TP53 gene
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Related entities (31)
Mentioned in (260)
Papers in which this entity is mentioned.
- A guide to transcriptomic deconvolution in cancer. (2026)
- Comprehensive repertoire of the chromosomal alteration and mutational signatures across 16 cancer types. (2026)
- Investigation of a global mouse methylome atlas reveals subtype-specific copy number alterations in pediatric cancer models. (2026)
- Integrated in vivo combinatorial functional genomics and spatial transcriptomics of tumours to decode genotype-to-phenotype relationships. (2026)
- Whole-genome landscapes of 1,364 breast cancers. (2026)
- Whole genome sequencing approach to assess homologous recombination deficiency in a pan-cancer cohort. (2026)
- Nanopore-based cell-free DNA fragmentation and methylation profiles from the cerebral spinal fluid of patients with lung cancer brain metastases. (2025)
- Stratified Medicine Pediatrics: Cell-Free DNA and Serial Tumor Sequencing Identifies Subtype-Specific Cancer Evolution and Epigenetic States. (2025)
- Extrachromosomal DNA-Driven Oncogene Spatial Heterogeneity and Evolution in Glioblastoma. (2025)
- Meta-analysis reveals differences in somatic alterations by genetic ancestry across common cancers. (2025)
- FET fusion oncoproteins disrupt physiologic DNA repair and create a targetable opportunity for ATR inhibitor therapy. (2025)
- Multigenerational cell tracking of DNA replication and heritable DNA damage. (2025)
- Tumour-wide RNA splicing aberrations generate actionable public neoantigens. (2025)
- Functional analysis of cancer-associated germline risk variants. (2025)
- Tracing the evolution of single-cell 3D genomes in Kras-driven cancers. (2025)
- MYC ecDNA promotes intratumour heterogeneity and plasticity in PDAC. (2025)
- Molecular profiling of 888 pediatric tumors informs future precision trials and data-sharing initiatives in pediatric cancer. (2024)
- CAGI, the Critical Assessment of Genome Interpretation, establishes progress and prospects for computational genetic variant interpretation methods. (2024)
- Sequence modeling and design from molecular to genome scale with Evo. (2024)
- Synthetic augmentation of cancer cell line multi-omic datasets using unsupervised deep learning. (2024)
- Insights for precision oncology from the integration of genomic and clinical data of 13,880 tumors from the 100,000 Genomes Cancer Programme. (2024)
- Analysis of 10,478 cancer genomes identifies candidate driver genes and opportunities for precision oncology. (2024)
- Alcohol exposure suppresses ribosome biogenesis and causes nucleolar stress in cranial neural crest cells. (2024)
- The Application of Long-Read Sequencing to Cancer. (2024)
- Combination of genomic instability score and TP53 status for prognosis prediction in lung adenocarcinoma. (2023)
- Comprehensive repertoire of the chromosomal alteration and mutational signatures across 16 cancer types from 10,983 cancer patients (2023)
- Heritable defects in telomere and mitotic function selectively predispose to sarcomas. (2023)
- Combined low-pass whole genome and targeted sequencing in liquid biopsies for pediatric solid tumors. (2023)
- Deterministic evolution and stringent selection during preneoplasia. (2023)
- Osteoclasts in Osteosarcoma: Mechanisms, Interactions, and Therapeutic Prospects. (2023)
- Comprehensive analysis of mutational signatures reveals distinct patterns and molecular processes across 27 pediatric cancers. (2023)
- Towards understandings of serine/arginine-rich splicing factors. (2023)
- RNA splicing dysregulation and the hallmarks of cancer. (2023)
- Chronic oligodendrocyte injury in central nervous system pathologies. (2022)
- Mapping clustered mutations in cancer reveals APOBEC3 mutagenesis of ecDNA. (2022)
- Nucleosome footprinting in plasma cell-free DNA for the pre-surgical diagnosis of ovarian cancer. (2022)
- Explainable multiview framework for dissecting spatial relationships from highly multiplexed data. (2022)
- Cell-free DNA technologies for the analysis of brain cancer. (2022)
- The pro-apoptotic Bax gene modifies susceptibility to craniofacial dysmorphology following gastrulation-stage alcohol exposure. (2022)
- Single-cell genomic variation induced by mutational processes in cancer. (2022)
- Hand2 delineates mesothelium progenitors and is reactivated in mesothelioma. (2022)
- Feasibility of whole genome and transcriptome profiling in pediatric and young adult cancers. (2022)
- Circulating Tumor DNA as a Biomarker in Patients With Stage III and IV Wilms Tumor: Analysis From a Children's Oncology Group Trial, AREN0533. (2022)
- Circulating Tumor DNA Is Associated with Response and Survival in Patients with Advanced Leiomyosarcoma. (2022)
- Integrating molecular profiles into clinical frameworks through the Molecular Oncology Almanac to prospectively guide precision oncology. (2021)
- Integrated analysis of multimodal single-cell data. (2021)
- Prospective pan-cancer germline testing using MSK-IMPACT informs clinical translation in 751 patients with pediatric solid tumors. (2021)
- Nanopore sequencing technology, bioinformatics and applications. (2021)
- Application of third-generation sequencing in cancer research. (2021)
- Evaluating the transcriptional fidelity of cancer models. (2021)
- Transcriptomic analyses of gastrulation-stage mouse embryos with differential susceptibility to alcohol. (2021)
- A Comprehensive Circulating Tumor DNA Assay for Detection of Translocation and Copy-Number Changes in Pediatric Sarcomas. (2021)
- Loss of tumor protein 53 protects against alcohol-induced facial malformations in mice and zebrafish. (2021)
- kataegis: an R package for identification and visualization of the genomic localized hypermutation regions using high-throughput sequencing. (2021)
- Biologically informed deep neural network for prostate cancer discovery. (2021)
- Accurate detection of circulating tumor DNA using nanopore consensus sequencing. (2021)
- Potential Role of S-Palmitoylation in Cancer Stem Cells of Lung Adenocarcinoma. (2021)
- Characterizing genetic intra-tumor heterogeneity across 2,658 human cancer genomes. (2021)
- Simultaneous single cell measurements of intranuclear proteins and gene expression (2021)
- Pan-cancer analysis of longitudinal metastatic tumors reveals genomic alterations and immune landscape dynamics associated with pembrolizumab sensitivity. (2021)
- Discovery of regulatory noncoding variants in individual cancer genomes by using cis-X. (2020)
- Immuno-genomic landscape of osteosarcoma. (2020)
- Genome-wide cell-free DNA mutational integration enables ultra-sensitive cancer monitoring. (2020)
- Pan-cancer analysis of whole genomes. (2020)
- Distinct Classes of Complex Structural Variation Uncovered across Thousands of Cancer Genome Graphs. (2020)
- Inferring structural variant cancer cell fraction. (2020)
- Frequency of Pathogenic Germline Variants in Cancer-Susceptibility Genes in Patients With Osteosarcoma. (2020)
- Emerging Roles of SRSF3 as a Therapeutic Target for Cancer. (2020)
- ABHD4-dependent developmental anoikis safeguards the embryonic brain. (2020)
- TGF-β/Smad3 Signalling Modulates GABA Neurotransmission: Implications in Parkinson's Disease. (2020)
- Transcriptome-Wide Regulation of Key Developmental Pathways in the Mouse Neural Tube by Prenatal Alcohol Exposure. (2020)
- Single-cell RNA landscape of intratumoral heterogeneity and immunosuppressive microenvironment in advanced osteosarcoma. (2020)
- Modification of stem cell states by alcohol and acetaldehyde. (2020)
- Effects of chronic intermittent ethanol exposure and withdrawal on neuroblastoma cell transcriptome. (2020)
- Comprehensive germline genomic profiles of children, adolescents and young adults with solid tumors. (2020)
- Longitudinal therapy monitoring of ALK-positive lung cancer by combined copy number and targeted mutation profiling of cell-free DNA. (2020)
- Provocative questions in osteosarcoma basic and translational biology: A report from the Children's Oncology Group. (2019)
- Single-Cell RNA-Seq Reveals AML Hierarchies Relevant to Disease Progression and Immunity. (2019)
- CHASMplus Reveals the Scope of Somatic Missense Mutations Driving Human Cancers. (2019)
- Super-enhancers: critical roles and therapeutic targets in hematologic malignancies. (2019)
- Passenger hotspot mutations in cancer driven by APOBEC3A and mesoscale genomic features. (2019)
- Whole-exome sequencing of cervical carcinomas identifies activating ERBB2 and PIK3CA mutations as targets for combination therapy. (2019)
- The Network of Cancer Genes (NCG): a comprehensive catalogue of known and candidate cancer genes from cancer sequencing screens. (2019)
- The mutational constraint spectrum quantified from variation in 141,456 humans (2019)
- Prenatal Particulate Air Pollution and DNA Methylation in Newborns: An Epigenome-Wide Meta-Analysis. (2019)
- The Clonal Evolution of Metastatic Osteosarcoma as Shaped by Cisplatin Treatment. (2019)
- The GenomeAsia 100K Project enables genetic discoveries across Asia. (2019)
- Whole-genome sequencing of triple-negative breast cancers in a population-based clinical study. (2019)
- Designing combination therapies with modeling chaperoned machine learning. (2019)
- Ethanol activates immune response in lymphoblastoid cells. (2019)
- Germline variants associated with leukocyte genes predict tumor recurrence in breast cancer patients. (2019)
- Genome-Informed Targeted Therapy for Osteosarcoma. (2019)
- Serial liquid biopsies for detection of treatment failure and profiling of resistance mechanisms in -rearranged lung cancer. (2019)
- Assessment of tumor mutation burden calculation from gene panel sequencing data. (2019)
- The role and robustness of the Gini coefficient as an unbiased tool for the selection of Gini genes for normalising expression profiling data. (2019)
- RNA sequence analysis reveals macroscopic somatic clonal expansion across normal tissues. (2019)
- Recurrent noncoding U1 snRNA mutations drive cryptic splicing in SHH medulloblastoma. (2019)
- A Compendium of Mutational Signatures of Environmental Agents. (2019)
- Hippocampal deficits in neurodevelopmental disorders. (2019)
- Pan-cancer whole-genome analyses of metastatic solid tumours. (2019)
- Alcohol and endogenous aldehydes damage chromosomes and mutate stem cells. (2018)
- The Cancer Spliceome: Reprograming of Alternative Splicing in Cancer. (2018)
- Driver Fusions and Their Implications in the Development and Treatment of Human Cancers. (2018)
- Pan-cancer genome and transcriptome analyses of 1,699 paediatric leukaemias and solid tumours. (2018)
- Rearrangement bursts generate canonical gene fusions in bone and soft tissue tumors. (2018)
- Detection of Somatic Structural Variants Enables Quantification and Characterization of Circulating Tumor DNA in Children With Solid Tumors. (2018)
- Quantification of subclonal selection in cancer from bulk sequencing data. (2018)
- Mutational processes shape the landscape of TP53 mutations in human cancer. (2018)
- Comprehensive Characterization of Cancer Driver Genes and Mutations. (2018)
- Enhanced detection of circulating tumor DNA by fragment size analysis. (2018)
- Genome doubling shapes the evolution and prognosis of advanced cancers. (2018)
- The Human Transcription Factors. (2018)
- Complex rearrangements and oncogene amplifications revealed by long-read DNA and RNA sequencing of a breast cancer cell line. (2018)
- The Immune Landscape of Cancer. (2018)
- Detection of circulating tumour DNA is associated with inferior outcomes in Ewing sarcoma and osteosarcoma: a report from the Children's Oncology Group. (2018)
- Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes. (2018)
- Tumor fraction in cell-free DNA as a biomarker in prostate cancer. (2018)
- Characterizing genetic intra-tumor heterogeneity across 2,658 human cancer genomes (2018)
- PI3K Signaling in Neurons: A Central Node for the Control of Multiple Functions. (2018)
- Clinical cancer genomic profiling by three-platform sequencing of whole genome, whole exome and transcriptome. (2018)
- Molecular profiling and sequential somatic mutation shift in hypermutator tumours harbouring POLE mutations. (2018)
- SvABA: genome-wide detection of structural variants and indels by local assembly. (2018)
- Patterns and mechanisms of structural variations in human cancer. (2018)
- Copy number signatures and mutational processes in ovarian carcinoma. (2018)
- Analysis of 100,000 human cancer genomes reveals the landscape of tumor mutational burden. (2017)
- OncoKB: A Precision Oncology Knowledge Base. (2017)
- HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational signatures. (2017)
- Universal Patterns of Selection in Cancer and Somatic Tissues. (2017)
- Integrated Molecular Meta-Analysis of 1,000 Pediatric High-Grade and Diffuse Intrinsic Pontine Glioma. (2017)
- Cerebral organoids reveal early cortical maldevelopment in schizophrenia-computational anatomy and genomics, role of FGFR1. (2017)
- One-Carbon Metabolism in Health and Disease. (2017)
- Integrative clustering of multi-level 'omic data based on non-negative matrix factorization algorithm. (2017)
- Patient-derived xenografts undergo mouse-specific tumor evolution. (2017)
- Integrated analysis of gene expression and copy number identified potential cancer driver genes with amplification-dependent overexpression in 1,454 solid tumors. (2017)
- A Next Generation Connectivity Map: L1000 Platform and the First 1,000,000 Profiles. (2017)
- Mutational landscape of metastatic cancer revealed from prospective clinical sequencing of 10,000 patients. (2017)
- CScape: a tool for predicting oncogenic single-point mutations in the cancer genome. (2017)
- Scalable whole-exome sequencing of cell-free DNA reveals high concordance with metastatic tumors. (2017)
- Transcriptome Profiling Identifies Ribosome Biogenesis as a Target of Alcohol Teratogenicity and Vulnerability during Early Embryogenesis. (2017)
- Recurrent mutation of IGF signalling genes and distinct patterns of genomic rearrangement in osteosarcoma. (2017)
- PGBD5 promotes site-specific oncogenic mutations in human tumors. (2017)
- Copy-number signatures and mutational processes in ovarian carcinoma (2017)
- Clinical Assessment and Diagnosis of Germline Predisposition to Hematopoietic Malignancies: The University of Chicago Experience. (2017)
- B lymphocytes and cancer: a love-hate relationship. (2016)
- Exploring genomic alteration in pediatric cancer using ProteinPaint. (2016)
- New insights into the generation and role of de novo mutations in health and disease. (2016)
- Association of germline variants in the APOBEC3 region with cancer risk and enrichment with APOBEC-signature mutations in tumors. (2016)
- Fragment Length of Circulating Tumor DNA. (2016)
- Landscape of somatic mutations in 560 breast cancer whole-genome sequences. (2016)
- Divergent clonal evolution of castration-resistant neuroendocrine prostate cancer. (2016)
- Development and clinical application of an integrative genomic approach to personalized cancer therapy. (2016)
- Dose-dependent teratogenicity of the synthetic cannabinoid CP-55,940 in mice. (2016)
- GenVisR: Genomic Visualizations in R. (2016)
- Establishment of human iPSC-based models for the study and targeting of glioma initiating cells. (2016)
- Genomic Characterization of Brain Metastases Reveals Branched Evolution and Potential Therapeutic Targets. (2015)
- The cell cycle regulator CCDC6 is a key target of RNA-binding protein EWS. (2015)
- Recurrent somatic mutations in regulatory regions of human cancer genomes. (2015)
- Integrative clinical genomics of advanced prostate cancer. (2015)
- Rise and fall of subclones from diagnosis to relapse in pediatric B-acute lymphoblastic leukaemia. (2015)
- ENVE: a novel computational framework characterizes copy-number mutational landscapes in colorectal cancers from African American patients. (2015)
- A Sleeping Beauty forward genetic screen identifies new genes and pathways driving osteosarcoma development and metastasis. (2015)
- Ube3a reinstatement identifies distinct developmental windows in a murine Angelman syndrome model. (2015)
- Integrative Clinical Sequencing in the Management of Refractory or Relapsed Cancer in Youth. (2015)
- Germline Mutations in Predisposition Genes in Pediatric Cancer. (2015)
- Reverse genetic screening reveals poor correlation between morpholino-induced and mutant phenotypes in zebrafish. (2015)
- Spontaneous ATM Gene Reversion in A-T iPSC to Produce an Isogenic Cell Line. (2015)
- Comprehensive genomic profiles of small cell lung cancer. (2015)
- Oncogenic fusion protein EWS-FLI1 is a network hub that regulates alternative splicing. (2015)
- MBASED: allele-specific expression detection in cancer tissues and cell lines. (2014)
- Unraveling the clonal hierarchy of somatic genomic aberrations. (2014)
- RADIA: RNA and DNA integrated analysis for somatic mutation detection. (2014)
- MAGeCK enables robust identification of essential genes from genome-scale CRISPR/Cas9 knockout screens. (2014)
- CDK9-mediated transcription elongation is required for MYC addiction in hepatocellular carcinoma. (2014)
- Programming of neural cells by (endo)cannabinoids: from physiological rules to emerging therapies. (2014)
- High-throughput transcriptome sequencing identifies candidate genetic modifiers of vulnerability to fetal alcohol spectrum disorders. (2014)
- PVT1 dependence in cancer with MYC copy-number increase. (2014)
- Low-dose maternal alcohol consumption: effects in the hearts of offspring in early life and adulthood. (2014)
- Effects of Acute Prenatal Exposure to Ethanol on microRNA Expression are Ameliorated by Social Enrichment. (2014)
- Genomic factors that shape craniofacial outcome and neural crest vulnerability in FASD. (2014)
- Genomic landscape of Ewing sarcoma defines an aggressive subtype with co-association of STAG2 and TP53 mutations. (2014)
- Neural crest development in fetal alcohol syndrome. (2014)
- Recurrent somatic structural variations contribute to tumorigenesis in pediatric osteosarcoma. (2014)
- An ultrasensitive method for quantitating circulating tumor DNA with broad patient coverage. (2014)
- Long noncoding RNA EWSAT1-mediated gene repression facilitates Ewing sarcoma oncogenesis. (2014)
- Involvement of p53 in the repair of DNA double strand breaks: multifaceted Roles of p53 in homologous recombination repair (HRR) and non-homologous end joining (NHEJ). (2014)
- Clonal evolution in hematological malignancies and therapeutic implications. (2014)
- TITAN: inference of copy number architectures in clonal cell populations from tumor whole-genome sequence data. (2014)
- EWS-FLI1 utilizes divergent chromatin remodeling mechanisms to directly activate or repress enhancer elements in Ewing sarcoma. (2014)
- A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP. (2014)
- The genomic landscape of the Ewing Sarcoma family of tumors reveals recurrent STAG2 mutation. (2014)
- Cancer genome landscapes. (2013)
- Neurodevelopmental alcohol exposure elicits long-term changes to gene expression that alter distinct molecular pathways dependent on timing of exposure. (2013)
- Alcohol metabolism and epigenetics changes. (2013)
- The sox family of transcription factors: versatile regulators of stem and progenitor cell fate. (2013)
- Integrative analysis of complex cancer genomics and clinical profiles using the cBioPortal. (2013)
- Signatures of mutational processes in human cancer. (2013)
- A rare population of CD24(+)ITGB4(+)Notch(hi) cells drives tumor propagation in NSCLC and requires Notch3 for self-renewal. (2013)
- Mutational heterogeneity in cancer and the search for new cancer-associated genes. (2013)
- Integrative Genomics Viewer (IGV): high-performance genomics data visualization and exploration. (2013)
- Novel oncogenic PDGFRA mutations in pediatric high-grade gliomas. (2013)
- Emerging landscape of oncogenic signatures across human cancers. (2013)
- Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas. (2013)
- RNA splicing: a new player in the DNA damage response. (2013)
- Computational approaches to identify functional genetic variants in cancer genomes. (2013)
- Proteomic and bioinformatic analysis of mammalian SWI/SNF complexes identifies extensive roles in human malignancy. (2013)
- The genomic landscape of hypodiploid acute lymphoblastic leukemia. (2013)
- Forebrain and hindbrain development in zebrafish is sensitive to ethanol exposure involving agrin, Fgf, and sonic hedgehog function. (2013)
- Pan-cancer patterns of somatic copy number alteration. (2013)
- Predicting the functional, molecular, and phenotypic consequences of amino acid substitutions using hidden Markov models. (2013)
- The Aplnr GPCR regulates myocardial progenitor development via a novel cell-non-autonomous, Gα(i/o) protein-independent pathway. (2012)
- Absolute quantification of somatic DNA alterations in human cancer. (2012)
- High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencing. (2012)
- Molecular genetics of B-precursor acute lymphoblastic leukemia. (2012)
- Integrative analysis reveals relationships of genetic and epigenetic alterations in osteosarcoma. (2012)
- Mutational processes molding the genomes of 21 breast cancers. (2012)
- Novel mutations target distinct subgroups of medulloblastoma. (2012)
- Patient-derived tumour xenografts as models for oncology drug development. (2012)
- Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations. (2012)
- Examination of a palatogenic gene program in zebrafish. (2011)
- A small-molecule smoothened agonist prevents glucocorticoid-induced neonatal cerebellar injury. (2011)
- A hippocampal insulin-growth factor 2 pathway regulates the extinction of fear memories. (2011)
- BRCA1 and BRCA2: different roles in a common pathway of genome protection. (2011)
- Rbfox-regulated alternative splicing is critical for zebrafish cardiac and skeletal muscle functions. (2011)
- Role of ubiquitin-proteasome-mediated proteolysis in nervous system disease. (2011)
- Functional consequences of developmentally regulated alternative splicing. (2011)
- Cranial neural crest cells on the move: their roles in craniofacial development. (2011)
- Mechanisms and consequences of alternative polyadenylation. (2011)
- Agrin function associated with ocular development is a target of ethanol exposure in embryonic zebrafish. (2011)
- Molecular mechanisms of long noncoding RNAs. (2011)
- Molecular insights into the pathogenesis of Alzheimer's disease and its relationship to normal aging. (2011)
- Allele-specific copy number analysis of tumors. (2010)
- The role of zinc in the modulation of neuronal proliferation and apoptosis. (2010)
- Linking functional decline of telomeres, mitochondria and stem cells during ageing. (2010)
- Craniofacial birth defects: The role of neural crest cells in the etiology and pathogenesis of Treacher Collins syndrome and the potential for prevention. (2010)
- Condensin complexes regulate mitotic progression and interphase chromatin structure in embryonic stem cells. (2010)
- Network of Cancer Genes: a web resource to analyze duplicability, orthology and network properties of cancer genes. (2010)
- Dyrk1A overexpression inhibits proliferation and induces premature neuronal differentiation of neural progenitor cells. (2010)
- The role of NOX enzymes in ethanol-induced oxidative stress and apoptosis in mouse embryos. (2010)
- Cellular metabolic stress: considering how cells respond to nutrient excess. (2010)
- Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. (2009)
- DNA methylation and methyl-CpG binding proteins: developmental requirements and function. (2009)
- Cancer-specific high-throughput annotation of somatic mutations: computational prediction of driver missense mutations. (2009)
- Activity-dependent neuroprotective protein-derived peptide, NAP, preventing alcohol-induced apoptosis in fetal brain of C57BL/6 mouse. (2009)
- MicroRNA Mirn140 modulates Pdgf signaling during palatogenesis. (2008)
- Modeling the impact of alcohol on cortical development in a dish: strategies from mapping neural stem cell fate. (2008)
- Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results. (2008)
- MMEJ repair of double-strand breaks (director's cut): deleted sequences and alternative endings. (2008)
- Effect of in utero and early-life conditions on adult health and disease. (2008)
- Competing interactions between micro-RNAs determine neural progenitor survival and proliferation after ethanol exposure: evidence from an ex vivo model of the fetal cerebral cortical neuroepithelium. (2007)
- MDM2 and MDM4: p53 regulators as targets in anticancer therapy. (2007)
- Neuroadaptations in human chronic alcoholics: dysregulation of the NF-kappaB system. (2007)
- Defects in embryonic neurogenesis and initial synapse formation in the forebrain of the Ts65Dn mouse model of Down syndrome. (2007)
- Choline: critical role during fetal development and dietary requirements in adults. (2006)
- Accurate and reliable high-throughput detection of copy number variation in the human genome. (2006)
- SNPs3D: candidate gene and SNP selection for association studies. (2006)
- Akt phosphorylation of p300 at Ser-1834 is essential for its histone acetyltransferase and transcriptional activity. (2005)
- Mammalian WDR12 is a novel member of the Pes1-Bop1 complex and is required for ribosome biogenesis and cell proliferation. (2005)
- Identification of cardiac malformations in mice lacking Ptdsr using a novel high-throughput magnetic resonance imaging technique. (2004)
- Identification of a small molecule inhibitor of the hedgehog signaling pathway: effects on basal cell carcinoma-like lesions. (2003)
- Transposable elements: targets for early nutritional effects on epigenetic gene regulation. (2003)
Merged raw entities (4)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| tp53 | gene | 260 | 1125 |
| p53kd | gene | — | — |
| p53 knockdown | gene | — | — |
| tumor protein p53 | gene | — | — |