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.
61 to 80 of 1,578
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Identification of novel variants in hereditary spherocytosis patients by whole-exome sequencing. | Clin Chim Acta | 2025 | 39378964 | PubTator, text mining | PubMed |
| Identification of a novel SPTB gene splicing mutation in hereditary spherocytosis: a case report and diagnostic insights. | Front Genet | 2024 | 39959857 | PubTator, text mining | PubMed |
| Complications of delayed diagnosis and challenges: successfully managed SPTB gene variant hereditary spherocytosis with hepatocellular jaundice-a case report. | J Med Case Rep | 2024 | 39627779 | PubTator, text mining | PubMed |
| DNA regulatory element cooperation and competition in transcription. | BMB Rep | 2024 | 39523506 | PubTator, text mining | PubMed |
| Identification and functional analysis of novel SPTB and ANK1 mutations in hereditary spherocytosis patients. | Sci Rep | 2024 | 39521890 | PubTator, text mining | PubMed |
| Erythroblast enucleation at a glance. | J Cell Sci | 2024 | 39397781 | PubTator, text mining | PubMed |
| Comprehensive Proteomic Analysis Reveals Distinct Features and a Diagnostic Biomarker Panel for Early Pregnancy Loss in Histological Subtypes. | Mol Cell Proteomics | 2024 | 39321873 | PubTator, text mining | PubMed |
| A Case of Adult Hereditary Spherocytosis Concomitant with Gilbert Syndrome Caused by Mutations in SPTB and UGT1A1. | J Inflamm Res | 2024 | 39247838 | PubTator, text mining | PubMed |
| Specific multivalent molecules boost CRISPR-mediated transcriptional activation. | Nat Commun | 2024 | 39174527 | PubTator, text mining | PubMed |
Gestation-dependent increase in cervicovaginal pro-inflammatory cytokines and cervical extracellular matrix proteins is associated with spontaneous preterm delivery within 2 weeks of index assessment in South African women. | Front Immunol | 2024 | 39165357 | PubTator, text mining | PubMed |
| The impact of common language on international trade: Evidence from Korean language. | PLoS One | 2024 | 39146302 | PubTator, text mining | PubMed |
| A novel variant in the SPTB gene underlying hereditary spherocytosis and a literature review of previous variants. | BMC Med Genomics | 2024 | 39135028 | PubTator, text mining | PubMed |
| Intragenic deletions in SPTB are associated with hereditary spherocytosis: Series of 12 cases. | Br J Haematol | 2024 | 39113354 | PubTator, text mining | PubMed |
| Clinical and genetic characteristics of Chinese pediatric and adult patients with hereditary spherocytosis. | Orphanet J Rare Dis | 2024 | 39044243 | PubTator, text mining | PubMed |
| Internal Psychometric Validation of an International Burden of Illness Survey for Idiopathic Multicentric Castleman Disease. | Oncol Ther | 2024 | 39012413 | PubTator, text mining | PubMed |
| Proteomic profiling of human plasma extracellular vesicles identifies PF4 and C1R as novel biomarker in sarcopenia. | J Cachexia Sarcopenia Muscle | 2024 | 39009419 | PubTator, text mining | PubMed |
| Coexistence of hereditary spherocytosis with SPTB P.Trp1150 gene variant and Gilbert syndrome: A case report and literature review. | Open Life Sci | 2024 | 38947766 | PubTator, text mining | PubMed |
| Hereditary Spherocytosis with Mitochondrial Retention, Increased Oxidative Stress, and Alterations to Bioactive Membrane Lipids. | J Pediatr Hematol Oncol | 2024 | 38934620 | PubTator, text mining | PubMed |
| An automated in vitro wound healing microscopy image analysis approach utilizing U-net-based deep learning methodology. | BMC Med Imaging | 2024 | 38914942 | PubTator, text mining | PubMed |
| Clinical Exome Sequencing Reveals Novel Mutations in SPTB Gene Associated with Hereditary Spherocytosis in Patients with Suspected Congenital Hemolytic Anemia. | Hemoglobin | 2024 | 38831725 | 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
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