Related references
Note: Only part of the references are listed.Antenatal mitochondrial disease caused by mitochondrial ribosomal protein (MRPS22) mutation
A. Saada et al.
JOURNAL OF MEDICAL GENETICS (2007)
Deleterious mutation in the mitochondrial arginyl-transfer RNA synthetase gene is associated with pontocerebellar hypoplasia
Simon Edvardson et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
mtRF1a is a human mitochondrial translation release factor decoding the major termination Codons UAA and UAG
Hamid Reza Soleimanpour-Lichaei et al.
MOLECULAR CELL (2007)
Reconstructing the evolution of the mitochondrial ribosomal proteome
Paulien Smits et al.
NUCLEIC ACIDS RESEARCH (2007)
Cytoplasmic and mitochondrial protein translation in axonal and dendritic terminal arborization
Takahiro Chihara et al.
NATURE NEUROSCIENCE (2007)
Mitochondrial translation initiation factor 3 gene polymorphism associated with Parkinson's disease
Nadine Abahuni et al.
NEUROSCIENCE LETTERS (2007)
Chaperone properties of mammalian mitochondrial translation elongation factor Tu
Hiroaki Suzuki et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
Mitochondrial aspartyl-tRNA synthetase deficiency causes leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation
Gert C. Scheper et al.
NATURE GENETICS (2007)
Translation matters: protein synthesis defects in inherited disease
Gert C. Scheper et al.
NATURE REVIEWS GENETICS (2007)
Infantile encephalopathy and defective mitochondrial DNA translation in patients with mutations of mitochondrial elongation factors EFG1 and EFTu
Lucia Valente et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Distinct clinical phenotypes associated with a mutation in the mitochondrial translation elongation factor EFTs
Jan A. M. Smeitink et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
The molecular basis for tissue specificity of the oxidative phosphorylation deficiencies in patients with mutations in the mitochondrial translation factor EFG1
Hana Antonicka et al.
HUMAN MOLECULAR GENETICS (2006)
High-resolution whole-genome association study of Parkinson disease
DM Maraganore et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
Nuclear genes and mitochondrial translation: a new class of genetic disease
HT Jacobs et al.
TRENDS IN GENETICS (2005)
Toward the full set of human mitochondrial aminoacyl-tRNA synthetases:: Characterization of AspRS and TyrRS
L Bonnefond et al.
BIOCHEMISTRY (2005)
Functional polypeptides can be synthesized from human mitochondrial transcripts lacking termination codons
ZMA Chrzanowska-Lightowlers et al.
BIOCHEMICAL JOURNAL (2004)
Characterization of the human mitochondrial methionyl-tRNA synthetase
AC Spencer et al.
BIOCHEMISTRY (2004)
Defective mitochondrial translation caused by a ribosomal protein (MRPS16) mutation
C Miller et al.
ANNALS OF NEUROLOGY (2004)
Diminished synthesis of subunit a (ATP6) and altered function of ATP synthase and cytochrome c oxidase due to the mtDNA 2 bp microdeletion of TA at positions 9205 and 9206
P Jesina et al.
BIOCHEMICAL JOURNAL (2004)
Down-regulation of the mitochondrial translation system during terminal differentiation of HL-60 cells by 12-O-tetradecanoyl-1-phorbol-13-acetate -: Comparison with the cytoplasmic translation system
N Takeuchi et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Disorders of mitochondrial protein synthesis
HT Jacobs
HUMAN MOLECULAR GENETICS (2003)
Investigation of a pathogenic mtDNA microdeletion reveals a translation-dependent deadenylation decay pathway in human mitochondria
RJ Temperley et al.
HUMAN MOLECULAR GENETICS (2003)
The large subunit of the mammalian mitochondrial ribosome - Analysis of the complement of ribosomal proteins present
EC Koc et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Proteomic analysis of the mammalian mitochondrial ribosome - Identification of protein components in the 28 S small subunit
T Suzuki et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Cell-free translation reconstituted with purified components
Y Shimizu et al.
NATURE BIOTECHNOLOGY (2001)
Structural compensation for the deficit of rRNA with proteins in the mammalian mitochondrial ribosome - Systematic analysis of protein components of the large ribosomal subunit from mammalian mitochondria
T Suzuki et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
The small subunit of the mammalian mitochondrial ribosome - Identification of the full complement of ribosomal proteins present
EC Koc et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
The human lysyl-tRNA synthetase gene encodes both the cytoplasmic and mitochondrial enzymes by means of an unusual alternative splicing of the primary transcript
E Tolkunova et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Interaction of mammalian mitochondrial ribosomes with the inner membrane
MQ Liu et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Characterization and tRNA recognition of mammalian mitochondrial seryl-tRNA synthetase
T Yokogawa et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Mammalian mitochondrial ribosomal proteins (4) - Amino acid sequencing, characterization, and identification of corresponding gene sequences
TW O'Brien et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)
Mimicry grasps reality in translation termination
Y Nakamura et al.
CELL (2000)
Expression and characterization of the human mitochondrial leucyl-tRNA synthetase
JM Bullard et al.
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION (2000)
Share Paper
