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.
581 to 600 of 2,261
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Mitochondrial Disease and Hearing Loss in Children: A Systematic Review. | Laryngoscope | 2022 | 35188226 | PubTator, text mining | PubMed |
| Knockdown of mitochondrial threonyl-tRNA synthetase 2 inhibits lung adenocarcinoma cell proliferation and induces apoptosis. | Bioengineered | 2022 | 35184682 | PubTator, text mining | PubMed |
| Mitochondria in tumour progression: a network of mtDNA variants in different types of cancer. | BMC Genom Data | 2022 | 35183124 | PubTator, text mining | PubMed |
| Racial Differences in XO (Xanthine Oxidase) and Mitochondrial DNA Damage-Associated Molecular Patterns in Resistant Hypertension. | Hypertension | 2022 | 35164526 | PubTator, text mining | PubMed |
| Functional Role of Mitochondrial DNA in Cancer Progression. | Int J Mol Sci | 2022 | 35163579 | PubTator, text mining | PubMed |
| Molecular Genetics Overview of Primary Mitochondrial Myopathies. | J Clin Med | 2022 | 35160083 | PubTator, text mining | PubMed |
| Complete mitochondrial genomes and phylogenetic analysis of four Baikal endemic Batrachocottus species (Scorpaeniformes: Cottoidei). | Mitochondrial DNA B Resour | 2022 | 35141404 | PubTator, text mining | PubMed |
| Next-generation sequencing of the whole mitochondrial genome identifies functionally deleterious mutations in patients with multiple sclerosis. | PLoS One | 2022 | 35130313 | PubTator, text mining | PubMed |
| Association between the single nucleotide variants of the mitochondrial cytochrome B gene (MT-CYB) and the male infertility. | Mol Biol Rep | 2022 | 35118571 | PubTator, text mining | PubMed |
| Suppression of non-small-cell lung cancer A549 tumor growth by an mtDNA mutation-targeting pyrrole-imidazole polyamide-triphenylphosphonium and a senolytic drug. | Cancer Sci | 2022 | 35112436 | PubTator, text mining | PubMed |
| ZBTB11 dysfunction: spectrum of brain abnormalities, biochemical signature and cellular consequences. | Brain | 2022 | 35104841 | PubTator, text mining | PubMed |
| Human cleaving embryos enable efficient mitochondrial base-editing with DdCBE. | Cell Discov | 2022 | 35102133 | PubTator, text mining | PubMed |
| Longitudinal Study of Optic Disk Perfusion and Retinal Structure in Leber's Hereditary Optic Neuropathy. | Invest Ophthalmol Vis Sci | 2022 | 35098304 | PubTator, text mining | PubMed |
| DNAJC30 disease-causing gene variants in a large Central European cohort of patients with suspected Leber's hereditary optic neuropathy and optic atrophy. | J Med Genet | 2022 | 35091433 | PubTator, text mining | PubMed |
| Mitochondrial dysfunction by TFAM depletion disrupts self-renewal and lineage differentiation of human PSCs by affecting cell proliferation and YAP response. | Redox Biol | 2022 | 35091324 | PubTator, text mining | PubMed |
| Comprehensive summary of mitochondrial DNA alterations in the postmortem human brain: A systematic review. | EBioMedicine | 2022 | 35085849 | PubTator, text mining | PubMed |
| Novel m.4268T>C mutation in the mitochondrial tRNAIle gene is associated with hearing loss in two Chinese families. | World J Clin Cases | 2022 | 35071519 | PubTator, text mining | PubMed |
| Genome-wide methylation analyses identifies Non-coding RNA genes dysregulated in breast tumours that metastasise to the brain. | Sci Rep | 2022 | 35058523 | PubTator, text mining | PubMed |
| Genetic Alterations in Mitochondrial DNA Are Complementary to Nuclear DNA Mutations in Pheochromocytomas. | Cancers (Basel) | 2022 | 35053433 | PubTator, text mining | PubMed |
| Low guanine content and biased nucleotide distribution in vertebrate mtDNA can cause overestimation of non-CpG methylation. | NAR Genom Bioinform | 2022 | 35047811 | 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/v1/4541/papers?page=30