about
Life extension in Drosophila by feeding a drug.Miro, MCU, and calcium: bridging our understanding of mitochondrial movement in axonsRegulation of lifespan by histone deacetylaseOverexpression of frataxin in the mitochondria increases resistance to oxidative stress and extends lifespan in DrosophilaIdentification of a phosphorylation site for calcium/calmodulindependent protein kinase II in the NR2B subunit of the N-methyl-D-aspartate receptorDSCR1 interacts with FMRP and is required for spine morphogenesis and local protein synthesisMitochondrial matrix Ca2+ as an intrinsic signal regulating mitochondrial motility in axons.Histone deacetylases suppress CGG repeat-induced neurodegeneration via transcriptional silencing in models of fragile X tremor ataxia syndrome.Meeting at the crossroads: common mechanisms in Fragile X and Down syndromeThe Drosophila homolog of Down's syndrome critical region 1 gene regulates learning: implications for mental retardation.Aberrant histone acetylation, altered transcription, and retinal degeneration in a Drosophila model of polyglutamine disease are rescued by CREB-binding proteinSir2 mediates apoptosis through JNK-dependent pathways in DrosophilaDynamics of Mitochondrial Transport in Axons.DSCR1 is required for both axonal growth cone extension and steering.Upregulation of three Drosophila homologs of human chromosome 21 genes alters synaptic function: implications for Down syndrome.Renaming the DSCR1/Adapt78 gene family as RCAN: regulators of calcineurin.Drosophila melanogaster homolog of Down syndrome critical region 1 is critical for mitochondrial function.Individual histone deacetylases in Drosophila modulate transcription of distinct genes.Drosophila as a model to study human brain degenerative diseases.IRES-mediated translation of cofilin regulates axonal growth cone extension and turning.MCU interacts with Miro1 to modulate mitochondrial functions in neurons.Progress in molecular biology and translational science. Animal models of human disease. Preface.Chemical synthesis and cloning of human beta-endorphin gene in Escherichia coli.σF, the first compartment-specific transcription factor of B. subtilis, is regulated by an anti-σ factor that is also a protein kinaseEcoRI variant N199H has enhanced specific activityDSCR1-mediated TET1 splicing regulates miR-124 expression to control adult hippocampal neurogenesisIncreased ER-mitochondria tethering promotes axon regeneration
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description
researcher
@en
wetenschapper
@nl
հետազոտող
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name
Kyung-Tai Min
@ast
Kyung-Tai Min
@en
Kyung-Tai Min
@es
Kyung-Tai Min
@nl
type
label
Kyung-Tai Min
@ast
Kyung-Tai Min
@en
Kyung-Tai Min
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Kyung-Tai Min
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prefLabel
Kyung-Tai Min
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Kyung-Tai Min
@en
Kyung-Tai Min
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Kyung-Tai Min
@nl
P108
P106
P108
P1153
7201466892
P31
P496
0000-0003-0983-4258