about
Keeping mtDNA in shape between generationsMaternal inheritance of mouse mtDNA in interspecific hybrids: segregation of the leaked paternal mtDNA followed by the prevention of subsequent paternal leakageEvolutionary defined role of the mitochondrial DNA in fertility, disease and ageingHeterogeneous tissue distribution of a mitochondrial DNA polymorphism in heteroplasmic subjects without mitochondrial disordersMutation and evolutionary rates in adélie penguins from the antarcticThe complete sequence of the mitochondrial genome of Nautilus macromphalus (Mollusca: Cephalopoda)Epistatic interactions modulate the evolution of mammalian mitochondrial respiratory complex components.New evidence confirms that the mitochondrial bottleneck is generated without reduction of mitochondrial DNA content in early primordial germ cells of mice.A wide range of 3243A>G/tRNALeu(UUR) (MELAS) mutation loads may segregate in offspring through the female germline bottleneck.Transmission of mitochondrial DNA diseases and ways to prevent them.Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcome.Evolutionary toxicology: contaminant-induced genetic mutations in mosquitofish from Sumgayit, Azerbaijan.A pedigree-based study of mitochondrial D-loop DNA sequence variation among Arabian horses.The strength and timing of the mitochondrial bottleneck in salmon suggests a conserved mechanism in vertebrates.Replacement of bovine mitochondrial DNA by a sequence variant within one generation.Mitochondrial genotype segregation in a mouse heteroplasmic lineage produced by embryonic karyoplast transplantation.Tissue- and cell-type-specific manifestations of heteroplasmic mtDNA 3243A>G mutation in human induced pluripotent stem cell-derived disease model.Mitochondrial disorders: genetics, counseling, prenatal diagnosis and reproductive options.Maternal age effect and severe germ-line bottleneck in the inheritance of human mitochondrial DNA.Mitochondrial genotype segregation during preimplantation development in mouse heteroplasmic embryos.Heteroplasmy and organelle gene dynamics.Replicative advantage and tissue-specific segregation of RR mitochondrial DNA between C57BL/6 and RR heteroplasmic miceSelective and continuous elimination of mitochondria microinjected into mouse eggs from spermatids, but not from liver cells, occurs throughout embryogenesisReactive oxygen species stimulate mitochondrial allele segregation toward homoplasmy in human cells.Lack of Structural Variation but Extensive Length Polymorphisms and Heteroplasmic Length Variations in the Mitochondrial DNA Control Region of Highly Inbred Crested Ibis, Nipponia nippon.Mhr1p-dependent concatemeric mitochondrial DNA formation for generating yeast mitochondrial homoplasmic cells.Segregation of point mutation heteroplasmy in the control region of dog mtDNA studied systematically in deep generation pedigrees.Lack of transmission of deleted mtDNA from a woman with Kearns-Sayre syndrome to her childSegregation and manifestations of the mtDNA tRNA(Lys) A-->G(8344) mutation of myoclonus epilepsy and ragged-red fibers (MERRF) syndromeDistribution and threshold expression of the tRNA(Lys) mutation in skeletal muscle of patients with myoclonic epilepsy and ragged-red fibers (MERRF).Transcription and translation of deleted mitochondrial genomes in Kearns-Sayre syndrome: implications for pathogenesisSegregation of mitochondrial genomes in a heteroplasmic lineage with Leber hereditary optic neuroretinopathy.Prenatal diagnosis of mitochondrial DNA8993 T----G disease.The contribution of mitochondrial function to reproductive aging.Molecular instability in the COII-tRNA(Lys) intergenic region of the human mitochondrial genome: multiple origins of the 9-bp deletion and heteroplasmy for expanded repeats.Homopolymeric tract heteroplasmy in mtDNA from tissues and single oocytes: support for a genetic bottleneck.Variable levels of a heteroplasmic point mutation in individual hair rootsSkewed segregation of the mtDNA nt 8993 (T-->G) mutation in human oocytesLength heteroplasmy in the first hypervariable segment of the human mtDNA control region.Rearranged mitochondrial genomes are present in human oocytes.
P2860
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P2860
description
1989 nî lūn-bûn
@nan
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
1989年论文
@zh
1989年论文
@zh-cn
name
Rapid segregation of heteroplasmic bovine mitochondria.
@ast
Rapid segregation of heteroplasmic bovine mitochondria.
@en
type
label
Rapid segregation of heteroplasmic bovine mitochondria.
@ast
Rapid segregation of heteroplasmic bovine mitochondria.
@en
prefLabel
Rapid segregation of heteroplasmic bovine mitochondria.
@ast
Rapid segregation of heteroplasmic bovine mitochondria.
@en
P2093
P2860
P356
P1476
Rapid segregation of heteroplasmic bovine mitochondria.
@en
P2093
M V Ashley
P J Laipis
W W Hauswirth
P2860
P304
P356
10.1093/NAR/17.18.7325
P407
P577
1989-09-01T00:00:00Z