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Peroxisome biogenesis disorders: identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13.
Shimozawa N, Suzuki Y, Zhang Z, Imamura A, Tsukamoto T, Osumi T, Tateishi K, Okumoto K, Fujiki Y, Orii T, Barth PG, Wanders RJ, Kondo N. Shimozawa N, et al. Among authors: okumoto k. Biochem Biophys Res Commun. 1998 Feb 13;243(2):368-71. doi: 10.1006/bbrc.1997.8067. Biochem Biophys Res Commun. 1998. PMID: 9480815
PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p.
Okumoto K, Shimozawa N, Kawai A, Tamura S, Tsukamoto T, Osumi T, Moser H, Wanders RJ, Suzuki Y, Kondo N, Fujiki Y. Okumoto K, et al. Mol Cell Biol. 1998 Jul;18(7):4324-36. doi: 10.1128/MCB.18.7.4324. Mol Cell Biol. 1998. PMID: 9632816 Free PMC article.
Rat PEX12 cDNA was isolated by functional complementation of peroxisome deficiency of a mutant CHO cell line, ZP109 (K. Okumoto, A. Bogaki, K. Tateishi, T. Tsukamoto, T. Osumi, N. ...
Rat PEX12 cDNA was isolated by functional complementation of peroxisome deficiency of a mutant CHO cell line, ZP109 (K. Okumoto …
141 results