Gene · 2775
Papers1,584
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
81 to 100 of 1,584
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Clinically Relevant Genes Identified in Cerebral Palsy Cohorts Following Evaluation of the Clinical Description and Phenotype: A Systematic Review. | J Child Neurol | 2024 | 39246294 | PubTator, text mining | PubMed |
| A neurodevelopmental disorder mutation locks G proteins in the transitory pre-activated state. | Nat Commun | 2024 | 39103320 | Swiss-Prot, curated | PubMed |
| Etiology of combined pituitary hormone deficiency: GNAO1 as a novel candidate gene. | Endocr Connect | 2024 | 39078873 | PubTator, text mining | PubMed |
| Gnao1 is a molecular switch that regulates the Rho signaling pathway in differentiating neurons. | Sci Rep | 2024 | 39048611 | PubTator, text mining | PubMed |
| First Immunohistochemical Demonstration of the Expression of a Type-2 Vomeronasal Receptor, V2R2, in Wild Canids. | Int J Mol Sci | 2024 | 39000398 | PubTator, text mining | PubMed |
| CircGNAO1 strengthens its host gene GNAO1 expression for suppression of hepatocarcinogenesis. | Heliyon | 2024 | 38988568 | PubTator, text mining | PubMed |
| The impact of developmental and epileptic encephalopathies on families: a qualitative study. | Eur J Pediatr | 2024 | 38965081 | PubTator, text mining | PubMed |
| Dyskinetic crisis in GNAO1-related disorders: clinical perspectives and management strategies. | Front Neurol | 2024 | 38903163 | PubTator, text mining | PubMed |
| Clinical and Molecular Profiling in GNAO1 Permits Phenotype-Genotype Correlation. | Mov Disord | 2024 | 38881224 | PubTator, text mining | PubMed |
| Neomorphic Gαo mutations gain interaction with Ric8 proteins in GNAO1 encephalopathies. | J Clin Invest | 2024 | 38874642 | PubTator, text mining | PubMed |
| AAV9-Mediated Intrastriatal Delivery of GNAO1 Reduces Hyperlocomotion in Gnao1 Heterozygous R209H Mutant Mice. | J Pharmacol Exp Ther | 2024 | 38866563 | PubTator, text mining | PubMed |
| Sleep and circadian rhythm dysfunctions in movement disorders beyond Parkinson's disease and atypical parkinsonisms. | Curr Opin Neurol | 2024 | 38809245 | PubTator, text mining | PubMed |
| Differential regulation of G protein-coupled receptor-associated proteins in the caudate and the putamen of cynomolgus macaques following chronic ethanol drinking. | J Neurochem | 2024 | 38783749 | PubTator, text mining | PubMed |
| Diverse faces of GNAO1: mild forms in epilepsy and autism. | J Neurol | 2024 | 38724739 | PubTator, text mining | PubMed |
| Bilateral Simultaneous Magnetic Resonance-Guided Focused Ultrasound Pallidotomy for Life-Threatening Status Dystonicus. | Mov Disord | 2024 | 38641910 | PubTator, text mining | PubMed |
| Molecular Dynamic Simulations to Determine Individualized Therapy: Tetrabenazine for the GNAO1 Encephalopathy E246K Variant. | Mol Diagn Ther | 2024 | 38581611 | PubTator, text mining | PubMed |
| Specific pharmacological and Gi/o protein responses of some native GPCRs in neurons. | Nat Commun | 2024 | 38443355 | PubTator, text mining | PubMed |
| Cortical neurons obtained from patient-derived iPSCs with GNAO1 p.G203R variant show altered differentiation and functional properties. | Heliyon | 2024 | 38434323 | PubTator, text mining | PubMed |
| A GNAI1 Pathogenic Variant in a Case with GNAO1-Isolated Dystonia: A Modifier of Disease Severity? | Mov Disord | 2024 | 38419191 | PubTator, text mining | PubMed |
| GNAO1 Mutations Affecting the N-Terminal α-Helix of Gαo Lead to Parkinsonism. | Mov Disord | 2024 | 38358016 | 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/v1/2775/papers?page=5