核编码的线粒体酶缺失时的基因剂量 - Suppr

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超能文献

Gene dosage in a deletion for a nuclear-coded, mitochondrial enzyme.

作者信息

Diamond R P, Erickson R P

出版信息

Nature. 1974 Mar 29;248(447):418-9. doi: 10.1038/248418a0.

DOI:10.1038/248418a0

PMID:4823666

Abstract

摘要

相似文献

Gene dosage in a deletion for a nuclear-coded, mitochondrial enzyme.核编码的线粒体酶缺失时的基因剂量

Nature. 1974 Mar 29;248(447):418-9. doi: 10.1038/248418a0.

Linkage of isozyyme loci in the mouse: phosphoglucomutase-2 (Pgm-2), mitochondrial NADP malate dehydrogenase (Mod-2), and dipeptidase-1 (Dip-1).小鼠中同工酶基因座的连锁：磷酸葡萄糖变位酶-2（Pgm-2）、线粒体NADP苹果酸脱氢酶（Mod-2）和二肽酶-1（Dip-1）。

Biochem Genet. 1971 Apr;5(2):101-10. doi: 10.1007/BF00485638.

Mitochondrial malate dehydrogenase (Mor-1) in the mouse: linkage to chromosome 5 markers.小鼠中的线粒体苹果酸脱氢酶（Mor-1）：与5号染色体标记的连锁关系。

Biochem Genet. 1975 Oct;13(9-10):519-25. doi: 10.1007/BF00484911.

Mitochondrial malate dehydrogenase and malic enzyme: Mendelian inherited electrophoretic variants in the mouse.线粒体苹果酸脱氢酶和苹果酸酶：小鼠中的孟德尔遗传电泳变体

Biochem Genet. 1970 Dec;4(6):707-18. doi: 10.1007/BF00486384.

Demonstration in mouse of X-ray induced deletions for a know enzyme structural locus.在小鼠中证明X射线诱导的已知酶结构基因座缺失。

Nature. 1974 Mar 29;248(447):416-8. doi: 10.1038/248416a0.

A new genetic variation of the malate dehydrogenase-like enzyme (MDL-1) in inbred rats and its possible linkage.近交系大鼠中苹果酸脱氢酶样酶（MDL-1）的一种新的基因变异及其可能的连锁关系。

Biochem Genet. 1982 Jun;20(5-6):443-8. doi: 10.1007/BF00484695.

Mitochondrial enzymatic alterations produced in the myocardium by anoxic cardiac arrest.

J Thorac Cardiovasc Surg. 1974 Apr;67(4):649-58.

Effect of gene dosage on expression of mitochondrial malic enzyme activity in the mouse.基因剂量对小鼠线粒体苹果酸酶活性表达的影响。

Nature. 1978 Feb 23;271(5647):748-50. doi: 10.1038/271748a0.

Onset of synthesis of mitochondrial enzymes during mouse development. Synchronous activation of parenteral alleles at the gene locus for the M-form of NADP-dependent malate dehydrogenase.

Humangenetik. 1973;20(2):133-40. doi: 10.1007/BF00284848.

Human malic enzyme: high-frequency polymorphism of the mitochondrial form.人类苹果酸酶：线粒体形式的高频多态性。

Biochem Genet. 1972 Dec;7(3):303-11. doi: 10.1007/BF00484830.

引用本文的文献

Mice homozygous for chromosomal deletions at the albino locus region lack specific polypeptides in two-dimensional gels.在白化病基因座区域存在染色体缺失的纯合小鼠，在二维凝胶中缺乏特定的多肽。

Proc Natl Acad Sci U S A. 1984 Apr;81(7):2132-6. doi: 10.1073/pnas.81.7.2132.

Glycogen storage diseases in animals and their potential value as models of human disease.动物中的糖原贮积病及其作为人类疾病模型的潜在价值。

J Inherit Metab Dis. 1983;6(1):3-16. doi: 10.1007/BF02391186.

Animal models of glycogen storage conditions. Their relation to human disease.糖原贮积症的动物模型。它们与人类疾病的关系。

West J Med. 1975 Sep;123(3):194-201.

Regulation of mitochondrial malic enzyme synthesis in mouse brain.小鼠脑中线粒体苹果酸酶合成的调控

Proc Natl Acad Sci U S A. 1979 Dec;76(12):6539-41. doi: 10.1073/pnas.76.12.6539.

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