Targeted disruption of the Mast syndrome gene SPG21 in mice impairs hind limb function and alters axon branching in cultured cortical neurons.
about
Loss of function of glucocerebrosidase GBA2 is responsible for motor neuron defects in hereditary spastic paraplegiaThe spectrum of KIAA0196 variants, and characterization of a murine knockout: implications for the mutational mechanism in hereditary spastic paraplegia type SPG8.Spg20-/- mice reveal multimodal functions for Troyer syndrome protein spartin in lipid droplet maintenance, cytokinesis and BMP signalingCellular pathways of hereditary spastic paraplegia.The glycosphingolipid hydrolases in the central nervous system.Exome sequencing reveals a novel homozygous mutation in ACP33 gene in the first Italian family with SPG21.Characterization of maspardin, responsible for human Mast syndrome, in an insect species and analysis of its evolution in metazoans.
P2860
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P2860
Targeted disruption of the Mast syndrome gene SPG21 in mice impairs hind limb function and alters axon branching in cultured cortical neurons.
description
2010 nî lūn-bûn
@nan
2010年の論文
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2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
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2010年論文
@zh-tw
2010年论文
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2010年论文
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2010年论文
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name
Targeted disruption of the Mas ...... in cultured cortical neurons.
@en
Targeted disruption of the Mas ...... in cultured cortical neurons.
@nl
type
label
Targeted disruption of the Mas ...... in cultured cortical neurons.
@en
Targeted disruption of the Mas ...... in cultured cortical neurons.
@nl
prefLabel
Targeted disruption of the Mas ...... in cultured cortical neurons.
@en
Targeted disruption of the Mas ...... in cultured cortical neurons.
@nl
P2093
P2860
P1433
P1476
Targeted disruption of the Mas ...... in cultured cortical neurons.
@en
P2093
Craig Blackstone
Cynthia Soderblom
Henri Jupille
Julia Stadler
Michael C Hanna
P2860
P2888
P304
P356
10.1007/S10048-010-0252-7
P577
2010-07-27T00:00:00Z