dbCRID

Names

More detailed information about this field from each metasource. ×

dbCRID

metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657

metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:28.075035

---

dbcrid

metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:28.075035

Close

Other names: dbcrid

Database of Chromosomal Rearrangements In Diseases

Webpage:

Publications:

Publications

More detailed information about this field from each metasource. ×

dbCRID: a database of chromosomal rearrangements in human diseases
PMID: 21051346

metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:28.075035

---

http://nar.oxfordjournals.org/content/39/suppl_1/D895

metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657

Close

• dbCRID: a database of chromosomal rearrangements in human diseases PubMed citations: 29.

  29 articles citing: dbCRID: a database of chromosomal rearrangements in human diseases

  ×

  Mechanism for inverted-repeat recombination induced by a replication fork barrier. PMID:35013185

  ---

  Chromosomal abnormality, laboratory techniques, tools and databases in molecular Cytogenetics. PMID:33104991

  ---

  Human transcription factor and protein kinase gene fusions in human cancer. PMID:32843691

  ---

  ChiTaRS 5.0: the comprehensive database of chimeric transcripts matched with druggable fusions and 3D chromatin maps. PMID:31747015

  ---

  Fusion Transcripts of Adjacent Genes: New Insights into the World of Human Complex Transcripts in Cancer. PMID:31652751

  ---

  ProtFus: A Comprehensive Method Characterizing Protein-Protein Interactions of Fusion Proteins. PMID:31437145

  ---

  HumCFS: a database of fragile sites in human chromosomes. PMID:30999860

  ---

  Parp3 promotes long-range end joining in murine cells. PMID:30213852

  ---

  Genome-wide mapping of sister chromatid exchange events in single yeast cells using Strand-seq. PMID:29231811

  ---

  Chimeric RNAs and their implications in cancer. PMID:29100211

  ---

  PARP3 is a promoter of chromosomal rearrangements and limits G4 DNA. PMID:28447610

  ---

  ChiTaRS-3.1-the enhanced chimeric transcripts and RNA-seq database matched with protein-protein interactions. PMID:27899596

  ---

  ChimerDB 3.0: an enhanced database for fusion genes from cancer transcriptome and literature data mining. PMID:27899563

  ---

  3Disease Browser: A Web server for integrating 3D genome and disease-associated chromosome rearrangement data. PMID:27734896

  ---

  RWCFusion: identifying phenotype-specific cancer driver gene fusions based on fusion pair random walk scoring method. PMID:27506935

  ---

  Discovering and understanding oncogenic gene fusions through data intensive computational approaches. PMID:27105842

  ---

  Mechanisms of Origin, Phenotypic Effects and Diagnostic Implications of Complex Chromosome Rearrangements. PMID:26732513

  ---

  Proteogenomics from a bioinformatics angle: A growing field. PMID:26670565

  ---

  FARE-CAFE: a database of functional and regulatory elements of cancer-associated fusion events. PMID:26384373

  ---

  ChiTaRS 2.1--an improved database of the chimeric transcripts and RNA-seq data with novel sense-antisense chimeric RNA transcripts. PMID:25414346

  ---

  Characterization of human chromosomal material exchange with regard to the chromosome translocations using next-generation sequencing data. PMID:25349267

  ---

  SIDD: a semantically integrated database towards a global view of human disease. PMID:24146757

  ---

  Fine mapping of V(D)J recombinase mediated rearrangements in human lymphoid malignancies. PMID:23957733

  ---

  Functional characterisation of human cells harbouring a novel t(2p;7p) translocation involving TNS3 and EXOC6B genes. PMID:23809228

  ---

  Genome-wide analysis of human hotspot intersected genes highlights the roles of meiotic recombination in evolution and disease. PMID:23368819

  ---

  Rare allelic forms of PRDM9 associated with childhood leukemogenesis. PMID:23222848

  ---

  ChiTaRS: a database of human, mouse and fruit fly chimeric transcripts and RNA-sequencing data. PMID:23143107

  ---

  Novel domain combinations in proteins encoded by chimeric transcripts. PMID:22689780

  ---

  Chimeras taking shape: potential functions of proteins encoded by chimeric RNA transcripts. PMID:22588898
• http://nar.oxfordjournals.org/content/39/suppl_1/D895

Tags:

Tags

More detailed information about this field from each metasource. ×

human genes and diseases

metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657

---

general human genetics databases

metasource: Nucleic Acid Research database catalogue
version: extracted_at: 2022-11-04T11:16:25.468657

---

pathology

metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:28.075035

---

dna

metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:28.075035

---

molecular interactions, pathways and networks

metasource: bio.tools
version: extracted_at: 2022-11-04T11:34:28.075035

Close

human genes and diseases general human genetics pathology dna molecular interactions, pathways and networks