Gene · 1134
Papers889
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 889
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| NMJ-associated transcriptomic remodeling correlates with disease severity in juvenile dermatomyositis. | Inflamm Res | 2026 | 42700229 | PubTator, text mining | PubMed |
| Multi-omics identifies promoter methylation and gene expression changes associated with human skeletal muscle atrophy. | Exp Physiol | 2026 | 42636425 | PubTator, text mining | PubMed |
| CHRNA gene alterations in epilepsy: A systematic review of alpha subunit associations with ADSHE, SeLIE, and SeLECTS. | Epilepsy Res | 2026 | 42607591 | PubTator, text mining | PubMed |
| Integrative multi-omics and machine learning identify CHRNA1 putative circadian-immune hub in COPD. | PLoS One | 2026 | 42536689 | PubTator, text mining | PubMed |
| Congenital myasthenic syndromes in a Southeast Asian adult neurology clinic: a long road to diagnosis and therapy. | BMC Neurol | 2026 | 42469681 | PubTator, text mining | PubMed |
| Hsa_circ_0065149 mediates the ceRNA network pathway: Research on the mechanism regulating myasthenia gravis. | J Mol Neurosci | 2026 | 42171932 | PubTator, text mining | PubMed |
| Hidden diagnoses among patients with double seronegative myasthenia gravis. | Front Neurol | 2026 | 41940306 | PubTator, text mining | PubMed |
| Non-pterygium Escobar syndrome from compound-heterozygous CHRNG variants: genotype-phenotype insights. | Hum Genome Var | 2026 | 41826296 | PubTator, text mining | PubMed |
| Telitacicept for refractory AChR-positive generalized myasthenia gravis: a retrospective real-world study. | Front Immunol | 2026 | 41737228 | PubTator, text mining | PubMed |
| PGVDA: a pathway-aggregated genetic dosage framework for interpretable disease classification using machine learning. | Brief Bioinform | 2026 | 41632594 | PubTator, text mining | PubMed |
| Exploring molecular signatures in PURA syndrome using muscle proteomics and serum biomarkers. | J Neurol | 2026 | 41575592 | PubTator, text mining | PubMed |
| Slow-Channel Congenital Myasthenic Syndrome due to a CHRNA1 Variant Masquerading as Atypical Anorexia Nervosa: A Case Report. | Cureus | 2025 | 41362569 | PubTator, text mining | PubMed |
| The Biological and Prognostic Implications of the Nicotinic Acetylcholine Receptor α3, α5, and α7 Subunits in Oral Squamous Cell Carcinoma. | Cancer Med | 2025 | 41201200 | PubTator, text mining | PubMed |
| mRNA Isoforms and Variants in Health and Disease. | Int J Mol Sci | 2025 | 41096623 | PubTator, text mining | PubMed |
| The new variant c.458C>G in CHRNA1 causes late-onset post-synaptic slow-channel congenital myasthenic syndrome. | Clinics (Sao Paulo) | 2025 | 40992289 | PubTator, text mining | PubMed |
| Biallelic CRELD1 variants cause severe muscle weakness and infantile epilepsy. | Brain Commun | 2025 | 40980404 | PubTator, text mining | PubMed |
| PAI-1 and CHRNA1-A new molecular axis and therapeutic target in primary focal hyperhidrosis. | Mol Ther Nucleic Acids | 2025 | 40896592 | PubTator, text mining | PubMed |
| Persistent Inflammation, Maladaptive Remodeling, and Fibrosis in the Kidney Following Long COVID-like MHV-1 Mouse Model. | Diseases | 2025 | 40863220 | PubTator, text mining | PubMed |
| Clinical and genetic features of congenital myasthenic syndrome due to the muscle acetylcholine receptor genes. | Brain Dev | 2025 | 40768883 | PubTator, text mining | PubMed |
| Reduction of the Ca2+ permeability of ligand-gated ion channels as a strategy against excitotoxicity. | Front Cell Neurosci | 2025 | 40740969 | 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/v1/1134/papers