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

In vivo manipulation of gene expression in non-human primates using lentiviral vectors as delivery vehicles

25 Jun 2009

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to RNA Interference and Gene Delivery
Share to Viral gastroenteritis research and epidemiology
Share to Virus-based gene therapy research

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 19559089
DOI: 10.1016/j.ymeth.2009.06.004

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

In vivo manipulation of gene expression in non-human primates using lentiviral vectors as delivery vehiclesPMID 19559089Read ↗

Lentiviruses as gene transfer agents for delivery to non-dividing cellsSemantic proximity Read ↗

Stable gene transfer to the nervous system using a non-primate lentiviral vectorSemantic proximity Read ↗

Lentiviruses in gene therapy clinical researchSemantic proximity Read ↗

The Era of Gene Therapy: The Advancement of Lentiviral Vectors and Their PseudotypingSemantic proximity Read ↗

The Inside Out of Lentiviral VectorsSemantic proximity Read ↗

The Era of Gene Therapy: The Advancement of Lentiviral Vectors and its PseudotypingSemantic proximity Read ↗

Viral Vectors in Gene TherapySemantic proximity Read ↗

Engineering targeted viral vectors for gene therapySemantic proximity Read ↗

Viral vectors for gene delivery to the central nervous systemSemantic proximity Read ↗

Progress and problems with the use of viral vectors for gene therapySemantic proximity Read ↗

Surface engineering of lentiviral vectors for gene transfer into gene therapy target cellsSemantic proximity Read ↗

Gene Therapy with Viral VectorsSemantic proximity Read ↗

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