-
1
-
-
0019423856
-
Sequence and organisation of the human mitochondrial genome
-
Anderson S, Bankier AT, Barrell BG, de Bruijn MHL, Coulson AR, Drouin J, Eperon IC, Nierlich DP, Roe BA, Sanger F, Schreier PH, Smith AJH, Staden R, Young IG (1981) Sequence and organisation of the human mitochondrial genome. Nature 290:457-465.
-
(1981)
Nature
, vol.290
, pp. 457-465
-
-
Anderson, S.1
Bankier, A.T.2
Barrell, B.G.3
De Bruijn, M.H.L.4
Coulson, A.R.5
Drouin, J.6
Eperon, I.C.7
Nierlich, D.P.8
Roe, B.A.9
Sanger, F.10
Schreier, P.H.11
Smith, A.J.H.12
Staden, R.13
Young, I.G.14
-
2
-
-
0002526279
-
Comparison of the human and bovine mitochondrial genomes
-
Slonimski P, Borst P, Attardi G (eds) Cold Spring Harbour, New York
-
Anderson S, Bankier AT, Barrell BG, deBruijn MHL, Coulson AR, Drouin J, Eperon IC, Nierlich DP, Roe BA, Sanger F, Schreier PH, Smith AJH, Staden R, Young IG (1982) Comparison of the human and bovine mitochondrial genomes In: Mitochondrial Genes. Slonimski P, Borst P, Attardi G (eds) Cold Spring Harbour, New York.
-
(1982)
Mitochondrial Genes
-
-
Anderson, S.1
Bankier, A.T.2
Barrell, B.G.3
DeBruijn, M.H.L.4
Coulson, A.R.5
Drouin, J.6
Eperon, I.C.7
Nierlich, D.P.8
Roe, B.A.9
Sanger, F.10
Schreier, P.H.11
Smith, A.J.H.12
Staden, R.13
Young, I.G.14
-
3
-
-
0025835296
-
Fast and sensitive silver staining of DNA in polyacrylamide gels
-
Bassam BJ, Caetano-Anolles G, Gresshoff PM (1991) Fast and sensitive silver staining of DNA in polyacrylamide gels. Anal Biochem 196:80-83.
-
(1991)
Anal Biochem
, vol.196
, pp. 80-83
-
-
Bassam, B.J.1
Caetano-Anolles, G.2
Gresshoff, P.M.3
-
4
-
-
0019837699
-
Sequence and gene organisation of mouse mitochondrial DNA
-
Bibb MJ, van Etten RA, Wright CT, Walberg MW, Clayton DA (1981) Sequence and gene organisation of mouse mitochondrial DNA. Cell 26:167-180.
-
(1981)
Cell
, vol.26
, pp. 167-180
-
-
Bibb, M.J.1
Van Etten, R.A.2
Wright, C.T.3
Walberg, M.W.4
Clayton, D.A.5
-
5
-
-
0026732706
-
A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues
-
Cortopassi GA, Shibata D, Soong N-W, Arnheim N (1992) A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues. Proc Natl Acad Sci USA 89:7370-7374.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 7370-7374
-
-
Cortopassi, G.A.1
Shibata, D.2
Soong, N.-W.3
Arnheim, N.4
-
6
-
-
0022492015
-
The mechanism of ATP synthase: A reassessment of the functions of the b and a subunits
-
Cox GB, Fimmel AL, Gibson F, Hatch L (1986) The mechanism of ATP synthase: a reassessment of the functions of the b and a subunits. Biochim Biophys Acta 849:62-69.
-
(1986)
Biochim Biophys Acta
, vol.849
, pp. 62-69
-
-
Cox, G.B.1
Fimmel, A.L.2
Gibson, F.3
Hatch, L.4
-
7
-
-
0028299566
-
Molecular biology of human male infertility: Links with aging, mitochondrial genetics, and oxidative stress?
-
Cummins JM, Jequier AM, Kan R (1993) Molecular biology of human male infertility: links with aging, mitochondrial genetics, and oxidative stress? Mol Reprod Devel 37:345-362.
-
(1993)
Mol Reprod Devel
, vol.37
, pp. 345-362
-
-
Cummins, J.M.1
Jequier, A.M.2
Kan, R.3
-
8
-
-
0025343497
-
Sequence and gene organisation of the chicken mitochondrial genome: A novel gene order in higher vertebrates
-
Desjardins P, Morais R (1990) Sequence and gene organisation of the chicken mitochondrial genome: a novel gene order in higher vertebrates. J Mol Biol 212:599-634.
-
(1990)
J Mol Biol
, vol.212
, pp. 599-634
-
-
Desjardins, P.1
Morais, R.2
-
9
-
-
0027379377
-
Mitochondrial disease and reduced sperm motility
-
Folgero T, Bertheussen K, Lindal S, Torbergsen T, Oian P (1993) Mitochondrial disease and reduced sperm motility. Hum Reprod 8:1863-1868.
-
(1993)
Hum Reprod
, vol.8
, pp. 1863-1868
-
-
Folgero, T.1
Bertheussen, K.2
Lindal, S.3
Torbergsen, T.4
Oian, P.5
-
10
-
-
0029026672
-
The 3243 MELAS mutation in a pedigree with MERFF
-
Folgero T, Torbergsen T, Oian P (1995) The 3243 MELAS mutation in a pedigree with MERFF. Eur Neurol 35:168-171.
-
(1995)
Eur Neurol
, vol.35
, pp. 168-171
-
-
Folgero, T.1
Torbergsen, T.2
Oian, P.3
-
11
-
-
0024352214
-
The complete nucleotide sequence of the Rattus norvegicus mitochondrial genome: Cryptic signals revealed by comparative analysis between vertebrates
-
Gadaleta G, Pepe G, De Candia G, Quagliariello C, Sbisa E, Saccone C (1989) The complete nucleotide sequence of the Rattus norvegicus mitochondrial genome: cryptic signals revealed by comparative analysis between vertebrates. J Mol Evol 28:497-516.
-
(1989)
J Mol Evol
, vol.28
, pp. 497-516
-
-
Gadaleta, G.1
Pepe, G.2
De Candia, G.3
Quagliariello, C.4
Sbisa, E.5
Saccone, C.6
-
12
-
-
0032495533
-
Recent developments in the molecular genetics of mitochondrial disorders
-
Graeber MB, Muller U (1998) Recent developments in the molecular genetics of mitochondrial disorders. J Neuro Sci 153:251-263.
-
(1998)
J Neuro Sci
, vol.153
, pp. 251-263
-
-
Graeber, M.B.1
Muller, U.2
-
14
-
-
0028359544
-
MELAS syndrome with mitochondrial tRNA leu (UUR) gene mutation in a Chinese family
-
Huang CC, Chen RS, Chen CM, Wang HS, Lee CC, Pang CY, Hsu HS, Lee HC, Wei YH (1994) MELAS syndrome with mitochondrial tRNA leu (UUR) gene mutation in a Chinese family. J Neurol Neurosurg Psychiatry 57:586-589.
-
(1994)
J Neurol Neurosurg Psychiatry
, vol.57
, pp. 586-589
-
-
Huang, C.C.1
Chen, R.S.2
Chen, C.M.3
Wang, H.S.4
Lee, C.C.5
Pang, C.Y.6
Hsu, H.S.7
Lee, H.C.8
Wei, Y.H.9
-
15
-
-
0031401759
-
Ageing-associated large-scale deletions of mitochondrial DNA in human hair follicles
-
Kao SH, Liu CS, Wang SY, Wei YH (1997) Ageing-associated large-scale deletions of mitochondrial DNA in human hair follicles. Biochem Mol Biol Int 42:285-298.
-
(1997)
Biochem Mol Biol Int
, vol.42
, pp. 285-298
-
-
Kao, S.H.1
Liu, C.S.2
Wang, S.Y.3
Wei, Y.H.4
-
16
-
-
0031826410
-
Multiple deletions of mitochondrial DNA are associated with the decline of motility and fertility of human spermatozoa
-
Kao SH, Chao HT, Wei YH (1998) Multiple deletions of mitochondrial DNA are associated with the decline of motility and fertility of human spermatozoa. Mol Hum Reprod 4:657-666.
-
(1998)
Mol Hum Reprod
, vol.4
, pp. 657-666
-
-
Kao, S.H.1
Chao, H.T.2
Wei, Y.H.3
-
17
-
-
0028908634
-
A mitochondrial mutation at nu9101 in the ATP synthase 6 gene associated with deficient oxidative phosphorylation in a family with Leber hereditary optic neuroretinopathy
-
Lamminen T, Majander A, Juvonen V, Wikström M, Aula P, Nikoskelainen E, Savontaus M-J (1995) A mitochondrial mutation at nu9101 in the ATP synthase 6 gene associated with deficient oxidative phosphorylation in a family with Leber hereditary optic neuroretinopathy. Am J Hum Genet 56:1238-1240.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 1238-1240
-
-
Lamminen, T.1
Majander, A.2
Juvonen, V.3
Wikström, M.4
Aula, P.5
Nikoskelainen, E.6
Savontaus, M.-J.7
-
18
-
-
0023913194
-
Simple non-invasive method to obtain DNA for gene analysis
-
Lench N, Stanier P, Williamson R (1988) Simple non-invasive method to obtain DNA for gene analysis. Lancet 18:1356-1358.
-
(1988)
Lancet
, vol.18
, pp. 1356-1358
-
-
Lench, N.1
Stanier, P.2
Williamson, R.3
-
19
-
-
0021876634
-
The complete nucleotide sequence of the Xenopus laevis mitochondrial genome
-
Roe BA, Ma D-P, Wilson RK, Wong JF-H (1985) The complete nucleotide sequence of the Xenopus laevis mitochondrial genome. J Biol Chem 260:9759-9774.
-
(1985)
J Biol Chem
, vol.260
, pp. 9759-9774
-
-
Roe, B.A.1
Ma, D.-P.2
Wilson, R.K.3
Wong, J.F.-H.4
-
20
-
-
0025338413
-
The proton-translocating ATPase of Escherichia coli
-
Senior AE (1990) The proton-translocating ATPase of Escherichia coli. Ann Rev Biophys Biophys Chem 19:7-42.
-
(1990)
Ann Rev Biophys Biophys Chem
, vol.19
, pp. 7-42
-
-
Senior, A.E.1
-
21
-
-
0026566850
-
Heteroplasmic mtDNA mutation (TG) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is high
-
Tatuch Y, Christodoulou J, Feigenbaum A, Clarke JTR, Wherret J, Smith C, Rudd N, Petrova-Benedict R, Robinson BH (1992) Heteroplasmic mtDNA mutation (TG) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is high. Am J Hum Genet 50:852-858.
-
(1992)
Am J Hum Genet
, vol.50
, pp. 852-858
-
-
Tatuch, Y.1
Christodoulou, J.2
Feigenbaum, A.3
Clarke, J.T.R.4
Wherret, J.5
Smith, C.6
Rudd, N.7
Petrova-Benedict, R.8
Robinson, B.H.9
-
22
-
-
0024726084
-
Variation in salmonid mitochondrial DNA: Evolutionary constraints and mechanisms of substitution
-
Thomas WK, Beckenbach AT (1989) Variation in salmonid mitochondrial DNA: evolutionary constraints and mechanisms of substitution. J Mol Evol 29:233-245.
-
(1989)
J Mol Evol
, vol.29
, pp. 233-245
-
-
Thomas, W.K.1
Beckenbach, A.T.2
-
23
-
-
0027936218
-
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
-
Trounce I, Neill S, Wallace DC (1994) 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 USA 91:8334-8338.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 8334-8338
-
-
Trounce, I.1
Neill, S.2
Wallace, D.C.3
-
24
-
-
0027512874
-
Mitochondrial diseases: Genotype versus phenotype
-
Wallace DC (1993) Mitochondrial diseases: genotype versus phenotype. Trends Genet 9:128-133.
-
(1993)
Trends Genet
, vol.9
, pp. 128-133
-
-
Wallace, D.C.1
|