Quantification of random mutations in the mitochondrial genome.
about
Mitochondrial DNA replication and disease: insights from DNA polymerase γ mutationsOxidative stress is not a major contributor to somatic mitochondrial DNA mutationsSingle-molecule LATE-PCR analysis of human mitochondrial genomic sequence variationsTranscellular degradation of axonal mitochondria.Targeted enrichment and high-resolution digital profiling of mitochondrial DNA deletions in human brain.Mitochondrial fusion is required for mtDNA stability in skeletal muscle and tolerance of mtDNA mutations.Ultra-sensitive sequencing reveals an age-related increase in somatic mitochondrial mutations that are inconsistent with oxidative damageA random mutation capture assay to detect genomic point mutations in mouse tissueEffects of CP-900691, a novel peroxisome proliferator-activated receptor α, agonist on diabetic nephropathy in the BTBR ob/ob mouseMaximizing signal-to-noise ratio in the random mutation capture assayCumulative mtDNA damage and mutations contribute to the progressive loss of RGCs in a rat model of glaucomaThe exonuclease activity of the yeast mitochondrial DNA polymerase γ suppresses mitochondrial DNA deletions between short direct repeats in Saccharomyces cerevisiaeSkeletal muscle action of estrogen receptor α is critical for the maintenance of mitochondrial function and metabolic homeostasis in femalesThe pathophysiology of mitochondrial disease as modeled in the mouse.Mitochondrial DNA exhibits resistance to induced point and deletion mutations.The identification of mitochondrial DNA variants in glioblastoma multiforme.Mitochondria in ageing: there is metabolism beyond the ROS.Age-related accumulation of phosphorylated mitofusin 2 protein in retinal ganglion cells correlates with glaucoma progression.Digital PCR Quantitation of Muscle Mitochondrial DNA: Age, Fiber Type, and Mutation-Induced Changes.Mitochondrial determinants of cancer health disparities.Successful tumour necrosis factor (TNF) blocking therapy suppresses oxidative stress and hypoxia-induced mitochondrial mutagenesis in inflammatory arthritis.Dysregulated bioenergetics: a key regulator of joint inflammation.Resolution of TLR2-induced inflammation through manipulation of metabolic pathways in Rheumatoid Arthritis.Thiamine deficiency induces oxidative stress in brain mitochondria of Mus musculus.Mitochondrial Dysfunction in Cardiovascular Aging.Reactive oxygen species stress increases accumulation of tyrosyl-DNA phsosphodiesterase 1 within mitochondria.Oxidative stress impairs energy metabolism in primary cells and synovial tissue of patients with rheumatoid arthritis.Hypoxia induces mitochondrial mutagenesis and dysfunction in inflammatory arthritis
P2860
Q24612561-3516013D-009F-49E5-B007-12201AF76AD6Q27319050-78778B25-28B0-4D9D-B5AA-8D93EE2CE84AQ28475515-F6C682A6-8F0C-4DCA-95F2-A46005569741Q30583027-FE5D9256-269A-496F-BFA6-BD4D8176467BQ33796548-8DC90978-042D-4455-8BDF-CCF6064A5D2DQ33877979-21C8950A-966A-482F-A99C-E4A884387D8BQ35004513-AB73CBCF-229D-48D5-B768-93206CE644D5Q35041017-63953C59-2840-4409-A23E-73E44AA12193Q35498269-C5512633-AE9C-49AF-88D8-812FD1B57D2CQ35823668-3D06EAA3-AF2E-4329-AD88-9D179E7A6AD7Q35911424-9E26CB23-D7C2-49C9-8F3C-A718FAF513D1Q36878648-1C803114-9BC3-48AD-9DC1-BD770ED25FA1Q37069670-F177DD52-21CC-4FED-B888-EBC159D28B5BQ37287583-66D8FDA8-B4AE-4348-9F62-D347008B64F7Q37336970-6EBCA513-A2DC-49A1-B82D-D69E41469CCCQ37551852-54AA0868-CAAC-41D8-8D66-5D7051CB4DBEQ38174328-FFE07FAC-C9C4-4164-8C6D-91CF6830A381Q38661781-48D7F581-D37C-48BA-81D8-61F029D8D334Q38811014-E78E094B-239D-469C-972B-F870C3F21D0FQ39294200-B2E59C3C-3A0B-48D3-8FE5-B6B9ADC07473Q39830600-903B3FFA-865D-4342-B2AF-08A6687A4FB3Q41829205-2F615C96-B9A8-471F-BC0B-8E2E266104B0Q42320463-C65DDD5F-3029-4743-AE3A-9A088E75E9C6Q43998674-2EEED3D2-4AF3-4C0C-A676-1C9491F185D2Q45060086-7FF10470-E64A-4E07-BED2-AB9F4FCC0D36Q52361042-85BF2C10-DA77-4F3C-A01D-D2394E897318Q54977825-5F6061B2-81AE-4342-8AEE-E6C0FFC28228Q59042062-15EB3D94-A9BD-47FD-A102-CE1D4E9B561A
P2860
Quantification of random mutations in the mitochondrial genome.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh-hant
name
Quantification of random mutations in the mitochondrial genome.
@en
Quantification of random mutations in the mitochondrial genome.
@nl
type
label
Quantification of random mutations in the mitochondrial genome.
@en
Quantification of random mutations in the mitochondrial genome.
@nl
prefLabel
Quantification of random mutations in the mitochondrial genome.
@en
Quantification of random mutations in the mitochondrial genome.
@nl
P2093
P2860
P1433
P1476
Quantification of random mutations in the mitochondrial genome.
@en
P2093
Jason H Bielas
Lawrence A Loeb
Marc Vermulst
P2860
P304
P356
10.1016/J.YMETH.2008.10.008
P577
2008-10-21T00:00:00Z