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Straight-forward synthesis of ringed particles

Chemical science (Cambridge), 2014-01, Vol.5 (5), p.1961

2014

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Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNC

Revue neurologique, 2016-10, Vol.172 (10), p.594-606

2016

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On noxious desmin: functional effects of a novel heterozygous desmin insertion mutation on the extrasarcomeric desmin cytoskeleton and mitochondria

Human molecular genetics, 2003-03, Vol.12 (6), p.657-669

2003

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Sealing hyaluronic acid microgels with oppositely-charged polypeptides: A simple strategy for packaging hydrophilic drugs with on-demand release

Journal of colloid and interface science, 2019-02, Vol.535, p.16-27

2019

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P2.18 A novel missense FLNC mutation causes arrhythmia and late onset myofibrillar myopathy with particular histopathology features

Neuromuscular disorders : NMD, 2010-10, Vol.20 (9), p.623-624

2010

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D.P.3.02 Desminopathies: What can we learn from a long term follow-up?

Neuromuscular disorders : NMD, 2008-10, Vol.18 (9), p.765-765

2008

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Forebrain-Specific Neuronal Inhibition of Nuclear Factor-κB Activity Leads to Loss of Neuroprotection

The Journal of neuroscience, 2003-10, Vol.23 (28), p.9403-9408

2003

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Pathogenic effects of a novel heterozygous R350P desmin mutation on the assembly of desmin intermediate filaments in vivo and in vitro

Human molecular genetics, 2005-05, Vol.14 (10), p.1251-1260

2005

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Variable pathogenic potentials of mutations located in the desmin alpha-helical domain

Human mutation, 2006-09, Vol.27 (9), p.906-913

2006

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IκBα/IκBε Deficiency Reveals That a Critical NF-κB Dosage Is Required for Lymphocyte Survival

Proceedings of the National Academy of Sciences - PNAS, 2003-12, Vol.100 (26), p.15800-15805

2003

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Small deletions disturb desmin architecture leading to breakdown of muscle cells and development of skeletal or cardioskeletal myopathy

Human genetics, 2004-02, Vol.114 (3), p.306-313

2004

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Hsp27-2D-gel electrophoresis is a diagnostic tool to differentiate primary desminopathies from myofibrillar myopathies

FEBS letters, 2005-07, Vol.579 (17), p.3777-3782

2005

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Myofibrillar (desmin-related) myopathy: clinico-pathological spectrum in 3 cases and review of the literature

Clinical neuropathology, 2002-09, Vol.21 (5), p.220

2002

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Structural and functional analysis of a new desmin variant causing desmin-related myopathy

Human mutation, 2001-11, Vol.18 (5), p.388-396

2001

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Respiratory insufficiency in desminopathy patients caused by introduction of proline residues in desmin c-terminal α-helical segment

Muscle & nerve, 2003-06, Vol.27 (6), p.669-675

2003

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Progressive skeletal myopathy, a phenotypic variant of desmin myopathy associated with desmin mutations

Neuromuscular disorders : NMD, 2003-03, Vol.13 (3), p.252-258

2003

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A novel desmin R355P mutation causes cardiac and skeletal myopathy

Neuromuscular disorders : NMD, 2005-08, Vol.15 (8), p.525-531

2005

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On noxious desmin: functional effects of a novel heterozygous desmin insertion mutation on the extrasarcomeric desmin cytoskeleton and mitochondria

Human molecular genetics, 2007-12, Vol.16 (23), p.2989-2990

2007

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Skeletal Muscles Express the Xenobiotic-metabolizing Enzyme Arylamine N-acetyltransferase

The journal of histochemistry and cytochemistry, 2003-06, Vol.51 (6), p.789-796

2003

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Expression of the intermediate filament protein synemin in myofibrillar myopathies and other muscle diseases

Acta neuropathologica, 2003-07, Vol.106 (1), p.1-7

2003

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IκBε-Deficient Mice: Reduction of One T Cell Precursor Subspecies and Enhanced Ig Isotype Switching and Cytokine Synthesis

The Journal of immunology (1950), 1999-12, Vol.163 (11), p.5994-6005

1999

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In vivo identification of lymphocyte subsets exhibiting transcriptionally active NF-κB/Rel complexes

International immunology, 2000-05, Vol.12 (5), p.613-621

2000

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In vivo identification of lymphocyte subsets exhibiting transcriptionally active NF-kappaB/Rel complexes

International immunology, 2000-05, Vol.12 (5), p.613-621

2000

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IkappaBepsilon-deficient mice: reduction of one T cell precursor subspecies and enhanced Ig isotype switching and cytokine synthesis

The Journal of immunology (1950), 1999-12, Vol.163 (11), p.5994-6005

1999

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Hidden diversity of soil giant viruses

Nature communications, 2018-11, Vol.9 (1), p.4881-9, Article 4881

2018

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Straight-forward synthesis of ringed particles

Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNC

On noxious desmin: functional effects of a novel heterozygous desmin insertion mutation on the extrasarcomeric desmin cytoskeleton and mitochondria

Sealing hyaluronic acid microgels with oppositely-charged polypeptides: A simple strategy for packaging hydrophilic drugs with on-demand release

P2.18 A novel missense FLNC mutation causes arrhythmia and late onset myofibrillar myopathy with particular histopathology features

D.P.3.02 Desminopathies: What can we learn from a long term follow-up?

Forebrain-Specific Neuronal Inhibition of Nuclear Factor-κB Activity Leads to Loss of Neuroprotection

Pathogenic effects of a novel heterozygous R350P desmin mutation on the assembly of desmin intermediate filaments in vivo and in vitro

Variable pathogenic potentials of mutations located in the desmin alpha-helical domain

IκBα/IκBε Deficiency Reveals That a Critical NF-κB Dosage Is Required for Lymphocyte Survival

Small deletions disturb desmin architecture leading to breakdown of muscle cells and development of skeletal or cardioskeletal myopathy

Hsp27-2D-gel electrophoresis is a diagnostic tool to differentiate primary desminopathies from myofibrillar myopathies

Myofibrillar (desmin-related) myopathy: clinico-pathological spectrum in 3 cases and review of the literature

Structural and functional analysis of a new desmin variant causing desmin-related myopathy

Respiratory insufficiency in desminopathy patients caused by introduction of proline residues in desmin c-terminal α-helical segment

Progressive skeletal myopathy, a phenotypic variant of desmin myopathy associated with desmin mutations

A novel desmin R355P mutation causes cardiac and skeletal myopathy

On noxious desmin: functional effects of a novel heterozygous desmin insertion mutation on the extrasarcomeric desmin cytoskeleton and mitochondria

Skeletal Muscles Express the Xenobiotic-metabolizing Enzyme Arylamine N-acetyltransferase

Expression of the intermediate filament protein synemin in myofibrillar myopathies and other muscle diseases

IκBε-Deficient Mice: Reduction of One T Cell Precursor Subspecies and Enhanced Ig Isotype Switching and Cytokine Synthesis

In vivo identification of lymphocyte subsets exhibiting transcriptionally active NF-κB/Rel complexes

In vivo identification of lymphocyte subsets exhibiting transcriptionally active NF-kappaB/Rel complexes

IkappaBepsilon-deficient mice: reduction of one T cell precursor subspecies and enhanced Ig isotype switching and cytokine synthesis

Hidden diversity of soil giant viruses

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