UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 29

Sortiert nach

WASP and WIP regulate podosomes in migrating leukocytes

Journal of microscopy (Oxford), 2008-09, Vol.231 (3), p.494-505

2008

Volltextzugriff (PDF)

Autologous Ex Vivo Lentiviral Gene Therapy for Adenosine Deaminase Deficiency

The New England journal of medicine, 2021-05, Vol.384 (21), p.2002-2013

2021

Volltextzugriff (PDF)

A Modified γ-Retrovirus Vector for X-Linked Severe Combined Immunodeficiency

The New England journal of medicine, 2014-10, Vol.371 (15), p.1407-1417

2014

Volltextzugriff (PDF)

Reconstitution of neutrophil NADPH oxidase activity in the cell-free system by four components: p67-phox, p47-phox, p21rac1, and cytochrome b-245

The Journal of biological chemistry, 1992-08, Vol.267 (24), p.16767-16770

1992

Volltextzugriff (PDF)

Current progress on gene therapy for primary immunodeficiencies

Gene therapy, 2013-10, Vol.20 (10), p.963-969

2013

Volltextzugriff (PDF)

278 Generation and clinical application of gene modified autologous epidermal sheets in Netherton syndrome – lessons learned from a phase 1 trial

Journal of investigative dermatology, 2019-09, Vol.139 (9), p.S262-S262

2019

Volltextzugriff (PDF)

Excess F-actin mechanically impedes mitosis leading to cytokinesis failure in X-linked neutropenia by exceeding Aurora B kinase error correction capacity

Blood, 2012-11, Vol.120 (18), p.3803-3811

2012

Volltextzugriff (PDF)

Correction of murine Rag1 deficiency by self-inactivating lentiviral vector-mediated gene transfer

Leukemia, 2011-09, Vol.25 (9), p.1471-1483

2011

Volltextzugriff (PDF)

Validation of a mutated PRE sequence allowing high and sustained transgene expression while abrogating WHV-X protein synthesis: application to the gene therapy of WAS

Gene therapy, 2009-05, Vol.16 (5), p.605-619

2009

Volltextzugriff (PDF)

Scale-up and manufacturing of clinical-grade self-inactivating γ-retroviral vectors by transient transfection

Gene therapy, 2012-03, Vol.19 (3), p.246-254

2012

Volltextzugriff (PDF)

Efficient gene delivery to the adult and fetal CNS using pseudotyped non-integrating lentiviral vectors

Gene therapy, 2009-04, Vol.16 (4), p.509-520

2009

Volltextzugriff (PDF)

Lentiviral transduction of the murine lung provides efficient pseudotype and developmental stage-dependent cell-specific transgene expression

Gene therapy, 2008-08, Vol.15 (16), p.1167-1175

2008

Volltextzugriff (PDF)

Critical Variables affecting clinical-grade production of the self-inactivating gamma-retroviral vector for the treatment of X-linked severe combined immunodeficiency

Gene therapy, 2012-08, Vol.19 (8), p.872-876

2012

Volltextzugriff (PDF)

Genetic Variants Associated With Neutrophil Function in Aggressive Periodontitis and Healthy Controls

Journal of periodontology (1970), 2010-04, Vol.81 (4), p.527-534

2010

Volltextzugriff (PDF)

S1632 SAFETY AND EFFICACY OF LENTIGLOBIN GENE THERAPY IN PATIENTS WITH TRANSFUSION‐DEPENDENT B‐THALASSAEMIA AND NON‐B0/B0 GENOTYPES IN THE PHASE 3 NORTHSTAR‐2 STUDY

HemaSphere, 2019-06, Vol.3 (S1), p.754-n/a

2019

Volltextzugriff (PDF)

Correction of SCID-X1 using an enhancerless Vav promoter

Human gene therapy, 2011-03, Vol.22 (3), p.263

2011

Volltextzugriff (PDF)

Dendritic Cells: The Bare Bones of Immunity

Current biology, 2004-11, Vol.14 (22), p.R965-R967

2004

Volltextzugriff (PDF)

Cell-specific and efficient expression in mouse and human B cells by a novel hybrid immunoglobulin promoter in a lentiviral vector

Gene therapy, 2007-12, Vol.14 (23), p.1623-1631

2007

Volltextzugriff (PDF)

Kinetics of transgene expression in mouse retina following sub-retinal injection of recombinant adeno-associated virus

Vision research (Oxford), 2002-02, Vol.42 (4), p.541-549

2002

Volltextzugriff (PDF)

Transgene optimization significantly improves SIN vector titers, [gp91.sup.phos] expression and reconstitution of superoxide production in X-CGD cells

Gene therapy, 2009-01, Vol.16 (1), p.111

2009

Volltextzugriff (PDF)

Improvement of neuronal visual responses in the superior colliculus in Prph2Rd2/Rd2 mice following gene therapy

Molecular and cellular neuroscience, 2004-01, Vol.25 (1), p.103-110

2004

Volltextzugriff (PDF)

Gene transfer to primary chronic granulomatous disease monocytes

The Lancet (British edition), 1995-07, Vol.346 (8967), p.92-93

1995

Volltextzugriff (PDF)

Intrinsic dendritic cell defects in Wiskott-Aldrich syndrome

Molecular immunology, 1998-08, Vol.35 (11), p.734-734

1998

Volltextzugriff (PDF)

Molecular studies towards gene therapy for chronic granulomatous disease

Thrasher, A.J

1995

Volltextzugriff (PDF)

Functional Reconstitution of the NADPH-Oxidase by Adeno-Associated Virus Gene Transfer

Blood, 1995-07, Vol.86 (2), p.761-765

1995

Volltextzugriff (PDF)

1 – 25 von 29

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(27)
Mit Volltextzugriff
(27)

Publikationsform

Artikel
(28)
Dissertationen
(1)

Sprache

Englisch
(29)
Japanisch
(4)

Erscheinungsjahr

n.n

Zeitschrift / Serie

Gene Therapy
(8)
Blood
(2)
The New England Journal Of Medicine
(2)
Cb/current Biology
(1)
Clinical And Experimental Immunology
(1)
Current Anaesthesia & Critical Care
(1)
Current Biology
(1)
Desalination
(1)
Hemasphere
(1)
Human Gene Therapy
(1)

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

WASP and WIP regulate podosomes in migrating leukocytes

Autologous Ex Vivo Lentiviral Gene Therapy for Adenosine Deaminase Deficiency

A Modified γ-Retrovirus Vector for X-Linked Severe Combined Immunodeficiency

Reconstitution of neutrophil NADPH oxidase activity in the cell-free system by four components: p67-phox, p47-phox, p21rac1, and cytochrome b-245

Current progress on gene therapy for primary immunodeficiencies

278 Generation and clinical application of gene modified autologous epidermal sheets in Netherton syndrome – lessons learned from a phase 1 trial

Excess F-actin mechanically impedes mitosis leading to cytokinesis failure in X-linked neutropenia by exceeding Aurora B kinase error correction capacity

Correction of murine Rag1 deficiency by self-inactivating lentiviral vector-mediated gene transfer

Validation of a mutated PRE sequence allowing high and sustained transgene expression while abrogating WHV-X protein synthesis: application to the gene therapy of WAS

Scale-up and manufacturing of clinical-grade self-inactivating γ-retroviral vectors by transient transfection

Efficient gene delivery to the adult and fetal CNS using pseudotyped non-integrating lentiviral vectors

Lentiviral transduction of the murine lung provides efficient pseudotype and developmental stage-dependent cell-specific transgene expression

Critical Variables affecting clinical-grade production of the self-inactivating gamma-retroviral vector for the treatment of X-linked severe combined immunodeficiency

Genetic Variants Associated With Neutrophil Function in Aggressive Periodontitis and Healthy Controls

S1632 SAFETY AND EFFICACY OF LENTIGLOBIN GENE THERAPY IN PATIENTS WITH TRANSFUSION‐DEPENDENT B‐THALASSAEMIA AND NON‐B0/B0 GENOTYPES IN THE PHASE 3 NORTHSTAR‐2 STUDY

Correction of SCID-X1 using an enhancerless Vav promoter

Dendritic Cells: The Bare Bones of Immunity

Cell-specific and efficient expression in mouse and human B cells by a novel hybrid immunoglobulin promoter in a lentiviral vector

Kinetics of transgene expression in mouse retina following sub-retinal injection of recombinant adeno-associated virus

Transgene optimization significantly improves SIN vector titers, [gp91.sup.phos] expression and reconstitution of superoxide production in X-CGD cells

Improvement of neuronal visual responses in the superior colliculus in Prph2Rd2/Rd2 mice following gene therapy

Gene transfer to primary chronic granulomatous disease monocytes

Intrinsic dendritic cell defects in Wiskott-Aldrich syndrome

Molecular studies towards gene therapy for chronic granulomatous disease

Functional Reconstitution of the NADPH-Oxidase by Adeno-Associated Virus Gene Transfer

Suchergebnisse filtern