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Gene · 2189

Papers1,427

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 1,427

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TitleJournalYearPMIDFound bySource
Combining targeted DNA repair inhibition and immune-oncology approaches for enhanced tumor control.Mol Cell202336669489PubTator, text miningPubMed
[Chinese expert consensus on the diagnosis and treatment of Fanconi anemia (version 2022)].Zhonghua Yi Xue Za Zhi202336660784PubTator, text miningPubMed
The FANCC-FANCE-FANCF complex is evolutionarily conserved and regulates meiotic recombination.Nucleic Acids Res202336652992PubTator, text miningPubMed
Exploring pradimicin-IRD antineoplastic mechanisms and related DNA repair pathways.Chem Biol Interact202336634904PubTator, text miningPubMed
Whole-exome sequencing identifies FANC heterozygous germline mutation as an adverse factor for immunosuppressive therapy in Chinese aplastic anemia patients aged 40 or younger: a single-center retrospective study.
Ann Hematol202336622392PubTator, text miningPubMed
Mutations of TP53 and genes related to homologous recombination repair in breast cancer with germline BRCA1/2 mutations.Hum Genomics202336604691PubTator, text miningPubMed
Cannabidiol-induced transcriptomic changes and cellular senescence in human Sertoli cells.Toxicol Sci202336519830PubTator, text miningPubMed
Specific mechanisms of translation initiation in higher eukaryotes: the eIF4G2 story.RNA202336517212PubTator, text miningPubMed
Mesenchymal stem/stromal cells from a transplanted, asymptomatic patient with Fanconi anemia exhibit an aging-like phenotype and dysregulated expression of genes implicated in hematopoiesis and myelodysplasia.
Cytotherapy202336481320PubTator, text miningPubMed
RosettaDDGPrediction for high-throughput mutational scans: From stability to binding.Protein Sci202336461907PubTator, text miningPubMed
Regorafenib with or without a programmed cell death protein 1 antibody as third-line treatment for microsatellite stable metastatic colorectal cancer.Cancer Med202336373163PubTator, text miningPubMed
Genetic analysis of a Fanconi anemia case revealed the presence of FANCF mutation (exon 1;469>C-T) with implications to develop acute myeloid leukemia.Mol Biol Rep202336369330PubTator, text miningPubMed
Investigation of mutations in Fanconi anemia genes and malignancy predisposition in Brazilian patients.Int J Lab Hematol202336333938PubTator, text miningPubMed
The kinetics of blast clearance are associated with copy number alterations in childhood B-cell acute lymphoblastic leukemia.Neoplasia202336288679PubTator, text miningPubMed
The First Case of Acute Myeloid Leukemia With Underlying Fanconi Anemia due to FANCF Variants in Korea.Ann Lab Med202336281516PubTator, text miningPubMed
Two decades of stem cell transplantation in patients with Fanconi anemia: Analysis of factors affecting transplant outcomes.Clin Transplant202336259220PubTator, text miningPubMed
DNA damage accumulation and repair defects in FLT3-ITD acute myeloid leukemia: Implications for clonal evolution and disease progression.Hematol Oncol202336131612PubTator, text miningPubMed
Genomic Signatures from Clinical Tumor Sequencing in Patients with Breast Cancer Having Germline BRCA1/2 Mutation.Cancer Res Treat202335681111PubTator, text miningPubMed
The genomic characteristics of RET fusion positive tumors in Chinese non-small cell lung cancer (NSCLC) patients.J Cancer Res Clin Oncol202335220468PubTator, text miningPubMed
Whole-exome sequencing and bioinformatic analyses revealed differences in gene mutation profiles in papillary thyroid cancer patients with and without benign thyroid goitre background.Front Endocrinol (Lausanne)202236686473PubTator, text miningPubMed

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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