User profiles for Suh Young Jeong
![]() | Suh Young JeongOregon Health & Science University Verified email at ohsu.edu Cited by 3652 |
Dysregulation of iron homeostasis in the central nervous system and the role of ferroptosis in neurodegenerative disorders
Significance: Iron accumulation occurs in the central nervous system (CNS) in a variety of
neurological conditions as diverse as spinal cord injury, stroke, multiple sclerosis, Parkinson's …
neurological conditions as diverse as spinal cord injury, stroke, multiple sclerosis, Parkinson's …
Glycosylphosphatidylinositol-anchored ceruloplasmin is required for iron efflux from cells in the central nervous system
Ceruloplasmin (Cp) is a ferroxidase that converts highly toxic ferrous iron to its non-toxic ferric
form. A glycosylphosphatidylinositol (GPI)-anchored form of this enzyme is expressed by …
form. A glycosylphosphatidylinositol (GPI)-anchored form of this enzyme is expressed by …
Ceruloplasmin regulates iron levels in the CNS and prevents free radical injury
BN Patel, RJ Dunn, SY Jeong, Q Zhu… - Journal of …, 2002 - jneurosci.org
Ceruloplasmin is a ferroxidase that oxidizes toxic ferrous iron to its nontoxic ferric form. We
have previously reported that a glycosylphosphatidylinositol-anchored form of ceruloplasmin …
have previously reported that a glycosylphosphatidylinositol-anchored form of ceruloplasmin …
Ferroxidase activity is required for the stability of cell surface ferroportin in cells expressing GPI‐ceruloplasmin
…, DMV Ward, MCB Di Patti, SY Jeong… - The EMBO …, 2007 - embopress.org
Ferroportin (Fpn), a ferrous iron Fe(II) transporter responsible for the entry of iron into plasma,
is regulated post‐translationally through internalization and degradation following binding …
is regulated post‐translationally through internalization and degradation following binding …
Iron accumulation in deep cortical layers accounts for MRI signal abnormalities in ALS: correlating 7 tesla MRI and pathology
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disorder characterized
by cortical and spinal motor neuron dysfunction. Routine magnetic resonance imaging (…
by cortical and spinal motor neuron dysfunction. Routine magnetic resonance imaging (…
Glutaredoxin 5 deficiency causes sideroblastic anemia by specifically impairing heme biosynthesis and depleting cytosolic iron in human erythroblasts
H Ye, SY Jeong, MC Ghosh, G Kovtunovych… - The Journal of clinical …, 2010 - jci.org
Glutaredoxin 5 (GLRX5) deficiency has previously been identified as a cause of anemia in a
zebrafish model and of sideroblastic anemia in a human patient. Here we report that GLRX5 …
zebrafish model and of sideroblastic anemia in a human patient. Here we report that GLRX5 …
[HTML][HTML] The glycolytic shift in fumarate-hydratase-deficient kidney cancer lowers AMPK levels, increases anabolic propensities and lowers cellular iron levels
WH Tong, C Sourbier, G Kovtunovych, SY Jeong… - Cancer cell, 2011 - cell.com
Inactivation of the TCA cycle enzyme, fumarate hydratase (FH), drives a metabolic shift to
aerobic glycolysis in FH-deficient kidney tumors and cell lines from patients with hereditary …
aerobic glycolysis in FH-deficient kidney tumors and cell lines from patients with hereditary …
Age-related changes in iron homeostasis and cell death in the cerebellum of ceruloplasmin-deficient mice
Iron is essential for a variety of cellular functions, but its levels and bioavailability must be
tightly regulated because of its toxic redox activity. A number of transporters, binding proteins, …
tightly regulated because of its toxic redox activity. A number of transporters, binding proteins, …
Dysregulation of iron homeostasis in the CNS contributes to disease progression in a mouse model of amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis (ALS), characterized by degeneration of spinal motor neurons,
consists of sporadic and familial forms. One cause of familial ALS is missense mutations in …
consists of sporadic and familial forms. One cause of familial ALS is missense mutations in …
PKAN pathogenesis and treatment
SJ Hayflick, SY Jeong, OCM Sibon - Molecular genetics and metabolism, 2022 - Elsevier
Studies aimed at supporting different treatment approaches for pantothenate kinase-associated
neurodegeneration (PKAN) have revealed the complexity of coenzyme A (CoA) …
neurodegeneration (PKAN) have revealed the complexity of coenzyme A (CoA) …