Jieun Seo

发表

Recurrent De Novo Mutations Disturbing the GTP/GDP Binding Pocket of RAB11B Cause Intellectual Disability and a Distinctive Brain Phenotype.

R. Pfundt, M. Reijnders, B. D. de Vries, 2017, American journal of human genetics.

Fatty-acid-induced FABP5/HIF-1 reprograms lipid metabolism and enhances the proliferation of liver cancer cells

J. Fukuda, Jieun Seo, Jong-Wan Park, 2020, Communications biology.

Genetic associations of in vivo pathology influence Alzheimer’s disease susceptibility

D. Y. Lee, Yu Kyeong Kim, C. Sohn, 2020, Alzheimer's Research & Therapy.

Comprehensive genetic analysis by whole exome sequencing in 352 Korean pediatric patients with unknown neurodevelopmental disorders

Murim Choi, J. Ko, Jieun Seo, 2018, bioRxiv.

Genomic profiling of 553 uncharacterized neurodevelopment patients reveals a high proportion of recessive pathogenic variant carriers in an outbred population

Murim Choi, J. Ko, Jieun Seo, 2020, Scientific Reports.

Genomic profiling of 553 uncharacterized neurodevelopment patients reveals a high proportion of recessive pathogenic variant carriers in an outbred population

Y. H. Lee, Murim Choi, J. Ko, 2019, Scientific Reports.

Neddylation of sterol regulatory element-binding protein 1c is a potential therapeutic target for nonalcoholic fatty liver treatment

Jieun Seo, J. B. Kim, Jong-Wan Park, 2020, Cell Death and Disease.

Neddylation blockade induces HIF-1α driven cancer cell migration via upregulation of ZEB1

Jieun Seo, Jong-Wan Park, Y. Chun, 2020, Scientific Reports.

The E3 ligase C-CBL inhibits cancer cell migration by neddylating the proto-oncogene c-Src

Masatoshi Watanabe, Jieun Seo, Jong-Wan Park, 2018, Oncogene.

Metastasis-on-a-chip reveals adipocyte-derived lipids trigger cancer cell migration via HIF-1α activation in cancer cells.

Ki Yong Hong, J. Fukuda, Hak Chang, 2020, Biomaterials.

Multi‐Omics‐Based Autophagy‐Related Untypical Subtypes in Patients with Cerebral Amyloid Pathology

D. Y. Lee, D. Hwang, Murim Choi, 2022, Advanced science.

Targeted Downregulation of kdm4a Ameliorates Tau-engendered Defects in Drosophila melanogaster

Jieun Seo, Y. Chun, Sung Yeon Park, 2019, Journal of Korean medical science.

Optical genome mapping identifies clinically relevant genomic rearrangements in prostate cancer biopsy sample

J. Choi, C. Park, Y. Choi, 2022, Cancer Cell International.

Uncovering the dosage-dependent roles of Arid1a in gastric tumorigenesis for combinatorial drug therapy

H. He, Haiyang Guo, L. Du, 2021, The Journal of experimental medicine.

Hypomorphic Mutations in TONSL Cause SPONASTRIME Dysplasia.

O. Mäkitie, Dongsup Kim, G. Stewart, 2019, American journal of human genetics.

University of Birmingham Hypomorphic Mutations in TONSL Cause SPONASTRIME Dysplasia

O. Mäkitie, Dongsup Kim, G. Stewart, 2019 .

Lipid metabolic reprogramming by hypoxia-inducible factor-1 in the hypoxic tumour microenvironment

Jieun Seo, Y. Chun, Jeong-Eun Yun, 2022, Pflügers Archiv - European Journal of Physiology.

Fatty-acid-induced FABP5/HIF-1 reprograms lipid metabolism and enhances the proliferation of liver cancer cells

J. Fukuda, Jieun Seo, Jong-Wan Park, 2020, Communications Biology.

Wiedemann-Steiner Syndrome With 2 Novel KMT2A Mutations

Murim Choi, T. Cho, Jieun Seo, 2017, Journal of child neurology.

SOFT syndrome caused by compound heterozygous mutations of POC1A and its skeletal manifestation

Murim Choi, J. Ko, T. Cho, 2016, Journal of Human Genetics.

Chimerism Assay Using Single Nucleotide Polymorphisms Adjacent and in Linkage-Disequilibrium Enables Sensitive Disease Relapse Monitoring after Hematopoietic Stem-Cell Transplantation.

J. Choi, Yu Jin Park, Jieun Seo, 2021, Clinical chemistry.

Wiedemann-Steiner Syndrome With 2 Novel KMT 2 A Mutations : Variable Severity in Psychomotor Development and Musculoskeletal Manifestation

Murim Choi, J. Ko, T. Cho, 2016 .

Tofacitinib relieves symptoms of stimulator of interferon genes (STING)-associated vasculopathy with onset in infancy caused by 2 de novo variants in TMEM173.

Dong Hun Lee, Murim Choi, June-Dong Park, 2017, The Journal of allergy and clinical immunology.

Histone demethylase PHF2 activates CREB and promotes memory consolidation

Hye-Jin Kim, Myoung-Hwan Kim, Jieun Seo, 2019, EMBO reports.

Biallelic mutations in ABCB1 display recurrent reversible encephalopathy

Murim Choi, J. Ku, J. Paeng, 2020, Annals of clinical and translational neurology.

The Genotype-Phenotype Correlation in Human 5α-Reductase Type 2 Deficiency: Classified and Analyzed from a SRD5A2 Structural Perspective

J. Choi, Jieun Seo, Saeam Shin, 2023, International journal of molecular sciences.

Hypoxia inducible factor-1α promotes trichogenic gene expression in human dermal papilla cells

J. Fukuda, Jieun Seo, Tatsuto Kageyama, 2023, Scientific Reports.

Development and validation of sensitive BCR::ABL1 fusion gene quantitation using next-generation sequencing

J. Choi, Jieun Seo, Saeam Shin, 2023, Cancer Cell International.

Genetic associations of in vivo pathology influence Alzheimer’s disease susceptibility

D. Y. Lee, Yu Kyeong Kim, C. Sohn, 2020, Alzheimer's research & therapy.

Analytical and Clinical Validation of Cell-Free Circulating Tumor DNA Assay for the Estimation of Tumor Mutational Burden.

J. Choi, H. Chung, S. Rha, 2022, Clinical chemistry.

Neddylation of sterol regulatory element-binding protein 1c is a potential therapeutic target for nonalcoholic fatty liver treatment

Jieun Seo, J. B. Kim, Jong-Wan Park, 2020, Cell Death & Disease.

Rare cases of congenital arthrogryposis multiplex caused by novel recurrent CHRNG mutations

Murim Choi, J. Ko, Y. Shin, 2015, Journal of Human Genetics.

Development and validation of sensitive BCR::ABL1 fusion gene quantitation using next-generation sequencing

J. Choi, Jieun Seo, Saeam Shin, 2023, Cancer Cell International.