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.
141 to 160 of 2,784
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| A coagulation-related long non-coding RNA signature to predict prognosis and immune features of breast cancer. | Discov Oncol | 2025 | 40317354 | PubTator, text mining | PubMed |
| Somatic mutations and outcomes in chronic myeloid leukemia adolescent and young adults compared to children, adults, and BCR::ABL1-positive acute lymphoblastic leukemia. | Leukemia | 2025 | 40295826 | PubTator, text mining | PubMed |
| Assessing the prognostic and therapeutic value of cuproptosis-related genes in colon adenocarcinoma patients. | Front Cell Dev Biol | 2025 | 40276654 | PubTator, text mining | PubMed |
| CHD7 binds distinct regions in the Sox11 locus to regulate neuronal differentiation. | bioRxiv | 2025 | 40236205 | PubTator, text mining | PubMed |
Circadian rhythm related genes identified through tumorigenesis and immune infiltration-guided strategies as predictors of prognosis, immunotherapy response, and candidate drugs in skin cutaneous malignant melanoma. | Front Immunol | 2025 | 40191195 | PubTator, text mining | PubMed |
| Gut Microbiome Pilot Study of Patients With CHARGE Syndrome and Sibling Controls. | Am J Med Genet A | 2025 | 40178132 | PubTator, text mining | PubMed |
| Mutation of CHD7 impairs the output of neuroepithelium transition that is reversed by the inhibition of EZH2. | Mol Psychiatry | 2025 | 40164694 | PubTator, text mining | PubMed |
| Atlas of imprinted and allele-specific DNA methylation in the human body. | Nat Commun | 2025 | 40069157 | PubTator, text mining | PubMed |
| [Clinical features of CHARGE syndrome in children]. | Zhonghua Yan Ke Za Zhi | 2025 | 40050103 | PubTator, text mining | PubMed |
| Management of anophthalmia, microphthalmia and coloboma in the newborn, shared care between neonatologist and ophthalmologist: a literature review. | Ital J Pediatr | 2025 | 40038803 | PubTator, text mining | PubMed |
| Genetic and Clinical Predictors of Hearing Loss Among Patients with CHARGE Syndrome. | J Am Acad Audiol | 2025 | 40015694 | PubTator, text mining | PubMed |
| Discovery of a new mitophagy-related gene signature for predicting the outlook and immunotherapy in triple-negative breast cancer. | Sci Rep | 2025 | 40000809 | PubTator, text mining | PubMed |
| Beyond CHD7 gene: unveiling genetic diversity in clinically suspected CHARGE syndrome. | J Hum Genet | 2025 | 40000719 | PubTator, text mining | PubMed |
| Pathogenic variants in chromatin-related genes: Linking immune dysregulation to neuroregression and acute neuropsychiatric disorders. | Dev Med Child Neurol | 2025 | 39985218 | PubTator, text mining | PubMed |
| Single-cell and Multi-omics Analysis Confirmed the Signature and Potential Targets of Cuproptosis in Colorectal Cancer. | J Cancer | 2025 | 39895793 | PubTator, text mining | PubMed |
| Cuproptosis gene characterizes the immune microenvironment of diabetic nephropathy. | Transpl Immunol | 2025 | 39892769 | PubTator, text mining | PubMed |
| Total syntheses of cyclohelminthol I-IV reveal a new cysteine-selective covalent reactive group. | Chem Sci | 2025 | 39886435 | PubTator, text mining | PubMed |
| Unveiling Cuproptosis-Driven Molecular Clusters and Immune Dysregulation in Ankylosing Spondylitis. | J Inflamm Res | 2025 | 39867949 | PubTator, text mining | PubMed |
| Construction of a novel cuproptosis-related gene signature and integrative analyses in cholangiocarcinoma. | Heliyon | 2025 | 39866451 | PubTator, text mining | PubMed |
| KMT2C Polymorphism in Familial Hypospadias. | Indian J Pediatr | 2025 | 39812948 | 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.
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GET https://conductscience.org/api/genes/v1/55636/papers?page=8