Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: ILK[original query] |
---|
Breast Cancer Clinical Trial of Chemotherapy and Trastuzumab: Potential Tool to Identify Cardiac Modifying Variants of Dilated Cardiomyopathy. Journal of cardiovascular development and disease 2018 1 4 (2): . Serie Daniel J, Crook Julia E, Necela Brian M, Axenfeld Bianca C, Dockter Travis J, Colon-Otero Gerardo, Perez Edith A, Thompson E Aubrey, Norton Nadi |
Rare genetic variants suggest dysregulation of signaling pathways in low- and high-risk patients developing severe ovarian hyperstimulation syndrome. Journal of assisted reproduction and genetics 2020 Sep . Borgwardt L, Olsen K W, Rossing M, Helweg-Larsen R Borup, Toftager M, Pinborg A, Bogstad J, Løssl K, Zedeler A, Grøndahl M |
Evaluation of the role of Nrf2/Keap1 pathway-associated novel mutations and gene expression on antioxidant status in patients with deep vein thrombosis. Experimental and therapeutic medicine 2020 8 20 (2): 868-881. Akin-Bali Dilara Fatma, Eroglu Tamer, Ilk Sedef, Egin Yonca, Kankilic Teom |
Multigene Panel Testing in Turkish Hereditary Cancer Syndrome Patients. Medeniyet medical journal 2022 6 37 (2): 150-158. Arslan Ates Esra, Turkyilmaz Ayberk, Alavanda Ceren, Yildirim Ozlem, Guney Ahmet Ilt |
Monoallelic deleterious MUTYH mutations generate colorectal cancer: A case report. Clinical case reports 2023 11 11 (12): e8229. Bei Zhao, Wenqi Sun, Yunrong Wang, Xinrong Wu, Yifan Li, Weiwei Wang, Muhan Ni, Peng Yan, Xiaotan Dou, Lei Wang, Min Ch |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: