Related references
Note: Only part of the references are listed.AAA+ Proteases: ATP-Fueled Machines of Protein Destruction
Robert T. Sauer et al.
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 80 (2011)
Hereditary spastic paraplegias: membrane traffic and the motor pathway (vol 12, pg 31, 2011)
Craig Blackstone et al.
NATURE REVIEWS NEUROSCIENCE (2011)
Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases
Tyler Mark Pierson et al.
PLOS GENETICS (2011)
Hereditary spastic paraplegia proteins REEP1, spastin, and atlastin-1 coordinate microtubule interactions with the tubular ER network
Seong H. Park et al.
JOURNAL OF CLINICAL INVESTIGATION (2010)
Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28
Daniela Di Bella et al.
NATURE GENETICS (2010)
Regulation of OPA1 processing and mitochondrial fusion by m-AAA protease isoenzymes and OMA1
Sarah Ehses et al.
JOURNAL OF CELL BIOLOGY (2009)
Misfolded Membrane Proteins Are Specifically Recognized by the Transmembrane Domain of the Hrd1p Ubiquitin Ligase
Brian K. Sato et al.
MOLECULAR CELL (2009)
An Intersubunit Signaling Network Coordinates ATP Hydrolysis by m-AAA Proteases
Steffen Augustin et al.
MOLECULAR CELL (2009)
Quality control of mitochondria: protection against neurodegeneration and ageing
Takashi Tatsuta et al.
EMBO JOURNAL (2008)
A clinical, genetic, and biochemical characterization of SPG7 mutations in a large cohort of patients with hereditary spastic paraplegia
Alessia Arnoldi et al.
HUMAN MUTATION (2008)
Hereditary Spastic Paraplegia-Associated Mutations in the NIPA1 Gene and Its Caenorhabditis elegans Homolog Trigger Neural Degeneration In Vitro and In Vivo through a Gain-of-Function Mechanism
Jiali Zhao et al.
JOURNAL OF NEUROSCIENCE (2008)
Characterization of seipin/BSCL2, a protein associated with spastic paraplegia 17
Daisuke Ito et al.
NEUROBIOLOGY OF DISEASE (2008)
Paraplegin mutations in sporadic adult-onset upper motor neuron syndromes
F. Brugman et al.
NEUROLOGY (2008)
The recognition and retrotranslocation of misfolded proteins from the endoplasmic reticulum
Kunio Nakatsukasa et al.
TRAFFIC (2008)
Signal integration in the endoplasmic reticulum unfolded protein response
David Ron et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2007)
Variable and tissue-specific subunit composition of mitochondrial m-AAA protease complexes linked to hereditary spastic paraplegia
Mirko Koppen et al.
MOLECULAR AND CELLULAR BIOLOGY (2007)
Distinct ubiquitin-ligase complexes define convergent pathways for the degradation of ER proteins
Pedro Carvalho et al.
CELL (2006)
Regulation of mitochondrial morphology through proteolytic cleavage of OPA1
Naotada Ishihara et al.
EMBO JOURNAL (2006)
Mutation analysis of the paraplegin gene (SPG7) in patients with hereditary spastic paraplegia
N Elleuch et al.
NEUROLOGY (2006)
Intramuscular viral delivery of paraplegin rescues peripheral axonopathy in a model of hereditary spastic paraplegia
M Pirozzi et al.
JOURNAL OF CLINICAL INVESTIGATION (2006)
The fluorescence protease protection (FPP) assay to determine protein localization and membrane topology
Holger Lorenz et al.
NATURE PROTOCOLS (2006)
The m-AAA protease defective in hereditary spastic paraplegia controls ribosome assembly in mitochondria
M Nolden et al.
CELL (2005)
Axonal degeneration in paraplegin-deficient mice is associated with abnormal mitochondria and impairment of axonal transport
F Ferreirinha et al.
JOURNAL OF CLINICAL INVESTIGATION (2004)
A clinical, genetic and biochemical study of SPG7 mutations in hereditary spastic paraplegia
PA Wilkinson et al.
BRAIN (2004)
Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia
L Atorino et al.
JOURNAL OF CELL BIOLOGY (2003)
Hereditary spastic paraplegia SPG13 is associated with a mutation in the gene encoding the mitochondrial chaperonin Hsp60
JJ Hansen et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics
A Errico et al.
HUMAN MOLECULAR GENETICS (2002)
Molecular and functional analyses of the human and mouse genes encoding AFG3L1, a mitochondrial metalloprotease homologous to the human spastic paraplegia protein
G Kremmidiotis et al.
GENOMICS (2001)
Mechanism of residence of cytochrome b(5), a tail-anchored protein, in the endoplasmic reticulum
E Pedrazzini et al.
JOURNAL OF CELL BIOLOGY (2000)
Share Paper
