Gene · 8243
Papers2,883
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
141 to 160 of 2,883
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Case Report of a DDX41 Germline Mutation in a Family with Multiple Relatives Suffering from Leukemia. | Biomedicines | 2023 | 38255170 | PubTator, text mining | PubMed |
| The Heart of Rett Syndrome: A Quantitative Analysis of Cardiac Repolarization. | Cardiol Res | 2023 | 38187509 | PubTator, text mining | PubMed |
| Genome-wide CRISPRi Screen in Human iNeurons to Identify Novel Focal Cortical Dysplasia Genes. | bioRxiv | 2023 | 38168415 | PubTator, text mining | PubMed |
| Retinitis pigmentosa GTPase regulator-related retinopathy and gene therapy. | Saudi J Ophthalmol | 2023 | 38155670 | PubTator, text mining | PubMed |
| PRAME Expression: A Target for Cancer Immunotherapy and a Prognostic Factor in Uveal Melanoma. | Invest Ophthalmol Vis Sci | 2023 | 38149971 | PubTator, text mining | PubMed |
| Cornelia de Lange Syndrome Caused by an Intragenic Heterozygous Deletion in RAD21 Detected through Very-High-Resolution Chromosomal Microarray Analysis. | Genes (Basel) | 2023 | 38137034 | PubTator, text mining | PubMed |
| BRD9 determines the cell fate of hematopoietic stem cells by regulating chromatin state. | Nat Commun | 2023 | 38102116 | PubTator, text mining | PubMed |
| Early onset developmental and epileptic encephalopathy and Rett-like phenotype in a 15-year-old girl affected by Cornelia de Lange syndrome type 2 due to a SMC1A gene mutation. | Epilepsy Behav Rep | 2023 | 38076278 | PubTator, text mining | PubMed |
| Epigenetic priming of an epithelial enhancer by p63 and CTCF controls expression of a skin-restricted gene XP33. | Cell Death Discov | 2023 | 38065940 | PubTator, text mining | PubMed |
| Defining a core configuration for human centromeres during mitosis. | Nat Commun | 2023 | 38040722 | PubTator, text mining | PubMed |
| The consequences of cohesin mutations in myeloid malignancies. | Front Mol Biosci | 2023 | 38033389 | PubTator, text mining | PubMed |
| RIT1 regulates mitosis and promotes proliferation by interacting with SMC3 and PDS5 in hepatocellular carcinoma. | J Exp Clin Cancer Res | 2023 | 38017479 | PubTator, text mining | PubMed |
| Venetoclax plus hypomethylating agents in newly diagnosed acute myeloid leukemia patients with RUNX1::RUNX1T1: a retrospective propensity score matching study. | Blood Cancer J | 2023 | 38012154 | PubTator, text mining | PubMed |
| A De Novo Frameshift Mutation in RPL5 with Classical Phenotype Abnormalities and Worsening Anemia Diagnosed in a Young Adult-A Case Report and Review of the Literature. | Medicina (Kaunas) | 2023 | 38004002 | PubTator, text mining | PubMed |
| Statistical Dissection of the Genetic Determinants of Phenotypic Heterogeneity in Genes with Multiple Associated Rare Diseases. | Genes (Basel) | 2023 | 38003043 | PubTator, text mining | PubMed |
| Joint epigenome profiling reveals cell-type-specific gene regulatory programmes in human cortical organoids. | Nat Cell Biol | 2023 | 37996647 | PubTator, text mining | PubMed |
| STAG2 Regulates Homologous Recombination Repair and Sensitivity to ATM Inhibition. | Adv Sci (Weinh) | 2023 | 37985839 | PubTator, text mining | PubMed |
| What AlphaFold tells us about cohesin's retention on and release from chromosomes. | Elife | 2023 | 37975572 | PubTator, text mining | PubMed |
| Profiling stress-triggered RNA condensation with photocatalytic proximity labeling. | Nat Commun | 2023 | 37968266 | PubTator, text mining | PubMed |
| Reference intervals of complete blood count and coagulation tests in Vietnamese pregnant women. | BMC Pregnancy Childbirth | 2023 | 37951881 | 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.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/genes/v1/8243/papers?page=8