Newly identified chinese hamster ovary cell mutants defective in peroxisome assembly represent complementation group A of human peroxisome biogenesis disorders and one novel group in mammals

Experimental Cell Research

Volumn 248, Issue 2, 1999, Pages 482-488

  Ghaedi, Kamran ^a   Itagaki, Atsushi ^a   Toyama, Ryusuke ^a   Tamura, Shigehiko ^a   Matsumura, Tsuyoshi ^a   Kawai, Atsushi ^a   Shimozawa, Nobuyuki ^b   Suzuki, Yasuyuki ^b   Kondo, Naomi ^b   Fujiki, Yukio ^a,c  

^a KYUSHU UNIVERSITY   (Japan)

^b GIFU UNIVERSITY   (Japan)

^c JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

CHO cell mutants; Complementation groups; Peroxin; Peroxisome biogenesis; Zellweger syndrome

Indexed keywords

CATALASE; COMPLEMENTARY DNA;

ANIMAL CELL; ARTICLE; CELL FUSION; CELL MUTANT; CHO CELL; DISORDERS OF PEROXISOMAL FUNCTIONS; ENZYME DEFICIENCY; GENETIC ANALYSIS; GENETIC COMPLEMENTATION; GENETIC TRANSFECTION; NONHUMAN; PEROXISOME; PRIORITY JOURNAL; TECHNIQUE; ZELLWEGER SYNDROME;

ANIMALIA; CRICETINAE; CRICETULUS GRISEUS; MAMMALIA;

EID: 0033134119     PISSN: 00144827     EISSN: None     Source Type: Journal    
DOI: 10.1006/excr.1999.4412     Document Type: Article

References (43)

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