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- 2005
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Mark
Development of cellular models for ribosomal protein S19 (RPS19)-deficient diamond-blackfan anemia using inducible expression of siRNA against RPS19.
(
- Contribution to journal › Article
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Mark
Deficiency of ribosomal protein S19 in CD34+ cells generated by siRNA blocks erythroid development and mimics defects seen in Diamond-Blackfan anemia.
(
- Contribution to journal › Article
- 2004
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Mark
Development of an adenoviral vector system with adenovirus serotype 35 tropism; efficient transient gene transfer into primary malignant hematopoietic cells.
(
- Contribution to journal › Article
- 2003
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Mark
Proliferation deficiency of multipotent hematopoietic progenitors in ribosomal protein S19 (RPS19)-deficient Diamond-Blackfan anemia improves following RPS19 gene transfer
(
- Contribution to journal › Article
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Mark
Bakslag for genterapi: två fall av leukemi i fransk studie [Setback for gene therapy: Two cases of leukemia in a French trial]
(
- Contribution to journal › Article
- 2002
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Mark
Gene transfer improves erythroid development in ribosomal protein S19-deficient Diamond-Blackfan anemia.
(
- Contribution to journal › Article
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Mark
Oncoretroviral gene transfer to NOD/SCID repopulating cells using three different viral envelopes
(
- Contribution to journal › Article
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Mark
Framgangsrik genterapi av barn med svar immundefekt. Forskningsgenombrott ger hopp om behandling aven av andra sjukdomar
(
- Contribution to journal › Article
- 2001
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Mark
Retroviral transduction of human CD34+ cells on fibronectin fragment CH-296 is inhibited by high concentrations of vector containing medium
(
- Contribution to journal › Article
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Mark
Clinical gene therapy in hematology: Past and future
(
- Contribution to journal › Article