相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Transition to Next Generation Analysis of the Whole Mitochondrial Genome: A Summary of Molecular Defects
Sha Tang et al.
HUMAN MUTATION (2013)
An Appraisal of Human Mitochondrial DNA Instability: New Insights into the Role of Non-Canonical DNA Structures and Sequence Motifs
Pedro H. Oliveira et al.
PLOS ONE (2013)
Repeated regions in mitochondrial genomes: Distribution, origin and evolutionary significance
Francesco Nardi et al.
MITOCHONDRION (2012)
Human mitochondrial DNA: roles of inherited and somatic mutations
Eric A. Schon et al.
NATURE REVIEWS GENETICS (2012)
Mitochondrial DNA deletions are associated with non-B DNA conformations
Joana Damas et al.
NUCLEIC ACIDS RESEARCH (2012)
Role of Direct Repeat and Stem-Loop Motifs in mtDNA Deletions: Cause or Coincidence?
Lakshmi Narayanan Lakshmanan et al.
PLOS ONE (2012)
Molecular Diagnosis of Infantile Mitochondrial Disease with Targeted Next-Generation Sequencing
Sarah E. Calvo et al.
SCIENCE TRANSLATIONAL MEDICINE (2012)
On the Sequence-Directed Nature of Human Gene Mutation: The Role of Genomic Architecture and the Local DNA Sequence Environment in Mediating Gene Mutations Underlying Human Inherited Disease
David N. Cooper et al.
HUMAN MUTATION (2011)
Mitochondrial DNA mutations in disease and aging
Chan Bae Park et al.
JOURNAL OF CELL BIOLOGY (2011)
Mitochondrial DNA mutations and human disease
Helen A. L. Tuppen et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS (2010)
Differential regulation of full-length genome and a single-stranded 7S DNA along the cell cycle in human mitochondria
Anita Antes et al.
NUCLEIC ACIDS RESEARCH (2010)
Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes
Bekim Sadikovic et al.
PLOS ONE (2010)
Repeats, longevity and the sources of mtDNA deletions: evidence from 'deletional spectra'
Xinhong Guo et al.
TRENDS IN GENETICS (2010)
Fragile Genomic Sites Are Associated with Origins of Replication
Sara C. Di Rienzi et al.
GENOME BIOLOGY AND EVOLUTION (2009)
CPEO and KSS differ in the percentage and location of the mtDNA deletion
Ester Lopez-Gallardo et al.
MITOCHONDRION (2009)
Mitochondrial DNA mutations and aging: devils in the details?
Konstantin Khrapko et al.
TRENDS IN GENETICS (2009)
Complex human chromosomal and genomic rearrangements
Feng Zhang et al.
TRENDS IN GENETICS (2009)
Nature of mitochondrial DNA deletions in substantial nigra neurons
Amy K. Reeve et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Evidence for Variable Selective Pressures at a Large Secondary Structure of the Human Mitochondrial DNA Control Region
Filipe Pereira et al.
MOLECULAR BIOLOGY AND EVOLUTION (2008)
What causes mitochondrial DNA deletions in human cells?
Kim J. Krishnan et al.
NATURE GENETICS (2008)
The yeast Holliday junction resolvase, CCE1, can restore wild-type mitochondrial DNA to human cells carrying rearranged mitochondrial DNA
Hiroshi Sembongi et al.
HUMAN MOLECULAR GENETICS (2007)
The role of mitochondrial DNA mutations in mammalian aging
Gregory C. Kujoth et al.
PLOS GENETICS (2007)
The AAA+ protein ATAD3 has displacement loop binding properties and is involved in mitochondrial nucleoid organization
Jiuya He et al.
JOURNAL OF CELL BIOLOGY (2007)
High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease
A Bender et al.
NATURE GENETICS (2006)
Mitochondrial DNA deletions are abundant and cause functional impairment in aged human substantia nigra neurons
Y Kraytsberg et al.
NATURE GENETICS (2006)
Replication of mitochondrial DNA occurs by strand displacement with alternative light-strand origins, not via a strand-coupled mechanism
TA Brown et al.
GENES & DEVELOPMENT (2005)
A bidirectional origin of replication maps to the major noncoding region of human mitochondrial DNA
T Yasukawa et al.
MOLECULAR CELL (2005)
Double-strand breaks of mouse muscle mtDNA promote large deletions similar to multiple mtDNA deletions in humans
S Srivastava et al.
HUMAN MOLECULAR GENETICS (2005)
Breakpoints of gross deletions coincide with non-B DNA conformations
A Bacolla et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
Two direct repeats cause most human mtDNA deletions
DC Samuels et al.
TRENDS IN GENETICS (2004)
Discovery of a major D-loop replication origin reveals two modes of human mtDNA synthesis
J Fish et al.
SCIENCE (2004)
ND5 is a hot-spot for multiple atypical mitochondrial DNA deletions in mitochondrial neurogastrointestinal encephalomyopathy
Y Nishigaki et al.
HUMAN MOLECULAR GENETICS (2004)
Twinkle and POLG defects enhance age-dependent accumulation of mutations in the control region of mtDNA
S Wanrooij et al.
NUCLEIC ACIDS RESEARCH (2004)
Mammalian mitochondrial DNA replicates bidirectionally from an initiation zone
M Bowmaker et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Human and mouse genomic sequences reveal extensive breakpoint reuse in mammalian evolution
P Pevzner et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
Pathogenic role of mtDNA duplications in mitochondrial diseases associated with mtDNA deletions
F Odoardi et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2003)
Frequency of duplications in the D-loop in patients with mitochondrial DNA deletions
CH Tengan et al.
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2002)
Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions
G Van Goethem et al.
NATURE GENETICS (2001)
Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene LF-like protein localized in mitochondria
JN Spelbrink et al.
NATURE GENETICS (2001)
Quantification and sequencing of somatic deleted mtDNA in single cells: evidence for partially duplicated mtDNA in aged human tissues
ND Bodyak et al.
HUMAN MOLECULAR GENETICS (2001)
Multiple deletions of mtDNA remove the light strand origin of replication
C Bank et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2000)
Human mtDNA sublimons resemble rearranged mitochondrial genoms found in pathological states
OA Kajander et al.
HUMAN MOLECULAR GENETICS (2000)
Maintenance of human rearranged mitochondrial DNAs in long-term cultured transmitochondrial cell lines
YY Tang et al.
MOLECULAR BIOLOGY OF THE CELL (2000)
分享论文
