Browsing by Keyword : Models, Genetic
Showing results 1 to 12 of 12
| Pub Year | | Title | AJOU Author(s) |
| 2001 | | Activated cAMP-response element-binding protein regulates neuronal expression of presenilin-1. | 이영돈 |
| 2004 | | B-cell translocation gene 2 (Btg2) regulates vertebral patterning by modulating bone morphogenetic protein/smad signaling. | 임인경 |
| 2021 | | Computational prediction and interpretation of cell-specific replication origin sites from multiple eukaryotes by exploiting stacking framework | Balachandran, Manavalan |
| 2021 | | Computational prediction of species-specific yeast DNA replication origin via iterative feature representation | Balachandran, Manavalan, Basith, Shaherin, 신태환, 이광 |
| 2011 | | Exploring genomic profiles of hepatocellular carcinoma | 우현구 |
| 2006 | | Genetic polymorphism of interferon-gamma, interferon-gamma receptor, and interferon regulatory factor-1 genes in patients with hepatitis B virus infection. | 김진홍, 여말희, 왕희정, 정재연, 조성원, 함기백 |
| 2005 | | Homocysteine levels--before and after methionine loading--in 51 Dutch families. | 이순영 |
| 2020 | | i6mA-Fuse: improved and robust prediction of DNA 6 mA sites in the Rosaceae genome by fusing multiple feature representation | Balachandran, Manavalan |
| 2021 | | Meta-i6mA: An interspecies predictor for identifying DNA N6-methyladenine sites of plant genomes by exploiting informative features in an integrative machine-learning framework | Balachandran, Manavalan, Basith, Shaherin, 이광 |
| 2003 | | Multiple mechanisms for oxygen-induced regulation of the Clara cell secretory protein gene. | 박문성 |
| 2005 | | Spontaneous fractures in the mouse mutant sfx are caused by deletion of the gulonolactone oxidase gene, causing vitamin C deficiency. | 정윤석 |
| 2005 | | Three novel VHL germline mutations in Korean patients with von Hippel-Lindau disease and pheochromocytomas. | 김대중, 이관우 |
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