Gene · 4607
Papers3,985
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
741 to 760 of 3,985
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Enhancing interaction of actin and actin-binding domain 1 of dystrophin with modulators: Toward improved gene therapy for Duchenne muscular dystrophy. | J Biol Chem | 2022 | 36372234 | PubTator, text mining | PubMed |
| Cryo-Electron Microscopy Reveals Cardiac Myosin Binding Protein-C M-Domain Interactions with the Thin Filament. | J Mol Biol | 2022 | 36370805 | PubTator, text mining | PubMed |
| RBPMS2 Is a Myocardial-Enriched Splicing Regulator Required for Cardiac Function. | Circ Res | 2022 | 36367103 | PubTator, text mining | PubMed |
| Alterations of the Sialylation Machinery in Brugada Syndrome. | Int J Mol Sci | 2022 | 36361941 | PubTator, text mining | PubMed |
| Challenging Occam's Razor: Dual Molecular Diagnoses Explain Entangled Clinical Pictures. | Genes (Basel) | 2022 | 36360260 | PubTator, text mining | PubMed |
| Mitochondrial Cardiomyopathy: Molecular Epidemiology, Diagnosis, Models, and Therapeutic Management. | Cells | 2022 | 36359908 | PubTator, text mining | PubMed |
| De novo and inherited variants in coding and regulatory regions in genetic cardiomyopathies. | Hum Genomics | 2022 | 36357925 | PubTator, text mining | PubMed |
| Five years' experience of the clinical exome sequencing in a Spanish single center. | Sci Rep | 2022 | 36357507 | PubTator, text mining | PubMed |
| MYBPC3 deficiency in cardiac fibroblasts drives their activation and contributes to fibrosis. | Cell Death Dis | 2022 | 36357371 | PubTator, text mining | PubMed |
| A novel likely pathogenic variant in the FBXO32 gene associated with dilated cardiomyopathy according to whole‑exome sequencing. | BMC Med Genomics | 2022 | 36344977 | PubTator, text mining | PubMed |
| Analysis of clinically relevant variants from ancestrally diverse Asian genomes. | Nat Commun | 2022 | 36335097 | PubTator, text mining | PubMed |
Infant with Loeys-Dietz syndrome treated for febrile status epilepticus with COVID-19 infection: first reported case of febrile status epilepticus and focal seizures in a patient with Loeys-Dietz syndrome and review of literature. | BMJ Case Rep | 2022 | 36328362 | PubTator, text mining | PubMed |
| Immune system disruptions implicated in whole blood epigenome-wide association study of depression among Parkinson's disease patients. | Brain Behav Immun Health | 2022 | 36325427 | PubTator, text mining | PubMed |
| Pathogenesis of Cardiomyopathy Caused by Variants in ALPK3, an Essential Pseudokinase in the Cardiomyocyte Nucleus and Sarcomere. | Circulation | 2022 | 36321451 | PubTator, text mining | PubMed |
| Validate the force-velocity relation of the Hill's muscle model from a molecular perspective. | Front Bioeng Biotechnol | 2022 | 36312549 | PubTator, text mining | PubMed |
Early Diagnosis of Abnormal Left Ventricular Systolic Functions of Rare Pathogenic Titin Mutation Gene Carriers in FHCM by Three-Dimensional Speckle Tracking Echocardiography Combined with Gene Detection. | Int J Clin Pract | 2022 | 36304977 | PubTator, text mining | PubMed |
| Subtypes and Mechanisms of Hypertrophic Cardiomyopathy Proposed by Machine Learning Algorithms. | Life (Basel) | 2022 | 36294999 | PubTator, text mining | PubMed |
| Unpredicted Aberrant Splicing Products Identified in Postmortem Sudden Cardiac Death Samples. | Int J Mol Sci | 2022 | 36293497 | PubTator, text mining | PubMed |
| Next-Generation Sequencing Gene Panels in Inheritable Cardiomyopathies and Channelopathies: Prevalence of Pathogenic Variants and Variants of Unknown Significance in Uncommon Genes. | Biomolecules | 2022 | 36291626 | PubTator, text mining | PubMed |
| Bioinformatics Analysis of Common Differential Genes of Viral Myocarditis and Dilated Cardiomyopathy: Screening for Potential Pharmacological Compounds. | J Cardiovasc Dev Dis | 2022 | 36286305 | 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/v1/4607/papers?page=38