AbstractEvidence is presented showing that in a patient with fatal neurological syndrome, the homozygous 5 bp duplication in the cDNA of the NDUFS4 18 kDa subunit of complex I abolishes cAMP-dependent phosphorylation of this protein and activation of the complex. These findings show for the first time that human complex I is regulated via phosphorylation of the subunit encoded by the NDUFS4 gene
A study is presented on the expression and activity of complex I, as well as of other complexes of t...
SummaryWe report the cDNA cloning, chromosomal localization, and a mutation in the human nuclear gen...
Mitochondrial complex I deficiency is the most frequently encountered defect of the oxidative phosph...
Evidence is presented showing that in a patient with fatal neurological syndrome, the homozygous 5 b...
Evidence is presented showing that in a patient with fatal neurological syndrome, the homozygous 5 ...
AbstractEvidence is presented showing that in a patient with fatal neurological syndrome, the homozy...
A cAMP-dependent protein kinase (PKA) is localized in mammalian mitochondria with the catalytic site...
Recent work has revealed cAMP-dependent phosphorylation of the 18-kDa IP subunit of the mammalian co...
Presented is a study of the impact on the structure and function of human complex I of three differe...
Presented is a study of the impact on the structure and function of human complex I of three differe...
Among the mitochondrial disorders, complex I deficiencies are encountered frequently. Although some ...
Sequence analysis of mitochondrial and nuclear candidate genes of complex I in children with deficie...
Sequence analysis of mitochondrial and nuclear candidate genes of complex I in children with deficie...
AbstractResults of studies on the role of the 18 kDa (IP) polypeptide subunit of complex I, encoded ...
Although deficiency of complex I of the mitochondrial respiratory chain is a frequent cause of encep...
A study is presented on the expression and activity of complex I, as well as of other complexes of t...
SummaryWe report the cDNA cloning, chromosomal localization, and a mutation in the human nuclear gen...
Mitochondrial complex I deficiency is the most frequently encountered defect of the oxidative phosph...
Evidence is presented showing that in a patient with fatal neurological syndrome, the homozygous 5 b...
Evidence is presented showing that in a patient with fatal neurological syndrome, the homozygous 5 ...
AbstractEvidence is presented showing that in a patient with fatal neurological syndrome, the homozy...
A cAMP-dependent protein kinase (PKA) is localized in mammalian mitochondria with the catalytic site...
Recent work has revealed cAMP-dependent phosphorylation of the 18-kDa IP subunit of the mammalian co...
Presented is a study of the impact on the structure and function of human complex I of three differe...
Presented is a study of the impact on the structure and function of human complex I of three differe...
Among the mitochondrial disorders, complex I deficiencies are encountered frequently. Although some ...
Sequence analysis of mitochondrial and nuclear candidate genes of complex I in children with deficie...
Sequence analysis of mitochondrial and nuclear candidate genes of complex I in children with deficie...
AbstractResults of studies on the role of the 18 kDa (IP) polypeptide subunit of complex I, encoded ...
Although deficiency of complex I of the mitochondrial respiratory chain is a frequent cause of encep...
A study is presented on the expression and activity of complex I, as well as of other complexes of t...
SummaryWe report the cDNA cloning, chromosomal localization, and a mutation in the human nuclear gen...
Mitochondrial complex I deficiency is the most frequently encountered defect of the oxidative phosph...