Stefan Karlsson
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- 2006
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Mark
HOXB4-induced self-renewal of hematopoietic stem cells is significantly enhanced by p21 deficiency.
(
- Contribution to journal › Article
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Mark
Neonatal hematopoietic stem cell transplantation cures oc/oc mice from osteopetrosis.
(
- Contribution to journal › Article
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Mark
Effective cell and gene therapy in a murine model of Gaucher disease.
(
- Contribution to journal › Article
- 2005
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Mark
Quiescence of hematopoietic stem cells and maintenance of the stem cell pool is not dependent on TGF-beta signaling in vivo.
(
- Contribution to journal › Article
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Mark
The role of Smad signaling in hematopoiesis.
(
- Contribution to journal › Scientific review
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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
Bone-marrow-derived cells contribute to the recruitment of microglial cells in response to beta-amyloid deposition in APP/PS1 double transgenic Alzheimer mice
(
- Contribution to journal › Article
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Mark
Gene therapy: efficient targeting of hematopoietic stem cells
(
- Contribution to journal › Debate/Note/Editorial
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Mark
TGF-{beta} type II receptor deficient thymocytes develop normally but demonstrate increased CD8+ proliferation in vivo.
(
- Contribution to journal › Article
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Mark
Compound developmental eye disorders following inactivation of TGFbeta signaling in neural-crest stem cells
(
- Contribution to journal › Article
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Mark
Inactivation of TGF beta signaling in neural crest stem cells leads to multiple defects reminiscent of DiGeorge syndrome
(
- Contribution to journal › Article
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Mark
Gene expression profiling demonstrates that TGF-{beta}1 signals exclusively through receptor complexes involving Alk5 and identifies targets of TGF-{beta} signaling.
(
- 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
Defective paracrine signalling by TGF beta in yolk sac vasculature of endoglin mutant mice: a paradigm for hereditary haemorrhagic telangiectasia
(
- Contribution to journal › Article
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Mark
Connective tissue growth factor expression and Smad signaling during mouse heart development and myocardial infarction
(
- Contribution to journal › Article
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Mark
Overexpression of CXCR4 on human CD34(+) progenitors increases their proliferation, migration, and NOD/SCID repopulation
(
- Contribution to journal › Article
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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
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Mark
Chance or necessity? Insertional mutagenesis in gene therapy and its consequences
(
- Contribution to journal › Scientific review
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Mark
Functionally distinct subpopulations of cord blood CD34+ cells are transduced by adenoviral vectors with serotype 5 or 35 tropism.
(
- Contribution to journal › Article
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Mark
Enforced expression of cyclin D2 enhances the proliferative potential of myeloid progenitors, accelerates in vivo myeloid reconstitution, and promotes rescue of mice from lethal myeloablation.
(
- Contribution to journal › Article
-
Mark
Targeted disruption of the ribosomal protein S19 gene is lethal prior to implantation
(
- Contribution to journal › Article
-
Mark
Stem cell expansion: success and complexities
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Hoxb4-deficient mice undergo normal hematopoietic development but exhibit a mild proliferation defect in hematopoietic stem cells
(
- Contribution to journal › Article
-
Mark
Intact signaling by transforming growth factor beta is not required for termination of liver regeneration in mice
(
- 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
-
Mark
Enforced adenoviral vector-mediated expression of HOXB4 in human umbilical cord blood CD34+ cells promotes myeloid differentiation but not proliferation.
(
- Contribution to journal › Article
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Mark
Activin receptor-like kinase (ALK)1 is an antagonistic mediator of lateral TGFP/ALK5 signaling
(
- Contribution to journal › Article
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Mark
Lentiviral vector transduction of NOD/SCID repopulating cells results in multiple vector integrations per transduced cell: risk of insertional mutagenesis.
(
- Contribution to journal › Article
-
Mark
Efficient characterization of retro-, lenti-, and foamyvector-transduced cell populations by high-accuracy insertion site sequencing
2003) HEMATOPOIETIC STEM CELLS 2002: GENETICS AND FUNCTION: Fourth International Symposium 996. p.112-121(
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
-
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
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Mark
Reduced proliferative capacity of hematopoietic stem cells deficient in hoxb3 and hoxb4.
(
- Contribution to journal › Article
-
Mark
TGF-{beta} signaling-deficient hematopoietic stem cells have normal self-renewal and regenerative ability in vivo despite increased proliferative capacity in vitro.
(
- Contribution to journal › Article
- 2002
-
Mark
Gene transfer improves erythroid development in ribosomal protein S19-deficient Diamond-Blackfan anemia.
(
- Contribution to journal › Article
-
Mark
Oncoretroviral gene transfer to NOD/SCID repopulating cells using three different viral envelopes
(
- Contribution to journal › Article
-
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
-
Mark
Framgangsrik genterapi av barn med svar immundefekt. Forskningsgenombrott ger hopp om behandling aven av andra sjukdomar
(
- Contribution to journal › Article
-
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.
(
- Contribution to journal › Article
-
Mark
Development of gene therapy for hematopoietic stem cells using lentiviral vectors.
(
- Contribution to journal › Scientific review
-
Mark
Development of gene therapy for blood disorders by gene transfer into haematopoietic stem cells.
(
- Contribution to journal › Article
-
Mark
Induced disruption of the transforming growth factor beta type II receptor gene in mice causes a lethal inflammatory disorder that is transplantable.
(
- Contribution to journal › Article
- 2001
-
Mark
High-titer lentivirus mediated gene transfer introduces multiple vector copies into the genome of primate and human hematopoietic repopulating cells
(
- Contribution to journal › Article
-
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
-
Mark
Proliferation of primitive myeloid progenitors can be reversibly induced by HOXA10
(
- Contribution to journal › Article
-
Mark
Impact of selective inactivation of transforming growth factor-beta type II receptor gene (TGFBR2) during viral hepatitis
(
- Contribution to journal › Article
-
Mark
Abnormal angiogenesis but intact hematopoietic potential in TGF-beta type I receptor-deficient mice
(
- Contribution to journal › Article
-
Mark
Clinical gene therapy in hematology: Past and future
(
- Contribution to journal › Article
- 2000
-
Mark
Low level of gene transfer to and engraftment of murine bone marrow cells from long-term bone marrow cultures
(
- Contribution to journal › Article
-
Mark
Lentiviral gene transfer into primary and secondary NOD/SCID repopulating cells
(
- Contribution to journal › Article
-
Mark
Lentivirus gene transfer in murine hematopoietic progenitor cells is compromised by a delay in proviral integration and results in transduction mosaicism and heterogeneous gene expression in progeny cells
(
- Contribution to journal › Article
-
Mark
Lentivirus vector gene expression during ES cell-derived hematopoietic development in vitro
(
- Contribution to journal › Article