-
1
-
-
0026624980
-
Diseases of the mitochondrial DNA
-
Wallace, D.C. Diseases of the mitochondrial DNA Annu. Rev. Biochem. 61, 1175-1212 (1992).
-
(1992)
Annu. Rev. Biochem.
, vol.61
, pp. 1175-1212
-
-
Wallace, D.C.1
-
2
-
-
0029638664
-
Mitochondrial DNA and disease
-
Johns, D.R. Mitochondrial DNA and disease. New Engl. J. Med. 333, 638-644 (1995).
-
(1995)
New Engl. J. Med.
, vol.333
, pp. 638-644
-
-
Johns, D.R.1
-
3
-
-
0026587335
-
Mitochondrial genetics: A paradigm for aging and degenerative diseases?
-
Wallace, D.C. Mitochondrial genetics: a paradigm for aging and degenerative diseases? Science 256, 628-632 (1992).
-
(1992)
Science
, vol.256
, pp. 628-632
-
-
Wallace, D.C.1
-
4
-
-
0029087931
-
Gene Therapy for mitochondrial DNA defects: Is it possible?
-
Chrzanowska-Lightowlers, Z.M.A., Lightowlers, R.N. & Turnbull, D.M. Gene Therapy for mitochondrial DNA defects: is it possible? Gene Therapy 2, 311-316 (1995).
-
(1995)
Gene Therapy
, vol.2
, pp. 311-316
-
-
Chrzanowska-Lightowlers, Z.M.A.1
Lightowlers, R.N.2
Turnbull, D.M.3
-
5
-
-
0026621445
-
Lys mutation in skeletal muscle of patients with myoclonus epilepsy and ragged-red fibres (MERRF)
-
Lys mutation in skeletal muscle of patients with myoclonus epilepsy and ragged-red fibres (MERRF). Am. J. Hum. Genet. 51, 1187-1200 (1992).
-
(1992)
Am. J. Hum. Genet.
, vol.51
, pp. 1187-1200
-
-
Boulet, L.1
Karpati, G.2
Shoubridge, E.A.3
-
6
-
-
0026608057
-
MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream or downstream mature transcripts
-
Chomyn, A. et al. MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream or downstream mature transcripts. Proc. Natl. Acad Sci. USA 89, 4221-4225 (1992).
-
(1992)
Proc. Natl. Acad Sci. USA
, vol.89
, pp. 4221-4225
-
-
Chomyn, A.1
-
7
-
-
0026573082
-
Leu(UUR) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes
-
Leu(UUR) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes. Mol. Cell. Biol. 12, 480-490 (1992).
-
(1992)
Mol. Cell. Biol.
, vol.12
, pp. 480-490
-
-
King, M.P.1
Koga, Y.2
Davidson, M.3
Schon, E.A.4
-
8
-
-
0026016180
-
Nuclear gadgets in mitochondrial DNA replication and transcription
-
Clayton, D.A. Nuclear gadgets in mitochondrial DNA replication and transcription. Trends Biochem. Sci. 16, 107-111 (1991).
-
(1991)
Trends Biochem. Sci.
, vol.16
, pp. 107-111
-
-
Clayton, D.A.1
-
9
-
-
0027058592
-
Transcription and replication of animal mitochondrial DNAs
-
Clayton, D.A. Transcription and replication of animal mitochondrial DNAs. Int. Rev. Cytol. 141, 217-232 (1992).
-
(1992)
Int. Rev. Cytol.
, vol.141
, pp. 217-232
-
-
Clayton, D.A.1
-
10
-
-
0026341239
-
Sequence-selective recognition of DNA by strand displacement with a thymine-substituted polyamide
-
Nielsen, P.E., Egholm, M., Berg, R.H. & Buchardt, O. Sequence-selective recognition of DNA by strand displacement with a thymine-substituted polyamide. Science 254, 1497-1500 (1991).
-
(1991)
Science
, vol.254
, pp. 1497-1500
-
-
Nielsen, P.E.1
Egholm, M.2
Berg, R.H.3
Buchardt, O.4
-
11
-
-
84990238662
-
Peptide nucleic acids (PNA). Oligonucleotide analogues with an achiral peptide backbone
-
Egholm, M., Buchardt, O., Nielsen, P.E. & Berg, R.H. Peptide nucleic acids (PNA). Oligonucleotide analogues with an achiral peptide backbone. J. Am. Chem. Soc. 114, 1895-1897 (1992).
-
(1992)
J. Am. Chem. Soc.
, vol.114
, pp. 1895-1897
-
-
Egholm, M.1
Buchardt, O.2
Nielsen, P.E.3
Berg, R.H.4
-
12
-
-
0027364174
-
PNA hybridizes to complementary oligonucleotides obeying the Watson-Crick hydrogen-bonding rules
-
Egholm, M. et al. PNA hybridizes to complementary oligonucleotides obeying the Watson-Crick hydrogen-bonding rules. Nature 365, 566-568 (1993).
-
(1993)
Nature
, vol.365
, pp. 566-568
-
-
Egholm, M.1
-
13
-
-
0028129843
-
Stability of peptide nucleic acids in human serum and cellular extracts
-
Demidov, V.V. et al. Stability of peptide nucleic acids in human serum and cellular extracts. Biochem. Pharmacol. 48, 1310-1313 (1994).
-
(1994)
Biochem. Pharmacol.
, vol.48
, pp. 1310-1313
-
-
Demidov, V.V.1
-
14
-
-
0023883150
-
Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies
-
Holt, I.J., Harding, A.E. & Morgan-Hughes, J.A. Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies. Nature 331, 717-719 (1988).
-
(1988)
Nature
, vol.331
, pp. 717-719
-
-
Holt, I.J.1
Harding, A.E.2
Morgan-Hughes, J.A.3
-
15
-
-
0024328462
-
Mitochondrial DNA deletions in progressive external opthalmoplegia and Kearns-Sayre syndrome
-
Moraes, C.T. et al. Mitochondrial DNA deletions in progressive external opthalmoplegia and Kearns-Sayre syndrome. New Engl. J. Med. 320, 1293-1299 (1989).
-
(1989)
New Engl. J. Med.
, vol.320
, pp. 1293-1299
-
-
Moraes, C.T.1
-
16
-
-
0024596946
-
A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA
-
Schon, E.A. et al. A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA. Science 244, 346-349 (1989).
-
(1989)
Science
, vol.244
, pp. 346-349
-
-
Schon, E.A.1
-
17
-
-
0027485066
-
Single base pair mutation analysis by PNA directed PCR clamping
-
Orum, H. et al. Single base pair mutation analysis by PNA directed PCR clamping. Nucleic Acids Res. 21, 5332-5336 (1993).
-
(1993)
Nucleic Acids Res.
, vol.21
, pp. 5332-5336
-
-
Orum, H.1
-
18
-
-
0022202524
-
Isolation and characterization of a DNA primase from human mitochondria
-
Wong, T.W. & Clayton, D.A. Isolation and characterization of a DNA primase from human mitochondria. J. Biol. Chem. 260, 11530-11536 (1985).
-
(1985)
J. Biol. Chem.
, vol.260
, pp. 11530-11536
-
-
Wong, T.W.1
Clayton, D.A.2
-
19
-
-
0025368281
-
Lys mutation
-
Lys mutation. Cell 61, 931-937 (1990).
-
(1990)
Cell
, vol.61
, pp. 931-937
-
-
Shoffner, J.M.1
-
20
-
-
0027190874
-
Clinical features associated with the A→G transition at nucleotide 8344 of mtDNA ("MERRF mutation")
-
Silvestri, G. et al. Clinical features associated with the A→G transition at nucleotide 8344 of mtDNA ("MERRF mutation"). Neurology 43, 1200-1206 (1993).
-
(1993)
Neurology
, vol.43
, pp. 1200-1206
-
-
Silvestri, G.1
-
21
-
-
0028199707
-
Single-stranded-DNA-binding proteins from human mitochondria and Escherichia coli have analogous physicochemical properties
-
Curth, U. et al. Single-stranded-DNA-binding proteins from human mitochondria and Escherichia coli have analogous physicochemical properties. Eur. J. Biochem. 221, 435-443 (1994).
-
(1994)
Eur. J. Biochem.
, vol.221
, pp. 435-443
-
-
Curth, U.1
-
22
-
-
0025124856
-
Structural and functional studies of the rat mitochondrial single strand DNA binding protein P16
-
Hoke, G.D., Pavco, P.A., Ledwith, B.J. & Van Tuyle, G.C. Structural and functional studies of the rat mitochondrial single strand DNA binding protein P16. Arch. Biochem. Biophys. 282, 116-124 (1990).
-
(1990)
Arch. Biochem. Biophys.
, vol.282
, pp. 116-124
-
-
Hoke, G.D.1
Pavco, P.A.2
Ledwith, B.J.3
Van Tuyle, G.C.4
-
23
-
-
0027874419
-
Stimulation of DNA polymerase gamma by a mitochondrial single-strand DNA binding protein
-
Genuario, R. & Wong, T.W. Stimulation of DNA polymerase gamma by a mitochondrial single-strand DNA binding protein. Cell. Mol. Biol. Res. 39, 625-634 (1993).
-
(1993)
Cell. Mol. Biol. Res.
, vol.39
, pp. 625-634
-
-
Genuario, R.1
Wong, T.W.2
-
24
-
-
0028959253
-
Stimulation of Drosophila mitochondrial DNA polymerase by single-stranded DNA-binding protein
-
Williams, A.J. & Kaguni, L.S. Stimulation of Drosophila mitochondrial DNA polymerase by single-stranded DNA-binding protein. J. Biol. Chem. 270, 860-865 (1995).
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 860-865
-
-
Williams, A.J.1
Kaguni, L.S.2
-
25
-
-
0021920551
-
Two binding modes in Escherichia coli single strand binding protein-single stranded DNA complexes
-
Lohman, T.M. & Overman, L.B. Two binding modes in Escherichia coli single strand binding protein-single stranded DNA complexes. J. Biol. Chem. 260, 3594-3603 (1985).
-
(1985)
J. Biol. Chem.
, vol.260
, pp. 3594-3603
-
-
Lohman, T.M.1
Overman, L.B.2
-
26
-
-
0024536726
-
DNA-protein conjugates can enter mitochondria via the protein import pathway
-
Vestweber, D. & Schatz, G. DNA-protein conjugates can enter mitochondria via the protein import pathway. Nature 338, 170-172 (1989).
-
(1989)
Nature
, vol.338
, pp. 170-172
-
-
Vestweber, D.1
Schatz, G.2
-
27
-
-
0028804570
-
Transfection of mitochondria: Strategy towards a gene therapy of mitochondrial DNA diseases
-
Seibel, P. et al. Transfection of mitochondria: strategy towards a gene therapy of mitochondrial DNA diseases. Nucl. Acids Res. 23, 10-17 (1995).
-
(1995)
Nucl. Acids Res.
, vol.23
, pp. 10-17
-
-
Seibel, P.1
-
29
-
-
0029055815
-
About the "Asian"-specific9-bp deletion of mtDNA
-
Torroni, A. et al. About the "Asian"-specific9-bp deletion of mtDNA.... Am. J. Hum. Genet. 57, 507-508 (1995).
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 507-508
-
-
Torroni, A.1
-
30
-
-
0019423856
-
Sequence and organisation of the human mitochondrial genome
-
Anderson, S. et al. Sequence and organisation of the human mitochondrial genome. Nature 290, 457-465 (1981).
-
(1981)
Nature
, vol.290
, pp. 457-465
-
-
Anderson, S.1
|