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Hyperalaninemia with pyruvicemia due to pyruvate carboxylase deficiency of the liver.

作者信息

Yoshida T, Tada K, Konno T, Arakawa T

出版信息

Tohoku J Exp Med. 1969 Oct;99(2):121-8. doi: 10.1620/tjem.99.121.

DOI:10.1620/tjem.99.121
PMID:5358431
Abstract
摘要

相似文献

1
Hyperalaninemia with pyruvicemia due to pyruvate carboxylase deficiency of the liver.由于肝脏丙酮酸羧化酶缺乏导致的高丙氨酸血症伴丙酮酸血症。
Tohoku J Exp Med. 1969 Oct;99(2):121-8. doi: 10.1620/tjem.99.121.
2
Hyperalaninemia with pyruvicemia in a patient suggestive of Leigh's encephalomyelopathy.一名患者出现高丙氨酸血症伴丙酮酸血症，提示 Leigh 脑脊髓病。
Tohoku J Exp Med. 1973 Jan;109(1):13-8. doi: 10.1620/tjem.109.13.
3
[Hyperalaninemia-pyruvicemia: chronic lactic acidosis].
Nihon Rinsho. 1973 Aug 10;31(8):2456-62.
4
Thiamine-responsive lactice acidosis in a patient with deficient low-KM pyruvate carboxylase activity in liver.
Pediatrics. 1972 Nov;50(5):702-11.
5
Effects of glucagon on carbohydrate synthesis and enzyme activity in rat liver.胰高血糖素对大鼠肝脏碳水化合物合成及酶活性的影响。
Endocrinology. 1968 Dec;83(6):1337-48. doi: 10.1210/endo-83-6-1337.
6
Development of some enzymes involved in gluconeogenesis in human liver.
Ann Med Exp Biol Fenn. 1969;47(2):146-50.
7
Abnormally high levels of lactate and pyruvate in cerebrospinal fluid of hyperalaninemia with hyperpyruvicemia.
Tohoku J Exp Med. 1970 Aug;101(4):375-8. doi: 10.1620/tjem.101.375.
8
Regulation of gluconeogenesis in the guinea pig liver.豚鼠肝脏中糖异生的调节
Eur J Biochem. 1970 Oct;16(2):289-302. doi: 10.1111/j.1432-1033.1970.tb01084.x.
9
Hyperalaninemia with pyruvicemia (preliminary report).
Tohoku J Exp Med. 1969 Jan;97(1):99-100. doi: 10.1620/tjem.97.99.
10
Intracellular localization of pyruvate carboxylase and phosphoenolpyruvate carboxykinase in rat liver.大鼠肝脏中丙酮酸羧化酶和磷酸烯醇式丙酮酸羧激酶的细胞内定位
Eur J Biochem. 1969 Mar;8(1):113-9. doi: 10.1111/j.1432-1033.1969.tb00503.x.

引用本文的文献

1
Specificity and selectivity in post-translational biotin addition.翻译后生物素添加中的特异性和选择性
Biochem Soc Trans. 2018 Dec 17;46(6):1577-1591. doi: 10.1042/BST20180425. Epub 2018 Oct 31.
2
The molecular basis of pyruvate carboxylase deficiency: mosaicism correlates with prolonged survival.丙酮酸羧化酶缺乏症的分子基础：嵌合体与延长生存期相关。
Mol Genet Metab. 2008 Sep-Oct;95(1-2):31-8. doi: 10.1016/j.ymgme.2008.06.006. Epub 2008 Aug 3.
3
Megavitamin therapy in inherited metabolic disorders.遗传性代谢紊乱中的大剂量维生素疗法。
Indian J Pediatr. 1981 Sep-Oct;48(394):635-46. doi: 10.1007/BF02821592.
4
Is pyruvate carboxylase involved in the renal tubular reabsorption of bicarbonate?丙酮酸羧化酶是否参与肾小管对碳酸氢盐的重吸收？
J Inherit Metab Dis. 1980;3(4):113-6. doi: 10.1007/BF02312544.
5
Evidence for two genetic complementation groups in pyruvate carboxylase-deficient human fibroblast cell lines.丙酮酸羧化酶缺陷型人成纤维细胞系中两个遗传互补组的证据。
Biochem Genet. 1980 Jun;18(5-6):617-24. doi: 10.1007/BF00484405.
6
The biotin-dependent carboxylase deficiencies.生物素依赖性羧化酶缺乏症
Am J Hum Genet. 1982 Sep;34(5):699-716.
7
Hyperalaninemia hyperpyruvicemia and lactic acidosis due to pyruvate carboxylase deficiency of the liver; treatment with thiamine and lipoic acid.由于肝脏丙酮酸羧化酶缺乏导致的高丙氨酸血症、高丙酮酸血症和乳酸酸中毒；硫胺素和硫辛酸治疗。
Eur J Pediatr. 1976 May 4;122(2):159-68. doi: 10.1007/BF00466274.
8
Congenital lactic acidosis due to pyruvate carboxylase deficiency: absence of an inhibitor of TPP-ATP phosphoryl transferase.
Eur J Pediatr. 1978 Jan 17;127(2):141-7. doi: 10.1007/BF00445770.
9
Fructose load test--an in vivo screening test designed to assess pyruvate dehydrogenase activity and interconversion.果糖负荷试验——一种旨在评估丙酮酸脱氢酶活性和相互转化的体内筛查试验。
J Inherit Metab Dis. 1978;1(4):163-5. doi: 10.1007/BF01805588.