about
RNA processing in human mitochondriaVisualization of RNA-protein interactions in living cells: FMRP and IMP1 interact on mRNAsLoss of the RNA-binding protein TACO1 causes late-onset mitochondrial dysfunction in miceStructure of the heterodimer of human NONO and paraspeckle protein component 1 and analysis of its role in subnuclear body formationAn artificial PPR scaffold for programmable RNA recognitionA bifunctional protein regulates mitochondrial protein synthesisMutation in MRPS34 compromises protein synthesis and causes mitochondrial dysfunctionConserved and novel functions for Arabidopsis thaliana MIA40 in assembly of proteins in mitochondria and peroxisomesEstrogen-mediated regulation of mitochondrial gene expression.Simultaneous processing and degradation of mitochondrial RNAs revealed by circularized RNA sequencingA network of orthogonal ribosome x mRNA pairs.The human mitochondrial transcriptomeLong noncoding RNAs are generated from the mitochondrial genome and regulated by nuclear-encoded proteins.SLIRP stabilizes LRPPRC via an RRM-PPR protein interface.Pentatricopeptide repeats: modular blocks for building RNA-binding proteins.Designer RNA-binding proteins: New tools for manipulating the transcriptome.Modular recognition of nucleic acids by PUF, TALE and PPR proteins.Specialization from synthesis: how ribosome diversity can customize protein function.Organelle transcriptomes: products of a deconstructed genome.Supernumerary proteins of mitochondrial ribosomes.MRPS27 is a pentatricopeptide repeat domain protein required for the translation of mitochondrially encoded proteins.Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia.Transcriptome-wide effects of a POLR3A gene mutation in patients with an unusual phenotype of striatal involvement.Hierarchical RNA Processing Is Required for Mitochondrial Ribosome Assembly.Transterm: a database of mRNAs and translational control elements.A gold(I) phosphine complex selectively induces apoptosis in breast cancer cells: implications for anticancer therapeutics targeted to mitochondria.Mapping of mitochondrial RNA-protein interactions by digital RNase footprinting.Adult-onset obesity is triggered by impaired mitochondrial gene expression.Mitochondria: Unusual features of the mammalian mitoribosome.Substrate and inhibitor specificities differ between human cytosolic and mitochondrial thioredoxin reductases: Implications for development of specific inhibitors.Regulation of a minimal transcriptome by repeat domain proteins.Engineered rRNA enhances the efficiency of selenocysteine incorporation during translation.Cellular logic with orthogonal ribosomes.LRPPRC-mediated folding of the mitochondrial transcriptome.Building a Parallel Metabolism within the Cell.Synthesizing cellular networks from evolved ribosome-mRNA pairs.A mutation in MT-TW causes a tRNA processing defect and reduced mitochondrial function in a family with Leigh syndrome.Mice lacking the mitochondrial exonuclease MGME1 accumulate mtDNA deletions without developing progeria.PTCD1 Is Required for 16S rRNA Maturation Complex Stability and Mitochondrial Ribosome Assembly.Defects in RNA metabolism in mitochondrial disease.
P50
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P50
description
Australian biochemist
@en
hulumtues
@sq
onderzoeker
@nl
հետազոտող
@hy
name
Oliver Rackham
@ast
Oliver Rackham
@en
Oliver Rackham
@es
Oliver Rackham
@nl
Oliver Rackham
@sl
type
label
Oliver Rackham
@ast
Oliver Rackham
@en
Oliver Rackham
@es
Oliver Rackham
@nl
Oliver Rackham
@sl
prefLabel
Oliver Rackham
@ast
Oliver Rackham
@en
Oliver Rackham
@es
Oliver Rackham
@nl
Oliver Rackham
@sl
P1053
E-1264-2013
P106
P1153
10243028300
P21
P31
P3829
P496
0000-0002-5301-9624