Peroxisomes are formed from complex membrane structures in PEX6-deficient CHO cells upon genetic complementation.
about
The assembly and maintenance of heterochromatin initiated by transgene repeats are independent of the RNA interference pathway in mammalian cellsDeficiency of a lipid droplet protein, perilipin 5, suppresses myocardial lipid accumulation, thereby preventing type 1 diabetes-induced heart malfunctionYeast pex1 cells contain peroxisomal ghosts that import matrix proteins upon reintroduction of Pex1.Tissue Specificity of Human Disease Module.Kidney-specific overexpression of Sirt1 protects against acute kidney injury by retaining peroxisome function.Super-resolution imaging reveals the sub-diffraction phenotype of Zellweger Syndrome ghosts and wild-type peroxisomes.
P2860
Peroxisomes are formed from complex membrane structures in PEX6-deficient CHO cells upon genetic complementation.
description
2002 nî lūn-bûn
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2002年の論文
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2002年論文
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2002年論文
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2002年論文
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2002年論文
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2002年論文
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2002年论文
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2002年论文
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2002年论文
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name
Peroxisomes are formed from co ...... upon genetic complementation.
@en
Peroxisomes are formed from co ...... upon genetic complementation.
@nl
type
label
Peroxisomes are formed from co ...... upon genetic complementation.
@en
Peroxisomes are formed from co ...... upon genetic complementation.
@nl
prefLabel
Peroxisomes are formed from co ...... upon genetic complementation.
@en
Peroxisomes are formed from co ...... upon genetic complementation.
@nl
P2093
P2860
P356
P1476
Peroxisomes are formed from co ...... s upon genetic complementation
@en
P2093
Noriyo Hashiguchi
Sadaki Yokota
Takashi Osumi
Tokuko Haraguchi
Tomoko Kojidani
Toshiro Tsukamoto
Tsuneo Imanaka
P2860
P304
P356
10.1091/MBC.01-10-0479
P577
2002-02-01T00:00:00Z