Associated Papers
Clinical perspectives on the value of testing for STK11 and KEAP1 mutations in advanced NSCLC.
Shiller M et al.
Frontiers in Oncology, 2024
39703851 (PubMed )
Supplement: DataSheet2.xlsx › Supplemental_data
Bioinformatic and computational analysis for predominant mutations of the Nrf2/Keap1 complex in pediatric leukemia.
Akın-Balı DF et al.
Journal of Biomolecular Structure & Dynamics, 2021
Evaluation of the role of Nrf2/Keap1 pathway-associated novel mutations and gene expression on antioxidant status in patients with deep vein thrombosis.
Akin-Bali DF et al.
Experimental and Therapeutic Medicine, 2020
Identification of novel Nrf2/Keap1 pathway mutations in pediatric acute lymphoblastic leukemia.
Akın-Balı DF et al.
Pediatric Hematology and Oncology, 2020
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