Gene · 70
Papers1,745
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
201 to 220 of 1,745
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Case-control association study of congenital heart disease from a tertiary paediatric cardiac centre from North India. | BMC Pediatr | 2023 | 37322441 | PubTator, text mining | PubMed |
| Is Hypertrophic Cardiomyopathy Always a Familial and Inherited Disease? | J Am Heart Assoc | 2023 | 37301765 | PubTator, text mining | PubMed |
| The actin cytoskeleton in hair bundle development and hearing loss. | Hear Res | 2023 | 37300948 | PubTator, text mining | PubMed |
| Identification and functional analysis of a novel de novo missense mutation located in the initiation codon of LAMP2 associated with early onset female Danon disease. | Mol Genet Genomic Med | 2023 | 37288668 | PubTator, text mining | PubMed |
| Proteomic profiling of sudden cardiac death with acquired cardiac hypertrophy. | Int J Legal Med | 2023 | 37284852 | PubTator, text mining | PubMed |
| A pathogenic nonsense mutation (c.1522C>T) of the MYBPC3 gene is implicated with hypertrophic cardiomyopathy. | ESC Heart Fail | 2023 | 37271167 | PubTator, text mining | PubMed |
| Left Ventricular Noncompaction Cardiomyopathy in an Elderly Patient: A Case Report and Literature Review. | Cureus | 2023 | 37261174 | PubTator, text mining | PubMed |
| Cardiac troponin T N-domain variant destabilizes the actin interface resulting in disturbed myofilament function. | Proc Natl Acad Sci U S A | 2023 | 37252999 | PubTator, text mining | PubMed |
| Personalized Management of Sudden Death Risk in Primary Cardiomyopathies: From Clinical Evaluation and Multimodality Imaging to Ablation and Cardioverter-Defibrillator Implant. | J Pers Med | 2023 | 37241047 | PubTator, text mining | PubMed |
| Arrhythmic Risk Stratification among Patients with Hypertrophic Cardiomyopathy. | J Clin Med | 2023 | 37240503 | PubTator, text mining | PubMed |
| Novel biphasic mechanism of the canonical Wnt signalling component PYGO2 promotes cardiomyocyte differentiation from hUC-MSCs. | Cell Tissue Res | 2023 | 37233752 | PubTator, text mining | PubMed |
| Integrated ACMG-approved genes and ICD codes for the translational research and precision medicine. | Database (Oxford) | 2023 | 37195695 | PubTator, text mining | PubMed |
| Direct Reprogramming of Resident Non-Myocyte Cells and Its Potential for In Vivo Cardiac Regeneration. | Cells | 2023 | 37190075 | PubTator, text mining | PubMed |
| Subcutaneous Adipose Tissue Transcriptome Highlights Specific Expression Profiles in Severe Pediatric Obesity: A Pilot Study. | Cells | 2023 | 37190014 | PubTator, text mining | PubMed |
| A case of infantile Barth syndrome with severe heart failure: Importance of splicing variants in the TAZ gene. | Mol Genet Genomic Med | 2023 | 37186429 | PubTator, text mining | PubMed |
| Palmitic Acid Upregulates Type I Interferon-Mediated Antiviral Response and Cholesterol Biosynthesis in Human Astrocytes. | Mol Neurobiol | 2023 | 37184765 | PubTator, text mining | PubMed |
| Role of non-coding variants in cardiovascular disease. | J Cell Mol Med | 2023 | 37183561 | PubTator, text mining | PubMed |
| Successful complex percutaneous intervention in patient with Fontan circulation and severe heart failure: A case report. | Clin Case Rep | 2023 | 37151951 | PubTator, text mining | PubMed |
| Novel immune cell infiltration-related biomarkers in atherosclerosis diagnosis. | PeerJ | 2023 | 37151293 | PubTator, text mining | PubMed |
| Insights into the genetic architecture of congenital heart disease from animal modeling. | Zool Res | 2023 | 37147909 | 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/v1/70/papers?page=11