Gene · 3908
Papers2,255
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 2,255
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Biallelic truncating variants in children with titinopathy represent a recognizable condition with distinctive muscular and cardiac characteristics: a report on five patients. | Front Cardiovasc Med | 2023 | 37576110 | PubTator, text mining | PubMed |
| SERPINB5 is a novel serum diagnostic biomarker for gastric high-grade intraepithelial neoplasia and plays a role in regulation of macrophage phenotypes. | Transl Oncol | 2023 | 37573714 | PubTator, text mining | PubMed |
| Editorial: The expanding clinical and genetic basis of adult inherited neurometabolic disorders. | Front Neurol | 2023 | 37560451 | PubTator, text mining | PubMed |
| Use of genome sequencing to hunt for cryptic second-hit variants: analysis of 31 cases recruited to the 100 000 Genomes Project. | J Med Genet | 2023 | 37558402 | PubTator, text mining | PubMed |
| Genetic findings in Czech patients with limb girdle muscular dystrophy. | Clin Genet | 2023 | 37526466 | PubTator, text mining | PubMed |
| Autophagy increase in Merosin-Deficient Congenital Muscular Dystrophy type 1A. | Eur J Transl Myol | 2023 | 37522802 | PubTator, text mining | PubMed |
| Identify and validate RUNX2 and LAMA2 as novel prognostic signatures and correlate with immune infiltrates in bladder cancer. | Front Oncol | 2023 | 37519798 | PubTator, text mining | PubMed |
| Whole Genome Sequencing Revealed Inherited Rare Oligogenic Variants Contributing to Schizophrenia and Major Depressive Disorder in Two Families. | Int J Mol Sci | 2023 | 37511534 | PubTator, text mining | PubMed |
| Limb-Girdle Muscular Dystrophies Classification and Therapies. | J Clin Med | 2023 | 37510884 | PubTator, text mining | PubMed |
| LAMA2-Related Muscular Dystrophy Across the Life Span: A Cross-sectional Study. | Neurol Genet | 2023 | 37476021 | PubTator, text mining | PubMed |
| Multi-omics in thoracic aortic aneurysm: the complex road to the simplification. | Cell Biosci | 2023 | 37475058 | PubTator, text mining | PubMed |
| Clearance of defective muscle stem cells by senolytics restores myogenesis in myotonic dystrophy type 1. | Nat Commun | 2023 | 37468473 | PubTator, text mining | PubMed |
| Transcriptomic patterns in early-secretory and mid-secretory endometrium in a natural menstrual cycle immediately before in vitro fertilization and embryo transfer. | Obstet Gynecol Sci | 2023 | 37460099 | PubTator, text mining | PubMed |
| Differences in the pathogenetic characteristics of prostate cancer in the transitional and peripheral zones and the possible molecular biological mechanisms. | Front Oncol | 2023 | 37456243 | PubTator, text mining | PubMed |
| Spatially resolved multiomics of human cardiac niches. | Nature | 2023 | 37438528 | PubTator, text mining | PubMed |
| In silico-in vitro modeling to uncover cues involved in establishing microglia identity: TGF-β3 and laminin can drive microglia signature gene expression. | Front Cell Neurosci | 2023 | 37435046 | PubTator, text mining | PubMed |
| History of international connections of myology in Europe. | Eur J Transl Myol | 2023 | 37428109 | PubTator, text mining | PubMed |
| Congenital Muscular Dystrophy Due to Merosin Deficiency: Report of a New Mutation. | Cureus | 2023 | 37416022 | PubTator, text mining | PubMed |
| Case report: Novel frameshift mutation in LAMA2 gene causing congenital muscular dystrophy type 1A. | Front Genet | 2023 | 37415604 | PubTator, text mining | PubMed |
| Characterization of Skeletal Muscle Biopsy and Derived Myoblasts in a Patient Carrying Arg14del Mutation in Phospholamban Gene. | Cells | 2023 | 37408239 | 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.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/genes/v1/3908/papers?page=11