SnoRNA Snord116 (Pwcr1/MBII-85) deletion causes growth deficiency and hyperphagia in mice.
Prader-Willi syndrome (PWS) is the leading genetic cause of obesity. After initial severe hypotonia, PWS children become hyperphagic and morbidly obese, if intake is not restricted. Short stature with abnormal growth hormone secretion, hypogonadism, cognitive impairment, anxiety and behavior problem...
Saved in:
Main Authors: | Feng Ding, Hong Hua Li, Shengwen Zhang, Nicola M Solomon, Sally A Camper, Pinchas Cohen, Uta Francke |
---|---|
Format: | article |
Language: | EN |
Published: |
Public Library of Science (PLoS)
2008
|
Subjects: | |
Online Access: | https://doaj.org/article/4d6067e8140b4bf6b481c8dbc8f16f07 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Snord116-dependent diurnal rhythm of DNA methylation in mouse cortex
by: Rochelle L. Coulson, et al.
Published: (2018) -
snoRNA, a novel precursor of microRNA in Giardia lamblia.
by: Ashesh A Saraiya, et al.
Published: (2008) -
Human miRNA precursors with box H/ACA snoRNA features.
by: Michelle S Scott, et al.
Published: (2009) -
Nuclear fate of yeast snoRNA is determined by co-transcriptional Rnt1 cleavage
by: Pawel Grzechnik, et al.
Published: (2018) -
Discovery of tumor immune infiltration-related snoRNAs for predicting tumor immune microenvironment status and prognosis in lung adenocarcinoma
by: Rongjun Wan, et al.
Published: (2021)