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?
- 17 April 1998
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 245 (2) , 599-606
- https://doi.org/10.1006/bbrc.1998.8486
Abstract
No abstract availableKeywords
This publication has 40 references indexed in Scilit:
- Deficiency of respiratory chain complex I is a common cause of leigh diseaseAnnals of Neurology, 1996
- Fatal mitochondrial myopathy, lactic acidosis, and complex I deficiency associated with a heteroplasmic A→G mutation at position 3251 in the mitochondrial tRNALeu(UUR) geneHuman Genetics, 1996
- The Mitochondrial DNA Mutation ND6*14,484C Associated with Leber Hereditary Optic Neuropathy, Leads to Deficiency of Complex I of the Respiratory ChainBiochemical and Biophysical Research Communications, 1995
- Maternally inherited hearing loss, ataxia and myoclonus associated with a novel point mutation in mitochondrial tRNA Ser(UCN) geneHuman Molecular Genetics, 1995
- Conservation of sequences of subunits of mitochondrial complex I and their relationships with other proteinsBiochimica et Biophysica Acta (BBA) - Bioenergetics, 1992
- Sequences of 20 subunits of NADH: Ubiquinone oxidoreductase from bovine heart mitochondriaJournal of Molecular Biology, 1992
- The respiratory‐chain NADH dehydrogenase (complex I) of mitochondriaEuropean Journal of Biochemistry, 1991
- Relationship between mitochondrial NADH-ubiquinone reductase and a bacterial NAD-reducing hydrogenaseBiochemistry, 1991
- Isolated and combined deficiencies of NADH dehydrogenase (complex I) in muscle tissue of children with mitochondrial myopathiesEuropean Journal of Pediatrics, 1990
- Purification and molecular and enzymic properties of mitochondrial NADH dehydrogenaseArchives of Biochemistry and Biophysics, 1979