Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I

Proceedings of the National Academy of Sciences of the United States of America

Volumn 95, Issue 8, 1998, Pages 4350-4355

  Tamura, Shigehiko ^a   Okumoto, Kanji ^a   Toyama, Ryusuke ^a   Shimozawa, Nobuyuki ^b   Tsukamoto, Toshiro ^c   Suzuki, Yasuyuki ^b   Osumi, Takashi ^c   Kondo, Naomi ^b   Fujiki, Yukio ^a,d  

^a KYUSHU UNIVERSITY   (Japan)

^b GIFU UNIVERSITY   (Japan)

^c UNIVERSITY OF HYOGO   (Japan)

^d JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ARTICLE; CHO CELL; CONTROLLED STUDY; GENETIC COMPLEMENTATION; HUMAN; HUMAN CELL; MOLECULAR CLONING; NONHUMAN; NUCLEOTIDE SEQUENCE; PEROXISOME; POINT MUTATION; PRIORITY JOURNAL; PROTEIN EXPRESSION; SIGNAL TRANSDUCTION; ZELLWEGER SYNDROME;

ADENOSINE TRIPHOSPHATASES; AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CELL LINE; CHO CELLS; CLONING, ORGANISM; CRICETINAE; FIBROBLASTS; GENETIC COMPLEMENTATION TEST; HUMANS; KINETICS; MEMBRANE PROTEINS; MICROBODIES; MOLECULAR SEQUENCE DATA; PICHIA; RECOMBINANT PROTEINS; SACCHAROMYCES CEREVISIAE; SACCHAROMYCES CEREVISIAE PROTEINS; SEQUENCE ALIGNMENT; SEQUENCE HOMOLOGY, AMINO ACID; SKIN; TRANSFECTION; ZELLWEGER SYNDROME;

ANIMALIA; CRICETINAE; CRICETULUS GRISEUS;

EID: 0032515992     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.95.8.4350     Document Type: Article

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