-
1
-
-
12344293822
-
Detection of mitochondrial DNA depletion in living human cells using PicoGreen staining
-
N. Ashley D. Harris J. Poulton Detection of mitochondrial DNA depletion in living human cells using PicoGreen staining Exp. Cell. Res. 303 2005 432-446
-
(2005)
Exp. Cell. Res.
, vol.303
, pp. 432-446
-
-
Ashley, N.1
Harris, D.2
Poulton, J.3
-
2
-
-
0027496432
-
Nuclear complementation restores mtDNA levels in cultured cells from a patient with mtDNA depletion
-
A.G. Bodnar J.M. Cooper I.J. Holt J.V. Leonard A.H. Schapira Nuclear complementation restores mtDNA levels in cultured cells from a patient with mtDNA depletion Am. J. Hum. Genet. 53 1993 663-669
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 663-669
-
-
Bodnar, A.G.1
Cooper, J.M.2
Holt, I.J.3
Leonard, J.V.4
Schapira, A.H.5
-
3
-
-
3042513691
-
Mitochondria dysfunction of Alzheimer's disease cybrids enhances Abeta toxicity
-
S.M. Cardoso I. Santana R.H. Swerdlow C.R. Oliveira Mitochondria dysfunction of Alzheimer's disease cybrids enhances Abeta toxicity J. Neurochem. 89 2004 1417-1426
-
(2004)
J. Neurochem.
, vol.89
, pp. 1417-1426
-
-
Cardoso, S.M.1
Santana, I.2
Swerdlow, R.H.3
Oliveira, C.R.4
-
4
-
-
0028238418
-
Platelet-mediated transformation of mtDNA-less human cells: Analysis of phenotypic variability among clones from normal individuals-and complementation behavior of the tRNALys mutation causing myoclonic epilepsy and ragged red fibers
-
A. Chomyn S.T. Lai R. Shakeley N. Bresolin G. Scarlato G. Attardi Platelet-mediated transformation of mtDNA-less human cells: Analysis of phenotypic variability among clones from normal individuals-and complementation behavior of the tRNALys mutation causing myoclonic epilepsy and ragged red fibers Am. J. Hum. Genet. 54 1994 966-974
-
(1994)
Am. J. Hum. Genet.
, vol.54
, pp. 966-974
-
-
Chomyn, A.1
Lai, S.T.2
Shakeley, R.3
Bresolin, N.4
Scarlato, G.5
Attardi, G.6
-
5
-
-
0031876808
-
The influence of nuclear background on the biochemical expression of 3460 Leber's hereditary optic neuropathy
-
H.R. Cock S.J. Tabrizi J.M. Cooper A.H. Schapira The influence of nuclear background on the biochemical expression of 3460 Leber's hereditary optic neuropathy Ann. Neurol. 44 1998 187-193
-
(1998)
Ann. Neurol.
, vol.44
, pp. 187-193
-
-
Cock, H.R.1
Tabrizi, S.J.2
Cooper, J.M.3
Schapira, A.H.4
-
6
-
-
0029079541
-
Different cellular backgrounds confer a marked advantage to either mutant or wild-type mitochondrial genomes
-
D.R. Dunbar P.A. Moonie H.T. Jacobs I.J. Holt Different cellular backgrounds confer a marked advantage to either mutant or wild-type mitochondrial genomes Proc. Natl Acad. Sci. USA 92 1995 6562-6566
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 6562-6566
-
-
Dunbar, D.R.1
Moonie, P.A.2
Jacobs, H.T.3
Holt, I.J.4
-
8
-
-
0025836655
-
Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction
-
J. Hayashi S. Ohta A. Kikuchi M. Takemitsu Y. Goto I. Nonaka Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction Proc. Natl Acad. Sci. USA 88 1991 10614-10618
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 10614-10618
-
-
Hayashi, J.1
Ohta, S.2
Kikuchi, A.3
Takemitsu, M.4
Goto, Y.5
Nonaka, I.6
-
9
-
-
0344564146
-
A novel mitochondrial DNA-like sequence in the human nuclear genome
-
C. Herrnstadt W. Clevenger S.S. Ghosh C. Anderson E. Fahy S. Miller N. Howell R.E. Davis A novel mitochondrial DNA-like sequence in the human nuclear genome Genomics 60 1999 67-77
-
(1999)
Genomics
, vol.60
, pp. 67-77
-
-
Herrnstadt, C.1
Clevenger, W.2
Ghosh, S.S.3
Anderson, C.4
Fahy, E.5
Miller, S.6
Howell, N.7
Davis, R.E.8
-
10
-
-
0030060823
-
Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14,459 that causes Leber hereditary optic neuropathy and dystonia
-
A.S. Jun I.A. Trounce M.D. Brown J.M. Shoffner D.C. Wallace Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14,459 that causes Leber hereditary optic neuropathy and dystonia Mol. Cell. Biol. 16 1996 771-777
-
(1996)
Mol. Cell. Biol.
, vol.16
, pp. 771-777
-
-
Jun, A.S.1
Trounce, I.A.2
Brown, M.D.3
Shoffner, J.M.4
Wallace, D.C.5
-
11
-
-
0030750574
-
Expanding the functional human mitochondrial DNA database by the establishment of primate xenomitochondrial cybrids
-
L. Kenyon C.T. Moraes Expanding the functional human mitochondrial DNA database by the establishment of primate xenomitochondrial cybrids Proc. Natl Acad. Sci. USA 94 1997 9131-9135
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 9131-9135
-
-
Kenyon, L.1
Moraes, C.T.2
-
12
-
-
0024448458
-
Human cells lacking mtDNA: Repopulation with exogenous mitochondria complementation
-
M.P. King G. Attardi Human cells lacking mtDNA: Repopulation with exogenous mitochondria complementation Science 246 1989 500-503
-
(1989)
Science
, vol.246
, pp. 500-503
-
-
King, M.P.1
Attardi, G.2
-
13
-
-
0026573082
-
Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes
-
M.P. King Y. Koga M. Davidson E.A. Schon Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes Mol. Cell. Biol. 12 1992 480-490
-
(1992)
Mol. Cell. Biol.
, vol.12
, pp. 480-490
-
-
King, M.P.1
Koga, Y.2
Davidson, M.3
Schon, E.A.4
-
15
-
-
0030059079
-
Aging-dependent functional alterations of mitochondrial DNA (mtDNA) from human fibroblasts transferred into mtDNA-less cells
-
K.A. Laderman J.R. Penny F. Mazzucchelli N. Bresolin G. Scarlato G. Attardi Aging-dependent functional alterations of mitochondrial DNA (mtDNA) from human fibroblasts transferred into mtDNA-less cells J. Biol. Chem. 271 1996 15891-15897
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 15891-15897
-
-
Laderman, K.A.1
Penny, J.R.2
Mazzucchelli, F.3
Bresolin, N.4
Scarlato, G.5
Attardi, G.6
-
16
-
-
0036559590
-
Nuclear mitochondrial interplay in the modulation of the homopolymeric tract length heteroplasmy in the control (D-loop) region of the mitochondrial DNA
-
S. Malik H. Sudoyo P. Pramoonjago H. Suryadi T. Sukarna M. Njunting E. Sahiratmadja S. Marzuki Nuclear mitochondrial interplay in the modulation of the homopolymeric tract length heteroplasmy in the control (D-loop) region of the mitochondrial DNA Hum. Genet. 110 2002 402-411
-
(2002)
Hum. Genet.
, vol.110
, pp. 402-411
-
-
Malik, S.1
Sudoyo, H.2
Pramoonjago, P.3
Suryadi, H.4
Sukarna, T.5
Njunting, M.6
Sahiratmadja, E.7
Marzuki, S.8
-
17
-
-
0028929372
-
In vitro analysis of mutations causing myoclonus epilepsy with ragged-red fibers in the mitochondrial tRNA(Lys)gene: Two genotypes produce similar phenotypes
-
J.P. Masucci M. Davidson Y. Koga E.A. Schon M.P. King In vitro analysis of mutations causing myoclonus epilepsy with ragged-red fibers in the mitochondrial tRNA(Lys)gene: Two genotypes produce similar phenotypes Mol. Cell. Biol. 15 1995 2872-2881
-
(1995)
Mol. Cell. Biol.
, vol.15
, pp. 2872-2881
-
-
Masucci, J.P.1
Davidson, M.2
Koga, Y.3
Schon, E.A.4
King, M.P.5
-
18
-
-
0029800941
-
Creation and characterization of mitochondrial DNA-depleted cell lines with 'neuronal-like' properties
-
S.W. Miller P.A. Trimmer W.D. Parker Jr R.E. Davis Creation and characterization of mitochondrial DNA-depleted cell lines with 'neuronal-like' properties J. Neurochem. 67 1996 1897-1907
-
(1996)
J. Neurochem.
, vol.67
, pp. 1897-1907
-
-
Miller, S.W.1
Trimmer, P.A.2
Parker Jr., W.D.3
Davis, R.E.4
-
19
-
-
0027219982
-
Ntera 2 cells: A human cell line with characteristics expected of a human committed neuronal progenitor cell
-
S.J. Pleasure V.M. Lee Ntera 2 cells: A human cell line with characteristics expected of a human committed neuronal progenitor cell J. Neurosci. Res. 35 1993 585-602
-
(1993)
J. Neurosci. Res.
, vol.35
, pp. 585-602
-
-
Pleasure, S.J.1
Lee, V.M.2
-
20
-
-
0026583471
-
Pure, postmitotic, polarized human neurons derived from NTera 2 cells provide a system for expressing exogenous proteins in terminally differentiated neurons
-
S.J. Pleasure C. Page V.M. Lee Pure, postmitotic, polarized human neurons derived from NTera 2 cells provide a system for expressing exogenous proteins in terminally differentiated neurons J. Neurosci. 12 1992 1802-1815
-
(1992)
J. Neurosci.
, vol.12
, pp. 1802-1815
-
-
Pleasure, S.J.1
Page, C.2
Lee, V.M.3
-
21
-
-
0031843532
-
Cybrids in Alzheimer's disease: A cellular model of the disease?
-
E.A. Schon E.A. Shoubridge C.T. Moraes Cybrids in Alzheimer's disease: A cellular model of the disease? Neurology 51 1998 326-327
-
(1998)
Neurology
, vol.51
, pp. 326-327
-
-
Schon, E.A.1
Shoubridge, E.A.2
Moraes, C.T.3
-
22
-
-
0033544323
-
Familial multisystem degeneration with parkinsonism associated with the 11,778 mitochondrial DNA mutation
-
D.K. Simon S.M. Pulst J.P. Sutton S.E. Browne M.F. Beal D.R. Johns Familial multisystem degeneration with parkinsonism associated with the 11,778 mitochondrial DNA mutation Neurology 53 1999 1787-1793
-
(1999)
Neurology
, vol.53
, pp. 1787-1793
-
-
Simon, D.K.1
Pulst, S.M.2
Sutton, J.P.3
Browne, S.E.4
Beal, M.F.5
Johns, D.R.6
-
23
-
-
0030960845
-
Atypical parkinsonism in a family of Portuguese ancestry: Absence of CAG repeat expansion in the MJD1 gene
-
J.P. Sutton S.M. Pulst Atypical parkinsonism in a family of Portuguese ancestry: Absence of CAG repeat expansion in the MJD1 gene Neurology 48 1997 1285-1290
-
(1997)
Neurology
, vol.48
, pp. 1285-1290
-
-
Sutton, J.P.1
Pulst, S.M.2
-
24
-
-
0036189213
-
Mitochondrial DNA-related mitochondrial dysfunction in neurodegenerative diseases
-
R.H. Swerdlow Mitochondrial DNA-related mitochondrial dysfunction in neurodegenerative diseases Arch. Pathol. Lab. Med. 126 2002 271-280
-
(2002)
Arch. Pathol. Lab. Med.
, vol.126
, pp. 271-280
-
-
Swerdlow, R.H.1
-
25
-
-
0029908226
-
Origin and functional consequences of the complex I defect in Parkinson's disease
-
R.H. Swerdlow J.K. Parks S.W. Miller J.B. Tuttle P.A. Trimmer J.P. Sheehan J.P. Bennett Jr. R.E. Davis W.D. Parker Jr. Origin and functional consequences of the complex I defect in Parkinson's disease Ann. Neurol. 40 1996 663-671
-
(1996)
Ann. Neurol.
, vol.40
, pp. 663-671
-
-
Swerdlow, R.H.1
Parks, J.K.2
Miller, S.W.3
Tuttle, J.B.4
Trimmer, P.A.5
Sheehan, J.P.6
Bennett Jr., J.P.7
Davis, R.E.8
Parker Jr., W.D.9
-
26
-
-
0030724118
-
Cybrids in Alzheimer's disease: A cellular model of the disease?
-
R.H. Swerdlow J.K. Parks D.S. Cassarino D.J. Maguire R.S. Maguire J.P. Bennett Jr. R.E. Davis W.D. Parker Jr. Cybrids in Alzheimer's disease: A cellular model of the disease? Neurology 49 1997 918-925
-
(1997)
Neurology
, vol.49
, pp. 918-925
-
-
Swerdlow, R.H.1
Parks, J.K.2
Cassarino, D.S.3
Maguire, D.J.4
Maguire, R.S.5
Bennett Jr., J.P.6
Davis, R.E.7
Parker Jr., W.D.8
-
27
-
-
0031716355
-
Mitochondria in sporadic amyotrophic lateral sclerosis
-
R.H. Swerdlow S.W. Miller J.K. Parks J.P. Sheehan D.S. Cassarino D.J. Maguire J.P. Sheehan R.S. Maguire G. Pattee V.C. Juel L.H. Phillips J.B. Tuttle J.P. Bennett Jr. R.E. Davis W.D. Parker Jr. Mitochondria in sporadic amyotrophic lateral sclerosis Exp. Neurol. 153 1998 135-142
-
(1998)
Exp. Neurol.
, vol.153
, pp. 135-142
-
-
Swerdlow, R.H.1
Miller, S.W.2
Parks, J.K.3
Sheehan, J.P.4
Cassarino, D.S.5
Maguire, D.J.6
Sheehan, J.P.7
Maguire, R.S.8
Pattee, G.9
Juel, V.C.10
Phillips, L.H.11
Tuttle, J.B.12
Bennett Jr., J.P.13
Davis, R.E.14
Parker Jr., W.D.15
-
28
-
-
0033822098
-
Mitochondrial dysfunction in cybrid lines expressing mitochondrial genes from patients with PSP
-
R.H. Swerdlow L.I. Golbe J.K. Parks D.S. Cassarino D.R. Binder A.E. Grawey I. Litvan J.P. Bennett Jr. G.F. Wooten W.D. Parker Mitochondrial dysfunction in cybrid lines expressing mitochondrial genes from patients with PSP J. Neurochem. 75 2000 1681-1684
-
(2000)
J. Neurochem.
, vol.75
, pp. 1681-1684
-
-
Swerdlow, R.H.1
Golbe, L.I.2
Parks, J.K.3
Cassarino, D.S.4
Binder, D.R.5
Grawey, A.E.6
Litvan, I.7
Bennett Jr., J.P.8
Wooten, G.F.9
Parker, W.D.10
-
30
-
-
33044509580
-
Development of a heteroplasmic mitochondrial DNA standard reference material for detection of heteroplasmy and low frequency mutations
-
[Online] Available online: www.nist.gov/sigmaxi/Posters00/abst/ Tully-abst.htm
-
Tully, L.A., Schwarz, F.P., Levin, B.C., 1999. Development of a heteroplasmic mitochondrial DNA standard reference material for detection of heteroplasmy and low frequency mutations [Online]. Available online: www.nist.gov/sigmaxi/Posters00/abst/Tully-abst.htm
-
(1999)
-
-
Tully, L.A.1
Schwarz, F.P.2
Levin, B.C.3
-
31
-
-
0027361386
-
Human neurons derived from a teratocarcinoma cell line express solely the 695-amino acid amyloid precursor protein and produce intracellular beta-amyloid or A4 peptides
-
A.M. Wertkin R.S. Turner S.J. Pleasure T.E. Golde S.G. Younkin J.Q. Trojanowski V.M. Lee Human neurons derived from a teratocarcinoma cell line express solely the 695-amino acid amyloid precursor protein and produce intracellular beta-amyloid or A4 peptides Proc. Natl Acad. Sci. USA 90 1993 9513-9517
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 9513-9517
-
-
Wertkin, A.M.1
Turner, R.S.2
Pleasure, S.J.3
Golde, T.E.4
Younkin, S.G.5
Trojanowski, J.Q.6
Lee, V.M.7
-
33
-
-
0026457825
-
Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy
-
M. Yoneda A. Chomyn A. Martinuzzi O. Hurko G. Attardi Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy Proc. Natl Acad. Sci. USA 89 1992 11164-11168
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 11164-11168
-
-
Yoneda, M.1
Chomyn, A.2
Martinuzzi, A.3
Hurko, O.4
Attardi, G.5
-
34
-
-
0027403522
-
Inducible expression of neuronal glutamate receptor channels in the NT2 human cell line
-
D.P. Younkin C.M. Tang M. Hardy U.R. Reddy Q.Y. Shi S.J. Pleasure V.M. Lee D. Pleasure Inducible expression of neuronal glutamate receptor channels in the NT2 human cell line Proc. Natl Acad. Sci. USA 90 1993 2174-2178
-
(1993)
Proc. Natl. Acad. Sci. USA
, vol.90
, pp. 2174-2178
-
-
Younkin, D.P.1
Tang, C.M.2
Hardy, M.3
Reddy, U.R.4
Shi, Q.Y.5
Pleasure, S.J.6
Lee, V.M.7
Pleasure, D.8
|