F. Desmet

发表

Human Splicing Finder: an online bioinformatics tool to predict splicing signals

C. Béroud, D. Hamroun, M. Claustres, 2009, Nucleic acids research.

Bioinformatics identification of splice site signals and prediction of mutation effects

Christophe Béroud, Mireille Claustres, C. Béroud, 2010 .

Identification of protein features encoded by alternative exons using Exon Ontology.

L. Tranchevent, E. Chautard, D. Auboeuf, 2017, Genome research.

[Genetic mutation databases: stakes and perspectives for orphan genetic diseases].

C. Béroud, D. Hamroun, M. Claustres, 2010, Pathologie-biologie.

RNA helicases DDX5 and DDX17 dynamically orchestrate transcription, miRNA, and splicing programs in cell differentiation.

L. Tranchevent, D. Auboeuf, F. Desmet, 2014, Cell reports.

A recently evolved class of alternative 3′-terminal exons involved in cell cycle regulation by topoisomerase inhibitors

D. Auboeuf, F. Desmet, H. Mortada, 2014, Nature Communications.

Endothelial, epithelial, and fibroblast cells exhibit specific splicing programs independently of their tissue of origin

L. Tranchevent, E. Chautard, D. Auboeuf, 2014, Genome research.

Genotype–phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD–DMD database: a model of nationwide knowledgebase

Christophe Béroud, Jamel Chelly, Mireille Claustres, 2009, Human mutation.

Thus, further studies of promoter and alternative splicing SNPs and altered BAFF expression in cGVHD are warranted.

C. Béroud, D. Hamroun, M. Claustres, 2017 .

Bioinformatics and mutations leading to exon skipping.

C Béroud, C. Béroud, F. Desmet, 2012, Methods in molecular biology.