Article

Applications of the PMO platform to genetic diseases

2015-01-01

Abstract excerpt

No abstract is available from the source.

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: 90eb7bab-66ab-52fa-8907-4c17116afb13
DOI: 10.1186/1750-1172-10-s2-o34
PMCID: PMC4652482

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Applications of the PMO platform to genetic diseasesDOI 10.1186/1750-1172-10-s2-o34Read

Omicron variant: Current insights and future directionsSemantic proximity Read

The characteristics of FBXO7 and its role in human diseasesSemantic proximity Read

Helicos BioSciences.Semantic proximity Read

Preparation for the challenge of heavily mutated Omicron variant.Semantic proximity Read

The phenotype and genotype experiment object model (PaGE-OM): a robust data structure for information related to DNA variation.Semantic proximity Read

Gephebase, a Database of Genotype-Phenotype Relationships for natural and domesticated variation in EukaryotesSemantic proximity Read

Function of a common FTO variant in vivo.Semantic proximity Read

Celera and Motorola brought in to aid hunt for disease genes.Semantic proximity Read

Mapping m6A and m1A with mutation signatures.Semantic proximity Read

Toward Next-Generation Phenomics: Precision Medicine, Spaceflight, Astronaut Omics, and Beyond.Semantic proximity Read

Genetic drift. "Omics"as the filtering gateway between environment and phenotype: The inflammatory bowel diseases example.Semantic proximity Read

The long walk toward the PKD1 gene. The European PKD1 Consortium.Semantic proximity Read