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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.

681 to 700 of 1,745

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TitleJournalYearPMIDFound bySource
Whole-Exome Sequencing and hiPSC Cardiomyocyte Models Identify MYRIP, TRAPPC11, and SLC27A6 of Potential Importance to Left Ventricular Hypertrophy in an African Ancestry Population.Front Genet202133679876PubTator, text miningPubMed
Prenatal diagnosis of a 15q11.2-q14 deletion of paternal origin associated with increased nuchal translucency, mosaicism for de novo multiple unbalanced translocations involving 15q11-q14, 5qter, 15qter, 17pter and 3qter and Prader-Willi syndrome.
Taiwan J Obstet Gynecol202133678338PubTator, text miningPubMed
Diagnostic yield of genetic testing in a heterogeneous cohort of 1376 HCM patients.BMC Cardiovasc Disord202133673806PubTator, text miningPubMed
Sarcomere mutation negative hypertrophic cardiomyopathy is associated with ageing and obesity.Open Heart202133637569PubTator, text miningPubMed
Harmonizing the Collection of Clinical Data on Genetic Testing Requisition Forms to Enhance Variant Interpretation in Hypertrophic Cardiomyopathy (HCM): A Study from the ClinGen Cardiomyopathy Variant Curation Expert Panel.
J Mol Diagn202133631351PubTator, text miningPubMed
Genetic Factors Underlying Sudden Infant Death Syndrome.Appl Clin Genet202133623412PubTator, text miningPubMed
Variant Spectrum of Formin Homology 2 Domain-Containing 3 Gene in Chinese Patients With Hypertrophic Cardiomyopathy.J Am Heart Assoc202133586461PubTator, text miningPubMed
Myogenesis modelled by human pluripotent stem cells: a multi-omic study of Duchenne myopathy early onset.J Cachexia Sarcopenia Muscle202133586340PubTator, text miningPubMed
Heat shock proteins and small nucleolar RNAs are dysregulated in a Drosophila model for feline hypertrophic cardiomyopathy.G3 (Bethesda)202133561224PubTator, text miningPubMed
Regional myocardial function at preclinical disease stage of hypertrophic cardiomyopathy in female gene variant carriers.Int J Cardiovasc Imaging202133559798PubTator, text miningPubMed
The origin of the expressed retrotransposed gene ACTBL2 and its influence on human melanoma cells' motility and focal adhesion formation.Sci Rep202133558623PubTator, text miningPubMed
Carbon nanomaterials for cardiovascular theranostics: Promises and challenges.Bioact Mater202133553814PubTator, text miningPubMed
Noonan syndrome patient-specific induced cardiomyocyte model carrying SOS1 gene variant c.1654A>G.Exp Cell Res202133549576PubTator, text miningPubMed
The canine activated platelet secretome (CAPS): A translational model of thrombin-evoked platelet activation response.Res Pract Thromb Haemost202133537530PubTator, text miningPubMed
Fetal programming of polycystic ovary syndrome: Effects of androgen exposure on prenatal ovarian development.J Steroid Biochem Mol Biol202133515680PubTator, text miningPubMed
Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies.Genet Med202133500567PubTator, text miningPubMed
Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity.Nat Genet202133495597PubTator, text miningPubMed
Vitamin D improves pulmonary function in a rat model for congenital diaphragmatic hernia.Arch Biochem Biophys202133484710PubTator, text miningPubMed
The Desmin (DES) Mutation p.A337P Is Associated with Left-Ventricular Non-Compaction Cardiomyopathy.Genes (Basel)202133478057PubTator, text miningPubMed
Exome Sequencing and Congenital Heart Disease in Sub-Saharan Africa.Circ Genom Precis Med202133448881PubTator, 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.

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