ScholarWorks@Korea University College of Medicine: Yoo, Yongjin

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Yoo, Yongjin (유용진)

College of Medicine (Department of Neuroscience)

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Wholeexome sequencing:2||Cell Therapy:2||Microglia:2||wholeexome sequencing:2||Atypical:1||Benign:1||Bone Marrow Cell:1||CALR:1||Degenerative Disease:1||Etiology:1||Functional Disease:1||GM3 synthase:1||Genetic Risk:1||HMGA2:1||Homeostasis:1||Human:1||Human Tissue:1||Intellectual disability:1||JAK2:1||Japanese myeloproliferative neoplasm patients:1||KMT2A:1||MAE:1||MECP2 mutation:1||MPL mutation:1||MYBPC1:1||Meningioma:1||Microglia Replacement:1||Mouse:1||Nerve Degeneration:1||Neurodegenerative Disease:1||Nonhuman:1||Pathogenesis:1||Pluripotent Stem Cell:1||Psychomotor retardation:1||RNA sequencing:1||Rett like:1||Rett syndrome:1||Rettlike phenotype:1||Review:1||SATB2:1||SATB2associated syndrome:1||SLC6A1:1||ST3GAL5:1||Trem2:1||WiedemannSteiner syndrome:1||arthrogryposis:1||cancer:1||circulationderived myeloid cells:1||congenital hip dislocation:1||dedifferentiated and welldifferentiated form:1||embryonic development:1||epilepsy:1||epilepsy genetics:1||fibromatosis colli:1||ganglioside:1||hematopoietic cell transplantation:1||histones:1||hypotonia:1||immune profiles:1||liposarcoma:1||lung adenocarcinoma:1||macrophages:1||microglia:1||myopathy:1||Alzheimer Disease:1||proteomics:1||psychomotor retardation:1||ribosome:1||ribosome heterogeneity:1||ribosomeassociated proteins:1||translational control:1||tremor:1||whole exome sequencing:1||myosin binding proteinC:1||Alzheimer's Disease:1||Alzheimer's disease:1||Animal Model:1||

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73, Goryeodae-ro, Seongbuk-gu, Seoul, Republic of Korea (02841)82-2-2286-1265

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