| Alternative splicing: a bioinformatics perspective |
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| Alternative splicing and genetic diversity: silencers are more frequently modified by SNVs associated with alternative exon/intron borders |
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| Alternative splicing enriched cDNA libraries identify breast cancer-associated transcripts |
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| AMIN domains have a predicted role in localization of diverse periplasmic protein complexes. |
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| Analysis of allelic differential expression in the human genome using allele-specific serial analysis of gene expression tags |
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| An anatomy of normal and malignant gene expression |
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| Assessment of somatic mutations in urine and plasma of Wilms tumor patients |
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| Automatic correspondence of tags and genes (ACTG): a tool for the analysis of SAGE, MPSS and SBS data. |
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| A bioinformatics analysis of alternative exon usage in human genes coding for extracellular matrix proteins |
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| Bioinformatics Analysis of the Human Surfaceome Reveals New Targets for a Variety of Tumor Types |
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| Building comprehensive MS-friendly databases for proteomic analysis of bacterial species of unknown genetic background |
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| Characterization of a cancer/testis (CT) antigen gene family capable of eliciting humoral response in cancer patients |
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| Complex Landscape of Germline Variants in Brazilian Patients With Hereditary and Early Onset Breast Cancer. |
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| A comprehensive in silico expression analysis of RNA binding proteins in normal and tumor tissue: Identification of potential players in tumor formation. |
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| The correlation between introns and the three-dimensional structure of proteins |
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| Delta-interacting protein A and the origin of hepatitis delta antigen |
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| Detection and evaluation of intron retention events in the human transcriptome. |
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| Different evolutionary strategies for the origin of caspase-1 inhibitors |
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| Dissecting the human spliceosome through bioinformatics and proteomics approaches |
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| Distinct patterns of somatic alterations in a lymphoblastoid and a tumor genome derived from the same individual |
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| Distribution and linkage disequilibrium of the enhancer SNP rs5758550 among Latin American populations: influence of continental ancestry |
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| Do introns favor or avoid regions of amino acid conservation? |
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| Domain shuffling and the increasing complexity of biological networks |
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| The emergence of a synthetic theory of intron evolution |
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| Essential Saccharomyces cerevisiae genome instability suppressing genes identify potential human tumor suppressors |
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| Evidence of Sleep Cycle Analogous to Vertebrate SWS/REM Alternation in the Octopus |
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| Evolutionary history of exon shuffling |
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| Exome Sequencing of Native Populations From the Amazon Reveals Patterns on the Peopling of South America |
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| Exon shuffling and the origin of the mitochondrial targeting function in plant cytochrome c1 precursor |
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| Exploiting ESTs in human health |
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| The FAPESP/LICR Human Cancer Genome Project: Perspectives on Integration |
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| Gene copy-number polymorphism caused by retrotransposition in humans |
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| Gene expression arrays in cancer research: methods and applications |
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| The generation and utilization of a cancer-oriented representation of the human transcriptome by using expressed sequence tags |
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| A genetic network that suppresses genome rearrangements in Saccharomyces cerevisiae and contains defects in cancers |
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| Genome-wide identification of cancer/testis genes and their association with prognosis in a pan-cancer analysis |
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| A genomic case study of desmoplastic small round cell tumor: comprehensive analysis reveals insights into potential therapeutic targets and development of a monitoring tool for a rare and aggressive disease. |
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| A goleada de Darwin: sobre o debate criacionismo/darwinismo |
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| The H-Invitational Database (H-InvDB), a comprehensive annotation resource for human genes and transcripts |
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| High-throughput sequencing of a South American Amerindian |
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| The Human Anatomic Gene Expression Library (H-ANGEL), the H-Inv integrative display of human gene expression across disparate technologies and platforms |
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| The human cell surfaceome of breast tumors |
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| Human gene discovery through experimental definition of transcribed regions of the human genome |
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| Identification and complete sequencing of novel human transcripts through the use of mouse orthologs and testis cDNA sequences. |
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| Identification of 9 novel transcripts and two RGSL genes within the hereditary prostate cancer region (HPC1) at 1q25. |
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| Identification of FAM46D as a novel cancer/testis antigen using EST data and serological analysis. |
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| Identification of human exons overexpressed in tumors through the use of genome and expressed sequence data |
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| Identification of new genes associated to senescent and tumorigenic phenotypes in mesenchymal stem cells. |
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| Identification of NUDT15 gene variants in Amazonian Amerindians and admixed individuals from northern Brazil |
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| Identification of rare alternative splicing events in MS/MS data reveals a significant fraction of alternative translation initiation sites |
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| The impact of SNPs on the interpretation of SAGE and MPSS experimental data |
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| In silico comparison of the transcriptome derived from purified normal breast cells and breast tumor cell lines reveals candidate upregulated genes in breast tumor cells |
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| Influence of BRCA1 Germline Mutations in the Somatic Mutational Burden of Triple-Negative Breast Cancer |
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| Insights into gliomagenesis: systems biology unravels key pathways |
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| Integrative annotation of 21,037 human genes validated by full-length cDNA clones |
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| Interacoes macromoleculares na matriz extracelular uma abordagem bioquimica e filogenetica |
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| Intron positions correlate with module boundaries in ancient proteins |
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| Long-range heterogeneity at the 3' ends of human mRNAs |
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| Modeling cancer: integration of "omics" information in dynamic systems |
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| Modeling tumor evolutionary dynamics |
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| Mutation Detection in Tumor-Derived Cell Free DNA Anticipates Progression in a Patient With Metastatic Colorectal Cancer |
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| neoANT-HILL: an integrated tool for identification of potential neoantigens |
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| A New Approach for Identification of Cancer-related Pathways using Protein Networks and Genomic Data. |
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| NFAT1 transcription factor regulates cell cycle progression and cyclin E expression in B lymphocytes |
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| On the Impact of the Pangenome and Annotation Discrepancies While Building Protein Sequence Databases for Bacteria Proteogenomics |
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| ORESTES are enriched in rare exon usage variants affecting the encoded proteins. |
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| Origin of Genes |
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| Populational landscape of INDELs affecting transcription factor-binding sites in humans |
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| PVALB, a new Hürthle adenoma diagnostic marker identified through gene expression |
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| Relationship between “proto-splice sites” and intron phases: Evidence from dicodon analysis |
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| Resveratrol decreases the expression of genes involved in inflammation through transcriptional regulation |
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| The role of exon shuffling in shaping protein-protein interaction networks |
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| S-score: a scoring system for the identification and prioritization of predicted cancer genes |
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| A score system for quality evaluation of RNA sequence tags: an improvement for gene expression profiling |
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| Sense-antisense pairs in mammals: functional and evolutionary considerations |
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| Sequence features responsible for intron retention in human |
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| Sex-biased gene expression in the frontal cortex of common marmosets (Callithrix jacchus) and potential behavioral correlates |
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| Signs of ancient and modern exon-shuffling are correlated to the distribution of ancient and modern domains along proteins |
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| Splicing Express: a software suite for alternative splicing analysis using next-generation sequencing data |
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| Splicing factors are differentially expressed in tumors |
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| SPLOOCE: a new portal for the analysis of human splicing variants. |
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| SurfaceomeDB: a cancer-orientated database for genes encoding cell surface proteins |
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| Systematic detection of putative tumor suppressor genes through the combined use of exome and transcriptome sequencing |
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| Testing for natural selection in human exonic splicing regulators associated with evolutionary rate shifts |
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| A tool for integrating genetic and mass spectrometry-based peptide data: Proteogenomics Viewer: PV: A genome browser-like tool, which includes MS data visualization and peptide identification parameters |
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| A transcript finishing initiative for closing gaps in the human transcriptome |
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| Transcriptome-guided characterization of genomic rearrangements in a breast cancer cell line |
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| Uncovering association networks through an eQTL analysis involving human miRNAs and lincRNAs |
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| Whole Genome Sequencing of the Pirarucu (Arapaima gigas) Supports Independent Emergence of Major Teleost Clades |
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| XPA deficiency affects the ubiquitin-proteasome system function |
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| The Yeast Splice Site Revisited: New Exon Consensus from Genomic Analysis |
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