Molecular defects in genetic diseases of peroxisomes

被引:60
作者
Fujiki, Y
机构
[1] Department of Biology, Fac. of Science, Kyushu University
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 1997年 / 1361卷 / 03期
关键词
peroxisome biogenesis disorder; Zellweger syndrome; complementation group; pathogenic gene; peroxisomal targeting signal; peroxisome biogenesis factor;
D O I
10.1016/S0925-4439(97)00051-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
[No abstract available]
引用
收藏
页码:235 / 250
页数:16
相关论文
共 166 条
[1]   2 CASES OF ACATALASIA IN SWITZERLAND [J].
AEBI, H ;
BUTLER, R ;
HEINIGER, JP ;
HASSIG, A .
EXPERIENTIA, 1961, 17 (10) :466-&
[2]   Pex14p, a peroxisomal membrane protein binding both receptors of the two PTS-dependent import pathways [J].
Albertini, M ;
Rehling, P ;
Erdmann, R ;
Girzalsky, W ;
Kiel, JAKW ;
Veenhuis, M ;
Kunau, WH .
CELL, 1997, 89 (01) :83-92
[3]  
Amara J F, 1992, Trends Cell Biol, V2, P145, DOI 10.1016/0962-8924(92)90101-R
[4]   PROTON IONOPHORES PREVENT ASSEMBLY OF A PEROXISOMAL PROTEIN [J].
BELLION, E ;
GOODMAN, JM .
CELL, 1987, 48 (01) :165-173
[5]   A NONMAMMALIAN HOMOLOG OF THE PAF1 GENE (ZELLWEGER-SYNDROME) DISCOVERED AS A GENE INVOLVED IN CARYOGAMY IN THE FUNGUS PODOSPORA-ANSERINA [J].
BERTEAUXLECELLIER, V ;
PICARD, M ;
THOMPSONCOFFE, C ;
ZICKLER, D ;
PANVIERADOUTTE, A ;
SIMONET, JM .
CELL, 1995, 81 (07) :1043-1051
[6]   GLYCOSOME ASSEMBLY IN TRYPANOSOMES - VARIATIONS IN THE ACCEPTABLE DEGENERACY OF A COOH-TERMINAL MICROBODY TARGETING SIGNAL [J].
BLATTNER, J ;
SWINKELS, B ;
DORSAM, H ;
PROSPERO, T ;
SUBRAMANI, S ;
CLAYTON, C .
JOURNAL OF CELL BIOLOGY, 1992, 119 (05) :1129-1136
[7]   NUCLEOTIDE-SEQUENCE OF HUMAN PEROXISOMAL 3-OXOACYL-COA THIOLASE [J].
BOUT, A ;
TEUNISSEN, Y ;
HASHIMOTO, T ;
BENNE, R ;
TAGER, JM .
NUCLEIC ACIDS RESEARCH, 1988, 16 (21) :10369-10369
[8]   DISORDERS OF PEROXISOME BIOGENESIS [J].
BRAVERMAN, N ;
DODT, G ;
GOULD, SJ ;
VALLE, D .
HUMAN MOLECULAR GENETICS, 1995, 4 :1791-1798
[9]   Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata [J].
Braverman, N ;
Steel, G ;
Obie, C ;
Moser, A ;
Moser, H ;
Gould, SJ ;
Valle, D .
NATURE GENETICS, 1997, 15 (04) :369-376
[10]   PEROXISOMAL DISORDERS - NEURODEVELOPMENTAL AND BIOCHEMICAL ASPECTS [J].
BROWN, FR ;
VOIGT, R ;
SINGH, AK ;
SINGH, I .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1993, 147 (06) :617-626