Gene · 6683
Papers1,637
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
1 to 20 of 1,637
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Phenotypic Spectrum and Clinical Approach to Early-Onset Hereditary Spastic Paraplegia. | Mov Disord Clin Pract | 2026 | 42764666 | PubTator, text mining | PubMed |
| Validation of a Cellular Imaging-Based Method as a Potential Biomarker for SPG4 Hereditary Spastic Paraplegia. | Ann Clin Transl Neurol | 2026 | 42687129 | PubTator, text mining | PubMed |
| Significant differences in phenotype and age of onset in an SPG4 family caused by whole SPAST deletion combined with a hemizygous S44L modifier. | Neurogenetics | 2026 | 42658319 | PubTator, text mining | PubMed |
| Late-Onset Hereditary Spastic Paraplegia with a Novel SPAST Intronic Variant. | Ann Lab Med | 2026 | 42613945 | PubTator, text mining | PubMed |
| SPG4-Associated Hereditary Spastic Paraplegia and Dilated Cardiomyopathy: Coincidence or Clue? | JACC Case Rep | 2026 | 42593014 | PubTator, text mining | PubMed |
| Microtubules in Spinal Cord Injury: From Cytoskeletal Dysregulation to Therapeutic Regeneration. | J Neurochem | 2026 | 42563243 | PubTator, text mining | PubMed |
| SPG4 Hereditary Spastic Paraplegia: From Etiology to Therapy. | Mov Disord | 2026 | 42538614 | PubTator, text mining | PubMed |
| Alu-mediated SPAST deletion impairs golgi zinc transport and reveals a druggable vulnerability. | Signal Transduct Target Ther | 2026 | 42521669 | PubTator, text mining | PubMed |
| Genotypic and Phenotypic Profile of Hereditary Spastic Paraplegia in Children: A Single-Centre Study from Northern India. | Indian Pediatr | 2026 | 42490029 | PubTator, text mining | PubMed |
| PTEN Negatively Regulates Spastin Ser210 Phosphorylation To Modulate GluA1 Surface Trafficking and Excitatory Synaptic Transmission. | ACS Chem Neurosci | 2026 | 42464651 | PubTator, text mining | PubMed |
| Clinical and genetic characteristics of pediatric hereditary spastic paraplegia in the Eastern Levant. | Eur J Paediatr Neurol | 2026 | 42462372 | PubTator, text mining | PubMed |
| Dilated Cardiomyopathy in a Woman With SPG4-Associated Hereditary Spastic Paraplegia. | JACC Case Rep | 2026 | 42233908 | PubTator, text mining | PubMed |
| Genetic landscape of hereditary spastic paraplegias in the Korean population. | Sci Rep | 2026 | 42225730 | PubTator, text mining | PubMed |
| Tubulin flux at spastin-induced nanodamage sites regulates microtubule rescue frequency and EB1 lifetimes. | Proc Natl Acad Sci U S A | 2026 | 42190000 | PubTator, text mining | PubMed |
| Genetic architecture of hereditary spastic paraplegia: from monogenic to oligogenic models. | J Neurogenet | 2026 | 42150761 | PubTator, text mining | PubMed |
| Expanding the genetic and clinical landscapes of hereditary spastic paraplegia (HSP): a cohort study of 103 families. | Orphanet J Rare Dis | 2026 | 42120987 | PubTator, text mining | PubMed |
| TRMT13 Facilitates SPAST Upregulation Through ceRNA Crosstalk and Modulates G3-YSD-Triggered Energy Metabolic Decline in Cardiomyocytes. | Clin Exp Pharmacol Physiol | 2026 | 42120960 | PubTator, text mining | PubMed |
| Genotype-structure-phenotype correlations define divergent natural history in early-onset spastic paraplegia type 4. | Brain | 2026 | 42083457 | PubTator, text mining | PubMed |
| Spastic Quadriplegia Resulting From a Pathogenic Variant in the SPAST Gene: A First Report. | Case Rep Neurol Med | 2026 | 42065018 | PubTator, text mining | PubMed |
| Expanding the clinical and mutational spectrum of hereditary spastic paraplegia type 4 in a cohort of patients from central China. | Front Genet | 2026 | 41978773 | 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.
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