(Q22009522)

GOA release 2020-03-11

R Triepels

1

R.

Triepels

1 reference

6 February 2023

J Smeitink

2

J.

Smeitink

1 reference

6 February 2023

J Loeffen

3

J.

Loeffen

1 reference

6 February 2023

R Smeets

4

R.

Smeets

1 reference

6 February 2023

C Buskens

5

C.

Buskens

1 reference

6 February 2023

F Trijbels

6

F.

Trijbels

1 reference

6 February 2023

L van den Heuvel

7

L.

Heuvel

1 reference

Journal of Inherited Metabolic Disease

6 February 2023

language of work or name

English

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publication date

April 1999

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published in

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volume

22

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issue

2

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page(s)

163-73

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cites work

Calcium-binding proteins: an overview

1 reference

12 December 2020

cDNA sequence and chromosomal localization of the remaining three human nuclear encoded iron sulphur protein (IP) subunits of complex I: the human IP fraction is completed

1 reference

12 December 2020

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

1 reference

12 December 2020

Presence of an acyl carrier protein in NADH:ubiquinone oxidoreductase from bovine heart mitochondria.

1 reference

12 December 2020

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

1 reference

12 December 2020

Normal mitochondrial genome in brain from patients with Parkinson's disease and complex I defect

1 reference

12 December 2020

A simple method for displaying the hydropathic character of a protein

1 reference

12 December 2020

Computational method to predict mitochondrially imported proteins and their targeting sequences

1 reference

12 December 2020

Molecular characterization and mutational analysis of the human B17 subunit of the mitochondrial respiratory chain complex I

1 reference

12 December 2020

The acyl-carrier protein in Neurospora crassa mitochondria is a subunit of NADH: ubiquinone reductase (complex I)

1 reference

12 December 2020

Hereditary tyrosinemia type 1: novel missense, nonsense and splice consensus mutations in the human fumarylacetoacetate hydrolase gene; variability of the genotype-phenotype relationship

1 reference

12 December 2020

Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystonia

1 reference

12 December 2020

Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes

1 reference

12 December 2020

Different respiratory-defective phenotypes of Neurospora crassa and Saccharomyces cerevisiae after inactivation of the gene encoding the mitochondrial acyl carrier protein.

1 reference

12 December 2020

Isolation, mapping, and genomic structure of an X-linked gene for a subunit of human mitochondrial complex I.

1 reference

12 December 2020

Studies on the mechanism of fatty acid synthesis. XIV. The prosthetic group of acyl carrier protein and the mode of its attachment to the protein

1 reference

12 December 2020

The human B22 subunit of the NADH-ubiquinone oxidoreductase maps to the region of chromosome 8 involved in branchio-oto-renal syndrome

1 reference

12 December 2020

Molecular cloning and characterization of the human mitochondrial NADH:oxidoreductase 10-kDa gene (NDUFV3)

1 reference

12 December 2020

Structural analysis of NADH: ubiquinone oxidoreductase from bovine heart mitochondria.

1 reference

12 December 2020

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

1 reference

12 December 2020

Determination of the cDNA sequence for the human mitochondrial 75-kDa Fe-S protein of NADH-coenzyme Q reductase

1 reference

12 December 2020

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

1 reference

12 December 2020

Cloning of the human cDNA sequence encoding the NADH:ubiquinone oxidoreductase MLRQ subunit

1 reference

12 December 2020

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

1 reference

12 December 2020

The investigation of mitochondrial respiratory chain disease

1 reference

12 December 2020

An unusually large multifunctional polypeptide in the erythromycin-producing polyketide synthase of Saccharopolyspora erythraea.

1 reference

12 December 2020

Cloning of the human mitochondrial 51 kDa subunit (NDUFV1) reveals a 100% antisense homology of its 3'UTR with the 5'UTR of the gamma-interferon inducible protein (IP-30) precursor: is this a link between mitochondrial myopathy and inflammation?

1 reference

12 December 2020

The 24-kDa subunit of the bovine mitochondrial NADH:ubiquinone oxidoreductase is a G protein

1 reference

12 December 2020

The characterization of a mitochondrial acyl carrier protein isoform isolated from Arabidopsis thaliana

1 reference

12 December 2020

The X-chromosomal NDUFA1 gene of complex I in mitochondrial encephalomyopathies: tissue expression and mutation detection

1 reference

12 December 2020

Identification of the subunits of bovine NADH dehydrogenase which are encoded by the mitochondrial genome

1 reference

12 December 2020

Identification and primary structure of five human NADH-ubiquinone oxidoreductase subunits

1 reference

12 December 2020

Benign mitochondrial encephalomyopathy in a patient with complex I deficiency

1 reference

12 December 2020

Common principles of protein translocation across membranes

1 reference

12 December 2020

Partial deficiency of complexes I and IV of the mitochondrial respiratory chain in skeletal muscle of two patients with mitochondrial myopathy

1 reference

12 December 2020

Lethal infantile mitochondrial disease with isolated complex I deficiency in fibroblasts but with combined complex I and IV deficiencies in muscle

1 reference

12 December 2020

Evidence for the existence of tissue specific isoenzymes of mitochondrial NADH dehydrogenase

1 reference

12 December 2020

Altered mitochondrial function in fibroblasts containing MELAS or MERRF mitochondrial DNA mutations.

1 reference

12 December 2020

Assignment of the PSST subunit gene of human mitochondrial complex I to chromosome 19p13

1 reference

12 December 2020

cDNA sequence and chromosomal localization of the NDUFS8 human gene coding for the 23 kDa subunit of the mitochondrial complex I.

1 reference

12 December 2020

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

1 reference

12 December 2020

A human cDNA encoding the homologue of NADH: ubiquinone oxidoreductase subunit B13

1 reference

12 December 2020

Deficiency of respiratory chain complex I is a common cause of Leigh disease.

1 reference

12 December 2020

The human NADH: ubiquinone oxidoreductase NDUFS5 (15 kDa) subunit: cDNA cloning, chromosomal localization, tissue distribution and the absence of mutations in isolated complex I-deficient patients

1 reference

12 December 2020

Electron transfer properties of NADH:ubiquinone reductase in the ND1/3460 and the ND4/11778 mutations of the Leber hereditary optic neuroretinopathy (LHON)

1 reference

12 December 2020

Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees

1 reference

12 December 2020

Complementary DNA sequencing: expressed sequence tags and human genome project

1 reference

12 December 2020

Identifiers

DOI

10.1023/A:1005402020569

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