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Operon structure and cotranslational subunit association direct protein assembly in bacteria

Science (American Association for the Advancement of Science), 2015-11, Vol.350 (6261), p.678-680

2015

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Manipulation of small Rho GTPases is a pathogen-induced process detected by NOD1

Nature (London), 2013-04, Vol.496 (7444), p.233-237

2013

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Corporate spin-offs’ success factors: management lessons from a comparative empirical analysis with research-based spin-offs

Review of managerial science, 2021-08, Vol.15 (6), p.1767-1796

2021

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The RNA-Binding Protein ATXN2 is Expressed during Megakaryopoiesis and May Control Timing of Gene Expression

International journal of molecular sciences, 2020-01, Vol.21 (3), p.967

2020

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Generation of four gene-edited human induced pluripotent stem cell lines with mutations in the ATM gene to model Ataxia-Telangiectasia

Stem cell research, 2023-12, Vol.73, p.103247-103247, Article 103247

2023

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Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesia

Neurology, 2007-05, Vol.68 (21), p.1782

2007

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The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathway

Human molecular genetics, 2004-12, Vol.13 (24), p.3161-3170

2004

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Spinocerebellar ataxia type 2

Handbook of Clinical Neurology, 2012, Vol.103, p.423-436

Auburger, Georg W.J.

2012

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The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathway

Human molecular genetics, 2004, Vol.13 (24), p.3161-3170

2004

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Therapeutic reduction of ataxin-2 extends lifespan and reduces pathology in TDP-43 mice

Nature (London), 2017-04, Vol.544 (7650), p.367-371

2017

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Mutations in CIZ1 cause adult onset primary cervical dystonia

Annals of neurology, 2012-04, Vol.71 (4), p.458-469

2012

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Ubiquitylome profiling of Parkin-null brain reveals dysregulation of calcium homeostasis factors ATP1A2, Hippocalcin and GNA11, reflected by altered firing of noradrenergic neurons

Neurobiology of disease, 2019-07, Vol.127, p.114-130

2019

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Generation of an Atxn2-CAG100 knock-in mouse reveals N-acetylaspartate production deficit due to early Nat8l dysregulation

Neurobiology of disease, 2019-12, Vol.132, p.104559-104559, Article 104559

2019

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Welcoming articles on genotype-dependent clinical features and diagnostics

Neurogenetics, 2021-05, Vol.22 (2), p.103-104

2021

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Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1

Science (American Association for the Advancement of Science), 2004-05, Vol.304 (5674), p.1158-1160

2004

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MPTP susceptibility in the mouse: behavioral, neurochemical, and histological analysis of gender and strain differences

Behavior genetics, 2000-05, Vol.30 (3), p.171-182

2000

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A53T-alpha-synuclein overexpression impairs dopamine signaling and striatal synaptic plasticity in old mice

PloS one, 2010-07, Vol.5 (7), p.e11464-e11464

2010

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Common variant near the endothelin receptor type A (EDNRA) gene is associated with intracranial aneurysm risk

Proceedings of the National Academy of Sciences - PNAS, 2011-12, Vol.108 (49), p.19707-19712

2011

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Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defect

Neurology, 2011-09, Vol.77 (10), p.959

2011

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Clinical and genetic differences between bipolar disorder type 1 and 2 in multiplex families

Translational psychiatry, 2021-01, Vol.11 (1), p.31-10, Article 31

2021

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A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants

Journal of medical genetics, 2012-11, Vol.49 (11), p.721-6

2012

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An approach to investigate the costs of herbicide-resistant Alopecurus myosuroides

Weed research, 2016-12, Vol.56 (6), p.407-414

2016

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Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families

Translational psychiatry, 2020-02, Vol.10 (1), p.57-57, Article 57

2020

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Factors associated with ATXN2 CAG/CAA repeat intergenerational instability in Spinocerebellar ataxia type 2

Clinical genetics, 2018-10, Vol.94 (3-4), p.346-350

2018

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Operon structure and cotranslational subunit association direct protein assembly in bacteria

Manipulation of small Rho GTPases is a pathogen-induced process detected by NOD1

Exome sequencing in large, multiplex bipolar disorder families from Cuba

Corporate spin-offs’ success factors: management lessons from a comparative empirical analysis with research-based spin-offs

The RNA-Binding Protein ATXN2 is Expressed during Megakaryopoiesis and May Control Timing of Gene Expression

Generation of four gene-edited human induced pluripotent stem cell lines with mutations in the ATM gene to model Ataxia-Telangiectasia

Genotype-phenotype correlation of paroxysmal nonkinesigenic dyskinesia

The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathway

Spinocerebellar ataxia type 2

The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathway

Therapeutic reduction of ataxin-2 extends lifespan and reduces pathology in TDP-43 mice

Mutations in CIZ1 cause adult onset primary cervical dystonia

Ubiquitylome profiling of Parkin-null brain reveals dysregulation of calcium homeostasis factors ATP1A2, Hippocalcin and GNA11, reflected by altered firing of noradrenergic neurons

Generation of an Atxn2-CAG100 knock-in mouse reveals N-acetylaspartate production deficit due to early Nat8l dysregulation

Welcoming articles on genotype-dependent clinical features and diagnostics

Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1

MPTP susceptibility in the mouse: behavioral, neurochemical, and histological analysis of gender and strain differences

A53T-alpha-synuclein overexpression impairs dopamine signaling and striatal synaptic plasticity in old mice

Common variant near the endothelin receptor type A (EDNRA) gene is associated with intracranial aneurysm risk

Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defect

Clinical and genetic differences between bipolar disorder type 1 and 2 in multiplex families

A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants

An approach to investigate the costs of herbicide-resistant Alopecurus myosuroides

Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families

Factors associated with ATXN2 CAG/CAA repeat intergenerational instability in Spinocerebellar ataxia type 2

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