2009 | | Calpain-mediated N-cadherin proteolytic processing in brain injury. | 문창현, 백은주, 이수환, 정이숙 |
2004 | | Casein kinase II-mediated phosphorylation regulates alpha-synuclein/synphilin-1 interaction and inclusion body formation. | 이광 |
2021 | | Caveolin-1 deficiency impairs synaptic transmission in hippocampal neurons | 박상면 |
2003 | | Cdk2-dependent phosphorylation of the NF-Y transcription factor and its involvement in the p53-p21 signaling pathway. | 최경숙 |
2010 | | Cell cycle-regulated expression and subcellular localization of a kinesin-8 member human KIF18B. | 김완기 |
2012 | | Characteristics of double heterozygosity for BRCA1 and BRCA2 germline mutations in Korean breast cancer patients | 김구상 |
2013 | | Characterization of human anti-heat shock protein 60 monoclonal autoantibody Fab fragments in atherosclerosis: genetic and functional analysis. | 장영주 |
2013 | | Characterization of mutations in multi- and extensive drug resistance among strains of Mycobacterium tuberculosis clinical isolates in Republic of Korea. | 황성철 |
2005 | | Characterization of thiol-specific antioxidant 1 (TSA1) of Candida albicans. | 김완기 |
2011 | | Clinical and genetic characteristics of Korean patients with Gaucher disease. | 김현주, 정선용 |
2013 | | Clinical and genetic spectrum of 18 unrelated Korean patients with Sotos syndrome: frequent 5q35 microdeletion and identification of four novel NSD1 mutations. | 손영배, 정선용, 진현석 |
2017 | | Clinical characteristics and mutation spectrum of GLA in Korean patients with Fabry disease by a nationwide survey: Underdiagnosis of late-onset phenotype | 손영배 |
2017 | | Clinical, biochemical and molecular characterization of Korean patients with mucolipidosis II/III and successful prenatal diagnosis | 손영배 |
2012 | | Clinical, biochemical, and genetic analysis of two korean patients with trichorhinophalangeal syndrome type I and growth hormone deficiency | 김옥화, 손영배 |
2017 | | Clinicopathologic Characteristics and Mutational Status of Succinate Dehydrogenase Genes in Paraganglioma of the Urinary Bladder: A Multi-Institutional Korean Study | 권지은 |
2023 | | Comparison of histological and molecular features of pediatric-type follicular lymphoma and pediatric nodal marginal zone lymphoma | 한재호 |
2011 | | Comparison of multiplex restriction fragment mass polymorphism and sequencing analyses for detecting entecavir resistance in chronic hepatitis B. | 조성원 |
1995 | | Contribution of B cell subsets to delayed development of MAIDS in xid mice. | 김완기 |
1997 | | Correlation between K-ras gene mutation and prognosis of patients with nonsmall cell lung carcinoma. | 이이형 |
2000 | | Correlation between structure of Bcl-2 and its inhibitory function of JNK and caspase activity in dopaminergic neuronal apoptosis. | 진병관 |
2019 | | CRISPR-Cas9-mediated therapeutic editing of Rpe65 ameliorates the disease phenotypes in a mouse model of Leber congenital amaurosis | 이기황 |
2015 | | Cross-strand binding of TFAM to a single mtDNA molecule forms the mitochondrial nucleoid. | 박찬배 |
2023 | | Deep brain stimulation in Parkinson disease with valosin-containing protein gene mutation | 박동규, 윤정한 |
2024 | | Deep learning–radiomics integrated noninvasive detection of epidermal growth factor receptor mutations in non-small cell lung cancer patients | 김철호, 노진, 유슬기, 허재성 |
2010 | | Definition of ubiquitination modulator COP1 as a novel therapeutic target in human hepatocellular carcinoma. | 우현구 |
2019 | | Deletion of exons 16-17b of CFTR is frequently identified in Korean patients with cystic fibrosis | 손영배, 장주영 |
2013 | | Dietary intake and breast cancer among carriers and noncarriers of BRCA mutations in the Korean Hereditary Breast Cancer Study. | 정용식 |
2018 | | Differences in prognosis and efficacy of chemotherapy by p53 expression in triple-negative breast cancer | 정용식 |
2024 | | Differential efficacy of tyrosine kinase inhibitors according to the types of EGFR mutations and agents in non-small cell lung cancer: a real-world study | 강석윤, 고영화, 김태환, 신승수, 안미선, 이현우, 최용원, 최진혁 |
2018 | | Diffusion-Weighted Imaging of Brain Metastasis from Lung Cancer: Correlation of MRI Parameters with the Histologic Type and Gene Mutation Status | 정우상 |
2020 | | Direct targeting of oncogenic RAS mutants with a tumor-specific cytosol-penetrating antibody inhibits RAS mutant-driven tumor growth | 이다근 |
2018 | | DJ-1 deficiency impairs synaptic vesicle endocytosis and reavailability at nerve terminals | 박상면, 조은혜, 주일로, 최동주, 하태영 |
2017 | | Does the efficacy of epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor differ according to the type of EGFR mutation in non-small cell lung cancer? | 최용원, 최진혁 |
2019 | | Drp1-Zip1 Interaction Regulates Mitochondrial Quality Surveillance System | 강호철 |
2023 | | Dual-phase 18F-FP-CIT positron emission tomography and cardiac 123I-MIBG scintigraphy of Parkinson's disease patients with GBA mutations: evidence of the body-first type? | 박동규, 안영실, 윤정한 |
2018 | | Dysregulated phosphorylation of Rab GTPases by LRRK2 induces neurodegeneration | 강호철 |
2014 | | Efficacy and safety of radotinib in chronic phase chronic myeloid leukemia patients with resistance or intolerance to BCR-ABL1 tyrosine kinase inhibitors. | 박준성, 정성현 |
2018 | | EGFR Exon 19 Deletion is Associated With Favorable Overall Survival After First-line Gefitinib Therapy in Advanced Non-Small Cell Lung Cancer Patients | 강석윤, 고영화, 박준성, 신승수, 이현우, 정성현, 최용원, 최진혁, 한재호 |
2006 | | ERK1/2 is an endogenous negative regulator of the gamma-secretase activity. | 백은주, 정민환 |
2000 | | Evidence that the 5'-end cap structure is essential for encapsidation of hepatitis B virus pregenomic RNA. | 윤계순 |
2014 | | First identified Korean family with Sotos syndrome caused by a novel intragenic mutation in NSD1. | 손영배 |
2019 | | Functional Genomic Complexity Defines Intratumor Heterogeneity and Tumor Aggressiveness in Liver Cancer | 권소미, 우현구 |
2016 | | G2385R and I2020T Mutations Increase LRRK2 GTPase Activity | 조은혜 |
2011 | | Genetic basis of congenital and infantile nephrotic syndromes. | 배기수 |
2013 | | Genetic investigation of patients with undetectable peaks of growth hormone after two provocation tests. | 손영배 |
2021 | | Genetic profiles of subcutaneous panniculitis-like t-cell lymphoma and clinicopathological impact of havcr2 mutations | 한재호 |
2017 | | Genetic variants of the gasdermin B gene associated with the development of aspirin-exacerbated respiratory diseases | 박해심 |
2023 | | Genomic analysis of plasma circulating tumor DNA in patients with heavily pretreated HER2 + metastatic breast cancer | 안미선 |
2023 | | Genotype–phenotype correlation of X-linked Alport syndrome observed in both genders: a multicenter study in South Korea | 배기수 |
2001 | | Hepatitis B virus X protein induced expression of the Nur77 gene. | 조혜성 |
2010 | | Hereditary palmoplantar keratoderma and deafness resulting from genetic mutation of Connexin 26. | 김유찬, 김현주, 정선용, 정연훈 |
2020 | | Hereditary spastic paraplegia SPG8 mutations impair CAV1-dependent, integrin-mediated cell adhesion | 장재락 |
2021 | | High SLC2A1 expression associated with suppressing CD8 T cells and B cells promoted cancer survival in gastric cancer | 고영화 |
1999 | | Histochemically reactive zinc in plaques of the Swedish mutant beta-amyloid precursor protein transgenic mice. | 묵인희 |
2002 | | Hrp3, a chromodomain helicase/ATPase DNA binding protein, is required for heterochromatin silencing in fission yeast. | 이명애 |
2013 | | Identification of a GDF5 mutation in a Korean patient with brachydactyly type C without foot involvement. | 김옥화 |
2019 | | Identification of a Novel Frameshift Variant of POU3F4 and Genetic Counseling of Korean Incomplete Partition Type III Subjects Based on Detailed Genotypes | 장정훈, 정연훈 |
2011 | | Identification of a novel recombinant mutation in Korean patients with Gaucher disease using a long-range PCR approach. | 김현주, 정선용 |
2018 | | Identification of a rare homozygous c.790C>T variation in the TFB2M gene in Korean patients with autism spectrum disorder | 김정현, 박찬배, 이영수, 임신영, 정선용 |
2018 | | Identification of genomic aberrations associated with lymph node metastasis in diffuse-type gastric cancer | 김영배, 우현구, 이다근, 최지혜, 한상욱 |