Loss of MAGEL2 in Prader-Willi syndrome leads to decreased secretory granule and neuropeptide production-Reference-Cited by-同舟云学术

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Loss of MAGEL2 in Prader-Willi syndrome leads to decreased secretory granule and neuropeptide production

Published:2020-09-03 Issue:17 Volume:5 Page:
ISSN:2379-3708
Container-title:JCI Insight
language:en
Short-container-title:

Author:

Chen Helen,Victor A. Kaitlyn^ORCID,Klein Jonathon,Tacer Klementina Fon^ORCID,Tai Derek J.C.^ORCID,de Esch Celine,Nuttle Alexander,Temirov Jamshid,Burnett Lisa C.,Rosenbaum Michael,Zhang Yiying,Ding Li,Moresco James J.^ORCID,Diedrich Jolene K.^ORCID,Yates John R.^ORCID,Tillman Heather S.,Leibel Rudolph L.,Talkowski Michael E.^ORCID,Billadeau Daniel D.,Reiter Lawrence T.^ORCID,Potts Patrick Ryan

Funder

Foundation for Prader-Willi Research

National Institute of General Medical Sciences

National Institute of Diabetes and Digestive and Kidney Diseases

St. Jude Children’s Research Hospital

Eagles 5th District Cancer Telethon Funds for Cancer Research

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Link

https://insight.jci.org/articles/view/138576/files/pdf

Reference79 articles.

1. Prader–Willi syndrome

2. Prader-Willi syndrome: consensus diagnostic criteria;Holm;Pediatrics,1993

3. Loss of Magel2 impairs the development of hypothalamic Anorexigenic circuits

4. The imprinted gene Magel2 regulates normal circadian output

5. Prader–Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain

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1. Truncated variants of MAGEL2 are involved in the etiologies of the Schaaf-Yang and Prader-Willi syndromes;The American Journal of Human Genetics;2024-07

2. MAGEL2 (patho‐)physiology and Schaaf–Yang syndrome;Developmental Medicine & Child Neurology;2024-07

3. Emerging Perspectives on Prime Editor Delivery to the Brain;Pharmaceuticals;2024-06-11

4. Acquiring Social Safety Engages Oxytocin Neurons in the Supraoptic Nucleus: Role of Magel2 Deficiency;Neuroendocrinology;2024-04-04

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

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