Gene · 5428
Papers4,408
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
121 to 140 of 4,408
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| The impact of induced burst suppression on outcomes in patients with POLG-related status epilepticus. | Seizure | 2025 | 40461324 | PubTator, text mining | PubMed |
| Delineating the mechanisms of cerebellar degeneration in paediatric and adult primary mitochondrial disease. | Acta Neuropathol | 2025 | 40445405 | PubTator, text mining | PubMed |
| The impact of VUS reclassification on reproductive decision making. | PLoS One | 2025 | 40424322 | PubTator, text mining | PubMed |
| Identification of common hub genes and construction of immune regulatory networks in aplastic anemia, myelodysplastic syndromes, and acute myeloid leukemia. | Front Immunol | 2025 | 40406144 | PubTator, text mining | PubMed |
| The Genetic Architecture of Parkinson's Disease in Morocco: Highlighting a Predominance of Mendelian Genes. | Neurodegener Dis | 2025 | 40393443 | PubTator, text mining | PubMed |
| [Morphological markers of mitochondrial dysfunction of the basal plate cytotrophoblast of the placenta in preeclampsia of varying severity]. | Arkh Patol | 2025 | 40289429 | PubTator, text mining | PubMed |
| Palatal tremor as the clue sign of POLG-related syndrome. | Neurol Sci | 2025 | 40254681 | PubTator, text mining | PubMed |
| Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed cases. | HGG Adv | 2025 | 40241304 | PubTator, text mining | PubMed |
| The POLγ Y951N patient mutation disrupts the switch between DNA synthesis and proofreading, triggering mitochondrial DNA instability. | Proc Natl Acad Sci U S A | 2025 | 40238457 | PubTator, text mining | PubMed |
| Knockdown of POLG Mimics the Neuronal Pathology of Polymerase-γ Spectrum Disorders in Human Neurons. | Cells | 2025 | 40214434 | PubTator, text mining | PubMed |
| Small molecules restore mutant mitochondrial DNA polymerase activity. | Nature | 2025 | 40205042 | PubTator, text mining | PubMed |
| Investigating the safety and efficacy of deoxycytidine/deoxythymidine in mitochondrial DNA depletion disorders: phase 2 open-label trial. | J Neurol | 2025 | 40175578 | PubTator, text mining | PubMed |
| Chromogen-based double immunohistochemical detection of mitochondrial respiratory chain deficiencies in human brain tissue. | Acta Neuropathol Commun | 2025 | 40114250 | PubTator, text mining | PubMed |
| Experiences from dual genome next-generation sequencing panel testing for mitochondrial disorders: a comprehensive molecular diagnosis. | Front Genet | 2025 | 40110048 | PubTator, text mining | PubMed |
| A steric gate prevents mutagenic dATP incorporation opposite 8-oxo-deoxyguanosine in mitochondrial DNA polymerases. | FEBS J | 2025 | 40070220 | PubTator, text mining | PubMed |
| Presentation, Treatment, and Outcome of a First Stroke-like Episode in a Carrier of the Compound Heterozygous Variants c.695G_A and c.2209G_C in POLG: A Case Report. | Cureus | 2025 | 40062103 | PubTator, text mining | PubMed |
| Mitochondrial damage in muscle specific PolG mutant mice activates the integrated stress response and disrupts the mitochondrial folate cycle. | Nat Commun | 2025 | 40057508 | PubTator, text mining | PubMed |
| Mitochondrial exonuclease EXOG supports DNA integrity by the removal of single-stranded DNA flaps. | Nucleic Acids Res | 2025 | 40042814 | PubTator, text mining | PubMed |
| The POLG Variant c.678G>C; p.(Gln226His) Is Associated with Mitochondrial Abnormalities in Fibroblasts Derived from a Patient Compared to a First-Degree Relative. | Genes (Basel) | 2025 | 40004527 | PubTator, text mining | PubMed |
| Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE) Phenotype Associated With Unique Compound Heterozygous POLG Variants: Case Presentation and Review of the Literature. | Pediatr Dev Pathol | 2025 | 39982139 | 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
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