about
CIViC is a community knowledgebase for expert crowdsourcing the clinical interpretation of variants in cancerEvaluation of Selected CYP51A1 Polymorphisms in View of Interactions with Substrate and Redox Partner.Succession of transiently active tumor-initiating cell clones in human pancreatic cancer xenografts.Giant desmoplastic cutaneous squamous cell carcinoma of the gluteal region.ChiPPI: a novel method for mapping chimeric protein-protein interactions uncovers selection principles of protein fusion events in cancer.Transcriptome modeling and phenotypic assays for cancer precision medicine.Characterisation of the novel deleterious RAD51C p.Arg312Trp variant and prioritisation criteria for functional analysis of RAD51C missense changes.A new twist in the coil: functions of the coiled-coil domain of structural maintenance of chromosome (SMC) proteins.HIT'nDRIVE: patient-specific multidriver gene prioritization for precision oncology.Similarity in gene-regulatory networks suggests that cancer cells share characteristics of embryonic neural cells.GenProBiS: web server for mapping of sequence variants to protein binding sites.Mutational landscape of metastatic cancer revealed from prospective clinical sequencing of 10,000 patients.Pancreatic Islet Protein Complexes and Their Dysregulation in Type 2 DiabetesIdentification and analysis of mutational hotspots in oncogenes and tumour suppressors.Breast cancer risk and germline genomic profiling of women with neurofibromatosis type 1 who developed breast cancer.Diagnostic value of CA19.9, circulating tumour DNA and circulating tumour cells in patients with solid pancreatic tumours.A PanorOmic view of personal cancer genomes.Prominent features of the amino acid mutation landscape in cancer.Copy number rather than epigenetic alterations are the major dictator of imprinted methylation in tumors.MELK is not necessary for the proliferation of basal-like breast cancer cells.Influence of DPH1 and DPH5 Protein Variants on the Synthesis of Diphthamide, the Target of ADPRibosylating Toxins.Resources for Interpreting Variants in Precision Genomic Oncology Applications.High mRNA expression of splice variant SYK short correlates with hepatic disease progression in chemonaive lymph node negative colon cancer patients.The ISB Cancer Genomics Cloud: A Flexible Cloud-Based Platform for Cancer Genomics Research.Improved prediction of breast cancer outcome by identifying heterogeneous biomarkers.SCENIC: single-cell regulatory network inference and clustering.Cancer-associated arginine-to-histidine mutations confer a gain in pH sensing to mutant proteins.Comprehensive bioinformatics analysis of the characterization and determination underlying mechanisms of over-expression and co-expression of genes residing on 20q in colorectal cancer.Ensemble-based modeling and rigidity decomposition of allosteric interaction networks and communication pathways in cyclin-dependent kinases: Differentiating kinase clients of the Hsp90-Cdc37 chaperone.Breast cancer: The translation of big genomic data to cancer precision medicine.MeT-DB V2.0: elucidating context-specific functions of N6-methyl-adenosine methyltranscriptome.iUUCD 2.0: an update with rich annotations for ubiquitin and ubiquitin-like conjugations.RMBase v2.0: deciphering the map of RNA modifications from epitranscriptome sequencing data.CRISPR-Mediated Base Editing Enables Efficient Disruption of Eukaryotic Genes through Induction of STOP Codons.Genomic analysis of the origins and evolution of multicentric diffuse lower-grade gliomas.Tumor-associated DNA mutation detection in individuals undergoing colonoscopy.VarCards: an integrated genetic and clinical database for coding variants in the human genome.The Dark Side of the Epitranscriptome: Chemical Modifications in Long Non-Coding RNAs.Perturbation of PALB2 function by the T413S mutation found in small cell lung cancer.Therapeutic target database update 2018: enriched resource for facilitating bench-to-clinic research of targeted therapeutics.
P2860
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P2860
description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年学术文章
@wuu
2016年学术文章
@zh-cn
2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
@yue
2016年學術文章
@zh
2016年學術文章
@zh-hant
name
COSMIC: somatic cancer genetics at high-resolution.
@en
COSMIC: somatic cancer genetics at high-resolution.
@nl
type
label
COSMIC: somatic cancer genetics at high-resolution.
@en
COSMIC: somatic cancer genetics at high-resolution.
@nl
prefLabel
COSMIC: somatic cancer genetics at high-resolution.
@en
COSMIC: somatic cancer genetics at high-resolution.
@nl
P2093
P2860
P50
P356
P1476
COSMIC: somatic cancer genetics at high-resolution.
@en
P2093
Chai Yin Kok
Charlotte G Cole
David Beare
Elisabeth Dawson
Harry Boutselakis
Laura Ponting
Mingming Jia
Nidhi Bindal
Peter J Campbell
P2860
P304
P356
10.1093/NAR/GKW1121
P407
P577
2016-11-28T00:00:00Z