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。Reduced mitochondrial DNA copy number is a biomarker of Parkinson's disease
Angela Pyle et al.
NEUROBIOLOGY OF AGING (2016)
Somatic mtDNA variation is an important component of Parkinson's disease
Jonathan Coxhead et al.
NEUROBIOLOGY OF AGING (2016)
Reduced Cerebrospinal Fluid Mitochondrial DNA Is a Biomarker for Early-Stage Parkinson's Disease
Angela Pyle et al.
ANNALS OF NEUROLOGY (2015)
Mitochondrial DNA mutations in neurodegeneration
Michael J. Keogh et al.
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS (2015)
Somatic mutation in single human neurons tracks developmental and transcriptional history
Michael A. Lodato et al.
SCIENCE (2015)
MToolBox: a highly automated pipeline for heteroplasmy annotation and prioritization analysis of human mitochondrial variants in high-throughput sequencing
Claudia Calabrese et al.
BIOINFORMATICS (2014)
Extraction and annotation of human mitochondrial genomes from 1000 Genomes Whole Exome Sequencing data
Maria Angela Diroma et al.
BMC GENOMICS (2014)
Recent Mitochondrial DNA Mutations Increase the Risk of Developing Common Late-Onset Human Diseases
Gavin Hudson et al.
PLOS GENETICS (2014)
Germline mitochondrial DNA mutations aggravate ageing and can impair brain development
Jaime M. Ross et al.
NATURE (2013)
Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease
Gavin Hudson et al.
NEUROLOGY (2013)
Somatic mitochondrial DNA mutations in early parkinson and incidental lewy body disease
Michael T. Lin et al.
ANNALS OF NEUROLOGY (2012)
HmtDB, a genomic resource for mitochondrion-based human variability studies
Francesco Rubino et al.
NUCLEIC ACIDS RESEARCH (2012)
The reference human nuclear mitochondrial sequences compilation validated and implemented on the UCSC genome browser
Domenico Simone et al.
BMC GENOMICS (2011)
Somatic Mitochondrial DNA Mutations in Mammalian Aging
Nils-Goeran Larsson
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 79 (2010)
DNA copy number, including telomeres and mitochondria, assayed using next-generation sequencing
John C. Castle et al.
BMC GENOMICS (2010)
A method and server for predicting damaging missense mutations
Ivan A. Adzhubei et al.
NATURE METHODS (2010)
Automated inference of molecular mechanisms of disease from amino acid substitutions
Biao Li et al.
BIOINFORMATICS (2009)
The Sequence Alignment/Map format and SAMtools
Heng Li et al.
BIOINFORMATICS (2009)
Fast and accurate short read alignment with Burrows-Wheeler transform
Heng Li et al.
BIOINFORMATICS (2009)
Updated Comprehensive Phylogenetic Tree of Global Human Mitochondrial DNA Variation
Mannis van Oven et al.
HUMAN MUTATION (2009)
Mitochondrial haplogroup H and Alzheimer's disease-Is there a connection?
Aleksandra Maruszak et al.
NEUROBIOLOGY OF AGING (2009)
An enhanced MITOMAP with a global mtDNA mutational phylogeny
Eduardo Ruiz-Pesini et al.
NUCLEIC ACIDS RESEARCH (2007)
High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease
A Bender et al.
NATURE GENETICS (2006)
Degenerate mitochondria
M van der Giezen et al.
EMBO REPORTS (2005)
Alzheimer's brains harbor somatic mtDNA control-region mutations that suppress mitochondrial transcription and replication
PE Coskun et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2004)
Stem cells, cancer, and cancer stem cells
T Reya et al.
NATURE (2001)
Random intracellular drift explains the clonal expansion of mitochondrial DNA mutations with age
JL Elson et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
Point mutations of the mtDNA control region in normal and neurodegenerative human brains
PF Chinnery et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2001)
Somatic and germline mosaic mutations in the doublecortin gene are associated with variable phenotypes
JG Gleeson et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2000)
mtDNA haplogroups and frequency patterns in Europe
A Torroni et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2000)
分享论文
