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Gene · 1285

Papers2,040

Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.

281 to 300 of 2,040

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TitleJournalYearPMIDFound bySource
Analysis of local extracellular matrix identifies different aetiologies behind bicuspid and tricuspid aortic valve degeneration and suggests therapies.Cell Mol Life Sci202337632572PubTator, text miningPubMed
The Potential Usefulness of the Expanded Carrier Screening to Identify Hereditary Genetic Diseases: A Case Report from Real-World Data.Genes (Basel)202337628702PubTator, text miningPubMed
A Role for Genetic Modifiers in Tubulointerstitial Kidney Diseases.Genes (Basel)202337628633PubTator, text miningPubMed
Genetic and molecular dynamics analysis of two variants of the COL4A5 gene causing Alport syndrome.BMC Med Genomics202337596645PubTator, text miningPubMed
Evaluation of the efficacy of Abelmoschus manihot (L.) on diabetic nephropathy by analyzing biomarkers in the glomeruli and proximal and distal convoluted tubules of the kidneys.Front Pharmacol202337587982PubTator, text miningPubMed
The ever wider clinical spectrum of RMND1-related disorders and limitedness of phenotype-based classifications.J Mol Med (Berl)202337584739PubTator, text miningPubMed
Reproductive Carrier Screening Results With Maternal Health Implications During Pregnancy.Obstet Gynecol202337562044PubTator, text miningPubMed
Alport Syndrome and Oral Mucous Membrane Pemphigoid: An Interesting Case.Cureus202337551211PubTator, text miningPubMed
SARS-CoV-2 accessory proteins involvement in inflammatory and profibrotic processes through IL11 signaling.Front Immunol202337545510PubTator, text miningPubMed
[COL4A5 genotypes and clinical characteristics of children with Alport syndrome].Zhongguo Dang Dai Er Ke Za Zhi202337529956PubTator, text miningPubMed
Case report: A case report of Alport syndrome caused by a novel mutation of COL4A5.Front Genet202337529776PubTator, text miningPubMed
Predictability of Nailfold Capillaroscopic Score in Diagnosing Retinopathy in Patients with Type 2 Diabetes Mellitus and its Utility as a Non-Invasive Tool for Differentiating from those Not Having Retinopathy: A Pilot Observational Cross-Sectional Analytical Study.
Indian J Dermatol202337529446PubTator, text miningPubMed
At-Risk Genomic Findings for Pediatric-Onset Disorders From Genome Sequencing vs Medically Actionable Gene Panel in Proactive Screening of Newborns and Children.JAMA Netw Open202337523181PubTator, text miningPubMed
Recent Advances in Proteinuric Kidney Disease/Nephrotic Syndrome: Lessons from Knockout/Transgenic Mouse Models.Biomedicines202337509442PubTator, text miningPubMed
Research progress on endoplasmic reticulum homeostasis in kidney diseases.Cell Death Dis202337500613PubTator, text miningPubMed
Pilot clinical trial and phenotypic analysis in chemotherapy-pretreated, metastatic triple-negative breast cancer patients treated with oral TAK-228 and TAK-117 (PIKTOR) to increase DNA damage repair deficiency followed by cisplatin and nab paclitaxel.
Biomark Res202337491309PubTator, text miningPubMed
A five-collagen-based risk model in lung adenocarcinoma: prognostic significance and immune landscape.Front Oncol202337476379PubTator, text miningPubMed
Clinical utility of genetic testing in Indian children with kidney diseases.BMC Nephrol202337464296PubTator, text miningPubMed
Contemporary Monoclonal Antibody Utilization in Glomerular Diseases.Mayo Clin Proc Innov Qual Outcomes202337448529PubTator, text miningPubMed
Albuminuria-Related Genetic Biomarkers: Replication and Predictive Evaluation in Individuals with and without Diabetes from the UK Biobank.Int J Mol Sci202337446387PubTator, text miningPubMed

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.

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