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J-GLOBAL ID：200902194465253780   Reference number：01A0522486

The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6.

ペルオキシンPex6p遺伝子は相補群6のペルオキシソーム生合成疾患において障害がある

Author (9)： MATSUMOTO N (Kyushu Univ. Graduate School, Fukuoka, JPN) ,  TAMURA S (Kyushu Univ. Graduate School, Fukuoka, JPN) ,  MOSER A (Johns Hopkins Univ., MD, USA) ,  MOSER H W (Johns Hopkins Univ., MD, USA) ,  BRAVERMAN N (Johns Hopkins Univ., MD, USA) ,  SUZUKI Y (Gifu Univ. School of Medicine, Gifu, JPN) ,  SHIMOZAWA N (Gifu Univ. School of Medicine, Gifu, JPN) ,  KONDO N (Gifu Univ. School of Medicine, Gifu, JPN) ,  FUJIKI Y (Kyushu Univ. Graduate School, Fukuoka, JPN)
Material： Journal of Human Genetics  (J Hum Genet)
Volume： 46  Issue： 5  Page： 273-277  Publication year： 2001 
JST Material Number： Z0756A  ISSN： 1434-5161  Document type： Article
Article type： 原著論文  Country of issue： United Kingdom (GBR)  Language： ENGLISH (EN)

Thesaurus term： *peroxisome ,...
Semi thesaurus term： ペルオキシソーム生合成障害 ,...

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JST classification (2)： Congenital diseases,deformities in general.  (GD03010V) ,  Structure and chemistry of genes  (EC02020U)

Reference (21)：

• FUJIKI, Y. Peroxisome biogenesis and peroxisome biogenesis disorders. FEBS Lett. 2000, 476, 42-46
• FUKUDA, S. Human peroxisome assembly factor-2 (PAF-2) : a gene responsible for group C peroxisome biogenesis disorder in humans. Am J Hum Genet. 1996, 59, 1210-1220
• GHAEDI, K. PEX3 is the causal gene responsibel for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G. Am J Hum Genet. 2000, 67, 976-981
• GHAEDI, K. Isolation and characterization of novel peroxisome biogenesis-defective Chinese hamster ovary cell mutants using green fluorescent protein. Exp Cell Res. 1999, 248, 489-497
• GOULD, SJ. Peroxisome biogenesis disorders : genetics and cell biology. Trends Genet. 2000, 16, 340-345

Terms in the title (6)： ペルオキシン ,  遺伝子 ,  ペルオキシソーム ,  生合成 ,  疾患 ,  障害