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A compound heterozygous mutation in HADHB gene causes an axonal Charcot-Marie-tooth diseaseCharacterization of 458 single nucleotide polymorphisms of disease candidate genes in the Korean populationHDAC6 Inhibitors Rescued the Defective Axonal Mitochondrial Movement in Motor Neurons Derived from the Induced Pluripotent Stem Cells of Peripheral Neuropathy Patients with HSPB1 MutationStructural and functional analyses of mutations of the human phenylalanine hydroxylase gene.Tissue-specific activation of mitogen-activated protein kinases for expression of transthyretin by phenylalanine and its metabolite, phenylpyruvic acid.Possible role of transforming growth factor-β1 and vascular endothelial growth factor in Fabry disease nephropathyDynamic transcriptional events in distal sural nerve revealed by transcriptome analysis.Characterization of Fabry mice treated with recombinant adeno-associated virus 2/8-mediated gene transfer.Enhanced sialylation and in vivo efficacy of recombinant human α-galactosidase through in vitro glycosylationLong-term enzymatic and phenotypic correction in the phenylketonuria mouse model by adeno-associated virus vector-mediated gene transfer.Proximal dominant hereditary motor and sensory neuropathy with proximal dominance association with mutation in the TRK-fused gene.The molecular basis of phenylketonuria in Koreans.miRGator v2.0: an integrated system for functional investigation of microRNAsAdeno-associated viral vector-mediated gene transfer results in long-term enzymatic and functional correction in multiple organs of Fabry mice.Tonsil-derived mesenchymal stem cells ameliorate CCl4-induced liver fibrosis in mice via autophagy activationGenome-wide scan of granular corneal dystrophy, type II: confirmation of chromosome 5q31 and identification of new co-segregated loci on chromosome 3q26.3.Epithelial-Mesenchymal Transition in Kidney Tubular Epithelial Cells Induced by Globotriaosylsphingosine and GlobotriaosylceramideA novel homozygous MPV17 mutation in two families with axonal sensorimotor polyneuropathy.Overexpression of mutant HSP27 causes axonal neuropathy in mice.High-density single-nucleotide polymorphism maps of the human genome.Substrate-specific gene expression profiles in different kidney cell types are associated with Fabry diseaseMyogenic differentiation potential of human tonsil-derived mesenchymal stem cells and their potential for use to promote skeletal muscle regeneration.Protective effect of recombinant adeno-associated virus 2/8-mediated gene therapy from the maternal hyperphenylalaninemia in offsprings of a mouse model of phenylketonuria.Recessive optic atrophy, sensorimotor neuropathy and cataract associated with novel compound heterozygous mutations in OPA1.PHEX gene mutations and genotype-phenotype analysis of Korean patients with hypophosphatemic rickets.Maternal Food Restriction during Pregnancy and Lactation Adversely Affect Hepatic Growth and Lipid Metabolism in Three-Week-Old Rat OffspringIn vitro differentiation of mouse embryonic stem cells: enrichment of endodermal cells in the embryoid body.Genetic basis of hearing loss associated with enlarged vestibular aqueducts in Koreans.Application of differentiated human tonsil-derived stem cells to trembler-J mice.DGAT2 Mutation in a Family with Autosomal-Dominant Early-Onset Axonal Charcot-Marie-Tooth Disease.Autophagy induction in the skeletal myogenic differentiation of human tonsil-derived mesenchymal stem cells.Tonsil-derived mesenchymal stromal cells: evaluation of biologic, immunologic and genetic factors for successful banking.Characterization of a novel mucopolysaccharidosis type II mouse model and recombinant AAV2/8 vector-mediated gene therapy.Altered brain gene expression profiles associated with the pathogenesis of phenylketonuria in a mouse model.Leukemia inhibitory factor blocks early differentiation of skeletal muscle cells by activating ERK.Long-term expression of the human glucocerebrosidase gene in vivo after transplantation of bone-marrow-derived cells transformed with a lentivirus vector.Feasibility of gene therapy in Gaucher disease using an adeno-associated virus vector.Expression and secretion of human glucocerebrosidase mediated by recombinant lentivirus vectors in vitro and in vivo: implications for gene therapy of Gaucher disease.Neuroleptic drugs alter the dopamine transporter-mediated uptake and release of dopamine: a possible mechanism for drug-induced tardive dyskinesia.Tonsil-derived mesenchymal stem cells alleviate concanavalin A-induced acute liver injury.
P50
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P50
description
hulumtues
@sq
researcher
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wetenschapper
@nl
հետազոտող
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name
Sung-Chul Jung
@ast
Sung-Chul Jung
@de
Sung-Chul Jung
@en
Sung-Chul Jung
@es
Sung-Chul Jung
@fr
Sung-Chul Jung
@nl
Sung-Chul Jung
@sl
type
label
Sung-Chul Jung
@ast
Sung-Chul Jung
@de
Sung-Chul Jung
@en
Sung-Chul Jung
@es
Sung-Chul Jung
@fr
Sung-Chul Jung
@nl
Sung-Chul Jung
@sl
prefLabel
Sung-Chul Jung
@ast
Sung-Chul Jung
@de
Sung-Chul Jung
@en
Sung-Chul Jung
@es
Sung-Chul Jung
@fr
Sung-Chul Jung
@nl
Sung-Chul Jung
@sl
P106
P1153
57008539100
P21
P31
P496
0000-0002-3174-8965
P569
2000-01-01T00:00:00Z