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.
681 to 700 of 3,985
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Comparative analysis of right ventricular strain in Fabry cardiomyopathy and sarcomeric hypertrophic cardiomyopathy. | Eur Heart J Cardiovasc Imaging | 2023 | 35900225 | PubTator, text mining | PubMed |
| Fluorescent hiPSC-derived MYH6-mScarlet cardiomyocytes for real-time tracking, imaging, and cardiotoxicity assays. | Cell Biol Toxicol | 2023 | 35870039 | PubTator, text mining | PubMed |
| Noncancer-related Secondary Findings in a Cohort of 231 Children With Cancer and Their Parents. | J Pediatr Hematol Oncol | 2023 | 35537032 | PubTator, text mining | PubMed |
| Cardiovascular Disease in South Asian Immigrants: a Review of Dysfunctional HDL as a Potential Marker. | J Racial Ethn Health Disparities | 2023 | 35449485 | PubTator, text mining | PubMed |
| Patterns and Persistence of Perioperative Plasma and Cerebrospinal Fluid Neuroinflammatory Protein Biomarkers After Elective Orthopedic Surgery Using SOMAscan. | Anesth Analg | 2023 | 35389379 | PubTator, text mining | PubMed |
| One gene, two modes of inheritance, four diseases: A systematic review of the cardiac manifestation of pathogenic variants in JPH2-encoded junctophilin-2. | Trends Cardiovasc Med | 2023 | 34861382 | PubTator, text mining | PubMed |
| Unique attributes of obesity in India: A narrative review. | Obes Med | 2022 | 38572212 | PubTator, text mining | PubMed |
| Site-specific genome editing in treatment of inherited diseases: possibility, progress, and perspectives. | Med Rev (2021) | 2022 | 37724161 | PubTator, text mining | PubMed |
| Evaluation of the DBA/2J mouse as a potential background strain for genetic models of cardiomyopathy. | J Mol Cell Cardiol Plus | 2022 | 37206988 | PubTator, text mining | PubMed |
| Low expression of the K280N TNNT2 mutation is sufficient to increase basal myofilament activation in human hypertrophy cardiomyopathy. | J Mol Cell Cardiol Plus | 2022 | 37159677 | PubTator, text mining | PubMed |
| Hypertrophic cardiomyopathy after Takeuchi procedure for anomalous origin of the left coronary artery from the pulmonary artery syndrome. | Ann Pediatr Cardiol | 2022 | 37152520 | PubTator, text mining | PubMed |
| Pathogenic Mechanisms Underlying Cirrhotic Cardiomyopathy. | Front Netw Physiol | 2022 | 36926084 | PubTator, text mining | PubMed |
| A Novel Loss-of-function Mutation in MYBPC3 Causes Familial Hypertrophic Cardiomyopathy with Extreme Intrafamilial Phenotypic Heterogeneity. | Balkan J Med Genet | 2022 | 36880031 | PubTator, text mining | PubMed |
| Contraction pressure analysis using optical imaging in normal and MYBPC3-mutated hiPSC-derived cardiomyocytes grown on matrices with tunable stiffness. | Biomater Biosyst | 2022 | 36824378 | PubTator, text mining | PubMed |
| Implications of S-glutathionylation of sarcomere proteins in cardiac disorders, therapies, and diagnosis. | Front Cardiovasc Med | 2022 | 36762302 | PubTator, text mining | PubMed |
| Cardiac calcium regulation in human induced pluripotent stem cell cardiomyocytes: Implications for disease modeling and maturation. | Front Cell Dev Biol | 2022 | 36742199 | PubTator, text mining | PubMed |
| Whole-Exome Sequencing Identifies Genetic Variants for Severe Adolescent Idiopathic Scoliosis in a Taiwanese Population. | J Pers Med | 2022 | 36675693 | PubTator, text mining | PubMed |
| Pacing Dynamics Determines the Arrhythmogenic Mechanism of the CPVT2-Causing CASQ2G112+5X Mutation in a Guinea Pig Ventricular Myocyte Computational Model. | Genes (Basel) | 2022 | 36672764 | PubTator, text mining | PubMed |
| Overlapping Phenotype of Adult-Onset ALPK3-Cardiomyopathy in the Setting of Two Novel Variants. | Cardiol Res | 2022 | 36660067 | PubTator, text mining | PubMed |
| Multimodality imaging fusion to guide stereotactic radioablation for refractory complex ventricular tachycardia. | HeartRhythm Case Rep | 2022 | 36620359 | 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
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GET https://conductscience.org/api/genes/v1/4607/papers?page=35