UB Paderborn / Katalog / Suche / in CDI

1 – 24 von 24

Sortiert nach

Successful gene therapy in utero for lethal murine hypophosphatasia

Human gene therapy, 2012-04, Vol.23 (4), p.399

2012

Link zum Volltext

Verfügbarkeit prüfen

The new self-inactivating lentiviral vector for thalassemia gene therapy combining two HPFH activating elements corrects human thalassemic hematopoietic stem cells

Human gene therapy, 2012-01, Vol.23 (1), p.15

2012

Link zum Volltext

Verfügbarkeit prüfen

Long-term luciferase expression monitored by bioluminescence imaging after adeno-associated virus-mediated fetal gene delivery in rhesus monkeys (Macaca mulatta)

Human gene therapy, 2010-02, Vol.21 (2), p.143

2010

Link zum Volltext

Verfügbarkeit prüfen

Stable transgene expression in primitive human CD34+ hematopoietic stem/progenitor cells, using the Sleeping Beauty transposon system

Human gene therapy, 2009-12, Vol.20 (12), p.1607

2009

Link zum Volltext

Verfügbarkeit prüfen

Fetal gene transfer using lentiviral vectors: in vivo detection of gene expression by microPET and optical imaging in fetal and infant monkeys

Human gene therapy, 2006-12, Vol.17 (12), p.1254

2006

Link zum Volltext

Verfügbarkeit prüfen

Regulatory and ethical issues for phase I in utero gene transfer studies

Human gene therapy, 2011-11, Vol.22 (11), p.1323

Strong, Carson

2011

Link zum Volltext

Verfügbarkeit prüfen

Transduction of human hematopoietic stem cells by lentiviral vectors pseudotyped with the RD114-TR chimeric envelope glycoprotein

Human gene therapy, 2007-09, Vol.18 (9), p.811

2007

Link zum Volltext

Verfügbarkeit prüfen

Repopulation of athymic mouse liver by cryopreserved early human fetal hepatoblasts

Human gene therapy, 2004-12, Vol.15 (12), p.1219-1228

2004

Link zum Volltext

Verfügbarkeit prüfen

In Utero injection of α-L-iduronidase-carrying retrovirus in canine mucopolysaccharidosis type I: Infection of multiple tissues and neonatal gene expression

Human gene therapy, 2002-10, Vol.13 (15), p.1809-1820

2002

Link zum Volltext

Verfügbarkeit prüfen

Efficient bone marrow transduction by gene transfer with allogeneic umbilical cord blood serum and plasma: an implication for clinical trials

Human gene therapy, 2008-07, Vol.19 (7), p.744

2008

Link zum Volltext

Verfügbarkeit prüfen

Differential transduction efficiency of SCID-repopulating cells derived from umbilical cord blood and granulocyte colony-stimulating factor-mobilized peripheral blood

Human gene therapy, 2001-11, Vol.12 (17), p.2095-2108

2001

Link zum Volltext

Verfügbarkeit prüfen

Gene therapy for canine α-l-iduronidase deficiency : In utero adoptive transfer of genetically corrected hematopoietic progenitors results in engraftment but not amelioration of disease

Human gene therapy, 1999-06, Vol.10 (9), p.1521-1532

1999

Link zum Volltext

Verfügbarkeit prüfen

Long-term engraftment of nonobese diabetic/severe combined immunodeficient mice with human CD34+ cells transduced by a self-inactivating human immunodeficiency virus type 1 vector

Human gene therapy, 2001-06, Vol.12 (9), p.1079-1089

2001

Link zum Volltext

Verfügbarkeit prüfen

Evaluation of peptide-mediated transduction in human CD34+ cells

Human gene therapy, 2004-04, Vol.15 (4), p.415-419

2004

Link zum Volltext

Verfügbarkeit prüfen

Human cord blood CD34+CD38- cell transduction via lentivirus-based gene transfer vectors

Human gene therapy, 1999-06, Vol.10 (9), p.1479-1489

1999

Link zum Volltext

Verfügbarkeit prüfen

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

Human gene therapy, 2002-06, Vol.13 (9), p.1061-1073

2002

Link zum Volltext

Verfügbarkeit prüfen

Limitations of informed consent for in utero gene transfer research : Implications for investigators and institutional review boards

Human gene therapy, 2000-05, Vol.11 (7), p.1057-1063

2000

Link zum Volltext

Verfügbarkeit prüfen

Stable transduction with lentiviral vectors and amplification of immature hematopoietic progenitors from cord blood of preterm human fetuses

Human gene therapy, 2001-03, Vol.12 (4), p.377-389

2001

Link zum Volltext

Verfügbarkeit prüfen

In vitro selection of lentivirus vector-transduced human CD34+ cells

Human gene therapy, 2000-09, Vol.11 (13), p.1949-1957

2000

Link zum Volltext

Verfügbarkeit prüfen

Optimization of retroviral gene transfer protocol to maintain the lymphoid potential of progenitor cells

Human gene therapy, 2001-02, Vol.12 (3), p.291-301

2001

Link zum Volltext

Verfügbarkeit prüfen

Efficient adenoviral vector transduction of human hematopoietic SCID-repopulating and long-term culture-initiating cells

Human gene therapy, 2000-06, Vol.11 (9), p.1313-1327

2000

Link zum Volltext

Verfügbarkeit prüfen

Retroviral vector-mediated gene expression in human CD34+CD38- cells expanded in vitro : Cis elements of FMEV are superior to those of Mo-MuLV

Human gene therapy, 2000-01, Vol.11 (2), p.271-284

2000

Link zum Volltext

Verfügbarkeit prüfen

Increased gene transfer into human cord blood cells by centrifugation-enhanced transduction in fibronectin fragment-coated tubes

Human gene therapy, 1999-11, Vol.10 (17), p.2859-2868

1999

Link zum Volltext

Verfügbarkeit prüfen

Inhibition of human immunodeficiency virus transmission to CD4+ T cells after gene transfer of constitutively expressed interferon β to dendritic cells

Human gene therapy, 2000-08, Vol.11 (12), p.1695-1703

2000

Link zum Volltext

Verfügbarkeit prüfen

1 – 24 von 24

Suche als RSS-Feed

Aktive Filter

Zeitschrift / SerieHuman Gene Therapy

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(24)
Mit Volltextzugriff
(16)

Publikationsform

Artikel
(24)

Sprache

Englisch
(24)
Japanisch
(1)

Erscheinungsjahr

n.n

Kollektion

IngentaConnect
(24)
IngentaConnect Journals
(2)

Zeitschrift / Serie

Hum Gene Ther
(1)
Hum. Gene Ther
(1)

Menü

Weitere Dienste

Einstellungen

Successful gene therapy in utero for lethal murine hypophosphatasia

The new self-inactivating lentiviral vector for thalassemia gene therapy combining two HPFH activating elements corrects human thalassemic hematopoietic stem cells

Long-term luciferase expression monitored by bioluminescence imaging after adeno-associated virus-mediated fetal gene delivery in rhesus monkeys (Macaca mulatta)

Stable transgene expression in primitive human CD34+ hematopoietic stem/progenitor cells, using the Sleeping Beauty transposon system

Fetal gene transfer using lentiviral vectors: in vivo detection of gene expression by microPET and optical imaging in fetal and infant monkeys

Regulatory and ethical issues for phase I in utero gene transfer studies

Transduction of human hematopoietic stem cells by lentiviral vectors pseudotyped with the RD114-TR chimeric envelope glycoprotein

Repopulation of athymic mouse liver by cryopreserved early human fetal hepatoblasts

In Utero injection of α-L-iduronidase-carrying retrovirus in canine mucopolysaccharidosis type I: Infection of multiple tissues and neonatal gene expression

Efficient bone marrow transduction by gene transfer with allogeneic umbilical cord blood serum and plasma: an implication for clinical trials

Differential transduction efficiency of SCID-repopulating cells derived from umbilical cord blood and granulocyte colony-stimulating factor-mobilized peripheral blood

Gene therapy for canine α-l-iduronidase deficiency : In utero adoptive transfer of genetically corrected hematopoietic progenitors results in engraftment but not amelioration of disease

Long-term engraftment of nonobese diabetic/severe combined immunodeficient mice with human CD34+ cells transduced by a self-inactivating human immunodeficiency virus type 1 vector

Evaluation of peptide-mediated transduction in human CD34+ cells

Human cord blood CD34+CD38- cell transduction via lentivirus-based gene transfer vectors

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

Limitations of informed consent for in utero gene transfer research : Implications for investigators and institutional review boards

Stable transduction with lentiviral vectors and amplification of immature hematopoietic progenitors from cord blood of preterm human fetuses

In vitro selection of lentivirus vector-transduced human CD34+ cells

Optimization of retroviral gene transfer protocol to maintain the lymphoid potential of progenitor cells

Efficient adenoviral vector transduction of human hematopoietic SCID-repopulating and long-term culture-initiating cells

Retroviral vector-mediated gene expression in human CD34+CD38- cells expanded in vitro : Cis elements of FMEV are superior to those of Mo-MuLV

Increased gene transfer into human cord blood cells by centrifugation-enhanced transduction in fibronectin fragment-coated tubes

Inhibition of human immunodeficiency virus transmission to CD4+ T cells after gene transfer of constitutively expressed interferon β to dendritic cells

Aktive Filter

Suchergebnisse filtern