Ryszard Kole
Kole, Ryszard
VIAF ID: 315225519 (Personal)
Permalink: http://viaf.org/viaf/315225519
Preferred Forms
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- 100 1 _ ‡a Kole, Ryszard
- 100 0 _ ‡a Ryszard Kole
4xx's: Alternate Name Forms (3)
Works
Title | Sources |
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Abstracts of papers presented at the 2010 meeting on RNA & oligonucleotide therapeutics, 2010: | |
Analysis of prostate-specific membrane antigen splice variants in LNCap cells | |
Applications of the PMO platform to genetic diseases. | |
Cellular response to an antisense-mediated shift of Bcl-x pre-mRNA splicing and antineoplastic agents | |
Dystromirs as serum biomarkers for monitoring the disease severity in Duchenne muscular Dystrophy | |
Effects of base modifications on antisense properties of 2'-O-methoxyethyl and PNA oligonucleotides | |
Exon skipping and dystrophin restoration in patients with Duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: an open-label, phase 2, dose-escalation study | |
High-level expression of hemoglobin A in human thalassemic erythroid progenitor cells following lentiviral vector delivery of an antisense snRNA. | |
HIV-1 preferentially binds receptors copatched with cell-surface elastase | |
The importance of Bcl-xL in the survival of human RPE cells | |
Long-term improvement in mdx cardiomyopathy after therapy with peptide-conjugated morpholino oligomers | |
Mismatched single stranded antisense oligonucleotides can induce efficient dystrophin splice switching | |
Modification of HER2 pre-mRNA alternative splicing and its effects on breast cancer cells | |
Oligorewolucja | |
Peptide-morpholino conjugate: a promising therapeutic for Duchenne muscular dystrophy | |
Prevention of dystrophic pathology in severely affected dystrophin/utrophin-deficient mice by morpholino-oligomer-mediated exon-skipping | |
Repair of a splicing defect in erythroid cells from patients with beta-thalassemia/HbE disorder | |
Restoration of correct β-globin mRNA splicing and HbA production by engineered U7 snRNA in β-thalassaemia/HbE erythroid cells | |
Restoration of human beta-globin gene expression in murine and human IVS2-654 thalassemic erythroid cells by free uptake of antisense oligonucleotides. | |
RNA modulation, repair and remodeling by splice switching oligonucleotides | |
Self-aggregating 1.8kDa polyethylenimines with dissolution switch at endosomal acidic pH are delivery carriers for plasmid DNA, mRNA, siRNA and exon-skipping oligonucleotides. | |
Short-term and long-term modulation of gene expression by antisense therapeutics | |
Size-uniform 200 nm particles: fabrication and application to magnetofection | |
Specific removal of the nonsense mutation from the mdx dystrophin mRNA using antisense oligonucleotides. | |
Splicing: hear and now! | |
Superoxide-dependent iron uptake: a new role for anion exchange protein 2. | |
Sustained dystrophin expression induced by peptide-conjugated morpholino oligomers in the muscles of mdx mice. | |
Switching on transgene expression by correcting aberrant splicing using multi-targeting steric-blocking oligonucleotides | |
Targeted correction of a thalassemia-associated beta-globin mutation induced by pseudo-complementary peptide nucleic acids | |
Targeted exon skipping to address "leaky" mutations in the dystrophin gene. | |
Targeting mRNA splicing as a potential treatment for Duchenne muscular dystrophy | |
Therapeutic potential of antisense oligonucleotides as modulators of alternative splicing | |
Znokautowane myszy pomagają w rozwikłaniu tajemnicy genów : Nagroda Nobla 2007 : Medycyna i Fizjologia |