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In vivo comparison of 2′- O-methyl phosphorothioate and morpholino antisense oligonucleotides for Duchenne muscular dystrophy exon skipping.
- Published in:
- Journal of Gene Medicine, 2009, v. 11, n. 3, p. 257, doi. 10.1002/jgm.1288
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- Publication type:
- Article
Dual exon skipping in myostatin and dystrophin for Duchenne muscular dystrophy.
- Published in:
- BMC Medical Genomics, 2011, v. 4, n. 1, p. 36, doi. 10.1186/1755-8794-4-36
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- Publication type:
- Article
Dystrophin expression in the developing conduction system of the human heart.
- Published in:
- Microscopy Research & Technique, 1995, v. 30, n. 6, p. 458, doi. 10.1002/jemt.1070300603
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- Publication type:
- Article
Low dystrophin levels increase survival and improve muscle pathology and function in dystrophin/utrophin double-knockout mice.
- Published in:
- FASEB Journal, 2013, v. 27, n. 6, p. 2484, doi. 10.1096/fj.12-224170
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- Publication type:
- Article
Cost-effective HRMA pre-sequence typing of clone libraries; application to phage display selection.
- Published in:
- BMC Biotechnology, 2009, v. 9, p. 1, doi. 10.1186/1472-6750-9-50
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- Publication type:
- Article
New insights in gene-derived therapy: the example of Duchenne muscular dystrophy.
- Published in:
- Annals of the New York Academy of Sciences, 2010, v. 1214, n. 1, p. 199, doi. 10.1111/j.1749-6632.2010.05836.x
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- Publication type:
- Article
Development of Antisense-Mediated Exon Skipping as a Treatment for Duchenne Muscular Dystrophy.
- Published in:
- Annals of the New York Academy of Sciences, 2009, v. 1175, n. 1, p. 71, doi. 10.1111/j.1749-6632.2009.04973.x
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- Publication type:
- Article
ADVANCES IN DUCHENNE MUSCULAR DYSTROPHY GENE THERAPY.
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- Nature Reviews Genetics, 2003, v. 4, n. 10, p. 774, doi. 10.1038/nrg1180
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- Publication type:
- Article
The Complete Genome Sequence of the Murine Pathobiont Helicobacter typhlonius.
- Published in:
- Frontiers in Microbiology, 2016, p. 1, doi. 10.3389/fmicb.2015.01549
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- Publication type:
- Article
A duplication at chromosome 11q12.2–11q12.3 is associated with spinocerebellar ataxia type 20.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 24, p. 3847, doi. 10.1093/hmg/ddn283
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- Publication type:
- Article
Prevention of oculopharyngeal muscular dystrophy-associated aggregation of nuclear poly(A)-binding protein with a single-domain intracellular antibody.
- Published in:
- Human Molecular Genetics, 2006, v. 15, n. 1, p. 105, doi. 10.1093/hmg/ddi432
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- Publication type:
- Article
BBMRI-ERIC as a resource for pharmaceutical and life science industries: the development of biobank-based Expert Centres.
- Published in:
- European Journal of Human Genetics, 2015, v. 23, n. 7, p. 893, doi. 10.1038/ejhg.2014.235
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- Publication type:
- Article
Gene expression variation between mouse inbred strains.
- Published in:
- BMC Genomics, 2004, v. 5, p. 57, doi. 10.1186/1471-2164-5-57
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- Publication type:
- Article
Human Papillomavirus (HPV) Upregulates the Cellular Deubiquitinase UCHL1 to Suppress the Keratinocyte's Innate Immune Response
- Published in:
- PLoS Pathogens, 2013, v. 9, n. 5, p. 1, doi. 10.1371/journal.ppat.1003384
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- Publication type:
- Article
Serrated adenomas and mixed polyposis caused by a splice acceptor deletion in the mouse Smad4 gene.
- Published in:
- Genes, Chromosomes & Cancer, 2003, v. 36, n. 3, p. 273, doi. 10.1002/gcc.10169
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- Publication type:
- Article
Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in the SDHD gene.
- Published in:
- Genes, Chromosomes & Cancer, 2001, v. 31, n. 3, p. 274, doi. 10.1002/gcc.1144
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- Publication type:
- Article
Scanning for Genes in Large Genomic Regions: Cosmid-Based Exon Trapping of Multiple Exons in a Single Product.
- Published in:
- Nucleic Acids Research, 1996, v. 24, n. 6, p. 1105, doi. 10.1093/nar/24.6.1105
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- Publication type:
- Article
Progress in therapeutic antisense applications for neuromuscular disorders.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 2, p. 146, doi. 10.1038/ejhg.2009.160
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- Publication type:
- Article
Reply to Nothnagel et al.
- Published in:
- 2008
- By:
- Publication type:
- Letter
Popper revisited: GWAS here, last year.
- Published in:
- 2008
- By:
- Publication type:
- Editorial
Copy number variation in regions flanked (or unflanked) by duplicons among patients with developmental delay and/or congenital malformations; detection of reciprocal and partial Williams-Beuren duplications.
- Published in:
- European Journal of Human Genetics, 2006, v. 14, n. 2, p. 180, doi. 10.1038/sj.ejhg.5201540
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- Publication type:
- Article
Genomics: The human genome, revisited.
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- European Journal of Human Genetics, 2005, v. 13, n. 3, p. 265, doi. 10.1038/sj.ejhg.5201348
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- Publication type:
- Article
Evidence for a QTL on chromosome 19 influencing LDL cholesterol levels in the general population.
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- European Journal of Human Genetics, 2003, v. 11, n. 11, p. 845, doi. 10.1038/sj.ejhg.5201053
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- Publication type:
- Article
New initiatives from EJHG, ESHG and Nature Publishing Group.
- Published in:
- 2002
- By:
- Publication type:
- Editorial
EDITORIAL.
- Published in:
- 2002
- By:
- Publication type:
- Editorial
Medical genomics.
- Published in:
- 2001
- By:
- Publication type:
- Editorial
2000: promises and plans.
- Published in:
- 2000
- By:
- Publication type:
- Editorial
Different localization of dystrophin in developing and adult human skeletal muscle.
- Published in:
- Muscle & Nerve, 1991, v. 14, n. 1, p. 1, doi. 10.1002/mus.880140102
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- Publication type:
- Article
Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome.
- Published in:
- Nature Genetics, 2012, v. 44, n. 4, p. 379, doi. 10.1038/ng.2217
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- Publication type:
- Article
Frequency of new copy number variation in humans.
- Published in:
- 2005
- By:
- Publication type:
- Letter
Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy.
- Published in:
- Nature Genetics, 2003, v. 35, n. 4, p. 315, doi. 10.1038/ng1262
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- Publication type:
- Article
DeepSAGE Reveals Genetic Variants Associated with Alternative Polyadenylation and Expression of Coding and Non-coding Transcripts.
- Published in:
- PLoS Genetics, 2013, v. 9, n. 6, p. 1, doi. 10.1371/journal.pgen.1003594
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- Publication type:
- Article
Preclinical PK and PD Studies on 2′-O-Methyl-phosphorothioate RNA Antisense Oligonucleotides in the mdx Mouse Model.
- Published in:
- Molecular Therapy, 2010, v. 18, n. 6, p. 1210, doi. 10.1038/mt.2010.72
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- Publication type:
- Article
Enhanced Exon-skipping Induced by U7 snRNA Carrying a Splicing Silencer Sequence: Promising Tool for DMD Therapy.
- Published in:
- Molecular Therapy, 2009, v. 17, n. 7, p. 1234, doi. 10.1038/mt.2009.113
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- Publication type:
- Article
Guidelines for Antisense Oligonucleotide Design and Insight Into Splice-modulating Mechanisms.
- Published in:
- Molecular Therapy, 2009, v. 17, n. 3, p. 548, doi. 10.1038/mt.2008.205
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- Publication type:
- Article
Exploring the Frontiers of Therapeutic Exon Skipping for Duchenne Muscular Dystrophy by Double Targeting within One or Multiple Exons.
- Published in:
- Molecular Therapy, 2006, v. 14, n. 3, p. 401, doi. 10.1016/j.ymthe.2006.02.022
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- Publication type:
- Article
Targeted Exon Skipping in Transgenic hDMD Mice: A Model for Direct Preclinical Screening of Human-Specific Antisense Oligonucleotides
- Published in:
- Molecular Therapy, 2004, v. 10, n. 2, p. 232, doi. 10.1016/j.ymthe.2004.05.031
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- Publication type:
- Article
Reproducibility of high-throughput mRNA and small RNA sequencing across laboratories.
- Published in:
- Nature Biotechnology, 2013, v. 31, n. 11, p. 1015, doi. 10.1038/nbt.2702
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- Publication type:
- Article
Literature-aided meta-analysis of microarray data: a compendium study on muscle development and disease.
- Published in:
- BMC Bioinformatics, 2008, v. 9, p. 1, doi. 10.1186/1471-2105-9-291
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- Publication type:
- Article
Interspecies Translation of Disease Networks Increases Robustness and Predictive Accuracy.
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- PLoS Computational Biology, 2011, v. 7, n. 11, p. 1, doi. 10.1371/journal.pcbi.1002258
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- Publication type:
- Article
Two-colour immunocytochemical staining of gamma (gamma) and epsilon (epsilon) type haemoglobin in fetal red cells.
- Published in:
- 1998
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- Publication type:
- journal article
Prenatal diagnosis of trisomy 13 on fetal cells obtained from maternal blood after minor enrichment.
- Published in:
- Prenatal Diagnosis, 1998, v. 18, n. 10, p. 1082, doi. 10.1002/(SICI)1097-0223(1998100)18:10<1082::AID-PD383>3.0.CO;2-D
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- Publication type:
- Article
Transcriptional Profiling of Human Familial Longevity Indicates a Role for ASF1A and IL7R.
- Published in:
- PLoS ONE, 2012, v. 7, n. 1, p. 1, doi. 10.1371/journal.pone.0027759
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- Publication type:
- Article
Targeting Several CAG Expansion Diseases by a Single Antisense Oligonucleotide.
- Published in:
- PLoS ONE, 2011, v. 6, n. 9, p. 1, doi. 10.1371/journal.pone.0024308
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- Publication type:
- Article
Human Papillomavirus Deregulates the Response of a Cellular Network Comprising of Chemotactic and Proinflammatory Genes.
- Published in:
- PLoS ONE, 2011, v. 6, n. 3, p. 1, doi. 10.1371/journal.pone.0017848
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- Publication type:
- Article
Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere.
- Published in:
- Nature Genetics, 2002, v. 32, n. 2, p. 235, doi. 10.1038/ng999
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- Publication type:
- Article
Ptprj is a candidate for the mouse colon-cancer susceptibility locus Scc1 and is frequently deleted in human cancers.
- Published in:
- Nature Genetics, 2002, v. 31, n. 3, p. 295, doi. 10.1038/ng903
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- Publication type:
- Article
Serum protein profiling in mice: Identification of Factor XIIIa as a potential biomarker for muscular dystrophy.
- Published in:
- Proteomics, 2008, v. 8, n. 8, p. 1552, doi. 10.1002/pmic.200700857
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- Publication type:
- Article
Huntington's disease blood and brain show a common gene expression pattern and share an immune signature with Alzheimer's disease.
- Published in:
- Scientific Reports, 2017, p. 44849, doi. 10.1038/srep44849
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- Publication type:
- Article
Deregulation of the ubiquitin-proteasome system is the predominant molecular pathology in OPMD animal models and patients.
- Published in:
- Skeletal Muscle, 2011, v. 1, n. 1, p. 2, doi. 10.1186/2044-5040-1-15
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- Publication type:
- Article