Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Mystery solved: VSV-G-LVs do not allow efficient gene transfer into unstimulated T cells, B cells, and HSCs because they lack the LDL receptor

27 Feb 2014

Abstract excerpt

International audience

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cytomegalovirus and herpesvirus research
Share to Viral Infections and Immunology Research
Share to Virus-based gene therapy research

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 24578496
DOI: 10.1182/blood-2013-11-540641

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mystery solved: VSV-G-LVs do not allow efficient gene transfer into unstimulated T cells, B cells, and HSCs because they lack the LDL receptorPMID 24578496Read ↗

Gene Therapy in Cardiovascular Disease: Recent Advances and Future Directions in Science: A Science Advisory From the American Heart AssociationSemantic proximity Read ↗

LDL receptor and its family members serve as the cellular receptors for vesicular stomatitis virusSemantic proximity Read ↗

An International Society for Cell & Gene Therapy working group short report on the future of expanded access to unapproved cell and gene therapiesSemantic proximity Read ↗

Progress in Pseudotyping Lentiviral Vectors Towards Cell-Specific Gene Delivery In VivoSemantic proximity Read ↗

Baboon envelope LVs efficiently transduced human adult, fetal, and progenitor T cells and corrected SCID-X1 T-cell deficiencySemantic proximity Read ↗

Targeted, safe, and efficient gene delivery to human hematopoietic stem and progenitor cells in vivo using the engineered AVID adenovirus vector platformSemantic proximity Read ↗

Baboon envelope pseudotyped LVs outperform VSV-G-LVs for gene transfer into early-cytokine-stimulated and resting HSCsSemantic proximity Read ↗

American society of gene therapy (ASGT) ad hoc subcommittee on retroviral-mediated gene transfer to hematopoietic stem cellsSemantic proximity Read ↗

Characterization of a third generation lentiviral vector pseudotyped with Nipah virus envelope proteins for endothelial cell transductionSemantic proximity Read ↗

Surface-Engineered Lentiviral Vectors for Selective Gene Transfer into Subtypes of LymphocytesSemantic proximity Read ↗

Efficient lentiviral transduction of different human and mouse cellsSemantic proximity Read ↗

Modulation of immune responses in lentiviral vector-mediated gene transferSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.