Gene · 825
Papers1,501
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
101 to 120 of 1,501
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Statistical Dissection of the Genetic Determinants of Phenotypic Heterogeneity in Genes with Multiple Associated Rare Diseases. | Genes (Basel) | 2023 | 38003043 | PubTator, text mining | PubMed |
| The Role and Therapeutic Implications of Inflammation in the Pathogenesis of Brain Arteriovenous Malformations. | Biomedicines | 2023 | 38001877 | PubTator, text mining | PubMed |
| Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients. | Orphanet J Rare Dis | 2023 | 37974208 | PubTator, text mining | PubMed |
| Novel mutations in the SGCA gene in unrelated Vietnamese patients with limb-girdle muscular dystrophies disease. | Front Genet | 2023 | 37900180 | PubTator, text mining | PubMed |
| Whole-Exome Sequencing of 24 Spanish Families: Candidate Genes for Non-Syndromic Pediatric Keratoconus. | Genes (Basel) | 2023 | 37895187 | PubTator, text mining | PubMed |
| Advances in immunotyping of colorectal cancer. | Front Immunol | 2023 | 37876934 | PubTator, text mining | PubMed |
| Functional enrichment analysis of mutated genes in children with hyperthyroidism. | Front Endocrinol (Lausanne) | 2023 | 37876543 | PubTator, text mining | PubMed |
| The role of TRIM family in metabolic associated fatty liver disease. | Front Endocrinol (Lausanne) | 2023 | 37867509 | PubTator, text mining | PubMed |
| MicroRNAs as a Tool for Differential Diagnosis of Neuromuscular Disorders. | Neuromolecular Med | 2023 | 37856057 | PubTator, text mining | PubMed |
| Single-centre experience with autosomal recessive limb-girdle muscular dystrophy: case series and literature review. | Arq Neuropsiquiatr | 2023 | 37852290 | PubTator, text mining | PubMed |
| Altered expression of proteins involved in metabolism in LGMDR1 muscle is lost in cell culture conditions. | Orphanet J Rare Dis | 2023 | 37817200 | PubTator, text mining | PubMed |
| Portrait of Dysferlinopathy: Diagnosis and Development of Therapy. | J Clin Med | 2023 | 37762951 | PubTator, text mining | PubMed |
| Calpain signaling: from biology to therapeutic opportunities in neurodegenerative disorders. | Front Vet Sci | 2023 | 37732142 | PubTator, text mining | PubMed |
| Towards the Identification of Biomarkers for Muscle Function Improvement in Myotonic Dystrophy Type 1. | J Neuromuscul Dis | 2023 | 37694373 | PubTator, text mining | PubMed |
| Combined sequence and copy number analysis improves diagnosis of limb girdle and other myopathies. | Ann Clin Transl Neurol | 2023 | 37688281 | PubTator, text mining | PubMed |
| Whole-Genome Sequencing Identified New Structural Variations in the DMD Gene That Cause Duchenne Muscular Dystrophy in Two Girls. | Int J Mol Sci | 2023 | 37686372 | PubTator, text mining | PubMed |
| Decoding the transcriptome of Duchenne muscular dystrophy to the single nuclei level reveals clinical-genetic correlations. | Cell Death Dis | 2023 | 37673877 | PubTator, text mining | PubMed |
| PROCEEDINGS OF THE XXIII CONGRESS OF THE ITALIAN ASSOCIATION OF MYOLOGY: PadovaJune 8-10, 2023. | Acta Myol | 2023 | 37650038 | PubTator, text mining | PubMed |
| Comparative Analysis of Muscle Atrophy During Spaceflight, Nutritional Deficiency and Disuse in the Nematode Caenorhabditis elegans. | Int J Mol Sci | 2023 | 37628820 | PubTator, text mining | PubMed |
| The Spectrum of the Heterozygous Effect in Biallelic Mendelian Diseases-The Symptomatic Heterozygote Issue. | Genes (Basel) | 2023 | 37628614 | 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/v1/825/papers?page=6