Using
CRISPR-Mhdcas13c
Prader-Willi syndrome
RNA detection
Sno-lncRNA3
Sno-lncRNAs
diagnostic marker
dried blood spot
whole blood samples
Journal
RNA biology
ISSN: 1555-8584
Titre abrégé: RNA Biol
Pays: United States
ID NLM: 101235328
Informations de publication
Date de publication:
01 2023
01 2023
Historique:
medline:
7
7
2023
pubmed:
5
7
2023
entrez:
5
7
2023
Statut:
ppublish
Résumé
The genetic disorder Prader-Willi syndrome (PWS) is mainly caused by the loss of multiple paternally expressed genes in chromosome 15q11-q13 (the PWS region). Early diagnosis of PWS is essential for timely treatment, leading to effectively easing some clinical symptoms. Molecular approaches for PWS diagnosis at the DNA level are available, but the diagnosis of PWS at the RNA level has been limited. Here, we show that a cluster of paternally transcribed snoRNA-ended long noncoding RNAs (
Identifiants
pubmed: 37405372
doi: 10.1080/15476286.2023.2230406
pmc: PMC10324448
doi:
Substances chimiques
RNA, Long Noncoding
0
RNA, Small Nucleolar
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
419-430Références
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