Related references
Note: Only part of the references are listed.ELAC2 Mutations Cause a Mitochondrial RNA Processing Defect Associated with Hypertrophic Cardiomyopathy
Tobias B. Haack et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2013)
GRSF1 Regulates RNA Processing in Mitochondrial RNA Granules
Alexis A. Jourdain et al.
CELL METABOLISM (2013)
The Mitochondrial RNA-Binding Protein GRSF1 Localizes to RNA Granules and Is Required for Posttranscriptional Mitochondrial Gene Expression
Hana Antonicka et al.
CELL METABOLISM (2013)
Human RNase H1 Is Associated with Protein P32 and Is Involved in Mitochondrial Pre-rRNA Processing
Hongjiang Wu et al.
PLOS ONE (2013)
Moonlighting is mainstream: Paradigm adjustment required
Shelley D. Copley
BIOESSAYS (2012)
HSD10 disease: clinical consequences of mutations in the HSD17B10 gene
Johannes Zschocke
JOURNAL OF INHERITED METABOLIC DISEASE (2012)
A subcomplex of human mitochondrial RNase P is a bifunctional methyltransferase-extensive moonlighting in mitochondrial tRNA biogenesis
Elisa Vilardo et al.
NUCLEIC ACIDS RESEARCH (2012)
Mitochondrial quality control: an integrated network of pathways
Fabian Fischer et al.
TRENDS IN BIOCHEMICAL SCIENCES (2012)
Human Mitochondrial tRNAs: Biogenesis, Function, Structural Aspects, and Diseases
Tsutomu Suzuki et al.
ANNUAL REVIEW OF GENETICS, VOL 45 (2011)
RNA processing in human mitochondria
Maria I. G. Lopez Sanchez et al.
CELL CYCLE (2011)
Maternally Inherited Essential Hypertension Is Associated With the Novel 4263A>G Mutation in the Mitochondrial tRNAIle Gene in a Large Han Chinese Family
Shiwen Wang et al.
CIRCULATION RESEARCH (2011)
Structure of MyTH4-FERM Domains in Myosin VIIa Tail Bound to Cargo
Lin Wu et al.
SCIENCE (2011)
Mechanism of neurodegeneration of neurons with mitochondrial DNA mutations
Andrey Y. Abramov et al.
BRAIN (2010)
A non-enzymatic function of 17β-hydroxysteroid dehydrogenase type 10 is required for mitochondrial integrity and cell survival
Katharina Rauschenberger et al.
EMBO MOLECULAR MEDICINE (2010)
Structures of the Human GTPase MMAA and Vitamin B12-dependent Methylmalonyl-CoA Mutase and Insight into Their Complex Formation
D. Sean Froese et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
A single Arabidopsis organellar protein has RNase P activity
Anthony Gobert et al.
NATURE STRUCTURAL & MOLECULAR BIOLOGY (2010)
SEDLIN Forms Homodimers: Characterisation of SEDLIN Mutations and Their Interactions with Transcription Factors MBP1, PITX1 and SF1
Jeshmi Jeyabalan et al.
PLOS ONE (2010)
Study of patients and carriers with 2-methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency: Difficulties in the diagnosis
Judit Garcia-Villoria et al.
CLINICAL BIOCHEMISTRY (2009)
tRNA recognition, processing, and disease: Hypotheses around an unorthodox type of RNase P in human mitochondria
Johann Holzmann et al.
MITOCHONDRION (2009)
RNase P without RNA: Identification and Functional Reconstitution of the Human Mitochondrial tRNA Processing Enzyme
Johann Holzmann et al.
CELL (2008)
The Dickkopf-homolog 3 is expressed in tumor endothelial cells and supports capillary formation
Gerold Untergasser et al.
INTERNATIONAL JOURNAL OF CANCER (2008)
The reduced expression of the HADH2 protein causes X-linked mental retardation, choreoathetosis, and abnormal behavior
Claus Lenski et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
HSD17B10: A gene involved in cognitive function through metabolism of isoleucine and neuroactive steroids
Song-Yu Yang et al.
MOLECULAR GENETICS AND METABOLISM (2007)
Molecular dysfunction associated with the human mitochondrial 3302A>G mutation in the MTTL1 (mt-tRNALeu(UUR)) gene
Katharina Maniura-Weber et al.
NUCLEIC ACIDS RESEARCH (2006)
2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency:: An x-linked inborn error of isoleucine metabolism that may mimic a mitochondrial disease
J García-Villoria et al.
PEDIATRIC RESEARCH (2005)
Multiple functions of type 10 17β-hydroxysteroid dehydrogenase
SY Yang et al.
TRENDS IN ENDOCRINOLOGY AND METABOLISM (2005)
Determination of stable housekeeping genes, differentially regulated target genes and sample integrity: BestKeeper - Excel-based tool using pair-wise correlations
MW Pfaffl et al.
BIOTECHNOLOGY LETTERS (2004)
2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency is caused by mutations in the HADH2 gene
R Ofman et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2003)
2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency in a 23-year-old man
SE Olpin et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2002)
A new mathematical model for relative quantification in real-time RT-PCR
MW Pfaffl
NUCLEIC ACIDS RESEARCH (2001)
Progressive infantile neurodegeneration caused by 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency: A novel inborn error of branched-chain fatty acid and isoleucine metabolism
J Zschocke et al.
PEDIATRIC RESEARCH (2000)