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Volumn 17, Issue 10, 2010, Pages 1525-1528
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A human mitochondriopathy caused by AIF mutation
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Author keywords
[No Author keywords available]
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Indexed keywords
APOPTOSIS INDUCING FACTOR;
CELL NUCLEUS DNA;
DNA;
FLAVINE ADENINE NUCLEOTIDE;
MITOCHONDRIAL DNA;
POLY(ADENOSINE DIPHOSPHATE RIBOSE);
CAENORHABDITIS ELEGANS;
CELL MEMBRANE PERMEABILITY;
CELL SURVIVAL;
CHROMATIN CONDENSATION;
CYTOPLASM;
CYTOSOL;
DISORDERS OF MITOCHONDRIAL FUNCTIONS;
DNA BINDING;
DNA DAMAGE;
DNA DEGRADATION;
DNA FRAGMENTATION;
DNA REPAIR;
DROSOPHILA MELANOGASTER;
EDITORIAL;
EMBRYO DEVELOPMENT;
ENZYME ACTIVITY;
GENE DELETION;
GENE LOCATION;
GENE MUTATION;
GENETIC COUNSELING;
HOMOLOGOUS RECOMBINATION;
HUMAN;
INCIDENCE;
INTRON;
MEMBRANE PERMEABILITY;
NERVE CELL;
NERVOUS SYSTEM DEVELOPMENT;
NONHUMAN;
OXIDATION REDUCTION STATE;
OXIDATIVE PHOSPHORYLATION;
OXIDATIVE STRESS;
PATHOGENESIS;
PRIORITY JOURNAL;
PROTEIN FOLDING;
RESPIRATORY CHAIN;
RETINA DETACHMENT;
SACCHAROMYCES CEREVISIAE;
SKELETAL MUSCLE;
X CHROMOSOME;
ANIMALS;
APOPTOSIS INDUCING FACTOR;
BINDING SITES;
COMPUTER SIMULATION;
GENE DELETION;
HUMANS;
MICE;
MITOCHONDRIAL DISEASES;
MUTAGENESIS, INSERTIONAL;
OLIGONUCLEOTIDES;
PROTEIN STRUCTURE, TERTIARY;
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EID: 77956698243
PISSN: 13509047
EISSN: 14765403
Source Type: Journal
DOI: 10.1038/cdd.2010.88 Document Type: Editorial |
Times cited : (10)
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References (12)
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