Stefan Karlsson
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- 2002
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Mark
Development of gene therapy for blood disorders by gene transfer into haematopoietic stem cells.
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- Contribution to journal › Article
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Mark
Efficient Oncoretroviral Transduction of Extended Long-Term Culture-Initiating Cells and NOD/SCID Repopulating Cells: Enhanced Reconstitution with Gene-Marked Cells Through an Ex Vivo Expansion Approach.
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- Contribution to journal › Article
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Mark
Development of gene therapy for hematopoietic stem cells using lentiviral vectors.
(
- Contribution to journal › Scientific review
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Mark
Framgangsrik genterapi av barn med svar immundefekt. Forskningsgenombrott ger hopp om behandling aven av andra sjukdomar
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- Contribution to journal › Article
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Mark
Transient disruption of autocrine TGF-beta signaling leads to enhanced survival and proliferation potential in single primitive human hemopoietic progenitor cells.
(
- Contribution to journal › Article
- 2001
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Mark
High-titer lentivirus mediated gene transfer introduces multiple vector copies into the genome of primate and human hematopoietic repopulating cells
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- Contribution to journal › Article
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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
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- Contribution to journal › Article
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Mark
Proliferation of primitive myeloid progenitors can be reversibly induced by HOXA10
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- Contribution to journal › Article
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Mark
Clinical gene therapy in hematology: Past and future
(
- Contribution to journal › Article
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Mark
Abnormal angiogenesis but intact hematopoietic potential in TGF-beta type I receptor-deficient mice
(
- Contribution to journal › Article