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The new genetic landscape of Alzheimer’s disease: from amyloid cascade to genetically driven synaptic failure hypothesis?

Acta neuropathologica, 2019-08, Vol.138 (2), p.221-236

2019

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The spindle assembly checkpoint: Preventing chromosome mis-segregation during mitosis and meiosis

FEBS letters, 2006-05, Vol.580 (12), p.2888-2895

2006

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Maternal expression of the checkpoint protein BubR1 is required for synchrony of syncytial nuclear divisions and polar body arrest in Drosophila melanogaster

Development (Cambridge), 2005-10, Vol.132 (20), p.4509-4520

2005

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Establishment and mitotic characterization of new Drosophila acentriolar cell lines from DSas-4 mutant

Biology open, 2013-03, Vol.2 (3), p.314-323

2013

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BIN1 recovers tauopathy-induced long-term memory deficits in mice and interacts with Tau through Thr.sup.348 phosphorylation

Acta neuropathologica, 2019-10, Vol.138 (4), p.631

2019

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Developmental Expression of 4-Repeat-Tau Induces Neuronal Aneuploidy in Drosophila Tauopathy Models

Scientific reports, 2017-01, Vol.7 (1), p.40764-40764, Article 40764

2017

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Tau phosphorylation regulates the interaction between BIN1's SH3 domain and Tau's proline-rich domain

Acta neuropathologica communications, 2015-09, Vol.3 (1), p.58-58, Article 58

2015

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Pyk2 overexpression in postsynaptic neurons blocks amyloid β1–42-induced synaptotoxicity in microfluidic co-cultures

Brain communications, 2020-07, Vol.2 (2)

2020

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EXPERIMENTAL IN VIVO EVIDENCE FOR TAU-INDUCED ANEUPLOIDY GENERATED DURING BRAIN DEVELOPMENT IN TAUOPATHIES

Alzheimer's & dementia, 2017-07, Vol.13 (7), p.P1292-P1293

2017

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Pyk2 overexpression in postsynaptic neurons blocks amyloid β 1-42 -induced synaptotoxicity in microfluidic co-cultures

Brain communications, 2020, Vol.2 (2), p.fcaa139

2020

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Drosophila BubR1 Is Essential for Meiotic Sister-Chromatid Cohesion and Maintenance of Synaptonemal Complex

Current biology, 2007-09, Vol.17 (17), p.1489-1497

2007

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polo Is Identified as a Suppressor of bubR1 Nondisjunction in a Deficiency Screen of the Third Chromosome in Drosophila melanogaster

G3 : genes - genomes - genetics, 2011-07, Vol.1 (2), p.161-169

2011

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Strategies for outcrossing and genetic manipulation of Drosophila compound autosome stocks

G3 : genes - genomes - genetics, 2013-01, Vol.3 (1), p.1-4

2013

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MOLECULAR CHARACTERISATION OF BRIDGING INTEGRATOR 1 (BIN1) INTERACTION WITH TAU

Alzheimer's & dementia, 2014-07, Vol.10 (4), p.P794-P794

2014

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P4‐032: MOLECULAR CHARACTERISATION OF BRIDGING INTEGRATOR 1 (BIN1) INTERACTION WITH TAU

Alzheimer's & dementia, 2014-07, Vol.10 (4S_Part_22), p.P794-P794

2014

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Drosophila melanogaster Prat, a purine de novo synthesis gene, has a pleiotropic maternal-effect phenotype

Genetics (Austin), 2004-12, Vol.168 (4), p.2011-2023

2004

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Identification of Trans-dominant Modifiers of Prat Expression in Drosophila melanogaster

Genetics (Austin), 2003-08, Vol.164 (4), p.1419-1433

2003

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The PRAT purine synthesis gene duplication in Drosophila melanogaster and Drosophila virilis is associated with a retrotransposition event and diversification of expression patterns

Journal of molecular evolution, 2003-05, Vol.56 (5), p.630-642

2003

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Purine de novo synthesis in Drosophila melanogaster: A study of Prat gene function, expression and evolution

Malmanche, Nicolas

2003

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The new genetic landscape of Alzheimer’s disease: from amyloid cascade to genetically driven synaptic failure hypothesis?

Alzheimer's genetic risk factor FERMT2 (Kindlin-2) controls axonal growth and synaptic plasticity in an APP-dependent manner

Correction to: Alzheimer's genetic risk factor FERMT2 (Kindlin-2) controls axonal growth and synaptic plasticity in an APP-dependent manner

The spindle assembly checkpoint: Preventing chromosome mis-segregation during mitosis and meiosis

Maternal expression of the checkpoint protein BubR1 is required for synchrony of syncytial nuclear divisions and polar body arrest in Drosophila melanogaster

Establishment and mitotic characterization of new Drosophila acentriolar cell lines from DSas-4 mutant

BIN1 recovers tauopathy-induced long-term memory deficits in mice and interacts with Tau through Thr.sup.348 phosphorylation

Developmental Expression of 4-Repeat-Tau Induces Neuronal Aneuploidy in Drosophila Tauopathy Models

BIN1 recovers tauopathy-induced long-term memory deficits in mice and interacts with Tau through Thr348 phosphorylation

Tau phosphorylation regulates the interaction between BIN1's SH3 domain and Tau's proline-rich domain

Pyk2 overexpression in postsynaptic neurons blocks amyloid β1–42-induced synaptotoxicity in microfluidic co-cultures

EXPERIMENTAL IN VIVO EVIDENCE FOR TAU-INDUCED ANEUPLOIDY GENERATED DURING BRAIN DEVELOPMENT IN TAUOPATHIES

Pyk2 overexpression in postsynaptic neurons blocks amyloid β 1-42 -induced synaptotoxicity in microfluidic co-cultures

Drosophila BubR1 Is Essential for Meiotic Sister-Chromatid Cohesion and Maintenance of Synaptonemal Complex

polo Is Identified as a Suppressor of bubR1 Nondisjunction in a Deficiency Screen of the Third Chromosome in Drosophila melanogaster

BIN1 recovers tauopathy-induced long-term memory deficits in mice and interacts with Tau through Thr 348 phosphorylation

Strategies for outcrossing and genetic manipulation of Drosophila compound autosome stocks

MOLECULAR CHARACTERISATION OF BRIDGING INTEGRATOR 1 (BIN1) INTERACTION WITH TAU

P4‐032: MOLECULAR CHARACTERISATION OF BRIDGING INTEGRATOR 1 (BIN1) INTERACTION WITH TAU

Drosophila melanogaster Prat, a purine de novo synthesis gene, has a pleiotropic maternal-effect phenotype

Identification of Trans-dominant Modifiers of Prat Expression in Drosophila melanogaster

The PRAT purine synthesis gene duplication in Drosophila melanogaster and Drosophila virilis is associated with a retrotransposition event and diversification of expression patterns

Purine de novo synthesis in Drosophila melanogaster: A study of Prat gene function, expression and evolution

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