Genetic factor in malignant melanoma.

PubWeight™: 1.00‹?› | Rank: Top 15%

🔗 View Article (PMID 5581515)

Published in Cancer on May 01, 1971

Authors

D C Wallace, L A Exton, G R McLeod

Articles by these authors

(truncated to the top 100)

Maternal inheritance of human mitochondrial DNA. Proc Natl Acad Sci U S A (1980) 9.48

Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutase. Nat Genet (1995) 7.17

Asian affinities and continental radiation of the four founding Native American mtDNAs. Am J Hum Genet (1993) 6.81

Radiation of human mitochondria DNA types analyzed by restriction endonuclease cleavage patterns. J Mol Evol (1983) 6.80

Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation. Cell (1990) 6.80

Classification of European mtDNAs from an analysis of three European populations. Genetics (1996) 6.28

Assessment of mitochondrial oxidative phosphorylation in patient muscle biopsies, lymphoblasts, and transmitochondrial cell lines. Methods Enzymol (1996) 5.40

Amerindian mitochondrial DNAs have rare Asian mutations at high frequencies, suggesting they derived from four primary maternal lineages. Am J Hum Genet (1990) 5.17

Dramatic founder effects in Amerindian mitochondrial DNAs. Am J Phys Anthropol (1985) 4.56

mtDNA and the origin of Caucasians: identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region. Am J Hum Genet (1994) 4.47

mtDNA variation of aboriginal Siberians reveals distinct genetic affinities with Native Americans. Am J Hum Genet (1993) 4.46

Analysis of mtDNA variation in African populations reveals the most ancient of all human continent-specific haplogroups. Am J Hum Genet (1995) 4.30

Southeast Asian mitochondrial DNA analysis reveals genetic continuity of ancient mongoloid migrations. Genetics (1992) 4.12

Mitochondrial mutations in cancer. Oncogene (2006) 3.86

Ethnic variation in Hpa 1 endonuclease cleavage patterns of human mitochondrial DNA. Proc Natl Acad Sci U S A (1981) 3.71

Mitochondrial DNA deletions in human brain: regional variability and increase with advanced age. Nat Genet (1992) 3.53

Extension of life-span with superoxide dismutase/catalase mimetics. Science (2000) 3.41

A novel neurological phenotype in mice lacking mitochondrial manganese superoxide dismutase. Nat Genet (1998) 3.41

Mitochondrial DNA analysis in Tibet: implications for the origin of the Tibetan population and its adaptation to high altitude. Am J Phys Anthropol (1994) 3.40

A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator. Nat Genet (1997) 3.26

Human mitochondrial DNA types in two Israeli populations--a comparative study at the DNA level. Am J Hum Genet (1986) 3.17

Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy. Genetics (1992) 2.94

Genome size and evolution. Chromosoma (1973) 2.93

Mitochondrial disease in superoxide dismutase 2 mutant mice. Proc Natl Acad Sci U S A (1999) 2.91

Mitochondrial DNA "clock" for the Amerinds and its implications for timing their entry into North America. Proc Natl Acad Sci U S A (1994) 2.86

Genetic studies on the Tharu population of Nepal: restriction endonuclease polymorphisms of mitochondrial DNA. Am J Hum Genet (1986) 2.80

The structure of human mitochondrial DNA variation. J Mol Evol (1991) 2.78

mtDNA and Y-chromosome polymorphisms in four Native American populations from southern Mexico. Am J Hum Genet (1994) 2.68

Increased mitochondrial oxidative stress in the Sod2 (+/-) mouse results in the age-related decline of mitochondrial function culminating in increased apoptosis. Proc Natl Acad Sci U S A (2001) 2.63

Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy. Proc Natl Acad Sci U S A (1989) 2.63

Mitochondrial disease in mouse results in increased oxidative stress. Proc Natl Acad Sci U S A (1999) 2.58

The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation. Am J Ophthalmol (1991) 2.57

Oxidative damage to mitochondrial DNA shows marked age-dependent increases in human brain. Ann Neurol (1993) 2.56

Mitochondrial DNA variation in Koryaks and Itel'men: population replacement in the Okhotsk Sea-Bering Sea region during the Neolithic. Am J Phys Anthropol (1999) 2.43

mtDNA variation in the South African Kung and Khwe-and their genetic relationships to other African populations. Am J Hum Genet (2000) 2.35

Hypoxemia is associated with mitochondrial DNA damage and gene induction. Implications for cardiac disease. JAMA (1991) 2.31

Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage. Am J Hum Genet (1997) 2.21

mtDNA haplogroup X: An ancient link between Europe/Western Asia and North America? Am J Hum Genet (1998) 2.16

Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion. Nat Genet (1992) 2.15

Amino acid change associated with the major polymorphic Hinc II site of Oriental and Caucasian mitochondrial DNAs. Am J Hum Genet (1983) 2.13

Structure and evolution of organelle genomes. Microbiol Rev (1982) 2.11

Differential expression of adenine nucleotide translocator isoforms in mammalian tissues and during muscle cell differentiation. J Biol Chem (1992) 2.08

Cytoplasmic inheritance of chloramphenicol resistance in mouse tissue culture cells. Proc Natl Acad Sci U S A (1974) 2.08

A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia. Proc Natl Acad Sci U S A (1994) 2.07

Mitochondrial oxidative phosphorylation defects in Parkinson's disease. Ann Neurol (1991) 2.06

Mitochondrial DNA variation in human populations and implications for detection of mitochondrial DNA mutations of pathological significance. J Bioenerg Biomembr (1994) 2.03

Mitochondrial DNA of chloramphenicol-resistant mouse cells contains a single nucleotide change in the region encoding the 3' end of the large ribosomal RNA. Proc Natl Acad Sci U S A (1981) 2.03

Coordinate induction of energy gene expression in tissues of mitochondrial disease patients. J Biol Chem (1999) 2.02

Variable genotype of Leber's hereditary optic neuropathy patients. Am J Ophthalmol (1990) 2.00

Association of mitochondrial DNA damage with aging and coronary atherosclerotic heart disease. Mutat Res (1992) 1.97

Maternally inherited mitochondrial myopathy and myoclonic epilepsy. Ann Neurol (1985) 1.94

A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy. N Engl J Med (1989) 1.91

mtDNA diversity in Chukchi and Siberian Eskimos: implications for the genetic history of Ancient Beringia and the peopling of the New World. Am J Hum Genet (1998) 1.91

A new manifestation of Leber's disease and a new explanation for the agency responsible for its unusual pattern of inheritance. Brain (1970) 1.91

Characterization of mitochondrial DNA in chloramphenicol-resistant interspecific hybrids and a cybrid. Somatic Cell Genet (1980) 1.88

Lifespan extension and rescue of spongiform encephalopathy in superoxide dismutase 2 nullizygous mice treated with superoxide dismutase-catalase mimetics. J Neurosci (2001) 1.86

Marked increase in the number and variety of mitochondrial DNA rearrangements in aging human skeletal muscle. Nucleic Acids Res (1995) 1.84

Novel mitochondrial DNA deletion found in a renal cell carcinoma. Genes Chromosomes Cancer (1996) 1.81

Mitochondrial DNA mutations and neuromuscular disease. Trends Genet (1989) 1.81

Combined use of biallelic and microsatellite Y-chromosome polymorphisms to infer affinities among African populations. Am J Hum Genet (1999) 1.81

Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations. Hum Mutat (1995) 1.80

Time trends of cutaneous melanoma in Queensland, Australia and Central Europe. Cancer (2000) 1.79

Mitochondrial DNA sequence diversity in bipolar affective disorder. Am J Psychiatry (2000) 1.77

Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystonia. Mol Cell Biol (1996) 1.76

Nonviability of cells with oxidative defects in galactose medium: a screening test for affected patient fibroblasts. Biochem Med Metab Biol (1992) 1.75

MITOMAP: a human mitochondrial genome database. Nucleic Acids Res (1996) 1.75

Dietary change through African American churches: baseline results and program description of the eat for life trial. J Cancer Educ (2000) 1.73

Mitochondrial DNA polymorphisms in Italy. I. Population data from Sardinia and Rome. Ann Hum Genet (1986) 1.73

Different nucleotide changes in the large rRNA gene of the mitochondrial DNA confer chloramphenicol resistance on two human cell lines. Nucleic Acids Res (1981) 1.72

MITOMAP: a human mitochondrial genome database--1998 update. Nucleic Acids Res (1998) 1.65

cDNA sequence of a human skeletal muscle ADP/ATP translocator: lack of a leader peptide, divergence from a fibroblast translocator cDNA, and coevolution with mitochondrial DNA genes. Proc Natl Acad Sci U S A (1987) 1.64

Prognostic value of quality of life scores in a trial of chemotherapy with or without interferon in patients with metastatic malignant melanoma. Eur J Cancer (1993) 1.64

Leber's hereditary optic neuropathy: a model for mitochondrial neurodegenerative diseases. FASEB J (1992) 1.62

Cytoplasmic transfer of chloramphenicol resistance in human tissue culture cells. J Cell Biol (1975) 1.62

Mitochondrial DNA polymorphisms in Italy. II. Molecular analysis of new and rare morphs from Sardinia and Rome. Ann Hum Genet (1988) 1.60

Evidence in a lethal infantile mitochondrial disease for a nuclear mutation affecting respiratory complexes I and IV. Neurology (1989) 1.57

Cytoplasmic transfer of the mtDNA nt 8993 T-->G (ATP6) point mutation associated with Leigh syndrome into mtDNA-less cells demonstrates cosegregation with a decrease in state III respiration and ADP/O ratio. Proc Natl Acad Sci U S A (1994) 1.57

Functional analysis of lymphoblast and cybrid mitochondria containing the 3460, 11778, or 14484 Leber's hereditary optic neuropathy mitochondrial DNA mutation. J Biol Chem (2000) 1.56

Maternal germ-line transmission of mutant mtDNAs from embryonic stem cell-derived chimeric mice. Proc Natl Acad Sci U S A (2000) 1.54

Y chromosome polymorphisms in native American and Siberian populations: identification of native American Y chromosome haplotypes. Hum Genet (1997) 1.52

Marked changes in mitochondrial DNA deletion levels in Alzheimer brains. Genomics (1994) 1.52

Expression and sequence analysis of the mouse adenine nucleotide translocase 1 and 2 genes. Gene (2000) 1.51

Heparinless partial cardiopulmonary bypass for the repair of aortic trauma. J Thorac Cardiovasc Surg (2000) 1.48

Increasing incidence of cutaneous melanoma in Queensland, Australia. J Natl Cancer Inst (1992) 1.47

Mitochondrial oxidative stress in mice lacking the glutathione peroxidase-1 gene. Free Radic Biol Med (2000) 1.47

The age-related accumulation of a mitochondrial DNA control region mutation in muscle, but not brain, detected by a sensitive PNA-directed PCR clamping based method. Nucleic Acids Res (2000) 1.44

Production of transmitochondrial mouse cell lines by cybrid rescue of rhodamine-6G pre-treated L-cells. Somat Cell Mol Genet (1996) 1.41

Oxidative phosphorylation diseases. Disorders of two genomes. Adv Hum Genet (1990) 1.38

Mitochondrial diabetes revisited. Nat Genet (1994) 1.33

Maternal inheritance of mitochondrial DNA polymorphisms in cultured human fibroblasts. Somatic Cell Genet (1981) 1.33

Assignment of two mitochondrially synthesized polypeptides to human mitochondrial DNA and their use in the study of intracellular mitochondrial interaction. Mol Cell Biol (1982) 1.33

A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit I. Am J Hum Genet (1992) 1.32

Radicals r'aging. Nat Genet (1998) 1.31

Visual recovery in patients with Leber's hereditary optic neuropathy and the 11778 mutation. J Clin Neuroophthalmol (1992) 1.30

Conformational mutations in human mitochondrial DNA. Nature (1987) 1.29

Evaluation of procedures for assaying oxidative phosphorylation enzyme activities in mitochondrial myopathy muscle biopsies. Biochim Biophys Acta (1990) 1.26

Leber's disease and dystonia: a mitochondrial disease. Neurology (1986) 1.25

Mitotic segregation of mitochondrial DNAs in human cell hybrids and expression of chloramphenicol resistance. Somat Cell Mol Genet (1986) 1.23

Multi-organ characterization of mitochondrial genomic rearrangements in ad libitum and caloric restricted mice show striking somatic mitochondrial DNA rearrangements with age. Nucleic Acids Res (1997) 1.20

Novel mtDNA mutations and oxidative phosphorylation dysfunction in Russian LHON families. Hum Genet (2001) 1.19