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Evaluating the prevalence of polyglutamine repeat expansions in amyotrophic lateral sclerosis

Neurology, 2011-06, Vol.76 (24), p.2062

2011

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Ataxin-2 intermediate-length polyglutamine expansions in European ALS patients

Human molecular genetics, 2011-05, Vol.20 (9), p.1697-1700

2011

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ALS-associated ataxin 2 polyQ expansions enhance stress-induced caspase 3 activation and increase TDP-43 pathological modifications

The Journal of neuroscience, 2012-07, Vol.32 (27), p.9133-9142

2012

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Defects in trafficking bridge Parkinson's disease pathology and genetics

Nature (London), 2016-11, Vol.539 (7628), p.207-216

2016

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Profilin 1 associates with stress granules and ALS-linked mutations alter stress granule dynamics

The Journal of neuroscience, 2014-06, Vol.34 (24), p.8083-8097

2014

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Kinetic analysis of npBAF to nBAF switching reveals exchange of SS18 with CREST and integration with neural developmental pathways

The Journal of neuroscience, 2013-06, Vol.33 (25), p.10348-10361

2013

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Neural crest migration and mouse models of congenital heart disease

Cold Spring Harbor Symposia on Quantitative Biology, 2002, Vol.67, p.57

2002

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Apakaochtodenes A and B: Two Tetrahalogenated Monoterpenes from the Red Marine Alga Portieria hornemannii

Journal of natural products (Washington, D.C.), 1999-10, Vol.62 (10), p.1376-1378

1999

Volltextzugriff (PDF)

Challenges of profiling motor neuron transcriptomes from human spinal cord

Neuron (Cambridge, Mass.), 2023-12, Vol.111 (23), p.3739-3741

2023

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Semaphorin-Plexin Signaling Guides Patterning of the Developing Vasculature

Developmental cell, 2004-07, Vol.7 (1), p.117-123

2004

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Insertion of Cre into the Pax3 locus creates a new allele of Splotch and identifies unexpected Pax3 derivatives

Developmental biology, 2005-04, Vol.280 (2), p.396-406

2005

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Cardiac hypertrophy and histone deacetylase–dependent transcriptional repression mediated by the atypical homeodomain protein Hop

The Journal of clinical investigation, 2003-09, Vol.112 (6), p.863-871

2003

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The novel Parkinson's disease linked mutation G51D attenuates in vitro aggregation and membrane binding of -synuclein, and enhances its secretion and nuclear localization in cells

Human molecular genetics, 2014-09, Vol.23 (17), p.4491-4509

2014

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Hop Is an Unusual Homeobox Gene that Modulates Cardiac Development

Cell, 2002-09, Vol.110 (6), p.713-723

2002

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Nf1 has an essential role in endothelial cells

Nature genetics, 2003-01, Vol.33 (1), p.75-79

2003

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Critical calpain-dependent ultrastructural alterations underlie the transformation of an axonal segment into a growth cone after axotomy of cultured Aplysia neurons

Journal of comparative neurology (1911), 2003-03, Vol.457 (3), p.293-312

2003

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Molecular markers of cardiac endocardial cushion development

Developmental dynamics, 2003-12, Vol.228 (4), p.643-650

2003

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Tie2-cre-induced inactivation of a conditional mutant Nf1 allele in mouse results in a myeloproliferative disorder that models juvenile myelomonocytic leukemia

Pediatric research, 2004-04, Vol.55 (4), p.581-584

2004

Volltextzugriff (PDF)

Distinct repertoires of microRNAs present in mouse astrocytes compared to astrocyte-secreted exosomes

PloS one, 2017-02, Vol.12 (2), p.e0171418-e0171418

2017

Volltextzugriff (PDF)

Neurodegenerative disease: models, mechanisms, and a new hope

Disease models & mechanisms, 2017-05, Vol.10 (5), p.499-502

2017

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Molecular determinants and genetic modifiers of aggregation and toxicity for the ALS disease protein FUS/TLS

PLoS biology, 2011-04, Vol.9 (4), p.e1000614

2011

Volltextzugriff (PDF)

Stress granules as crucibles of ALS pathogenesis

The Journal of cell biology, 2013-04, Vol.201 (3), p.361-372

2013

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There has been an awakening: Emerging mechanisms of C9orf72 mutations in FTD/ALS

Brain research, 2016-09, Vol.1647, p.19-29

2016

Volltextzugriff (PDF)

Neurotoxic reactive astrocytes induce cell death via saturated lipids

Nature (London), 2021-11, Vol.599 (7883), p.102-107

2021

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The tip of the iceberg: RNA-binding proteins with prion-like domains in neurodegenerative disease

Brain research, 2012-06, Vol.1462, p.61-80

2012

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Evaluating the prevalence of polyglutamine repeat expansions in amyotrophic lateral sclerosis

Ataxin-2 intermediate-length polyglutamine expansions in European ALS patients

ALS-associated ataxin 2 polyQ expansions enhance stress-induced caspase 3 activation and increase TDP-43 pathological modifications

Defects in trafficking bridge Parkinson's disease pathology and genetics

Profilin 1 associates with stress granules and ALS-linked mutations alter stress granule dynamics

Kinetic analysis of npBAF to nBAF switching reveals exchange of SS18 with CREST and integration with neural developmental pathways

Neural crest migration and mouse models of congenital heart disease

Apakaochtodenes A and B: Two Tetrahalogenated Monoterpenes from the Red Marine Alga Portieria hornemannii

Challenges of profiling motor neuron transcriptomes from human spinal cord

Semaphorin-Plexin Signaling Guides Patterning of the Developing Vasculature

Insertion of Cre into the Pax3 locus creates a new allele of Splotch and identifies unexpected Pax3 derivatives

Cardiac hypertrophy and histone deacetylase–dependent transcriptional repression mediated by the atypical homeodomain protein Hop

The novel Parkinson's disease linked mutation G51D attenuates in vitro aggregation and membrane binding of -synuclein, and enhances its secretion and nuclear localization in cells

Hop Is an Unusual Homeobox Gene that Modulates Cardiac Development

Nf1 has an essential role in endothelial cells

Critical calpain-dependent ultrastructural alterations underlie the transformation of an axonal segment into a growth cone after axotomy of cultured Aplysia neurons

Molecular markers of cardiac endocardial cushion development

Tie2-cre-induced inactivation of a conditional mutant Nf1 allele in mouse results in a myeloproliferative disorder that models juvenile myelomonocytic leukemia

Distinct repertoires of microRNAs present in mouse astrocytes compared to astrocyte-secreted exosomes

Neurodegenerative disease: models, mechanisms, and a new hope

Molecular determinants and genetic modifiers of aggregation and toxicity for the ALS disease protein FUS/TLS

Stress granules as crucibles of ALS pathogenesis

There has been an awakening: Emerging mechanisms of C9orf72 mutations in FTD/ALS

Neurotoxic reactive astrocytes induce cell death via saturated lipids

The tip of the iceberg: RNA-binding proteins with prion-like domains in neurodegenerative disease

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