-
1
-
-
0025854490
-
Importance of maternal history of non-insulin-dependent diabetic patients
-
Alcolado JC, Alcolado R: Importance of maternal history of non-insulin-dependent diabetic patients. BMJ 302:1178-1180, 1991
-
(1991)
BMJ
, vol.302
, pp. 1178-1180
-
-
Alcolado, J.C.1
Alcolado, R.2
-
2
-
-
0000204255
-
Maternal inheritance of human mitochondrial DNA
-
Giles RE, Blanc H, Cann HM, Wallace DC: Maternal inheritance of human mitochondrial DNA. Proc Natl Acad Sci U S A 77:6715-6719, 1980
-
(1980)
Proc Natl Acad Sci U S A
, vol.77
, pp. 6715-6719
-
-
Giles, R.E.1
Blanc, H.2
Cann, H.M.3
Wallace, D.C.4
-
3
-
-
0030046495
-
Mitochondria and diabetes: Genetic, biochemical, and clinical implications of the cellular energy circuit
-
Gerbitz KD, Gempel K, Brdiczka D: Mitochondria and diabetes: genetic, biochemical, and clinical implications of the cellular energy circuit. Diabetes 45:113-126, 1996
-
(1996)
Diabetes
, vol.45
, pp. 113-126
-
-
Gerbitz, K.D.1
Gempel, K.2
Brdiczka, D.3
-
4
-
-
0026906885
-
Leu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness
-
Leu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness. Nat Genet 1:368-371, 1992
-
(1992)
Nat Genet
, vol.1
, pp. 368-371
-
-
Van Den Ouweland, J.M.1
Lemkes, H.H.2
Ruitenbeek, W.3
Sandkuijl, L.A.4
De Vijlder, M.F.5
Struyvenberg, P.A.6
Van De Kamp, J.J.7
Maassen, J.A.8
-
5
-
-
0028258021
-
Leu(UUR) gene mutation in Japanese patients
-
Leu(UUR) gene mutation in Japanese patients. Diabetologia 37:504-510, 1994
-
(1994)
Diabetologia
, vol.37
, pp. 504-510
-
-
Katagiri, H.1
Asano, T.2
Ishihara, H.3
Inukai, K.4
Anai, M.5
Yamanouchi, T.6
Tsukuda, K.7
Kikuchi, M.8
Kitaoka, H.9
Ohsawa, N.10
Yazaki, Y.11
Oka, Y.12
-
7
-
-
0031938224
-
New mitochondrial DNA homoplasmic mutations associated with Japanese patients with type 2 diabetes
-
Tawata M, Ohtaka M, Iwase E, Ikegishi Y, Aida K, Onaya T: New mitochondrial DNA homoplasmic mutations associated with Japanese patients with type 2 diabetes. Diabetes 47:276-277, 1998
-
(1998)
Diabetes
, vol.47
, pp. 276-277
-
-
Tawata, M.1
Ohtaka, M.2
Iwase, E.3
Ikegishi, Y.4
Aida, K.5
Onaya, T.6
-
8
-
-
0019423856
-
Sequence and organization of the human mitochondrial genome
-
Anderson S, Bankier AT, Barrell BG, de Buijn MHL, Coulson AR, Drouin J, Eperon IC, Nierlich DP, Roe BA, Sanger F, Schreier PH, Smith AJH, Staden R, Young IG: Sequence and organization of the human mitochondrial genome. Nature 290:457-465, 1981
-
(1981)
Nature
, vol.290
, pp. 457-465
-
-
Anderson, S.1
Bankier, A.T.2
Barrell, B.G.3
De Buijn, 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
-
9
-
-
0032868141
-
Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA
-
Andrews RM, Kubacka I, Chinnery PF, Lightowlers RN, Turnbull DM, Howell N: Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA (Letter). Nat Genet 23:147, 1999
-
(1999)
Nat Genet
, vol.23
, pp. 147
-
-
Andrews, R.M.1
Kubacka, I.2
Chinnery, P.F.3
Lightowlers, R.N.4
Turnbull, D.M.5
Howell, N.6
-
10
-
-
0026592540
-
Native american mitochondrial DNA analysis indicates that the Amerind and the Nadene populations were founded by two independent migrations
-
Torroni A, Schurr TG, Yang CC, Szathmary EJE, Williams RC, Schanfield MS, Troup GA, Knowler WC, Lawrence DN, Weiss KM, Wallace DC: Native American mitochondrial DNA analysis indicates that the Amerind and the Nadene populations were founded by two independent migrations. Genetics 130:153-162, 1992
-
(1992)
Genetics
, vol.130
, pp. 153-162
-
-
Torroni, A.1
Schurr, T.G.2
Yang, C.C.3
Szathmary, E.J.E.4
Williams, R.C.5
Schanfield, M.S.6
Troup, G.A.7
Knowler, W.C.8
Lawrence, D.N.9
Weiss, K.M.10
Wallace, D.C.11
-
11
-
-
0032539447
-
Mitochondrial genotype associated with longevity
-
Tanaka M, Gong J-S, Zhang J, Yoneda M, Yagi K: Mitochondrial genotype associated with longevity. Lancet 351:185-186, 1998
-
(1998)
Lancet
, vol.351
, pp. 185-186
-
-
Tanaka, M.1
Gong, J.-S.2
Zhang, J.3
Yoneda, M.4
Yagi, K.5
-
12
-
-
0028365120
-
Functional and morphological abnormalities of mitochondrial in human cells containing mitochondrial DNA with pathogenic point mutations in tRNA genes
-
Hayashi J-I, Ohta S, Kagawa Y, Takai D, Miyabayashi S, Tada K, Fukushima H, Inui K, Okada S, Goto Y-I, Nonaka I: Functional and morphological abnormalities of mitochondrial in human cells containing mitochondrial DNA with pathogenic point mutations in tRNA genes. J Biol Chem 269:19060-19066, 1994
-
(1994)
J Biol Chem
, vol.269
, pp. 19060-19066
-
-
Hayashi, J.-I.1
Ohta, S.2
Kagawa, Y.3
Takai, D.4
Miyabayashi, S.5
Tada, K.6
Fukushima, H.7
Inui, K.8
Okada, S.9
Goto, Y.-I.10
Nonaka, I.11
-
13
-
-
0026608057
-
MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts
-
Chomyn A, Martinuzzi A, Yoneda M, Daga A, Hurko O, Johns D, Lai ST, Nonaka I, Angelini C, Attardi G: MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts. Proc Natl Acad Sci U S A 89:4221-4225, 1992
-
(1992)
Proc Natl Acad Sci U S A
, vol.89
, pp. 4221-4225
-
-
Chomyn, A.1
Martinuzzi, A.2
Yoneda, M.3
Daga, A.4
Hurko, O.5
Johns, D.6
Lai, S.T.7
Nonaka, I.8
Angelini, C.9
Attardi, G.10
-
14
-
-
0029908226
-
Origin and functional consequences of the complex I defect in Parkinson's disease
-
Swerdlow RH, Parks JK, Miller SW, Turtle JB, Trimmer PA, Sheehan JP, Bennett JP Jr, Davis RE, Parker WD Jr: Origin and functional consequences of the complex I defect in Parkinson's disease. Ann Neurol 40:663-671, 1996
-
(1996)
Ann Neurol
, vol.40
, pp. 663-671
-
-
Swerdlow, R.H.1
Parks, J.K.2
Miller, S.W.3
Turtle, J.B.4
Trimmer, P.A.5
Sheehan, J.P.6
Bennett J.P., Jr.7
Davis, R.E.8
Parker W.D., Jr.9
-
15
-
-
0028342847
-
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
-
Albert SJ, Brown MD, Wallace DC: 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 91:6206-6210, 1994
-
(1994)
Proc Natl Acad Sci U S A
, vol.91
, pp. 6206-6210
-
-
Albert, S.J.1
Brown, M.D.2
Wallace, D.C.3
-
16
-
-
0024448458
-
Human cells lacking mtDNA: Repopulation with exogenous mitochondria by complementation
-
King MP, Attardi G: Human cells lacking mtDNA: repopulation with exogenous mitochondria by complementation. Science 246:500-503, 1989
-
(1989)
Science
, vol.246
, pp. 500-503
-
-
King, M.P.1
Attardi, G.2
-
17
-
-
0025836655
-
Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction
-
Hayashi J-I, Ohta S, Kikuchi A, Takemitsu M, Goto Y, Nonaka I: Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction. Proc Natl Acad Sci U S A 88:10614-10618, 1991
-
(1991)
Proc Natl Acad Sci U S A
, vol.88
, pp. 10614-10618
-
-
Hayashi, J.-I.1
Ohta, S.2
Kikuchi, A.3
Takemitsu, M.4
Goto, Y.5
Nonaka, I.6
-
18
-
-
0032543370
-
Long-term postmortem survival of mitochondrial genomes in mouse synaptosomes and their rescue in a mitochondrial DNA-less mouse cell line
-
Ito S, Inoue K, Yanagisawa N, Kaneko M, Hayashi J-I: Long-term postmortem survival of mitochondrial genomes in mouse synaptosomes and their rescue in a mitochondrial DNA-less mouse cell line. Biochem Biophys Res Commun 247:432-435, 1998
-
(1998)
Biochem Biophys Res Commun
, vol.247
, pp. 432-435
-
-
Ito, S.1
Inoue, K.2
Yanagisawa, N.3
Kaneko, M.4
Hayashi, J.-I.5
-
19
-
-
0024814593
-
Defective pattern of mitochondrial respiratory enzymes in mitochondrial myopathy
-
Miyabayashi S, Haginoya K, Hanamizu H, Iinum K, Narisawa K, Tada K: Defective pattern of mitochondrial respiratory enzymes in mitochondrial myopathy. J Inherit Metab Dis 12:373-377, 1989
-
(1989)
J Inherit Metab Dis
, vol.12
, pp. 373-377
-
-
Miyabayashi, S.1
Haginoya, K.2
Hanamizu, H.3
Iinum, K.4
Narisawa, K.5
Tada, K.6
-
20
-
-
0021162972
-
Cytochrome c oxidase deficiency in two siblings with Leigh encephalomyelopathy
-
Miyabayashi S, Narisawa K, Iinuma K, Tada K, Sakai K, Kobayashi K, Kobayashi Y, Morinaga S: Cytochrome c oxidase deficiency in two siblings with Leigh encephalomyelopathy. Brain Dev 6:362-372, 1984
-
(1984)
Brain Dev
, vol.6
, pp. 362-372
-
-
Miyabayashi, S.1
Narisawa, K.2
Iinuma, K.3
Tada, K.4
Sakai, K.5
Kobayashi, K.6
Kobayashi, Y.7
Morinaga, S.8
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