AJOU Open Repository: Medical Genetics

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Medical Genetics242

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AJOU Authors Title Publication Year Keyword Keyword (Historical Materials) Journal

Pub Year	Title	Author(s)
2012	Inhibition of Bcl-xL by ABT-737 enhances chemotherapy sensitivity in neurofibromatosis type 1-associated malignant peripheral nerve sheath tumor cells	김보영, 김현주, 임현이, 정선용, 진현석, 한재호
2022	Inhibitory Effect of Ulmus davidiana and Cornus officinalis Extracts on Osteoporotic Bone Loss In Vitro and In Vivo	김정현, 박은국, 정선용
2023	Inhibitory Effects of Loganin on Adipogenesis In Vitro and In Vivo	김정현, 박은국, 정선용
2013	Interaction of motor training and intermittent theta burst stimulation in modulating motor cortical plasticity: influence of BDNF Val66Met polymorphism.	김병곤, 정선용
2015	Isolated patchy heterochromia of the scalp hair.	김유찬, 손성향, 손영배
2010	KISS1 gene analysis in Korean girls with central precocious puberty: a polymorphism, p.P110T, suggested to exert a protective effect.	고정민, 황진순
2020	Loss of Heterozygosity at Chromosome 16q Is a Negative Prognostic Factor in Korean Pediatric Patients with Favorable Histology Wilms Tumor: A Report of the Korean Pediatric Hematology Oncology Group (K-PHOG)	노오규, 박준은, 이용희, 정선용
2010	Loss of Y chromosome in the malignant peripheral nerve sheet tumor of a patient with Neurofibromatosis type 1.	김현주, 정선용
2016	Low Frequency of MKRN3 Mutations in Central Precocious Puberty Among Korean Girls	권은별, 이해상, 정선용, 황진순
2013	Low-frequency Mosaicism of Trisomy 14, Missed by Array CGH	손영배
2018	Makorin 1 Regulates Developmental Timing in Drosophila	김은영, 이해상, 정선용, 황진순
2007	Mitochondrial fission and fusion mediators, hFis1 and OPA1, modulate cellular senescence.	김수정, 정선용, 조혜성
2008	Molecular diagnosis of fragile X syndrome in a female child	김현주, 정선용
2012	Molecular genetic analysis of TWIST1 and FGFR3 genes in Korean patients with coronal synostosis: identification of three novel TWIST1 mutations	박동하, 윤수한, 정선용
2013	Mutation spectrum of NF1 and clinical characteristics in 78 Korean patients with neurofibromatosis type 1.	김현주, 손영배, 정선용
2012	Mutation spectrum of the TYR and SLC45A2 genes in patients with oculocutaneous albinism	김현주, 정선용
2007	National survey for genetic counseling and demands for Professional genetic counselor	김현주, 정윤석
2021	Neurofibromin deficiency causes epidermal growth factor receptor upregulation through the activation of Ras/ERK/SP1 signaling pathway in neurofibromatosis type 1-associated malignant peripheral nerve sheet tumor	김정현, 박건후, 박은국, 이창근, 정선용
2019	Neuronopathic Gaucher disease presenting with microcytic hypochromic anemia	손영배
2018	Neuroprotective Effects of Schisandra chinensis and Ribes fasciculatum Extract on Hydrogen Peroxide-Mediated Oxidative Stress in Neuroblastic SH-SY5Y Cell Line	박은국, 정선용

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