Gene · 1286
Papers1,462
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
61 to 80 of 1,462
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Coexistence of Alport Syndrome and Fabry Disease in a Female with R112H Variant: Early Progression of Fabry Nephropathy. | Int J Mol Sci | 2025 | 41516147 | PubTator, text mining | PubMed |
| Expanding carrier screening: beyond the genes, to include underrepresented ancestries. | NPJ Genom Med | 2025 | 41453871 | PubTator, text mining | PubMed |
| Case Report: Neonatal nephropathy with polycystic appearance in child harboring WT1 variant. | Front Pediatr | 2025 | 41450889 | PubTator, text mining | PubMed |
| Anticodon-edited tRNA enables translational readthrough of COL4A5 premature termination codons. | PLoS One | 2025 | 41417821 | PubTator, text mining | PubMed |
| Clinical features of hearing loss and genotype-phenotype correlations in Alport syndrome caused by COL4A4 or COL4A5 variants. | Sci Rep | 2025 | 41398421 | PubTator, text mining | PubMed |
| Biomimetic fractal topography enhances podocyte maturation in vitro. | Nat Commun | 2025 | 41398144 | PubTator, text mining | PubMed |
| Increased in vivo transduction of AAV-9 cargo in Alport podocytes. | Wellcome Open Res | 2025 | 41394796 | PubTator, text mining | PubMed |
| Case Report: A novel TTN gene variant and a concurrent rare COL4A4 gene variant in a Chinese patient with dilated cardiomyopathy. | Front Cardiovasc Med | 2025 | 41306271 | PubTator, text mining | PubMed |
| A case of concurrent Alport syndrome and Nail-patella syndrome posing diagnostic challenge without genetic testing. | BMC Nephrol | 2025 | 41299396 | PubTator, text mining | PubMed |
| Autosomal Dominant Alport Syndrome Diagnosed in an Elderly Man. | Cureus | 2025 | 41257164 | PubTator, text mining | PubMed |
| Placental Malperfusion Is Associated With Adverse Outcomes in Congenital Heart Disease and With Genetic Variants in Placental Developmental Pathways. | J Am Coll Cardiol | 2025 | 41193091 | PubTator, text mining | PubMed |
| Case Report: Evaluation of COL4A5 non-canonical splicing variants in two families. | Front Med (Lausanne) | 2025 | 41090128 | PubTator, text mining | PubMed |
| Expanding the COL4A4 variant spectrum: genotype-phenotype correlation in 19 Chinese children using updated Alport kidney disease classification. | Ren Fail | 2025 | 41087309 | PubTator, text mining | PubMed |
| An Elusive Diagnosis of Autosomal Dominant Alport Syndrome: Genomic Sequencing Is a Game Changer. | Cureus | 2025 | 41069567 | PubTator, text mining | PubMed |
| Age at disease onset and risk of chronic kidney disease in patients with heterozygous disease-causing variants in COL4A3 and COL4A4. | Clin Kidney J | 2025 | 41059411 | PubTator, text mining | PubMed |
| Severe Clinical Phenotype in Alport Syndrome Due to 2 COL4A4 Exon-Skipping Events. | Kidney Med | 2025 | 41050124 | PubTator, text mining | PubMed |
| The microenvironment of ocular surface in keratoconus: a systematic review. | Eye Vis (Lond) | 2025 | 40993744 | PubTator, text mining | PubMed |
| Targeted exome sequencing for molecular diagnosis of pediatric Alport syndrome in Southwest China. | Front Genet | 2025 | 40949880 | PubTator, text mining | PubMed |
| High Prevalence of Autosomal Recessive Alport Syndrome in Roma Population of Eastern Slovakia. | Biomedicines | 2025 | 40868214 | PubTator, text mining | PubMed |
| Novel COL4A3-COL4A5 variants and digenic inheritance in pediatric Alport syndrome from Southwestern China. | Sci Rep | 2025 | 40855356 | 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/v1/1286/papers?page=4