Gene · 85358
Papers2,252
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
121 to 140 of 2,252
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| SHANK3 depletion leads to ERK signalling overdose and cell death in KRAS-mutant cancers. | Nat Commun | 2024 | 39266533 | PubTator, text mining | PubMed |
| Variants in LRRC7 lead to intellectual disability, autism, aggression and abnormal eating behaviors. | Nat Commun | 2024 | 39256359 | Swiss-Prot, curated | PubMed |
| [Clinical features and genetic analysis of four children with Phelan-McDermid syndrome]. | Zhonghua Yi Xue Yi Chuan Xue Za Zhi | 2024 | 39217483 | PubTator, text mining | PubMed |
| Specific multivalent molecules boost CRISPR-mediated transcriptional activation. | Nat Commun | 2024 | 39174527 | PubTator, text mining | PubMed |
| Whole-genome sequencing identifies novel genes for autism in Chinese trios. | Sci China Life Sci | 2024 | 39126614 | PubTator, text mining | PubMed |
| Cardiovascular abnormalities in patients with SHANK3 pathogenic variants: Beyond neurodevelopmental disorders and epilepsy. | Eur J Med Genet | 2024 | 39094681 | PubTator, text mining | PubMed |
| Correction: Differentially altered social dominance- and cooperative-like behaviors in Shank2- and Shank3-mutant mice. | Mol Autism | 2024 | 39080803 | PubTator, text mining | PubMed |
| Clinical description and evaluation of 30 pediatric patients with ultra-rare diseases: A multicenter study with real-world data from Saudi Arabia. | PLoS One | 2024 | 39024300 | PubTator, text mining | PubMed |
| RevGraphVAMP: A protein molecular simulation analysis model combining graph convolutional neural networks and physical constraints. | Methods | 2024 | 38972499 | PubTator, text mining | PubMed |
| Transcriptional determinism and stochasticity contribute to the complexity of autism-associated SHANK family genes. | Cell Rep | 2024 | 38900637 | PubTator, text mining | PubMed |
| Clinicopathological characteristics and genomic profiling of pure mucinous breast cancer. | Breast | 2024 | 38896982 | PubTator, text mining | PubMed |
| Conditional knockout of Shank3 in the ventral CA1 by quantitative in vivo genome-editing impairs social memory in mice. | Nat Commun | 2024 | 38866749 | PubTator, text mining | PubMed |
| Pharmacological modulation of developmental and synaptic phenotypes in human SHANK3 deficient stem cell-derived neuronal models. | Transl Psychiatry | 2024 | 38858349 | PubTator, text mining | PubMed |
| The effect of LNCRNA SHANK3 on the malignant development of gastric cancer cells by regulating the miR-4530/MNX1. | Transl Oncol | 2024 | 38852278 | PubTator, text mining | PubMed |
| Clinical, genetic, and cognitive correlates of seizure occurrences in Phelan-McDermid syndrome. | J Neurodev Disord | 2024 | 38730350 | PubTator, text mining | PubMed |
| Measurement Invariance in Intellectual and Developmental Disability Research. | Am J Intellect Dev Disabil | 2024 | 38657963 | PubTator, text mining | PubMed |
| Shank3 deficiency elicits autistic-like behaviors by activating p38α in hypothalamic AgRP neurons. | Mol Autism | 2024 | 38570876 | PubTator, text mining | PubMed |
| Correction: Neuron type-specific proteomics reveals distinct Shank3 proteoforms in iSPNs and dSPNs lead to striatal synaptopathy in Shank3B-/- mice. | Mol Psychiatry | 2024 | 38548985 | PubTator, text mining | PubMed |
| Caregiver perspectives on patient-focused drug development for Phelan-McDermid syndrome. | Orphanet J Rare Dis | 2024 | 38532502 | PubTator, text mining | PubMed |
| De novo copy number variations in candidate genomic regions in patients of severe autism spectrum disorder in Vietnam. | PLoS One | 2024 | 38451970 | 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/v1/85358/papers?page=7