ConductScience.org, home

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.

81 to 100 of 2,035

Download this page as JSON
TitleJournalYearPMIDFound bySource
A survey on mutation spectrum in Iranian patients with limb-girdle muscular dystrophies.Hum Genomics202540361203PubTator, text miningPubMed
Multiple sclerosis severity variant in DYSF-ZNF638 locus associates with neuronal loss and inflammation.iScience202540352730PubTator, text miningPubMed
Decoding the role of microtubules: a trafficking road for vesicle.Theranostics202540303338PubTator, text miningPubMed
Machine Learning Identification of Neutrophil Extracellular Trap-Related Genes as Potential Biomarkers and Therapeutic Targets for Bronchopulmonary Dysplasia.Int J Mol Sci202540244055PubTator, text miningPubMed
Treatabolome for finely targeting muscle pathology in LGMD.Acta Myol202540183440PubTator, text miningPubMed
The Association Between Statin Drugs and Rhabdomyolysis: An Analysis of FDA Adverse Event Reporting System (FAERS) Data and Transcriptomic Profiles.Genes (Basel)202540149400PubTator, text miningPubMed
Identification of glucocorticoid-related genes in systemic lupus erythematosus using bioinformatics analysis and machine learning.PLoS One202540131879PubTator, text miningPubMed
High-throughput screening identifies bazedoxifene as a potential therapeutic for dysferlin-deficient limb girdle muscular dystrophy.Br J Pharmacol202540108832PubTator, text miningPubMed
Muscle MRI Pattern in Dysferlinopathy and its Correlation with Dysferlin Gait.Ann Indian Acad Neurol202540079678PubTator, text miningPubMed
Limb-Girdle Muscular Dystrophy Type 2 Caused by a Novel Homozygous Mutation in DYSF in a Consanguineous Family.Int J Rheum Dis202540062450PubTator, text miningPubMed
Antisense oligonucleotide-mediated exon 27 skipping restores dysferlin function in dysferlinopathy patient-derived muscle cells.Mol Ther Nucleic Acids202539991471PubTator, text miningPubMed
Antisense oligonucleotide-mediated exon 27 skipping restores dysferlin function in dysferlinopathy patient-derived muscle cells.Mol Ther Nucleic Acids202539967852PubTator, text miningPubMed
[Ultrastructural changes of skeletal muscle tissue of patients with dysferlinopathy].Arkh Patol202539943726PubTator, text miningPubMed
Analysis of Exon Skipping Applicability for Dysferlinopathies.Cells202539936969PubTator, text miningPubMed
Whole genome sequencing identifies novel candidate genetic variants in canine stomatocytosis.Gene202539929273PubTator, text miningPubMed
Limb-Girdle Muscular Dystrophies (LGMD): Clinical features, diagnosis and genetic variability through next generation sequencing.Glob Med Genet202539925440PubTator, text miningPubMed
Rapid Quantitative Assessment of Muscle Sodium Dynamics After Exercise Using 23Na-MRI in Dysferlinopathy and Healthy Controls.J Cachexia Sarcopenia Muscle202539900102PubTator, text miningPubMed
Bioinformatics approach reveals the critical role of inflammation-related genes in age-related hearing loss.Sci Rep202539837906PubTator, text miningPubMed
Chronic pain as a presenting feature of dysferlinopathy.Neuromuscul Disord202539798170PubTator, text miningPubMed
Clinical features, mutation spectrum and factors related to reaching molecular diagnosis in a cohort of patients with distal myopathies.J Neurol202539775307PubTator, text miningPubMed

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/v1/8291/papers?page=5