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정, 선용(Jeong, Seon Yong) Currently indexed
[School of Medicine / Graduate School of Medicine] - [Medical Genetics]

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-
ISNI
0000000463373664
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Showing results 41 to 60 of 79

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Pub YearTitleAuthor(s)
2012Correlation Between Unidentified Bright Objects on Brain Magnetic Resonance Imaging (MRI) and Cerebral Glucose Metabolism in Patients with Neurofibromatosis Type 1김현주, 손영배, 안영실, 이수진, 정선용, 최진욱
2012Histone deacetylase inhibitors induce mitochondrial elongation정선용
2012Molecular genetic analysis of TWIST1 and FGFR3 genes in Korean patients with coronal synostosis: identification of three novel TWIST1 mutations박동하, 윤수한, 정선용
2012Mutation spectrum of the TYR and SLC45A2 genes in patients with oculocutaneous albinism김현주, 정선용
2012Inhibition of Bcl-xL by ABT-737 enhances chemotherapy sensitivity in neurofibromatosis type 1-associated malignant peripheral nerve sheath tumor cells김보영, 김현주, 임현이, 정선용, 진현석, 한재호
2012Pathologic diagnosis of recurrent glioblastoma: morphologic, immunohistochemical, and molecular analysis of 20 paired cases김보영, 김세혁, 김영배, 김장희, 신승수, 이기범, 이현우, 정선용, 한재호
2011Two Children with Saethre-Chotzen Syndrome Confirmed by the TWIST1 Gene Analysis윤수한, 정선용
2011Age-dependent association of the polymorphisms in the mitochondria-shaping gene, OPA1, with blood pressure and hypertension in Korean population.정선용, 진현석
2011Replicated association between genetic variation in the PARK2 gene and blood pressure.정선용, 진현석
2011In Vitro and In Vivo Inhibition of Glucocorticoid-induced Osteoporosis by the Hexane Extract of Poncirus trifoliata.정선용, 정윤석
2011Identification of a novel recombinant mutation in Korean patients with Gaucher disease using a long-range PCR approach.김현주, 정선용
2011Clinical and genetic characteristics of Korean patients with Gaucher disease.김현주, 정선용
2011Poncirin promotes osteoblast differentiation but inhibits adipocyte differentiation in mesenchymal stem cells.정선용, 정윤석
2010A case of donor-derived granulocytic sarcoma after allogeneic hematopoietic stem cell transplantation강석윤, 박준성, 이현우, 정선용, 정성현, 최진혁, 한재호
2010A novel homozygous MMP2 mutation in a patient with Torg-Winchester syndrome.김옥화, 김현주, 정선용
2010De novo pericentric inversion of chromosome 9 in congenital anomaly.정선용
2010Loss of Y chromosome in the malignant peripheral nerve sheet tumor of a patient with Neurofibromatosis type 1.김현주, 정선용
2010Hereditary palmoplantar keratoderma and deafness resulting from genetic mutation of Connexin 26.김유찬, 김현주, 정선용, 정연훈
2009Glucocorticoid induces apoptosis of osteoblast cells through the activation of glycogen synthase kinase 3beta.정선용, 정윤석
2009The cell death-inducing activity of the peptide containing Noxa mitochondrial-targeting domain is associated with calcium release.정선용
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