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Now showing items 1-18 of 18
A network analysis to identify mediators of germline-driven differences in breast cancer prognosis.
An expanded evaluation of protein function prediction methods shows an improvement in accuracy
Analysis of the genome content of Lactococcus garvieae by genomic interspecies microarray hybridization
Comparative transcriptomics of human multipotent stem cells during adipogenesis and osteoblastogenesis
Computational characterization of the peptidome in transporter associated with antigen processing (TAP)-deficient cells
Conservation of coevolving protein interfaces bridges prokaryote-eukaryote homologies in the twilight zone
Data integration and exploration for the identification of molecular mechanisms in tumor-immune cells interaction
Enrichment of neural-related genes in human mesenchymal stem cells from neuroblastoma patients.
Finding gene regulatory network candidates using the gene expression knowledge base
GOplot: an R package for visually combining expression data with functional analysis
Identification of 88 regulatory small RNAs in the TIGR4 strain of the human pathogen Streptococcus pneumoniae
Integrating epigenomic data and 3D genomic structure with a new measure of chromatin assortativity
Linked Registries: Connecting Rare Diseases Patient Registries through a Semantic Web Layer
Modeling human endometrial decidualization from the interaction between proteome and secretome
Modifications in host cell cytoskeleton structure and function mediated by intracellular HIV-1 Tat protein are greatly dependent on the second coding exon
Molecular cloning and characterisation of the RESA gene, a marker of genetic diversity of Plasmodium falciparum
Recommendations for Improving the Quality of Rare Disease Registries
The RD-Connect Registry & Biobank Finder: a tool for sharing aggregated data and metadata among rare disease researchers.