Gene · 1287
Papers2,056
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
121 to 140 of 2,056
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Molecular dynamics simulations of intrinsically disordered protein regions enable biophysical interpretation of variant effect predictors. | bioRxiv | 2025 | 40462930 | PubTator, text mining | PubMed |
| Ocular cues to a larger picture! | Indian J Ophthalmol | 2025 | 40434453 | PubTator, text mining | PubMed |
| Transcriptomic characterization of the synergy between human induced pluripotent stem cells-derived liver- and pancreas-on-chip coculture. | Mol Cell Endocrinol | 2025 | 40409528 | PubTator, text mining | PubMed |
| A case report of atypical autosomal dominant polycystic kidney disease presenting as glomerulocystic kidney superimposed with thin basement membrane nephropathy. | BMC Nephrol | 2025 | 40375172 | PubTator, text mining | PubMed |
| RNA m5C modification: from physiology to pathology and its biological significance. | Front Immunol | 2025 | 40370440 | PubTator, text mining | PubMed |
| Circular RNA LDLRAD3 promotes gastric cancer progression by upregulating COL4A5 through sponging miR-137: Erratum. | J Chin Med Assoc | 2025 | 40368838 | PubTator, text mining | PubMed |
Transcriptome-Wide Analysis and Experimental Validation from FFPE Tissue Identifies Stage-Specific Gene Expression Profiles Differentiating Adenoma, Carcinoma In-Situ and Adenocarcinoma in Colorectal Cancer Progression. | Int J Mol Sci | 2025 | 40362431 | PubTator, text mining | PubMed |
| [New Genetic Variants Involved in the Pathogenesis of Autosomal Dominant Alport Syndrome: A Familial Case Report]. | G Ital Nefrol | 2025 | 40332975 | PubTator, text mining | PubMed |
| Genetic and biomarker approaches to uterine fibroids: toward precision medicine. | Front Glob Womens Health | 2025 | 40330123 | PubTator, text mining | PubMed |
| Clinical differences between female monozygotic twins with X-linked Alport syndrome with somatic mosaicism. | Pediatr Nephrol | 2025 | 40299036 | PubTator, text mining | PubMed |
| Phenotype-genotype correlations in patients with Alport syndrome from the Polish population. | J Nephrol | 2025 | 40237890 | PubTator, text mining | PubMed |
| Whole exome sequencing shows novel COL4A3 and COL4A4 variants as causes of Alport syndrome in Rio Grande do Norte, Brazil. | BMC Genomics | 2025 | 40169949 | PubTator, text mining | PubMed |
| Increased HA/CD44/TGFβ signaling implicates in renal fibrosis of a Col4a5 mutant Alport mice. | Mol Med | 2025 | 40075271 | PubTator, text mining | PubMed |
| Identification of novel COL4A5 variants and prenatal diagnosis in three large families. | Sci Rep | 2025 | 40057613 | PubTator, text mining | PubMed |
| Pathogenic variants in the Alport genes are prevalent in the Singapore multiethnic population with highest frequency in the Chinese. | Sci Rep | 2025 | 40044766 | PubTator, text mining | PubMed |
| Understanding the early molecular changes associated with radiation therapy-A preliminary bulk RNA sequencing study. | PLoS One | 2025 | 40029831 | PubTator, text mining | PubMed |
| Molecular Review of Suspected Alport Syndrome Patients-A Single-Centre Experience. | Genes (Basel) | 2025 | 40004525 | PubTator, text mining | PubMed |
| COL4A5 Intronic Variants at Third to Fifth Nucleotides Cause Alport Syndrome. | Kidney Int Rep | 2025 | 39990911 | PubTator, text mining | PubMed |
| Alport Syndrome May contribute to Grand Multiparity in a Typical Low Income Setting. | Ethiop J Health Sci | 2025 | 39981328 | PubTator, text mining | PubMed |
| Corneal endothelial neovascularization and glaucoma in X-linked Alport syndrome. | Eur J Ophthalmol | 2025 | 39949076 | 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/v1/1287/papers?page=7