相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Loss of Mfn2 results in progressive, retrograde degeneration of dopaminergic neurons in the nigrostriatal circuit
Anh H. Pham et al.
HUMAN MOLECULAR GENETICS (2012)
Neuromuscular effects of G93A-SOD1 expression in zebrafish
Stacey A. Sakowski et al.
MOLECULAR NEURODEGENERATION (2012)
The ADHD-susceptibility gene lphn3.1 modulates dopaminergic neuron formation and locomotor activity during zebrafish development
M. Lange et al.
MOLECULAR PSYCHIATRY (2012)
EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humans
Annelies Van Hoecke et al.
NATURE MEDICINE (2012)
A novel mitofusin 2 mutation causes canine fetal-onset neuroaxonal dystrophy
John C. Fyfe et al.
NEUROGENETICS (2011)
Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations
J. M. Polke et al.
NEUROLOGY (2011)
Developmental defects and neuromuscular alterations due to mitofusin 2 gene (MFN2) silencing in zebrafish: a new model for Charcot-Marie-Tooth type 2A neuropathy
Andrea Vettori et al.
NEUROMUSCULAR DISORDERS (2011)
An Unusual Splice Defect in the Mitofusin 2 Gene (MFN2) Is Associated with Degenerative Axonopathy in Tyrolean Grey Cattle
Cord Drogemuller et al.
PLOS ONE (2011)
A genetic model of amyotrophic lateral sclerosis in zebrafish displays phenotypic hallmarks of motoneuron disease
Tennore Ramesh et al.
DISEASE MODELS & MECHANISMS (2010)
Mitofusin 2 Is Necessary for Transport of Axonal Mitochondria and Interacts with the Miro/Milton Complex
Albert Misko et al.
JOURNAL OF NEUROSCIENCE (2010)
Zebrafish atlastin controls motility and spinal motor axon architecture via inhibition of the BMP pathway
Coralie Fassier et al.
NATURE NEUROSCIENCE (2010)
Drosophila Parkin requires PINK1 for mitochondrial translocation and ubiquitinates Mitofusin
Elena Ziviani et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2010)
Role of mitofusin 2 mutations in the physiopathology of Charcot-Marie-Tooth disease type 2A
Romain Cartoni et al.
EXPERIMENTAL NEUROLOGY (2009)
Zebrafish survival motor neuron mutants exhibit presynaptic neuromuscular junction defects
Kum-Loong Boon et al.
HUMAN MOLECULAR GENETICS (2009)
Direct evidence for axonal transport defects in a novel mouse model of mutant spastin-induced hereditary spastic paraplegia (HSP) and human HSP patients
Paul. R. Kasher et al.
JOURNAL OF NEUROCHEMISTRY (2009)
The PINK1/Parkin pathway regulates mitochondrial morphology
Angela C. Poole et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2008)
Hindlimb gait defects due to motor axon loss and reduced distal muscles in a transgenic mouse model of Charcot-Marie-Tooth type 2A
Scott A. Detmer et al.
HUMAN MOLECULAR GENETICS (2008)
Familial amyotrophic lateral sclerosis-linked SOD1 mutants perturb fast axonal transport to reduce axonal mitochondria content
Kurt J. De Vos et al.
HUMAN MOLECULAR GENETICS (2007)
Mitochondrial fusion protects against neurodegeneration in the cerebellum
Hsiuchen Chen et al.
CELL (2007)
Altered axonal mitochondrial transport in the pathogenesis of Charcot-Marie-Tooth disease from mitofusin 2 mutations
Robert H. Baloh et al.
JOURNAL OF NEUROSCIENCE (2007)
Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2
S Züchner et al.
ANNALS OF NEUROLOGY (2006)
Mitochondrial function and actin regulate dynamin-related protein 1-dependent mitochondrial fission
KJ De Vos et al.
CURRENT BIOLOGY (2005)
A syntaxin 1, Gαo, and N-type calcium channel complex at a presynaptic nerve terminal:: Analysis by quantitative immunocolocalization
Q Li et al.
JOURNAL OF NEUROSCIENCE (2004)
Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A
S Züchner et al.
NATURE GENETICS (2004)
Knockdown of the survival motor neuron (Smn) protein in zebrafish causes defects in motor axon outgrowth and pathfinding
ML McWhorter et al.
JOURNAL OF CELL BIOLOGY (2003)
Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development
HC Chen et al.
JOURNAL OF CELL BIOLOGY (2003)