서을주 교수
#세포유전학 #분자유전
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학력
1995 .03 ~ 1999 .02울산대학교 의학 박사
1993 .03 ~ 1995 .02울산대학교 의학 석사
1984 .03 ~ 1990 .02경북대학교 의학 학사
1993 .03 ~ 1995 .02울산대학교 의학 석사
1984 .03 ~ 1990 .02경북대학교 의학 학사
경력
2011 .09 ~ 현재울산의대 서울아산병원 진단검사의학과 교수
2006 .04 ~ 2011 .08울산의대 서울아산병원 진단검사의학과 부교수
2004 .02 ~ 2005 .01The Centre for Applied Genomics, Department of Geneties and Genomics Biology, The Hospital for Sick Children, University of Toronto, Canada, Visiting Scientist
2002 .03 ~ 2006 .03울산의대 서울아산병원 진단검사의학과 조교수
2000 .03 ~ 2002 .02울산의대 서울아산병원 임상병리과 전임강사
1999 .03 ~ 2000 .02울산의대 서울아산병원 임상병리과 촉탁의
1995 .03 ~ 1999 .02울산의대 서울아산병원 임상병리과 전임의
1991 .03 ~ 1995 .02울산의대 서울아산병원 임상병리과 전공의
1990 .03 ~ 1991 .02울산의대 서울아산병원 인턴
2006 .04 ~ 2011 .08울산의대 서울아산병원 진단검사의학과 부교수
2004 .02 ~ 2005 .01The Centre for Applied Genomics, Department of Geneties and Genomics Biology, The Hospital for Sick Children, University of Toronto, Canada, Visiting Scientist
2002 .03 ~ 2006 .03울산의대 서울아산병원 진단검사의학과 조교수
2000 .03 ~ 2002 .02울산의대 서울아산병원 임상병리과 전임강사
1999 .03 ~ 2000 .02울산의대 서울아산병원 임상병리과 촉탁의
1995 .03 ~ 1999 .02울산의대 서울아산병원 임상병리과 전임의
1991 .03 ~ 1995 .02울산의대 서울아산병원 임상병리과 전공의
1990 .03 ~ 1991 .02울산의대 서울아산병원 인턴
논문
Is Whole Exome Sequencing Clinically Practical in the Management of Pediatric Crohn's Disease?
A Case of Acute Myeloid Leukemia Concurrent With Untreated Chronic Lymphocytic Leukemia.
A Case of Primary Bone Marrow Diffuse Large B-cell Lymphoma Presenting With Fibrillar Projections and Hemophagocytic Lymphohistiocytosis.
Familial Hemophagocytic Lymphohistiocytosis Type 2 in a Korean Infant With Compound Heterozygous PRF1 Defects Involving a PRF1 Mutation, c.1091T>G.
Frequency and Distinct Characteristics of Acute Myeloid Leukemia Lacking HLA-DR and CD34 Expression: Features Intermediate between Typical Acute Myeloid Leukemia and Acute Promyelocytic Leukemia
GAB2 Amplification in Squamous Cell Lung Cancer of Non-Smokers.
Increased circulating plasma cells detected by flow cytometry predicts poor prognosis in patients with plasma cell myeloma.
Prognostic significance of recurrent additional chromosomal abnormalities in adult patients with Philadelphia chromosome-positive acute lymphoblastic leukemia.
The First Case of Therapy-Related Myelomastocytic Leukemia Based on the WHO 2008 Classification and the Recently Proposed Diagnostic Criteria.
Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay.
Myelodysplasia-Related Features of Acute Myeloid Leukemia Evolving From Philadelphia-Negative Myeloproliferative Neoplasms.
The added values of multiplex reverse transcriptase-PCR followed by mutation screening in the initial evaluation of acute leukemia.
A t(8;9)(p22;p24)/PCM1-JAK2 translocation in a patient with myeloproliferative neoplasm and myeloid sarcoma: first report in Korea.
Concurrent Hematologic and Metastatic Epithelial Malignancies in the Bone Marrow: Report of Three Cases.
JAK2 V617F, MPL, and CALR Mutations in Korean Patients with Essential Thrombocythemia and Primary Myelofibrosis.
Loss of mismatched HLA detected in the peripheral blood of an AML patient who relapsed after haploidentical hematopoietic stem cell transplantation.
Monosomal karyotype in acute myeloid leukemia and the role of allogeneic hematopoietic cell transplantation.
Phenotypic variability of a terminal 7q deletion/8q duplication in Korean siblings.
Straightforward identification of masked polycythemia vera based on proposed revision of World Health Organization diagnostic criteria for BCR-ABL1-negative myeloproliferative neoplasms.
Turner syndrome presented with tall stature due to overdosage of the SHOX gene.
A Case of Acute Myeloid Leukemia Concurrent With Untreated Chronic Lymphocytic Leukemia.
A Case of Primary Bone Marrow Diffuse Large B-cell Lymphoma Presenting With Fibrillar Projections and Hemophagocytic Lymphohistiocytosis.
Familial Hemophagocytic Lymphohistiocytosis Type 2 in a Korean Infant With Compound Heterozygous PRF1 Defects Involving a PRF1 Mutation, c.1091T>G.
Frequency and Distinct Characteristics of Acute Myeloid Leukemia Lacking HLA-DR and CD34 Expression: Features Intermediate between Typical Acute Myeloid Leukemia and Acute Promyelocytic Leukemia
GAB2 Amplification in Squamous Cell Lung Cancer of Non-Smokers.
Increased circulating plasma cells detected by flow cytometry predicts poor prognosis in patients with plasma cell myeloma.
Prognostic significance of recurrent additional chromosomal abnormalities in adult patients with Philadelphia chromosome-positive acute lymphoblastic leukemia.
The First Case of Therapy-Related Myelomastocytic Leukemia Based on the WHO 2008 Classification and the Recently Proposed Diagnostic Criteria.
Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay.
Myelodysplasia-Related Features of Acute Myeloid Leukemia Evolving From Philadelphia-Negative Myeloproliferative Neoplasms.
The added values of multiplex reverse transcriptase-PCR followed by mutation screening in the initial evaluation of acute leukemia.
A t(8;9)(p22;p24)/PCM1-JAK2 translocation in a patient with myeloproliferative neoplasm and myeloid sarcoma: first report in Korea.
Concurrent Hematologic and Metastatic Epithelial Malignancies in the Bone Marrow: Report of Three Cases.
JAK2 V617F, MPL, and CALR Mutations in Korean Patients with Essential Thrombocythemia and Primary Myelofibrosis.
Loss of mismatched HLA detected in the peripheral blood of an AML patient who relapsed after haploidentical hematopoietic stem cell transplantation.
Monosomal karyotype in acute myeloid leukemia and the role of allogeneic hematopoietic cell transplantation.
Phenotypic variability of a terminal 7q deletion/8q duplication in Korean siblings.
Straightforward identification of masked polycythemia vera based on proposed revision of World Health Organization diagnostic criteria for BCR-ABL1-negative myeloproliferative neoplasms.
Turner syndrome presented with tall stature due to overdosage of the SHOX gene.
저서
진단검사의학
진단검사의학 완전개정 3판
임상병리학 교과서 제3판
진단검사의학 완전개정 3판
임상병리학 교과서 제3판
보도자료
"DTC 유전자검사 업체 전문성 관리 필요"
https://news.mt.co.kr/mtview.php?no=2019123011111820726
https://news.mt.co.kr/mtview.php?no=2019123011111820726
포스팅
Characteristics of MYC Gene Aberrations in Multiple Myeloma
Myeloid-Derived Suppressor Cells in Chronic Myelogenous Leukemia
Frequent Detection of Chromothripsis in Acute Myeloid Leukemia with Complex Karyotype and Marker Chromosomes
Myeloid Neoplasms Involving Body Fluid: an Unusual Presentation and Case Series in a Single Tertiary Care Center in Korea
A Case of Myelomastocytic Leukemia Based on the Recently Proposed Criteria
Prognostic Impact of Mutant Allele Ratio, Not Conferred by Duplicated Fragment Length, of FMS-like
Tyrosine Kinase 3 Internal Tandem Duplication in Patients with Acute Myeloid Leukemia
Frequency, Characteristics and Prognostic Significance of RUNX1 Mutations in Patients with Acute Myeloid Leukemia, Not Otherwise Specified
Identification of novel fusion genes and differentially expressed genes in acute leukemia through transcriptome analysis
Characterization of Plasma Cell Myeloma Patients Based on Plasma Cell Labeling Index: An Old Marker Revisited with Updated Guideline for Risk Stratification
Frequency, Characteristics, and Prognostic Significance of RUNX1 Mutations in Patients with Acute Myeloid Leukemia, Not Otherwise Specified
Influence of Quantitative Chromosomal Changes at the Polymorphic Short Tandem Repeat Loci on Chimerism in Patients with Hematologic Malignancies
Bone Marrow Histopathology with Gene Mutational Correlation in Patients with Essential Thrombocythemia and Primary Myelofibrosis
Alternating Appearance of Acute Promyelocytic Leukemia and Secondary Myelodysplastic Syndrome: Case Report
A Rare Case of Familial Hemophagocytic Lymphohistiocytosis Resulting from a Compound Heterozygous PRF1 Defect
The t(8;9)(p22;p24) Translocation in Myeloproliferative Neoplasm associated with Myeloid Sarcoma
Adding value to multiplex RT-PCR followed by mutation screening in the initial evaluation of acute leukemia
Straightforward identification of masked polycythemia vera based on proposed revision of WHO diagnostic criteria for BCR-ABL1-negative myeloproliferative neopla는
Predictive Value of Post-transplant Molecular Minimal Residual Disease Monitoring Versus Pretreatment
Risk Factors in Patients with Favorable Risk Acute Myeloid Leukemia Following Hematopoietic Stem Cell Transplantation
The Practical Utility of Risk Stratification via Molecular Testing in Patients with Acute Leukemia
Features and Outcomes of Rare Cases with the t(9;22) Occurring in Acute Myeloid Leukemia without a Preceding History of Chronic Myelogenous Leukemia
Myeloid-Derived Suppressor Cells in Chronic Myelogenous Leukemia
Frequent Detection of Chromothripsis in Acute Myeloid Leukemia with Complex Karyotype and Marker Chromosomes
Myeloid Neoplasms Involving Body Fluid: an Unusual Presentation and Case Series in a Single Tertiary Care Center in Korea
A Case of Myelomastocytic Leukemia Based on the Recently Proposed Criteria
Prognostic Impact of Mutant Allele Ratio, Not Conferred by Duplicated Fragment Length, of FMS-like
Tyrosine Kinase 3 Internal Tandem Duplication in Patients with Acute Myeloid Leukemia
Frequency, Characteristics and Prognostic Significance of RUNX1 Mutations in Patients with Acute Myeloid Leukemia, Not Otherwise Specified
Identification of novel fusion genes and differentially expressed genes in acute leukemia through transcriptome analysis
Characterization of Plasma Cell Myeloma Patients Based on Plasma Cell Labeling Index: An Old Marker Revisited with Updated Guideline for Risk Stratification
Frequency, Characteristics, and Prognostic Significance of RUNX1 Mutations in Patients with Acute Myeloid Leukemia, Not Otherwise Specified
Influence of Quantitative Chromosomal Changes at the Polymorphic Short Tandem Repeat Loci on Chimerism in Patients with Hematologic Malignancies
Bone Marrow Histopathology with Gene Mutational Correlation in Patients with Essential Thrombocythemia and Primary Myelofibrosis
Alternating Appearance of Acute Promyelocytic Leukemia and Secondary Myelodysplastic Syndrome: Case Report
A Rare Case of Familial Hemophagocytic Lymphohistiocytosis Resulting from a Compound Heterozygous PRF1 Defect
The t(8;9)(p22;p24) Translocation in Myeloproliferative Neoplasm associated with Myeloid Sarcoma
Adding value to multiplex RT-PCR followed by mutation screening in the initial evaluation of acute leukemia
Straightforward identification of masked polycythemia vera based on proposed revision of WHO diagnostic criteria for BCR-ABL1-negative myeloproliferative neopla는
Predictive Value of Post-transplant Molecular Minimal Residual Disease Monitoring Versus Pretreatment
Risk Factors in Patients with Favorable Risk Acute Myeloid Leukemia Following Hematopoietic Stem Cell Transplantation
The Practical Utility of Risk Stratification via Molecular Testing in Patients with Acute Leukemia
Features and Outcomes of Rare Cases with the t(9;22) Occurring in Acute Myeloid Leukemia without a Preceding History of Chronic Myelogenous Leukemia
영상자료
영상자료 내용이 없습니다.
발표자료
정상 핵형을 보인 성인 급성골수성백혈병에서의 nucleophosmin 엑손 12 돌연변이 선별의 임상적 의의
급성백혈병에서 다중 역전사중합효소연쇄반응을 이용한 분자생물학적 선별과 세포유전학적 분석과의 비교
유방암 환자에서 Topoisomerase II 억제제 치료 후 발생한 이차성 급성백혈병
골수형성이상증후군 골수생검에서 면역조직화학염색으로 시행한 CD34 및 p53 발현양상과 예후와의 연관성
골수형성이상증후군에서 4색 유세포분석의 진단적 유용성
진성적혈구증다증에서 hydroxyurea 치료 후 골수증식성질환/골수이형성증후군-미분류로 전환된 1례 보고
der(4)t(4;11)이 추가된 t(4;11)을 가지는 급성단모구성백혈병 1예
CD34 및 p53 면역조직화학염색을 이용한 저세포성 골수형성이상증후군과 재생불량성빈혈의 감별진단
A case of leukemic manifestation in anaplastic large cell lymphoma
급성백혈병에서의 형질 전환
급성백혈병에서 다중 역전사중합효소연쇄반응을 이용한 분자생물학적 선별과 세포유전학적 분석과의 비교
유방암 환자에서 Topoisomerase II 억제제 치료 후 발생한 이차성 급성백혈병
골수형성이상증후군 골수생검에서 면역조직화학염색으로 시행한 CD34 및 p53 발현양상과 예후와의 연관성
골수형성이상증후군에서 4색 유세포분석의 진단적 유용성
진성적혈구증다증에서 hydroxyurea 치료 후 골수증식성질환/골수이형성증후군-미분류로 전환된 1례 보고
der(4)t(4;11)이 추가된 t(4;11)을 가지는 급성단모구성백혈병 1예
CD34 및 p53 면역조직화학염색을 이용한 저세포성 골수형성이상증후군과 재생불량성빈혈의 감별진단
A case of leukemic manifestation in anaplastic large cell lymphoma
급성백혈병에서의 형질 전환