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Steven P. Gygi

Researcher at Harvard University

Publications -  778
Citations -  147003

Steven P. Gygi is an academic researcher from Harvard University. The author has contributed to research in topics: Proteome & Phosphorylation. The author has an hindex of 172, co-authored 704 publications receiving 129173 citations. Previous affiliations of Steven P. Gygi include University of Rochester Medical Center & Cell Signaling Technology.

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Journal ArticleDOI

The skeletal phenotype of achondrogenesis type 1A is caused exclusively by cartilage defects

TL;DR: Conditional inactivation of the cis-Golgin GMAP-210 reveals that the skeletal phenotype in achondrogenesis type-1A, which is caused by mutations in GMap-210, is solely due to impaired protein trafficking by chondrocytes.
Posted ContentDOI

Improved Monoisotopic Mass Estimation for Deeper Proteome Coverage

TL;DR: This work presents a performant, open-source, cross-platform algorithm, Monocle, for the rapid reassignment of instrument assigned precursor peaks to monoisotopic peptide assignments and demonstrates that the present algorithm can be integrated into many common proteomics pipelines and provides rapid conversion from multiple data source types.
Patent

Non-affinity based isotope tagged peptides and methods for using the same

TL;DR: In this article, non-affinity based isotope tagged peptides, chemistries for making peptides and methods for using these peptides are described. But the peptide reagents can be used for rapid and quantitative analysis of proteins or protein function.
Journal ArticleDOI

Global proteomics of Ubqln2-based murine models of ALS.

TL;DR: The proteomic landscape of ALS-related Ubqln2 mutants is charted and candidate client proteins that are altered in vivo in disease models and whose degradation is promoted by UBQLN2 are identified.
Journal ArticleDOI

Rixosomal RNA degradation contributes to silencing of Polycomb target genes

TL;DR: In this article , the rixosome contributes to silencing of many Polycomb targets in human cells and is enriched at promoters of Polycomb target genes, suggesting that direct recruitment of the RIXosome to chromatin is required for silencing.