-
2
-
-
0037080987
-
CREB activation induced by mitochondrial dysfunction is a new signaling pathway that impairs cell proliferation
-
COI: 1:CAS:528:DC%2BD38XpsFCjtw%3D%3D, PID: 11782425
-
Arnould T, Vankoningsloo S, Renard P, Houbion A, Ninane N, Demazy C et al (2002) CREB activation induced by mitochondrial dysfunction is a new signaling pathway that impairs cell proliferation. EMBO J 21:53–63
-
(2002)
EMBO J
, vol.21
, pp. 53-63
-
-
Arnould, T.1
Vankoningsloo, S.2
Renard, P.3
Houbion, A.4
Ninane, N.5
Demazy, C.6
-
3
-
-
43549098268
-
Calcium cycling and signaling in cardiac myocytes
-
COI: 1:CAS:528:DC%2BD1cXkt1eqsbg%3D, PID: 17988210
-
Bers DM (2008) Calcium cycling and signaling in cardiac myocytes. Annu Rev Physiol 70:23–49
-
(2008)
Annu Rev Physiol
, vol.70
, pp. 23-49
-
-
Bers, D.M.1
-
4
-
-
23644436504
-
Mitochondria-to-nucleus stress signaling in mammalian cells: nature of nuclear gene targets, transcription regulation, and induced resistance to apoptosis
-
COI: 1:CAS:528:DC%2BD2MXntlSgs7o%3D, PID: 15978749
-
Biswas G, Guha M, Avadhani NG (2005) Mitochondria-to-nucleus stress signaling in mammalian cells: nature of nuclear gene targets, transcription regulation, and induced resistance to apoptosis. Gene 354:132–139
-
(2005)
Gene
, vol.354
, pp. 132-139
-
-
Biswas, G.1
Guha, M.2
Avadhani, N.G.3
-
5
-
-
1842665662
-
Mitochondrial signaling: the retrograde response
-
COI: 1:CAS:528:DC%2BD2cXjvVaqsbs%3D, PID: 15068799
-
Butow RA, Avadhani NG (2004) Mitochondrial signaling: the retrograde response. Mol Cell 14:1–15
-
(2004)
Mol Cell
, vol.14
, pp. 1-15
-
-
Butow, R.A.1
Avadhani, N.G.2
-
6
-
-
1942425120
-
Human mitochondrial transcription factor B1 as a modifier gene for hearing loss associated with the mitochondrial A1555G mutation
-
COI: 1:CAS:528:DC%2BD2cXjtl2murs%3D, PID: 15110318
-
Bykhovskaya Y, Mengesha E, Wang D, Yang H, Estivill X, Shohat M et al (2004) Human mitochondrial transcription factor B1 as a modifier gene for hearing loss associated with the mitochondrial A1555G mutation. Mol Genet Metab 82:27–32
-
(2004)
Mol Genet Metab
, vol.82
, pp. 27-32
-
-
Bykhovskaya, Y.1
Mengesha, E.2
Wang, D.3
Yang, H.4
Estivill, X.5
Shohat, M.6
-
7
-
-
33745274726
-
Mitochondria: dynamic organelles in disease, aging, and development
-
COI: 1:CAS:528:DC%2BD28XmvVGrsrk%3D, PID: 16814712
-
Chan DC (2006) Mitochondria: dynamic organelles in disease, aging, and development. Cell 125:1241–1252
-
(2006)
Cell
, vol.125
, pp. 1241-1252
-
-
Chan, D.C.1
-
8
-
-
0037972522
-
Mitochondrial respiratory-chain diseases
-
COI: 1:CAS:528:DC%2BD3sXkvVSksbw%3D, PID: 12826641
-
DiMauro S, Schon EA (2003) Mitochondrial respiratory-chain diseases. N Engl J Med 348:2656–2668
-
(2003)
N Engl J Med
, vol.348
, pp. 2656-2668
-
-
DiMauro, S.1
Schon, E.A.2
-
9
-
-
84904406653
-
VARS2 and TARS2 mutations in patients with mitochondrial encephalomyopathies
-
COI: 1:CAS:528:DC%2BC2cXhtF2lt7fE, PID: 24827421
-
Diodato D, Melchionda L, Haack TB, Dallabona C, Baruffini E, Donnini C et al (2014) VARS2 and TARS2 mutations in patients with mitochondrial encephalomyopathies. Hum Mutat 35:983–989
-
(2014)
Hum Mutat
, vol.35
, pp. 983-989
-
-
Diodato, D.1
Melchionda, L.2
Haack, T.B.3
Dallabona, C.4
Baruffini, E.5
Donnini, C.6
-
10
-
-
0029059067
-
MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNA(Lys) and premature translation termination
-
COI: 1:CAS:528:DyaK2MXlsVymtr8%3D, PID: 7647790
-
Enriquez JA, Chomyn A, Attardi G (1995) MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNA(Lys) and premature translation termination. Nat Genet 10:47–55
-
(1995)
Nat Genet
, vol.10
, pp. 47-55
-
-
Enriquez, J.A.1
Chomyn, A.2
Attardi, G.3
-
11
-
-
84893842173
-
Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy
-
Giordano C, Iommarini L, Giordano L, Maresca A, Pisano A, Valentino ML et al (2014) Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy. Brain 137:335–353
-
(2014)
Brain
, vol.137
, pp. 335-353
-
-
Giordano, C.1
Iommarini, L.2
Giordano, L.3
Maresca, A.4
Pisano, A.5
Valentino, M.L.6
-
12
-
-
84893442805
-
Declining NAD+ induces a pseudohypoxic state disrupting nuclear-mitochondrial communication during aging
-
COI: 1:CAS:528:DC%2BC3sXhvFylurrJ, PID: 24360282
-
Gomes AP, Price NL, Ling AJY, Moslehi JJ, Montgomery MK, Rajman L et al (2013) Declining NAD+ induces a pseudohypoxic state disrupting nuclear-mitochondrial communication during aging. Cell 155:1624–1638
-
(2013)
Cell
, vol.155
, pp. 1624-1638
-
-
Gomes, A.P.1
Price, N.L.2
Ling, A.J.Y.3
Moslehi, J.J.4
Montgomery, M.K.5
Rajman, L.6
-
13
-
-
0025666322
-
A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
-
COI: 1:CAS:528:DyaK3MXls1Kqsw%3D%3D, PID: 2102678
-
Goto Y, Nonaka I, Horai S (1990) A mutation in the tRNALeu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies. Nature 348:651–653
-
(1990)
Nature
, vol.348
, pp. 651-653
-
-
Goto, Y.1
Nonaka, I.2
Horai, S.3
-
14
-
-
0030016359
-
Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation
-
COI: 1:CAS:528:DyaK28Xkt1Cnt78%3D, PID: 8817331
-
Guan M-X, Fischel-Ghodsian N, Attardi G (1996) Biochemical evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation. Hum Mol Genet 5:963–971
-
(1996)
Hum Mol Genet
, vol.5
, pp. 963-971
-
-
Guan, M.-X.1
Fischel-Ghodsian, N.2
Attardi, G.3
-
15
-
-
0035869153
-
Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation
-
COI: 1:CAS:528:DC%2BD3MXit1ehtb0%3D, PID: 11230176
-
Guan MX, Fischel-Ghodsian N, Attardi G (2001) Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation. Hum Mol Genet 10:573–580
-
(2001)
Hum Mol Genet
, vol.10
, pp. 573-580
-
-
Guan, M.X.1
Fischel-Ghodsian, N.2
Attardi, G.3
-
16
-
-
33746559647
-
Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations
-
COI: 1:CAS:528:DC%2BD28XnsVOktrY%3D, PID: 16826519
-
Guan MX, Yan Q, Li X, Bykhovskaya Y, Gallo-Teran J, Hajek P et al (2006) Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations. Am J Hum Genet 79:291–302
-
(2006)
Am J Hum Genet
, vol.79
, pp. 291-302
-
-
Guan, M.X.1
Yan, Q.2
Li, X.3
Bykhovskaya, Y.4
Gallo-Teran, J.5
Hajek, P.6
-
17
-
-
84884337715
-
Mitochondrial retrograde signaling at the crossroads of tumor bioenergetics, genetics and epigenetics
-
COI: 1:CAS:528:DC%2BC3sXhslaiurfM, PID: 24004957
-
Guha M, Avadhani NG (2013) Mitochondrial retrograde signaling at the crossroads of tumor bioenergetics, genetics and epigenetics. Mitochondrion 13:577–591
-
(2013)
Mitochondrion
, vol.13
, pp. 577-591
-
-
Guha, M.1
Avadhani, N.G.2
-
18
-
-
84907932106
-
Genetic modifiers of Huntington’s disease
-
COI: 1:CAS:528:DC%2BC2cXhsFGhtrfL, PID: 25154728
-
Gusella JF, MacDonald ME, Lee J-M (2014) Genetic modifiers of Huntington’s disease. Mov Disord 29:1359–1365
-
(2014)
Mov Disord
, vol.29
, pp. 1359-1365
-
-
Gusella, J.F.1
MacDonald, M.E.2
Lee, J.-M.3
-
19
-
-
0029064615
-
Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutation
-
COI: 1:CAS:528:DyaK2MXnsVersr0%3D, PID: 7611298
-
Harding AE, Sweeney MG, Govan GG, Riordan-Eva P (1995) Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutation. Am J Hum Genet 57:77–86
-
(1995)
Am J Hum Genet
, vol.57
, pp. 77-86
-
-
Harding, A.E.1
Sweeney, M.G.2
Govan, G.G.3
Riordan-Eva, P.4
-
20
-
-
0023883150
-
Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies
-
COI: 1:STN:280:DyaL1c7ktlWmtQ%3D%3D, PID: 2830540
-
Holt IJ, Harding AE, Morgan-Hughes JA (1988) Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies. Nature 331:717–719
-
(1988)
Nature
, vol.331
, pp. 717-719
-
-
Holt, I.J.1
Harding, A.E.2
Morgan-Hughes, J.A.3
-
21
-
-
84858693597
-
Monogenic mitochondrial disorders
-
COI: 1:CAS:528:DC%2BC38XktlCqtb4%3D, PID: 22435372
-
Koopman WJ, Willems PH, Smeitink JA (2012) Monogenic mitochondrial disorders. N Engl J Med 366:1132–1141
-
(2012)
N Engl J Med
, vol.366
, pp. 1132-1141
-
-
Koopman, W.J.1
Willems, P.H.2
Smeitink, J.A.3
-
22
-
-
0345415102
-
Identification and characterization of mouse GTPBP3 gene encoding a mitochondrial GTP-binding protein involved in tRNA modification
-
COI: 1:CAS:528:DC%2BD3sXpt1Wjtrk%3D, PID: 14680828
-
Li X, Guan M-X (2003) Identification and characterization of mouse GTPBP3 gene encoding a mitochondrial GTP-binding protein involved in tRNA modification. Biochem Biophys Res Commun 312:747–754
-
(2003)
Biochem Biophys Res Commun
, vol.312
, pp. 747-754
-
-
Li, X.1
Guan, M.-X.2
-
23
-
-
0037178851
-
Isolation and characterization of the putative nuclear modifier gene MTO1 involved in the pathogenesis of deafness-associated mitochondrial 12 S rRNA A1555G mutation
-
COI: 1:CAS:528:DC%2BD38XlvV2itb0%3D, PID: 12011058
-
Li X, Li R, Lin X, Guan MX (2002) Isolation and characterization of the putative nuclear modifier gene MTO1 involved in the pathogenesis of deafness-associated mitochondrial 12 S rRNA A1555G mutation. J Biol Chem 277:27256–27264
-
(2002)
J Biol Chem
, vol.277
, pp. 27256-27264
-
-
Li, X.1
Li, R.2
Lin, X.3
Guan, M.X.4
-
24
-
-
84922545670
-
The severity of retinal pathology in homozygous Crb1rd8/rd8 mice is dependent on additional genetic factors
-
Luhmann UF, Carvalho LS, Holthaus SM, Cowing JA, Greenaway S, Chu CJ et al (2015) The severity of retinal pathology in homozygous Crb1rd8/rd8 mice is dependent on additional genetic factors. Hum Mol Genet 24:128–141
-
(2015)
Hum Mol Genet
, vol.24
, pp. 128-141
-
-
Luhmann, U.F.1
Carvalho, L.S.2
Holthaus, S.M.3
Cowing, J.A.4
Greenaway, S.5
Chu, C.J.6
-
25
-
-
84931829244
-
Congenital visual impairment and progressive microcephaly due to lysyl-transfer ribonucleic acid (rna) synthetase (kars) mutations: the expanding phenotype of aminoacyl-transfer RNA synthetase mutations in human disease. J Child Neurol
-
McMillan HJ, Humphreys P, Smith A, Schwartzentruber J, Chakraborty P, Bulman DE, et al. (2014) Congenital visual impairment and progressive microcephaly due to lysyl-transfer ribonucleic acid (rna) synthetase (kars) mutations: the expanding phenotype of aminoacyl-transfer RNA synthetase mutations in human disease. J Child Neurol. doi:10.1177/0883073814553272
-
(2014)
doi:10.1177/0883073814553272
-
-
McMillan, H.J.1
Humphreys, P.2
Smith, A.3
Schwartzentruber, J.4
Chakraborty, P.5
Bulman, D.E.6
-
26
-
-
84922588679
-
The ROS-sensitive microRNA-9/9* controls the expression of mitochondrial tRNA-modifying enzymes and is involved in the molecular mechanism of MELAS syndrome
-
Meseguer S, Martinez-Zamora A, Garcia-Arumi E, Andreu AL, Armengod ME (2015) The ROS-sensitive microRNA-9/9* controls the expression of mitochondrial tRNA-modifying enzymes and is involved in the molecular mechanism of MELAS syndrome. Hum Mol Genet 24:167–184
-
(2015)
Hum Mol Genet
, vol.24
, pp. 167-184
-
-
Meseguer, S.1
Martinez-Zamora, A.2
Garcia-Arumi, E.3
Andreu, A.L.4
Armengod, M.E.5
-
27
-
-
84899559302
-
A novel homozygous YARS2 mutation causes severe myopathy, lactic acidosis, and sideroblastic anemia 2
-
COI: 1:CAS:528:DC%2BC2cXntVSgsb0%3D, PID: 24430573
-
Nakajima J, Eminoglu TF, Vatansever G, Nakashima M, Tsurusaki Y, Saitsu H et al (2014) A novel homozygous YARS2 mutation causes severe myopathy, lactic acidosis, and sideroblastic anemia 2. J Hum Genet 59:229–232
-
(2014)
J Hum Genet
, vol.59
, pp. 229-232
-
-
Nakajima, J.1
Eminoglu, T.F.2
Vatansever, G.3
Nakashima, M.4
Tsurusaki, Y.5
Saitsu, H.6
-
28
-
-
0037459081
-
Mitochondria: releasing power for life and unleashing the machineries of death
-
COI: 1:CAS:528:DC%2BD3sXhs1SnsLs%3D, PID: 12600312
-
Newmeyer DD, Ferguson-Miller S (2003) Mitochondria: releasing power for life and unleashing the machineries of death. Cell 112:481–490
-
(2003)
Cell
, vol.112
, pp. 481-490
-
-
Newmeyer, D.D.1
Ferguson-Miller, S.2
-
29
-
-
84858376953
-
Mitochondria: in sickness and in health
-
COI: 1:CAS:528:DC%2BC38Xkt1Gitrg%3D, PID: 22424226
-
Nunnari J, Suomalainen A (2012) Mitochondria: in sickness and in health. Cell 148:1145–1159
-
(2012)
Cell
, vol.148
, pp. 1145-1159
-
-
Nunnari, J.1
Suomalainen, A.2
-
30
-
-
84886786722
-
Muscle mitohormesis promotes longevity via systemic repression of insulin signaling
-
COI: 1:CAS:528:DC%2BC3sXhs1yqt77K, PID: 24243023
-
Owusu-Ansah E, Song W, Perrimon N (2013) Muscle mitohormesis promotes longevity via systemic repression of insulin signaling. Cell 155:699–712
-
(2013)
Cell
, vol.155
, pp. 699-712
-
-
Owusu-Ansah, E.1
Song, W.2
Perrimon, N.3
-
31
-
-
0023106633
-
The mitochondrial genotype can influence nuclear gene expression in yeast
-
COI: 1:CAS:528:DyaL2sXhsFSmsL0%3D, PID: 3027892
-
Parikh VS, Morgan MM, Scott R, Clements LS, Butow RA (1987) The mitochondrial genotype can influence nuclear gene expression in yeast. Science 235:576–580
-
(1987)
Science
, vol.235
, pp. 576-580
-
-
Parikh, V.S.1
Morgan, M.M.2
Scott, R.3
Clements, L.S.4
Butow, R.A.5
-
32
-
-
34247892408
-
Extended guidelines for mtDNA typing of population data in forensic science
-
COI: 1:CAS:528:DC%2BD2sXhtlOitbvF, PID: 19083723
-
Parson W, Bandelt HJ (2007) Extended guidelines for mtDNA typing of population data in forensic science. Forensic Sci Int Genet 1:13–19
-
(2007)
Forensic Sci Int Genet
, vol.1
, pp. 13-19
-
-
Parson, W.1
Bandelt, H.J.2
-
33
-
-
84871734834
-
Signaling the mitochondrial unfolded protein response
-
COI: 1:CAS:528:DC%2BC38XltValt7g%3D
-
Pellegrino MW, Nargund AM, Haynes CM (2013) Signaling the mitochondrial unfolded protein response. Biochim et Biophys Acta 1833:410–416
-
(2013)
Biochim et Biophys Acta
, vol.1833
, pp. 410-416
-
-
Pellegrino, M.W.1
Nargund, A.M.2
Haynes, C.M.3
-
34
-
-
84893777996
-
The isolated carboxy-terminal domain of human mitochondrial leucyl-tRNA synthetase rescues the pathological phenotype of mitochondrial tRNA mutations in human cells
-
COI: 1:CAS:528:DC%2BC2cXitFWktbs%3D, PID: 24413190
-
Perli E, Giordano C, Pisano A, Montanari A, Campese AF, Reyes A et al (2014) The isolated carboxy-terminal domain of human mitochondrial leucyl-tRNA synthetase rescues the pathological phenotype of mitochondrial tRNA mutations in human cells. EMBO Mol Med 6:169–182
-
(2014)
EMBO Mol Med
, vol.6
, pp. 169-182
-
-
Perli, E.1
Giordano, C.2
Pisano, A.3
Montanari, A.4
Campese, A.F.5
Reyes, A.6
-
35
-
-
84907267817
-
Progressive increase in mtDNA 3243A>G heteroplasmy causes abrupt transcriptional reprogramming
-
COI: 1:CAS:528:DC%2BC2cXhsVyrtb7E, PID: 25192935
-
Picard M, Zhang J, Hancock S, Derbeneva O, Golhar R, Golik P et al (2014) Progressive increase in mtDNA 3243A>G heteroplasmy causes abrupt transcriptional reprogramming. Proc Natl Acad Sci USA 111:E4033–E4042
-
(2014)
Proc Natl Acad Sci USA
, vol.111
, pp. E4033-E4042
-
-
Picard, M.1
Zhang, J.2
Hancock, S.3
Derbeneva, O.4
Golhar, R.5
Golik, P.6
-
36
-
-
0027226069
-
Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness
-
COI: 1:CAS:528:DyaK3sXmtVWjt78%3D, PID: 7689389
-
Prezant TR, Agapian JV, Bohlman MC, Bu X, Oztas S, Qiu WQ et al (1993) Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness. Nat Genet 4:289–294
-
(1993)
Nat Genet
, vol.4
, pp. 289-294
-
-
Prezant, T.R.1
Agapian, J.V.2
Bohlman, M.C.3
Bu, X.4
Oztas, S.5
Qiu, W.Q.6
-
37
-
-
84899907186
-
Mitochondrial pathology: stress signals from the energy factory
-
COI: 1:CAS:528:DC%2BC2cXhvFGhur4%3D, PID: 24508276
-
Raimundo N (2014) Mitochondrial pathology: stress signals from the energy factory. Trends Mol Med 20:282–292
-
(2014)
Trends Mol Med
, vol.20
, pp. 282-292
-
-
Raimundo, N.1
-
38
-
-
84857343794
-
Mitochondrial stress engages E2F1 apoptotic signaling to cause deafness
-
COI: 1:CAS:528:DC%2BC38XjtFSgtLk%3D, PID: 22341444
-
Raimundo N, Song L, Shutt TE, McKay SE, Cotney J, Guan MX et al (2012) Mitochondrial stress engages E2F1 apoptotic signaling to cause deafness. Cell 148:716–726
-
(2012)
Cell
, vol.148
, pp. 716-726
-
-
Raimundo, N.1
Song, L.2
Shutt, T.E.3
McKay, S.E.4
Cotney, J.5
Guan, M.X.6
-
39
-
-
0028949749
-
The clinical features of Leber’s hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation
-
PID: 7735876
-
Riordan-Eva P, Sanders MD, Govan GG, Sweeney MG, Da Costa J, Harding AE (1995) The clinical features of Leber’s hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation. Brain 118(Pt 2):319–337
-
(1995)
Brain
, vol.118
, pp. 319-337
-
-
Riordan-Eva, P.1
Sanders, M.D.2
Govan, G.G.3
Sweeney, M.G.4
Da Costa, J.5
Harding, A.E.6
-
40
-
-
84884416043
-
Germline mitochondrial DNA mutations aggravate ageing and can impair brain development
-
COI: 1:CAS:528:DC%2BC3sXhtlCgtL3L, PID: 23965628
-
Ross JM, Stewart JB, Hagstrom E, Brene S, Mourier A, Coppotelli G et al (2013) Germline mitochondrial DNA mutations aggravate ageing and can impair brain development. Nature 501:412–415
-
(2013)
Nature
, vol.501
, pp. 412-415
-
-
Ross, J.M.1
Stewart, J.B.2
Hagstrom, E.3
Brene, S.4
Mourier, A.5
Coppotelli, G.6
-
41
-
-
84931346628
-
Maternally transmitted mitochondrial DNA mutations can reduce lifespan
-
COI: 1:CAS:528:DC%2BC2MXksVyru78%3D, PID: 25299268
-
Ross JM, Coppotelli G, Hoffer BJ, Olson L (2014) Maternally transmitted mitochondrial DNA mutations can reduce lifespan. Sci Rep 4:6569
-
(2014)
Sci Rep
, vol.4
, pp. 6569
-
-
Ross, J.M.1
Coppotelli, G.2
Hoffer, B.J.3
Olson, L.4
-
42
-
-
80052303130
-
Autophagy and aging
-
COI: 1:CAS:528:DC%2BC3MXhtFakurzM, PID: 21884931
-
Rubinsztein DC, Marino G, Kroemer G (2011) Autophagy and aging. Cell 146:682–695
-
(2011)
Cell
, vol.146
, pp. 682-695
-
-
Rubinsztein, D.C.1
Marino, G.2
Kroemer, G.3
-
43
-
-
34250811284
-
Mitochondrial-nuclear communications
-
COI: 1:CAS:528:DC%2BD2sXhtVehtbzL, PID: 17227225
-
Ryan MT, Hoogenraad NJ (2007) Mitochondrial-nuclear communications. Annu Rev Biochem 76:701–722
-
(2007)
Annu Rev Biochem
, vol.76
, pp. 701-722
-
-
Ryan, M.T.1
Hoogenraad, N.J.2
-
44
-
-
4143081492
-
Two direct repeats cause most human mtDNA deletions
-
COI: 1:CAS:528:DC%2BD2cXmsl2isLw%3D, PID: 15313545
-
Samuels DC, Schon EA, Chinnery PF (2004) Two direct repeats cause most human mtDNA deletions. Trends Genet 20:393–398
-
(2004)
Trends Genet
, vol.20
, pp. 393-398
-
-
Samuels, D.C.1
Schon, E.A.2
Chinnery, P.F.3
-
45
-
-
80755169463
-
Human mitochondrial tRNAs: biogenesis, function, structural aspects, and diseases
-
COI: 1:CAS:528:DC%2BC3MXhs1ahtrrP, PID: 21910628
-
Suzuki T, Nagao A (2011) Human mitochondrial tRNAs: biogenesis, function, structural aspects, and diseases. Annu Rev Genet 45:299–329
-
(2011)
Annu Rev Genet
, vol.45
, pp. 299-329
-
-
Suzuki, T.1
Nagao, A.2
-
46
-
-
17744393686
-
Mitochondrial DNA mutations in human disease
-
COI: 1:CAS:528:DC%2BD2MXjs1OksLY%3D, PID: 15861210
-
Taylor RW, Turnbull DM (2005) Mitochondrial DNA mutations in human disease. Nat Rev Genet 6:389–402
-
(2005)
Nat Rev Genet
, vol.6
, pp. 389-402
-
-
Taylor, R.W.1
Turnbull, D.M.2
-
47
-
-
0026906885
-
Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness
-
PID: 1284550
-
van den Ouweland JMW, Lemkes HHPJ, Ruitenbeek W, Sandkuijl LA, de Vijlder MF, Struyvenberg PAA et al (1992) Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness. Nat Genet 1:368–371
-
(1992)
Nat Genet
, vol.1
, pp. 368-371
-
-
van den 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
-
48
-
-
23844558266
-
A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine
-
COI: 1:CAS:528:DC%2BD28Xlt1Wrtw%3D%3D, PID: 16285865
-
Wallace DC (2005) A mitochondrial paradigm of metabolic and degenerative diseases, aging, and cancer: a dawn for evolutionary medicine. Annu Rev Genet 39:359–407
-
(2005)
Annu Rev Genet
, vol.39
, pp. 359-407
-
-
Wallace, D.C.1
-
49
-
-
84866665390
-
Mitochondria and cancer. Nature reviews
-
COI: 1:CAS:528:DC%2BC38Xhtlylsb%2FO, PID: 23001348
-
Wallace DC (2012) Mitochondria and cancer. Nature reviews. Cancer 12:685–698
-
(2012)
Cancer
, vol.12
, pp. 685-698
-
-
Wallace, D.C.1
-
50
-
-
84901382660
-
Mitochondrial DNA genetics and the heteroplasmy conundrum in evolution and disease
-
PID: 24186072
-
Wallace DC, Chalkia D (2013) Mitochondrial DNA genetics and the heteroplasmy conundrum in evolution and disease. Cold Spring Harb Perspect Biol 5:a021220
-
(2013)
Cold Spring Harb Perspect Biol
, vol.5
, pp. a021220
-
-
Wallace, D.C.1
Chalkia, D.2
-
51
-
-
0033968067
-
Defect in modification at the anticodon wobble nucleotide of mitochondrial tRNA(Lys) with the MERRF encephalomyopathy pathogenic mutation
-
COI: 1:CAS:528:DC%2BD3cXpsFyguw%3D%3D, PID: 10675533
-
Yasukawa T, Suzuki T, Ishii N, Ueda T, Ohta S, Watanabe K (2000a) Defect in modification at the anticodon wobble nucleotide of mitochondrial tRNA(Lys) with the MERRF encephalomyopathy pathogenic mutation. FEBS Lett 467:175–178
-
(2000)
FEBS Lett
, vol.467
, pp. 175-178
-
-
Yasukawa, T.1
Suzuki, T.2
Ishii, N.3
Ueda, T.4
Ohta, S.5
Watanabe, K.6
-
52
-
-
0034635519
-
Modification defect at anticodon wobble nucleotide of mitochondrial tRNAs(Leu)(UUR) with pathogenic mutations of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
-
COI: 1:CAS:528:DC%2BD3cXht12gtLo%3D, PID: 10660592
-
Yasukawa T, Suzuki T, Ueda T, Ohta S, Watanabe K (2000b) Modification defect at anticodon wobble nucleotide of mitochondrial tRNAs(Leu)(UUR) with pathogenic mutations of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes. J Biol Chem 275:4251–4257
-
(2000)
J Biol Chem
, vol.275
, pp. 4251-4257
-
-
Yasukawa, T.1
Suzuki, T.2
Ueda, T.3
Ohta, S.4
Watanabe, K.5
-
53
-
-
37549048249
-
The BCL-2 protein family: opposing activities that mediate cell death
-
COI: 1:CAS:528:DC%2BD2sXhsVKrsrrP, PID: 18097445
-
Youle RJ, Strasser A (2008) The BCL-2 protein family: opposing activities that mediate cell death. Nat Rev Mol Cell Biol 9:47–59
-
(2008)
Nat Rev Mol Cell Biol
, vol.9
, pp. 47-59
-
-
Youle, R.J.1
Strasser, A.2
-
54
-
-
0347003512
-
Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family
-
COI: 1:CAS:528:DC%2BD2cXlvVOrtw%3D%3D, PID: 14681830
-
Zhao H, Li R, Wang Q, Yan Q, Deng JH, Han D et al (2004) Maternally inherited aminoglycoside-induced and nonsyndromic deafness is associated with the novel C1494T mutation in the mitochondrial 12S rRNA gene in a large Chinese family. Am J Hum Genet 74:139–152
-
(2004)
Am J Hum Genet
, vol.74
, pp. 139-152
-
-
Zhao, H.1
Li, R.2
Wang, Q.3
Yan, Q.4
Deng, J.H.5
Han, D.6
|