Molecular Neurobiology Laboratory,
Psychiatry,
Molecular Neurobiology Laboratory, Psychiatry
Chun-Hyung Kim has not added Biography.
If you are Chun-Hyung Kim and would like to personalize this page please email our Author Liaison for assistance.
Mutations in the dopamine beta-hydroxylase gene are associated with human norepinephrine deficiency.
American journal of medical genetics Mar, 2002 | Pubmed ID: 11857564
A proximal promoter domain containing a homeodomain-binding core motif interacts with multiple transcription factors, including HoxA5 and Phox2 proteins, and critically regulates cell type-specific transcription of the human norepinephrine transporter gene.
The Journal of neuroscience : the official journal of the Society for Neuroscience Apr, 2002 | Pubmed ID: 11923423
A direct role of the homeodomain proteins Phox2a/2b in noradrenaline neurotransmitter identity determination.
Journal of neurochemistry Mar, 2002 | Pubmed ID: 11948255
Effects of desipramine treatment on norepinephrine transporter gene expression in the cultured SK-N-BE(2)M17 cells and rat brain tissue.
Journal of neurochemistry Jul, 2002 | Pubmed ID: 12091475
Genetic basis of clinical catecholamine disorders.
Annals of the New York Academy of Sciences Oct, 2002 | Pubmed ID: 12438171
Orphan nuclear receptor Nurr1 directly transactivates the promoter activity of the tyrosine hydroxylase gene in a cell-specific manner.
Journal of neurochemistry May, 2003 | Pubmed ID: 12694388
Variations in the dopamine beta-hydroxylase gene are not associated with the autonomic disorders, pure autonomic failure, or multiple system atrophy.
American journal of medical genetics. Part A Jul, 2003 | Pubmed ID: 12833405
A revised allele frequency estimate and haplotype analysis of the DBH deficiency mutation IVS1+2T --> C in African- and European-Americans.
American journal of medical genetics. Part A Dec, 2003 | Pubmed ID: 14598346
Mitochondrial cyclic AMP response element-binding protein (CREB) mediates mitochondrial gene expression and neuronal survival.
The Journal of biological chemistry Dec, 2005 | Pubmed ID: 16207717
A polymorphism in the norepinephrine transporter gene alters promoter activity and is associated with attention-deficit hyperactivity disorder.
Proceedings of the National Academy of Sciences of the United States of America Dec, 2006 | Pubmed ID: 17146058
Functional gene variation in the human norepinephrine transporter: association with attention deficit hyperactivity disorder.
Annals of the New York Academy of Sciences , 2008 | Pubmed ID: 18591486
Generation of human induced pluripotent stem cells by direct delivery of reprogramming proteins.
Cell stem cell Jun, 2009 | Pubmed ID: 19481515
Association studies of -3081(A/T) polymorphism of norepinephrine transporter gene with attention deficit/hyperactivity disorder in Korean population.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics Mar, 2010 | Pubmed ID: 19685476
Wnt1-lmx1a forms a novel autoregulatory loop and controls midbrain dopaminergic differentiation synergistically with the SHH-FoxA2 pathway.
Cell stem cell Dec, 2009 | Pubmed ID: 19951692
Direct reprogramming of rat neural precursor cells and fibroblasts into pluripotent stem cells.
PloS one , 2010 | Pubmed ID: 20352099
Norepinephrine deficiency is caused by combined abnormal mRNA processing and defective protein trafficking of dopamine beta-hydroxylase.
The Journal of biological chemistry Mar, 2011 | Pubmed ID: 21209083
Protein-based human iPS cells efficiently generate functional dopamine neurons and can treat a rat model of Parkinson disease.
The Journal of clinical investigation Jun, 2011 | Pubmed ID: 21576821
Lmx1a regulates dopamine transporter gene expression during ES cell differentiation and mouse embryonic development.
Journal of neurochemistry Jul, 2012 | Pubmed ID: 22564125
Korean mistletoe (Viscum album coloratum) extract improves endurance capacity in mice by stimulating mitochondrial activity.
Journal of medicinal food Jul, 2012 | Pubmed ID: 22612297
Transcription elongation factor Tcea3 regulates the pluripotent differentiation potential of mouse embryonic stem cells via the Lefty1-Nodal-Smad2 pathway.
Stem cells (Dayton, Ohio) Feb, 2013 | Pubmed ID: 23169579
Altered expression of norepinephrine transporter and norepinephrine in human placenta cause pre-eclampsia through regulated trophoblast invasion.
Clinical and experimental reproductive medicine Mar, 2013 | Pubmed ID: 23614111
Pitx3 deficient mice as a genetic animal model of co-morbid depressive disorder and parkinsonism.
Brain research Mar, 2014 | Pubmed ID: 24480473
Increased genomic integrity of an improved protein-based mouse induced pluripotent stem cell method compared with current viral-induced strategies.
Stem cells translational medicine May, 2014 | Pubmed ID: 24763686
Correlation between orphan nuclear receptor Nurr1 expression and amyloid deposition in 5XFAD mice, an animal model of Alzheimer's disease.
Journal of neurochemistry Jan, 2015 | Pubmed ID: 25156412
Nuclear receptor Nurr1 agonists enhance its dual functions and improve behavioral deficits in an animal model of Parkinson's disease.
Proceedings of the National Academy of Sciences of the United States of America Jul, 2015 | Pubmed ID: 26124091
SOBRE A JoVE
Copyright © 2024 MyJoVE Corporation. Todos os direitos reservados