Gene · 6710
Papers1,578
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
21 to 40 of 1,578
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Clinical Characteristics and Gene Mutations of Hereditary Spherocytosis in 59 Chinese Children. | Mol Genet Genomic Med | 2026 | 41721551 | PubTator, text mining | PubMed |
| Placental iron utilisation in fetal growth restriction: alterations in mitochondrial haem synthesis and iron-sulphur cluster assembly pathways. | J Physiol | 2026 | 41697720 | PubTator, text mining | PubMed |
| Case Report: Clinical and genetic analysis of a family with hereditary spherocytosis combined with familial chylomicronemia syndrome. | Front Genet | 2026 | 41660043 | PubTator, text mining | PubMed |
| Sex differences in molecular pathways underlying cardiovascular health in Black Americans. | Res Sq | 2026 | 41658954 | PubTator, text mining | PubMed |
| Density transitions in the regulation of transcription. | Mol Cell | 2026 | 41653921 | PubTator, text mining | PubMed |
| Genetic Analysis of 23 SNVs of Nine Genes Involved in RBC Membranopathies with the Hematological Parameters of Mexican Patients. | Genet Test Mol Biomarkers | 2026 | 41631466 | PubTator, text mining | PubMed |
| IL-37 alleviates inflammatory effects and NLRP3 inflammasome activation in LPS-induced preterm birth. | Sci Rep | 2026 | 41629351 | PubTator, text mining | PubMed |
| How England got to mandatory biodiversity net gain: A timeline. | Ambio | 2026 | 41335314 | PubTator, text mining | PubMed |
| Influence of the intramolecular disulfide Cys46-Cys55 bridge on the interaction of human neuroglobin with SDS. | J Inorg Biochem | 2026 | 41101060 | PubTator, text mining | PubMed |
| Genetic Mutations of Congenital Red Cell Membrane Defects in Hydrops Fetalis. | Fetal Diagn Ther | 2026 | 40875716 | PubTator, text mining | PubMed |
| Uncovering the genetic architecture of ME/CFS: a precision approach reveals impact of rare monogenic variation. | J Transl Med | 2025 | 41444612 | PubTator, text mining | PubMed |
| Nonsense Variant in the β-Spectrin Gene Causing Hereditary Spherocytosis Identified by Whole-Exome Sequencing in a Child. | Hemoglobin | 2025 | 41423346 | PubTator, text mining | PubMed |
| Case Report: Identification and functional characterization of a novel heterozygous splice-donor (c.647+1G>A) site mutation in the SPTB gene that causes hereditary spherocytosis with hemolytic anemia. | Front Genet | 2025 | 41321563 | PubTator, text mining | PubMed |
| The application of next-generation sequencing technology in congenital haemolytic anaemia: a systematic review and meta-analysis. | Clin Exp Med | 2025 | 41217551 | PubTator, text mining | PubMed |
| Unraveling the role of coagulation-related genes in esophageal squamous cell carcinoma: development of a prognostic model and exploration of potential clinical significance. | Front Oncol | 2025 | 41127022 | PubTator, text mining | PubMed |
| A novel ANK1 frameshift mutation associated with neonatal hereditary spherocytosis: a case report. | Front Pediatr | 2025 | 41050359 | PubTator, text mining | PubMed |
| Coexistence of Hereditary Spherocytosis, Beta-Thalassemia Trait and Gilbert Syndrome in a Newborn: A Rare Genetic Profile. | Fetal Pediatr Pathol | 2025 | 41014001 | PubTator, text mining | PubMed |
| A Review of Gait Analysis Using Gyroscopes and Inertial Measurement Units. | Sensors (Basel) | 2025 | 40969016 | PubTator, text mining | PubMed |
| Shared Inflammatory Genetic Susceptibility Underlying Spontaneous Preterm Birth and Periodontitis: A Case-Control Study. | J Clin Med | 2025 | 40943955 | PubTator, text mining | PubMed |
| Genotype clinical phenotype analysis of 35 cases of hereditary spherocytosis in children. | Front Pediatr | 2025 | 40909430 | 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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