

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The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

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Neurogranin, a link between calcium/calmodulin and protein kinase C signaling in synaptic plasticity

(2010) F. Javier Díez-Guerra   IUBMB LIFE

Increased caspase activation and decreased TDP-43 solubility in progranulin knockout cortical cultures

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A method and server for predicting damaging missense mutations

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Neurosteroid biosynthetic pathways changes in prefrontal cortex in Alzheimer's disease

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Minimal Peroxide Exposure of Neuronal Cells Induces Multifaceted Adaptive Responses

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Filamins in cell signaling, transcription and organ development

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Fast and accurate short read alignment with Burrows-Wheeler transform

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Amyotrophic lateral sclerosis, frontotemporal dementia and beyond: the TDP-43 diseases

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Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources

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Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His

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Filamins Regulate Cell Spreading and Initiation of Cell Migration

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Simultaneous mutation and copy number variation (CNV) detection by multiplex PCR-based GS-FLX sequencing

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iTRAQ Analysis of Complex Proteome Alterations in 3xTgAD Alzheimer's Mice: Understanding the Interface between Physiology and Disease

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Selective age-related changes in the PKC-sensitive, calmodulin-binding protein, neurogranin, in the mouse brain

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