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Priming DNA Replication from Triple Helix Oligonucleotides: Possible Threestranded DNA in DNA Polymerases

Molecular Biology International, 2011-01, Vol.2011 (2011), p.206-214

2011

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Are there three polynucleotide strands in the catalytic centre of DNA polymerases?

Biochimie, 2009-11, Vol.91 (11), p.1523-1530

Lestienne, Patrick P.

2009

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Mitochondrial DNA mutations in human diseases: a review

Biochimie, 1992-02, Vol.74 (2), p.123-130

Lestienne, P.

1992

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Mitochondrial DNA expression in mitochondrial myopathies and coordinated expression of nuclear genes involved in ATP production

The Journal of biological chemistry, 1993-06, Vol.268 (16), p.12156-12163

1993

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Initiation of DNA Replication by a Third Parallel DNA Strand Bound in a Triple-Helix Manner Leads to Strand Invasion

Biochemistry (Easton), 2008-05, Vol.47 (21), p.5689-5698

2008

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Normal Mitochondrial Genome in Brain from Patients with Parkinson's Disease and Complex I Defect

Journal of neurochemistry, 1990-11, Vol.55 (5), p.1810-1812

1990

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Replication of mitochondrial DNA occurs throughout the mitochondria of cultured human cells

Experimental cell research, 2003-09, Vol.289 (1), p.133-142

2003

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Mitochondrial DNA alterations and genetic diseases: a review

Biomedicine & pharmacotherapy, 1994, Vol.48 (5), p.199-214

1994

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Kearns-Sayre syndrome with muscle mitochondrial DNA deletion

The Lancet (British edition), 1988-04, Vol.1 (8590), p.885-885

1988

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Partial Triplication of mtDNA in Maternally Transmitted Diabetes Mellitus and Deafness

American journal of human genetics, 1998-10, Vol.63 (4), p.1227-1232

1998

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Different mechanisms inferred from sequences of human mitochondrial DNA deletions in ocular myopathies

Nucleic acids research, 1991-02, Vol.19 (3), p.493-496

1991

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Three DNA strands in the catalytic center of DNA polymerases

M.S. Médecine sciences, 2004-10, Vol.20 (10), p.854-856

Lestienne, Patrick

2004

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Mitochondrial DNA in Postmortem Brain from Patients with Parkinson's Disease

Journal of neurochemistry, 1991-05, Vol.56 (5), p.1819-1819

1991

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Self-organisation of an oligodeoxynucleotide containing the G- and C-rich stretches of the direct repeats of the human mitochondrial DNA

Biochimie, 2005-08, Vol.87 (8), p.725-735

2005

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Elongation of oligonucleotide primers forming a triple helix on double-stranded DNA templates by purified DNA polymerases

Biochemical and biophysical research communications, 2003-11, Vol.311 (2), p.380-385

2003

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Evolution of new tRNA-synthetase classes

Nature (London), 1988-10, Vol.335 (6190), p.503-504

LESTIENNE, PATRICK P

1988

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Self-organisation of an oligodeoxynucleotide containing the G- and C-rich stretches of the direct repeats of the human mitochondrial DNA

Biochimie, 2005-08, Vol.87 (8), p.725-735

2005

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Molecular Cloning of Human Calmitine, a Mitochondrial Calcium Binding Protein, Reveals Identity with Calsequestrine

Biochemical and biophysical research communications, 1994-09, Vol.203 (3), p.1477-1482

1994

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Oligoasthenospermia associated with multiple mitochondrial DNA rearrangements

Molecular human reproduction, 1997-09, Vol.3 (9), p.811-814

1997

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Deletions of mitochondrial DNA in Kearns-Sayre syndrome and ocular myopathies: Genetic, biochemical and morphological studies

Journal of the neurological sciences, 1991-02, Vol.101 (2), p.168-177

1991

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Base composition at mtDNA boundaries suggests a DNA triple helix model for human mitochondrial DNA large-scale rearrangements

Molecular genetics and metabolism, 2002-06, Vol.76 (2), p.123-132

2002

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Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromes

Journal of neurology, 1990-02, Vol.237 (1), p.5-10

1990

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Kearns-Sayre syndrome with sideroblastic anemia: molecular investigations

Neuropediatrics, 1992-08, Vol.23 (4), p.199-205

1992

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Different copy numbers of apparently identically deleted mitochondrial DNA in tissues from a patient with Kearns-Sayre syndrome detected by PCR

Biochemical and biophysical research communications, 1990-06, Vol.169 (3), p.1007-1015

1990

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Initiation of DNA Replication by a Third Parallel DNA Strand Bound in a Triple-Helix Manner Leads to Strand Invasion super([dagger])

Biochemistry (Easton), 2008-01, Vol.47 (21), p.5689-5698

2008

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Priming DNA Replication from Triple Helix Oligonucleotides: Possible Threestranded DNA in DNA Polymerases

Are there three polynucleotide strands in the catalytic centre of DNA polymerases?

Mitochondrial DNA mutations in human diseases: a review

Mitochondrial DNA expression in mitochondrial myopathies and coordinated expression of nuclear genes involved in ATP production

Initiation of DNA Replication by a Third Parallel DNA Strand Bound in a Triple-Helix Manner Leads to Strand Invasion

Normal Mitochondrial Genome in Brain from Patients with Parkinson's Disease and Complex I Defect

Replication of mitochondrial DNA occurs throughout the mitochondria of cultured human cells

Mitochondrial DNA alterations and genetic diseases: a review

Kearns-Sayre syndrome with muscle mitochondrial DNA deletion

Partial Triplication of mtDNA in Maternally Transmitted Diabetes Mellitus and Deafness

Different mechanisms inferred from sequences of human mitochondrial DNA deletions in ocular myopathies

Three DNA strands in the catalytic center of DNA polymerases

Mitochondrial DNA in Postmortem Brain from Patients with Parkinson's Disease

Self-organisation of an oligodeoxynucleotide containing the G- and C-rich stretches of the direct repeats of the human mitochondrial DNA

Elongation of oligonucleotide primers forming a triple helix on double-stranded DNA templates by purified DNA polymerases

Evolution of new tRNA-synthetase classes

Self-organisation of an oligodeoxynucleotide containing the G- and C-rich stretches of the direct repeats of the human mitochondrial DNA

Molecular Cloning of Human Calmitine, a Mitochondrial Calcium Binding Protein, Reveals Identity with Calsequestrine

Oligoasthenospermia associated with multiple mitochondrial DNA rearrangements

Deletions of mitochondrial DNA in Kearns-Sayre syndrome and ocular myopathies: Genetic, biochemical and morphological studies

Base composition at mtDNA boundaries suggests a DNA triple helix model for human mitochondrial DNA large-scale rearrangements

Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromes

Kearns-Sayre syndrome with sideroblastic anemia: molecular investigations

Different copy numbers of apparently identically deleted mitochondrial DNA in tissues from a patient with Kearns-Sayre syndrome detected by PCR

Initiation of DNA Replication by a Third Parallel DNA Strand Bound in a Triple-Helix Manner Leads to Strand Invasion super([dagger])

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