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

Redirecting Lentiviral Vectors Pseudotyped with Sindbis Virus-Derived Envelope Proteins to DC-SIGN by Modification of N-Linked Glycans of Envelope Proteins

19 May 2010

Abstract excerpt

Redirecting the tropism of viral vectors enables specific transduction of selected cells by direct administration of vectors. We previously developed targeting lentiviral vectors by pseudotyping with modified Sindbis virus envelope proteins. These modified Sindbis virus envelope proteins have mutations in their original receptor-binding regions to eliminate their natural tropisms, and they are conjugated with...

Read the complete abstract on PubMed

Topics

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

Share to Herpesvirus Infections and Treatments
Share to Viral gastroenteritis research and epidemiology
Share to Virus-based gene therapy research

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 20484510
DOI: 10.1128/jvi.00435-10

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

Redirecting Lentiviral Vectors Pseudotyped with Sindbis Virus-Derived Envelope Proteins to DC-SIGN by Modification of N-Linked Glycans of Envelope ProteinsPMID 20484510Read ↗

Production of lentiviral vectors with enhanced efficiency to target dendritic cells by attenuating mannosidase activity of mammalian cellsSemantic proximity Read ↗

West Nile virus discriminates between DC-SIGN and DC-SIGNR for cellular attachment and infection.Semantic proximity Read ↗

Lentiviral Vector Pseudotypes: Precious Tools to Improve Gene Modification of Hematopoietic Cells for Research and Gene TherapySemantic proximity Read ↗

Design of a Novel Integration-deficient Lentivector Technology That Incorporates Genetic and Posttranslational Elements to Target Human Dendritic CellsSemantic proximity Read ↗

Antibody-Directed Targeting of Retroviral Vectors via Cell Surface AntigensSemantic proximity Read ↗

DARPins: An Efficient Targeting Domain for Lentiviral VectorsSemantic proximity Read ↗

Human Immunodeficiency Virus Type 1-Derived Lentivirus Vectors Pseudotyped with Envelope Glycoproteins Derived from Ross River Virus and Semliki Forest VirusSemantic proximity Read ↗

Pseudotyping lentiviral vectors with the wild-type measles virus glycoproteins improves titer and selectivitySemantic proximity Read ↗

The Dual-Pseudotyped Lentiviral Vector with VSV-G and Sendai Virus HN Enhances Infection Efficiency through the Synergistic Effect of the Envelope ProteinsSemantic proximity Read ↗

DC-SIGN as a receptor for phleboviruses.Semantic proximity Read ↗

Differential Use of the C‐Type Lectins L‐<scp>SIGN</scp> and <scp>DC‐SIGN</scp> for Phlebovirus EndocytosisSemantic proximity Read ↗

Targeted Cell Entry of Lentiviral VectorsSemantic proximity Read ↗

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