Gene · 5314
Papers1,363
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
21 to 40 of 1,363
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Molecular genetic diagnosis of autosomal dominant polycystic kidney disease - A systematic review. | Glob Med Genet | 2026 | 41938343 | PubTator, text mining | PubMed |
| [Research advances in the diagnosis and treatment of Polycystic kidney disease]. | Zhonghua Yi Xue Yi Chuan Xue Za Zhi | 2026 | 41916891 | PubTator, text mining | PubMed |
| Phenotype-Driven Next-Generation Sequencing and Structure-Based In Silico Analysis Reveal Disease-Specific Diagnostic Yield and Genotype-Phenotype Correlations in Inherited Kidney Diseases. | Life (Basel) | 2026 | 41901018 | PubTator, text mining | PubMed |
| Clinical outcomes in Caroli disease and Caroli syndrome: a longitudinal observational cohort study. | Sci Rep | 2026 | 41888235 | PubTator, text mining | PubMed |
| Pegcetacoplan-induced remission in pediatric immune-complex membranoproliferative glomerulonephritis with comorbid autosomal recessive polycystic kidney disease: a case report. | Front Med (Lausanne) | 2026 | 41884136 | PubTator, text mining | PubMed |
| GGPS1 Promoter Variant (rs3806394) Is Associated With Larger Simple Renal Cysts via Reduced GGPPS Expression. | Hum Mutat | 2026 | 41800173 | PubTator, text mining | PubMed |
| Caroli disease associated with autosomal recessive polycystic kidney disease: CT imaging features of a case report. | Radiol Case Rep | 2026 | 41798673 | PubTator, text mining | PubMed |
| Monogenic Etiologies of Kidney Cysts in the Pediatric Population: An Observational Cohort Study. | Clin J Am Soc Nephrol | 2026 | 41790507 | PubTator, text mining | PubMed |
| Exome sequencing in patients with medullary sponge kidney. | Nephrol Dial Transplant | 2026 | 41790480 | PubTator, text mining | PubMed |
| Unmasking of a Heterozygous SLC12A3 Variant. | Kidney Med | 2026 | 41767689 | PubTator, text mining | PubMed |
| Next-Generation Sequencing Defines a Molecularly Confirmed ARPKD Core Within the Broader PKHD1-Associated Disease Spectrum. | Genes (Basel) | 2026 | 41751613 | PubTator, text mining | PubMed |
| Deciphering the Impact of RAC1-SPTAN1 in ARPKD Cystogenesis Using Multifaceted Models. | Adv Sci (Weinh) | 2026 | 41742835 | PubTator, text mining | PubMed |
| Dentofacial Malocclusion and Salivary Biomarkers in Asthmatic Patients: A Scoping Review. | Int Dent J | 2026 | 41740246 | PubTator, text mining | PubMed |
| Novel compound heterozygous PKHD1 mutations in a Chinese ARPKD pedigree and analysis of genotype-phenotype correlations. | Front Med (Lausanne) | 2026 | 41728609 | PubTator, text mining | PubMed |
| Screening for genetic kidney diseases in a dialysis cohort via exome sequencing. | Clin Kidney J | 2026 | 41725785 | PubTator, text mining | PubMed |
| Disruption of the human cystin-1 myristoyl-electrostatic switch causes polycystic kidney disease that phenocopies autosomal recessive polycystic kidney disease. | Kidney Int | 2026 | 41720266 | PubTator, text mining | PubMed |
| Pediatric Cholestatic Diseases in the Era of Ileal Bile Acid Transporter (IBAT) Inhibitors. | Pediatr Rep | 2026 | 41718432 | PubTator, text mining | PubMed |
| Rare Combination of PKD and precocious puberty in a HNF1B mutated little girl. | Urol Case Rep | 2026 | 41716527 | PubTator, text mining | PubMed |
| Transcriptomic profiling of porcine duodenal, jejunal, and ileal organoids in response to porcine epidemic diarrhea virus. | J Anim Sci Technol | 2026 | 41695673 | PubTator, text mining | PubMed |
| Delineating the Genetic Basis of RNF213-related vasculopathies: The association of PKHD1 variants with bilateral cerebral vasculopathy. | Eur J Hum Genet | 2026 | 41680453 | 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
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