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백승태 사진
교원에 대한 정보를 나타내는 표입니다.
성명 백승태
소속 생명과학과
전화번호 054-279-2360
E-mail sbaek@postech.ac.kr
Homepage https://sites.google.com/site/baeklabpostech/

학력

  • 2008.08 ~ 2012.08 Univ. of Texas Southwestern Medical Center (박사-Genetics and Development)
  • 2005.08 ~ 2007.08 충남대학교 (석사-)
  • 1995.03 ~ 1999.02 충남대학교 (학사-)

주요경력

  • 2014.07 ~ 2017.01 : THE ROCKEFELLER UNIV. LAB. OF PEDIATRIC BRAIN DISEASE
  • 2012.09 ~ 2014.06 : UNIV. OF CALIFORNIA, SAN DIEGO DEPT. OF NEUROSCIENCES

전문분야

학술지

국제전문학술지

  • Loss of the neural-specific BAF subunit ACTL6B relieves repression of early response genes and causes recessive autism., Proceedings of the National Academy of Sciences of the United States of America, , 117, 10055-10066 (2020)
  • Downregulation of Human DAB2IP Gene Expression in Renal Cell Carcinoma Results in Resistance to Ionizing Radiation, CLINICAL CANCER RESEARCH, , 25, 4542-4551 (2019)
  • Neurodevelopmental Aspects of RASopathies, MOLECULES AND CELLS, , 42, 441-447 (2019)
  • Sequential phosphorylation of NDEL1 by the DYRK2-GSK3 beta complex is critical for neuronal morphogenesis, ELIFE, , 8, - (2019)
  • Biallelic loss of human CTNNA2, encoding αN-catenin, leads to ARP2/3 complex overactivity and disordered cortical neuronal migration., NATURE GENETICS, , 50, 1093-1101 (2018)
  • An AKT3-FOXG1-reelin network underlies defective migration in human focal malformations of cortical development., NATURE MEDICINE, , 21, 1445-1454 (2015)
  • Clinical and Genetic Aspects of the Segmental Overgrowth Spectrum Due to Somatic Mutations in PIK3CA, JOURNAL OF PEDIATRICS, , 167, 957-962 (2015)
  • Focal dysplasia of the cerebral cortex and infantile spasms associated with somatic 1q21.1-q44 duplication including the AKT3 gene, CLINICAL GENETICS, , 88, 214-247 (2015)
  • DAB2IP regulates cancer stem cell phenotypes through modulating stem cell factor receptor and ZEB1, ONCOGENE, , 34, 2741-2752 (2015)
  • An AKT3-FOXG1-Reelin network underlies defective migration in human focal malformations of cortical development, NATURE MEDICINE, , 21, 1445-+ (2015)
  • DAB2IP regulates cancer stem cell phenotypes through modulating stem cell factor receptor and ZEB1, ONCOGENE, , 34, 2741-2752 (2015)
  • Off-Target Effect of doublecortin Family shRNA on Neuronal Migration Associated with Endogenous MicroRNA Dysregulation, NEURON, , 82, 1255-1262 (2014)
  • The Sacred Disease: The Puzzling Genetics of Epileptic Disorders, NEURON, , 80, 9-11 (2013)
  • Hemimegalencephaly, a paradigm for somatic postzygotic neurodevelopmental disorders, CURRENT OPINION IN NEUROLOGY, , 26, 122-127 (2013)
  • The bHLH transcription factor Tcf21 is required for lineage-specific EMT of cardiac fibroblast progenitors, DEVELOPMENT, , 139, 2139-2149 (2012)
  • Nf1 limits epicardial derivative expansion by regulating epithelial to mesenchymal transition and proliferation, DEVELOPMENT, , 139, 2040-2049 (2012)
  • Efficient Inducible Cre-Mediated Recombination in Tcf21 Cell Lineages in the Heart and Kidney, GENESIS, , 49, 870-877 (2011)
  • Epicardial-Derived Cell Epithelial-to-Mesenchymal Transition and Fate Specification Require PDGF Receptor Signaling, CIRCULATION RESEARCH, , 108, 15-28 (2011)
  • Analysis of a genome-wide set of gene deletions in the fission yeast Schizosaccharomyces pombe, NATURE BIOTECHNOLOGY, , 28, 617-U111 (2010)
  • Genome-wide identification of haploinsufficiency in fission yeast, JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, , 18, 1059-1063 (2008)
  • Genome-wide drug-induced haploinsufficiency screening of fission yeast for identification of hydrazinocurcumin targets, JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, , 18, 263-269 (2008)
  • Cl- -channel is essential for LDL-induced cell proliferation via the activation of Erk1/2 and PI3k/Akt and the upregulation of Egr-1 in human aortic smooth muscle cells, Molecules and cells, , 26, 468-473 (2008)
  • Activation of PKC beta(II) and PKC theta is essential for LDL-induced cell proliferation of human aortic smooth muscle cells via Gi-mediated Erk1/2 activation and Egr-1 upregulation, Biochemical and biophysical research communications, , 368, 126-131 (2008)
  • PPAR gamma activation abolishes LDL-induced proliferation of human aortic smooth muscle cells via SOD-mediated down-regulation of superoxide, Biochemical and biophysical research communications, , 359, 1017-1023 (2007)

국내전문학술지

일반학술지

학술회의논문

  • Cellular and molecular mechanisms of epilepsy in focal brain malformations, KJPP2018, 0, 0, - (2018)
  • Developmental mechanisms of child epileptic syndrome caused by dysregulation of RAS/MAPK pathway, KSBNS 2018, 0, 0, - (2018)

학회발표

  • Genetic landscape of neurodevelopmental disorders associated with cortical malformation, ICGSK 2019, 0, 0, - (2019)
  • Investigating mitochondrial dynamic change caused by domain-specific missense mutations in DNM1L associated with a varying degree of neurological phenotypes in patients, SFN 2019, 0, 0, - (2019)
  • Developmental mechanisms of sebaceous nevus syndrome caused by dysregulation of RAS/MAPK pathway., IBRO 2019, 0, 0, - (2019)
  • Ectopic expression of HRAS gain-of-function mutation resulted in neurological abnormalities associated with nevus sebaceous syndrome in developing mouse brain, IBRO 2019, 0, 0, - (2019)
  • Molecular decoding of post traumatic stress disorder via time-resolved measurement of newly synthesized and existing RNA, IBRO 2019, 0, 0, - (2019)
  • Developmental mechanisms of epilepsy in sebaceous nevus syndrome caused by dysregulation of RAS/MAPK pathway, 뇌신경발생분과 2019, 0, 0, - (2019)
  • Developmental mechanisms of sebaceous nevus syndrome caused by dysregulation of RAS/MAPK pathway, SFN2018, 0, 0, - (2018)
  • Perturbation of overall activity of mTOR pathway in mouse model of focal cortical dysplasia, SFN2018, 0, 0, - (2018)
  • Development of therapeutic intervention to post traumatic stress disorder via systematic analysis of neural circuitry, KSBNS 2018, 0, 0, - (2018)
  • Insights into intractable epilepsy from focal cortical malformation, 2018 KSBMB, 0, 0, - (2018)
  • Transcriptional approaches to decode the mechanisms of intractable, 2017 RNA SUMMER SYMPOSIUM, 0, 0, - (2017)
  • Decoding the developmental and pathologic mechanisms of intractable seizure, 2017 CELL CYCLE & CILIA JOINT SYMPOSIUM, 0, 0, - (2017)
  • Insights into neuronal development from focal cortical malformation, 제 9회 뇌신경발생학분과 하계심포지엄, 0, 0, - (2017)
  • An AKT3-FOXG1-Reelin Network Underlies Defective Migration in Human Focal Malformations of Cortical Development, ., 0, 0, - (2016)
  • An AKT3-FOXG1-Reelin Network Underlies Human Focal Malformations of Cortical Development, ., 0, 0, - (2015)

단행본

연구실적

  • 백승태_신규부임교수 기자재지원(1차_대학), 포항공과대학교 (2017-2018)
  • 백승태_신규부임교수 연구비지원(1차_대학), 포항공과대학교 (2017-2018)
  • 백승태_신규부임교수 교수아파트 입주 지원금[삭제], 포항공과대학교 (2017-2017)
  • 난치성 뇌전증 치료법 개발을 위한 신경줄기세포 질환모델 수립, 포항공과대학교 (2017-2018)
  • 신경줄기세포 질병모델을 이용한 난치성 뇌전증의 병증기반 치료 분자타겟 개발, 재단법인한국연구재단 (2017-2018)
  • 백승태_신규부임교수 연구비지원(2차_학과), 포항공과대학교 (2018-2019)
  • 백승태_신규부임교수 연구비지원(2차_대학), 포항공과대학교 (2018-2019)
  • 백승태_신규부임교수 기자재지원(2차_학과), 포항공과대학교 (2018-2019)
  • 백승태_신규부임교수 연구비지원(2차_학과), 포항공과대학교 (2018-2019)
  • 신경줄기세포 질병모델을 이용한 난치성 뇌전증의 병증기반 치료 분자타겟 개발, 재단법인한국연구재단 (2018-2019)
  • [CW]대구경북 뇌과학 합동 심포지움, 포항공과대학교 (2018-2019)
  • 학생인건비통합관리과제, 포항공대산학협력단 (2019-2040)
  • 백승태_신규부임교수 연구비지원(3차_대학), 포항공과대학교 (2019-2020)
  • 백승태_신규부임교수 연구비지원(3차_학과), 포항공과대학교 (2019-2020)
  • 신경줄기세포 질병모델을 이용한 난치성 뇌전증의 병증기반 치료 분자타겟 개발, 재단법인한국연구재단 (2019-2019)
  • [BSRI-CW]제20회 포스텍 브레인 윈터스쿨, 포항공과대학교 (2019-2020)
  • RAS 신호전달계 이상에 의한 희귀 발작질환의 병리기전 규명, 재단법인한국연구재단 (2019-2020)
  • 백승태_신규부임교수 기자재지원(3차_학과), 포항공과대학교 (2019-2020)
  • RAS 신호전달계 이상에 의한 희귀 발작질환의 병리기전 규명, 재단법인한국연구재단 (2020-2021)
  • [BSRI-CW]제 20회 포스텍 브레인 윈터스쿨 2021, 포항공과대학교 (2020-2021)
  • 4.18366 이월과제, 재단법인한국연구재단 (2020-2021)
  • RAS 신호전달계 이상에 의한 희귀 발작질환의 병리기전 규명, 재단법인한국연구재단 (2021-2022)
  • 4.0019483/4.0020482_이월과제, 재단법인한국연구재단 (2021-2022)
  • RAS 질환 신경병증의 가역성 조절 및 기전 규명, 재단법인한국연구재단 (2022-2023)
  • RAS 신호전달계 이상에 의한 희귀 발작질환의 병리기전 규명, 재단법인한국연구재단 (2022-2022)
  • [UGRP]FICK'S LAW를 이용한 미생물의 이동속도 측정, 포항공과대학교 (2022-2023)
  • 생명과학과 화재 관련 부서연구관리비 직접 지원(백승태), 포항공과대학교 (2022-2023)

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