Gene · 8291
Papers2,035
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 2,035
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| A novel biallelic mutation in the DYSF gene as a cause of Miyoshi myopathy. | Neurol Sci | 2026 | 42047868 | PubTator, text mining | PubMed |
| Dysferlinopathies: phenotypic study of a Moroccan series of 28 cases. | Acta Myol | 2026 | 41954144 | PubTator, text mining | PubMed |
| Full length TECPR1 displays 'cis' Dysferlin domain architecture. | bioRxiv | 2026 | 41889887 | PubTator, text mining | PubMed |
| Dysferlin stabilizes membrane nanodomains of cardiomyocytes after myocardial infarction. | Sci Rep | 2026 | 41882145 | PubTator, text mining | PubMed |
| The genetics of multiple sclerosis: an updated perspective. | Curr Opin Neurol | 2026 | 41873214 | PubTator, text mining | PubMed |
| DAB2 in LGMD R2: a molecular link between disease progression and lipid dysregulation. | JCI Insight | 2026 | 41869723 | PubTator, text mining | PubMed |
| A Novel Dysferlin-Binding Kinase CK2α Promotes Plasma Membrane Repair in Dysferlinopathy. | FASEB J | 2026 | 41824290 | PubTator, text mining | PubMed |
| TMEM259/MEMBRALIN is a non-canonical ER-phagy receptor that associates with MAN1B1 and VCP to eliminate viral glycoproteins. | Autophagy Rep | 2026 | 41799849 | PubTator, text mining | PubMed |
| The Clinical, Histological, and Genetic Spectrum of RYR1 Variants-A Multi-Center Israeli Cohort Study. | J Clin Med | 2026 | 41753076 | PubTator, text mining | PubMed |
| Implementing a Tiered Genetic Testing Strategy for Muscular Dystrophies in Morocco: From Targeted Assays to Exome Sequencing. | Mol Genet Genomic Med | 2026 | 41742649 | PubTator, text mining | PubMed |
| Advances in electrical stimulation-based therapeutic technologies for sarcopenia prevention and treatment. | Bioact Mater | 2026 | 41727275 | PubTator, text mining | PubMed |
| Dysferlinopathy due to a homozygous DYSF DysF-domain variant in a non-consanguineous Tunisian family. | Mol Biol Rep | 2026 | 41721951 | PubTator, text mining | PubMed |
| Novel Insights into the Enigmatic Genetics of Male Breast Cancer in China. | Pathophysiology | 2026 | 41718387 | PubTator, text mining | PubMed |
| Linking Oxidative Stress to Placental Dysfunction: The Key Role of Mitochondria in Trophoblast Function. | Med Sci (Basel) | 2026 | 41718100 | PubTator, text mining | PubMed |
| DYSF gene variant spectrum in Arab populations across eight countries: A systematic review. | Biomol Biomed | 2026 | 41677014 | PubTator, text mining | PubMed |
| Myopathy With Exercise-Induced Intolerance due to Novel Biallelic Variants in OBSCN-A Clinical, Morphological and Molecular Analysis. | Neuropathol Appl Neurobiol | 2026 | 41645489 | PubTator, text mining | PubMed |
| Muscle RING finger-1 facilitates skeletal muscle regeneration via regulating myoblast proliferation and differentiation. | J Transl Med | 2026 | 41606616 | PubTator, text mining | PubMed |
| Enhancing the Performance of a Blood-Based Diagnostic Screening Tool for Dysferlinopathy: Optimising an Immunoassay Across Continents. | Neuropathol Appl Neurobiol | 2026 | 41605519 | PubTator, text mining | PubMed |
| The proteome of goat meat exudate: Temporal proteomics as a new way to uncover the underlying mechanisms of meat tenderization. | Meat Sci | 2026 | 41605078 | PubTator, text mining | PubMed |
| A novel case of compound heterozygous GFPT1 congenital myasthenic syndrome with a coexisting heterozygous DYSF mutation: clinical and pathological insights. | Neurol Sci | 2026 | 41546777 | 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/v1/8291/papers?page=2