Gene · 4541
Papers2,261
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
561 to 580 of 2,261
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Ultra-deep whole genome bisulfite sequencing reveals a single methylation hotspot in human brain mitochondrial DNA. | Epigenetics | 2022 | 35253628 | PubTator, text mining | PubMed |
| Mussel Unio douglasiae MG from the Chihe River: mitogenome description and phylogenetic analysis. | Mitochondrial DNA B Resour | 2022 | 35252570 | PubTator, text mining | PubMed |
| Overexpression of cytosolic long noncoding RNA cytb protects against pressure-overload-induced heart failure via sponging microRNA-103-3p. | Mol Ther Nucleic Acids | 2022 | 35251768 | PubTator, text mining | PubMed |
| Expression signature of the Leigh syndrome French-Canadian type. | Mol Genet Metab Rep | 2022 | 35242578 | PubTator, text mining | PubMed |
| Genetics and Brain Transcriptomics of Completed Suicide. | Am J Psychiatry | 2022 | 35236118 | PubTator, text mining | PubMed |
| Exploring the Anti-Pulmonary Fibrosis Mechanism of Jingyin Granule by Network Pharmacology Strategy. | Front Pharmacol | 2022 | 35222040 | PubTator, text mining | PubMed |
| Maternally transmitted nonsyndromic hearing impairment may be associated with mitochondrial tRNAAla 5601C>T and tRNALeu(CUN) 12311T>C mutations. | J Clin Lab Anal | 2022 | 35218233 | PubTator, text mining | PubMed |
| m.3685T > C is a novel mitochondrial DNA variant that causes Leigh syndrome. | Cold Spring Harb Mol Case Stud | 2022 | 35217561 | PubTator, text mining | PubMed |
| Early developmental delay in Leigh syndrome spectrum disorders is associated with poor clinical prognosis. | Mol Genet Metab | 2022 | 35216885 | PubTator, text mining | PubMed |
| Association of variants m.T16172C and m.T16519C in whole mtDNA sequences with high altitude pulmonary edema in Han Chinese lowlanders. | BMC Pulm Med | 2022 | 35216582 | PubTator, text mining | PubMed |
| The Mitochondrial Epigenome: An Unexplored Avenue to Explain Unexplained Myopathies? | Int J Mol Sci | 2022 | 35216315 | PubTator, text mining | PubMed |
| Genome-Wide Expression and Anti-Proliferative Effects of Electric Field Therapy on Pediatric and Adult Brain Tumors. | Int J Mol Sci | 2022 | 35216098 | PubTator, text mining | PubMed |
| New Insights on Rotenone Resistance of Complex I Induced by the m.11778G>A/MT-ND4 Mutation Associated with Leber's Hereditary Optic Neuropathy. | Molecules | 2022 | 35209128 | PubTator, text mining | PubMed |
| Pathogenic Biallelic Mutations in ECHS1 in a Case with Short-Chain Enoyl-CoA Hydratase (SCEH) Deficiency-Case Report and Literature Review. | Int J Environ Res Public Health | 2022 | 35206276 | PubTator, text mining | PubMed |
| Diagnostic Modalities of Non-Alcoholic Fatty Liver Disease: From Biochemical Biomarkers to Multi-Omics Non-Invasive Approaches. | Diagnostics (Basel) | 2022 | 35204498 | PubTator, text mining | PubMed |
| Mitochondrial Fragmentation in a High Homocysteine Environment in Diabetic Retinopathy. | Antioxidants (Basel) | 2022 | 35204246 | PubTator, text mining | PubMed |
| The Mitochondrial Genome in Aging and Disease and the Future of Mitochondrial Therapeutics. | Biomedicines | 2022 | 35203698 | PubTator, text mining | PubMed |
| Single-Cell RNA-Seq Analysis of Olfactory Mucosal Cells of Alzheimer's Disease Patients. | Cells | 2022 | 35203328 | PubTator, text mining | PubMed |
| Mitochondrial Neurodegeneration. | Cells | 2022 | 35203288 | PubTator, text mining | PubMed |
| Low-input RNase footprinting for simultaneous quantification of cytosolic and mitochondrial translation. | Genome Res | 2022 | 35193938 | 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/v1/4541/papers?page=29