UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Efficient construction of producer cell lines for a SIN lentiviral vector for SCID-X1 gene therapy by concatemeric array transfection

Blood, 2009-05, Vol.113 (21), p.5104-5110

2009

Volltextzugriff (PDF)

Correction of Murine Hemophilia a by Hematopoietic Stem Cell Gene Therapy

Molecular therapy, 2005-12, Vol.12 (6), p.1034-1042

2005

Volltextzugriff (PDF)

Development and Implementation of Real-Time Web-Based Dashboards in a Multisite Transfusion Service

Journal of pathology informatics, 2019, Vol.10 (1), p.3-3, Article 3

2019

Volltextzugriff (PDF)

Transfusion confusion: hemolysis or eltrombopag?

Transfusion (Philadelphia, Pa.), 2020-02, Vol.60 (2), p.235-236

2020

Volltextzugriff (PDF)

Impact of new myeloma agents on the transfusion laboratory

Pathology, 2021-04, Vol.53 (3), p.427-437

2021

Volltextzugriff (PDF)

Recognition of α2-Macroglobulin by the Low Density Lipoprotein Receptor-related Protein Requires the Cooperation of Two Ligand Binding Cluster Regions

The Journal of biological chemistry, 2001-10, Vol.276 (42), p.39484-39491

2001

Volltextzugriff (PDF)

Investigating Transfusion-related Sepsis Using Culture-Independent Metagenomic Sequencing

Clinical infectious diseases, 2020-08, Vol.71 (5), p.1179-1185

2020

Volltextzugriff (PDF)

Abstract 1888: Anti-CD38 interference with blood compatibility testing: Differentiating isatuximab and daratumumab via functional epitope mapping

Cancer research (Chicago, Ill.), 2021-07, Vol.81 (13_Supplement), p.1888-1888

2021

Volltextzugriff (PDF)

Anti‐CD38 monoclonal antibody interference with blood compatibility testing: Differentiating isatuximab and daratumumab via functional epitope mapping

Transfusion (Philadelphia, Pa.), 2022-11, Vol.62 (11), p.2334-2348

2022

Volltextzugriff (PDF)

Sepsis from an apheresis platelet contaminated with Acinetobacter calcoaceticus/baumannii complex bacteria and Staphylococcus saprophyticus after pathogen reduction

Transfusion (Philadelphia, Pa.), 2020-09, Vol.60 (9), p.1960-1969

2020

Volltextzugriff (PDF)

Comparison of GeneXpert FluA PCR to Direct Fluorescent Antibody and Respiratory Viral Panel PCR Assays for Detection of 2009 Novel H1N1 Influenza Virus

Journal of clinical microbiology, 2010-12, Vol.48 (12), p.4684-4685

2010

Volltextzugriff (PDF)

Development of improved factor VIII molecules and new gene transfer approaches for hemophilia A

Current gene therapy, 2003-02, Vol.3 (1), p.27-41

2003

Volltextzugriff (PDF)

Transfer of a TCR gene derived from a patient with a marked antitumor response conveys highly active T-cell effector functions

Human gene therapy, 2005-04, Vol.16 (4), p.457-472

2005

Volltextzugriff (PDF)

Prolonged ceftriaxone-induced immune thrombocytopenia due to impaired drug clearance: a case report

Transfusion (Philadelphia, Pa.), 2013-11, Vol.53 (11), p.2715-2721

2013

Volltextzugriff (PDF)

Sustained Phenotypic Correction of Hemophilia A Mice Following Oncoretroviral-Mediated Expression of a Bioengineered Human Factor VIII Gene in Long-Term Hematopoietic Repopulating Cells

Molecular therapy, 2004-11, Vol.10 (5), p.892-902

2004

Volltextzugriff (PDF)

Correction of Murine Hemophilia A by Hematopoietic Stem Cell Gene Therapy

Blood, 2005-11, Vol.106 (11), p.1291-1291

2005

Volltextzugriff (PDF)

Correction of Human X-Linked Chronic Granulomatous Disease (X-CGD) Following Transduction of X-CGD CD34+ Cells with a Modified RD114-Pseudotyped Simian Immunodeficiency Virus Lentiviral Vector in a NOD/SCID Mouse Xenograft Model

Blood, 2006-11, Vol.108 (11), p.3278-3278

2006

Volltextzugriff (PDF)

Improvement of Canine XSCID by In Vivo Gene Therapy Using RD114/TR-Pseudotyped SIV Lentiviral Vectors

Blood, 2006-11, Vol.108 (11), p.3275-3275

2006

Volltextzugriff (PDF)

Simian immundeficiency virus lentivector corrects human X-linked chronic granulomatous disease in the NOD/SCID mouse xenograft

Gene therapy, 2007-08, Vol.14 (21), p.1513-1524

2007

Volltextzugriff (PDF)

468. Evaluation of Factors Influencing the Production Titers of SIV-Derived Lentiviral Vectors

Molecular therapy, 2006-05, Vol.13 (S1), p.S181-S181

2006

Volltextzugriff (PDF)

671. SIV-Derived Lentiviral Vectors Pseudotyped with Modified RD114 Envelope and Containing Mutant MGMT Efficiently Transduce Human CD34+ PBSCs and Allow Selection

Molecular therapy, 2006-05, Vol.13 (S1), p.S259-S259

2006

Volltextzugriff (PDF)

Gene therapy for hemophilia A: Targeting long-term hematopoietic repopulating cells with a retroviral vector expressing a bioengineered human factor VIII gene

Moayeri, Morvarid

2005

Volltextzugriff (PDF)

Update on gene therapy for Chronic Granulomatous Disease: Current studies and future approaches

Blood cells, molecules, & diseases, 2008-03, Vol.40 (2), p.274-275

2008

Volltextzugriff (PDF)

Recognition of Î±2-Macroglobulin by the Low Density Lipoprotein Receptor-related Protein Requires the Cooperation of Two Ligand Binding Cluster Regions

The Journal of biological chemistry, 2001-10, Vol.276 (42), p.39484

2001

Volltextzugriff (PDF)

1 – 25 von 26

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(23)
Mit Volltextzugriff
(24)

Publikationsform

Sprache

Englisch
(26)

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(11)
Science & Technology
(11)
Humans
(7)
Gene Therapy
(6)
Animals
(4)
Biological And Medical Sciences
(4)
Hematology
(4)
Mice
(4)
Patients
(4)
Biotechnology & Applied Microbiology
(3)
Factor Viii - Genetics
(3)
Genetic Therapy - Methods
(3)
Genetics & Heredity
(3)
Genomes
(3)
Hemophilia A - Therapy
(3)
Infectious Diseases
(3)
Medical Sciences
(3)
Medicine, Research & Experimental
(3)
Research & Experimental Medicine
(3)
Transfusion
(3)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Efficient construction of producer cell lines for a SIN lentiviral vector for SCID-X1 gene therapy by concatemeric array transfection

Correction of Murine Hemophilia a by Hematopoietic Stem Cell Gene Therapy

Development and Implementation of Real-Time Web-Based Dashboards in a Multisite Transfusion Service

Transfusion confusion: hemolysis or eltrombopag?

Impact of new myeloma agents on the transfusion laboratory

Recognition of α2-Macroglobulin by the Low Density Lipoprotein Receptor-related Protein Requires the Cooperation of Two Ligand Binding Cluster Regions

Investigating Transfusion-related Sepsis Using Culture-Independent Metagenomic Sequencing

Abstract 1888: Anti-CD38 interference with blood compatibility testing: Differentiating isatuximab and daratumumab via functional epitope mapping

Anti‐CD38 monoclonal antibody interference with blood compatibility testing: Differentiating isatuximab and daratumumab via functional epitope mapping

Sepsis from an apheresis platelet contaminated with Acinetobacter calcoaceticus/baumannii complex bacteria and Staphylococcus saprophyticus after pathogen reduction

Comparison of GeneXpert FluA PCR to Direct Fluorescent Antibody and Respiratory Viral Panel PCR Assays for Detection of 2009 Novel H1N1 Influenza Virus

Development of improved factor VIII molecules and new gene transfer approaches for hemophilia A

Transfer of a TCR gene derived from a patient with a marked antitumor response conveys highly active T-cell effector functions

Prolonged ceftriaxone-induced immune thrombocytopenia due to impaired drug clearance: a case report

Sepsis Attributed to Bacterial Contamination of Platelets Associated with a Potential Common Source — Multiple States, 2018

Sustained Phenotypic Correction of Hemophilia A Mice Following Oncoretroviral-Mediated Expression of a Bioengineered Human Factor VIII Gene in Long-Term Hematopoietic Repopulating Cells

Correction of Murine Hemophilia A by Hematopoietic Stem Cell Gene Therapy

Correction of Human X-Linked Chronic Granulomatous Disease (X-CGD) Following Transduction of X-CGD CD34+ Cells with a Modified RD114-Pseudotyped Simian Immunodeficiency Virus Lentiviral Vector in a NOD/SCID Mouse Xenograft Model

Improvement of Canine XSCID by In Vivo Gene Therapy Using RD114/TR-Pseudotyped SIV Lentiviral Vectors

Simian immundeficiency virus lentivector corrects human X-linked chronic granulomatous disease in the NOD/SCID mouse xenograft

468. Evaluation of Factors Influencing the Production Titers of SIV-Derived Lentiviral Vectors

671. SIV-Derived Lentiviral Vectors Pseudotyped with Modified RD114 Envelope and Containing Mutant MGMT Efficiently Transduce Human CD34+ PBSCs and Allow Selection

Gene therapy for hemophilia A: Targeting long-term hematopoietic repopulating cells with a retroviral vector expressing a bioengineered human factor VIII gene

Update on gene therapy for Chronic Granulomatous Disease: Current studies and future approaches

Recognition of Î±2-Macroglobulin by the Low Density Lipoprotein Receptor-related Protein Requires the Cooperation of Two Ligand Binding Cluster Regions

Suchergebnisse filtern