Gene · 5205
Papers1,828
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
1 to 20 of 1,828
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Genetic and clinical spectrum of progressive familial intrahepatic cholestasis type 1: novel ATP8B1 variants and genotype-phenotype correlations. | Eur J Pediatr | 2026 | 42760445 | PubTator, text mining | PubMed |
| Novel genetic variants and atypical phenotypes in pediatric progressive familial intrahepatic cholestasis. | Pediatr Res | 2026 | 42754724 | PubTator, text mining | PubMed |
| Subtype-Dependent Transcriptional Coupling Between DNMT1 and E2F-Linked Proliferative Programs in Breast Cancer: A Dual-Cohort Transcriptomic Analysis. | J Cancer | 2026 | 42741635 | PubTator, text mining | PubMed |
| TFAP2B and FOXC1 are associated with biologically and clinically distinct differentiation states in triple-negative breast cancer. | Sci Rep | 2026 | 42728354 | PubTator, text mining | PubMed |
| A comparative evaluation of quantum machine learning architectures for breast cancer classification using clinical and genomic data. | Front Artif Intell | 2026 | 42591753 | PubTator, text mining | PubMed |
| Use of Next-Generation Sequencing and Whole-Exome Sequencing in the Diagnosis of Adult-Onset Familial Intrahepatic Cholestasis: Challenges in Interpreting Variants of Uncertain Significance. | Diagnostics (Basel) | 2026 | 42587573 | PubTator, text mining | PubMed |
| Tertiary lymphoid structure transcriptomic signatures show limited and cohort-dependent value for predicting axillary nodal involvement in oestrogen receptor-positive luminal breast cancer. | Anticancer Drugs | 2026 | 42542556 | PubTator, text mining | PubMed |
| Multi-omic Profiling of Recurrence Risk Across Breast Cancer Subtypes. | medRxiv | 2026 | 42528523 | PubTator, text mining | PubMed |
| Mechanistic Insights into Autoinhibition of the Human Flippase ATP8B1. | J Membr Biol | 2026 | 42517958 | PubTator, text mining | PubMed |
| Case Report: Recurrent intrahepatic cholestasis: two rare cases with their novel variants of ATB8B1 and atypical clinical findings. | Front Med (Lausanne) | 2026 | 42500542 | PubTator, text mining | PubMed |
| Adult-Onset BAAT p.Glu401Asp Mutation Linking Intrahepatic Cholestasis of Pregnancy to FXR-SREBP Dysregulation. | J Clin Exp Hepatol | 2026 | 42495515 | PubTator, text mining | PubMed |
| Genotype-Phenotype Correlations of Monoallelic PFIC Variants in Pediatric Liver Disease: A Multicenter Retrospective Cohort Study. | Am J Med Genet A | 2026 | 42477309 | PubTator, text mining | PubMed |
| The toxin-antitoxin complex Fic-1-AntF functions as a deAMPylase that regulates the activity of DNA gyrase. | mLife | 2026 | 42394850 | PubTator, text mining | PubMed |
| Cell-cell junction gene signatures as subtype-specific prognostic biomarkers in breast cancer. | PLoS One | 2026 | 42371976 | PubTator, text mining | PubMed |
| Domain-Level Distribution of Pathogenic BRCA1/2 Somatic Mutations Shows No Evidence of Large Subtype-Specific Enrichment in Breast Cancer: A Three-Cohort Analysis Supporting Broad BRCA Testing. | Genes (Basel) | 2026 | 42353852 | PubTator, text mining | PubMed |
| Use of genetic analysis in adult cholestatic liver disease: lessons from progressive paediatric syndromes and cohort studies. | Gut | 2026 | 42309808 | PubTator, text mining | PubMed |
| Searching for New Genes That Cause Usher Syndrome. | Am J Ophthalmol | 2026 | 42309414 | PubTator, text mining | PubMed |
| CBFB mutations predict endocrine therapy benefit in estrogen receptor-positive breast cancer. | medRxiv | 2026 | 42238456 | PubTator, text mining | PubMed |
| Tumor hypoxia is associated with global copy-number alteration burden and subtype-dependent overall survival in breast cancer: Evidence from TCGA and METABRIC. | PLoS One | 2026 | 42228744 | PubTator, text mining | PubMed |
| A Cross-Species Single-Cell Atlas Reveals Conserved Regulatory Networks and Candidate Hearing Loss Genes in the Cochlea. | Genes (Basel) | 2026 | 42074555 | PubTator, text mining | PubMed |
gene-search-2026-11-11-0.2.0
Sources 12
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ChEMBL, through Open TargetsCC BY-SA 3.0
- ClinicalTrials.govNo license stated
- EMBL-EBI's patent proteinsNo added restrictions. Attribution expected
- GenBank's patent filesNo restrictions from NCBI. Submitters may hold rights
- HGNCCC0
- NCBI GenePublic domain (US government)
- NIH's project files and grant-paper linksPublic domain
- Open TargetsCC0 1.0
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- ClinicalTrials.govnone stated
- EMBL-EBI's patent proteinsEMBL-EBI's patent protein files from the EPO, JPO, KIPO and USPTO. EMBL-EBI: "EMBL-EBI itself places no additional restrictions on the use or redistribution of the data available via its Data Resources and Tools other than those provided by the original data owners" and "EMBL-EBI expects attribution (e.g. in publications, services or products) for the use of any of its Data Resources and Tools." Read on 11 Nov 2026 at https://www.ebi.ac.uk/about/terms-of-use
- GenBank's patent filesGenBank's patent files. NCBI: "NCBI places no restrictions on the use or distribution of the GenBank data. However, some submitters may claim patent, copyright, or other intellectual property rights in all or a portion of the data they have submitted." Read on 11 Nov 2026 at https://www.ncbi.nlm.nih.gov/genbank/about/
- HGNCCC0: https://www.genenames.org/about/license/
- NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- NIH's project files and grant-paper linksPublic domain (NIH RePORTER)
- Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
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