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

Ex Vivo Improvement of a von Willebrand Disease Type 2A Phenotype Using an Allele-Specific Small Interfering RNA.

Thrombosis and haemostasis - 1 Nov 2020

Mannhalter Christine

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 Alleles
Share to Phenotype
Share to RNA, Small Interfering
Share to von Willebrand Disease, Type 2

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to von Willebrand Diseases

Source

Identifiers

PMID: 33086399
DOI: 10.1055/s-0040-1718412

Provenance

PubMed metadata and Literature Corpus relationships.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Ex Vivo Improvement of a von Willebrand Disease Type 2A Phenotype Using an Allele-Specific Small Interfering RNA.PMID 33086399Read ↗

Ex vivo Improvement of a von Willebrand Disease Type 2A Phenotype Using an Allele-Specific Small-Interfering RNA.Semantic proximity Read ↗

Correction of a dominant-negative von Willebrand factor multimerization defect by small interfering RNA-mediated allele-specific inhibition of mutant von Willebrand factor.Semantic proximity Read ↗

Translational medicine advances in von Willebrand diseaseSemantic proximity Read ↗

Allele-selective disruption of pathogenic VWF variants in type 2 von Willebrand disease using CRISPR/Cas9.Semantic proximity Read ↗

In vivo modulation of a dominant-negative variant in mouse models of von Willebrand disease type 2A.Semantic proximity Read ↗

Treatment of von Willebrand's Disease.Semantic proximity Read ↗

Amelioration of a von Willebrand disease type 2B phenotype in vivo upon treatment with allele-selective siRNAsSemantic proximity Read ↗

First identification and expression of a type 2N von Willebrand disease mutation (E1078K) located in exon 25 of von Willebrand factor gene.Semantic proximity Read ↗

Identification of a new nonsense mutation in the von Willebrand factor gene in patients with von Willebrand disease type III.Semantic proximity Read ↗

Small interfering RNA-mediated allele-selective silencing of von Willebrand factor in vitro and in vivo.Semantic proximity Read ↗

Impact of allele-selective silencing of von Willebrand factor in mice based on a single nucleotide allelic difference in von Willebrand factor.Semantic proximity Read ↗

Phenotype correction of hemophilia A mice by spliceosome-mediated RNA trans-splicing.Semantic proximity Read ↗

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