Role of direct repeat and stem-loop motifs in mtDNA deletions: cause or coincidence? - Wikidata - wikimedia - TriplyDB

Role of direct repeat and stem-loop motifs in mtDNA deletions: cause or coincidence?

Role of direct repeat and stem-loop motifs in mtDNA deletions: cause or coincidence?

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Association of G-quadruplex forming sequences with human mtDNA deletion breakpoints.An appraisal of human mitochondrial DNA instability: new insights into the role of non-canonical DNA structures and sequence motifs.Somatic mtDNA mutation spectra in the aging human putamen.Are mutagenic non D-loop direct repeat motifs in mitochondrial DNA under a negative selection pressure?Transcription could be the key to the selection advantage of mitochondrial deletion mutants in aging.Mitochondrial DNA rearrangements in health and disease--a comprehensive study.Technical adequacy of bisulfite sequencing and pyrosequencing for detection of mitochondrial DNA methylation: Sources and avoidance of false-positive detection.Resolving the Enigma of the Clonal Expansion of mtDNA Deletions.

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P2860

Role of direct repeat and stem-loop motifs in mtDNA deletions: cause or coincidence?

http://www.wikidata.org/entity/Q31058320

description

2012 nî lūn-bûn

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2012 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի ապրիլին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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name

Role of direct repeat and stem-loop motifs in mtDNA deletions: cause or coincidence?

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Role of direct repeat and stem-loop motifs in mtDNA deletions: cause or coincidence?

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type

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Role of direct repeat and stem-loop motifs in mtDNA deletions: cause or coincidence?

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Role of direct repeat and stem-loop motifs in mtDNA deletions: cause or coincidence?

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Role of direct repeat and stem-loop motifs in mtDNA deletions: cause or coincidence?

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Role of direct repeat and stem-loop motifs in mtDNA deletions: cause or coincidence?

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Role of direct repeat and stem-loop motifs in mtDNA deletions: cause or coincidence?

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Barry Halliwell

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Jan Gruber

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Lakshmi Narayanan Lakshmanan

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P2860

Sequence homology at the breakpoint and clinical phenotype of mitochondrial DNA deletion syndromes

High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease

Mitochondrial DNA deletion mutations are concomitant with ragged red regions of individual, aged muscle fibers: analysis by laser-capture microdissection.

Molecular analyses of mtDNA deletion mutations in microdissected skeletal muscle fibers from aged rhesus monkeys.

Accumulation of mitochondrial DNA deletion mutations in aged muscle fibers: evidence for a causal role in muscle fiber loss

Repeats, longevity and the sources of mtDNA deletions: evidence from 'deletional spectra'.

Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy.

Life span is related to the free energy of mitochondrial DNA.

UNAFold: software for nucleic acid folding and hybridization.

Mitochondrial DNA-deletion mutations accumulate intracellularly to detrimental levels in aged human skeletal muscle fibers.

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