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.
41 to 60 of 1,813
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Heart rate variability: longitudinal cardioautonomic physiomarker in congenital central hypoventilation syndrome. | Ann Am Thorac Soc | 2026 | 41721744 | PubTator, text mining | PubMed |
| Shake and bake: a robust and cost-effective proteomic sample preparation workflow for plasma and cerebrospinal fluid. | Clin Proteomics | 2026 | 41692724 | PubTator, text mining | PubMed |
| Germline duplication of MYCN predisposes to childhood embryonal tumours. | EBioMedicine | 2026 | 41621405 | PubTator, text mining | PubMed |
| GABAergic Inhibition from the Nucleus Tractus Solitarius to Ventrolateral Medulla Phox2b Neurons Modulates Central Respiratory Chemoreflex and Ventilatory Homeostasis. | Neurosci Bull | 2026 | 41588273 | PubTator, text mining | PubMed |
| Transjugular Leadless Pacemaker Implantation in an Adolescent With Central Hypoventilation Syndrome: A Case Report. | Pacing Clin Electrophysiol | 2026 | 41582863 | PubTator, text mining | PubMed |
| Regulation of PHOX2B gene expression by the long non-coding natural antisense RNA PHOX2B-AS1. | FEBS J | 2026 | 41578938 | PubTator, text mining | PubMed |
| A novel molecular classifier enabling identification and prediction on immunotherapeutic response for MYCN-low pediatric neuroblastoma. | Cell Oncol (Dordr) | 2026 | 41553393 | PubTator, text mining | PubMed |
| Aberrant neural crest cells migration leads to melanocyte presence in the umbilical cord. | Placenta | 2026 | 41548465 | PubTator, text mining | PubMed |
| CAR T cells: the missing piece needed to improve outcomes for children with cancer? | J Immunother Cancer | 2026 | 41545304 | PubTator, text mining | PubMed |
| Sympathetic nerve dysfunction exacerbates skin inflammation in atopic dermatitis. | J Allergy Clin Immunol | 2026 | 41448402 | PubTator, text mining | PubMed |
| Central control of gastrointestinal functions in health and disease. | Physiol Rev | 2026 | 41432726 | PubTator, text mining | PubMed |
Generation of iPSC lines (UMILi032-A, UMILi033-A, UMILi034-A, UMILi035-A, UMILi036-A) from five Congenital Central Hypoventilation Syndrome patients carrying different poly-alanine expansion mutations in the PHOX2B gene. | Stem Cell Res | 2026 | 41420984 | PubTator, text mining | PubMed |
| Hirschsprung Disease on Fetal Autopsy Leading to the Diagnosis of Congenital Central Hypoventilation Syndrome in a Stillborn Fetus. | Clin Genet | 2026 | 41253684 | PubTator, text mining | PubMed |
| PHOX2B deletion in congenital central hypoventilation syndrome: is this sufficient for pathogenesis? | J Hum Genet | 2026 | 41188450 | PubTator, text mining | PubMed |
| SOX2 Is the Most Sensitive Biomarker in Testicular and Gynecologic Embryonic-type Neuroectodermal Tumors (ENT) Based on a Comprehensive Evaluation of Biomarker Expression. | Am J Surg Pathol | 2026 | 40922405 | PubTator, text mining | PubMed |
| Composite gangliocytoma/neuroma and neuroendocrine tumor: a clinicopathologic, immunohistochemical, and molecular genetic study of 11 cases. | Virchows Arch | 2026 | 40665162 | PubTator, text mining | PubMed |
| Recognition of Hyperinsulinaemic Hypoglycaemia in Infants with Congenital Central Hypoventilation Syndrome. | Horm Res Paediatr | 2026 | 39447557 | PubTator, text mining | PubMed |
| Paired-Like Homeobox 2B (PHOX2B) Mutation and the Hidden Endocrine Puzzle: Hyperinsulinism in Congenital Central Hypoventilation Syndrome. | Cureus | 2025 | 41531556 | PubTator, text mining | PubMed |
| Minimal Residual Disease Detection in Peripheral Blood of Patients With High-Risk Neuroblastoma Correlates With Outcome in the International GPOH-DCOG Prospective Validation Study. | JCO Precis Oncol | 2025 | 41411610 | PubTator, text mining | PubMed |
| Ventilatory Complexity Persists in Phox2b Mutant Mice Lacking the Retrotrapezoid Nucleus/Parafacial Respiratory Group (RTN/pFRG) and in Humans With Congenital Central Hypoventilation Syndrome. | J Comp Neurol | 2025 | 41335011 | 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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