Gene · 8243
Papers2,883
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 2,883
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Expression Patterns of Escape Genes in Turner Syndrome Fibroblasts and Induced Pluripotent Stem Cells. | Int J Mol Sci | 2025 | 39940742 | PubTator, text mining | PubMed |
Increased interferon I signaling, DNA damage response and evidence of T-cell exhaustion in a patient with combined interferonopathy (Aicardi-Goutières Syndrome, AGS) and cohesinopathy (Cornelia de Lange Syndrome, CdLS). | Pediatr Rheumatol Online J | 2025 | 39871364 | PubTator, text mining | PubMed |
| Association of Structural Maintenance of Chromosome-1A Phosphorylation with Progression of Breast Cancer. | Cells | 2025 | 39851557 | PubTator, text mining | PubMed |
| A dual role of Cohesin in DNA DSB repair. | Nat Commun | 2025 | 39833168 | PubTator, text mining | PubMed |
| A De Novo Frameshift Variant in SMC1A Causes Non-Classic Cornelia de Lange Syndrome With Epilepsy: A Case Report and Literature Review. | Mol Genet Genomic Med | 2025 | 39831465 | PubTator, text mining | PubMed |
| A de-novo loss-of-function variant of SMC1A gene in a girl with epilepsy and neurodevelopmental delay. | Clin Dysmorphol | 2025 | 39807618 | PubTator, text mining | PubMed |
| Sensory-Motor Polyneuropathy in an 11-year- old Girl with a Pathogenic Variant in SMC1A: A Case Report. | Neuropediatrics | 2025 | 39542017 | PubTator, text mining | PubMed |
| Highlighting the different facets of SMC1A truncating variants: Two patients with novel SMC1A pathogenic variants. | Epileptic Disord | 2025 | 39513746 | PubTator, text mining | PubMed |
| Untangling the loops of STAG2 mutations in myelodysplastic syndrome. | Leuk Lymphoma | 2025 | 39264305 | PubTator, text mining | PubMed |
| Cornelia de Lange Syndrome Accompanied by Cholelithiasis and Nephrolithiasis: A Case Report. | Children (Basel) | 2024 | 39767862 | PubTator, text mining | PubMed |
| Genome Instability and Senescence Are Markers of Cornelia de Lange Syndrome Cells. | Cells | 2024 | 39682772 | PubTator, text mining | PubMed |
| The Benefits of Whole-Exome Sequencing in the Differential Diagnosis of Hypophosphatasia. | Int J Mol Sci | 2024 | 39519277 | PubTator, text mining | PubMed |
| Curating genomic disease-gene relationships with Gene2Phenotype (G2P). | Genome Med | 2024 | 39506859 | PubTator, text mining | PubMed |
| Sleep correlates of behavior functioning in Cornelia de Lange syndrome. | Am J Med Genet A | 2024 | 39394947 | PubTator, text mining | PubMed |
| Cytogenetic bands and sharp peaks of Alu underlie large-scale segmental regulation of nuclear genome architecture. | Nucleus | 2024 | 39377317 | PubTator, text mining | PubMed |
| Hsa_circ_0000092 up-regulates IL24 by SMC1A to induce macrophages M2 polarization. | Heliyon | 2024 | 39296099 | PubTator, text mining | PubMed |
| Cohesin mutations in acute myeloid leukemia. | Leukemia | 2024 | 39251741 | PubTator, text mining | PubMed |
| The cohesin ATPase cycle is mediated by specific conformational dynamics and interface plasticity of SMC1A and SMC3 ATPase domains. | Cell Rep | 2024 | 39240714 | PubTator, text mining | PubMed |
| The physical chemistry of interphase loop extrusion. | bioRxiv | 2024 | 39229088 | PubTator, text mining | PubMed |
| A novel STAG1 variant associated with congenital clubfoot and microphthalmia: A case report. | SAGE Open Med Case Rep | 2024 | 39224759 | 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/v1/8243/papers?page=5