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Human papillomavirus (HPV) upregulates the cellular deubiquitinase UCHL1 to suppress the keratinocyte's innate immune response

PLoS pathogens, 2013-05, Vol.9 (5), p.e1003384-e1003384

2013

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Human papillomavirus deregulates the response of a cellular network comprising of chemotactic and proinflammatory genes

PloS one, 2011-03, Vol.6 (3), p.e17848

2011

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The Pathogenesis and Therapy of Muscular Dystrophies

Annual review of genomics and human genetics, 2015-08, Vol.16 (1), p.281-308

2015

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Targeting several CAG expansion diseases by a single antisense oligonucleotide

PloS one, 2011-09, Vol.6 (9), p.e24308

2011

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In vivo comparison of 2′-O-methyl phosphorothioate and morpholino antisense oligonucleotides for Duchenne muscular dystrophy exon skipping

The journal of gene medicine, 2009-03, Vol.11 (3), p.257-266

2009

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Systemic Administration of PRO051 in Duchenne's Muscular Dystrophy

The New England journal of medicine, 2011-04, Vol.364 (16), p.1513-1522

2011

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Deep sequencing-based expression analysis shows major advances in robustness, resolution and inter-lab portability over five microarray platforms

Nucleic acids research, 2008-12, Vol.36 (21), p.e141-e141

2008

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Entries in the Leiden Duchenne muscular dystrophy mutation database: An overview of mutation types and paradoxical cases that confirm the reading-frame rule

Muscle & nerve, 2006-08, Vol.34 (2), p.135-144

2006

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Phenotypically Concordant and Discordant Monozygotic Twins Display Different DNA Copy-Number-Variation Profiles

American journal of human genetics, 2008-03, Vol.82 (3), p.763-771

2008

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Ataxin-3 protein modification as a treatment strategy for spinocerebellar ataxia type 3: Removal of the CAG containing exon

Neurobiology of disease, 2013-10, Vol.58, p.49-56

2013

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Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in Both the CBP and EP300 Genes Cause Disease

American journal of human genetics, 2005-04, Vol.76 (4), p.572-580

2005

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An immune response network associated with blood lipid levels

PLoS genetics, 2010-09, Vol.6 (9), p.e1001113-e1001113

2010

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Preclinical PK and PD Studies on 2′-O-Methyl-phosphorothioate RNA Antisense Oligonucleotides in the mdx Mouse Model

Molecular therapy, 2010-06, Vol.18 (6), p.1210-1217

2010

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Comprehensive Detection of Genomic Duplications and Deletions in the DMD Gene, by Use of Multiplex Amplifiable Probe Hybridization

American journal of human genetics, 2002-08, Vol.71 (2), p.365-374

2002

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Assessment of the feasibility of exon 45-55 multiexon skipping for Duchenne muscular dystrophy

BMC medical genetics, 2008-12, Vol.9 (1), p.105-105, Article 105

2008

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Serum protein profiling in mice: Identification of Factor XIIIa as a potential biomarker for muscular dystrophy

Proteomics (Weinheim), 2008-04, Vol.8 (8), p.1552-1563

2008

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Comparison of skeletal muscle pathology and motor function of dystrophin and utrophin deficient mouse strains

Neuromuscular disorders : NMD, 2012-05, Vol.22 (5), p.406-417

2012

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Antisense-mediated exon skipping: a versatile tool with therapeutic and research applications

RNA (Cambridge), 2007-10, Vol.13 (10), p.1609-1624

2007

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Familial Resemblance for Serum Metabolite Concentrations

Twin research and human genetics, 2013-10, Vol.16 (5), p.948-961

2013

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Antisense-Induced Multiexon Skipping for Duchenne Muscular Dystrophy Makes More Sense

American journal of human genetics, 2004-01, Vol.74 (1), p.83-92

2004

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Enhanced Exon-skipping Induced by U7 snRNA Carrying a Splicing Silencer Sequence: Promising Tool for DMD Therapy

Molecular therapy, 2009-07, Vol.17 (7), p.1234-1240

2009

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Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome

Nature genetics, 2012-04, Vol.44 (4), p.379-380

2012

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Integrated analysis of DNA copy number and gene expression microarray data using gene sets

BMC bioinformatics, 2009-06, Vol.10 (1), p.203-203, Article 203

2009

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Local Dystrophin Restoration with Antisense Oligonucleotide PRO051

The New England journal of medicine, 2007-12, Vol.357 (26), p.2677-2686

2007

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Low dystrophin levels increase survival and improve muscle pathology and function in dystrophin/utrophin double‐knockout mice

The FASEB journal, 2013-06, Vol.27 (6), p.2484-2495

2013

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Human papillomavirus (HPV) upregulates the cellular deubiquitinase UCHL1 to suppress the keratinocyte's innate immune response

Human papillomavirus deregulates the response of a cellular network comprising of chemotactic and proinflammatory genes

The Pathogenesis and Therapy of Muscular Dystrophies

Targeting several CAG expansion diseases by a single antisense oligonucleotide

In vivo comparison of 2′-O-methyl phosphorothioate and morpholino antisense oligonucleotides for Duchenne muscular dystrophy exon skipping

Systemic Administration of PRO051 in Duchenne's Muscular Dystrophy

Deep sequencing-based expression analysis shows major advances in robustness, resolution and inter-lab portability over five microarray platforms

Entries in the Leiden Duchenne muscular dystrophy mutation database: An overview of mutation types and paradoxical cases that confirm the reading-frame rule

Phenotypically Concordant and Discordant Monozygotic Twins Display Different DNA Copy-Number-Variation Profiles

Ataxin-3 protein modification as a treatment strategy for spinocerebellar ataxia type 3: Removal of the CAG containing exon

Genetic Heterogeneity in Rubinstein-Taybi Syndrome: Mutations in Both the CBP and EP300 Genes Cause Disease

An immune response network associated with blood lipid levels

Preclinical PK and PD Studies on 2′-O-Methyl-phosphorothioate RNA Antisense Oligonucleotides in the mdx Mouse Model

Comprehensive Detection of Genomic Duplications and Deletions in the DMD Gene, by Use of Multiplex Amplifiable Probe Hybridization

Assessment of the feasibility of exon 45-55 multiexon skipping for Duchenne muscular dystrophy

Serum protein profiling in mice: Identification of Factor XIIIa as a potential biomarker for muscular dystrophy

Comparison of skeletal muscle pathology and motor function of dystrophin and utrophin deficient mouse strains

Antisense-mediated exon skipping: a versatile tool with therapeutic and research applications

Familial Resemblance for Serum Metabolite Concentrations

Antisense-Induced Multiexon Skipping for Duchenne Muscular Dystrophy Makes More Sense

Enhanced Exon-skipping Induced by U7 snRNA Carrying a Splicing Silencer Sequence: Promising Tool for DMD Therapy

Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome

Integrated analysis of DNA copy number and gene expression microarray data using gene sets

Local Dystrophin Restoration with Antisense Oligonucleotide PRO051

Low dystrophin levels increase survival and improve muscle pathology and function in dystrophin/utrophin double‐knockout mice

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