-
1
-
-
0019423856
-
Sequence and organization of the human mitochondrial genome
-
(1981)
Nature
, vol.290
, pp. 457-465
-
-
Anderson, S.1
Bankier, A.T.2
Barrell, B.G.3
De Bruijn, M.H.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.12
Staden, R.13
Young, I.G.14
-
4
-
-
0027490348
-
Reaching for the ring: The study of mitochondrial genome structure
-
(1993)
Curr Genet
, vol.24
, pp. 279-290
-
-
Bendich, A.J.1
-
11
-
-
0032914642
-
Early onset of diabetes mellitus associated with the mitochondrial DNA T14709C point mutation: Patient report and literature review
-
(1999)
J Pediatr Endocrinol Metab
, vol.12
, pp. 207-213
-
-
Damore, M.E.1
Speiser, P.W.2
Slonim, A.E.3
New, M.I.4
Shanske, S.5
Xia, W.6
Santorelli, F.M.7
DiMauro, S.8
-
12
-
-
0027311861
-
The expanding clinical spectrum of mitochondrial diseases
-
(1993)
Brain Dev
, vol.15
, pp. 1-22
-
-
DeVivo, D.C.1
-
19
-
-
0031598833
-
Cardiolipin: Biosynthesis, remodeling and trafficking in the heart and mammalian cells
-
(1998)
Int J Mol Med
, vol.1
, pp. 33-41
-
-
Hatch, G.M.1
-
22
-
-
0033646471
-
Evolutionary origin and consequences of uniparental genetic transmission
-
(2000)
Hum Reprod
, vol.15
, Issue.SUPPL. 2
, pp. 102-111
-
-
Hoekstra, R.1
-
24
-
-
0030806721
-
Leber hereditary optic neuropathy: Mitochondrial mutations and degeneration of the optic nerve
-
(1997)
Vision Res
, vol.37
, pp. 3495-3507
-
-
Howell, N.1
-
38
-
-
0018577688
-
Mechanism of mitochondrial DNA replication in mouse L-cells: Localization and sequence of the light-strand origin of replication
-
(1979)
J Mol Biol
, vol.135
, pp. 327-351
-
-
Martens, P.A.1
Clayton, D.A.2
-
42
-
-
0008758805
-
The mitochondrial DNA depletion syndromes
-
Nyhan WL, Ozand P (eds) Atlas of metabolic disease. Chapman & Hall, Lon
-
(1999)
-
-
Naviaux, R.K.1
-
48
-
-
0031736203
-
Somatic mutations of the mitochondrial genome in human colorectal tumours
-
(1998)
Nat Genet
, vol.20
, pp. 91-93
-
-
Polyak, K.1
Li, Y.2
Zhu, H.3
Lengauer, C.4
Willson, J.K.5
Markowitz, S.D.6
Trush, M.A.7
Kinzler, K.W.8
Vogelstein, B.9
-
49
-
-
4243651720
-
Pathogenesis of mitochondrial disease
-
Applegarth DA, Dimmick JE, Hall JG (eds) Organelle diseases. Chapman & Hall, New York
-
(1997)
, pp. 305-340
-
-
Poulton, J.1
-
51
-
-
0032511112
-
2+ responses
-
(1998)
Science
, vol.280
, pp. 1763-1766
-
-
Rizzuto, R.1
Pinton, P.2
Carrington, W.3
Fay, F.S.4
Fogarty, K.E.5
Lifshitz, L.M.6
Tuft, R.A.7
Pozzan, T.8
-
62
-
-
0033525773
-
Mitochondrial diseases in man and mouse
-
(1999)
Science
, vol.283
, pp. 1482-1488
-
-
Wallace, D.C.1
-
63
-
-
0024242545
-
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy
-
(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.6
Elsas II, L.J.7
Nikoskelainen, E.K.8
-
66
-
-
0031036872
-
Prevention of apoptosis by Bcl-2: Release of cytochrome c from mitochondria blocked
-
(1997)
Science
, vol.275
, pp. 1129-1132
-
-
Yang, J.1
Liu, X.2
Bhalla, K.3
Kim, C.N.4
Ibrado, A.M.5
Cai, J.6
Peng, T.I.7
Jones, D.P.8
Wang, X.9
|