Gene · 8929
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.
121 to 140 of 1,813
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Airway obstruction in two children with congenital central hypoventilation syndrome and review of the literature. | Arch Pediatr | 2024 | 38538464 | PubTator, text mining | PubMed |
| Recurrence of CCHS-associated PHOX2B Poly-Alanine expansion variant due to paternal mosaicism. | Gene | 2024 | 38467313 | PubTator, text mining | PubMed |
| PHOX2B: a diagnostic cornerstone in neurocristopathies and neuroblastomas. | J Clin Pathol | 2024 | 38458747 | PubTator, text mining | PubMed |
| Pulmonary hypertension in an adult patient with congenital central hypoventilation syndrome: a case report. | Eur Heart J Case Rep | 2024 | 38454954 | PubTator, text mining | PubMed |
| Alternative low-populated conformations prompt phase transitions in polyalanine repeat expansions. | Nat Commun | 2024 | 38431667 | PubTator, text mining | PubMed |
| Identifying a novel PHOX2B gene variant in a neuroblastoma family: A case report. | Heliyon | 2024 | 38420445 | PubTator, text mining | PubMed |
| Hand2 Immunohistochemistry in the Diagnosis of Paragangliomas and Other Neuroendocrine Neoplasms. | Endocr Pathol | 2024 | 38416360 | PubTator, text mining | PubMed |
| An unusual ophthalmologic finding in a patient with congenital central hypoventilation syndrome. | Eur J Ophthalmol | 2024 | 38403966 | PubTator, text mining | PubMed |
| Further description of two individuals with de novo p.(Glu127Lys) missense variant in the ASCL1 gene. | Clin Genet | 2024 | 38287449 | PubTator, text mining | PubMed |
| Molecular autopsy for sudden death in Japan. | J Toxicol Pathol | 2024 | 38283375 | PubTator, text mining | PubMed |
| ROHHAD syndrome spectrum in an adult: a possible new variant. | ERJ Open Res | 2024 | 38259814 | PubTator, text mining | PubMed |
| Reanalysis of Trio Whole-Genome Sequencing Data Doubles the Yield in Autism Spectrum Disorder: De Novo Variants Present in Half. | Int J Mol Sci | 2024 | 38256266 | PubTator, text mining | PubMed |
| 17q Gain in Neuroblastoma: A Review of Clinical and Biological Implications. | Cancers (Basel) | 2024 | 38254827 | PubTator, text mining | PubMed |
| Predicting Neuroblastoma Patient Risk Groups, Outcomes, and Treatment Response Using Machine Learning Methods: A Review. | Med Sci (Basel) | 2024 | 38249081 | PubTator, text mining | PubMed |
| Computer-aided diagnostic screen for Congenital Central Hypoventilation Syndrome with facial phenotype. | Pediatr Res | 2024 | 38238566 | PubTator, text mining | PubMed |
| Mutually exclusive teams-like patterns of gene regulation characterize phenotypic heterogeneity along the noradrenergic-mesenchymal axis in neuroblastoma. | Cancer Biol Ther | 2024 | 38230570 | PubTator, text mining | PubMed |
| Human iPSC modeling recapitulates in vivo sympathoadrenal development and reveals an aberrant developmental subpopulation in familial neuroblastoma. | iScience | 2024 | 38222111 | PubTator, text mining | PubMed |
| Genetic variants of m7G modification genes influence neuroblastoma susceptibility. | Heliyon | 2024 | 38173492 | PubTator, text mining | PubMed |
| [Study of GCN repeats of PHOX2B gene among individuals from southwest China and diagnosis of two patients with Congenital central hypoventilation syndrome]. | Zhonghua Yi Xue Yi Chuan Xue Za Zhi | 2024 | 38171556 | PubTator, text mining | PubMed |
| Delivery of average assured pressure support (AVAPS) through tracheostomy in paediatric patients. | Respirol Case Rep | 2024 | 38074920 | 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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