Gene · 2294
Papers1,430
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 1,430
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Composition and function of the nuchal hump of male Xiphophorus multilineatus. | Fish Physiol Biochem | 2025 | 40742476 | PubTator, text mining | PubMed |
| Molecular mechanism, diagnosis, and treatment of VACTERL association. | Front Pediatr | 2025 | 40692799 | PubTator, text mining | PubMed |
| Single-cell RNA sequencing: new insights for pulmonary endothelial cells. | Front Cell Dev Biol | 2025 | 40599812 | PubTator, text mining | PubMed |
| A Hedgehog-Foxf axis coordinates dental follicle-derived alveolar bone formation. | Nat Commun | 2025 | 40593802 | PubTator, text mining | PubMed |
| Co-development of mesoderm and endoderm enables organotypic vascularization in lung and gut organoids. | Cell | 2025 | 40592324 | PubTator, text mining | PubMed |
| Molecular Targets in Alveolar Rhabdomyosarcoma: A Narrative Review of Progress and Pitfalls. | Int J Mol Sci | 2025 | 40508013 | PubTator, text mining | PubMed |
| Genetic features of alveolar capillary dysplasia with misalignment of pulmonary veins in Japanese infants. | Early Hum Dev | 2025 | 40480017 | PubTator, text mining | PubMed |
| Bronchopulmonary dysplasia with pulmonary hypertension associates with semaphorin signaling loss and functionally decreased FOXF1 expression. | Nat Commun | 2025 | 40442177 | PubTator, text mining | PubMed |
| Why some and not others? Understanding vascular phenotypes in genetic developmental lung diseases. | Curr Opin Pediatr | 2025 | 40172258 | PubTator, text mining | PubMed |
| Decreased Level of TMEM100 in Neonates With Lethal Lung Developmental Disorders due to Abnormalities in SHH-FOXF1 and TBX4-FGF10 Signaling Pathways. | Am J Med Genet A | 2025 | 40145339 | PubTator, text mining | PubMed |
| Familial Alveolar Capillary Dysplasia With Misalignment of Pulmonary Veins Caused by Paternal FOXF1 Upstream Enhancer Deletion: A Case Report. | Am J Med Genet A | 2025 | 40114448 | PubTator, text mining | PubMed |
| FOXF1 promotes ovarian cancer metastasis by facilitating HMGA2-mediated USP30-dependent S100A6 deubiquitination. | Biochim Biophys Acta Mol Basis Dis | 2025 | 39694080 | PubTator, text mining | PubMed |
| Genetic burden in neonatal and pediatric-onset pulmonary hypertension: A single-center retrospective study using exome sequencing in a Chinese population. | Pediatr Neonatol | 2025 | 39542781 | PubTator, text mining | PubMed |
| Modeling and predicting single-cell multi-gene perturbation responses with scLAMBDA. | bioRxiv | 2024 | 39677694 | PubTator, text mining | PubMed |
| Chromatin accessibility: biological functions, molecular mechanisms and therapeutic application. | Signal Transduct Target Ther | 2024 | 39627201 | PubTator, text mining | PubMed |
| An organotypic atlas of human vascular cells. | Nat Med | 2024 | 39566559 | PubTator, text mining | PubMed |
| The molecular consequences of FOXF1 missense mutations associated with alveolar capillary dysplasia with misalignment of pulmonary veins. | J Biomed Sci | 2024 | 39497128 | PubTator, text mining | PubMed |
| Elucidating the roles of SOD3 correlated genes and reactive oxygen species in rare human diseases using a bioinformatic-ontology approach. | PLoS One | 2024 | 39480826 | PubTator, text mining | PubMed |
| Alveolar capillary dysplasia with misalignment of the pulmonary veins: A surgical lung biopsy and autopsy in a full-term newborn. | Rev Esp Patol | 2024 | 39393900 | PubTator, text mining | PubMed |
| FOXF1 inhibits invasion and metastasis of lung adenocarcinoma cells and enhances anti-tumor immunity via MFAP4/FAK signal axis. | Sci Rep | 2024 | 39271782 | 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.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/genes/v1/2294/papers?page=3