Cargando…
A novel mutation in the mouse Pcsk1 gene showing obesity and diabetes
The proprotein convertase subtilisin/Kexin type 1 (PCSK1/PC1) protein processes inactive pro-hormone precursors into biologically active hormones in a number of neuroendocrine and endocrine cell types. Patients with recessive mutations in PCSK1 exhibit a complex spectrum of traits including obesity,...
Autores principales: | Muhsin, Nor I. A., Bentley, Liz, Bai, Ying, Goldsworthy, Michelle, Cox, Roger D. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7060156/ https://www.ncbi.nlm.nih.gov/pubmed/31974728 http://dx.doi.org/10.1007/s00335-020-09826-4 |
Ejemplares similares
-
Severe obesity and diabetes insipidus in a patient with PCSK1 deficiency()
por: Frank, Graeme R., et al.
Publicado: (2013) -
A Wars2 mutant mouse shows a sex and diet specific change in fat distribution, reduced food intake and depot-specific upregulation of WAT browning
por: Mušo, Milan, et al.
Publicado: (2022) -
Mouse models and the interpretation of human GWAS in type 2 diabetes and obesity
por: Cox, Roger D., et al.
Publicado: (2011) -
Monitoring type 2 diabetes from volatile faecal metabolome in Cushing’s syndrome and single Afmid mouse models via a longitudinal study
por: Lourenço, Célia, et al.
Publicado: (2019) -
Novel Homozygous Inactivating Mutation in the PCSK1 Gene in an Infant with Congenital Malabsorptive Diarrhea
por: Aerts, Laetitia, et al.
Publicado: (2021)