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

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ORCID
-
ISNI
0000000463373664
WOS
-
SCOPUS
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Showing results 41 to 60 of 101

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Pub YearTitleAuthor(s)
2015A reply to a commentary on identification of the rare compound heterozygous variants in the NEB gene in a Korean family with intellectual disability, epilepsy and early-childhood-onset generalized muscle weakness.임신영, 정선용
2015Experimental study of the potential hazards of surgical smoke from powered instruments.김철호, 김현준, 정선용, 한재호
2015Association of the I264T variant in the sulfide quinone reductase-like (SQRDL) gene with osteoporosis in Korean postmenopausal women.김범택, 김정현, 박은국, 정선용
2015Targeted inhibition of mitochondrial Hsp90 induces mitochondrial elongation in Hep3B hepatocellular carcinoma cells undergoing apoptosis by increasing the ROS level.정선용
2015VE1 antibody is not highly specific for the BRAF V600E mutation in thyroid cytology categories with the exception of malignant cases.김대중, 김장희, 소의영, 신승수, 이기범, 이정훈, 임현이, 정선용, 정윤석, 한재호
2014The effect of Lycii Radicis Cortex extract on bone formation in vitro and in vivo.김정현, 박은국, 정선용, 정윤석, 조두연
2014TAGLN expression is upregulated in NF1-associated malignant peripheral nerve sheath tumors by hypomethylation in its promoter and subpromoter regions.손영배, 임현이, 정선용, 한재호
2014Identification of KMT2D and KDM6A mutations by exome sequencing in Korean patients with Kabuki syndrome.손영배, 정선용
2014Retinal pigment epithelial cells undergoing mitotic catastrophe are vulnerable to autophagy inhibition.정선용
2014The PARK2 gene is involved in the maintenance of pancreatic β-cell functions related to insulin production and secretion.강엽, 정선용, 진현석
2014Identification of the rare compound heterozygous variants in the NEB gene in a Korean family with intellectual disability, epilepsy and early-childhood-onset generalized muscle weakness.이기영, 임신영, 정선용
2014TIMP-1 modulates chemotaxis of human neural stem cells through CD63 and integrin signalling.이명애, 정선용
2014A Korean case of neurofibromatosis type 1 with an exonic splicing enhancer site mutation박상욱, 손영배, 정선용
2013Ocular Abnormality of Korean Patients with Molecular Genetically Confirmed Gaucher Disease김현주, 정선용
2013Mutation spectrum of NF1 and clinical characteristics in 78 Korean patients with neurofibromatosis type 1.김현주, 손영배, 정선용
2013Clinical and genetic spectrum of 18 unrelated Korean patients with Sotos syndrome: frequent 5q35 microdeletion and identification of four novel NSD1 mutations.손영배, 정선용, 진현석
2013p21(WAF¹/C¹P¹) deficiency induces mitochondrial dysfunction in HCT116 colon cancer cells.정선용
2013An unusual presentation of diabetic ketoacidosis in familial hajdu-cheney syndrome: a case report.손영배, 정선용, 정윤석
2013Association between the SPRY1 gene polymorphism and obesity-related traits and osteoporosis in Korean women.김보영, 정선용, 정윤석, 진현석
2013Interaction of motor training and intermittent theta burst stimulation in modulating motor cortical plasticity: influence of BDNF Val66Met polymorphism.김병곤, 정선용
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