Heteroplasmic point mutations in the human mtDNA control region.
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The pedigree rate of sequence divergence in the human mitochondrial genome: there is a difference between phylogenetic and pedigree ratesHypervariable sites in the mtDNA control region are mutational hotspotsThe mutation rate in the human mtDNA control regionHeterogeneous tissue distribution of a mitochondrial DNA polymorphism in heteroplasmic subjects without mitochondrial disordersReply to Macauley et alPersistent heteroplasmy of a mutation in the human mtDNA control region: hypermutation as an apparent consequence of simple-repeat expansion/contractionThe strength and timing of the mitochondrial bottleneck in salmon suggests a conserved mechanism in vertebrates.Uncovering the profile of somatic mtDNA mutations in Chinese colorectal cancer patients.Heteroplasmy of the human mtDNA control region remains constant during life.Random genetic drift determines the level of mutant mtDNA in human primary oocytesA sensitive denaturing gradient-Gel electrophoresis assay reveals a high frequency of heteroplasmy in hypervariable region 1 of the human mtDNA control region.The frequency of heteroplasmy in the HVII region of mtDNA differs across tissue types and increases with age.The identification of the Romanovs: Can we (finally) put the controversies to rest?Mitochondrial genetics '98 is the bottleneck cracked?mtDNA diversity in Chukchi and Siberian Eskimos: implications for the genetic history of Ancient Beringia and the peopling of the New World.Germline bottlenecks and the evolutionary maintenance of mitochondrial genomes.Heteroplasmy and organelle gene dynamics.Contrasting patterns of nonneutral evolution in proteins encoded in nuclear and mitochondrial genomes.Neutral mitochondrial heteroplasmy and the influence of aging.Segregation of point mutation heteroplasmy in the control region of dog mtDNA studied systematically in deep generation pedigrees.Second generation sequencing allows for mtDNA mixture deconvolution and high resolution detection of heteroplasmy.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.The molecular genetics of European ancestry.Variable levels of a heteroplasmic point mutation in individual hair rootsWhy do older women have poor implantation rates? A possible role of the mitochondria.Mitochondrial COX2 G7598A mutation may have a modifying role in the phenotypic manifestation of aminoglycoside antibiotic-induced deafness associated with 12S rRNA A1555G mutation in a Han Chinese pedigree.Transmission of human mtDNA heteroplasmy in the Genome of the Netherlands families: support for a variable-size bottleneck.Paleolithic and Neolithic lineages in the European mitochondrial gene pool.Sequence variations of mitochondrial DNA D-loop region in patients with acute myeloid leukemia.Reply to Cavalli-Sforza and Minch.The causes of mutation accumulation in mitochondrial genomes
P2860
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P2860
Heteroplasmic point mutations in the human mtDNA control region.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
Heteroplasmic point mutations in the human mtDNA control region.
@ast
Heteroplasmic point mutations in the human mtDNA control region.
@en
type
label
Heteroplasmic point mutations in the human mtDNA control region.
@ast
Heteroplasmic point mutations in the human mtDNA control region.
@en
prefLabel
Heteroplasmic point mutations in the human mtDNA control region.
@ast
Heteroplasmic point mutations in the human mtDNA control region.
@en
P2093
P2860
P1476
Heteroplasmic point mutations in the human mtDNA control region
@en
P2093
K E Bendall
V A Macaulay
P2860
P304
P407
P577
1996-12-01T00:00:00Z