Human NADH:ubiquinone oxidoreductase.

PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT

1951 • 319,299 citations

[1] Citrate synthase

1969 • 1,958 citations

The NADH:ubiquinone oxidoreductase (complex I) of respiratory chains

1992 • 772 citations

Isolated complex I deficiency in children: Clinical, biochemical and genetic aspects

2000 • 284 citations

Demonstration of a New Pathogenic Mutation in Human Complex I Deficiency: A 5-bp Duplication in the Nuclear Gene Encoding the 18-kD (AQDQ) Subunit

1998 • 262 citations

Respiratory chain complex I deficiency

1999 • 255 citations

Leigh syndrome associated with a mutation in the NDUFS7 (PSST) nuclear encoded subunit of complex I

1999 • 191 citations

Human Mitochondrial Complex I in Health and Disease

1999 • 153 citations

Membrane-bound ribosomes in HeLa cells

1969 • 148 citations

The nuclear‐encoded 18 kDa (IP) AQDQ subunit of bovine heart complex I is phosphorylated by the mitochondrial cAMP‐dependent protein kinase

1996 • 120 citations

A mitochondrial myopathy with a deficiency of respiratory chain NADH-CoQ reductase activity

1979 • 113 citations

Clinical features, investigation, and management of patients with defects of mitochondrial DNA

1997 • 107 citations

Leigh disease caused by the mitochondrial DNA G14459A mutation in unrelated families

2000 • 99 citations

Mutation in the NDUFS4 gene of complex I abolishes cAMP‐dependent activation of the complex in a child with fatal neurological syndrome

2001 • 94 citations

The oxidative phosphorylation (OXPHOS) system: nuclear genes and human genetic diseases

2001 • 83 citations

cDNA of Eight Nuclear Encoded Subunits of NADH:Ubiquinone Oxidoreductase: Human Complex I cDNA Characterization Completed

1998 • 82 citations

Investigation of mitochondrial metabolism in small human skeletal muscle biopsy specimens. Improvement of preparation procedure

1985 • 71 citations

Nuclear genes of human complex I of the mitochondrial electron transport chain: state of the art

1998 • 70 citations

Lacticacidemia

1993 • 69 citations

NADH‐coenzyme Q reductase (complex I) deficiency: heterogeneity in phenotype and biochemical findings

1996 • 64 citations

NADH:ubiquinone oxidoreductase from bovine heart mitochondria: sequence of a novel 17.2‐kDa subunit

1998 • 61 citations

Human Complex I Defects Can Be Resolved by Monoclonal Antibody Analysis into Distinct Subunit Assembly Patterns

2001 • 61 citations

Disorders of the mitochondrial respiratory chain: clinical manifestations and diagnostic approach

1988 • 60 citations

Isolation, Mapping, and Genomic Structure of an X-Linked Gene for a Subunit of Human Mitochondrial Complex I

1996 • 49 citations

Problems with the biochemical diagnosis in mitochondrial (encephalo-)myopathies

1993 • 46 citations

Molecular cloning and characterization of the active human mitochondrial NADH:ubiquinone oxidoreductase 24-kDa gene (NDUFV2) and its pseudogene

1995 • 39 citations

Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblasts

1999 • 37 citations

Molecular Cloning and Characterization of the Human Mitochondrial NADH:Oxidoreductase 10-kDa Gene (NDUFV3)

1997 • 33 citations

Determination of enzyme activities for prenatal diagnosis of respiratory chain deficiency

2000 • 33 citations

Biochemical, genetic and immunoblot analyses of 17 patients with an isolated cytochrome c oxidase deficiency

1999 • 32 citations

Determination of enzyme activities for prenatal diagnosis of respiratory chain deficiency

2000 • 32 citations

Practical problems in detecting abnormal mitochondrial function and genomes

2000 • 31 citations

Genomic structure of the human NDUFS8 gene coding for the iron–sulfur TYKY subunit of the mitochondrial NADH:ubiquinone oxidoreductase

1998 • 24 citations

Structural Organization and Chromosomal Localization of the Human Nuclear Gene (NDUFV2) for the 24-kDa Iron-Sulfur Subunit of Complex I in Mitochondrial Respiratory Chain

1995 • 24 citations

lntron based radiation hybrid mapping of 15 complex I genes of the human electron transport chain

1998 • 23 citations

Cloning of the Human Mitochondrial 51 kDa Subunit (NDUFV1) Reveals a 100% Antisense Homology of Its 3′UTR with the 5′UTR of the γ-Interferon Inducible Protein (IP-30) Precursor: Is This a Link between Mitochondrial Myopathy and Inflammation?

1998 • 23 citations

Human NDUFB9 Gene: Genomic Organization and a Possible Candidate Gene Associated with Deafness Disorder Mapped to Chromosome 8q13

1999 • 17 citations

Characterization of the human complex I NDUFB7 and 17.2-kDa cDNAs and mutational analysis of 19 genes of the HP fraction in complex I-deficient-patients

2000 • 16 citations

Human NDUFS3 gene coding for the 30-kDa subunit of mitochondrial Complex I: genomic organization and expression

2000 • 16 citations

Mapping<footref rid="foot01"><sup>1</sup></footref> of the NDUFA2, NDUFA6, NDUFA7, NDUFB8, and NDUFS8 electron transport chain genes by intron based radiation hybrid mapping

1998 • 15 citations

A Prognostic Index as Diagnostic Strategy in Children Suspected of Mitochondriocytopathy

2000 • 15 citations

The structure of the human NDUFV1 gene encoding the 51-kDa subunit of mitochondrial complex I 61, A305, 1997.-->

1999 • 5 citations