Hypothalamic loss of Snord116 recapitulates the hyperphagia of Prader-Willi syndrome-Reference-Cited by-同舟云学术

Hypothalamic loss of Snord116 recapitulates the hyperphagia of Prader-Willi syndrome

Published:2018-01-29 Issue:3 Volume:128 Page:960-969
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:

Author:

Polex-Wolf Joseph,Lam Brian Y.H.,Larder Rachel,Tadross John^ORCID,Rimmington Debra,Bosch Fàtima,Cenzano Verónica Jiménez,Ayuso Eduard,Ma Marcella K.L.,Rainbow Kara^ORCID,Coll Anthony P.,O’Rahilly Stephen,Yeo Giles S.H.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Link

https://www.jci.org/articles/view/97007/files/pdf

Reference57 articles.

1. Prader-Willi syndrome

2. Prevalence of, and risk factors for, physical ill-health in people with Prader-Willi syndrome: a population-based study

3. Nutritional phases in Prader-Willi syndrome;Miller;Am J Med Genet A,2011

4. Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster

5. Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader–Willi syndrome

Cited by 85 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Newly developed oral bioavailable EHMT2 inhibitor as a potential epigenetic therapy for Prader-Willi syndrome;Molecular Therapy;2024-08

2. Similar metabolic pathways are affected in both Congenital Myasthenic Syndrome-22 and Prader-Willi Syndrome;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2024-06

3. SNORA69 is up-regulated in the lateral habenula of individuals with major depressive disorder;Scientific Reports;2024-04-09

4. Neuromodulation for the treatment of Prader-Willi syndrome – A systematic review;Neurotherapeutics;2024-04

5. Microglial phagolysosome dysfunction and altered neural communication amplify phenotypic severity in Prader-Willi Syndrome with larger deletion;Acta Neuropathologica;2024-03-31