Gene · 6792
Papers1,482
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 1,482
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Real-world experience of diagnosis, disability, and daily management in parents of children with different genetic developmental and epileptic encephalopathies: a qualitative study. | Ann Med | 2025 | 39731461 | PubTator, text mining | PubMed |
| Chromosome X-wide common variant association study in autism spectrum disorder. | Am J Hum Genet | 2025 | 39706197 | PubTator, text mining | PubMed |
| RETRACTION: CDKL5 Promotes Proliferation, Migration, and Chemotherapeutic Drug Resistance of Glioma Cells via Activation of the PI3K/AKT Signaling Pathway. | FEBS Open Bio | 2025 | 39643919 | PubTator, text mining | PubMed |
| Deletions in the CDKL5 5' untranslated region lead to CDKL5 deficiency disorder. | Am J Med Genet A | 2025 | 39205479 | PubTator, text mining | PubMed |
| Characterisation of sleep apneas and respiratory circuitry in mice lacking CDKL5. | J Sleep Res | 2025 | 39049436 | PubTator, text mining | PubMed |
| Revealing the complex role of CDKL5 in developmental epilepsy through a calcium channel related vision. | Acta Epileptol | 2024 | 40217367 | PubTator, text mining | PubMed |
| Engineered tRNAs efficiently suppress CDKL5 premature termination codons. | Sci Rep | 2024 | 39738338 | PubTator, text mining | PubMed |
| The genetic landscape of autism spectrum disorder in an ancestrally diverse cohort. | NPJ Genom Med | 2024 | 39632905 | PubTator, text mining | PubMed |
| A new knockin mouse carrying the E364X patient mutation for CDKL5 deficiency disorder: neurological, behavioral and molecular profiling. | Heliyon | 2024 | 39583831 | PubTator, text mining | PubMed |
| Generation of a human induced pluripotent stem cell (iPSC) line from a patient with a CDKL5 gene mutation. | Stem Cell Res | 2024 | 39541770 | PubTator, text mining | PubMed |
| A case of CDKL5 deficiency disorder with a novel intragenic multi-exonic duplication. | Hum Genome Var | 2024 | 39511144 | PubTator, text mining | PubMed |
| Therapeutic implications of etiology-specific diagnosis of early-onset developmental and epileptic encephalopathies (EO-DEEs): A nationwide Turkish cohort study. | Seizure | 2024 | 39447234 | PubTator, text mining | PubMed |
| Longitudinal, multidimensional, observational study of 15 patients with CDKL5 Deficiency Disorder. | Clin Neurol Neurosurg | 2024 | 39433014 | PubTator, text mining | PubMed |
| Correction: Novel CDKL5 targets identified in human iPSC-derived neurons. | Cell Mol Life Sci | 2024 | 39254686 | PubTator, text mining | PubMed |
| The long odyssey for the DEE-CDKL5 diagnosis: A call for action. | Epilepsia Open | 2024 | 39248178 | PubTator, text mining | PubMed |
| Analysis of the causes of neonatal death and genetic variations in congenital anomalies: a multi-center study. | Front Pediatr | 2024 | 39205667 | PubTator, text mining | PubMed |
| Bacterial Production of CDKL5 Catalytic Domain: Insights in Aggregation, Internal Translation and Phosphorylation Patterns. | Int J Mol Sci | 2024 | 39201578 | PubTator, text mining | PubMed |
| Novel CDKL5 targets identified in human iPSC-derived neurons. | Cell Mol Life Sci | 2024 | 39136782 | PubTator, text mining | PubMed |
| Chromosome X-Wide Common Variant Association Study (XWAS) in Autism Spectrum Disorder. | medRxiv | 2024 | 39108515 | PubTator, text mining | PubMed |
| Preclinical studies of gene replacement therapy for CDKL5 deficiency disorder. | Mol Ther | 2024 | 39033321 | 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/v1/6792/papers?page=5