CTNNB1 gene

Aliases

CNTTB1, Ctnnb1, beta-catenin, ctnnb1, β-catenin

External links

NCBI Gene · Ensembl · GeneCards · UniProt

No related entities found.

Mentioned in (66)

Papers in which this entity is mentioned.

• Integrated in vivo combinatorial functional genomics and spatial transcriptomics of tumours to decode genotype-to-phenotype relationships. (2026)
• 3D spatial organization of heterogeneous nkx2.5+ progenitors in the zebrafish heart field pre-patterns cardiovascular development. (2025)
• Molecular profiling of 888 pediatric tumors informs future precision trials and data-sharing initiatives in pediatric cancer. (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)
• Combined low-pass whole genome and targeted sequencing in liquid biopsies for pediatric solid tumors. (2023)
• Multiomic prioritisation of risk genes for anorexia nervosa. (2023)
• Towards understandings of serine/arginine-rich splicing factors. (2023)
• Mapping clustered mutations in cancer reveals APOBEC3 mutagenesis of ecDNA. (2022)
• Single-cell analysis of hepatoblastoma identifies tumor signatures that predict chemotherapy susceptibility using patient-specific tumor spheroids. (2022)
• Cross-tissue transcriptome-wide association studies identify susceptibility genes shared between schizophrenia and inflammatory bowel disease. (2022)
• Single-cell genomic variation induced by mutational processes in cancer. (2022)
• Construction and validation of a novel gene signature for predicting the prognosis of osteosarcoma. (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)
• Integrated Genomic Analysis Identifies Driver Genes and Cisplatin-Resistant Progenitor Phenotype in Pediatric Liver Cancer. (2021)
• Atrial and Sinoatrial Node Development in the Zebrafish Heart. (2021)
• Inferring structural variant cancer cell fraction. (2020)
• Emerging Roles of SRSF3 as a Therapeutic Target for Cancer. (2020)
• Folding Keratin Gene Clusters during Skin Regional Specification. (2020)
• Super-enhancers: critical roles and therapeutic targets in hematologic malignancies. (2019)
• Canonical Wnt5b Signaling Directs Outlying Nkx2.5+ Mesoderm into Pacemaker Cardiomyocytes. (2019)
• De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies. (2019)
• Epigenetics and depression
. (2019)
• RNA sequence analysis reveals macroscopic somatic clonal expansion across normal tissues. (2019)
• Pan-cancer whole-genome analyses of metastatic solid tumours. (2019)
• Comprehensive Characterization of Cancer Driver Genes and Mutations. (2018)
• Mental Illnesses-Associated Fxr1 and Its Negative Regulator Gsk3β Are Modulators of Anxiety and Glutamatergic Neurotransmission. (2018)
• The Immune Landscape of Cancer. (2018)
• Characterizing genetic intra-tumor heterogeneity across 2,658 human cancer genomes (2018)
• Wnt5a is essential for hippocampal dendritic maintenance and spatial learning and memory in adult mice. (2017)
• Early pathogenic event of Alzheimer's disease documented in iPSCs from patients with PSEN1 mutations. (2017)
• Transcriptome Profiling Identifies Ribosome Biogenesis as a Target of Alcohol Teratogenicity and Vulnerability during Early Embryogenesis. (2017)
• Medulloblastoma-associated DDX3 variant selectively alters the translational response to stress. (2016)
• Small molecule inhibition of cAMP response element binding protein in human acute myeloid leukemia cells. (2016)
• Integrative clinical genomics of advanced prostate cancer. (2015)
• Early steps in inner ear development: induction and morphogenesis of the otic placode. (2015)
• The role of BAF (mSWI/SNF) complexes in mammalian neural development. (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)
• An evolutionarily conserved mechanism of calcium-dependent neurotoxicity in a zebrafish model of fetal alcohol spectrum disorders. (2014)
• Genomic factors that shape craniofacial outcome and neural crest vulnerability in FASD. (2014)
• Neural crest development in fetal alcohol syndrome. (2014)
• Cancer genome landscapes. (2013)
• The sox family of transcription factors: versatile regulators of stem and progenitor cell fate. (2013)
• Hand in glove: brain and skull in development and dysmorphogenesis. (2013)
• Proteomic and bioinformatic analysis of mammalian SWI/SNF complexes identifies extensive roles in human malignancy. (2013)
• Zebrafish models of human liver development and disease. (2013)
• LIN28B promotes growth and tumorigenesis of the intestinal epithelium via Let-7. (2013)
• Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units. (2012)
• High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencing. (2012)
• Novel mutations target distinct subgroups of medulloblastoma. (2012)
• Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. (2012)
• DISC1 at 10: connecting psychiatric genetics and neuroscience. (2011)
• Cranial neural crest cells on the move: their roles in craniofacial development. (2011)
• Epicardial-derived cell epithelial-to-mesenchymal transition and fate specification require PDGF receptor signaling. (2011)
• Mechanisms that underlie co-variation of the brain and face. (2011)
• Calcium-mediated repression of β-catenin and its transcriptional signaling mediates neural crest cell death in an avian model of fetal alcohol syndrome. (2011)
• Integrative analysis of the melanoma transcriptome. (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)
• FGF signaling regulates otic placode induction and refinement by controlling both ectodermal target genes and hindbrain Wnt8a. (2010)
• Primary contribution to zebrafish heart regeneration by gata4(+) cardiomyocytes. (2010)
• Evolution of the neocortex: a perspective from developmental biology. (2009)
• Common and rare variants in multifactorial susceptibility to common diseases. (2008)
• Adrenomedullin signaling is necessary for murine lymphatic vascular development. (2008)
• Identification of novel bone-specific molecular targets of binge alcohol and ibandronate by transcriptome analysis. (2008)
• Perlecan controls neurogenesis in the developing telencephalon. (2007)

Merged raw entities (3)

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.