Gene · 6709
Papers1,635
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 1,635
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| [Overlap of neuropathy and myopathy genes: convergence of two entities]. | Med Sci (Paris) | 2025 | 41313053 | PubTator, text mining | PubMed |
| Oxidative Stress and Antioxidant Therapies in Friedreich's Ataxia. | Cells | 2025 | 41002373 | PubTator, text mining | PubMed |
| TRIM52 Ubiquitin Ligase Acts as a Key Recognition Component of the Mammalian fMet/N-degron Pathway. | J Mol Biol | 2025 | 40976346 | PubTator, text mining | PubMed |
| Calpain in Traumatic Brain Injury: From Cinderella to Central Player. | Cells | 2025 | 40862734 | PubTator, text mining | PubMed |
| Triglycerides and T Cells in Cardiovascular Risk: Inflammatory Transcriptomic Profile in Hypertriglyceridemia Patients' T Cells. | JACC Basic Transl Sci | 2025 | 40845480 | PubTator, text mining | PubMed |
| Loss-of-function variants in SPTAN1 and SPTBN4 cause early-onset hereditary myopathy. | J Physiol | 2025 | 40842327 | PubTator, text mining | PubMed |
| [Sjögren disease complicated by primary breast lymphoma: A case report]. | Beijing Da Xue Xue Bao Yi Xue Ban | 2025 | 40754924 | PubTator, text mining | PubMed |
| Exome Study of Single Nucleotide Variations in Patients with Syndromic and Non-Syndromic Autism Reveals Potential Candidate Genes for Diagnostics and Novel Single Nucleotide Variants. | Cells | 2025 | 40558542 | PubTator, text mining | PubMed |
| Expansion of the Epilepsy Genotype-Phenotype Spectrum: Genetic and Clinical Characterization of 288 Children with Epilepsy in China. | Seizure | 2025 | 40554313 | PubTator, text mining | PubMed |
| Role of alphaII-spectrin and XPF interaction in Hepatocellular carcinoma. | Gene | 2025 | 40466963 | PubTator, text mining | PubMed |
| FGF21 alleviates α-II-spectrin breakdown in a model of oxygen-glucose deprivation and modulates global protein phosphorylation in hippocampal neurons. | Neuropharmacology | 2025 | 40447258 | PubTator, text mining | PubMed |
| Phenotypic and molecular characterization of a recurrent SPTAN1 mutation causing SPG91. | Mol Biol Rep | 2025 | 40397273 | PubTator, text mining | PubMed |
| Critical role of alpha spectrin in DNA repair: the importance of μ-calpain and Fanconi anemia proteins. | Exp Biol Med (Maywood) | 2025 | 40375875 | PubTator, text mining | PubMed |
| SPTAN1-Results of a Caregiver Survey. | J Child Adolesc Psychopharmacol | 2025 | 40261672 | PubTator, text mining | PubMed |
| Comprehensive Proteomics and Machine Learning Analysis to Distinguish Follicular Adenoma and Follicular Thyroid Carcinoma from Indeterminate Thyroid Nodules. | Endocrinol Metab (Seoul) | 2025 | 40205804 | PubTator, text mining | PubMed |
| Insights into the clinical and immunological significance of anti-α-fodrin antibodies in systemic lupus erythematosus. | Rheumatol Immunol Res | 2025 | 40191471 | PubTator, text mining | PubMed |
| Heterozygous loss-of-function variants in SPTAN1 cause an early childhood onset distal myopathy. | Genet Med | 2025 | 40023774 | PubTator, text mining | PubMed |
| Loss of Function SPTAN1 Variants Result in Ataxia and Intellectual Disability. | Clin Genet | 2025 | 39988451 | PubTator, text mining | PubMed |
| The up-regulation of SPTAN1 expression in Pancreatic adenocarcinoma is associated with tumor immune invasion and poor clinical prognosis. | BMC Gastroenterol | 2025 | 39762747 | PubTator, text mining | PubMed |
| Multi-Omics Approach Reveals Genes and Pathways Affected in Miller-Dieker Syndrome. | Mol Neurobiol | 2025 | 39508990 | 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/v1/6709/papers?page=2