Browsing "Journal Papers" by Keyword : Mutation
Showing results 181 to 192 of 192
Pub Year | | Title | Author(s) |
2004 | | Three novel cis-acting elements required for efficient plus-strand DNA synthesis of the hepatitis B virus genome. | 윤계순 |
2005 | | Three novel VHL germline mutations in Korean patients with von Hippel-Lindau disease and pheochromocytomas. | 김대중, 이관우 |
2023 | | Three-Year Safety, Tolerability, and Health-Related Quality of Life Outcomes of Adjuvant Osimertinib in Patients With Resected Stage IB to IIIA EGFR-Mutated NSCLC: Updated Analysis From the Phase 3 ADAURA Trial | 최진혁 |
2015 | | Timely Degradation of Wip1 Phosphatase by APC/C Activator Protein Cdh1 is Necessary for Normal Mitotic Progression. | 조혜성 |
2015 | | Tolerance to acetic acid is improved by mutations of the TATA-binding protein gene. | 김완기 |
2003 | | Transmodulation between phospholipase D and c-Src enhances cell proliferation. | 최경숙 |
2010 | | TRPV4-pathy, a novel channelopathy affecting diverse systems. | 김옥화 |
2013 | | TWINKLE is an essential mitochondrial helicase required for synthesis of nascent D-loop strands and complete mtDNA replication. | 박찬배 |
2024 | | Unveiling local and global conformational changes and allosteric communications in SOD1 systems using molecular dynamics simulation and network analyses | Basith, Shaherin, 이광 |
2015 | | VE1 antibody is not highly specific for the BRAF V600E mutation in thyroid cytology categories with the exception of malignant cases. | 김대중, 김장희, 소의영, 신승수, 이기범, 이정훈, 임현이, 정선용, 정윤석, 한재호 |
1999 | | Very long chain acyl coenzyme A dehydrogenase deficiency in a 5-month-old Korean boy: identification of a novel mutation. | 정조원, 한시훈, 홍창호 |
2011 | | Whole-exome sequencing detects somatic mutations of IDH1 in metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria (MC-HGA). | 김옥화 |