Gene · 3767
Papers4,332
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
781 to 800 of 4,332
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Why Is Only Type 1 Electrocardiogram Diagnostic of Brugada Syndrome? Mechanistic Insights From Computer Modeling. | Circ Arrhythm Electrophysiol | 2022 | 34963310 | PubTator, text mining | PubMed |
| Investigating Genetic Mutations in a Large Cohort of Iranian Patients with Congenital Hyperinsulinism | J Clin Res Pediatr Endocrinol | 2022 | 34927408 | PubTator, text mining | PubMed |
| An Investigation of the Knowledge Overlap between Pharmacogenomics and Disease Genetics. | Pac Symp Biocomput | 2022 | 34890165 | PubTator, text mining | PubMed |
| Young-onset diabetes patients in Thailand: Data from Thai Type 1 Diabetes and Diabetes diagnosed Age before 30 years Registry, Care and Network (T1DDAR CN). | J Diabetes Investig | 2022 | 34890117 | PubTator, text mining | PubMed |
| Quantile-Dependent Heritability of Glucose, Insulin, Proinsulin, Insulin Resistance, and Glycated Hemoglobin. | Lifestyle Genom | 2022 | 34872092 | PubTator, text mining | PubMed |
| Invaluable Role of Consanguinity in Providing Insight into Paediatric Endocrine Conditions: Lessons Learnt from Congenital Hyperinsulinism, Monogenic Diabetes, and Short Stature. | Horm Res Paediatr | 2022 | 34847552 | PubTator, text mining | PubMed |
| Clinical characteristics, growth patterns, and long-term diabetes complications of 24 patients with neonatal diabetes mellitus: A single center experience. | Pediatr Diabetes | 2022 | 34837310 | PubTator, text mining | PubMed |
| Next- generation sequencing is an effective method for diagnosing patients with different forms of monogenic diabetes. | Diabetes Res Clin Pract | 2022 | 34826540 | PubTator, text mining | PubMed |
| ATP-sensitive potassium channels in zebrafish cardiac and vascular smooth muscle. | J Physiol | 2022 | 34820842 | PubTator, text mining | PubMed |
| The manifold roles of protein S-nitrosylation in the life of insulin. | Nat Rev Endocrinol | 2022 | 34789923 | PubTator, text mining | PubMed |
| Somatostatin-evoked Aβ catabolism in the brain: Mechanistic involvement of α-endosulfine-KATP channel pathway. | Mol Psychiatry | 2022 | 34737456 | PubTator, text mining | PubMed |
| The coincidence of two rare diseases with opposite metabolic phenotype: a child with congenital hyperinsulinism and Bloom syndrome. | J Pediatr Endocrinol Metab | 2022 | 34700371 | PubTator, text mining | PubMed |
| CYP2C19 Loss-of-function Polymorphisms are Associated with Reduced Risk of Sulfonylurea Treatment Failure in Chinese Patients with Type 2 Diabetes. | Clin Pharmacol Ther | 2022 | 34656068 | PubTator, text mining | PubMed |
| A 646C > G (rs41423247) polymorphism of the glucocorticoid receptor as a risk factor for hyperglycaemia diagnosed in pregnancy-data from an observational study. | Acta Diabetol | 2022 | 34648084 | PubTator, text mining | PubMed |
| Diabetes: discovery of insulin, genetic, epigenetic and viral infection mediated regulation. | Nucleus (Calcutta) | 2022 | 34629548 | PubTator, text mining | PubMed |
| D-bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia. | Am J Med Genet A | 2022 | 34623748 | PubTator, text mining | PubMed |
| Ischemic postconditioning reduces spinal cord ischemia-reperfusion injury through ATP-sensitive potassium channel. | Spinal Cord | 2022 | 34616009 | PubTator, text mining | PubMed |
| Evolution of inwardly rectifying potassium channels and their gene expression in zebrafish embryos. | Dev Dyn | 2022 | 34558132 | PubTator, text mining | PubMed |
| Congenital hyperinsulinism: recent updates on molecular mechanisms, diagnosis and management. | J Pediatr Endocrinol Metab | 2022 | 34547194 | PubTator, text mining | PubMed |
| Genomic editing of metformin efficacy-associated genetic variants in SLC47A1 does not alter SLC47A1 expression. | Hum Mol Genet | 2022 | 34505146 | 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
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