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神经学缺陷:表型模拟中的锰与内耳遗传异常的预防

Neurological defect: manganese in phenocopy and prevention of a genetic abnormality of inner ear.

作者信息

Erway L, Hurley L S, Fraser A

出版信息

Science. 1966 Jun 24;152(3730):1766-8. doi: 10.1126/science.152.3730.1766.

DOI:10.1126/science.152.3730.1766
PMID:5949342
Abstract

A specific congenital ataxia may be caused by presence of mutant genes and by manganese deficiency during prenatal development in normal mice. Supplementation of the diet of mutant mice with manganese during prenatal development rectifies the aberrant development, resulting in normal behavior. The congential ataxa results from defective development of the the otoliths.

摘要

在正常小鼠中,特定的先天性共济失调可能由突变基因的存在以及产前发育期间锰缺乏引起。在产前发育期间给突变小鼠的饮食补充锰可纠正异常发育,从而产生正常行为。先天性共济失调是由耳石发育缺陷导致的。

相似文献

1
Neurological defect: manganese in phenocopy and prevention of a genetic abnormality of inner ear.神经学缺陷:表型模拟中的锰与内耳遗传异常的预防
Science. 1966 Jun 24;152(3730):1766-8. doi: 10.1126/science.152.3730.1766.
2
Prevention of congenital otolith defect in pallid mutant mice by manganese supplementation.通过补充锰预防苍白突变小鼠的先天性耳石缺陷。
Genetics. 1971 Jan;67(1):97-108. doi: 10.1093/genetics/67.1.97.
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Anomalous development of otoliths associated with postural defects in manganese-deficient guinea-pigs.缺锰豚鼠耳石异常发育与姿势缺陷相关
J Nutr. 1967 Apr;91(4):453-60. doi: 10.1093/jn/91.4.453.
4
Congenital ataxia and otolith defects due to manganese deficiency in mice.
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Trace elements and teratogenesis.微量元素与致畸作用
Med Clin North Am. 1976 Jul;60(4):771-8. doi: 10.1016/s0025-7125(16)31860-0.
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Mucopolysaccharide synthesis in the developing inner ear of manganese-deficient and pallid mutant mice.
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Genetic influence on response to dietary manganese deficiency in mice.基因对小鼠饮食性锰缺乏反应的影响。
J Nutr. 1974 Jan;104(1):133-7. doi: 10.1093/jn/104.1.133.
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Prevention of otolith defect in pastel mink by manganese supplementation.通过补充锰预防彩色水貂耳石缺陷。
J Hered. 1973 May-Jun;64(3):111-9. doi: 10.1093/oxfordjournals.jhered.a108366.
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Genes, manganese, and zinc in formation of otoconia: labeling, recovery, and maternal effects.基因、锰和锌在耳石形成中的作用:标记、回收及母体效应。
Scan Electron Microsc. 1986(Pt 4):1681-94.
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Effects of dichlorophenamide, zinc, and manganese on otolith development in mice.
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引用本文的文献

1
The effects of manganese deficiency during prenatal and postnatal development on mitochondrial structure and function in the rat.孕期和产后发育期锰缺乏对大鼠线粒体结构和功能的影响。
Biol Trace Elem Res. 1985 Feb;7(1):31-48. doi: 10.1007/BF02916545.
2
Deletion mapping of the head tilt (het) gene in mice: a vestibular mutation causing specific absence of otoliths.小鼠头部倾斜(het)基因的缺失图谱:一种导致耳石特异性缺失的前庭突变。
Genetics. 1998 Oct;150(2):815-22. doi: 10.1093/genetics/150.2.815.
3
Hyperoxia and hypoxia in pregnancy: simple experimental manipulation alters the incidence of cleft lip and palate in CL/Fr mice.
孕期的高氧和低氧:简单的实验操作改变了CL/Fr小鼠唇腭裂的发生率。
Proc Natl Acad Sci U S A. 1981 Sep;78(9):5722-3. doi: 10.1073/pnas.78.9.5722.
4
Unilateral agenesis of the diaphragm.单侧膈肌发育不全
Humangenetik. 1968;5(3):226-30. doi: 10.1007/BF00281959.
5
Genetic aspects of negative geotaxis in mice.小鼠负趋地性的遗传因素
Behav Genet. 1970 Feb;1(1):21-34. doi: 10.1007/BF01067368.
6
Neurochemical correlates of the waltzing-shaker syndrome in the Varitint-waddler mouse.变色素摇摆小鼠中华尔兹 - 摇晃综合征的神经化学关联
Psychopharmacologia. 1972;24(3):384-96. doi: 10.1007/BF00402533.
7
Inherited diseases of the inner ear in man in the light of studies on the mouse.基于对小鼠的研究看人类内耳的遗传性疾病
J Med Genet. 1968 Jun;5(2):137-58. doi: 10.1136/jmg.5.2.137.
8
Slow turnover of manganese in active rheumatoid arthritis accelerated by prednisone.泼尼松加速活动性类风湿关节炎中锰的缓慢周转。
J Clin Invest. 1968 May;47(5):992-1001. doi: 10.1172/JCI105814.
9
Effects of calcium preloading on the growth of calcium carbonate crystals in the endolymphatic sac of the tree frog, Hyla arborea japonica.
Cell Tissue Res. 1988 Jun;252(3):679-82. doi: 10.1007/BF00216656.