-
1
-
-
0000204255
-
Maternal inheritance of human mtDNA
-
Giles RE, Blanc H, Cann HM, Wallace DC. Maternal inheritance of human mtDNA. 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
-
2
-
-
0026624980
-
Diseases of the mtDNA
-
Wallace DC. Diseases of the mtDNA. Annu Rev Biochem 61:1175-1212, 1992.
-
(1992)
Annu Rev Biochem
, vol.61
, pp. 1175-1212
-
-
Wallace, D.C.1
-
3
-
-
0022555846
-
Biogenesis of mitochondrial genetics
-
Tzagoloff A, Myers AM. Biogenesis of mitochondrial genetics. Annu Rev Biochem 55:249-285, 1986.
-
(1986)
Annu Rev Biochem
, vol.55
, pp. 249-285
-
-
Tzagoloff, A.1
Myers, A.M.2
-
4
-
-
0019423856
-
Sequence and organization of the human mitochondrial genome
-
Anderson S, Bankier AT, Barrell BG, Bruijin MHL, Coulsen 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
Bruijin, M.H.L.4
Coulsen, 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
-
5
-
-
0018954657
-
Mapping the nascent light and heavy strand transcripts on the physical map of HeLa cell mtDNA
-
Cantatore P, Attardi G. Mapping the nascent light and heavy strand transcripts on the physical map of HeLa cell mtDNA. Nucleic Acids Res 8:2605-2625, 1980.
-
(1980)
Nucleic Acids Res
, vol.8
, pp. 2605-2625
-
-
Cantatore, P.1
Attardi, G.2
-
6
-
-
0021399823
-
Precise identification of individual promoters for transcription of each strand of human mtDNA
-
Chang DD, Clayton DA. Precise identification of individual promoters for transcription of each strand of human mtDNA. Cell 36:635-643, 1984.
-
(1984)
Cell
, vol.36
, pp. 635-643
-
-
Chang, D.D.1
Clayton, D.A.2
-
7
-
-
0025697303
-
Direct repeats in the noncoding region of rabbit mtDNA: Involvement in the generation of intra- and inter-individual heterogeneity
-
Mignotte F, Gueride A, Champagne AM, Mounolou JC. Direct repeats in the noncoding region of rabbit mtDNA: Involvement in the generation of intra- and inter-individual heterogeneity. Eur J Biochem 194:561-571, 1990.
-
(1990)
Eur J Biochem
, vol.194
, pp. 561-571
-
-
Mignotte, F.1
Gueride, A.2
Champagne, A.M.3
Mounolou, J.C.4
-
8
-
-
0022534679
-
Nucleotide sequence identity of mitochondrial DNA from different human tissues
-
Monnat RJ, Reay DT. Nucleotide sequence identity of mitochondrial DNA from different human tissues. Gene 43:205-211, 1986.
-
(1986)
Gene
, vol.43
, pp. 205-211
-
-
Monnat, R.J.1
Reay, D.T.2
-
9
-
-
0028037791
-
Oxidative phosphorylation disease and mitochondrial DNA mutations: Diagnosis and treatment
-
Shoffner JM, Wallace DC. Oxidative phosphorylation disease and mitochondrial DNA mutations: Diagnosis and treatment. Annu Rev Nutr 14:535-568, 1994.
-
(1994)
Annu Rev Nutr
, vol.14
, pp. 535-568
-
-
Shoffner, J.M.1
Wallace, D.C.2
-
10
-
-
0023621390
-
ATP synthase from bovine mitochondria: Sequences of imported precursors of oligomycin sensitivity conferral protein, factor 6, and adenosinetriphosphatase inhibitor protein
-
Walker JE, Gay NJ, Powell SJ, Kostina M, Dyer MR. ATP synthase from bovine mitochondria: Sequences of imported precursors of oligomycin sensitivity conferral protein, factor 6, and adenosinetriphosphatase inhibitor protein. Biochemistry 26:8613-8619, 1987.
-
(1987)
Biochemistry
, vol.26
, pp. 8613-8619
-
-
Walker, J.E.1
Gay, N.J.2
Powell, S.J.3
Kostina, M.4
Dyer, M.R.5
-
11
-
-
0023645444
-
ATP synthase from bovine mitochondria: The characterization and sequence analysis of two membrane-associated subunits and of corresponding cDNAs
-
Walker JE, Runswick MJ, Poulter L. ATP synthase from bovine mitochondria: The characterization and sequence analysis of two membrane-associated subunits and of corresponding cDNAs. J Mol Biol 197:89-100, 1987.
-
(1987)
J Mol Biol
, vol.197
, pp. 89-100
-
-
Walker, J.E.1
Runswick, M.J.2
Poulter, L.3
-
12
-
-
0014407722
-
Repeated sequences in DNA: Hundreds of thousands of copies of DNA sequences have been incorporated into the genomes of higher organisms
-
Britten RJ, Kohne DE. Repeated sequences in DNA: Hundreds of thousands of copies of DNA sequences have been incorporated into the genomes of higher organisms. Science 161:529-540, 1968.
-
(1968)
Science
, vol.161
, pp. 529-540
-
-
Britten, R.J.1
Kohne, D.E.2
-
13
-
-
0021964548
-
Initiation of transcription from each of the two human mitochondrial promoters requires unique nucleotide as transcriptional start sites
-
Hixson JE, Clayton A. Initiation of transcription from each of the two human mitochondrial promoters requires unique nucleotide as transcriptional start sites. Proc Natl Acad Sci U S A 82:2660-2664, 1985.
-
(1985)
Proc Natl Acad Sci U S A
, vol.82
, pp. 2660-2664
-
-
Hixson, J.E.1
Clayton, A.2
-
14
-
-
0024352214
-
The complete nucleotide sequence of the Rattus norvegicus mitochondrial genome: Cryptic signals revealed by comparative analysis between vertebrates
-
Gadaleta G, Pepe G, DeCandia G, Quagliariello C, Sbissá E, Saccone C. 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.
-
(1989)
J Mol Evol
, vol.28
, pp. 497-516
-
-
Gadaleta, G.1
Pepe, G.2
DeCandia, G.3
Quagliariello, C.4
Sbissá, E.5
Saccone, C.6
-
16
-
-
0023943474
-
Comparisons of ape and human sequences that regulate mtDNA transcription and D-loop DNA synthesis
-
Foran DR, Hixson JE, Brown WM. Comparisons of ape and human sequences that regulate mtDNA transcription and D-loop DNA synthesis. Nucleic Acid Res 16:5841-5861, 1988.
-
(1988)
Nucleic Acid Res
, vol.16
, pp. 5841-5861
-
-
Foran, D.R.1
Hixson, J.E.2
Brown, W.M.3
-
17
-
-
0022274030
-
Animal mitochondrial DNA: An extreme example of genetic economy
-
Attardi G. Animal mitochondrial DNA: An extreme example of genetic economy, Int Rev Cytol 93:93-145, 1985.
-
(1985)
Int Rev Cytol
, vol.93
, pp. 93-145
-
-
Attardi, G.1
-
18
-
-
0025885770
-
Replication and transcription of vertebrate mitochondrial DNA
-
Clayton DA. Replication and transcription of vertebrate mitochondrial DNA. Annu Rev Cell Biol 7:453-478, 1991.
-
(1991)
Annu Rev Cell Biol
, vol.7
, pp. 453-478
-
-
Clayton, D.A.1
-
20
-
-
0013936167
-
Codon-anticodon pairing: The wobble hypothesis
-
Crick FHC. Codon-anticodon pairing: The wobble hypothesis. J Mol Biol 19:548, 1966.
-
(1966)
J Mol Biol
, vol.19
, pp. 548
-
-
Crick, F.H.C.1
-
21
-
-
2542497311
-
Transfer RNA: The translational adaptor
-
Cambridge, MA: Cell Press
-
Lewin B. Transfer RNA: The translational adaptor. In: Genes IV. Cambridge, MA: Cell Press, pp 137-170, 1990.
-
(1990)
Genes IV
, pp. 137-170
-
-
Lewin, B.1
-
22
-
-
0018577407
-
A different genetic code in human mitochondria
-
Barrell BG, Bankier AT, Drouin J. A different genetic code in human mitochondria. Nature 282:189-194, 1979.
-
(1979)
Nature
, vol.282
, pp. 189-194
-
-
Barrell, B.G.1
Bankier, A.T.2
Drouin, J.3
-
23
-
-
25344458167
-
Adaptation of tRNA population to codon usage in cellular organelles
-
Hatfield D, Lee B, Pirthe H, Eds. Boca Raton, FL: CRC Press
-
Marèchal-Douard L, Dietrich A, Wiel JH. Adaptation of tRNA population to codon usage in cellular organelles. In: Hatfield D, Lee B, Pirthe H, Eds. Transfer RNA in Protein Synthesis. Boca Raton, FL: CRC Press, pp 125-140, 1992.
-
(1992)
Transfer RNA in Protein Synthesis
, pp. 125-140
-
-
Marèchal-Douard, L.1
Dietrich, A.2
Wiel, J.H.3
-
24
-
-
0021604866
-
A nuclear mutation that post-transcriptionally blocks accumulation of a yeast mitochondrial gene product can be suppressed by a mitochondrial gene rearrangement
-
Muller PP, Reif MK, Zoughou S, Sengstag C, Mason TL, Fox TD. A nuclear mutation that post-transcriptionally blocks accumulation of a yeast mitochondrial gene product can be suppressed by a mitochondrial gene rearrangement. J Mol Biol 174:431-452, 1984.
-
(1984)
J Mol Biol
, vol.174
, pp. 431-452
-
-
Muller, P.P.1
Reif, M.K.2
Zoughou, S.3
Sengstag, C.4
Mason, T.L.5
Fox, T.D.6
-
25
-
-
0021327772
-
Assembly of the mitochondrial membrane system: Nuclear sequence of yeast gene (CBPl) involved in 5′ processing of cytochrome b pre-mRNA
-
Dieckmann CL, Homison G, Tzagoloff AJ. Assembly of the mitochondrial membrane system: Nuclear sequence of yeast gene (CBPl) involved in 5′ processing of cytochrome b pre-mRNA. J Biol Chem 259:4732-738, 1984.
-
(1984)
J Biol Chem
, vol.259
, pp. 4732-4738
-
-
Dieckmann, C.L.1
Homison, G.2
Tzagoloff, A.J.3
-
26
-
-
0021099817
-
Assembly of the mitochondrial membrane system: Characterization of a yeast nuclear gene involved in processing of cytochrome b pre-mRNA
-
McGraw P, Tzagoloff A. Assembly of the mitochondrial membrane system: Characterization of a yeast nuclear gene involved in processing of cytochrome b pre-mRNA. J Biol Chem 258:9459-9468, 1983.
-
(1983)
J Biol Chem
, vol.258
, pp. 9459-9468
-
-
McGraw, P.1
Tzagoloff, A.2
-
27
-
-
0021099701
-
Expression of the "split-gene" cob in yeast mtDNA: Nuclear mutations specifically block the excision of different introns from its primary transcript
-
Pillar T, Lang BF, Steinberger I, Vogt B, Kaudewitz F. Expression of the "split-gene" cob in yeast mtDNA: Nuclear mutations specifically block the excision of different introns from its primary transcript. J Biol Chem 258:7954-7959, 1983.
-
(1983)
J Biol Chem
, vol.258
, pp. 7954-7959
-
-
Pillar, T.1
Lang, B.F.2
Steinberger, I.3
Vogt, B.4
Kaudewitz, F.5
-
28
-
-
0021913292
-
Assembly of the mitochondrial membrane system: CBP6, a yeast nuclear gene necessary for synthesis of cytochrome b
-
Dieckmann CL, Tzagoloff AJ. Assembly of the mitochondrial membrane system: CBP6, a yeast nuclear gene necessary for synthesis of cytochrome b. J Biol Chem 260:1513-1520, 1985.
-
(1985)
J Biol Chem
, vol.260
, pp. 1513-1520
-
-
Dieckmann, C.L.1
Tzagoloff, A.J.2
-
29
-
-
0015251707
-
Biogenesis of mitochondrial inner membrane in bakers' yeast
-
Schatz G, Groot GS, Mason T, Rouslin W, Wharton DC, Salitzgaber J. Biogenesis of mitochondrial inner membrane in bakers' yeast. Fed Proc 31:21-29, 1972.
-
(1972)
Fed Proc
, vol.31
, pp. 21-29
-
-
Schatz, G.1
Groot, G.S.2
Mason, T.3
Rouslin, W.4
Wharton, D.C.5
Salitzgaber, J.6
-
30
-
-
0030809575
-
Regulation of mitochondrial transcription by mitochondrial transcription factor A
-
Montoya J, Perez-Martos A, Garstka HL, Wiesner RJ. Regulation of mitochondrial transcription by mitochondrial transcription factor A. Mol Cell Biochem 174:227-230, 1997.
-
(1997)
Mol Cell Biochem
, vol.174
, pp. 227-230
-
-
Montoya, J.1
Perez-Martos, A.2
Garstka, H.L.3
Wiesner, R.J.4
-
31
-
-
0029975942
-
Mitochondrial genes as sites of primary action of steroid hormones
-
Demonacos CV, Karayanni N, Hatzoglou E, Tsiriyiotis C, Spandidos DA. Mitochondrial genes as sites of primary action of steroid hormones. Steroids 61:226-232, 1996.
-
(1996)
Steroids
, vol.61
, pp. 226-232
-
-
Demonacos, C.V.1
Karayanni, N.2
Hatzoglou, E.3
Tsiriyiotis, C.4
Spandidos, D.A.5
-
32
-
-
0026026191
-
Different mechanisms inferred from sequences of human mitochondrial DNA deletions in ocular myopathies
-
Degoul F, Nelson I, Amselem S, Romero N, Obermaier-Kusser B, Ponsot G, Marsac C, Lestienne P. Different mechanisms inferred from sequences of human mitochondrial DNA deletions in ocular myopathies. Nucleic Acids Res 19:493-496, 1990.
-
(1990)
Nucleic Acids Res
, vol.19
, pp. 493-496
-
-
Degoul, F.1
Nelson, I.2
Amselem, S.3
Romero, N.4
Obermaier-Kusser, B.5
Ponsot, G.6
Marsac, C.7
Lestienne, P.8
-
33
-
-
0025807222
-
Maternally inherited myopathy and cardiomyopathy: Association with mutation in mitochondrial DNA tRNA(Leu)(UUR)
-
Zeviani M, Gellera C, Antozzi C, Rimoldi M, Morandi L, Villani F, Tiranti V, DiDonato S. Maternally inherited myopathy and cardiomyopathy: Association with mutation in mitochondrial DNA tRNA(Leu)(UUR). Lancet 338:143-147, 1991.
-
(1991)
Lancet
, vol.338
, pp. 143-147
-
-
Zeviani, M.1
Gellera, C.2
Antozzi, C.3
Rimoldi, M.4
Morandi, L.5
Villani, F.6
Tiranti, V.7
DiDonato, S.8
-
34
-
-
0025056701
-
Length heteroplasmy of sturgeon mtDNA: An illegitimate elongation model
-
Buroker NE, Brown JR, Gilbert TA, O'Hara PJ, Beckenback AT, Thomas WK, Smith MJ. Length heteroplasmy of sturgeon mtDNA: An illegitimate elongation model. Genetics 124:157-163, 1991.
-
(1991)
Genetics
, vol.124
, pp. 157-163
-
-
Buroker, N.E.1
Brown, J.R.2
Gilbert, T.A.3
O'Hara, P.J.4
Beckenback, A.T.5
Thomas, W.K.6
Smith, M.J.7
-
35
-
-
0027166063
-
In vivo and in vitro evidence for slipped mispairing in mammalian mitochondria
-
Madsen CS, Ghivizzani SC, Hauswirth WW. In vivo and in vitro evidence for slipped mispairing in mammalian mitochondria. Proc Natl Acad Sci U S A 90:7671-7675, 1993.
-
(1993)
Proc Natl Acad Sci U S A
, vol.90
, pp. 7671-7675
-
-
Madsen, C.S.1
Ghivizzani, S.C.2
Hauswirth, W.W.3
-
36
-
-
0026074885
-
Hypoxemia is associated with mtDNA damage and gene induction. Implications for cardiac disease
-
Corral-Debrinski M, Stepien G, Shoffner JM, Lott MT, Kanter K, Wallace DC. Hypoxemia is associated with mtDNA damage and gene induction. Implications for cardiac disease. JAMA 266:1812-1816, 1991.
-
(1991)
JAMA
, vol.266
, pp. 1812-1816
-
-
Corral-Debrinski, M.1
Stepien, G.2
Shoffner, J.M.3
Lott, M.T.4
Kanter, K.5
Wallace, D.C.6
-
37
-
-
0002959109
-
Mitochondrial DNA mutations and lipid peroxidation in human aging
-
(Berdanier CD, ed). Boca Raton, FL: CRC Press
-
Wei Y-H, Kao S-H. Mitochondrial DNA mutations and lipid peroxidation in human aging. In: Nutrients and Gene Expression (Berdanier CD, ed). Boca Raton, FL: CRC Press, pp 165-188, 1996.
-
(1996)
Nutrients and Gene Expression
, pp. 165-188
-
-
Wei, Y.-H.1
Kao, S.-H.2
-
38
-
-
0026553006
-
Age-dependent 6-kb deletion in human mitochondrial DNA
-
Yen TC, Pang CY, Hsieh RH, Su CH, King KL, Wei YH. Age-dependent 6-kb deletion in human mitochondrial DNA. Biochem Mol Biol Int 26:457-468, 1992.
-
(1992)
Biochem Mol Biol Int
, vol.26
, pp. 457-468
-
-
Yen, T.C.1
Pang, C.Y.2
Hsieh, R.H.3
Su, C.H.4
King, K.L.5
Wei, Y.H.6
-
39
-
-
0025741445
-
Aging-associated 5-kb deletion in human liver mitochondrial DNA
-
Yen TC, Su HH, King KL, Wei YH. Aging-associated 5-kb deletion in human liver mitochondrial DNA. Biochem Biophys Res Commun 178:124-131, 1991.
-
(1991)
Biochem Biophys Res Commun
, vol.178
, pp. 124-131
-
-
Yen, T.C.1
Su, H.H.2
King, K.L.3
Wei, Y.H.4
-
40
-
-
0026528416
-
Mitochondrial DNA mutations in human diseases: A review
-
Lestienne P. Mitochondrial DNA mutations in human diseases: A review. Biochimie 74:123-130, 1992.
-
(1992)
Biochimie
, vol.74
, pp. 123-130
-
-
Lestienne, P.1
-
41
-
-
0025250482
-
Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: A new autosomal dominant disease
-
Zeviani M, Bresolin N, Gellera C, Bordoni A, Pannacci M, Amati P, Moggio M, Servidei S, Scarlato G, DiDonato S. Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: A new autosomal dominant disease. Am J Hum Genet 47:904-914, 1990.
-
(1990)
Am J Hum Genet
, vol.47
, pp. 904-914
-
-
Zeviani, M.1
Bresolin, N.2
Gellera, C.3
Bordoni, A.4
Pannacci, M.5
Amati, P.6
Moggio, M.7
Servidei, S.8
Scarlato, G.9
DiDonato, S.10
-
42
-
-
0027297967
-
Transcribed heteroplasmic repeated sequences in porcine mtDNA D-loop region
-
Ghivizzani SC, Mackay SD, Madsen CS, Laipis PJ, Hauswirth WW. Transcribed heteroplasmic repeated sequences in porcine mtDNA D-loop region. J Mol Evol 137:36-47, 1993.
-
(1993)
J Mol Evol
, vol.137
, pp. 36-47
-
-
Ghivizzani, S.C.1
Mackay, S.D.2
Madsen, C.S.3
Laipis, P.J.4
Hauswirth, W.W.5
-
43
-
-
0026471872
-
Accumulation of deletions in human mitochondria during normal aging: Analysis by quantitative PCR
-
Simonetti S, Chen X, DiMauro S, Schon EA. Accumulation of deletions in human mitochondria during normal aging: Analysis by quantitative PCR. Biochem Biophys Acta 1180:113-122, 1992.
-
(1992)
Biochem Biophys Acta
, vol.1180
, pp. 113-122
-
-
Simonetti, S.1
Chen, X.2
DiMauro, S.3
Schon, E.A.4
-
44
-
-
0027431036
-
Age dependency of mtDNA decrease differs in different tissues of rat
-
Asano K, Nakamura M, Sato T, Tauchi H, Asano A. Age dependency of mtDNA decrease differs in different tissues of rat. J Biochem 114:303-306, 1993.
-
(1993)
J Biochem
, vol.114
, pp. 303-306
-
-
Asano, K.1
Nakamura, M.2
Sato, T.3
Tauchi, H.4
Asano, A.5
-
45
-
-
0027244097
-
Mitochondrial DNA remains intact during Drosophila aging, but the levels of mitochondrial transcripts are significantly reduced
-
Calleja M, Pena P, Ugalde C, Ferreiro C, Marco R, Garesse R. Mitochondrial DNA remains intact during Drosophila aging, but the levels of mitochondrial transcripts are significantly reduced. J Biol Chem 268:1891-1898, 1993.
-
(1993)
J Biol Chem
, vol.268
, pp. 1891-1898
-
-
Calleja, M.1
Pena, P.2
Ugalde, C.3
Ferreiro, C.4
Marco, R.5
Garesse, R.6
-
46
-
-
0026463740
-
Does the mitochondrial DNA play a role in the pathogenesis of diabetes?
-
Gerbitz KD. Does the mitochondrial DNA play a role in the pathogenesis of diabetes? Diabetologia 35:1181-1186, 1992.
-
(1992)
Diabetologia
, vol.35
, pp. 1181-1186
-
-
Gerbitz, K.D.1
-
47
-
-
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
-
48
-
-
0027511591
-
Diabetes mellitus is one of the heterogeneous phenotypic features of a mtDNA point mutation within the tRNA leu gene
-
Gerbitz KD, Paprotta A, Jaksch M, Zierz S, Drechsel J. Diabetes mellitus is one of the heterogeneous phenotypic features of a mtDNA point mutation within the tRNA leu gene. FEES Lett 321:194-196, 1993.
-
(1993)
FEES Lett
, vol.321
, pp. 194-196
-
-
Gerbitz, K.D.1
Paprotta, A.2
Jaksch, M.3
Zierz, S.4
Drechsel, J.5
-
49
-
-
0026462744
-
Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA
-
Reardon W, Ross RJ, Sweeney MG, Luxon LM, Pembry ME, Harding AE, Trembath RC. Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA. Lancet 340:1376-1379, 1992.
-
(1992)
Lancet
, vol.340
, pp. 1376-1379
-
-
Reardon, W.1
Ross, R.J.2
Sweeney, M.G.3
Luxon, L.M.4
Pembry, M.E.5
Harding, A.E.6
Trembath, R.C.7
-
50
-
-
0027496790
-
Substitution rate variation among sites in hypervariable region 1 of human mtDNA
-
Wakeley J. Substitution rate variation among sites in hypervariable region 1 of human mtDNA. J Mol Evol 37:613-623, 1993.
-
(1993)
J Mol Evol
, vol.37
, pp. 613-623
-
-
Wakeley, J.1
-
51
-
-
0026654907
-
The sequence of human mtDNA: The question of errors versus polymorphisms
-
Howell N, McCullough DA, Kubacka I, Halvorson S, Mackey D. The sequence of human mtDNA: The question of errors versus polymorphisms. Am J Human Genet 50:1333-1337, 1992.
-
(1992)
Am J Human Genet
, vol.50
, pp. 1333-1337
-
-
Howell, N.1
McCullough, D.A.2
Kubacka, I.3
Halvorson, S.4
Mackey, D.5
-
52
-
-
0023201498
-
Concordance for type 2 (noninsulin-dependent) diabetes mellitus in male twins
-
Newman B, Shelby JV, King MC, Selmenda C, Fabsitz R, Friedman GD. Concordance for type 2 (noninsulin-dependent) diabetes mellitus in male twins. Diabetologia 30:763-768, 1987.
-
(1987)
Diabetologia
, vol.30
, pp. 763-768
-
-
Newman, B.1
Shelby, J.V.2
King, M.C.3
Selmenda, C.4
Fabsitz, R.5
Friedman, G.D.6
-
53
-
-
0002806616
-
Genetics of diabetes mellitus
-
Alberti KGMM, Defronzo RA, Keen H, Zimmlet P, Chichester T, Eds. New York: Wiley
-
Vanheim CM, Rotter JI. Genetics of diabetes mellitus. In: Alberti KGMM, Defronzo RA, Keen H, Zimmlet P, Chichester T, Eds. International Textbook of Diabetes Mellitus. New York: Wiley, pp 31-98, 1992.
-
(1992)
International Textbook of Diabetes Mellitus
, pp. 31-98
-
-
Vanheim, C.M.1
Rotter, J.I.2
-
54
-
-
0026639928
-
Human glucokinase gene: Isolation, characterization and identification of two missense mutations linked to early-onset noninsulin-dependent (type 2) diabetes mellitus
-
Stoffel M, Froguel PH, Takeda J, Zouali H, Vionnet N, Nishi S, Weber IT, Harrison RW, Pilkis SJ, Lesage S, Vaxillaire M. Velho G, Sun F, Iris F, Passa PH, Cohen D, Bell GI. Human glucokinase gene: Isolation, characterization and identification of two missense mutations linked to early-onset noninsulin-dependent (type 2) diabetes mellitus. Proc Natl Acad Sci U S A 89:7698-7702, 1992.
-
(1992)
Proc Natl Acad Sci U S A
, vol.89
, pp. 7698-7702
-
-
Stoffel, M.1
Froguel, P.H.2
Takeda, J.3
Zouali, H.4
Vionnet, N.5
Nishi, S.6
Weber, I.T.7
Harrison, R.W.8
Pilkis, S.J.9
Lesage, S.10
Vaxillaire, M.11
Velho, G.12
Sun, F.13
Iris, F.14
Passa, P.H.15
Cohen, D.16
Bell, G.I.17
-
55
-
-
0027312093
-
Mutations in the human glucokinase gene and diabetes mellitus
-
Bell GI, Froguel P, Nishi S, Pilkis SJ, Stoffel M, Takeda J, Vionnet N, Yasuda K. Mutations in the human glucokinase gene and diabetes mellitus. Trends Endocrinol Metab 4:86-90, 1993.
-
(1993)
Trends Endocrinol Metab
, vol.4
, pp. 86-90
-
-
Bell, G.I.1
Froguel, P.2
Nishi, S.3
Pilkis, S.J.4
Stoffel, M.5
Takeda, J.6
Vionnet, N.7
Yasuda, K.8
-
56
-
-
0027523052
-
Glucokinase gene variants in the common form of NIDDM
-
Chiu KC, Tanizawa Y, Permutt MA. Glucokinase gene variants in the common form of NIDDM. Diabetes 42:579-582, 1993.
-
(1993)
Diabetes
, vol.42
, pp. 579-582
-
-
Chiu, K.C.1
Tanizawa, Y.2
Permutt, M.A.3
-
57
-
-
0027358380
-
Glucokinase as pancreatic β-cell, glucose sensor and diabetes gene
-
Matschinsky FM, Liang Y, Keavan P, Wang L, Froguel P, Velho G, Cohen D, Permutt MA, Tanizawa Y, Jetton TL, Niswender K, Magnuson MA. Glucokinase as pancreatic β-cell, glucose sensor and diabetes gene. J Clin Invest 2:2092-2098, 1993.
-
(1993)
J Clin Invest
, vol.2
, pp. 2092-2098
-
-
Matschinsky, F.M.1
Liang, Y.2
Keavan, P.3
Wang, L.4
Froguel, P.5
Velho, G.6
Cohen, D.7
Permutt, M.A.8
Tanizawa, Y.9
Jetton, T.L.10
Niswender, K.11
Magnuson, M.A.12
-
58
-
-
8044260804
-
Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families
-
Velho G, Blanche H, Vaxillaire M, Bellanne-Chantelot C, Pardini VC, Timsit J, Passa P, Deschamps I, Robert JJ, Weber IT, Marotta D, Pilkis SJ, Lipkind GM, Bell GI, Froguel P. Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families. Diabetologia 40:217-224, 1997.
-
(1997)
Diabetologia
, vol.40
, pp. 217-224
-
-
Velho, G.1
Blanche, H.2
Vaxillaire, M.3
Bellanne-Chantelot, C.4
Pardini, V.C.5
Timsit, J.6
Passa, P.7
Deschamps, I.8
Robert, J.J.9
Weber, I.T.10
Marotta, D.11
Pilkis, S.J.12
Lipkind, G.M.13
Bell, G.I.14
Froguel, P.15
-
59
-
-
0030765909
-
Evidence for association between the class 1 subset of the insulin gene minisatellite (IDDM 2 locus) and IDDM in the Japanese population
-
Awata T, Kurihara S, Kikuchi C, Takai S-I, Inoue I, Ishii C, Takahashi K, Negishi K, Yoshida Y, Hagura R, Kanazawa Y, Katayama S. Evidence for association between the class 1 subset of the insulin gene minisatellite (IDDM 2 locus) and IDDM in the Japanese population. Diabetes 46:1637-1642, 1997.
-
(1997)
Diabetes
, vol.46
, pp. 1637-1642
-
-
Awata, T.1
Kurihara, S.2
Kikuchi, C.3
Takai, S.-I.4
Inoue, I.5
Ishii, C.6
Takahashi, K.7
Negishi, K.8
Yoshida, Y.9
Hagura, R.10
Kanazawa, Y.11
Katayama, S.12
-
60
-
-
0030662718
-
Release of incompletely processed proinsulin is the cause of the disproportionate proinsulinemia of NIDDM
-
Kahn SE, Halban PA. Release of incompletely processed proinsulin is the cause of the disproportionate proinsulinemia of NIDDM. Diabetes 46:1725-1732, 1997.
-
(1997)
Diabetes
, vol.46
, pp. 1725-1732
-
-
Kahn, S.E.1
Halban, P.A.2
-
61
-
-
0022625728
-
Prolonged plasma half-life of insulin in patients with a genetic defect of high affinity binding sites
-
Dreyer M, Matthaei S, Kuhnau J, Rudiger HW. Prolonged plasma half-life of insulin in patients with a genetic defect of high affinity binding sites. Horm Metab Res 18:247-249, 1986.
-
(1986)
Horm Metab Res
, vol.18
, pp. 247-249
-
-
Dreyer, M.1
Matthaei, S.2
Kuhnau, J.3
Rudiger, H.W.4
-
62
-
-
0027286436
-
Uncoupling of mitochondrial oxidative phosphorylation abolishes the stimulatory action of insulin on the binding of glycolytic enzymes to muscle cytoskeleton
-
Livnat TM, Chen-Zion M, Beitner R. Uncoupling of mitochondrial oxidative phosphorylation abolishes the stimulatory action of insulin on the binding of glycolytic enzymes to muscle cytoskeleton. Int J Biochem 25:993-997, 1993.
-
(1993)
Int J Biochem
, vol.25
, pp. 993-997
-
-
Livnat, T.M.1
Chen-Zion, M.2
Beitner, R.3
-
63
-
-
0029813021
-
2+, substrate, and ADP
-
2+, substrate, and ADP. Biochem J 318:615-621, 1996.
-
(1996)
Biochem J
, vol.318
, pp. 615-621
-
-
Civelek, V.N.1
Deeney, J.T.2
Shalosky, N.J.3
Tornheim, K.4
Hansford, R.G.5
Prentki, M.6
Corkey, B.E.7
-
64
-
-
0030016913
-
Adenosine diphosphate as an intracellular regulator of insulin secretion
-
Nichols CG, Shyng SL, Nestorowicz A, Glaser B, Clement JP IV, Gonzalez G, Aguilar-Bryan L, Permutt MA, Bryan J. Adenosine diphosphate as an intracellular regulator of insulin secretion. Science 272:1785-1787, 1996.
-
(1996)
Science
, vol.272
, pp. 1785-1787
-
-
Nichols, C.G.1
Shyng, S.L.2
Nestorowicz, A.3
Glaser, B.4
Clement IV, J.P.5
Gonzalez, G.6
Aguilar-Bryan, L.7
Permutt, M.A.8
Bryan, J.9
-
66
-
-
0030254594
-
Impaired glucose tolerance in the young
-
Isshiki G. Impaired glucose tolerance in the young. Nippon Rinsho 54:2766-2772, 1997.
-
(1997)
Nippon Rinsho
, vol.54
, pp. 2766-2772
-
-
Isshiki, G.1
-
67
-
-
0025854490
-
Importance of maternal history of noninsulin-dependent diabetic patients
-
Alcolado JC, Alcolado R. Importance of maternal history of noninsulin-dependent diabetic patients. BMJ 302:1178-1180, 1991.
-
(1991)
BMJ
, vol.302
, pp. 1178-1180
-
-
Alcolado, J.C.1
Alcolado, R.2
-
68
-
-
0028279885
-
Mitochondrial gene defects in patients with NIDDM
-
Alcolado JC, Majid A, Brockington M, Sweeney MG, Morgan R, Rees A, Harding AE, Barnett AH. Mitochondrial gene defects in patients with NIDDM. Diabetologia 37:372-376, 1994.
-
(1994)
Diabetologia
, vol.37
, pp. 372-376
-
-
Alcolado, J.C.1
Majid, A.2
Brockington, M.3
Sweeney, M.G.4
Morgan, R.5
Rees, A.6
Harding, A.E.7
Barnett, A.H.8
-
69
-
-
0028888396
-
Maternally inherited diabetes mellitus: The role of mitochondrial DNA defects
-
Alcolado JC, Thomas AW. Maternally inherited diabetes mellitus: The role of mitochondrial DNA defects. Diabet Med 12:102-108, 1995.
-
(1995)
Diabet Med
, vol.12
, pp. 102-108
-
-
Alcolado, J.C.1
Thomas, A.W.2
-
70
-
-
0028528250
-
Clinical characterization of diabetes mellitus in the families with mitochondrial encephalomyopathies
-
Suzuki S. Clinical characterization of diabetes mellitus in the families with mitochondrial encephalomyopathies. Nippon Rinsho 52:2606-2610, 1994.
-
(1994)
Nippon Rinsho
, vol.52
, pp. 2606-2610
-
-
Suzuki, S.1
-
71
-
-
0028153078
-
Lys mutation
-
Lys mutation. Diabetes Care 17:1428-1432, 1994.
-
(1994)
Diabetes Care
, vol.17
, pp. 1428-1432
-
-
Suzuki, S.1
Hinokio, Y.2
Hirai, S.3
Onoda, M.4
Matsumoto, M.5
Ohtomo, M.6
Kawasaki, H.7
Satoh, Y.8
Akai, H.9
Abe, K.10
-
72
-
-
0030279938
-
Clinical picture of a case of diabetes with mitochondrial tRNA mutation at position 3271
-
Suzuki Y, Tsukuda K, Atsumi Y, Goto Y, Hosokawa K, Asahina T, Nonaka I, Matsuoka K, Oka Y. Clinical picture of a case of diabetes with mitochondrial tRNA mutation at position 3271. Diabetes Care 19:1304-1305, 1996.
-
(1996)
Diabetes Care
, vol.19
, pp. 1304-1305
-
-
Suzuki, Y.1
Tsukuda, K.2
Atsumi, Y.3
Goto, Y.4
Hosokawa, K.5
Asahina, T.6
Nonaka, I.7
Matsuoka, K.8
Oka, Y.9
-
73
-
-
0029008728
-
A new mitochondrial DNA deletion associated with diabetic amyotrophy, diabetic myoatrophy and diabetic fatty liver
-
Hinokio Y, Suzuki S, Komatu K, Ohtomo M, Onoda M, Matsumoto M, Hirai S, Sato Y, Akai H, Abe K, Miyabayasi S, Abe R, Toyoto T. A new mitochondrial DNA deletion associated with diabetic amyotrophy, diabetic myoatrophy and diabetic fatty liver. Muscle Nerve 3:S142-S149, 1995.
-
(1995)
Muscle Nerve
, vol.3
-
-
Hinokio, Y.1
Suzuki, S.2
Komatu, K.3
Ohtomo, M.4
Onoda, M.5
Matsumoto, M.6
Hirai, S.7
Sato, Y.8
Akai, H.9
Abe, K.10
Miyabayasi, S.11
Abe, R.12
Toyoto, T.13
-
74
-
-
0028952456
-
Insulin sensitivity and mitochondrial gene mutation
-
Walker M, Taylor RW, Stewart MW, Bindoff LA, Jackson MJ, Alberti GK, Turnbull DM. Insulin sensitivity and mitochondrial gene mutation. Diabetes Care 18:273-275, 1995.
-
(1995)
Diabetes Care
, vol.18
, pp. 273-275
-
-
Walker, M.1
Taylor, R.W.2
Stewart, M.W.3
Bindoff, L.A.4
Jackson, M.J.5
Alberti, G.K.6
Turnbull, D.M.7
-
75
-
-
0024787573
-
Normal insulin receptors in mitochondrial myopathies with ophthalmoplegia
-
Piccolo G, Aschei M, Ricordi A, Banfi P, Lo Curto F, Fratino P. Normal insulin receptors in mitochondrial myopathies with ophthalmoplegia. J Neurol Sci 94:163-172, 1989.
-
(1989)
J Neurol Sci
, vol.94
, pp. 163-172
-
-
Piccolo, G.1
Aschei, M.2
Ricordi, A.3
Banfi, P.4
Lo Curto, F.5
Fratino, P.6
-
76
-
-
0029867177
-
Insulin resistance associated with maternally inherited diabetes and deafness
-
Gebhart SS, Shoffner JM, Koontz D, Kaufman A, Wallace D. Insulin resistance associated with maternally inherited diabetes and deafness. Metabolism 45:526-531, 1996.
-
(1996)
Metabolism
, vol.45
, pp. 526-531
-
-
Gebhart, S.S.1
Shoffner, J.M.2
Koontz, D.3
Kaufman, A.4
Wallace, D.5
-
77
-
-
0029818009
-
β-cell loss and glucose-induced signaling defects in diabetes mellitus caused by mitochondrial tRNA(Leu(UUR)) gene mutation
-
Oka Y, Katagiri H, Ishihara H, Asano T, Kobayashi T, Kikuchi M. β-cell loss and glucose-induced signaling defects in diabetes mellitus caused by mitochondrial tRNA(Leu(UUR)) gene mutation. Diabet Med 13.S98-S102, 1996.
-
(1996)
Diabet Med
, vol.13
-
-
Oka, Y.1
Katagiri, H.2
Ishihara, H.3
Asano, T.4
Kobayashi, T.5
Kikuchi, M.6
-
78
-
-
0030067124
-
A lesson in metabolic regulation inspired by the glucokinase glucose sensor paradigm
-
Matschinsky FM. A lesson in metabolic regulation inspired by the glucokinase glucose sensor paradigm. Diabetes 45:223-241, 1996.
-
(1996)
Diabetes
, vol.45
, pp. 223-241
-
-
Matschinsky, F.M.1
-
79
-
-
0027145131
-
Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis: Is the tRNA(Leu(UUR)) gene an etiologic hot spot?
-
Moraes CT, Ciacci F, Bonilla E, Jansen C, Hirano M, Rao N, Locelace RE, Rowland LP, Schon EA, DiMauro S. Two novel pathogenic mitochondrial DNA mutations affecting organelle number and protein synthesis: Is the tRNA(Leu(UUR)) gene an etiologic hot spot? J Clin Invest 92:2909-2915, 1993.
-
(1993)
J Clin Invest
, vol.92
, pp. 2909-2915
-
-
Moraes, C.T.1
Ciacci, F.2
Bonilla, E.3
Jansen, C.4
Hirano, M.5
Rao, N.6
Locelace, R.E.7
Rowland, L.P.8
Schon, E.A.9
DiMauro, S.10
-
80
-
-
0027715020
-
A new point mutation associated with mitochondrial encephalomyopathy
-
Morten KJ, Cooper JM, Brown GK, Lake BD, Pike D, Poulton J. A new point mutation associated with mitochondrial encephalomyopathy. Hum Mol Genet 2:2081-2087, 1993.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 2081-2087
-
-
Morten, K.J.1
Cooper, J.M.2
Brown, G.K.3
Lake, B.D.4
Pike, D.5
Poulton, J.6
-
81
-
-
0003182407
-
Maternal inherited diabetes deafness of the young (MIDDY), a new mitochondrial syndrome
-
Lempkes HHPJ, de Vijlder M, Struyvenberg PAA, van de Kamp JJP, Frolich M. Maternal inherited diabetes deafness of the young (MIDDY), a new mitochondrial syndrome. Diabetologia 32:509A, 1989.
-
(1989)
Diabetologia
, vol.32
-
-
Lempkes, H.H.P.J.1
De Vijlder, M.2
Struyvenberg, P.A.A.3
Van De Kamp, J.J.P.4
Frolich, M.5
-
82
-
-
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 Der Ouweland, J.M.W.1
Lemkes, H.H.P.J.2
Ruitenbeek, W.3
Sandkuijl, L.A.4
De Vijlder, M.F.5
Struyvenberg, P.A.A.6
Van De Kamp, J.J.P.7
Maassen, J.A.8
-
83
-
-
0029875834
-
Leu(UUR) gene mutation
-
Leu(UUR) gene mutation. Diabetes 45:478-487, 1996.
-
(1996)
Diabetes
, vol.45
, pp. 478-487
-
-
Velho, G.1
Byrne, M.M.2
Clement, K.3
Sturis, J.4
Pueyo, M.E.5
Blanche, H.6
Vionnet, N.7
Fiet, J.8
Passa, P.9
Robert, J.J.10
Polonsky, K.S.11
Froguel, P.12
-
84
-
-
0026585685
-
Endocrine abnormalities in mitochondrial myopathy with external ophthalmoplegia
-
Quade A, Zierz S, Klingmuller D. Endocrine abnormalities in mitochondrial myopathy with external ophthalmoplegia. Clin Invest 70:396-402, 1992.
-
(1992)
Clin Invest
, vol.70
, pp. 396-402
-
-
Quade, A.1
Zierz, S.2
Klingmuller, D.3
-
85
-
-
0027381483
-
Maternally transmitted partial direct tandem duplication of mitochondrial DNA associated with diabetes mellitus
-
Dunbar DR, Moonie PA, Swingler RJ, Davidson D, Roberts R, Holt IJ. Maternally transmitted partial direct tandem duplication of mitochondrial DNA associated with diabetes mellitus. Hum Mol Genet 2:1619-1624, 1993.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1619-1624
-
-
Dunbar, D.R.1
Moonie, P.A.2
Swingler, R.J.3
Davidson, D.4
Roberts, R.5
Holt, I.J.6
-
86
-
-
0024499802
-
Duplications of mitochondrial DNA in mitochondrial myopathy
-
Poulton J, Deadman ME, Gardiner RM. Duplications of mitochondrial DNA in mitochondrial myopathy. Lancet 1:236-240, 1989.
-
(1989)
Lancet
, vol.1
, pp. 236-240
-
-
Poulton, J.1
Deadman, M.E.2
Gardiner, R.M.3
-
87
-
-
0028286575
-
Are duplications of mitochondrial DNA characteristic of Kearns-Sayre syndrome?
-
Poulton J, Morten KJ, Weber K, Brown GK, Bindoff L. Are duplications of mitochondrial DNA characteristic of Kearns-Sayre syndrome? Hum Mol Genet 3:947-951, 1994.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 947-951
-
-
Poulton, J.1
Morten, K.J.2
Weber, K.3
Brown, G.K.4
Bindoff, L.5
-
88
-
-
0029040769
-
Mitochondrial DNA, diabetes, and pancreatic pathology in Kearns-Sayre syndrome
-
Poulton J, O'Rahilly S, Morten KJ, Clark A. Mitochondrial DNA, diabetes, and pancreatic pathology in Kearns-Sayre syndrome. Diabetologia 38:868-871, 1995.
-
(1995)
Diabetologia
, vol.38
, pp. 868-871
-
-
Poulton, J.1
O'Rahilly, S.2
Morten, K.J.3
Clark, A.4
-
89
-
-
0026569283
-
Maternally inherited duplication of the mitochondrial genome in a syndrome of proximal tubulopathy, diabetes mellitus, and cerebellar ataxia
-
Rotig A, Bessis JL, Romero N, Cormier V, Saudubray JM, Narcy P, Lenoir G, Rustin P, Munnich A. Maternally inherited duplication of the mitochondrial genome in a syndrome of proximal tubulopathy, diabetes mellitus, and cerebellar ataxia. Am J Hum Genet 50:364-370, 1992.
-
(1992)
Am J Hum Genet
, vol.50
, pp. 364-370
-
-
Rotig, A.1
Bessis, J.L.2
Romero, N.3
Cormier, V.4
Saudubray, J.M.5
Narcy, P.6
Lenoir, G.7
Rustin, P.8
Munnich, A.9
-
90
-
-
0026041854
-
Congenital hypoplastic anemia, diabetes, and severe renal tubular dysfunction associated with a mitochondrial DNA deletion
-
Majander A, Suomaleinen A, Vettebranta K, Sarioly H, Pekkio M, Holmberg C, Pihko H. Congenital hypoplastic anemia, diabetes, and severe renal tubular dysfunction associated with a mitochondrial DNA deletion. Pediatr Res 30:327-330, 1991.
-
(1991)
Pediatr Res
, vol.30
, pp. 327-330
-
-
Majander, A.1
Suomaleinen, A.2
Vettebranta, K.3
Sarioly, H.4
Pekkio, M.5
Holmberg, C.6
Pihko, H.7
-
91
-
-
0027310104
-
Pearson bone marrow-pancreas syndrome with insulin-dependent diabetes, progressive renal tubulopathy, organic aciduria, and elevated fetal haemoglobin caused by deletion and duplication of mitochondrial DNA
-
Superti-Furga A, Schoenle E, Tuchschmid P, Caduff R, Sabato V, DeMattia D, Gitzelmann R, Steinmann B. Pearson bone marrow-pancreas syndrome with insulin-dependent diabetes, progressive renal tubulopathy, organic aciduria, and elevated fetal haemoglobin caused by deletion and duplication of mitochondrial DNA. Eur J Pediatr 152:44-50, 1993.
-
(1993)
Eur J Pediatr
, vol.152
, pp. 44-50
-
-
Superti-Furga, A.1
Schoenle, E.2
Tuchschmid, P.3
Caduff, R.4
Sabato, V.5
DeMattia, D.6
Gitzelmann, R.7
Steinmann, B.8
-
92
-
-
2542453285
-
Progressive ocular myopathy with ovarian insufficiency and diabetes mellitus: Report of a case
-
Lankin M, Locke S. Progressive ocular myopathy with ovarian insufficiency and diabetes mellitus: Report of a case. Diabetes 10:228-231, 1961.
-
(1961)
Diabetes
, vol.10
, pp. 228-231
-
-
Lankin, M.1
Locke, S.2
-
93
-
-
0019524247
-
Mitochondrial myopathy: A study of clinically affected and asymptomatic members of a six-generation family
-
Mechler F, Fawcett PRW, Mastaglia FL, Hudgson P. Mitochondrial myopathy: A study of clinically affected and asymptomatic members of a six-generation family. J Neurol Sci 50:191-200, 1981.
-
(1981)
J Neurol Sci
, vol.50
, pp. 191-200
-
-
Mechler, F.1
Fawcett, P.R.W.2
Mastaglia, F.L.3
Hudgson, P.4
-
94
-
-
0029555574
-
Mitochondrial encephalomyopathies: 3243 mutation as a central matter
-
Goto Y, Nonaka I. Mitochondrial encephalomyopathies: 3243 mutation as a central matter. Rinsho Shinkeigaku 35:1425-1426, 1995.
-
(1995)
Rinsho Shinkeigaku
, vol.35
, pp. 1425-1426
-
-
Goto, Y.1
Nonaka, I.2
-
95
-
-
0027915545
-
Mitochondrial gene mutations and diabetes mellitus
-
Schulz JB, Klockgether T, Dichgans J, Seibel P, Reichmann H. Mitochondrial gene mutations and diabetes mellitus. Lancet 341:438-449, 1993.
-
(1993)
Lancet
, vol.341
, pp. 438-449
-
-
Schulz, J.B.1
Klockgether, T.2
Dichgans, J.3
Seibel, P.4
Reichmann, H.5
-
96
-
-
0027477373
-
Mitochondrial gene mutations and diabetes mellitus
-
Sue CM, Holmes-Walker DJ, Morris JGL, Bovages SC, Crimmins DS, Byrne E. Mitochondrial gene mutations and diabetes mellitus. Lancet 341:437-438, 1993.
-
(1993)
Lancet
, vol.341
, pp. 437-438
-
-
Sue, C.M.1
Holmes-Walker, D.J.2
Morris, J.G.L.3
Bovages, S.C.4
Crimmins, D.S.5
Byrne, E.6
-
97
-
-
0026849690
-
Maternally transmitted diabetes and deafness associated with a 10.4-kb mitochondrial DNA deletion
-
Ballinger SW, Shoffner JM, Hedaya EV, Trounce I, Polak MA, Koontz DA, Wallace DC. Maternally transmitted diabetes and deafness associated with a 10.4-kb mitochondrial DNA deletion. Nat Genet 1:11-15, 1992.
-
(1992)
Nat Genet
, vol.1
, pp. 11-15
-
-
Ballinger, S.W.1
Shoffner, J.M.2
Hedaya, E.V.3
Trounce, I.4
Polak, M.A.5
Koontz, D.A.6
Wallace, D.C.7
-
98
-
-
0027935776
-
Mitochondrial diabetes revisted
-
Ballinger SW, Shoffner JM, Gebhart S, Koontz DA, Wallace DC. Mitochondrial diabetes revisted. Nat Genet 7:458-459, 1994.
-
(1994)
Nat Genet
, vol.7
, pp. 458-459
-
-
Ballinger, S.W.1
Shoffner, J.M.2
Gebhart, S.3
Koontz, D.A.4
Wallace, D.C.5
-
99
-
-
0027474477
-
Mitochondrial DNA deletion in human myocardium
-
Takeda N, Tanamura A, Iwai T, Nakamura I, Kato M, Ohkuba T, Noma K. Mitochondrial DNA deletion in human myocardium. Mol Cell Biochem 119:105-108, 1993.
-
(1993)
Mol Cell Biochem
, vol.119
, pp. 105-108
-
-
Takeda, N.1
Tanamura, A.2
Iwai, T.3
Nakamura, I.4
Kato, M.5
Ohkuba, T.6
Noma, K.7
-
100
-
-
0029611068
-
A point mutation in the mitochondrial DNA of diabetes prone BHE/Cdb rats
-
Mathews CE, McGraw RA, Berdanier CD. A point mutation in the mitochondrial DNA of diabetes prone BHE/Cdb rats. FASEB J 9:1638-1642, 1995.
-
(1995)
FASEB J
, vol.9
, pp. 1638-1642
-
-
Mathews, C.E.1
McGraw, R.A.2
Berdanier, C.D.3
-
101
-
-
0342395722
-
Mutations in mitochondrial ATPase 8 gene are associated with NIDDM
-
Anderson C, Hermstadt C, Miller C, Olefsky J, Davis R. Mutations in mitochondrial ATPase 8 gene are associated with NIDDM. Diabetes 46:174A, 1997.
-
(1997)
Diabetes
, vol.46
-
-
Anderson, C.1
Hermstadt, C.2
Miller, C.3
Olefsky, J.4
Davis, R.5
-
102
-
-
0020482020
-
Energy requirements for protein synthesis in isolated rat liver mitochondria
-
Mutvei A, Nelson BD. Energy requirements for protein synthesis in isolated rat liver mitochondria. Biochem Biophys Res Comm 105:916-921, 1982.
-
(1982)
Biochem Biophys Res Comm
, vol.105
, pp. 916-921
-
-
Mutvei, A.1
Nelson, B.D.2
-
103
-
-
0026606220
-
Glucose sensing by the pancreatic β cell. The mitochondrial part
-
Malaisse WJ. Glucose sensing by the pancreatic β cell. The mitochondrial part. Int J Biochem 24:693-701, 1992.
-
(1992)
Int J Biochem
, vol.24
, pp. 693-701
-
-
Malaisse, W.J.1
-
104
-
-
33749714153
-
Inheritance of a mitochondrial DNA defect and impaired glucose tolerance in BHE/Cdb rats
-
in press
-
Mathews CE, Berdanier CD. Inheritance of a mitochondrial DNA defect and impaired glucose tolerance in BHE/Cdb rats. Diabetologia (in press).
-
Diabetologia
-
-
Mathews, C.E.1
Berdanier, C.D.2
-
105
-
-
0011790119
-
Analysis of a DNA segment from rat liver mitochondria containing genes for the cytochrome oxidase subunits I, II, and ATPase 6 and several tRNA genes
-
Grosskopf R, Feldmann H. Analysis of a DNA segment from rat liver mitochondria containing genes for the cytochrome oxidase subunits I, II, and ATPase 6 and several tRNA genes. Curr Genet 4:151-158, 1981.
-
(1981)
Curr Genet
, vol.4
, pp. 151-158
-
-
Grosskopf, R.1
Feldmann, H.2
-
106
-
-
0025732931
-
The BHE rat: An animal model for the study of noninsulin-dependent diabetes mellitus
-
Berdanier CD. The BHE rat: An animal model for the study of noninsulin-dependent diabetes mellitus. FASEB J 5:2139-2144, 1991.
-
(1991)
FASEB J
, vol.5
, pp. 2139-2144
-
-
Berdanier, C.D.1
-
107
-
-
0006429090
-
Diet can influence mitochondrial respiration in genetically diabetic BHE/Cdb rats: A review
-
Berdanier CD. Diet can influence mitochondrial respiration in genetically diabetic BHE/Cdb rats: A review. Res Trends Endocrinol 12:103-115, 1993.
-
(1993)
Res Trends Endocrinol
, vol.12
, pp. 103-115
-
-
Berdanier, C.D.1
-
108
-
-
0002210892
-
Noninsulin-dependent diabetes in the non-obese BHE/ Cdb rat
-
Shafrir E, Ed. London: Smith Gordon Publishers
-
Berdanier CD. Noninsulin-dependent diabetes in the non-obese BHE/ Cdb rat. In: Shafrir E, Ed. Recent Advances in Animal Diabetes. London: Smith Gordon Publishers, pp 231-246, 1994.
-
(1994)
Recent Advances in Animal Diabetes
, pp. 231-246
-
-
Berdanier, C.D.1
-
109
-
-
0026778034
-
Lifespan is shortened in BHE/Cdb rats fed a diet containing 9% menhaden oil and 1% corn oil
-
Berdanier Cd, Johnson B, Hartle DK, Crowell WA. Lifespan is shortened in BHE/Cdb rats fed a diet containing 9% menhaden oil and 1% corn oil. J Nutr 122:1109-1131, 1992.
-
(1992)
J Nutr
, vol.122
, pp. 1109-1131
-
-
Berdanier, C.D.1
Johnson, B.2
Hartle, D.K.3
Crowell, W.A.4
-
110
-
-
0031693596
-
Whole egg delays the age-related impaired glucose tolerance of BHE/Cdb rats
-
Berdanier CD, Kras KM, Wickwire K, Hall DG. Whole egg delays the age-related impaired glucose tolerance of BHE/Cdb rats. Proc Soc Exp Biol Med 219:28-36, 1998.
-
(1998)
Proc Soc Exp Biol Med
, vol.219
, pp. 28-36
-
-
Berdanier, C.D.1
Kras, K.M.2
Wickwire, K.3
Hall, D.G.4
-
111
-
-
0001929885
-
Progressive glucose intolerance and renal disease in aging rats
-
Berdanier CD, Kras KM, Hall DG, Gunnett C, Hartle D. Progressive glucose intolerance and renal disease in aging rats. Int J Diabetes 5:27-38, 1997.
-
(1997)
Int J Diabetes
, vol.5
, pp. 27-38
-
-
Berdanier, C.D.1
Kras, K.M.2
Hall, D.G.3
Gunnett, C.4
Hartle, D.5
-
112
-
-
0017694118
-
Comarative studies on lipogenesis and cholesterogenesis in lipemic BHE rats and normal Wistar rats
-
Lakshmanan MR, Berdanier CD, Veech RL. Comarative studies on lipogenesis and cholesterogenesis in lipemic BHE rats and normal Wistar rats. Arch Biochem Biophys 183:355-360, 1977.
-
(1977)
Arch Biochem Biophys
, vol.183
, pp. 355-360
-
-
Lakshmanan, M.R.1
Berdanier, C.D.2
Veech, R.L.3
-
113
-
-
0017843164
-
Studies on the metabolism of glycerol by hyperlipemic and normolipemic rats
-
Berdanier CD, Tobin RB, DeVore V, Wurdeman R. Studies on the metabolism of glycerol by hyperlipemic and normolipemic rats. Proc Soc Exp Biol Med 157:5-11, 1978.
-
(1978)
Proc Soc Exp Biol Med
, vol.157
, pp. 5-11
-
-
Berdanier, C.D.1
Tobin, R.B.2
DeVore, V.3
Wurdeman, R.4
-
114
-
-
0020070421
-
Rat strain differences in gluconeogenesis by isolated hepatocytes
-
Berdanier CD. Rat strain differences in gluconeogenesis by isolated hepatocytes. Proc Soc Exp Biol Med 169:74-79, 1982.
-
(1982)
Proc Soc Exp Biol Med
, vol.169
, pp. 74-79
-
-
Berdanier, C.D.1
-
115
-
-
0022987432
-
Comparative studies on mitochondrial respiration in four strains of rats Rattus norvegicus
-
Berdanier CD, Thomson AR. Comparative studies on mitochondrial respiration in four strains of rats Rattus norvegicus. Comp Biochem Physiol 85B:531-535, 1986.
-
(1986)
Comp Biochem Physiol
, vol.85 B
, pp. 531-535
-
-
Berdanier, C.D.1
Thomson, A.R.2
-
116
-
-
0343940812
-
Low-dose intakes of mitochondrial uncouplers differentially affect hepatic lipogenesis in BHE/Cdb and Sprague-Dawley rats
-
Fowler K, Berdanier CD. Low-dose intakes of mitochondrial uncouplers differentially affect hepatic lipogenesis in BHE/Cdb and Sprague-Dawley rats. Biochemistry Archives 7:269-274, 1991.
-
(1991)
Biochemistry Archives
, vol.7
, pp. 269-274
-
-
Fowler, K.1
Berdanier, C.D.2
-
117
-
-
0022444751
-
Effects of type of dietary fat and carbohydrate on gluconeogenesis in isolated hepatocytes from BHE rats
-
Wander RC, Berdanier CD. Effects of type of dietary fat and carbohydrate on gluconeogenesis in isolated hepatocytes from BHE rats. J Nutr 116:1156-1164, 1986.
-
(1986)
J Nutr
, vol.116
, pp. 1156-1164
-
-
Wander, R.C.1
Berdanier, C.D.2
-
118
-
-
0027232363
-
Hyperthyroidism does not induce an increase in mitochondrial respiration
-
Berdanier CD, Kim M-J C. Hyperthyroidism does not induce an increase in mitochondrial respiration. J Nutr Biochem 4:10-19, 1993.
-
(1993)
J Nutr Biochem
, vol.4
, pp. 10-19
-
-
Berdanier, C.D.1
Kim, M.-J.C.2
-
119
-
-
0022493282
-
Diet effects on membrane phospholipid fatty acids and mitochondrial function in BHE rats
-
Deaver OE Jr., Wander RC, McCusker RH, Berdanier CD. Diet effects on membrane phospholipid fatty acids and mitochondrial function in BHE rats. J Nutr 116:1148-1155, 1986.
-
(1986)
J Nutr
, vol.116
, pp. 1148-1155
-
-
Deaver Jr., O.E.1
Wander, R.C.2
McCusker, R.H.3
Berdanier, C.D.4
-
120
-
-
0027280434
-
Glucose homeostasis in thyroxine-treated BHE/Cdb rats fed corn oil or hydrogenated coconut oil
-
Kim MC, Berdanier CD. Glucose homeostasis in thyroxine-treated BHE/Cdb rats fed corn oil or hydrogenated coconut oil. J Nutr Biochem 4:10-19, 1993.
-
(1993)
J Nutr Biochem
, vol.4
, pp. 10-19
-
-
Kim, M.C.1
Berdanier, C.D.2
-
121
-
-
0031952581
-
Nutrient-gene interactions determine mitochondrial function: Effect of dietary fat
-
Kim MC, Berdanier CD. Nutrient-gene interactions determine mitochondrial function: Effect of dietary fat. FASEB J 12:112-118, 1998.
-
(1998)
FASEB J
, vol.12
, pp. 112-118
-
-
Kim, M.C.1
Berdanier, C.D.2
-
122
-
-
0026793865
-
Effect of thyroid status on the expression of metabolic enzymes during chronic stimulation
-
Hood DA, Simoneau J-A, Kelly AM, Pette D. Effect of thyroid status on the expression of metabolic enzymes during chronic stimulation. Am J Physiol 263:C788-C793, 1992.
-
(1992)
Am J Physiol
, vol.263
-
-
Hood, D.A.1
Simoneau, J.-A.2
Kelly, A.M.3
Pette, D.4
-
123
-
-
0027260708
-
Thyroid hormone action on mitochondrial energy transfer
-
Soboll S. Thyroid hormone action on mitochondrial energy transfer. Biochim Biophys Acta 1144:1-16, 1993.
-
(1993)
Biochim Biophys Acta
, vol.1144
, pp. 1-16
-
-
Soboll, S.1
-
124
-
-
0025313377
-
Thyroid hormone and dexamethasone increase the levels of a messenger ribonucleic acid for a mitochondrially encoded subunit but not for a nuclear-encoded subunit of cytochrome-c oxidase
-
Van Itallie CM. Thyroid hormone and dexamethasone increase the levels of a messenger ribonucleic acid for a mitochondrially encoded subunit but not for a nuclear-encoded subunit of cytochrome-c oxidase. Endocrinology 127:55-62, 1990.
-
(1990)
Endocrinology
, vol.127
, pp. 55-62
-
-
Van Itallie, C.M.1
-
125
-
-
0026549468
-
Control of respiration and ATP synthesis in mammalian mitochondria and cells
-
Brown GC. Control of respiration and ATP synthesis in mammalian mitochondria and cells. Biochem J 284:1-13, 1992.
-
(1992)
Biochem J
, vol.284
, pp. 1-13
-
-
Brown, G.C.1
-
126
-
-
0025007883
-
Control of respiration and oxidative phosphorylation in isolated rat liver cells
-
Brown GC, Lakin-Thomas PL, Brand MD. Control of respiration and oxidative phosphorylation in isolated rat liver cells. Eur J Biochem 192:355-362, 1990.
-
(1990)
Eur J Biochem
, vol.192
, pp. 355-362
-
-
Brown, G.C.1
Lakin-Thomas, P.L.2
Brand, M.D.3
-
127
-
-
0025238864
-
Analysis of the control of respiration rate, phosphorylation rate, proton leak rate, and protonmotive force in isolated mitochondria using the "top-down" approach of metabolic control theory
-
Hafner RP, Brown GC, Brand MD. Analysis of the control of respiration rate, phosphorylation rate, proton leak rate, and protonmotive force in isolated mitochondria using the "top-down" approach of metabolic control theory. Eur J Biochem 188:313-319, 1990.
-
(1990)
Eur J Biochem
, vol.188
, pp. 313-319
-
-
Hafner, R.P.1
Brown, G.C.2
Brand, M.D.3
-
128
-
-
2542487796
-
-
PhD dissertation (Berdanier CD, Director), University of Georgia
-
0ATPaSe of BHE/Cdb rats. PhD dissertation (Berdanier CD, Director), University of Georgia, 1997.
-
(1997)
0ATPaSe of BHE/Cdb Rats
-
-
Kim, S.-B.1
-
129
-
-
33749690485
-
Further studies on oxidative phosphorylation in diabetes-prone BHE/Cdb rats: Increased sensitivity to the calcium ion
-
in press
-
Kim S-B, Berdanier CD. Further studies on oxidative phosphorylation in diabetes-prone BHE/Cdb rats: Increased sensitivity to the calcium ion. J Nutr Biochem (in press).
-
J Nutr Biochem
-
-
Kim, S.-B.1
Berdanier, C.D.2
-
130
-
-
0029807647
-
Frontiers in ATP synthase research: Understanding the relationship between subunit movements and ATP synthesis
-
Pedersen PL. Frontiers in ATP synthase research: Understanding the relationship between subunit movements and ATP synthesis. J Bioenerg Biomembr 28:389-395, 1996.
-
(1996)
J Bioenerg Biomembr
, vol.28
, pp. 389-395
-
-
Pedersen, P.L.1
-
132
-
-
0028278040
-
In situ glucose uptake and glucokinase activity of pancreatic islets in diabetic and obese rodents
-
Liang Y, Bonner-Weir S, Wu Y-J, Berdanier CD, Bemer DK, Efrat S, Matschinsky F. In situ glucose uptake and glucokinase activity of pancreatic islets in diabetic and obese rodents. J Clin Invest 93:2473-2481, 1994.
-
(1994)
J Clin Invest
, vol.93
, pp. 2473-2481
-
-
Liang, Y.1
Bonner-Weir, S.2
Wu, Y.-J.3
Berdanier, C.D.4
Bemer, D.K.5
Efrat, S.6
Matschinsky, F.7
-
133
-
-
25344460306
-
Early manifestation of pancreatic islet dysfunction in the BHE/Cdb rat, a model of type II diabetes caused by a genetic mitochondrial defect
-
Collins H, Li G, Najafi H, Doliba N, Berdanier CD, Matschinsky FM. Early manifestation of pancreatic islet dysfunction in the BHE/Cdb rat, a model of type II diabetes caused by a genetic mitochondrial defect. Diabetes 47:A58, 1998.
-
(1998)
Diabetes
, vol.47
-
-
Collins, H.1
Li, G.2
Najafi, H.3
Doliba, N.4
Berdanier, C.D.5
Matschinsky, F.M.6
|