-
1
-
-
0019423856
-
Sequence and organization of the human mitochondrial genome
-
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 (1981) Sequence and organization 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
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
-
2
-
-
0027282274
-
Abnormal RNa processing associated with a novel tRNa mutation in mitochondrial DNA. a potential disease mechanism
-
Bindoff LA, Howell N, Poulton J, McCullough DA, Morten KJ, Lightowlers RN, Turnbull DM, Weber K (1993) Abnormal RNA processing associated with a novel tRNA mutation in mitochondrial DNA. A potential disease mechanism. J Biol Chem 268:19559-19564
-
(1993)
J Biol Chem
, vol.268
, pp. 19559-19564
-
-
Bindoff, L.A.1
Howell, N.2
Poulton, J.3
McCullough, D.A.4
Morten, K.J.5
Lightowlers, R.N.6
Turnbull, D.M.7
Weber, K.8
-
3
-
-
0029587469
-
Molecular genetic aspects of human mitochondrial disorders
-
Larsson NG, Clayton DA (1995) Molecular genetic aspects of human mitochondrial disorders. Annu Rev Genet 29:151-178
-
(1995)
Annu Rev Genet
, vol.29
, pp. 151-178
-
-
Larsson, N.G.1
Clayton, D.A.2
-
4
-
-
0027145131
-
Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNALeu(UUR) gene an etiologic hot spot?
-
Moraes CT, Ciacci F, Bonilla E, Jansen C, Hirano M, Rao N, Lovelace RE, Rowland LP, Schon EA, DiMauro S (1993) Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis. Is the tRNALeu(UUR) gene an etiologic hot spot? J Clin Invest 92:2906-2915
-
(1993)
J Clin Invest
, vol.92
, pp. 2906-2915
-
-
Moraes, C.T.1
Ciacci, F.2
Bonilla, E.3
Jansen, C.4
Hirano, M.5
Rao, N.6
Lovelace, R.E.7
Rowland, L.P.8
Schon, E.A.9
DiMauro, S.10
-
6
-
-
0027238740
-
Large-scale production of DNA sequencing templates by microtitre format PCR
-
Rosenthal A, Coutelle O, Craxton M (1993) Large-scale production of DNA sequencing templates by microtitre format PCR. Nucleic Acids Res 21:173-174
-
(1993)
Nucleic Acids Res
, vol.21
, pp. 173-174
-
-
Rosenthal, A.1
Coutelle, O.2
Craxton, M.3
-
7
-
-
0029048832
-
Human mitochondrial tRNA processing
-
Rossmanith W, Tullo A, Potuschak T, Karwan R, Sbisa E (1995) Human mitochondrial tRNA processing. J Biol Chem 270: 12885-12891
-
(1995)
J Biol Chem
, vol.270
, pp. 12885-12891
-
-
Rossmanith, W.1
Tullo, A.2
Potuschak, T.3
Karwan, R.4
Sbisa, E.5
-
8
-
-
0028908586
-
Deletion of mitochondrial DNA in patient with chronic tubulointerstitial nephritis
-
Rötig A, Goutieres F, Niaudet P, Rustin P, Chretien D, Guest G, Mikol J, Gubler MC, Munnich A (1995) Deletion of mitochondrial DNA in patient with chronic tubulointerstitial nephritis. J Pediatr 126:597-601
-
(1995)
J Pediatr
, vol.126
, pp. 597-601
-
-
Rötig, A.1
Goutieres, F.2
Niaudet, P.3
Rustin, P.4
Chretien, D.5
Guest, G.6
Mikol, J.7
Gubler, M.C.8
Munnich, A.9
-
9
-
-
0028258316
-
Mitochondrial DNa deletion: A cause of chronic tubulointerstitial nephropathy
-
Szabolcs MJ, Seigle R, Shanske S, Bonilla E, DiMauro S, D'Agati V (1994) Mitochondrial DNA deletion: a cause of chronic tubulointerstitial nephropathy. Kidney Int 45:1388-1396
-
(1994)
Kidney Int
, vol.45
, pp. 1388-1396
-
-
Szabolcs, M.J.1
Seigle, R.2
Shanske, S.3
Bonilla, E.4
DiMauro, S.5
D'Agati, V.6
-
10
-
-
0027982001
-
Comparative sensitivity of alternative single-strand conformation polymorphism (SSCP) methods
-
Vidal-Puig A, Moller DE (1994) Comparative sensitivity of alternative single-strand conformation polymorphism (SSCP) methods. BioTechniques 17:490-496
-
(1994)
BioTechniques
, vol.17
, pp. 490-496
-
-
Vidal-Puig, A.1
Moller, D.E.2
-
11
-
-
0024242545
-
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy
-
Wallace DC, Singh G, Lott MT, Hodge JA, Schurr TG, Lezza AMS, Elsas LJII, Nikoskelainen EK (1988) Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. Science 242:1427-1430
-
(1988)
Science
, vol.242
, pp. 1427-1430
-
-
Wallace, D.C.1
Singh, G.2
Lott, M.T.3
Hodge, J.A.4
Schurr, T.G.5
Lezza, A.M.S.6
Elsas, L.7
Nikoskelainen, E.K.8
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