Phenotype - Genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction

Biochemical Journal

Volumn 357, Issue 2, 2001, Pages 417-426

  Tamura, S ^a   Matsumoto, N ^a   Imamura, A ^a   Shimozawa, N ^a   Suzuki, Y ^a   Kondo, N ^a   Fujiki, Y ^a  

^a KYUSHU UNIVERSITY   (Japan)

Author keywords

AAA ATPase; Infantile Refsum disease; Temperature sensitivity; Zellweger syndrome

Indexed keywords

BIOSYNTHESIS; GENES; HORMONES; MUTAGENS; PATIENT MONITORING;

BIOGENESIS;

DISEASES;

CELL PROTEIN; PEROXIN; PEX1 PROTEIN; PEX6 PROTEIN; UNCLASSIFIED DRUG;

ADRENOLEUKODYSTROPHY; ANIMAL CELL; ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; FIBROBLAST; GENE MUTATION; GENOTYPE; HUMAN; HUMAN CELL; NONHUMAN; NUCLEOTIDE SEQUENCE; PEROXISOME; PHENOTYPE; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN PROTEIN INTERACTION; PROTEIN STABILITY; REFSUM DISEASE; TEMPERATURE SENSITIVITY; ZELLWEGER SYNDROME;

ADENOSINE TRIPHOSPHATASES; AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CELLS, CULTURED; CHO CELLS; CODON, TERMINATOR; CRICETINAE; DNA MUTATIONAL ANALYSIS; EXONS; FIBROBLASTS; GENETIC COMPLEMENTATION TEST; GENOTYPE; HUMANS; MEMBRANE PROTEINS; MUTAGENESIS, SITE-DIRECTED; MUTATION; PEROXISOMAL DISORDERS; PEROXISOMES; PHENOTYPE; POLYMERASE CHAIN REACTION; RECOMBINANT PROTEINS; REFERENCE VALUES; SKIN; TRANSFECTION; ZELLWEGER SYNDROME;

ANIMALIA;

EID: 0035878969     PISSN: 02646021     EISSN: None     Source Type: Journal    
DOI: 10.1042/0264-6021:3570417     Document Type: Article

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