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Showing results 108 to 167 of 194

Pub YearTitleAuthor(s)
2019Makorin 1 is required for Drosophila oogenesis by regulating insulin/Tor signaling김은영
2018Makorin 1 Regulates Developmental Timing in Drosophila김은영, 이해상, 정선용, 황진순
2001Methylation of O(6)-methylguanine-DNA methyltransferase gene is associated significantly with K-ras mutation, lymph node invasion, tumor staging, and disease free survival in patients with gastric carcinoma.김영배, 백운기, 임인경, 조용관, 한상욱
2016MicroRNA Expression Signatures Associated With BRAF-Mutated Versus KRAS-Mutated Colorectal Cancers김영배, 서광욱, 이다근, 이현우, 최용원
2016Minor BCR-ABL1-Positive Acute Myeloid Leukemia Associated With the NPM1 Mutation and FLT3 Internal Tandem Duplication정성현, 조성란, 한재호
2011Mitochondrial DNA mutations in disease and aging.박찬배
2016Mitochondrial E3 Ubiquitin Protein Ligase 1 Mediates Cigarette Smoke-Induced Endothelial Cell Death and Dysfunction김선용
2001Mitogen-activated protein kinase signalling in oligodendrocytes: a comparison of primary cultures and CG-4.김승업
2004Mitotic aberration coupled with centrosome amplification is induced by hepatitis B virus X oncoprotein via the Ras-mitogen-activated protein/extracellular signal-regulated kinase-mitogen-activated protein pathway.이재호, 조혜성
2003Modulation of the N-type calcium channel gene expression by the alpha subunit of Go.김성환, 서해영, 이영돈
2023Molecular and Clinical Features of Fluconazole Non-susceptible Candida albicans Bloodstream Isolates Recovered in Korean Multicenter Surveillance Studies이위교
2021Molecular correlates and nuclear features of encapsulated follicular-patterned thyroid neoplasms김장희
2019Molecular diagnosis of hereditary spherocytosis by multi-gene target sequencing in Korea: matching with osmotic fragility test and presence of spherocyte박준은, 정현주
2012Molecular genetic analysis of TWIST1 and FGFR3 genes in Korean patients with coronal synostosis: identification of three novel TWIST1 mutations박동하, 윤수한, 정선용
2018mRNA Expression of SLC5A5 and SLC2A Family Genes in Papillary Thyroid Cancer: An Analysis of The Cancer Genome Atlas장전엽
2004Mutant p53 protein in the serum of patients with cervical carcinoma: correlation with the level of serum epidermal growth factor receptor and prognostic significance.최진혁
2005Mutation analysis of the MCM gene in Korean patients with MMA.김성환, 박준은, 정조원, 황진순
2022Mutation spectrum and genotype–phenotype correlations in 157 Korean CADASIL patients: a multicenter study박서진
2013Mutation spectrum of NF1 and clinical characteristics in 78 Korean patients with neurofibromatosis type 1.김현주, 손영배, 정선용
2012Mutation spectrum of the TYR and SLC45A2 genes in patients with oculocutaneous albinism김현주, 정선용
2018Mutational and phenotypic spectrum of OTOF-related auditory neuropathy in Koreans: eliciting reciprocal interaction between bench and clinics장정훈, 정연훈
2015Mutations in the Spliceosomal Machinery Genes SRSF2, U2AF1, and ZRSR2 and Response to Decitabine in Myelodysplastic Syndrome.박준성
2013Mutations of the TATA-binding protein confer enhanced tolerance to hyperosmotic stress in Saccharomyces cerevisiae.김완기
2006Neuronal nitric oxide synthase (nNOS) modulates the JNK1 activity through redox mechanism: a cGMP independent pathway.곽병주
2014Non-thermal atmospheric pressure plasma induces apoptosis in oral cavity squamous cell carcinoma: Involvement of DNA-damage-triggering sub-G(1) arrest via the ATM/p53 pathway.강성운, 김철호, 신유섭
2020Normal presynaptic dopaminergic neurons in corticobasal syndrome with MAPT gene mutation박동규, 안영실, 윤정한
2000Novel 67-bp insertional mutation in the ASS gene in a patient with citrullinemia.한시훈
2004Novel and recurrent mutations of the LDL receptor gene in Korean patients with familial hypercholesterolemia.김현주
2010Novel and recurrent TRPV4 mutations and their association with distinct phenotypes within the TRPV4 dysplasia family.김옥화
2010Novel mutation in SLC6A19 causing late-onset seizures in Hartnup disorder.고정민
2020Osimertinib for Patients With Non-Small-Cell Lung Cancer Harboring Uncommon EGFR Mutations: A Multicenter, Open-Label, Phase II Trial (KCSG-LU15-09)안미선
2013Osteogenesis imperfecta type V: clinical and radiographic manifestations in mutation confirmed patients.김옥화
2015Ovarian microcystic stromal tumor: A novel extracolonic tumor in familial adenomatous polyposis.고영화
2014Overgrowth syndrome associated with a gain-of-function mutation of the natriuretic peptide receptor 2 (NPR2) gene.김옥화
2016Pacemaker-neuron-dependent disturbance of the molecular clockwork by a Drosophila CLOCK mutant homologous to the mouse Clock mutation김은영, 조은주
2017Pan-cancer analysis of systematic batch effects on somatic sequence variations우현구
2012PAPSS2 mutations cause autosomal recessive brachyolmia김옥화
2019Parkinson's disease-associated LRRK2-G2019S mutant acts through regulation of SERCA activity to control ER stress in astrocytes김현미, 박상면, 이지훈, 조은혜, 주일로
2020PCAF-Mediated Histone Acetylation Promotes Replication Fork Degradation by MRE11 and EXO1 in BRCA-Deficient Cells우현구, 최지혜
2015Phase II Trial of Nilotinib in Patients With Metastatic Malignant Melanoma Harboring KIT Gene Aberration: A Multicenter Trial of Korean Cancer Study Group (UN10-06).안미선
2014Phosphoacceptors threonine 162 and serines 170 and 178 within the carboxyl-terminal RRRS/T motif of the hepatitis B virus core protein make multiple contributions to hepatitis B virus replication.김경민, 박선, 신호준, 정재성, 최용준
2014Phosphorylation of a central clock transcription factor is required for thermal but not photic entrainment.김은영
2005Phosphorylation of serine 147 of tis21/BTG2/pc3 by p-Erk1/2 induces Pin-1 binding in cytoplasm and cell death.유민숙, 임인경
2016Position statements on genetic test for peritoneal, ovarian, and fallopian tubal cancers: Korean Society of Gynecologic Oncology (KSGO)장석준
2021Presence of TERT ± BRAF V600E mutation is not a risk factor for the clinical management of patients with papillary thyroid microcarcinoma김형규, 노진, 이정훈, 하은주
1999Presenilin 1 mediates protein kinase C dependent alpha-secretase derived amyloid precursor protein secretion and mitogen-activated protein kinase activation in presenilin 1 transfected human embryonic kidney 293 cell.묵인희
2012Prevalence of BRCA1 and BRCA2 mutations in non-familial breast cancer patients with high risks in Korea: the Korean Hereditary Breast Cancer (KOHBRA) Study김구상, 정용식
2011Prevalence of plasmid-mediated quinolone resistance and mutations in the gyrase and topoisomerase IV genes in Salmonella isolated from 12 tertiary-care hospitals in Korea.이위교
2014Profiling of exome mutations associated with progression of HBV-related hepatocellular carcinoma.김순선, 안선주, 우현구, 정재연, 조성원, 조효정
2019Proteogenomic Characterization of Human Early-Onset Gastric Cancer한상욱
2018Recapitulation of pharmacogenomic data reveals that invalidation of SULF2 enhance sorafenib susceptibility in liver cancer김혁훈, 왕희정, 우현구, 윤사라
2004Regulation of Semliki Forest virus RNA replication: a model for the control of alphavirus pathogenesis in invertebrate hosts.김경민
2015Relation Between F-18 FDG Uptake of PET/CT and BRAFV600E Mutation in Papillary Thyroid Cancer.김장희, 소의영, 안영실, 윤준기, 이수진, 정윤석
2016Resistance Mechanisms and Clinical Features of Fluconazole-Nonsusceptible Candida tropicalis Isolates Compared with Fluconazole-Less-Susceptible Isolates이위교
2000Reversion from precore/core promoter mutants to wild-type hepatitis B virus during the course of lamivudine therapy.김진홍, 조성원, 함기백
2018Roles of TNS3 gene in tumor progression of Neurofibromatosis Type 1안수용
2016Self-clearance mechanism of mitochondrial E3 ligase MARCH5 contributes to mitochondria quality control유영석, 조혜성
2021Small heterodimer partner (SHP) aggravates ER stress in Parkinson’s disease-linked LRRK2 mutant astrocyte by regulating XBP1 SUMOylation이지훈, 조은혜, 주일로
2010Spondylo-epiphyseal dysplasia, Maroteaux type (pseudo-Morquio syndrome type 2), and parastremmatic dysplasia are caused by TRPV4 mutations.김옥화
2005Spontaneous fractures in the mouse mutant sfx are caused by deletion of the gulonolactone oxidase gene, causing vitamin C deficiency.정윤석
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