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Gene · 55636

Papers2,784

Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.

TitleJournalYearPMIDFound bySource
Oncogenic DNMT3B as a therapeutic target for cervical cancer.Chin Med J (Engl)202642402721PubTator, text miningPubMed
Isolated absent pulmonary valve syndrome with intact ventricular septum in a child with CHARGE syndrome: a rare case report and review of the literature.Front Cardiovasc Med202642395886PubTator, text miningPubMed
Analysis of end-stage renal disease mediated by cuproptosis-related genes.Clin Nephrol202642383521PubTator, text miningPubMed
A Novel Variant of the CHD8 Gene in a Patient with Autism Spectrum Disorder.Genes (Basel)202642353758PubTator, text miningPubMed
Supratentorial intraparenchymal schwannoma: Systematic review of the literature with an illustrative case.J Clin Neurosci202642330744PubTator, text miningPubMed
Role of CHD chromatin remodelers in heart development.World J Pediatr202642323439PubTator, text miningPubMed
Corrigendum to: A Novel Cuproptosis-Related Gene Signature Predicts Prognosis in Papillary Thyroid Carcinoma Patients.Comb Chem High Throughput Screen202642294634PubTator, text miningPubMed
CHARGE Syndrome Associated With Persistent Hyperplastic Primary Vitreous: A Case Report.Case Rep Ophthalmol Med202642266710PubTator, text miningPubMed
Differential Transcriptome Analysis of Intrauterine UPD6pat Fetuses With Distinct Phenotypes.Mol Genet Genomic Med202642260905PubTator, text miningPubMed
CHARGE Syndrome: A Narrative Review and Update on Diagnosis, Assessment and Management.J Paediatr Child Health202642219920PubTator, text miningPubMed
Single-Cell and Integrative Analyses Uncover Therapeutic Potential of RFX1-Mediated Cuproptosis in PitNETs.J Integr Neurosci202642216643PubTator, text miningPubMed
Molecular Characterization of Syndromic Hearing Loss in North African Moroccan Families.Biomolecules202642193970PubTator, text miningPubMed
Integrated analysis of cell-in-cell related genes and immune microenvironment in heart failure.Front Cell Dev Biol202642181687PubTator, text miningPubMed
Beyond GH stimulation tests: genetic heterogeneity and treatment response in children with diagnosed GH deficiency.J Endocr Soc202642181673PubTator, text miningPubMed
Monogenic kidney disease and monogenic diabetes are present in renal clinic patients with non-genetic diagnoses.Sci Rep202642141127PubTator, text miningPubMed
Trio Whole-Genome Sequencing for Diagnosis of Neonates with Multiple Congenital Anomalies.Neonatology202642139173PubTator, text miningPubMed
Integration of transcriptome and DNA methylation reveals the mechanism of cilia-related genes in recurrent miscarriage.Sci Rep202642106497PubTator, text miningPubMed
Carrageenan-Acyclovir Complex and Its Liposomal Form.Int J Mol Sci202642074011PubTator, text miningPubMed
Phenocopies of 22q11.2DS: revealing genetic diversity in clinically suspected 22q11.2 deletion syndrome.Mol Cell Pediatr202642056684PubTator, text miningPubMed
[Genetic variants analysis of 17 female patients with idiopathic hypogonadotropic hypogonadism].Beijing Da Xue Xue Bao Yi Xue Ban202641978403PubTator, 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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