Gene · 6326
Papers4,098
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
901 to 920 of 4,098
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Assessing the landscape of STXBP1-related disorders in 534 individuals. | Brain | 2022 | 35190816 | PubTator, text mining | PubMed |
| Genomic variations and epigenomic landscape of the Medaka Inbred Kiyosu-Karlsruhe (MIKK) panel. | Genome Biol | 2022 | 35189951 | PubTator, text mining | PubMed |
| A Novel SCN8A mutation in a case of early-onset infantile epileptic encephalopathy: A Case Report. | Acta Biomed | 2022 | 35188110 | PubTator, text mining | PubMed |
| Iron from nanostructured ferric phosphate: absorption and biodistribution in mice and bioavailability in iron deficient anemic women. | Sci Rep | 2022 | 35181698 | PubTator, text mining | PubMed |
| A Multi-Target and Multi-Channel Mechanism of Action for Jiawei Yinhuo Tang in the Treatment of Social Communication Disorders in Autism: Network Pharmacology and Molecular Docking Studies. | Evid Based Complement Alternat Med | 2022 | 35178102 | PubTator, text mining | PubMed |
| Structural and functional insights into the inhibition of human voltage-gated sodium channels by μ-conotoxin KIIIA disulfide isomers. | J Biol Chem | 2022 | 35167877 | PubTator, text mining | PubMed |
| Analysis of Factors That May Affect the Effectiveness of Ketogenic Diet Treatment in Pediatric and Adolescent Patients. | J Clin Med | 2022 | 35160058 | PubTator, text mining | PubMed |
| Rare diseases - rare outcomes: Assessing communication abilities for the developmental and epileptic encephalopathies. | Epilepsy Behav | 2022 | 35158285 | PubTator, text mining | PubMed |
| Neonatal Screening for Sickle Cell Disease in Congo. | Anemia | 2022 | 35154827 | PubTator, text mining | PubMed |
| A tale of two cohorts: Differing outcomes in infantile-onset focal epilepsy. | Epilepsia | 2022 | 35146752 | PubTator, text mining | PubMed |
| Divergent allostery reveals critical differences between structurally homologous regulatory domains of Plasmodium falciparum and human protein kinase G. | J Biol Chem | 2022 | 35143840 | PubTator, text mining | PubMed |
| Cilia proteins are biomarkers of altered flow in the vasculature. | JCI Insight | 2022 | 35143420 | PubTator, text mining | PubMed |
| DECIPHER: Supporting the interpretation and sharing of rare disease phenotype-linked variant data to advance diagnosis and research. | Hum Mutat | 2022 | 35143074 | PubTator, text mining | PubMed |
| Genetic Analysis of Sodium Channel Genes in Pediatric Epilepsy Patients of Pakistan. | Genet Res (Camb) | 2022 | 35136380 | PubTator, text mining | PubMed |
| Evaluation of phenotype-driven gene prioritization methods for Mendelian diseases. | Brief Bioinform | 2022 | 35134823 | PubTator, text mining | PubMed |
| Disentangling glial diversity in peripheral nerves at single-nuclei resolution. | Nat Neurosci | 2022 | 35115729 | PubTator, text mining | PubMed |
| Genomic and neuroimaging approaches to bipolar disorder. | BJPsych Open | 2022 | 35101157 | PubTator, text mining | PubMed |
| Thermal dysregulation in patients with multiple sclerosis during SARS-CoV-2 infection. The potential therapeutic role of exercise. | Mult Scler Relat Disord | 2022 | 35092946 | PubTator, text mining | PubMed |
| Diagnostic preferences include discussion of etiology for adults with cerebral palsy and their caregivers. | Dev Med Child Neurol | 2022 | 35092695 | PubTator, text mining | PubMed |
| The EPIGENE network: A French initiative to harmonize and improve the nationwide diagnosis of monogenic epilepsies. | Eur J Med Genet | 2022 | 35091117 | 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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GET https://conductscience.org/api/genes/v1/6326/papers?page=46