Gene · 1630
Papers3,713
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
181 to 200 of 3,713
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| PUResNetV2.0: a deep learning model leveraging sparse representation for improved ligand binding site prediction. | J Cheminform | 2024 | 38849917 | PubTator, text mining | PubMed |
| Disproportionate neuroanatomical effects of DCC haploinsufficiency in adolescence compared with adulthood: links to dopamine, connectivity, covariance, and gene expression brain maps in mice. | J Psychiatry Neurosci | 2024 | 38692693 | PubTator, text mining | PubMed |
| Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder. | Nat Genet | 2024 | 38637617 | PubTator, text mining | PubMed |
| Response of human peripheral blood monocyte-derived macrophages (PBMM) to demineralized and decellularized bovine bone graft substitutes. | PLoS One | 2024 | 38635511 | PubTator, text mining | PubMed |
Report of a Novel Homozygous Intragenic DCC Duplication and a Review of Literature of Developmental Split-Brain Syndrome aka Horizontal Gaze Palsy with Progressive Scoliosis-2 with Impaired Intellectual Development Syndrome. | Mol Syndromol | 2024 | 38585553 | PubTator, text mining | PubMed |
| NME1 and DCC variants are associated with susceptibility and tumor characteristics in Mexican patients with colorectal cancer. | J Egypt Natl Canc Inst | 2024 | 38556604 | PubTator, text mining | PubMed |
| UNC5C: Novel Gene Associated with Psychiatric Disorders Impacts Dysregulation of Axon Guidance Pathways. | Genes (Basel) | 2024 | 38540364 | PubTator, text mining | PubMed |
| Methylation analysis of DCC gene in saliva samples is an efficient method for non-invasive detection of superficial hypopharyngeal cancer. | Br J Cancer | 2024 | 38538728 | PubTator, text mining | PubMed |
| Learnt representations of proteins can be used for accurate prediction of small molecule binding sites on experimentally determined and predicted protein structures. | J Cheminform | 2024 | 38486231 | PubTator, text mining | PubMed |
| Identification of specific codon 201 mutation of the DCC Gene in the colonoscopic specimen of colorectal cancer. | J Pak Med Assoc | 2024 | 38419228 | PubTator, text mining | PubMed |
| Paroxysmal Dystonic Posturing Mimicking Nocturnal Leg Cramps as a Presenting Sign in an Infant with DCC Mutation, Callosal Agenesis and Mirror Movements. | J Clin Med | 2024 | 38398422 | PubTator, text mining | PubMed |
| Adhesion-clutch between DCC and netrin-1 mediates netrin-1-induced axonal haptotaxis. | Front Mol Neurosci | 2024 | 38375502 | PubTator, text mining | PubMed |
| Development of Receptor for Advanced Glycation End Products (RAGE) ligands through target directed dynamic combinatorial chemistry: a novel class of possible antagonists. | Chemistry | 2024 | 38317623 | PubTator, text mining | PubMed |
| Epigenetics in the diagnosis and prognosis of head and neck cancer: A systematic review. | J Oral Pathol Med | 2024 | 38316046 | PubTator, text mining | PubMed |
| Defining the Genetic Landscape of Congenital Mirror Movements in 80 Affected Individuals. | Mov Disord | 2024 | 38314870 | Swiss-Prot, curated | PubMed |
| Molecular signature of stem-like glioma cells (SLGCs) from human glioblastoma and gliosarcoma. | PLoS One | 2024 | 38306361 | PubTator, text mining | PubMed |
| Retrospective analysis of the prognostic factors of fetal corpus callosum dysplasia. | BMC Pregnancy Childbirth | 2024 | 38302905 | PubTator, text mining | PubMed |
| Neuronal DSCAM regulates the peri-synaptic localization of GLAST in Bergmann glia for functional synapse formation. | Nat Commun | 2024 | 38302444 | PubTator, text mining | PubMed |
| New candidate region for mirror hand movements: two patients with terminal 9p deletion and 20p duplication. | Mol Biol Rep | 2024 | 38300327 | PubTator, text mining | PubMed |
| Molecular landscape of congenital vertebral malformations: recent discoveries and future directions. | Orphanet J Rare Dis | 2024 | 38291488 | 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/v1/1630/papers?page=10