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.
181 to 200 of 2,056
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Identification of potential shared gene signatures between gastric cancer and type 2 diabetes: a data-driven analysis. | Front Med (Lausanne) | 2024 | 38903804 | PubTator, text mining | PubMed |
| Single-cell RNA transcriptomic reveal the mechanism of MSC derived small extracellular vesicles against DKD fibrosis. | J Nanobiotechnology | 2024 | 38890734 | PubTator, text mining | PubMed |
| Exploring the link between Alport syndrome and multiple intracranial artery stenoses: A case report of COL4A5 mutation. | J Stroke Cerebrovasc Dis | 2024 | 38880363 | PubTator, text mining | PubMed |
| Aberrant Splicing of COL4A5 Intronic Variant Contribute to the Pathogenesis of X-Linked Alport Syndrome: A Case Series. | Int J Nephrol Renovasc Dis | 2024 | 38855711 | PubTator, text mining | PubMed |
| The NM_033380.2 transcript of the COL4A5 gene contains a variable splice site c.4822-10T>C, which has been identified as a causative factor for Alport syndrome. | Front Genet | 2024 | 38818038 | PubTator, text mining | PubMed |
| A Novel COL4A5 Pathogenic Variant Joins the Dots in a Family with a Synchronous Diagnosis of Alport Syndrome and Polycystic Kidney Disease. | Genes (Basel) | 2024 | 38790225 | PubTator, text mining | PubMed |
| An unusual case of nephrotic syndrome. | Pediatr Nephrol | 2024 | 38780768 | PubTator, text mining | PubMed |
| Identification of potential candidate genes for the Huoyan trait in developing Wulong goose embryos by transcriptomic analysis. | Br Poult Sci | 2024 | 38727584 | PubTator, text mining | PubMed |
| Benfotiamine improves dystrophic pathology and exercise capacity in mdx mice by reducing inflammation and fibrosis. | Hum Mol Genet | 2024 | 38710523 | PubTator, text mining | PubMed |
| Kidney Cysts in Children With Alport Syndrome: A Report of 3 Cases. | Kidney Med | 2024 | 38680391 | PubTator, text mining | PubMed |
| A novel COL4A5 splicing mutation causes alport syndrome in a Chinese family. | BMC Med Genomics | 2024 | 38671472 | PubTator, text mining | PubMed |
| X-linked Alport syndrome presenting in mother and son with the same unique histopathological features. | J Nephrol | 2024 | 38668984 | PubTator, text mining | PubMed |
| Trimerization profile of type IV collagen COL4A5 exon deletion in X-linked Alport syndrome. | Clin Exp Nephrol | 2024 | 38658441 | PubTator, text mining | PubMed |
| Cellular and Transcriptional Response of Human Astrocytes to Hybrid Protein Materials. | ACS Appl Bio Mater | 2024 | 38632900 | PubTator, text mining | PubMed |
| Reclassification of Genetic Testing Results: A Case Report Demonstrating the Need for Structured Re-Evaluation of Genetic Findings. | Can J Kidney Health Dis | 2024 | 38623282 | PubTator, text mining | PubMed |
| Genetic reprogramming with stem cells regenerates glomerular epithelial podocytes in Alport syndrome. | Life Sci Alliance | 2024 | 38561223 | PubTator, text mining | PubMed |
| Trigenic COL4A3/COL4A4/COL4A5 Pathogenic Variants in Alport Syndrome: A Case Report. | Nephron | 2024 | 38547857 | PubTator, text mining | PubMed |
| Introducing Exome Sequencing as Part of the Diagnostic Algorithm for Pediatric Nephrology Patients in Bulgaria: A Single-Center Experience. | Nephron | 2024 | 38547852 | PubTator, text mining | PubMed |
| Alport syndrome and Alport kidney diseases - elucidating the disease spectrum. | Curr Opin Nephrol Hypertens | 2024 | 38477333 | PubTator, text mining | PubMed |
| Genetic diagnosis of Alport syndrome in 16 Chinese families. | Mol Genet Genomic Med | 2024 | 38433557 | 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=10