-
1
-
-
0026514891
-
Familial aggregation of arterial blood pressure and possible genetic influence
-
Brandao A.P., Brandao A.A., Araujo E.M., and Oliveira R.C. Familial aggregation of arterial blood pressure and possible genetic influence. Hypertension 19 (1992) II214-II217
-
(1992)
Hypertension
, vol.19
-
-
Brandao, A.P.1
Brandao, A.A.2
Araujo, E.M.3
Oliveira, R.C.4
-
2
-
-
0033981680
-
Mitochondrial defects in cardiomyopathy and neuromuscular disease
-
Wallace D.C. Mitochondrial defects in cardiomyopathy and neuromuscular disease. Am. Heart J. 139 (2000) S70-S85
-
(2000)
Am. Heart J.
, vol.139
-
-
Wallace, D.C.1
-
4
-
-
0034874355
-
Mitochondrial DNA mutations in black Americans with hypertension-associated end-stage renal disease
-
Watson Jr. B., Khan M.A., Desmond R.A., and Bergman S. Mitochondrial DNA mutations in black Americans with hypertension-associated end-stage renal disease. Am. J. Kidney Dis. 38 (2001) 529-536
-
(2001)
Am. J. Kidney Dis.
, vol.38
, pp. 529-536
-
-
Watson Jr., B.1
Khan, M.A.2
Desmond, R.A.3
Bergman, S.4
-
5
-
-
3042541718
-
Mitochondrial genome mutations in hypertensive individuals
-
Schwartz F., Duka A., Sun F., Cui J., Manolis A., and Gavras H. Mitochondrial genome mutations in hypertensive individuals. Am. J. Hypertens. 17 (2004) 629-635
-
(2004)
Am. J. Hypertens.
, vol.17
, pp. 629-635
-
-
Schwartz, F.1
Duka, A.2
Sun, F.3
Cui, J.4
Manolis, A.5
Gavras, H.6
-
6
-
-
0033366515
-
Maternally inherited cardiomyopathy: an atypical presentation of the mtDNA 12S rRNA gene A1555G mutation
-
Santorelli F.M., Tanji K., Manta P., Casali C., Krishna S., Hays A.P., Mancini D.M., DiMauro S., and Hirano M. Maternally inherited cardiomyopathy: an atypical presentation of the mtDNA 12S rRNA gene A1555G mutation. Am. J. Hum. Genet. 64 (1999) 295-300
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 295-300
-
-
Santorelli, F.M.1
Tanji, K.2
Manta, P.3
Casali, C.4
Krishna, S.5
Hays, A.P.6
Mancini, D.M.7
DiMauro, S.8
Hirano, M.9
-
7
-
-
0025807222
-
Leu(UUR)
-
Leu(UUR). Lancet 338 (1991) 143-147
-
(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
-
9
-
-
0034939410
-
Lys gene with severe ultrastructural alterations of mitochondria in cardiomyocytes
-
Lys gene with severe ultrastructural alterations of mitochondria in cardiomyocytes. Jpn. Circ. J. 65 (2001) 691-694
-
(2001)
Jpn. Circ. J.
, vol.65
, pp. 691-694
-
-
Terasaki, F.1
Tanaka, M.2
Kawamura, K.3
Kanzaki, Y.4
Okabe, M.5
Hayashi, T.6
Shimomura, H.7
Ito, T.8
Suwa, M.9
Gong, J.S.10
Zhang, J.11
Kitaura, Y.12
-
10
-
-
0029962873
-
Lys gene (G8363A)
-
Lys gene (G8363A). Am. J. Hum. Genet. 58 (1996) 933-939
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 933-939
-
-
Santorelli, F.M.1
Mak, S.C.2
El-Schahawi, M.3
Casali, C.4
Shanske, S.5
Baram, T.Z.6
Madrid, R.E.7
DiMauro, S.8
-
11
-
-
0029835998
-
An additional mitochondrial tRNA(Ile) point mutation (A-to-G at nucleotide 4295) causing hypertrophic cardiomyopathy
-
Merante F., Myint T., Tein I., Benson L., and Robinson B.H. An additional mitochondrial tRNA(Ile) point mutation (A-to-G at nucleotide 4295) causing hypertrophic cardiomyopathy. Hum. Mut. 8 (1996) 216-222
-
(1996)
Hum. Mut.
, vol.8
, pp. 216-222
-
-
Merante, F.1
Myint, T.2
Tein, I.3
Benson, L.4
Robinson, B.H.5
-
12
-
-
0035573734
-
Phylogenetic analysis of mitochondrial DNA in patients with an occipital stroke. Evaluation of mutations by using sequence data on the entire coding region
-
Finnila S., Hassinen I.E., and Majamaa K. Phylogenetic analysis of mitochondrial DNA in patients with an occipital stroke. Evaluation of mutations by using sequence data on the entire coding region. Mut. Res. 458 (2001) 31-39
-
(2001)
Mut. Res.
, vol.458
, pp. 31-39
-
-
Finnila, S.1
Hassinen, I.E.2
Majamaa, K.3
-
13
-
-
0038238874
-
A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy
-
Taylor R.W., Giordano C., Davidson M.M., d'Amati G., Bain H., Hayes C.M., Leonard H., Barron M.J., Casali C., Santorelli F.M., Hirano M., Lightowlers R.N., DiMauro S., and Turnbull D.M. A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy. J. Am. Coll. Cardiol. 41 (2003) 1786-1796
-
(2003)
J. Am. Coll. Cardiol.
, vol.41
, pp. 1786-1796
-
-
Taylor, R.W.1
Giordano, C.2
Davidson, M.M.3
d'Amati, G.4
Bain, H.5
Hayes, C.M.6
Leonard, H.7
Barron, M.J.8
Casali, C.9
Santorelli, F.M.10
Hirano, M.11
Lightowlers, R.N.12
DiMauro, S.13
Turnbull, D.M.14
-
14
-
-
8444228909
-
A cluster of metabolic defects caused by mutation in a mitochondrial tRNA
-
Wilson F.H., Hariri A., Farhi A., Zhao H., Petersen K.F., Toka H.R., Nelson-Williams C., Raja K.M., Kashgarian M., Shulman G.I., Scheinman S.J., and Lifton R.P. A cluster of metabolic defects caused by mutation in a mitochondrial tRNA. Science 306 (2004) 1190-1194
-
(2004)
Science
, vol.306
, pp. 1190-1194
-
-
Wilson, F.H.1
Hariri, A.2
Farhi, A.3
Zhao, H.4
Petersen, K.F.5
Toka, H.R.6
Nelson-Williams, C.7
Raja, K.M.8
Kashgarian, M.9
Shulman, G.I.10
Scheinman, S.J.11
Lifton, R.P.12
-
15
-
-
0030713021
-
-
The sixth report of the Joint National Committee on Prevention, Detection, Evaluation and Treatment of High Blood Pressure, Arch. Intern. Med. 157 (1997) 2413-2446.
-
The sixth report of the Joint National Committee on Prevention, Detection, Evaluation and Treatment of High Blood Pressure, Arch. Intern. Med. 157 (1997) 2413-2446.
-
-
-
-
16
-
-
0033069767
-
-
1999 World Health Organization-International Society of Hypertension Guidelines for the Management of Hypertension. Guidelines Subcommittee. J. Hypertens. 17 (1999) 151-183.
-
1999 World Health Organization-International Society of Hypertension Guidelines for the Management of Hypertension. Guidelines Subcommittee. J. Hypertens. 17 (1999) 151-183.
-
-
-
-
17
-
-
0032519307
-
Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome
-
Rieder M.J., Taylor S.L., Tobe V.O., and Nickerson D.A. Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome. Nucleic Acids Res. 26 (1981) 967-973
-
(1981)
Nucleic Acids Res.
, vol.26
, pp. 967-973
-
-
Rieder, M.J.1
Taylor, S.L.2
Tobe, V.O.3
Nickerson, D.A.4
-
18
-
-
0019423856
-
Sequence and organization of the human mitochondrial genome
-
Anderson S., Bankier A.T., Barrell B.G., deBruijn M.H.L., Coulson A.R., Drouin J., Eperon I.C., Nierlich D.P., Rose B.A., Sanger F., Schreier P.H., Smith A.J.H., Staden R., and Young I. Sequence and organization of the human mitochondrial genome. Nature 290 (1981) 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
Rose, B.A.9
Sanger, F.10
Schreier, P.H.11
Smith, A.J.H.12
Staden, R.13
Young, I.14
-
19
-
-
0031804156
-
Compilation of tRNA sequences and sequences of tRNA genes
-
Sprinzl M., Horn C., Brown M., Ioudovitch A., and Steinberg S. Compilation of tRNA sequences and sequences of tRNA genes. Nucleic Acids Res. 26 (1998) 148-153
-
(1998)
Nucleic Acids Res.
, vol.26
, pp. 148-153
-
-
Sprinzl, M.1
Horn, C.2
Brown, M.3
Ioudovitch, A.4
Steinberg, S.5
-
20
-
-
0013084592
-
Human mitochondrial tRNAs in health and disease
-
Florentz C., Sohm B., Tryoen-Toth P., Putz J., and Sissler M. Human mitochondrial tRNAs in health and disease. Cell. Mol. Life Sci. 60 (2003) 1356-1375
-
(2003)
Cell. Mol. Life Sci.
, vol.60
, pp. 1356-1375
-
-
Florentz, C.1
Sohm, B.2
Tryoen-Toth, P.3
Putz, J.4
Sissler, M.5
-
21
-
-
0002495140
-
tRNA: structure, biosynthesis and function
-
Söll D., and RajBhandary U.L. (Eds), ASM Press, Washington, DC
-
Björk G.R. tRNA: structure, biosynthesis and function. In: Söll D., and RajBhandary U.L. (Eds). tRNA: Structure, Biosynthesis and Function (1995), ASM Press, Washington, DC 165-206
-
(1995)
tRNA: Structure, Biosynthesis and Function
, pp. 165-206
-
-
Björk, G.R.1
-
22
-
-
6344259029
-
Mitochondrial genome variation in eastern Asia and the peopling of Japan
-
Tanaka M., Cabrera V.M., Gonzalez A.M., Larruga J.M., Takeyasu T., Fuku N., Guo L.J., Hirose R., Fujita Y., Kurata M., Shinoda K., Umetsu K., Yamada Y., Oshida Y., Sato Y., Hattori N., Mizuno Y., Arai Y., Hirose N., Ohta S., Ogawa O., Tanaka Y., Kawamori R., Shamoto-Nagai M., Maruyama W., Shimokata H., Suzuki R., and Shimodaira H. Mitochondrial genome variation in eastern Asia and the peopling of Japan. Genome Res. (2004) 1832-1850
-
(2004)
Genome Res.
, pp. 1832-1850
-
-
Tanaka, M.1
Cabrera, V.M.2
Gonzalez, A.M.3
Larruga, J.M.4
Takeyasu, T.5
Fuku, N.6
Guo, L.J.7
Hirose, R.8
Fujita, Y.9
Kurata, M.10
Shinoda, K.11
Umetsu, K.12
Yamada, Y.13
Oshida, Y.14
Sato, Y.15
Hattori, N.16
Mizuno, Y.17
Arai, Y.18
Hirose, N.19
Ohta, S.20
Ogawa, O.21
Tanaka, Y.22
Kawamori, R.23
Shamoto-Nagai, M.24
Maruyama, W.25
Shimokata, H.26
Suzuki, R.27
Shimodaira, H.28
more..
-
23
-
-
13444256467
-
MITOMAP: a human mitochondrial genome database-2004 update
-
Brandon M.C., Lott M.T., Nguyen K.C., Spolim S., Navathe S.B., Baldi P., and Wallace D.C. MITOMAP: a human mitochondrial genome database-2004 update. Nucleic Acids Res. 33 (2005) D611-D613
-
(2005)
Nucleic Acids Res.
, vol.33
-
-
Brandon, M.C.1
Lott, M.T.2
Nguyen, K.C.3
Spolim, S.4
Navathe, S.B.5
Baldi, P.6
Wallace, D.C.7
-
24
-
-
0019837699
-
Sequence and gene organization of mouse mitochondrial DNA
-
Bibb M.J., Van Etten R.A., Wright C.T., Walberg M.W., and Clayton D.A. Sequence and gene organization of mouse mitochondrial DNA. Cell 26 (1981) 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
-
25
-
-
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., and Saccone C. The complete nucleotide sequence of the Rattus norvegicus mitochondrial genome: cryptic signals revealed by comparative analysis between vertebrates. J. Mol. Evol. 28 (1989) 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
-
26
-
-
0021876634
-
The complete nucleotide sequence of the Xenopus laevis mitochondrial genome
-
Roe A., Ma D.P., Wilson R.K., and Wong J.F. The complete nucleotide sequence of the Xenopus laevis mitochondrial genome. J. Biol. Chem. 260 (1985) 9759-9774
-
(1985)
J. Biol. Chem.
, vol.260
, pp. 9759-9774
-
-
Roe, A.1
Ma, D.P.2
Wilson, R.K.3
Wong, J.F.4
-
27
-
-
29244483946
-
Leber's hereditary optic neuropathy is associated with the mitochondrial ND4 G11696A mutation in five Chinese families
-
Zhou X., Wei Q., Yang L., Tong Y., Zhao F., Lu C., Qian Y., Sun Y., Lu F., Qu J., and Guan M.X. Leber's hereditary optic neuropathy is associated with the mitochondrial ND4 G11696A mutation in five Chinese families. Biochem. Biophys. Res. Commun. 340 (2006) 69-75
-
(2006)
Biochem. Biophys. Res. Commun.
, vol.340
, pp. 69-75
-
-
Zhou, X.1
Wei, Q.2
Yang, L.3
Tong, Y.4
Zhao, F.5
Lu, C.6
Qian, Y.7
Sun, Y.8
Lu, F.9
Qu, J.10
Guan, M.X.11
-
28
-
-
0035019225
-
Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disorders
-
Sternberg D., Chatzoglou E., Laforet P., Fayet G., Jardel C., Blondy P., Fardeau M., Amselem S., Eymard B., and Lombes A. Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disorders. Brain 124 (2001) 984-994
-
(2001)
Brain
, vol.124
, pp. 984-994
-
-
Sternberg, D.1
Chatzoglou, E.2
Laforet, P.3
Fayet, G.4
Jardel, C.5
Blondy, P.6
Fardeau, M.7
Amselem, S.8
Eymard, B.9
Lombes, A.10
-
29
-
-
0242300145
-
MELAS with point mutations involving tRNALeu (A3243G) and tRNAGlu (A14693G)
-
Tzen C.Y., Thajeb P., Wu T.Y., and Chen S.C. MELAS with point mutations involving tRNALeu (A3243G) and tRNAGlu (A14693G). Muscle Nerve 28 (2003) 575-581
-
(2003)
Muscle Nerve
, vol.28
, pp. 575-581
-
-
Tzen, C.Y.1
Thajeb, P.2
Wu, T.Y.3
Chen, S.C.4
-
30
-
-
33749463802
-
Thr may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss
-
Thr may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss. Am. J. Med. Genet. A 140 (2006) 2188-2197
-
(2006)
Am. J. Med. Genet. A
, vol.140
, pp. 2188-2197
-
-
Young, W.Y.1
Zhao, L.2
Qian, Y.3
Li, R.4
Chen, J.5
Dai, P.6
Zhai, S.7
Han, D.8
Guan, M.X.9
-
31
-
-
34247092566
-
Glu A14693G mutation may influence the phenotypic manifestation of ND1 G3460A mutation in a Chinese family with Leber's hereditary optic neuropathy
-
Glu A14693G mutation may influence the phenotypic manifestation of ND1 G3460A mutation in a Chinese family with Leber's hereditary optic neuropathy. Biochem. Biophys. Res. Commun. 357 (2007) 524-530
-
(2007)
Biochem. Biophys. Res. Commun.
, vol.357
, pp. 524-530
-
-
Tong, Y.1
Mao, Y.2
Zhou, X.3
Yang, L.4
Zhang, J.5
Cai, W.6
Zhao, F.7
Wang, X.8
Lu, F.9
Qu, J.10
Guan, M.X.11
-
32
-
-
0002365884
-
Modified nucleosides and codon recognition
-
Söll D., and RajBhandary U.L. (Eds), ASM Press, Washington, DC
-
Yokoyama S., and Nishimura S. Modified nucleosides and codon recognition. In: Söll D., and RajBhandary U.L. (Eds). tRNA: Structure, Biosynthesis and Function (1995), ASM Press, Washington, DC 207-224
-
(1995)
tRNA: Structure, Biosynthesis and Function
, pp. 207-224
-
-
Yokoyama, S.1
Nishimura, S.2
-
34
-
-
0031571595
-
Three modified nucleosides present in the anticodon stem and loop influence the in vivo aa-tRNA selection in a tRNA-dependent manner
-
Li J., Esberg B., Curran J.F., and Bjork G.R. Three modified nucleosides present in the anticodon stem and loop influence the in vivo aa-tRNA selection in a tRNA-dependent manner. J. Mol. Biol. 271 (1997) 209-221
-
(1997)
J. Mol. Biol.
, vol.271
, pp. 209-221
-
-
Li, J.1
Esberg, B.2
Curran, J.F.3
Bjork, G.R.4
-
35
-
-
0020489739
-
Iron mediated methylthiolation of tRNA as a regulator of operon expression in Escherichia coli
-
Buck M., and Griffiths F. Iron mediated methylthiolation of tRNA as a regulator of operon expression in Escherichia coli. Nucleic Acids Res. 10 (1982) 2024-2609
-
(1982)
Nucleic Acids Res.
, vol.10
, pp. 2024-2609
-
-
Buck, M.1
Griffiths, F.2
-
36
-
-
0035801515
-
Improvement of reading frame maintenance is a common function for several tRNA modifications
-
Urbonavicius J., Qian Q., Durand J.M., Hagervall T.G., and Bjork G.R. Improvement of reading frame maintenance is a common function for several tRNA modifications. EMBO J. 20 (2001) 4863-4873
-
(2001)
EMBO J.
, vol.20
, pp. 4863-4873
-
-
Urbonavicius, J.1
Qian, Q.2
Durand, J.M.3
Hagervall, T.G.4
Bjork, G.R.5
-
37
-
-
0023036918
-
Actions of the anticodon arm in translation on the phenotypes of RNA mutants
-
Yarus M., Cline S.W., Wier P., Breeden L., and Thompson R.C. Actions of the anticodon arm in translation on the phenotypes of RNA mutants. J. Mol. Biol. 192 (1986) 235-255
-
(1986)
J. Mol. Biol.
, vol.192
, pp. 235-255
-
-
Yarus, M.1
Cline, S.W.2
Wier, P.3
Breeden, L.4
Thompson, R.C.5
-
38
-
-
33644868369
-
The novel A4435G mutation in the mitochondrial tRNAMet may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutation
-
Qu J., Li R., Zhou X., Tong Y., Lu F., Qian Y., Hu Y., Mo J.Q., West C.E., and Guan M.X. The novel A4435G mutation in the mitochondrial tRNAMet may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutation. Invest. Ophthalmol. Vis. Sci. 47 (2006) 475-483
-
(2006)
Invest. Ophthalmol. Vis. Sci.
, vol.47
, pp. 475-483
-
-
Qu, J.1
Li, R.2
Zhou, X.3
Tong, Y.4
Lu, F.5
Qian, Y.6
Hu, Y.7
Mo, J.Q.8
West, C.E.9
Guan, M.X.10
-
39
-
-
33847689427
-
Cosegregation of the ND4 G11696A mutation with the LHON-associated ND4 G11778A mutation in a four generation Chinese family
-
Qu J., Li R., Zhou X., Tong Y., Yang L., Chen J., Zhao F., Lu C., Qian Y., Lu F., and Guan M.X. Cosegregation of the ND4 G11696A mutation with the LHON-associated ND4 G11778A mutation in a four generation Chinese family. Mitochondrion 7 (2007) 140-146
-
(2007)
Mitochondrion
, vol.7
, pp. 140-146
-
-
Qu, J.1
Li, R.2
Zhou, X.3
Tong, Y.4
Yang, L.5
Chen, J.6
Zhao, F.7
Lu, C.8
Qian, Y.9
Lu, F.10
Guan, M.X.11
|