Gene · 779
Papers2,128
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
1,021 to 1,040 of 2,128
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Effects of Beetroot Juice Supplementation on Performance and Fatigue in a 30-s All-Out Sprint Exercise: A Randomized, Double-Blind Cross-Over Study. | Nutrients | 2018 | 30181436 | PubTator, text mining | PubMed |
| STAC3 variants cause a congenital myopathy with distinctive dysmorphic features and malignant hyperthermia susceptibility. | Hum Mutat | 2018 | 30168660 | PubTator, text mining | PubMed |
| In vitro and in vivo phosphorylation of the Cav2.3 voltage-gated R-type calcium channel. | Channels (Austin) | 2018 | 30165790 | PubTator, text mining | PubMed |
| Correlation of phenotype with genotype and protein structure in RYR1-related disorders. | J Neurol | 2018 | 30155738 | PubTator, text mining | PubMed |
| A Rare Case of Severe Congenital RYR1-Associated Myopathy. | Case Rep Genet | 2018 | 30155320 | PubTator, text mining | PubMed |
| Review of Drug Repositioning Approaches and Resources. | Int J Biol Sci | 2018 | 30123072 | PubTator, text mining | PubMed |
| Comparative 1D Blue-Native electrophoresis analysis of Plasmodium falciparum and human proteins associated with cytoadherence. | Malar J | 2018 | 30103779 | PubTator, text mining | PubMed |
| Centronuclear myopathies under attack: A plethora of therapeutic targets. | J Neuromuscul Dis | 2018 | 30103348 | PubTator, text mining | PubMed |
| Pathogenic and rare deleterious variants in multiple genes suggest oligogenic inheritance in recurrent exertional rhabdomyolysis. | Mol Genet Metab Rep | 2018 | 30094188 | PubTator, text mining | PubMed |
| Phenotypical Variation with Same Genetic Mutation in Familial Hypokalemic Periodic Paralysis. | J Pediatr Neurosci | 2018 | 30090141 | PubTator, text mining | PubMed |
| STAC3 incorporation into skeletal muscle triads occurs independent of the dihydropyridine receptor. | J Cell Physiol | 2018 | 30071129 | PubTator, text mining | PubMed |
| Exciting perspectives for Translational Myology in the Abstracts of the 2018Spring PaduaMuscleDays: Giovanni Salviati Memorial - Chapter II - Abstracts of March 15, 2018. | Eur J Transl Myol | 2018 | 30057726 | PubTator, text mining | PubMed |
| Germline mutations in young non-smoking women with lung adenocarcinoma. | Lung Cancer | 2018 | 30032850 | PubTator, text mining | PubMed |
| Influences: Sodium channel excitement. | J Gen Physiol | 2018 | 30030300 | PubTator, text mining | PubMed |
| Matrix Stiffening and EGFR Cooperate to Promote the Collective Invasion of Cancer Cells. | Cancer Res | 2018 | 30026329 | PubTator, text mining | PubMed |
| Voltage sensing mechanism in skeletal muscle excitation-contraction coupling: coming of age or midlife crisis? | Skelet Muscle | 2018 | 30025545 | PubTator, text mining | PubMed |
| Role of putative voltage-sensor countercharge D4 in regulating gating properties of CaV1.2 and CaV1.3 calcium channels. | Channels (Austin) | 2018 | 30001160 | PubTator, text mining | PubMed |
| NaV1.4 DI-S4 periodic paralysis mutation R222W enhances inactivation and promotes leak current to attenuate action potentials and depolarize muscle fibers. | Sci Rep | 2018 | 29991727 | PubTator, text mining | PubMed |
| Role of defective Ca2+ signaling in skeletal muscle weakness: Pharmacological implications. | J Cell Commun Signal | 2018 | 29982883 | PubTator, text mining | PubMed |
| Whole-exome sequencing identifies novel pathogenic mutations and putative phenotype-influencing variants in Polish limb-girdle muscular dystrophy patients. | Hum Genomics | 2018 | 29970176 | 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/v1/779/papers?page=52