Gene · 3785
Papers2,279
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 2,279
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Identification of a de novo CACNA1B variant and a start-loss ADRA2B variant in paroxysmal kinesigenic dyskinesia. | Heliyon | 2024 | 38571653 | PubTator, text mining | PubMed |
| PI3K/Akt/FoxO Pathway Mediates Antagonistic Toxicity in HepG2 Cells Coexposed to Deoxynivalenol and Enniatins. | J Agric Food Chem | 2024 | 38557103 | PubTator, text mining | PubMed |
| Genetic Advancements in Infantile Epileptic Spasms Syndrome and Opportunities for Precision Medicine. | Genes (Basel) | 2024 | 38540325 | PubTator, text mining | PubMed |
| Genetic determinants of global developmental delay and intellectual disability in Ukrainian children. | J Neurodev Disord | 2024 | 38539105 | PubTator, text mining | PubMed |
| MLe-KCNQ2: An Artificial Intelligence Model for the Prognosis of Missense KCNQ2 Gene Variants. | Int J Mol Sci | 2024 | 38474157 | PubTator, text mining | PubMed |
| Glial KCNQ K+ channels control neuronal output by regulating GABA release from glia in C. elegans. | Neuron | 2024 | 38460523 | PubTator, text mining | PubMed |
| Molecular subtype identification and prognosis stratification by a immunogenic cell death-related gene expression signature in colorectal cancer. | Expert Rev Anticancer Ther | 2024 | 38407877 | PubTator, text mining | PubMed |
| Genetic and phenotypic landscape of pediatric-onset epilepsy in 142 Indian families: Counseling and therapeutic implications. | Clin Genet | 2024 | 38374498 | PubTator, text mining | PubMed |
| The importance of routine genetic testing in pediatric epilepsy surgery. | Epilepsia Open | 2024 | 38366963 | PubTator, text mining | PubMed |
| Newly discovered variants in unexplained neonatal encephalopathy. | Mol Genet Genomic Med | 2024 | 38284441 | PubTator, text mining | PubMed |
| Combining Off-flow, a Nextflow-coded program, and whole genome sequencing reveals unintended genetic variation in CRISPR/Cas-edited iPSCs. | Comput Struct Biotechnol J | 2024 | 38283851 | PubTator, text mining | PubMed |
| iPSC-derived models of PACS1 syndrome reveal transcriptional and functional deficits in neuron activity. | Nat Commun | 2024 | 38280846 | PubTator, text mining | PubMed |
| Genetic Epilepsies and Developmental Epileptic Encephalopathies with Early Onset: A Multicenter Study. | Int J Mol Sci | 2024 | 38279250 | PubTator, text mining | PubMed |
| Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy. | bioRxiv | 2024 | 38260608 | PubTator, text mining | PubMed |
| Phenotypic and functional assessment of two novel KCNQ2 gain-of-function variants Y141N and G239S and effects of amitriptyline treatment. | Neurotherapeutics | 2024 | 38241158 | PubTator, text mining | PubMed |
| Effect of a sensing charge mutation on the deactivation of KV7.2 channels. | J Gen Physiol | 2024 | 38236165 | PubTator, text mining | PubMed |
| Phase separation as a possible mechanism for dosage sensitivity. | Genome Biol | 2024 | 38225666 | PubTator, text mining | PubMed |
| A small-molecule activation mechanism that directly opens the KCNQ2 channel. | Nat Chem Biol | 2024 | 38167918 | PubTator, text mining | PubMed |
| Neurodevelopmental outcomes in a cohort of Australian families with self-limited familial epilepsy of neonatal/infantile onset. | Seizure | 2024 | 38160512 | PubTator, text mining | PubMed |
| Improved classification and pathogenicity assessment by comprehensive functional studies in a large data set of KCNQ2 variants. | Life Sci | 2024 | 38142737 | 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.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/genes/v1/3785/papers?page=10