Cargando…
Insulin secretion deficits in a Prader-Willi syndrome β-cell model are associated with a concerted downregulation of multiple endoplasmic reticulum chaperones
Prader-Willi syndrome (PWS) is a multisystem disorder with neurobehavioral, metabolic, and hormonal phenotypes, caused by loss of expression of a paternally-expressed imprinted gene cluster. Prior evidence from a PWS mouse model identified abnormal pancreatic islet development with retention of aged...
Autores principales: | Koppes, Erik A., Johnson, Marie A., Moresco, James J., Luppi, Patrizia, Lewis, Dale W., Stolz, Donna B., Diedrich, Jolene K., Yates, John R., Wek, Ronald C., Watkins, Simon C., Gollin, Susanne M., Park, Hyun Jung, Drain, Peter, Nicholls, Robert D. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10138222/ https://www.ncbi.nlm.nih.gov/pubmed/37068109 http://dx.doi.org/10.1371/journal.pgen.1010710 |
Ejemplares similares
-
Loss of MAGEL2 in Prader-Willi syndrome leads to decreased secretory granule and neuropeptide production
por: Chen, Helen, et al.
Publicado: (2020) -
Three Siblings with Prader-Willi Syndrome: Brief Review of Sleep and Prader-Willi Syndrome
por: Bingeliene, Arina, et al.
Publicado: (2015) -
Genetics of Prader-Willi syndrome and Prader-Will-Like syndrome
por: Cheon, Chong Kun
Publicado: (2016) -
Epigenetics in Prader-Willi Syndrome
por: Mendiola, Aron Judd P., et al.
Publicado: (2021) -
Prader-Willi Syndrome: Clinical Aspects
por: Elena, Grechi, et al.
Publicado: (2012)