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Details on Person Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I
| Class:Id | LiteratureReference:9033849 |
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| _displayName | Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I |
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| _timestamp | 2017-12-28 17:57:22 |
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| author | [Person:9033835] Tamura, S
[Person:9033872] Okumoto, K
[Person:9033842] Toyama, R
[Person:2458314] Shimozawa, N
[Person:77531] Tsukamoto, T
[Person:2285500] Suzuki, Y
[Person:5320202] Osumi, T
[Person:2458321] Kondo, N
[Person:5321239] Fujiki, Y |
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| created | [InstanceEdit:9033817] May, Bruce, 2017-12-28 |
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| journal | Proc. Natl. Acad. Sci. U.S.A. |
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| pages | 4350-5 |
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| pubMedIdentifier | 9539740 |
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| title | Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I |
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| volume | 95 |
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| year | 1998 |
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| (literatureReference) | [BlackBoxEvent:9033499] PEX1:PEX6:PEX26:ZFAND6 dissociates Ub:PEX5L and PEX7 from PEX14:PEX13:PEX2:PEX10:PEX12 and translocates PEX5L and PEX7 from the peroxisomal membrane to the cytosol [Homo sapiens]
[BlackBoxEvent:9033505] PEX1:PEX6:PEX26:ZFAND6:Ub:PEX5S,L:PEX14:PEX13:PEX2:PEX10:PEX12 dissociates yielding cytosolic Ub:PEX5S,L and membrane PEX14:PEX13:PEX2:PEX10:PEX12 [Homo sapiens] |
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