Published in EMBO J on May 18, 2010
Making heads or tails of phospholipids in mitochondria. J Cell Biol (2011) 2.55
Metabolism and regulation of glycerolipids in the yeast Saccharomyces cerevisiae. Genetics (2012) 1.98
Mitochondrial phosphatase PTPMT1 is essential for cardiolipin biosynthesis. Cell Metab (2011) 1.97
The conserved GTPase Gem1 regulates endoplasmic reticulum-mitochondria connections. Proc Natl Acad Sci U S A (2011) 1.75
The complexity of cardiolipin in health and disease. Trends Biochem Sci (2011) 1.61
Regulation of phospholipid synthesis in the yeast Saccharomyces cerevisiae. Annu Rev Biochem (2011) 1.51
Hallmarks of a new era in mitochondrial biochemistry. Genes Dev (2013) 1.15
Three phosphatidylglycerol-phosphate phosphatases in the inner membrane of Escherichia coli. J Biol Chem (2010) 1.07
Role for two conserved intermembrane space proteins, Ups1p and Ups2p, [corrected] in intra-mitochondrial phospholipid trafficking. J Biol Chem (2012) 1.03
Seven functional classes of Barth syndrome mutation. Hum Mol Genet (2012) 1.00
Unremodeled and remodeled cardiolipin are functionally indistinguishable in yeast. J Biol Chem (2013) 0.98
Tam41 is a CDP-diacylglycerol synthase required for cardiolipin biosynthesis in mitochondria. Cell Metab (2013) 0.98
Structural and functional analysis of PTPMT1, a phosphatase required for cardiolipin synthesis. Proc Natl Acad Sci U S A (2011) 0.98
Disorders of phospholipid metabolism: an emerging class of mitochondrial disease due to defects in nuclear genes. Front Genet (2015) 0.95
Phospholipid transport via mitochondria. Traffic (2014) 0.93
Lipid transport between the endoplasmic reticulum and mitochondria. Cold Spring Harb Perspect Biol (2013) 0.92
The topology and regulation of cardiolipin biosynthesis and remodeling in yeast. Chem Phys Lipids (2013) 0.91
Deacylation on the matrix side of the mitochondrial inner membrane regulates cardiolipin remodeling. Mol Biol Cell (2013) 0.91
Deletion of the cardiolipin-specific phospholipase Cld1 rescues growth and life span defects in the tafazzin mutant: implications for Barth syndrome. J Biol Chem (2013) 0.91
A retrospective: use of Escherichia coli as a vehicle to study phospholipid synthesis and function. Biochim Biophys Acta (2012) 0.90
Processing and topology of the yeast mitochondrial phosphatidylserine decarboxylase 1. J Biol Chem (2012) 0.89
Phosphatidylethanolamine biosynthesis in mitochondria: phosphatidylserine (PS) trafficking is independent of a PS decarboxylase and intermembrane space proteins UPS1P and UPS2P. J Biol Chem (2012) 0.87
Cardiolipin remodeling: a regulatory hub for modulating cardiolipin metabolism and function. J Bioenerg Biomembr (2014) 0.85
The functions of cardiolipin in cellular metabolism-potential modifiers of the Barth syndrome phenotype. Chem Phys Lipids (2014) 0.83
Structural and mechanistic insights into phospholipid transfer by Ups1-Mdm35 in mitochondria. Nat Commun (2015) 0.83
The post-translational modification of the Clostridium difficile flagellin affects motility, cell surface properties and virulence. Mol Microbiol (2014) 0.82
The Role of Cardiolipin in Cardiovascular Health. Biomed Res Int (2015) 0.82
Identification of critical host mitochondrion-associated genes during Ehrlichia chaffeensis infections. Infect Immun (2012) 0.81
Genome-Wide Screens in Saccharomyces cerevisiae Highlight a Role for Cardiolipin in Biogenesis of Mitochondrial Outer Membrane Multispan Proteins. Mol Cell Biol (2015) 0.81
Barth Syndrome: From Mitochondrial Dysfunctions Associated with Aberrant Production of Reactive Oxygen Species to Pluripotent Stem Cell Studies. Front Genet (2016) 0.80
Functional Diversity of Haloacid Dehalogenase Superfamily Phosphatases from Saccharomyces cerevisiae: BIOCHEMICAL, STRUCTURAL, AND EVOLUTIONARY INSIGHTS. J Biol Chem (2015) 0.80
The power of yeast to model diseases of the powerhouse of the cell. Front Biosci (Landmark Ed) (2013) 0.80
Biosynthesis and roles of phospholipids in mitochondrial fusion, division and mitophagy. Cell Mol Life Sci (2014) 0.79
Mechanism for Remodeling of the Acyl Chain Composition of Cardiolipin Catalyzed by Saccharomyces cerevisiae Tafazzin. J Biol Chem (2016) 0.78
Biosynthesis, remodeling and turnover of mitochondrial cardiolipin. Biochim Biophys Acta (2016) 0.77
Identification of a mammalian-type phosphatidylglycerophosphate phosphatase in the Eubacterium Rhodopirellula baltica. J Biol Chem (2013) 0.76
Power(2): the power of yeast genetics applied to the powerhouse of the cell. Trends Endocrinol Metab (2015) 0.76
In Vivo and in Vitro Synthesis of Phosphatidylglycerol by an Escherichia coli Cardiolipin Synthase. J Biol Chem (2016) 0.76
Functional Specificity of Cardiolipin Synthase Revealed by the Identification of a Cardiolipin Synthase CrCLS1 in Chlamydomonas reinhardtii. Front Microbiol (2016) 0.75
Successful management of Barth syndrome: a systematic review highlighting the importance of a flexible and multidisciplinary approach. J Multidiscip Healthc (2015) 0.75
Structural Insight into Substrate Selection and Catalysis of Lipid Phosphate Phosphatase PgpB in the Cell Membrane. J Biol Chem (2016) 0.75
Analysis of sphingolipids, sterols and phospholipids in human pathogenic Cryptococcus strains. J Lipid Res (2017) 0.75
A rapid method of total lipid extraction and purification. Can J Biochem Physiol (1959) 173.74
Designer deletion strains derived from Saccharomyces cerevisiae S288C: a useful set of strains and plasmids for PCR-mediated gene disruption and other applications. Yeast (1998) 23.00
Two dimensional then layer chromatographic separation of polar lipids and determination of phospholipids by phosphorus analysis of spots. Lipids (1970) 11.81
Subcellular localization of the yeast proteome. Genes Dev (2002) 7.93
Mitochondria: more than just a powerhouse. Curr Biol (2006) 6.76
Getting started with yeast. Methods Enzymol (2002) 6.60
An ER-mitochondria tethering complex revealed by a synthetic biology screen. Science (2009) 6.14
Quantitative analysis of biological membrane lipids at the low picomole level by nano-electrospray ionization tandem mass spectrometry. Proc Natl Acad Sci U S A (1997) 4.61
Function and biogenesis of iron-sulphur proteins. Nature (2009) 4.56
A novel X-linked gene, G4.5. is responsible for Barth syndrome. Nat Genet (1996) 3.58
A common lipid links Mfn-mediated mitochondrial fusion and SNARE-regulated exocytosis. Nat Cell Biol (2006) 3.56
Cardiolipin stabilizes respiratory chain supercomplexes. J Biol Chem (2003) 3.16
Gluing the respiratory chain together. Cardiolipin is required for supercomplex formation in the inner mitochondrial membrane. J Biol Chem (2002) 2.92
Yeast mitochondrial F1F0-ATP synthase exists as a dimer: identification of three dimer-specific subunits. EMBO J (1998) 2.67
Association between the endoplasmic reticulum and mitochondria of yeast facilitates interorganelle transport of phospholipids through membrane contact. Eur J Biochem (1999) 2.40
A new class of phosphotransferases phosphorylated on an aspartate residue in an amino-terminal DXDX(T/V) motif. J Biol Chem (1998) 2.29
Structures and physiological roles of 13 integral lipids of bovine heart cytochrome c oxidase. EMBO J (2007) 2.28
Absence of cardiolipin in the crd1 null mutant results in decreased mitochondrial membrane potential and reduced mitochondrial function. J Biol Chem (2000) 2.26
Specific roles of protein-phospholipid interactions in the yeast cytochrome bc1 complex structure. EMBO J (2001) 2.24
The genetic interactome of prohibitins: coordinated control of cardiolipin and phosphatidylethanolamine by conserved regulators in mitochondria. J Cell Biol (2009) 2.22
Cardiolipin synthesis for the assembly of bacterial and mitochondrial membranes. J Lipid Res (2007) 2.21
Cardiolipin defines the interactome of the major ADP/ATP carrier protein of the mitochondrial inner membrane. J Cell Biol (2008) 2.18
Barth syndrome, a human disorder of cardiolipin metabolism. FEBS Lett (2006) 2.17
Evidence for segregation of sphingomyelin and cholesterol during formation of COPI-coated vesicles. J Cell Biol (2000) 2.13
Cardiolipin provides an essential activating platform for caspase-8 on mitochondria. J Cell Biol (2008) 2.06
Quantitative determination of phospholipid compositions by ESI-MS: effects of acyl chain length, unsaturation, and lipid concentration on instrument response. J Lipid Res (2001) 1.92
Aberrant cardiolipin metabolism in the yeast taz1 mutant: a model for Barth syndrome. Mol Microbiol (2004) 1.90
Isolation and characterization of the gene (CLS1) encoding cardiolipin synthase in Saccharomyces cerevisiae. J Biol Chem (1998) 1.82
The membrane domains occupied by glycosylphosphatidylinositol-anchored prion protein and Thy-1 differ in lipid composition. J Biol Chem (2003) 1.73
Subcellular and submitochondrial localization of phospholipid-synthesizing enzymes in Saccharomyces cerevisiae. J Bacteriol (1986) 1.71
Mitochondrial cardiolipin involved in outer-membrane protein biogenesis: implications for Barth syndrome. Curr Biol (2009) 1.62
Synthetic lethal interaction of the mitochondrial phosphatidylethanolamine and cardiolipin biosynthetic pathways in Saccharomyces cerevisiae. J Biol Chem (2005) 1.58
Ups1p and Ups2p antagonistically regulate cardiolipin metabolism in mitochondria. J Cell Biol (2009) 1.55
Cardiolipin deficiency releases cytochrome c from the inner mitochondrial membrane and accelerates stimuli-elicited apoptosis. Cell Death Differ (2006) 1.55
The PEL1 gene (renamed PGS1) encodes the phosphatidylglycero-phosphate synthase of Saccharomyces cerevisiae. J Biol Chem (1998) 1.42
Cardiolipin is synthesized on the matrix side of the inner membrane in rat liver mitochondria. J Biol Chem (1993) 1.41
The reconstituted ADP/ATP carrier activity has an absolute requirement for cardiolipin as shown in cysteine mutants. J Biol Chem (1994) 1.35
The enigmatic role of tafazzin in cardiolipin metabolism. Biochim Biophys Acta (2009) 1.35
Cellular functions of cardiolipin in yeast. Biochim Biophys Acta (2008) 1.32
The translocator maintenance protein Tam41 is required for mitochondrial cardiolipin biosynthesis. J Cell Biol (2008) 1.32
Newly made phosphatidylserine and phosphatidylethanolamine are preferentially translocated between rat liver mitochondria and endoplasmic reticulum. J Biol Chem (1991) 1.32
Cardiolipin is not essential for the growth of Saccharomyces cerevisiae on fermentable or non-fermentable carbon sources. Mol Microbiol (1997) 1.30
Identification of Tam41 maintaining integrity of the TIM23 protein translocator complex in mitochondria. J Cell Biol (2006) 1.30
Supercomplexes and subcomplexes of mitochondrial oxidative phosphorylation. Biochim Biophys Acta (2006) 1.29
Characterization of a microsomal subfraction associated with mitochondria of the yeast, Saccharomyces cerevisiae. Involvement in synthesis and import of phospholipids into mitochondria. Biochim Biophys Acta (1995) 1.28
Prohibitins interact genetically with Atp23, a novel processing peptidase and chaperone for the F1Fo-ATP synthase. Mol Biol Cell (2006) 1.26
The CDS1 gene encoding CDP-diacylglycerol synthase in Saccharomyces cerevisiae is essential for cell growth. J Biol Chem (1996) 1.20
Ups1p, a conserved intermembrane space protein, regulates mitochondrial shape and alternative topogenesis of Mgm1p. J Cell Biol (2006) 1.20
Identification of a cardiolipin-specific phospholipase encoded by the gene CLD1 (YGR110W) in yeast. J Biol Chem (2009) 1.20
Characterization of Mmp37p, a Saccharomyces cerevisiae mitochondrial matrix protein with a role in mitochondrial protein import. Mol Biol Cell (2006) 1.20
Loss of function of KRE5 suppresses temperature sensitivity of mutants lacking mitochondrial anionic lipids. Mol Biol Cell (2004) 1.11
Substrate specificity and membrane topology of Escherichia coli PgpB, an undecaprenyl pyrophosphate phosphatase. J Biol Chem (2008) 1.08
The pgpA and pgpB genes of Escherichia coli are not essential: evidence for a third phosphatidylglycerophosphate phosphatase. J Bacteriol (1992) 1.04
Phosphatidylserine decarboxylases, key enzymes of lipid metabolism. IUBMB Life (2009) 1.03
Characterization and regulation of phosphatidylglycerolphosphate phosphatase in Saccharomyces cerevisiae. Biochim Biophys Acta (1990) 0.99
Bacterial expression and purification of interleukin-2 tyrosine kinase: single step separation of the chaperonin impurity. Protein Expr Purif (2008) 0.98
Molecular cloning of the PEL1 gene of Saccharomyces cerevisiae that is essential for the viability of petite mutants. Curr Genet (1993) 0.95
The pel1 mutant of Saccharomyces cerevisiae is deficient in cardiolipin and does not survive the disruption of the CHO1 gene encoding phosphatidylserine synthase. FEMS Microbiol Lett (1996) 0.91
Post-translational regulation of phosphatidylglycerolphosphate synthase in response to inositol. Mol Microbiol (2004) 0.91
Loss of mitochondrial DNA in the yeast cardiolipin synthase crd1 mutant leads to up-regulation of the protein kinase Swe1p that regulates the G2/M transition. J Biol Chem (2010) 0.90
Phosphatidylglycerolphosphate synthase encoded by the PEL1/PGS1 gene in Saccharomyces cerevisiae is localized in mitochondria and its expression is regulated by phospholipid precursors. Curr Genet (1998) 0.89
Yeast Pgc1p (YPL206c) controls the amount of phosphatidylglycerol via a phospholipase C-type degradation mechanism. J Biol Chem (2008) 0.88
One-dimensional thin-layer chromatography of all known D-3 and D-4 isomers of phosphoinositides. Anal Biochem (1996) 0.86
Molecular anatomy of a trafficking organelle. Cell (2006) 11.47
Ceramide triggers budding of exosome vesicles into multivesicular endosomes. Science (2008) 9.42
The HIV lipidome: a raft with an unusual composition. Proc Natl Acad Sci U S A (2006) 4.15
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
High cholesterol level is essential for myelin membrane growth. Nat Neurosci (2005) 2.34
Journeys through the Golgi--taking stock in a new era. J Cell Biol (2009) 2.30
Axonal loss and neuroinflammation caused by peroxisome-deficient oligodendrocytes. Nat Genet (2007) 2.30
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
Biochemical and morphological properties of hepatitis C virus particles and determination of their lipidome. J Biol Chem (2010) 2.05
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
The structures of COPI-coated vesicles reveal alternate coatomer conformations and interactions. Science (2012) 1.90
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
Membrane curvature induced by Arf1-GTP is essential for vesicle formation. Proc Natl Acad Sci U S A (2008) 1.63
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
A critical role for ceramide synthase 2 in liver homeostasis: I. alterations in lipid metabolic pathways. J Biol Chem (2010) 1.56
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
The Sur7p family defines novel cortical domains in Saccharomyces cerevisiae, affects sphingolipid metabolism, and is involved in sporulation. Mol Cell Biol (2002) 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
Molecular recognition of a single sphingolipid species by a protein's transmembrane domain. Nature (2012) 1.42
Arf1-GTP-induced tubule formation suggests a function of Arf family proteins in curvature acquisition at sites of vesicle budding. J Biol Chem (2008) 1.40
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
COPI budding within the Golgi stack. Cold Spring Harb Perspect Biol (2011) 1.33
Oligomeric state and stoichiometry of p24 proteins in the early secretory pathway. J Biol Chem (2002) 1.31
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
Translating m-AAA protease function in mitochondria to hereditary spastic paraplegia. Trends Mol Med (2006) 1.24
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
Functional reconstitution of COPI coat assembly and disassembly using chemically defined components. Proc Natl Acad Sci U S A (2003) 1.20
A global circadian repressor controls antiphasic expression of metabolic genes in Neurospora. Mol Cell (2011) 1.19
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
Identification and characterization of a novel human plant pathogenesis-related protein that localizes to lipid-enriched microdomains in the Golgi complex. J Cell Sci (2002) 1.18
Dual roles of the transmembrane protein p23/TMP21 in the modulation of amyloid precursor protein metabolism. Mol Neurodegener (2007) 1.18
Unconventional secretion of fibroblast growth factor 2 is mediated by direct translocation across the plasma membrane of mammalian cells. J Biol Chem (2003) 1.17
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
Vesicle coats: structure, function, and general principles of assembly. Trends Cell Biol (2013) 1.15
Mitofusin 2 builds a bridge between ER and mitochondria. Cell (2008) 1.14
Coatomer, the coat protein of COPI transport vesicles, discriminates endoplasmic reticulum residents from p24 proteins. Mol Cell Biol (2006) 1.13
Vesicular transport: the core machinery of COPI recruitment and budding. J Cell Sci (2002) 1.13
Identification and biophysical characterization of a very-long-chain-fatty-acid-substituted phosphatidylinositol in yeast subcellular membranes. Biochem J (2004) 1.13
Differential localization of coatomer complex isoforms within the Golgi apparatus. Proc Natl Acad Sci U S A (2007) 1.12
Specificity of intramembrane protein-lipid interactions. Cold Spring Harb Perspect Biol (2011) 1.12
Cholesterol regulates the endoplasmic reticulum exit of the major membrane protein P0 required for peripheral myelin compaction. J Neurosci (2009) 1.12
Comparative lipidomics analysis of HIV-1 particles and their producer cell membrane in different cell lines. Cell Microbiol (2013) 1.11
Autocatalytic processing of m-AAA protease subunits in mitochondria. Mol Biol Cell (2009) 1.11
Differential roles of ArfGAP1, ArfGAP2, and ArfGAP3 in COPI trafficking. J Cell Biol (2008) 1.10
Involvement of a Golgi-resident GPI-anchored protein in maintenance of the Golgi structure. Mol Biol Cell (2007) 1.09
Functional evaluation of paraplegin mutations by a yeast complementation assay. Hum Mutat (2010) 1.09
Formation and nuclear export of tRNA, rRNA and mRNA is regulated by the ubiquitin ligase Rsp5p. EMBO Rep (2003) 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
Human immunodeficiency virus type 1 Nef protein modulates the lipid composition of virions and host cell membrane microdomains. Retrovirology (2007) 1.08
Ugo1 and Mdm30 act sequentially during Fzo1-mediated mitochondrial outer membrane fusion. J Cell Sci (2011) 1.07
Probing HIV-1 membrane liquid order by Laurdan staining reveals producer cell-dependent differences. J Biol Chem (2009) 1.07
Loss of prohibitin membrane scaffolds impairs mitochondrial architecture and leads to tau hyperphosphorylation and neurodegeneration. PLoS Genet (2012) 1.07
Peroxisomal alterations in Alzheimer's disease. Acta Neuropathol (2011) 1.06
Coatomer and dimeric ADP ribosylation factor 1 promote distinct steps in membrane scission. J Cell Biol (2011) 1.04
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