Browsing by Keyword : Mutation

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Showing results 181 to 194 of 194

Pub YearTitleAuthor(s)
2013The prevalence of BRCA mutations among familial breast cancer patients in Korea: results of the Korean Hereditary Breast Cancer study.김구상, 정용식
2003The putative transcriptional activator MSN1 promotes chromium accumulation in Saccharomyces cerevisiae.김경민
2004Three novel cis-acting elements required for efficient plus-strand DNA synthesis of the hepatitis B virus genome.윤계순
2005Three novel VHL germline mutations in Korean patients with von Hippel-Lindau disease and pheochromocytomas.김대중, 이관우
2023Three-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 Trial최진혁
2015Timely Degradation of Wip1 Phosphatase by APC/C Activator Protein Cdh1 is Necessary for Normal Mitotic Progression.조혜성
2015Tolerance to acetic acid is improved by mutations of the TATA-binding protein gene.김완기
2003Transmodulation between phospholipase D and c-Src enhances cell proliferation.최경숙
2010TRPV4-pathy, a novel channelopathy affecting diverse systems.김옥화
2013TWINKLE is an essential mitochondrial helicase required for synthesis of nascent D-loop strands and complete mtDNA replication.박찬배
2024Unveiling local and global conformational changes and allosteric communications in SOD1 systems using molecular dynamics simulation and network analysesBasith, Shaherin, 이광
2015VE1 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
1999Very long chain acyl coenzyme A dehydrogenase deficiency in a 5-month-old Korean boy: identification of a novel mutation.정조원, 한시훈, 홍창호
2011Whole-exome sequencing detects somatic mutations of IDH1 in metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria (MC-HGA).김옥화
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