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Notch2 signaling promotes biliary epithelial cell fate specification and tubulogenesis during bile duct development in mice

Hepatology (Baltimore, Md.), 2009-09, Vol.50 (3), p.871-879

2009

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CaMKIIβ deregulation contributes to neuromuscular junction destabilization in Myotonic Dystrophy type I

Skeletal muscle, 2024-05, Vol.14 (1), p.11-11, Article 11

2024

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Molecular targets to treat muscular dystrophies

Swiss medical weekly, 2014-02, Vol.144, p.w13916

2014

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Calsyntenin-1 docks vesicular cargo to kinesin-1

Molecular biology of the cell, 2006-08, Vol.17 (8), p.3651-3663

2006

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An essential role of MAG in mediating axon–myelin attachment in Charcot–Marie–Tooth 1A disease

Neurobiology of disease, 2013-01, Vol.49, p.221-231

2013

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Impaired explorative behavior and neophobia in genetically modified mice lacking or overexpressing the extracellular serine protease inhibitor neuroserpin

Molecular and cellular neuroscience, 2003-07, Vol.23 (3), p.473-494

2003

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DNA aptamers against the DUX4 protein reveal novel therapeutic implications for FSHD

The FASEB journal, 2020-03, Vol.34 (3), p.4573-4590

2020

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Withdrawal: Proteasomal inhibition restores biological function of mis-sense mutated dysferlin in patient-derived muscle cells

The Journal of biological chemistry, 2017-07, Vol.292 (30), p.12542-12542

2017

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Proteasomal inhibition restores biological function of mis-sense mutated dysferlin in patient-derived muscle cells

The Journal of biological chemistry, 2017-07, Vol.292 (30), p.12542-12542

2017

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CaMKII[beta] deregulation contributes to neuromuscular junction destabilization in Myotonic Dystrophy type I

Skeletal muscle, 2024-05, Vol.14 (1)

2024

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Proteasomal Inhibition Restores Biological Function of Mis-sense Mutated Dysferlin in Patient-derived Muscle Cells

The Journal of biological chemistry, 2012-03, Vol.287 (13), p.10344-10354

2012

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Identification of Plant-derived Alkaloids with Therapeutic Potential for Myotonic Dystrophy Type I

The Journal of biological chemistry, 2016-08, Vol.291 (33), p.17165-17177

2016

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Differential gene expression in nerve biopsies of inflammatory neuropathies

Journal of the peripheral nervous system, 2011-06, Vol.16 (s1), p.30-33

2011

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Genetic characterization and improved genotyping of the dysferlin-deficient mouse strain Dysf (tm1Kcam)

Skeletal muscle, 2015-10, Vol.5, p.32-32

2015

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Genetic characterization and improved genotyping of the dysferlin-deficient mouse strain Dysf tm1Kcam

Skeletal muscle, 2015-10, Vol.5 (1), Article 32

2015

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Accumulation of Mutant Neuroserpin Precedes Development of Clinical Symptoms in Familial Encephalopathy with Neuroserpin Inclusion Bodies

The American journal of pathology, 2007-04, Vol.170 (4), p.1305-1313

2007

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Gene expression profiling in nerve biopsy of vasculitic neuropathy

Journal of neuroimmunology, 2010-08, Vol.225 (1), p.184-189

2010

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Genetic characterization and improved genotyping of the dysferlin-deficient mouse strain Dysftm1Kcam

Skeletal muscle, 2015-10, Vol.5

2015

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Novel valosin containing protein mutation in a Swiss family with hereditary inclusion body myopathy and dementia

Neuromuscular disorders : NMD, 2013-02, Vol.23 (2), p.149-154

2013

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Calsyntenin-1, a Proteolytically Processed Postsynaptic Membrane Protein with a Cytoplasmic Calcium-Binding Domain

Molecular and cellular neuroscience, 2001-01, Vol.17 (1), p.151-166

2001

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HuD binds to three AU-rich sequences in the 3'-UTR of neuroserpin mRNA and promotes the accumulation of neuroserpin mRNA and protein

Nucleic acids research, 2002-05, Vol.30 (10), p.2202-2211

2002

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Familial dementia caused by polymerization of mutant neuroserpin

Nature (London), 1999-09, Vol.401 (6751), p.376-379

1999

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A Chronic Relapsing Animal Model for Multiple Sclerosis

2008

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Notch2 signaling promotes biliary epithelial cell fate specification and tubulogenesis during bile duct development in mice

CaMKIIβ deregulation contributes to neuromuscular junction destabilization in Myotonic Dystrophy type I

Molecular targets to treat muscular dystrophies

Calsyntenin-1 docks vesicular cargo to kinesin-1

An essential role of MAG in mediating axon–myelin attachment in Charcot–Marie–Tooth 1A disease

Impaired explorative behavior and neophobia in genetically modified mice lacking or overexpressing the extracellular serine protease inhibitor neuroserpin

DNA aptamers against the DUX4 protein reveal novel therapeutic implications for FSHD

Withdrawal: Proteasomal inhibition restores biological function of mis-sense mutated dysferlin in patient-derived muscle cells

Proteasomal inhibition restores biological function of mis-sense mutated dysferlin in patient-derived muscle cells

CaMKII[beta] deregulation contributes to neuromuscular junction destabilization in Myotonic Dystrophy type I

Proteasomal Inhibition Restores Biological Function of Mis-sense Mutated Dysferlin in Patient-derived Muscle Cells

Identification of Plant-derived Alkaloids with Therapeutic Potential for Myotonic Dystrophy Type I

Differential gene expression in nerve biopsies of inflammatory neuropathies

Genetic characterization and improved genotyping of the dysferlin-deficient mouse strain Dysf (tm1Kcam)

Genetic characterization and improved genotyping of the dysferlin-deficient mouse strain Dysf tm1Kcam

Accumulation of Mutant Neuroserpin Precedes Development of Clinical Symptoms in Familial Encephalopathy with Neuroserpin Inclusion Bodies

Gene expression profiling in nerve biopsy of vasculitic neuropathy

Genetic characterization and improved genotyping of the dysferlin-deficient mouse strain Dysftm1Kcam

Novel valosin containing protein mutation in a Swiss family with hereditary inclusion body myopathy and dementia

Calsyntenin-1, a Proteolytically Processed Postsynaptic Membrane Protein with a Cytoplasmic Calcium-Binding Domain

HuD binds to three AU-rich sequences in the 3'-UTR of neuroserpin mRNA and promotes the accumulation of neuroserpin mRNA and protein

Familial dementia caused by polymerization of mutant neuroserpin

A Chronic Relapsing Animal Model for Multiple Sclerosis

An Analysis of Pharmaceutical Experience with Decades of Rat Carcinogenicity Testing: Support for a Proposal to Modify Current Regulatory Guidelines

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