Cargando…
Systematic proteome and proteostasis profiling in human Trisomy 21 fibroblast cells
Down syndrome (DS) is mostly caused by a trisomy of the entire Chromosome 21 (Trisomy 21, T21). Here, we use SWATH mass spectrometry to quantify protein abundance and protein turnover in fibroblasts from a monozygotic twin pair discordant for T21, and to profile protein expression in 11 unrelated DS...
Autores principales: | Liu, Yansheng, Borel, Christelle, Li, Li, Müller, Torsten, Williams, Evan G., Germain, Pierre-Luc, Buljan, Marija, Sajic, Tatjana, Boersema, Paul J., Shao, Wenguang, Faini, Marco, Testa, Giuseppe, Beyer, Andreas, Antonarakis, Stylianos E., Aebersold, Ruedi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663699/ https://www.ncbi.nlm.nih.gov/pubmed/29089484 http://dx.doi.org/10.1038/s41467-017-01422-6 |
Ejemplares similares
-
Systematic characterization of pan‐cancer mutation clusters
por: Buljan, Marija, et al.
Publicado: (2018) -
The burden of trisomy 21 disrupts the proteostasis network in Down syndrome
por: Aivazidis, Stefanos, et al.
Publicado: (2017) -
A computational framework for the inference of protein complex remodeling from whole-proteome measurements
por: Buljan, Marija, et al.
Publicado: (2023) -
The Evolving Contribution of Mass Spectrometry to Integrative Structural Biology
por: Faini, Marco, et al.
Publicado: (2016) -
DNA-Methylation Patterns in Trisomy 21 Using Cells from Monozygotic Twins
por: Sailani, M. Reza, et al.
Publicado: (2015)