New DNA-binding activity of rat mitochondrial transcription termination factor (mTERF).

PubWeight™: 0.78‹?›

🔗 View Article (PMID 15671493)

Published in J Biochem on December 01, 2004

Authors

Ascensión Prieto-Martín1, Julio Montoya, Francisco Martínez-Azorín

Author Affiliations

1: Departamento de Bioquímica y Biología Molecular y Celular, Universidad de Zaragoza, Miguel Servet 177, E-50013 Zaragoza, Spain.

Articles by these authors

Platelet cytochrome c oxidase activity and quantity in septic patients. Crit Care Med (2011) 2.23

Replication and transcription of mammalian mitochondrial DNA. Exp Physiol (2003) 1.99

Unmasking the causes of multifactorial disorders: OXPHOS differences between mitochondrial haplogroups. Hum Mol Genet (2010) 1.79

Transient overexpression of mitochondrial transcription factor A (TFAM) is sufficient to stimulate mitochondrial DNA transcription, but not sufficient to increase mtDNA copy number in cultured cells. Nucleic Acids Res (2004) 1.53

Human mitochondrial transcription factor A induces a U-turn structure in the light strand promoter. Nat Struct Mol Biol (2011) 1.51

An intragenic suppressor in the cytochrome c oxidase I gene of mouse mitochondrial DNA. Hum Mol Genet (2003) 1.44

A randomised controlled trial of motivational interviewing for smoking cessation. Br J Gen Pract (2006) 1.27

Differences of sperm motility in mitochondrial DNA haplogroup U sublineages. Gene (2005) 1.21

Human mitochondrial haplogroup H: the highest VO2max consumer--is it a paradox? Mitochondrion (2009) 1.18

Tissue-specific differences in mitochondrial activity and biogenesis. Mitochondrion (2010) 1.17

Cerebral folate deficiency and leukoencephalopathy caused by a mitochondrial DNA deletion. Ann Neurol (2006) 1.12

Import of mitochondrial transcription factor A (TFAM) into rat liver mitochondria stimulates transcription of mitochondrial DNA. Nucleic Acids Res (2003) 1.12

Human mitochondrial mTERF wraps around DNA through a left-handed superhelical tandem repeat. Nat Struct Mol Biol (2010) 1.12

Oxidative phosphorylation differences between mitochondrial DNA haplogroups modify the risk of Leber's hereditary optic neuropathy. Biochim Biophys Acta (2012) 1.11

Bilateral striatal necrosis associated with a novel mutation in the mitochondrial ND6 gene. Ann Neurol (2003) 1.10

Transcriptomic profiling of TK2 deficient human skeletal muscle suggests a role for the p53 signalling pathway and identifies growth and differentiation factor-15 as a potential novel biomarker for mitochondrial myopathies. BMC Genomics (2014) 1.04

Human mitochondrial variants influence on oxygen consumption. Mitochondrion (2008) 1.01

Whole-exome sequencing identifies a variant of the mitochondrial MT-ND1 gene associated with epileptic encephalopathy: west syndrome evolving to Lennox-Gastaut syndrome. Hum Mutat (2013) 1.00

Kearns-Sayre syndrome: cerebral folate deficiency, MRI findings and new cerebrospinal fluid biochemical features. Mitochondrion (2010) 0.97

Association of mitochondrial haplogroup J and mtDNA oxidative damage in two different North Spain elderly populations. Biogerontology (2008) 0.95

Liver failure caused by herpes simplex virus thymidine kinase plus ganciclovir therapy is associated with mitochondrial dysfunction and mitochondrial DNA depletion. Hum Gene Ther (2003) 0.94

Cisplatin-mediated impairment of mitochondrial DNA metabolism inversely correlates with glutathione levels. Biochem J (2008) 0.91

CPEO and KSS differ in the percentage and location of the mtDNA deletion. Mitochondrion (2009) 0.90

Genetic causes of cerebral folate deficiency: clinical, biochemical and therapeutic aspects. Drug Discov Today (2012) 0.89

A new mutation in the gene encoding mitochondrial seryl-tRNA synthetase as a cause of HUPRA syndrome. BMC Nephrol (2013) 0.89

Mitochondrial gene expression is regulated at multiple levels and differentially in the heart and liver by thyroid hormones. Curr Genet (2008) 0.89

Mitochondrial diseases mimicking neurotransmitter defects. Mitochondrion (2008) 0.88

Autism associated to a deficiency of complexes III and IV of the mitochondrial respiratory chain. Invest Clin (2010) 0.88

The P1/P2 proteins of the human ribosomal stalk are required for ribosome binding and depurination by ricin in human cells. FEBS J (2012) 0.88

Mitochondrial DNA depletion syndrome: new descriptions and the use of citrate synthase as a helpful tool to better characterise the patients. Mol Genet Metab (2012) 0.86

Survival and mitochondrial function in septic patients according to mitochondrial DNA haplogroup. Crit Care (2012) 0.86

In vitro transcription termination activity of the Drosophila mitochondrial DNA-binding protein DmTTF. Biochem Biophys Res Commun (2005) 0.86

Mitochondrial DNA content of human spermatozoa. Biol Reprod (2003) 0.86

The A8344G mutation in mitochondrial DNA associated with stroke-like episodes and gastrointestinal dysfunction. Acta Neuropathol (2002) 0.85

New mitochondrial DNA mutations in tRNA associated with three severe encephalopamyopathic phenotypes: neonatal, infantile, and childhood onset. Neurogenetics (2012) 0.85

Mitochondrial antibiograms in personalized medicine. Hum Mol Genet (2012) 0.84

Altered expression of master regulatory genes of adipogenesis in lipomas from patients bearing tRNA(Lys) point mutations in mitochondrial DNA. Mol Genet Metab (2006) 0.84

Steady exercise removes VO(2max) difference between mitochondrial genomic variants. Mitochondrion (2009) 0.84

Coenzyme Q₁₀ deficiency in mitochondrial DNA depletion syndromes. Mitochondrion (2013) 0.83

Severe septic patients with mitochondrial DNA haplogroup JT show higher survival rates: a prospective, multicenter, observational study. PLoS One (2013) 0.83

Coenzyme Q10 deficiency associated with a mitochondrial DNA depletion syndrome: a case report. Clin Biochem (2008) 0.83

Macular lesion resembling adult-onset vitelliform macular dystrophy in Kearns-Sayre syndrome with multiple mtDNA deletions. Clin Experiment Ophthalmol (2010) 0.82

Association of human mitochondrial DNA variants with plasma LDL levels. Mitochondrion (2008) 0.82

Rebooting the human mitochondrial phylogeny: an automated and scalable methodology with expert knowledge. BMC Bioinformatics (2011) 0.82

Phosphorylation of rat mitochondrial transcription termination factor (mTERF) is required for transcription termination but not for binding to DNA. Nucleic Acids Res (2004) 0.82

Moroccan mitochondrial genetic background suggests prehistoric human migrations across the Gibraltar Strait. Mitochondrion (2009) 0.81

OXPHOS toxicogenomics and Parkinson's disease. Mutat Res (2011) 0.80

Hearing loss in a patient with the myopathic form of mitochondrial DNA depletion syndrome and a novel mutation in the TK2 gene. Pediatr Res (2010) 0.80

Free radicals-mediated damage in transmitochondrial cells harboring the T14487C mutation in the ND6 gene of mtDNA. FEBS Lett (2005) 0.80

Higher platelet cytochrome oxidase specific activity in surviving than in non-surviving septic patients. Crit Care (2014) 0.79

Expression of the Drosophila melanogaster ATP synthase alpha subunit gene is regulated by a transcriptional element containing GAF and Adf-1 binding sites. Eur J Biochem (2004) 0.79

Mitochondrial pharmacogenomics: barcode for antibiotic therapy. Drug Discov Today (2009) 0.78

Mitochondrial pharma-Q-genomics: targeting the OXPHOS cytochrome b. Drug Discov Today (2010) 0.78

'Progress' renders detrimental an ancient mitochondrial DNA genetic variant. Hum Mol Genet (2011) 0.78

Biochemical parameters to assess choroid plexus dysfunction in Kearns-Sayre syndrome patients. Mitochondrion (2011) 0.78

[Pearson syndrome. Case report]. Invest Clin (2011) 0.77

Maternally inherited susceptibility to cancer. Biochim Biophys Acta (2010) 0.77

A new pathologic mitochondrial DNA mutation in the cytochrome oxidase subunit I (MT-CO1). Hum Mutat (2008) 0.77

Mitochondrial ribosome and Ménière's disease: a pilot study. Eur Arch Otorhinolaryngol (2012) 0.77

Mitochondria from ejaculated human spermatozoa do not synthesize proteins. FEBS Lett (2003) 0.76

A MELAS/MERRF phenotype associated with the mitochondrial DNA 5521G>A mutation. J Neurol Neurosurg Psychiatry (2010) 0.76

FK506 affects mitochondrial protein synthesis and oxygen consumption in human cells. Cell Biol Toxicol (2013) 0.76

Influence of mtDNA genetic variation on antibiotic therapy. Pharmacogenomics (2010) 0.75

Effects of Tributyltin Chloride on Cybrids with or without an ATP Synthase Pathologic Mutation. Environ Health Perspect (2016) 0.75

Folate analysis for the differential diagnosis of profound cerebrospinal fluid folate deficiency. Clin Biochem (2011) 0.75

New MT-ND1 pathologic mutation for Leber hereditary optic neuropathy. Clin Experiment Ophthalmol (2014) 0.75

[Deletions of the mitochondrial DNA associated to chronic progressive external ophthalmoplegia with ragged-red fibers in 2 Brazilian patients]. Med Clin (Barc) (2006) 0.75

Stressed cybrids model demyelinated axons in multiple sclerosis. Metab Brain Dis (2013) 0.75

Phylogenetic analysis of mitochondrial DNA in a patient with Kearns-Sayre syndrome containing a novel 7629-bp deletion. Mitochondrial DNA (2013) 0.75

Peripheral neuropathy with ataxia in childhood as a result of the G8363A mutation in mitochondrial DNA. Pediatr Res (2004) 0.75

Read-through therapy for mitochondrial DNA nonsense mutations. Drug Discov Today (2012) 0.75

De Toni-Debré-Fanconi syndrome due to a palindrome-flanked deletion in mitochondrial DNA. Pediatr Nephrol (2004) 0.75