Related references
Note: Only part of the references are listed.Association Between Mitochondrial DNA Content in Leukocytes and Colorectal Cancer Risk
Falin Qu et al.
CANCER (2011)
Leber's Hereditary Optic Neuropathy-Gene Therapy: From Benchtop to Bedside
Rajeshwari D. Koilkonda et al.
JOURNAL OF OPHTHALMOLOGY (2011)
Novel heteroplasmic mutation in the anticodon stem of mitochondrial tRNALys associated with dystonia and stroke-like episodes
A. Gal et al.
ACTA NEUROLOGICA SCANDINAVICA (2010)
Mitochondrial NADH-dehydrogenase subunit 3 (ND3) polymorphism (A10398G) and sporadic breast cancer in Poland
Anna M. Czarnecka et al.
BREAST CANCER RESEARCH AND TREATMENT (2010)
Mitochondrial DNA copy number and lung cancer risk in a prospective cohort study
H. Dean Hosgood et al.
CARCINOGENESIS (2010)
The Background of Mitochondrial DNA Haplogroup J Increases the Sensitivity of Leber's Hereditary Optic Neuropathy Cells to 2,5-Hexanedione Toxicity
Anna Ghelli et al.
PLOS ONE (2009)
Mitochondrial DNA variant interactions modify breast cancer risk
Daniel Covarrubias et al.
JOURNAL OF HUMAN GENETICS (2008)
Mitochondrial genetic background modifies breast cancer risk
Ren-Kui Bai et al.
CANCER RESEARCH (2007)
Mitochondrial DNA G10398A polymorphism imparts maternal Haplogroup N a risk for breast and esophageal cancer
Katayoon Darvishi et al.
CANCER LETTERS (2007)
Molecular dysfunction associated with the human mitochondrial 3302A>G mutation in the MTTL1 (mt-tRNALeu(UUR)) gene
Katharina Maniura-Weber et al.
NUCLEIC ACIDS RESEARCH (2006)
North American white mitochondrial haplogroups in prostate and renal cancer
LM Booker et al.
JOURNAL OF UROLOGY (2006)
Saami and Berbers - An unexpected mitochondrial DNA link
A Achilli et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
mtDNA mutations increase tumorigenicity in prostate cancer
JA Petros et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
Effects of purifying and adaptive selection on regional variation in human mtDNA
E Ruiz-Pesini et al.
SCIENCE (2004)
Assigning pathogenicity to mitochondrial tRNA mutations: when 'definitely maybe' is not good enough
R McFarland et al.
TRENDS IN GENETICS (2004)
Novel point mutations in the mitochondrial DNA detected in patients with dilated cardiomyopathy by screening the whole mitochondrial genome
V Ruppert et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2004)
Mitochondrial A12308G polymorphism affects clinical features in patients with single mtDNA macrodeletion
M Crimi et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2003)
Increased variation in mtDNA in patients with familial sensorineural hearing impairment
MS Lehtonen et al.
HUMAN GENETICS (2003)
Natural selection shaped regional mtDNA variation in humans
D Mishmar et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups
C Herrnstadt et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
The mitochondrial DNA mutation T12297C affects a highly conserved nucleotide of tRNALeu(CUN) and is associated with dilated cardiomyopathy
M Grasso et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2001)
Search for characteristic structural features of mammalian mitochondrial tRNAs
M Helm et al.
RNA (2000)