Gene · 215
Papers2,145
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
81 to 100 of 2,145
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Incidental diagnosis of primary adrenal insufficiency precipitated by positive ABCD1 gene mutation detected on cascade screening. | BMJ Case Rep | 2025 | 40759493 | PubTator, text mining | PubMed |
| Critical analysis of translational potential of rodent models of white matter pathology across a wide spectrum of human diseases. | Cell Death Dis | 2025 | 40744926 | PubTator, text mining | PubMed |
| Japanese experience of newborn screening for lysosomal storage diseases and adrenoleukodystrophy. | Orphanet J Rare Dis | 2025 | 40708026 | PubTator, text mining | PubMed |
| ALDP-FL for adaptive local differential privacy in federated learning. | Sci Rep | 2025 | 40696085 | PubTator, text mining | PubMed |
| Clinical Variation and Neuroimaging Patterns in Monozygotic Twins With Arrested X-Linked Adrenoleukodystrophy: A Case Report. | Cureus | 2025 | 40693081 | PubTator, text mining | PubMed |
| Hemizygous contiguous gene deletion within Xq28 that includes BCAP31, ABCD1, SRPK3 and SSR4: case report and literature review. | Glob Med Genet | 2025 | 40662097 | PubTator, text mining | PubMed |
| Overview of genetic mutations causing adrenoleukodystrophy: A case-series study. | Mol Genet Metab Rep | 2025 | 40655266 | PubTator, text mining | PubMed |
| Extracellular Aldehyde Sensing Probes for In Vivo Imaging. | Acc Chem Res | 2025 | 40580095 | PubTator, text mining | PubMed |
| Twenty years of misdiagnosis of X-linked adrenoleukodystrophy: a case report. | Am J Transl Res | 2025 | 40535651 | PubTator, text mining | PubMed |
| Strategic partnership for Health in All Policies and sustainable transport in Scotland: a case study evaluation. | Public Health Pract (Oxf) | 2025 | 40491550 | PubTator, text mining | PubMed |
| [Molecular genetics in pediatric endocrinology: 35 years of research]. | Probl Endokrinol (Mosk) | 2025 | 40411325 | PubTator, text mining | PubMed |
| Neurofilament light chain as a biomarker to indicate early activation of cerebral disease in boys with adrenoleukodystrophy. | Commun Med (Lond) | 2025 | 40410561 | PubTator, text mining | PubMed |
| [A clinical case of X-linked adrenoleukodystrophy]. | Zh Nevrol Psikhiatr Im S S Korsakova | 2025 | 40350736 | PubTator, text mining | PubMed |
| Mosaic X-linked adrenoleukodystrophy in males identified by newborn screening and next-generation sequencing. | NPJ Genom Med | 2025 | 40346069 | PubTator, text mining | PubMed |
| Using structural equation model to analyse the effect of psychological pressure on the patients with essential hypertension blood pressure and blood biochemical indicators. | BMC Cardiovasc Disord | 2025 | 40325421 | PubTator, text mining | PubMed |
| XXVI Reunión Anual de la Sociedad Extremeña de Neurología. Comunicaciones Orales y Póster. | Rev Neurol | 2025 | 40296540 | PubTator, text mining | PubMed |
| Adult-onset cerebral X-linked adrenoleukodystrophy presenting with frontal lobe syndrome caused by a de novo ABCD1 gene mutation (c.1415_1416delAG, p.Gln472fs*83). | Neurol Perspect | 2025 | 40256457 | PubTator, text mining | PubMed |
| Novel ABCD1 Variants in X-Linked Adrenoleukodystrophy. | Clin Genet | 2025 | 40210590 | PubTator, text mining | PubMed |
| Reporting ABCD1 variants as actionable secondary findings on exome and genome sequencing. | Genet Med | 2025 | 40202052 | PubTator, text mining | PubMed |
| Genotypic and Phenotypic Characteristics of Pediatric X-Adrenoleukodystrophy in a Chinese Cohort. | Neuropsychiatr Dis Treat | 2025 | 40165924 | 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/v1/215/papers?page=5