scispace - formally typeset
O

Olivier Lichtarge

Researcher at Baylor College of Medicine

Publications -  198
Citations -  14363

Olivier Lichtarge is an academic researcher from Baylor College of Medicine. The author has contributed to research in topics: Gene & G protein-coupled receptor. The author has an hindex of 50, co-authored 184 publications receiving 12145 citations. Previous affiliations of Olivier Lichtarge include University of California, San Francisco & Boston Children's Hospital.

Papers
More filters
Journal ArticleDOI

Comprehensive and Integrative Genomic Characterization of Hepatocellular Carcinoma

Adrian Ally, +235 more
- 15 Jun 2017 - 
TL;DR: Integrative molecular HCC subtyping incorporating unsupervised clustering of five data platforms identified three subtypes, one of which was associated with poorer prognosis in three HCC cohorts and development of a p53 target gene expression signature correlating with poor survival was enabled.
Journal ArticleDOI

An evolutionary trace method defines binding surfaces common to protein families

TL;DR: The evolutionary trace method is a systematic, transparent and novel predictive technique that identifies active sites and functional interfaces in proteins with known structure and provides an evolutionary perspective for judging the functional or structural role of each residue in protein structure.
Journal ArticleDOI

A large-scale evaluation of computational protein function prediction

Predrag Radivojac, +107 more
- 01 Mar 2013 - 
TL;DR: Today's best protein function prediction algorithms substantially outperform widely used first-generation methods, with large gains on all types of targets, and there is considerable need for improvement of currently available tools.
Journal ArticleDOI

β-Arrestin-dependent, G Protein-independent ERK1/2 Activation by the β2 Adrenergic Receptor

TL;DR: It is demonstrated that the β2AR can signal to ERK via a GRK5/6-β-arrestin-dependent pathway, which is independent of G protein coupling, and GRK2, membrane translocation of which requires Gβγ release upon G protein activation, was ineffective unless it was constitutively targeted to the plasma membrane by a prenylation signal.