Published in Trends Mol Med on May 02, 2006
Quality control of mitochondria: protection against neurodegeneration and ageing. EMBO J (2008) 3.39
Progressive parkinsonism in mice with respiratory-chain-deficient dopamine neurons. Proc Natl Acad Sci U S A (2007) 2.77
Inherited mitochondrial optic neuropathies. J Med Genet (2008) 2.50
Mitochondrial translation and beyond: processes implicated in combined oxidative phosphorylation deficiencies. J Biomed Biotechnol (2010) 2.01
Variable and tissue-specific subunit composition of mitochondrial m-AAA protease complexes linked to hereditary spastic paraplegia. Mol Cell Biol (2006) 2.00
Quality control of mitochondrial proteostasis. Cold Spring Harb Perspect Biol (2011) 1.55
m-AAA protease-driven membrane dislocation allows intramembrane cleavage by rhomboid in mitochondria. EMBO J (2007) 1.54
Spastic paraplegia gene 7 in patients with spasticity and/or optic neuropathy. Brain (2012) 1.34
Autocatalytic processing of m-AAA protease subunits in mitochondria. Mol Biol Cell (2009) 1.11
The role of mitochondria in neurodegenerative diseases. J Neurol (2011) 1.05
SPG7 Is an Essential and Conserved Component of the Mitochondrial Permeability Transition Pore. Mol Cell (2015) 0.96
The crystal structure of apo-FtsH reveals domain movements necessary for substrate unfolding and translocation. Proc Natl Acad Sci U S A (2009) 0.92
Congenital bovine spinal dysmyelination is caused by a missense mutation in the SPAST gene. Neurogenetics (2009) 0.86
Crystal structure of the ATPase domain of the human AAA+ protein paraplegin/SPG7. PLoS One (2009) 0.82
New roles for OMA1 metalloprotease: From mitochondrial proteostasis to metabolic homeostasis. Adipocyte (2013) 0.75
Mitochondrial ClpP activity is required for cisplatin resistance in human cells. Biochim Biophys Acta (2015) 0.75
Predominant cerebellar phenotype in spastic paraplegia 7 (SPG7). Hum Genome Var (2015) 0.75
The m-AAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondria. Cell (2005) 3.72
SLP-2 is required for stress-induced mitochondrial hyperfusion. EMBO J (2009) 3.61
Quality control of mitochondria: protection against neurodegeneration and ageing. EMBO J (2008) 3.39
Prohibitins control cell proliferation and apoptosis by regulating OPA1-dependent cristae morphogenesis in mitochondria. Genes Dev (2008) 2.76
Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28. Nat Genet (2010) 2.66
Regulation of OPA1 processing and mitochondrial fusion by m-AAA protease isoenzymes and OMA1. J Cell Biol (2009) 2.65
Making heads or tails of phospholipids in mitochondria. J Cell Biol (2011) 2.55
The genetic interactome of prohibitins: coordinated control of cardiolipin and phosphatidylethanolamine by conserved regulators in mitochondria. J Cell Biol (2009) 2.22
Protein degradation within mitochondria: versatile activities of AAA proteases and other peptidases. Crit Rev Biochem Mol Biol (2007) 2.18
Lung stress and strain during mechanical ventilation: any difference between statics and dynamics? Crit Care Med (2013) 2.14
The E3 ligase parkin maintains mitochondrial integrity by increasing linear ubiquitination of NEMO. Mol Cell (2013) 2.12
An intersubunit signaling network coordinates ATP hydrolysis by m-AAA proteases. Mol Cell (2009) 2.12
Variable and tissue-specific subunit composition of mitochondrial m-AAA protease complexes linked to hereditary spastic paraplegia. Mol Cell Biol (2006) 2.00
Maternal and offspring pools of osteocalcin influence brain development and functions. Cell (2013) 2.00
Prohibitin function within mitochondria: essential roles for cell proliferation and cristae morphogenesis. Biochim Biophys Acta (2008) 1.96
Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia. J Cell Biol (2003) 1.95
Formation of membrane-bound ring complexes by prohibitins in mitochondria. Mol Biol Cell (2004) 1.92
Two deubiquitylases act on mitofusin and regulate mitochondrial fusion along independent pathways. Mol Cell (2013) 1.90
OPA1 processing reconstituted in yeast depends on the subunit composition of the m-AAA protease in mitochondria. Mol Biol Cell (2007) 1.87
Mitochondrial quality control: a matter of life and death for neurons. EMBO J (2012) 1.83
Lung stress and strain during mechanical ventilation: any safe threshold? Am J Respir Crit Care Med (2011) 1.77
NMR characterization of kinase p38 dynamics in free and ligand-bound forms. Angew Chem Int Ed Engl (2006) 1.61
Membrane protein degradation by AAA proteases in mitochondria. Biochim Biophys Acta (2002) 1.57
Quality control of mitochondrial proteostasis. Cold Spring Harb Perspect Biol (2011) 1.55
Time to generate ventilator-induced lung injury among mammals with healthy lungs: a unifying hypothesis. Intensive Care Med (2011) 1.55
m-AAA protease-driven membrane dislocation allows intramembrane cleavage by rhomboid in mitochondria. EMBO J (2007) 1.54
Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases. PLoS Genet (2011) 1.54
Characterization of peptides released from mitochondria: evidence for constant proteolysis and peptide efflux. J Biol Chem (2004) 1.53
Impaired folding of the mitochondrial small TIM chaperones induces clearance by the i-AAA protease. J Mol Biol (2012) 1.51
Prohibitins and the functional compartmentalization of mitochondrial membranes. J Cell Sci (2009) 1.49
Effects of reduced dialysate calcium on calcium-phosphorus product and bone metabolism in hemodialysis patients. Nephron Clin Pract (2004) 1.46
Regulation of mitochondrial fusion by the F-box protein Mdm30 involves proteasome-independent turnover of Fzo1. J Cell Biol (2006) 1.44
Oma1, a novel membrane-bound metallopeptidase in mitochondria with activities overlapping with the m-AAA protease. J Biol Chem (2003) 1.42
Intramitochondrial transport of phosphatidic acid in yeast by a lipid transfer protein. Science (2012) 1.36
The i-AAA protease YME1L and OMA1 cleave OPA1 to balance mitochondrial fusion and fission. J Cell Biol (2014) 1.34
Clinical review: Extracorporeal membrane oxygenation. Crit Care (2011) 1.34
A mitochondrial phosphatase required for cardiolipin biosynthesis: the PGP phosphatase Gep4. EMBO J (2010) 1.26
Prohibitins interact genetically with Atp23, a novel processing peptidase and chaperone for the F1Fo-ATP synthase. Mol Biol Cell (2006) 1.26
Using wavelet de-noised spectra in NMR screening. J Magn Reson (2005) 1.25
Regulation of mitochondrial phospholipids by Ups1/PRELI-like proteins depends on proteolysis and Mdm35. EMBO J (2010) 1.24
AAA proteases in mitochondria: diverse functions of membrane-bound proteolytic machines. Res Microbiol (2009) 1.22
Nonredundant roles of mitochondria-associated F-box proteins Mfb1 and Mdm30 in maintenance of mitochondrial morphology in yeast. Mol Biol Cell (2006) 1.19
Emerging health technologies: informing and supporting health policy early. Health Policy (2008) 1.18
TRIAP1/PRELI complexes prevent apoptosis by mediating intramitochondrial transport of phosphatidic acid. Cell Metab (2013) 1.16
Stress-induced OMA1 activation and autocatalytic turnover regulate OPA1-dependent mitochondrial dynamics. EMBO J (2014) 1.15
Mitofusin 2 builds a bridge between ER and mitochondria. Cell (2008) 1.14
Autocatalytic processing of m-AAA protease subunits in mitochondria. Mol Biol Cell (2009) 1.11
Functional evaluation of paraplegin mutations by a yeast complementation assay. Hum Mutat (2010) 1.09
Role of the novel metallopeptidase Mop112 and saccharolysin for the complete degradation of proteins residing in different subcompartments of mitochondria. J Biol Chem (2005) 1.08
Ugo1 and Mdm30 act sequentially during Fzo1-mediated mitochondrial outer membrane fusion. J Cell Sci (2011) 1.07
Loss of prohibitin membrane scaffolds impairs mitochondrial architecture and leads to tau hyperphosphorylation and neurodegeneration. PLoS Genet (2012) 1.07
Substrate recognition by AAA+ ATPases: distinct substrate binding modes in ATP-dependent protease Yme1 of the mitochondrial intermembrane space. Mol Cell Biol (2007) 1.04
Substrate specific consequences of central pore mutations in the i-AAA protease Yme1 on substrate engagement. J Struct Biol (2006) 1.03
The mitochondrial electron transport chain is dispensable for proliferation and differentiation of epidermal progenitor cells. Stem Cells (2011) 1.03
Mitochondrial AAA proteases--towards a molecular understanding of membrane-bound proteolytic machines. Biochim Biophys Acta (2011) 1.02
Studying proteolysis within mitochondria. Methods Mol Biol (2007) 1.01
NMR analysis of a Tau phosphorylation pattern. J Am Chem Soc (2006) 1.00
The human Cdc37.Hsp90 complex studied by heteronuclear NMR spectroscopy. J Biol Chem (2008) 1.00
Evidence for a novel mitochondria-to-nucleus signalling pathway in respiring cells lacking i-AAA protease and the ABC-transporter Mdl1. Gene (2006) 0.98
Towards ultraprotective mechanical ventilation. Curr Opin Anaesthesiol (2012) 0.96
Discovery of Mycobacterium tuberculosis protein tyrosine phosphatase A (MptpA) inhibitors based on natural products and a fragment-based approach. Chembiochem (2005) 0.96
Proteolytic control of mitochondrial function and morphogenesis. Biochim Biophys Acta (2012) 0.96
AFG3L2 supports mitochondrial protein synthesis and Purkinje cell survival. J Clin Invest (2012) 0.95
Presequence-dependent folding ensures MrpL32 processing by the m-AAA protease in mitochondria. EMBO J (2011) 0.94
Membrane protein turnover by the m-AAA protease in mitochondria depends on the transmembrane domains of its subunits. EMBO Rep (2004) 0.94
Electron cryomicroscopy structure of a membrane-anchored mitochondrial AAA protease. J Biol Chem (2010) 0.93
NMR backbone assignment of the mitogen-activated protein (MAP) kinase p38. J Biomol NMR (2005) 0.93
Low-dose chest computed tomography for quantitative and visual anatomical analysis in patients with acute respiratory distress syndrome. Intensive Care Med (2014) 0.92
Noninvasive carbon dioxide monitoring in a porcine model of acute lung injury due to smoke inhalation and burns. Shock (2013) 0.91
Dynamic survey of mitochondria by ubiquitin. EMBO Rep (2014) 0.90
The mitochondrial amidoxime-reducing component (mARC1) is a novel signal-anchored protein of the outer mitochondrial membrane. J Biol Chem (2012) 0.89
Loss of prohibitin induces mitochondrial damages altering β-cell function and survival and is responsible for gradual diabetes development. Diabetes (2013) 0.89
A novel function for the 90 kDa heat-shock protein (Hsp90): facilitating nuclear export of 60 S ribosomal subunits. Biochem J (2002) 0.89
Familial Alzheimer's disease-associated presenilin-1 alters cerebellar activity and calcium homeostasis. J Clin Invest (2014) 0.88
Reversible assembly of the ATP-binding cassette transporter Mdl1 with the F1F0-ATP synthase in mitochondria. J Biol Chem (2004) 0.87
Targeting capacity and conservation of PreP homologues localization in mitochondria of different species. J Mol Biol (2011) 0.85
The life of proteins: the good, the mostly good and the ugly. Nat Struct Mol Biol (2011) 0.84
In vitro study of drug-eluting stent coatings based on poly(L-lactide) incorporating cyclosporine A - drug release, polymer degradation and mechanical integrity. J Mater Sci Mater Med (2007) 0.84
[Quality indicators for National Disease Management Guidelines using the example of the National Disease Management Guideline for "Chronic Heart Failure"]. Z Evid Fortbild Qual Gesundhwes (2011) 0.83
Loss of the m-AAA protease subunit AFG₃L₂ causes mitochondrial transport defects and tau hyperphosphorylation. EMBO J (2014) 0.82
How psychological framing affects economic market prices in the lab and field. Proc Natl Acad Sci U S A (2013) 0.81
Pseudotumor cerebri due to proximal haemodialysis fistula. Nephrol Dial Transplant (2006) 0.81
Mitochondrial shaping cuts. Biochim Biophys Acta (2006) 0.80
Low-dose CT for quantitative analysis in acute respiratory distress syndrome. Crit Care (2013) 0.80
Mitochondrial lipid transport at a glance. J Cell Sci (2013) 0.79
NMR backbone assignment of the N-terminal domain of human HSP90. J Biomol NMR (2006) 0.79
StAR enhances transcription of genes encoding the mitochondrial proteases involved in its own degradation. Mol Endocrinol (2013) 0.79
Microadenomas of the pituitary gland in children with and without hypophyseal dysfunction in magnetic resonance imaging. J Pediatr Endocrinol Metab (2002) 0.79
Intravenous balanced solutions: from physiology to clinical evidence. Anaesthesiol Intensive Ther (2015) 0.78
Distinct seasonal growth patterns of the bacterium Planktotalea frisia in the North Sea and specific interaction with phytoplankton algae. FEMS Microbiol Ecol (2013) 0.78
[Sonographic findings in the diagnostic course of vascular access for hemodialysis]. Med Klin (Munich) (2005) 0.78
Backbone NMR assignment of the low-molecular-weight protein tyrosine phosphatase (MPtpA) from Mycobacterium tuberculosis. J Biomol NMR (2005) 0.77
Acute lung injury/acute respiratory distress syndrome pathophysiology: what we have learned from computed tomography scanning. Curr Opin Crit Care (2008) 0.77
1H, 13C and 15N backbone resonance assignment of the integrin alpha2 I-domain. J Biomol NMR (2003) 0.77
Information service on new and emerging health technologies: identification and prioritization processes for a European union-wide newsletter. Int J Technol Assess Health Care (2009) 0.77
1,2-N-migration in a gold-catalysed synthesis of functionalised indenes by the 1,1-carboalkoxylation of ynamides. Chemistry (2014) 0.77
1H, 13C and 15N backbone resonance assignment of the peptidyl-prolyl cis-trans isomerase Pin1. J Biomol NMR (2002) 0.76
Albumin in critically ill patients: the ideal colloid? Curr Opin Crit Care (2015) 0.76
Prone position ameliorates lung elastance and increases functional residual capacity independently from lung recruitment. Intensive Care Med Exp (2015) 0.76
How much NMR data is required to determine a protein-ligand complex structure? Chembiochem (2005) 0.76