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Biochemical Medicine and Metabolic Biology|December 1, 1993
Copper effects on metal regulatory factors of cultured human fibroblastsS H Hahn, W A GahlJournal of Korean Medical Science|May 10, 2000
HFE gene mutation, C282Y causing hereditary hemochromatosis in Caucasian is extremely rare in Korean populationJ Y Lee, K H Yoo, S H HahnJournal of Inherited Metabolic Disease|July 30, 2009
A cognitively normal PDH-deficient 18-year-old man carrying the R263G mutation in the PDHA1 geneR Bachmann-Gagescu, J Lawrence Merritt, S H HahnMitochondrion|September 21, 2010
Altered redox status of coenzyme Q9 reflects mitochondrial electron transport chain deficiencies in Caenorhabditis elegansV Vasta, M Sedensky, P Morgan, et al.Journal of Inherited Metabolic Disease|April 8, 2006
Stabilization of hypoglycosylation in a patient with congenital disorder of glycosylation type IaS H Hahn, S J Minnich, J F O'BrienExperimental & Molecular Medicine|April 27, 2001
Effect of metal ions on the stability of metallothionein in the degradation by cellular fractions in vitroS H Hahn, O J Yoo, W A GahlJournal of Inherited Metabolic Disease|July 23, 2003
Mutation analysis of copper transporter genes in patients with ethylmalonic encephalopathy, mitochondriopathies and copper deficiency phenotypesX Fu, P Rinaldo, S H Hahn, et al.Biochemical and Molecular Medicine|April 1, 1995
Normal metallothionein synthesis in fibroblasts obtained from children with Indian childhood cirrhosis or copper-associated childhood cirrhosisS H Hahn, M S Tanner, D M Danks, et al.Molecules and Cells|February 24, 2001
The first successful prenatal diagnosis on a Korean family with citrullinemiaK M Hong, M K Paik, O J Yoo, et al.The Review of Scientific Instruments|November 8, 2018
Considerations of the q-profile control in KSTAR for advanced tokamak operation scenariosJ Chung, J Ko, S-H Hahn, et al.Pageof 4