천성민 부교수
#병리과
|
학력
1999 .03 ~ 2007 .08고려대학교 분자생물학 박사
1997 .03 ~ 1999 .02고려대학교 분자생물학 석사
1993 .03 ~ 1997 .02단국대학교 분자생물학 학사
1997 .03 ~ 1999 .02고려대학교 분자생물학 석사
1993 .03 ~ 1997 .02단국대학교 분자생물학 학사
경력
2018 .03 ~ 현재서울아산병원 병리과 임상부교수
2011 .03 ~ 2018 .02서울아산병원 특수전문학자
2010 .03 ~ 2011 .02고대안암병원 연구교수
2008 .09 ~ 2009 .08울산대학교 연구교수
2007 .09 ~ 2010 .02아산생명과학연구소 박사후연구원
2011 .03 ~ 2018 .02서울아산병원 특수전문학자
2010 .03 ~ 2011 .02고대안암병원 연구교수
2008 .09 ~ 2009 .08울산대학교 연구교수
2007 .09 ~ 2010 .02아산생명과학연구소 박사후연구원
논문
Detection of chromosome structural variation by targeted next-generation sequencing and a deep learning application
Immunogenomic landscape of hepatocellular carcinoma with immune cell stroma and EBV-positive tumor-infiltrating lymphocytes.
Mutational profile of papillary thyroid microcarcinoma with extensive lymph node metastasis.
Genomic profiles of lung cancer associated with idiopathic pulmonary fibrosis.
Mutation Burden and I Index for Detection of Microsatellite Instability in Colorectal Cancer by Targeted Next-Generation Sequencing.
Mutational Profiling of Malignant Mesothelioma Revealed Potential Therapeutic Targets in EGFR and NRAS.
Next-Generation Sequencing Using S1 Nuclease for Poor-Quality Formalin-Fixed, Paraffin-Embedded Tumor Specimens.
Feasibility of multiplexed gene mutation detection in plasma samples of colorectal cancer patients by mass spectrometric genotyping.
Good Laboratory Standards for Clinical Next-Generation Sequencing Cancer Panel Tests.
HER2 Amplification and Cetuximab Efficacy in Patients With Metastatic Colorectal Cancer Harboring Wild-type RAS and BRAF.
Hypermethylation of adjacent CpG sites is negatively correlated with the expression of lineage oncogene ASCL1 in pulmonary neuroendocrine tumors.
KRAS and PIK3CA mutations in colorectal adenocarcinomas correlate with aggressive histological features and behavior.
Lynch syndrome-related small intestinal adenocarcinomas.
Use of a High-Throughput Genotyping Platform (OncoMap) for RAS Mutational Analysis to Predict Cetuximab Efficacy in Patients with Metastatic Colorectal Cancer.
Association between the CpG island methylator phenotype and its prognostic significance in primary pulmonary adenocarcinoma.
Genomic alterations of anaplastic thyroid carcinoma detected by targeted massive parallel sequencing in a BRAFV600E mutation-prevalent area.
Paired Primary and Metastatic Tumor Analysis of Somatic Mutations in Synchronous and Metachronous Colorectal Cancer.
Reappraisal of hMLH1 promoter methylation and protein expression status in the serrated neoplasia pathway.
The somatic POLE P286R mutation defines a unique subclass of colorectal cancer featuring hypermutation, representing a potential genomic biomarker for immunotherapy.
Use of a High-Throughput Genotyping Platform (OncoMap) for RAS Mutational Analysis to Predict
Cetuximab Efficacy in Patients with Metastatic Colorectal Cancer
Comprehensive genomic profiles of small cell lung cancer.
Epigenetic modulation with HDAC inhibitor CG200745 induces anti-proliferation in non-small cell lung cancer cells.
Multiple resistant factors in lung cancer with primary resistance to EGFR-TK inhibitors confer poor survival.
Sessile serrated adenoma/polyps with a depressed surface: a rare form of sessile serrated adenoma/polyp.
Analysis and comparison of somatic mutations in paired primary and recurrent epithelial ovarian cancer samples.
Development and characterization of a colon PDX model that reproduces drug responsiveness and the mutation profiles of its original tumor.
Epigenetic silencing of microRNA-373 to epithelial-mesenchymal transition in non-small cell lung cancer through IRAK2 and LAMP1 axes.
Genomic Alterations in the RB Pathway Indicate Prognostic Outcomes of Early-Stage Lung Adenocarcinoma.
Genomic portrait of resectable hepatocellular carcinomas: implications of RB1 and FGF19 aberrations for patient stratification.
Protuberant fibro-osseous lesions of the temporal bone: two additional case reports.
Immunogenomic landscape of hepatocellular carcinoma with immune cell stroma and EBV-positive tumor-infiltrating lymphocytes.
Mutational profile of papillary thyroid microcarcinoma with extensive lymph node metastasis.
Genomic profiles of lung cancer associated with idiopathic pulmonary fibrosis.
Mutation Burden and I Index for Detection of Microsatellite Instability in Colorectal Cancer by Targeted Next-Generation Sequencing.
Mutational Profiling of Malignant Mesothelioma Revealed Potential Therapeutic Targets in EGFR and NRAS.
Next-Generation Sequencing Using S1 Nuclease for Poor-Quality Formalin-Fixed, Paraffin-Embedded Tumor Specimens.
Feasibility of multiplexed gene mutation detection in plasma samples of colorectal cancer patients by mass spectrometric genotyping.
Good Laboratory Standards for Clinical Next-Generation Sequencing Cancer Panel Tests.
HER2 Amplification and Cetuximab Efficacy in Patients With Metastatic Colorectal Cancer Harboring Wild-type RAS and BRAF.
Hypermethylation of adjacent CpG sites is negatively correlated with the expression of lineage oncogene ASCL1 in pulmonary neuroendocrine tumors.
KRAS and PIK3CA mutations in colorectal adenocarcinomas correlate with aggressive histological features and behavior.
Lynch syndrome-related small intestinal adenocarcinomas.
Use of a High-Throughput Genotyping Platform (OncoMap) for RAS Mutational Analysis to Predict Cetuximab Efficacy in Patients with Metastatic Colorectal Cancer.
Association between the CpG island methylator phenotype and its prognostic significance in primary pulmonary adenocarcinoma.
Genomic alterations of anaplastic thyroid carcinoma detected by targeted massive parallel sequencing in a BRAFV600E mutation-prevalent area.
Paired Primary and Metastatic Tumor Analysis of Somatic Mutations in Synchronous and Metachronous Colorectal Cancer.
Reappraisal of hMLH1 promoter methylation and protein expression status in the serrated neoplasia pathway.
The somatic POLE P286R mutation defines a unique subclass of colorectal cancer featuring hypermutation, representing a potential genomic biomarker for immunotherapy.
Use of a High-Throughput Genotyping Platform (OncoMap) for RAS Mutational Analysis to Predict
Cetuximab Efficacy in Patients with Metastatic Colorectal Cancer
Comprehensive genomic profiles of small cell lung cancer.
Epigenetic modulation with HDAC inhibitor CG200745 induces anti-proliferation in non-small cell lung cancer cells.
Multiple resistant factors in lung cancer with primary resistance to EGFR-TK inhibitors confer poor survival.
Sessile serrated adenoma/polyps with a depressed surface: a rare form of sessile serrated adenoma/polyp.
Analysis and comparison of somatic mutations in paired primary and recurrent epithelial ovarian cancer samples.
Development and characterization of a colon PDX model that reproduces drug responsiveness and the mutation profiles of its original tumor.
Epigenetic silencing of microRNA-373 to epithelial-mesenchymal transition in non-small cell lung cancer through IRAK2 and LAMP1 axes.
Genomic Alterations in the RB Pathway Indicate Prognostic Outcomes of Early-Stage Lung Adenocarcinoma.
Genomic portrait of resectable hepatocellular carcinomas: implications of RB1 and FGF19 aberrations for patient stratification.
Protuberant fibro-osseous lesions of the temporal bone: two additional case reports.
저서
저서 내용이 없습니다.
보도자료
보도자료 내용이 없습니다.
포스팅
포스팅 내용이 없습니다.
영상자료
영상자료 내용이 없습니다.
발표자료
Understanding of clinical NGS data
NGS System: Technology & wet-lab
Establishment of lung cancer organoid lines as a new preclinical model for lung cancer.
Liquid biopsy for clinical trial
NGS 기술의 개요
임상 NGS 검사의 wet-lab 전과정 이해
유전체병리 검사실의 질관리 프로그램
NGS-Platforms-current and future (WGS, WES, WTS, Targeted panel sequencing)
Identification of genomic aberrations in Large Cell Neuroendocrine Carcinoma of Lung by targeted next-generation sequencing
A novel allele specific enrichment method for ultra-high sensitive mutation detection
NGS System: Technology & wet-lab
Establishment of lung cancer organoid lines as a new preclinical model for lung cancer.
Liquid biopsy for clinical trial
NGS 기술의 개요
임상 NGS 검사의 wet-lab 전과정 이해
유전체병리 검사실의 질관리 프로그램
NGS-Platforms-current and future (WGS, WES, WTS, Targeted panel sequencing)
Identification of genomic aberrations in Large Cell Neuroendocrine Carcinoma of Lung by targeted next-generation sequencing
A novel allele specific enrichment method for ultra-high sensitive mutation detection