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PEROXISOMAL DISORDERS - COMPLEMENTATION ANALYSIS USING BETA-OXIDATION OF VERY LONG-CHAIN FATTY-ACIDS
被引:25
作者
:
MCGUINNESS, MC
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT NEUROL,BALTIMORE,MD 21205
JOHNS HOPKINS UNIV,SCH MED,DEPT NEUROL,BALTIMORE,MD 21205
MCGUINNESS, MC
[
1
]
MOSER, AB
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT NEUROL,BALTIMORE,MD 21205
JOHNS HOPKINS UNIV,SCH MED,DEPT NEUROL,BALTIMORE,MD 21205
MOSER, AB
[
1
]
MOSER, HW
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT NEUROL,BALTIMORE,MD 21205
JOHNS HOPKINS UNIV,SCH MED,DEPT NEUROL,BALTIMORE,MD 21205
MOSER, HW
[
1
]
WATKINS, PA
论文数:
0
引用数:
0
h-index:
0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT NEUROL,BALTIMORE,MD 21205
JOHNS HOPKINS UNIV,SCH MED,DEPT NEUROL,BALTIMORE,MD 21205
WATKINS, PA
[
1
]
机构
:
[1]
JOHNS HOPKINS UNIV,SCH MED,DEPT NEUROL,BALTIMORE,MD 21205
来源
:
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
|
1990年
/ 172卷
/ 01期
关键词
:
D O I
:
10.1016/S0006-291X(05)80218-9
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
:
Complementation studies, using fused cell lines from patients with peroxisomal disorders, have shown correction of defective plasmalogen synthesis and phytanic acid oxidation as wll as an increase in the number of peroxisomes. At least six complementation groups have been reported. We demostrate here that complementing cell lines also acquire the ability to oxidize very long chain fatty acids (VLCFA), and that complementation groups defined with this technique are identical to those reported previously when plasmalogen synthesis was used as the criterion for complementation. This VLCFA complementation technique is of particular value in the study of patients in whom defective VLCFA is the only or major enzymatic defect, and we show complementation between cell lines from two patients each with an isolated defect in one of the peroxisomal fatty acid beta-oxidation enzymes. © 1990 Academic Press, Inc.
引用
收藏
页码:364 / 369
页数:6
相关论文
共 13 条
[1]
GENETIC-HETEROGENEITY IN THE CEREBROHEPATORENAL (ZELLWEGER) SYNDROME AND OTHER INHERITED DISORDERS WITH A GENERALIZED IMPAIRMENT OF PEROXISOMAL FUNCTIONS - A STUDY USING COMPLEMENTATION ANALYSIS
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0
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[1]
GENETIC-HETEROGENEITY IN THE CEREBROHEPATORENAL (ZELLWEGER) SYNDROME AND OTHER INHERITED DISORDERS WITH A GENERALIZED IMPAIRMENT OF PEROXISOMAL FUNCTIONS - A STUDY USING COMPLEMENTATION ANALYSIS
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