Gene · 7148
Papers1,502
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
1 to 20 of 1,502
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Degradomic and transcriptomic profiling reveal pleiotropic roles of extracellular granzyme B in scarring and fibrosis. | Matrix Biol | 2026 | 42777922 | PubTator, text mining | PubMed |
| Connective tissue and genetics in the pathogenesis of rectal prolapse: A scoping review. | Colorectal Dis | 2026 | 42765168 | PubTator, text mining | PubMed |
| Long-Read Sequencing Resolves Complex CYP21A2 Variants and Identifies 2+0 Carriers in 21-Hydroxylase Deficiency. | J Mol Diagn | 2026 | 42727689 | PubTator, text mining | PubMed |
| Discovery of potential new drug targets for cystitis and chronic cystitis: A drug target Mendelian randomization study. | Fr J Urol | 2026 | 42700931 | PubTator, text mining | PubMed |
| Screening Potential Diagnostic Biomarkers of Lung Adenocarcinoma Related to Immune Infiltration Based on Single-Cell Proteomic Integration Analysis. | Can Respir J | 2026 | 42608948 | PubTator, text mining | PubMed |
| The Effects of Protein Environments on the Geometries and Energies of Hydrogen Bond Enhanced Halogen Bonds. | J Med Chem | 2026 | 42593916 | PubTator, text mining | PubMed |
| Syndromic dilated cardiomyopathy suggestive of an oligogenic background with CD36 and TNXB variants: a case report. | Eur Heart J Case Rep | 2026 | 42559185 | PubTator, text mining | PubMed |
| Mechanisms of blood-induced joint disease in hemophilia and potential novel targets for interventions. | Haematologica | 2026 | 42489065 | PubTator, text mining | PubMed |
| snRNA-seq of acral melanoma reveals heterogeneity and identifies novel progression marker and cancer-associated fibroblasts subpopulation. | NPJ Precis Oncol | 2026 | 42469458 | PubTator, text mining | PubMed |
| Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome. | Mol Syndromol | 2026 | 42445465 | PubTator, text mining | PubMed |
| Splicing Alterations Associated with Multiple Homozygous TNXB Variants in a Patient with Suspected Classical-Like Ehlers-Danlos Syndrome. | Biochem Genet | 2026 | 42295573 | PubTator, text mining | PubMed |
| Proteome-wide Mendelian Randomization and Colocalization Nominate CD58, PARP1, and Immune Co-stimulatory Pathways as Genetically Supported Targets for Multiple Sclerosis. | Curr Neuropharmacol | 2026 | 42227395 | PubTator, text mining | PubMed |
| Novel cardiac abnormalities observed in CAH patients with tenascin-X haploinsufficiency. | Front Endocrinol (Lausanne) | 2026 | 42222075 | PubTator, text mining | PubMed |
| Comment on: "Proteome-wide Mendelian randomization identifies APOM and TNXB as actionable mediators of steroid-sensitive nephrotic syndrome". | Pediatr Nephrol | 2026 | 42209839 | PubTator, text mining | PubMed |
| Identification of novel genomic variants in diabetic nephropathy patients using whole-exome sequencing: a pilot investigation. | Front Endocrinol (Lausanne) | 2026 | 41970998 | PubTator, text mining | PubMed |
| Methylation of tenascin XB mediated by methyltransferase-like 3 can effectively suppress neural injury and cellular apoptosis induced by ischemic stroke. | Int J Neurosci | 2026 | 41968052 | PubTator, text mining | PubMed |
| Proteome-wide Mendelian randomization identifies APOM and TNXB as actionable mediators of steroid-sensitive nephrotic syndrome. | Pediatr Nephrol | 2026 | 41961272 | PubTator, text mining | PubMed |
| Bilateral optic neuritis and multiple nerve sheath tumors in a patient with genetically characterized Ehlers-Danlos syndrome: A rare co-occurrence. | Radiol Case Rep | 2026 | 41960132 | PubTator, text mining | PubMed |
| Insights into TNXB-Related Classical-Like Ehlers-Danlos Syndrome: A Study of Polish Patients. | Open Access Rheumatol | 2026 | 41913751 | PubTator, text mining | PubMed |
| Live Births Following IVF-FET in Two Adult Sisters with Nonclassic P450 Oxidoreductase Deficiency: A Case Report Identifying a Novel POR Variant. | Int J Womens Health | 2026 | 41809679 | 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.
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