Gene · 778
Papers843
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
1 to 20 of 843
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Targeting Lung Cancer Stem Cells with Trimebutine: Synergistic Antitumor Activity in Combination with Cisplatin. | Int J Mol Sci | 2026 | 42794641 | PubTator, text mining | PubMed |
| AAV-mediated age- and circuit-dependent restoration of photoreceptor synaptic structure and function in α2δ4-associated retinal synaptopathy. | bioRxiv | 2026 | 42539265 | PubTator, text mining | PubMed |
| Diagnostic discovery of structural variants causing foveal hypoplasia using SVRare and long-read nanopore sequencing. | Eur J Hum Genet | 2026 | 42477408 | PubTator, text mining | PubMed |
| Diagnostic Yield and Clinical Impact of Comprehensive WES/WGS Testing Beyond Common Genetic Causes in Hereditary Optic Atrophy. | Clin Genet | 2026 | 42363686 | PubTator, text mining | PubMed |
| Genetic and Clinical Heterogeneity of Polish Patients with Congenital Stationary Night Blindness (CSNB). | Int J Mol Sci | 2026 | 42278384 | PubTator, text mining | PubMed |
| Genotype-phenotype correlations in Chinese patients with congenital stationary night blindness and early-onset high myopia: evidence from electrophysiology and whole-exome sequencing. | Int J Ophthalmol | 2026 | 42211199 | PubTator, text mining | PubMed |
| Expanding the Genotypic Landscape of Congenital Stationary Night Blindness in an Ethnically Diverse Canadian Population. | Hum Mutat | 2026 | 42147812 | PubTator, text mining | PubMed |
| Electronegative electroretinography in inherited retinal disease: a systematic review of genotype-phenotype correlations. | BMC Ophthalmol | 2026 | 42106701 | PubTator, text mining | PubMed |
| Mutation Screening of ARR3, CACNA1F, P4HA2, TRPM1, COL2A1, COL11A1 and PAX6 in a Chinese Cohort of 37 Patients with Early-Onset High Myopia. | Genes (Basel) | 2026 | 42074509 | PubTator, text mining | PubMed |
| L-type calcium channel-mediated lipid metabolic reprogramming in gastric adenocarcinoma progression. | Transl Oncol | 2026 | 41861661 | PubTator, text mining | PubMed |
| Advances in calcium signalling research for the diagnosis and treatment of depression. | Ann Med | 2026 | 41787814 | PubTator, text mining | PubMed |
| Genetic Architecture of Myopia and Its Implications for Risk Stratification and Prognosis. | Diagnostics (Basel) | 2026 | 41750685 | PubTator, text mining | PubMed |
| Clinical and Molecular Characteristics of Foveal Sparing Phenotype in Chinese Patients With Inherited Retinal Diseases. | Transl Vis Sci Technol | 2026 | 41700794 | PubTator, text mining | PubMed |
| Inhibition of CaV1.4 channels by CaV3 channel antagonists ML218 and Z944. | J Gen Physiol | 2026 | 41489546 | PubTator, text mining | PubMed |
| Incomplete congenital stationary night blindness associated with a novel variant in the CACNA1F gene. | Doc Ophthalmol | 2026 | 41201761 | PubTator, text mining | PubMed |
| Integrating biological regulatory network analysis and structural bioinformatics to probe CABP4 transcriptional regulation in night blindness. | J Biomol Struct Dyn | 2026 | 40975890 | PubTator, text mining | PubMed |
| Fast ERG 15 Hz flicker protocol for assessing functional changes in the rod system. | Doc Ophthalmol | 2026 | 40715895 | PubTator, text mining | PubMed |
| Identification of a Novel Splice-Site Variant in CACNA1F With Variable Phenotypic Expression in a Chinese Family. | Mol Genet Genomic Med | 2025 | 41381383 | PubTator, text mining | PubMed |
| Genetic Spectrum of Negative Electroretinograms in a Predominantly Pediatric Cohort of 177 Patients. | Invest Ophthalmol Vis Sci | 2025 | 41342616 | PubTator, text mining | PubMed |
| Inherited Retinal Diseases with High Myopia: A Review. | Genes (Basel) | 2025 | 41153400 | 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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