The determination of complete human mitochondrial DNA sequences in single cells: implications for the study of somatic mitochondrial DNA point mutations.
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Counting the founders: the matrilineal genetic ancestry of the Jewish DiasporaThe Druze: a population genetic refugium of the Near EastNDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiencyPhylogeny of mitochondrial DNA macrohaplogroup N in India, based on complete sequencing: implications for the peopling of South AsiaThe matrilineal ancestry of Ashkenazi Jewry: portrait of a recent founder eventPronuclear transfer in human embryos to prevent transmission of mitochondrial DNA diseaseMutations in FBXL4 cause mitochondrial encephalopathy and a disorder of mitochondrial DNA maintenanceMaternal traces of deep common ancestry and asymmetric gene flow between Pygmy hunter-gatherers and Bantu-speaking farmersThe dawn of human matrilineal diversityMutation in mitochondrial complex I ND6 subunit is associated with defective response to hypoxia in human glioma cellsAbsence of pathogenic mitochondrial DNA mutations in mouse brain tumorsSomatic mutations in the mitochondria of rheumatoid arthritis synoviocytesFunctional consequences of mitochondrial tRNA Trp and tRNA Arg mutations causing combined OXPHOS defects.Epithelial mesenchymal-like transition occurs in a subset of cells in castration resistant prostate cancer bone metastases.Towards clinical application of pronuclear transfer to prevent mitochondrial DNA disease.Production of transmitochondrial cybrids containing naturally occurring pathogenic mtDNA variants.External contamination in single cell mtDNA analysis.Investigation of the role of mitochondrial DNA in multiple sclerosis susceptibility.Performance of mitochondrial DNA mutations detecting early stage cancer.Sequencing strategy for the whole mitochondrial genome resulting in high quality sequences.Variation in OPA1 does not explain the incomplete penetrance of Leber hereditary optic neuropathy.Mitochondrial DNA levels in Huntington disease leukocytes and dermal fibroblasts.Defects in multiple complexes of the respiratory chain are present in ageing human colonic crypts.Somatic mitochondrial DNA deletions accumulate to high levels in aging human extraocular muscles.Mitochondrial DNA mutations are established in human colonic stem cells, and mutated clones expand by crypt fission.Decreased mitochondrial DNA mutagenesis in human colorectal cancer.Variation in MAPT is not a contributing factor to the incomplete penetrance in LHON.Respiratory chain complex I deficiency caused by mitochondrial DNA mutations.Investigating mitochondria as a target for treating age-related macular degenerationCell lineage tracing in human epithelial tissues using mitochondrial DNA mutations as clonal markers.Mitochondrial DNA as a cancer biomarkerCharacterization of mtDNA variation in a cohort of South African paediatric patients with mitochondrial disease.Mitochondrial heteroplasmy in vertebrates using ChIP-sequencing dataMutations in the mitochondrial tRNA Ser(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy.Mutations in mitochondrial DNA causing tubulointerstitial kidney disease.Mitochondrial DNA mutations in human colonic crypt stem cells.Cerebral hypoxia and ischemia: the forensic point of view: a review.Mitochondrial DNA damage in non-melanoma skin cancerMitochondrial DNA mutations and aging.Mitochondrial and inflammatory changes in sporadic inclusion body myositis
P2860
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P2860
The determination of complete human mitochondrial DNA sequences in single cells: implications for the study of somatic mitochondrial DNA point mutations.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
2001年论文
@zh
2001年论文
@zh-cn
name
The determination of complete ...... chondrial DNA point mutations.
@en
The determination of complete ...... chondrial DNA point mutations.
@nl
type
label
The determination of complete ...... chondrial DNA point mutations.
@en
The determination of complete ...... chondrial DNA point mutations.
@nl
prefLabel
The determination of complete ...... chondrial DNA point mutations.
@en
The determination of complete ...... chondrial DNA point mutations.
@nl
P2093
P2860
P356
P1476
The determination of complete ...... chondrial DNA point mutations.
@en
P2093
P2860
P356
10.1093/NAR/29.15.E74
P407
P577
2001-08-01T00:00:00Z