Gene · 4647
Papers1,877
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
301 to 320 of 1,877
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Human regulatory T cells locally differentiate and are functionally heterogeneous within the inflamed arthritic joint. | Clin Transl Immunology | 2022 | 36204213 | PubTator, text mining | PubMed |
| AAV vectors: The Rubik's cube of human gene therapy. | Mol Ther | 2022 | 36203359 | PubTator, text mining | PubMed |
| De novo variants are a common cause of genetic hearing loss. | Genet Med | 2022 | 36194208 | PubTator, text mining | PubMed |
| Eyes on CHARGE syndrome: Roles of CHD7 in ocular development. | Front Cell Dev Biol | 2022 | 36172288 | PubTator, text mining | PubMed |
| Outcomes of Gene Panel Testing for Sensorineural Hearing Loss in a Diverse Patient Cohort. | JAMA Netw Open | 2022 | 36166228 | PubTator, text mining | PubMed |
| Regulation of the rhythmic diversity of daily photoreceptor outer segment phagocytosis in vivo. | FASEB J | 2022 | 36165194 | PubTator, text mining | PubMed |
| Novel compound heterozygous synonymous and missense variants in the MYO7A gene identified by next-generation sequencing in a Chinese family with nonsyndromic hearing loss. | J Clin Lab Anal | 2022 | 36164746 | PubTator, text mining | PubMed |
| Does senescence play a role in age-related macular degeneration? | Exp Eye Res | 2022 | 36150544 | PubTator, text mining | PubMed |
| Genomic study of nonsyndromic hearing loss in unaffected individuals: Frequency of pathogenic and likely pathogenic variants in a Brazilian cohort of 2,097 genomes. | Front Genet | 2022 | 36147510 | PubTator, text mining | PubMed |
| Analysis of the Results of Cytomegalovirus Testing Combined with Genetic Testing in Children with Congenital Hearing Loss. | J Clin Med | 2022 | 36142981 | PubTator, text mining | PubMed |
| GenOtoScope: Towards automating ACMG classification of variants associated with congenital hearing loss. | PLoS Comput Biol | 2022 | 36129964 | PubTator, text mining | PubMed |
| Ti3 C2 Tx MXene Composite 3D Hydrogel Potentiates mTOR Signaling to Promote the Generation of Functional Hair Cells in Cochlea Organoids. | Adv Sci (Weinh) | 2022 | 36117048 | PubTator, text mining | PubMed |
| Neural signatures of auditory hypersensitivity following acoustic trauma. | Elife | 2022 | 36111669 | PubTator, text mining | PubMed |
| A novel nonsense variant in the CENPP gene segregates in a Swiss family with autosomal dominant low-frequency sensorineural hearing loss. | Eur J Hum Genet | 2022 | 36071244 | PubTator, text mining | PubMed |
| Protocol for the isolation of CD8+ tumor-infiltrating lymphocytes from human tumors and their characterization by single-cell immune profiling and multiome. | STAR Protoc | 2022 | 36065294 | PubTator, text mining | PubMed |
| Mutation spectrum of non-syndromic hearing loss in the UAE, a retrospective cohort study and literature review. | Mol Genet Genomic Med | 2022 | 36056583 | PubTator, text mining | PubMed |
| de novo variant calling identifies cancer mutation signatures in the 1000 Genomes Project. | Hum Mutat | 2022 | 36054329 | PubTator, text mining | PubMed |
| Lentiviral Vectors for Ocular Gene Therapy. | Pharmaceutics | 2022 | 36015231 | PubTator, text mining | PubMed |
| Inherited Retinal Dystrophy in Southeastern United States: Characterization of South Carolina Patients and Comparative Literature Review. | Genes (Basel) | 2022 | 36011402 | PubTator, text mining | PubMed |
| Phenotypic and Genetic Characteristics in a Cohort of Patients with Usher Genes. | Genes (Basel) | 2022 | 36011334 | 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/v1/4647/papers?page=16