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TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration

Proceedings of the National Academy of Sciences - PNAS, 2010-02, Vol.107 (8), p.3858-3863

2010

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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

Lancet neurology, 2012, Vol.11 (1), p.54-65

2012

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Common pathobiochemical hallmarks of progranulin-associated frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis

Acta neuropathologica, 2014-06, Vol.127 (6), p.845-860

2014

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Passive immunotherapy with a novel antibody against 3pE-modified Aβ demonstrates potential for enhanced efficacy and favorable safety in combination with BACE inhibitor treatment in plaque-depositing mice

Neurobiology of disease, 2021-07, Vol.154, p.105365-105365, Article 105365

2021

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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

Molecular neurobiology, 2013-08, Vol.48 (1), p.22-35

2013

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

Human molecular genetics, 2013-10, Vol.22 (R1), p.R77-R87

2013

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hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations

Acta neuropathologica, 2013-03, Vol.125 (3), p.413-423

2013

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Cellular ageing, increased mortality and FTLD-TDP-associated neuropathology in progranulin knockout mice

The Journal of pathology, 2012-09, Vol.228 (1), p.67-76

2012

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GIT2-A keystone in ageing and age-related disease

Ageing research reviews, 2018-05, Vol.43, p.46-63

2018

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Informatic deconvolution of biased GPCR signaling mechanisms from in vivo pharmacological experimentation

Methods (San Diego, Calif.), 2016-01, Vol.92, p.51-63

2016

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Altered learning, memory, and social behavior in type 1 taste receptor subunit 3 knock-out mice are associated with neuronal dysfunction

The Journal of biological chemistry, 2017-07, Vol.292 (27), p.11508-11530

2017

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The RXFP3‐GIT2 signaling system represents a potential multidimensional therapeutic target in age‐related disorders

The FASEB journal, 2018-04, Vol.32 (S1), p.533.111-533.111

2018

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The role of mutant TAR DNA-binding protein 43 in amyotrophic lateral sclerosis and frontotemporal lobar degeneration

Biochemical Society transactions, 2011-08, Vol.39 (4), p.954-959

2011

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Genomic deletion of GIT2 induces a premature age-related thymic dysfunction and systemic immune system disruption

Aging (Albany, NY.), 2017-03, Vol.9 (3), p.706-740

2017

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Systems-Level G Protein-Coupled Receptor Therapy Across a Neurodegenerative Continuum by the GLP-1 Receptor System

Frontiers in endocrinology (Lausanne), 2014-01, Vol.5, p.142-142

2014

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The synergistic GIT2-RXFP3 system in the brain and its importance in age-related disorders

Frontiers in aging neuroscience, 2016, Vol.8

2016

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GIT2 Acts as a Systems-Level Coordinator of Neurometabolic Activity and Pathophysiological Aging

Frontiers in endocrinology (Lausanne), 2016-01, Vol.6, p.191-191

2016

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Investigating the role of sweet taste receptors in age-related neurodegeneration

Frontiers in aging neuroscience, 2016, Vol.8

2016

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

Acta neuropathologica communications, 2015-11, Vol.3 (68), p.68-68, Article 68

2015

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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 identifi cation study

Lancet neurology, 2012-01, Vol.11 (1), p.54

2012

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S4‐04‐02: Overexpression of Wild‐type TDP‐43 Leads to Motor Neuron Degeneration and Spastic Quadriplegia in Germline Transgenic Mice

Alzheimer's & dementia, 2009-07, Vol.5 (4S_Part_5), p.e4-e4

2009

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Overexpression of Wild-type TDP-43 Leads to Motor Neuron Degeneration and Spastic Quadriplegia in Germline Transgenic Mice

Alzheimer's & dementia, 2009-07, Vol.5 (4), p.e4-e4

2009

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Concepts, Techniques, and Models of Computer Programming by Peter Van Roy and Seif Haridi, MIT Press, 2004, hard cover: ISBN 0-262-22069-5, xxvii + 900 pages, 55

Theory and Practice of Logic Programming, 2005-07, Vol.5 (4-5), p.595-600

Deville, Yves

2005

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Uranium Biominerals Precipitated by an Environmental Isolate of Serratia under Anaerobic Conditions

PloS one, 2015-07, Vol.10 (7), p.e0132392-e0132392

2015

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TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration

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

Common pathobiochemical hallmarks of progranulin-associated frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis

Passive immunotherapy with a novel antibody against 3pE-modified Aβ demonstrates potential for enhanced efficacy and favorable safety in combination with BACE inhibitor treatment in plaque-depositing mice

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

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

hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations

Cellular ageing, increased mortality and FTLD-TDP-associated neuropathology in progranulin knockout mice

GIT2-A keystone in ageing and age-related disease

Informatic deconvolution of biased GPCR signaling mechanisms from in vivo pharmacological experimentation

Altered learning, memory, and social behavior in type 1 taste receptor subunit 3 knock-out mice are associated with neuronal dysfunction

The RXFP3‐GIT2 signaling system represents a potential multidimensional therapeutic target in age‐related disorders

The role of mutant TAR DNA-binding protein 43 in amyotrophic lateral sclerosis and frontotemporal lobar degeneration

Genomic deletion of GIT2 induces a premature age-related thymic dysfunction and systemic immune system disruption

Systems-Level G Protein-Coupled Receptor Therapy Across a Neurodegenerative Continuum by the GLP-1 Receptor System

The synergistic GIT2-RXFP3 system in the brain and its importance in age-related disorders

GIT2 Acts as a Systems-Level Coordinator of Neurometabolic Activity and Pathophysiological Aging

Investigating the role of sweet taste receptors in age-related neurodegeneration

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

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

S4‐04‐02: Overexpression of Wild‐type TDP‐43 Leads to Motor Neuron Degeneration and Spastic Quadriplegia in Germline Transgenic Mice

Overexpression of Wild-type TDP-43 Leads to Motor Neuron Degeneration and Spastic Quadriplegia in Germline Transgenic Mice

Concepts, Techniques, and Models of Computer Programming by Peter Van Roy and Seif Haridi, MIT Press, 2004, hard cover: ISBN 0-262-22069-5, xxvii + 900 pages, 55

The SGLT2 inhibitor empagliflozin in patients hospitalized for acute heart failure: a multinational randomized trial

Uranium Biominerals Precipitated by an Environmental Isolate of Serratia under Anaerobic Conditions

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