Mechanisms of human mitochondrial DNA maintenance: the determining role of primary sequence and length over function.
about
Human mitochondrial DNA with large deletions repopulates organelles faster than full-length genomes under relaxed copy number control.Mitochondrial fragmentation in neurodegenerationA novel syndrome affecting multiple mitochondrial functions, located by microcell-mediated transfer to chromosome 2p14-2p13.Conflicting levels of selection in the accumulation of mitochondrial defects in Saccharomyces cerevisiae.Absolute quantitation of a heteroplasmic mitochondrial DNA deletion using a multiplex three-primer real-time PCR assay.Detection of heteroplasmy in individual mitochondrial particlesModulation of mitochondrial transcription in response to mtDNA depletion and repletion in HeLa cellsDiseases caused by nuclear genes affecting mtDNA stability.Divergent mitochondrial biogenesis responses in human cardiomyopathyGermline bottlenecks, biparental inheritance and selection on mitochondrial variants: a two-level selection modelRearrangements of human mitochondrial DNA (mtDNA): new insights into the regulation of mtDNA copy number and gene expressionMaintenance of human rearranged mitochondrial DNAs in long-term cultured transmitochondrial cell lines.Context-Dependent Role of Mitochondrial Fusion-Fission in Clonal Expansion of mtDNA MutationsMitochondrial targeting of recombinant RNAs modulates the level of a heteroplasmic mutation in human mitochondrial DNA associated with Kearns Sayre SyndromeThe mitochondrial genome sequence of Mus terricolor: comparison with Mus musculus domesticus and implications for xenomitochondrial mouse modeling.Simultaneous quantification of mitochondrial DNA copy number and deletion ratio: a multiplex real-time PCR assay.Selfish drive can trump function when animal mitochondrial genomes compete.Intra- and inter-molecular recombination of mitochondrial DNA after in vivo induction of multiple double-strand breaks.Homeostatic Responses Regulate Selfish Mitochondrial Genome Dynamics in C. elegans.Release of replication termination controls mitochondrial DNA copy number after depletion with 2',3'-dideoxycytidine.Obtaining mice that carry human mitochondrial DNA transmitted to the progeny.Expression of Rattus norvegicus mtDNA in Mus musculus cells results in multiple respiratory chain defects.Functional constraints of nuclear-mitochondrial DNA interactions in xenomitochondrial rodent cell lines.Aberrant nucleo-cytoplasmic cross-talk results in donor cell mtDNA persistence in cloned embryos.Lipopolysaccharide stimulates mitochondrial biogenesis via activation of nuclear respiratory factor-1.On the relevance of mitochondrial fusions for the accumulation of mitochondrial deletion mutants: a modelling study.
P2860
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P2860
Mechanisms of human mitochondrial DNA maintenance: the determining role of primary sequence and length over function.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
1999年论文
@zh
1999年论文
@zh-cn
name
Mechanisms of human mitochondr ...... ence and length over function.
@en
type
label
Mechanisms of human mitochondr ...... ence and length over function.
@en
prefLabel
Mechanisms of human mitochondr ...... ence and length over function.
@en
P2093
P2860
P356
P1476
Mechanisms of human mitochondr ...... ence and length over function.
@en
P2093
P2860
P304
P356
10.1091/MBC.10.10.3345
P577
1999-10-01T00:00:00Z