Gene · 6708
Papers1,813
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
681 to 700 of 1,813
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| β-Globin Lentiviral Vectors Have Reduced Titers due to Incomplete Vector RNA Genomes and Lowered Virion Production. | Stem Cell Reports | 2021 | 33186538 | PubTator, text mining | PubMed |
| Hereditary red blood cell membrane defects. Detection of PIEZO1 mutations associated with SPTA1 mutations. An unusual clinical case of hereditary xerocytosis. | Pediatr Hematol Oncol | 2021 | 33136529 | PubTator, text mining | PubMed |
| Approaching environmental human thermophysiological thresholds for the case of Ankara, Turkey. | Theor Appl Climatol | 2021 | 33132470 | PubTator, text mining | PubMed |
| Generation and Identification of the Linear OCBNO and OBNCO Molecules with 24 Valence Electrons. | Chemistry | 2021 | 33104262 | PubTator, text mining | PubMed |
| A systematic review of monogenic etiologies of nonimmune hydrops fetalis. | Genet Med | 2021 | 33082562 | PubTator, text mining | PubMed |
| Proteomic and Genomic Methylation Signatures of Idiopathic Subglottic Stenosis. | Laryngoscope | 2021 | 32619300 | PubTator, text mining | PubMed |
| A Novel α-Spectrin Pathogenic Variant in Trans to α-Spectrin LELY Causing Neonatal Jaundice With Hemolytic Anemia From Hereditary Pyropoikilocytosis Coexisting With Gilbert Syndrome. | J Pediatr Hematol Oncol | 2021 | 32287101 | PubTator, text mining | PubMed |
| The Coup-TFII orphan nuclear receptor is an activator of the γ-globin gene. | Haematologica | 2021 | 32107331 | PubTator, text mining | PubMed |
| G-Protein coupled receptors: structure and function in drug discovery. | RSC Adv | 2020 | 35517958 | PubTator, text mining | PubMed |
| A Small Key for a Heavy Door: Genetic Therapies for the Treatment of Hemoglobinopathies. | Front Genome Ed | 2020 | 34713239 | PubTator, text mining | PubMed |
| Genomic Mutations of Primary and Metastatic Lung Adenocarcinoma in Chinese Patients. | J Oncol | 2020 | 33488709 | PubTator, text mining | PubMed |
| Pediatric weight estimation: validation of the PAWPER XL tape and the PAWPER XL tape mid-arm circumference method in a South African hospital. | Clin Exp Emerg Med | 2020 | 33440107 | PubTator, text mining | PubMed |
| Genetics and Genomics Approaches for Diagnosis and Research Into Hereditary Anemias. | Front Physiol | 2020 | 33414725 | PubTator, text mining | PubMed |
| Whole-genome sequencing of recurrent neuroblastoma reveals somatic mutations that affect key players in cancer progression and telomere maintenance. | Sci Rep | 2020 | 33384420 | PubTator, text mining | PubMed |
| Atypical hereditary spherocytosis phenotype associated with pseudohypokalaemia and a new variant in the band 3 protein. | BMJ Case Rep | 2020 | 33298499 | PubTator, text mining | PubMed |
| DNA methylation patterns of β-globin cluster in β-thalassemia patients. | Clin Epigenetics | 2020 | 33272312 | PubTator, text mining | PubMed |
| Unique genomic features and prognostic value of COSMIC mutational signature 4 in lung adenocarcinoma and lung squamous cell carcinoma. | Ann Transl Med | 2020 | 33241025 | PubTator, text mining | PubMed |
| Correlation of genetic alterations by whole-exome sequencing with clinical outcomes of glioblastoma patients from the Lebanese population. | PLoS One | 2020 | 33237934 | PubTator, text mining | PubMed |
| Hereditary spherocytosis overlooked for 7 years in a pediatric patient with β-thalassemia trait and novel compound heterozygous mutations of SPTA1 gene. | Hematology | 2020 | 33210974 | PubTator, text mining | PubMed |
| KRAS G12C mutations in Asia: a landscape analysis of 11,951 Chinese tumor samples. | Transl Lung Cancer Res | 2020 | 33209599 | 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/v1/6708/papers?page=35