Gene · 4210
Papers4,381
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
321 to 340 of 4,381
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Implementation of long-read sequencing for routine molecular diagnosis of familial mediterranean fever. | Pract Lab Med | 2024 | 39228674 | PubTator, text mining | PubMed |
| Heterozygous MEFV Mutation Leading to Renal Failure: A Case Study. | Glob Pediatr Health | 2024 | 39219559 | PubTator, text mining | PubMed |
| NLRP3 Negative Regulation Mechanisms in the Resting State and Its Implications for Therapeutic Development. | Int J Mol Sci | 2024 | 39201704 | PubTator, text mining | PubMed |
| How do gene mutation diversity and disease severity scoring affect physical capacity and quality of life in children/adolescents with Familial Mediterranean Fever? | Reumatol Clin (Engl Ed) | 2024 | 39160007 | PubTator, text mining | PubMed |
| Potential association between M694V homozygous mutation in familial Mediterranean fever and eosinophilic intestinal inflammation: a pediatric case series. | Front Pediatr | 2024 | 39156024 | PubTator, text mining | PubMed |
| E148Q variant: a familial Mediterranean fever-causing mutation or a sequence variant? | Eur J Pediatr | 2024 | 39143349 | PubTator, text mining | PubMed |
| A narrative review on the role of cytokines in the pathogenesis and treatment of familial Mediterranean fever: an emphasis on pediatric cases. | Front Pediatr | 2024 | 39132307 | PubTator, text mining | PubMed |
| The Impact of Different MEFV Genotypes on Clinical Phenotype of Patients with Familial Mediterranean Fever: Special Emphasis on Joint Involvement. | Eur J Pediatr | 2024 | 39112805 | PubTator, text mining | PubMed |
Health Technology Assessment Reports for Non-Oncology Medications in Canada from 2018 to 2022: Methodological Critiques on Manufacturers' Submissions and a Comparison between Manufacturer and Canadian Agency for Drugs and Technologies in Health (CADTH) Analyses. | Pharmacoecon Open | 2024 | 39103675 | PubTator, text mining | PubMed |
| Clinical Associations of E148Q Heterozygosity: What to Expect From E148Q? | J Clin Rheumatol | 2024 | 39093307 | PubTator, text mining | PubMed |
| The increased chromosomal DNA damage in patients with Familial Mediterranean Fever. | Biotech Histochem | 2024 | 39092615 | PubTator, text mining | PubMed |
| Exploring factors for predicting colchicine responsiveness in children with PFAPA. | Eur J Pediatr | 2024 | 39085658 | PubTator, text mining | PubMed |
| Pyrin-associated autoinflammation with neutrophilic dermatosis: A case report. | J Dermatol | 2024 | 39072843 | PubTator, text mining | PubMed |
| Genomic Landscape of Susceptibility to Severe COVID-19 in the Slovenian Population. | Int J Mol Sci | 2024 | 39062917 | PubTator, text mining | PubMed |
Familial Mediterranean fever gene variations could trigger VPS16-associated early-onset dystonia and diabetes mellitus: clinical identification of a family with MEFV and VPS16 genetic variation association. | Rheumatol Adv Pract | 2024 | 39055541 | PubTator, text mining | PubMed |
| Sacroiliitis in familial Mediterranean fever: A rare joint involvement of the disease. | J Paediatr Child Health | 2024 | 39051573 | PubTator, text mining | PubMed |
| Molecular analyses of MEFV gene mutation variants in Turkish population. | Mol Biol Rep | 2024 | 39042260 | PubTator, text mining | PubMed |
| TNFRSF11A variants contribute to systemic autoinflammatory diseases: A case series of 12 patients. | Semin Arthritis Rheum | 2024 | 39003954 | PubTator, text mining | PubMed |
| Plasminogen activator inhibitor-1 genotype 4G/5G associates with skin involvement in Armenian familial Mediterranean fever patients. | Rheumatol Int | 2024 | 38976029 | PubTator, text mining | PubMed |
| Human Inborn Errors of Immunity in Pyoderma Gangrenosum: A Systematic Review. | Am J Clin Dermatol | 2024 | 38951460 | 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/v1/4210/papers?page=17