PEROXISOME BIOGENESIS REVISITED

被引:167
作者
BORST, P
机构
关键词
D O I
10.1016/0167-4781(89)90163-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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页码:1 / 13
页数:13
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  • [1] PARTIAL DISASSEMBLY OF PEROXISOMES
    ALEXSON, SEH
    FUJIKI, Y
    SHIO, H
    LAZAROW, PB
    [J]. JOURNAL OF CELL BIOLOGY, 1985, 101 (01) : 294 - 304
  • [2] CDNA-DERIVED AMINO-ACID-SEQUENCE OF RAT MITOCHONDRIAL 3-OXOACYL-COA THIOLASE WITH NO TRANSIENT PRESEQUENCE - STRUCTURAL RELATIONSHIP WITH PEROXISOMAL ISOZYME
    ARAKAWA, H
    TAKIGUCHI, M
    AMAYA, Y
    NAGATA, S
    HAYASHI, H
    MORI, M
    [J]. EMBO JOURNAL, 1987, 6 (05) : 1361 - 1366
  • [3] BELL GI, 1986, NUCLEIC ACIDS RES, V14, P5561
  • [4] PROTON IONOPHORES PREVENT ASSEMBLY OF A PEROXISOMAL PROTEIN
    BELLION, E
    GOODMAN, JM
    [J]. CELL, 1987, 48 (01) : 165 - 173
  • [5] TRANSLOCATION IN YEAST AND MAMMALIAN-CELLS - NOT ALL SIGNAL SEQUENCES ARE FUNCTIONALLY EQUIVALENT
    BIRD, P
    GETHING, MJ
    SAMBROOK, J
    [J]. JOURNAL OF CELL BIOLOGY, 1987, 105 (06) : 2905 - 2914
  • [8] BORST P, 1989, IN PRESS NATO ASI SE
  • [9] NUCLEOTIDE-SEQUENCE OF HUMAN PEROXISOMAL 3-OXOACYL-COA THIOLASE
    BOUT, A
    TEUNISSEN, Y
    HASHIMOTO, T
    BENNE, R
    TAGER, JM
    [J]. NUCLEIC ACIDS RESEARCH, 1988, 16 (21) : 10369 - 10369
  • [10] GENETIC-HETEROGENEITY IN THE CEREBROHEPATORENAL (ZELLWEGER) SYNDROME AND OTHER INHERITED DISORDERS WITH A GENERALIZED IMPAIRMENT OF PEROXISOMAL FUNCTIONS - A STUDY USING COMPLEMENTATION ANALYSIS
    BRUL, S
    WESTERVELD, A
    STRIJLAND, A
    WANDERS, RJA
    SCHRAM, AW
    HEYMANS, HSA
    SCHUTGENS, RBH
    VANDENBOSCH, H
    TAGER, JM
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1988, 81 (06) : 1710 - 1715