II型酪氨酸血症中的肝酪氨酸转氨酶 - Suppr

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Hepatic tyrosine aminotransferase in tyrosinaemia type II.

作者信息

Kida K, Takahashi M, Fujisawa Y, Matsuda H, Machino H, Miki Y

出版信息

J Inherit Metab Dis. 1982;5(4):229-30. doi: 10.1007/BF02179149.

DOI:10.1007/BF02179149

PMID:6133036

Abstract

摘要

相似文献

Hepatic tyrosine aminotransferase in tyrosinaemia type II.II型酪氨酸血症中的肝酪氨酸转氨酶

J Inherit Metab Dis. 1982;5(4):229-30. doi: 10.1007/BF02179149.

Tyrosinosis (tyrosinaemia).酪氨酸血症

Indian Pediatr. 1975 Mar;12(3):209-10.

A new variant form of hypertyrosinaemia due to 4-hydroxyphenylpyruvic acid oxidase deficiency.一种由于4-羟基苯丙酮酸氧化酶缺乏导致的新型高酪氨酸血症变异型。

J Inherit Metab Dis. 1982;5(4):237-8. doi: 10.1007/BF02179153.

Putative genetic deficiency of 4-hydroxyphenylpyruvic acid dioxygenase in mice: a murine model for hereditary tyrosinaemia type III.小鼠中4-羟基苯丙酮酸双加氧酶的假定基因缺陷：III型遗传性酪氨酸血症的小鼠模型。

J Inherit Metab Dis. 1990;13(5):780-2. doi: 10.1007/BF01799587.

Development of tyrosine aminotransferase and para-hydroxyphenylpyruvate dioxygenase activities in fetal and neonatal human liver.胎儿及新生儿肝脏中酪氨酸转氨酶和对羟基苯丙酮酸双加氧酶活性的发育

J Clin Invest. 1982 Jul;70(1):198-200. doi: 10.1172/jci110593.

Enzyme defect in a case of tyrosinemia type I, acute form.1型酪氨酸血症急性型的酶缺陷病例

Pediatr Res. 1984 May;18(5):463-6. doi: 10.1203/00006450-198405000-00014.

Defect in soluble tyrosine aminotransferase in skin fibroblasts of a patient with tyrosinemia.

Pediatr Res. 1980 Jul;14(7):896-8. doi: 10.1203/00006450-198007000-00013.

Tyrosinemia type III: diagnosis and ten-year follow-up.III型酪氨酸血症：诊断与十年随访

Acta Paediatr. 1997 Sep;86(9):1013-5. doi: 10.1111/j.1651-2227.1997.tb15192.x.

Parahydroxyphenylpyruvicacidemia in tyrosinosis.酪氨酸血症中的对羟基苯丙酮酸血症

Indian Pediatr. 1978 Nov;15(11):893-9.

Hepatic enzymes of tyrosine metabolism in tyrosinemia II.酪氨酸血症II型中酪氨酸代谢的肝脏酶

J Invest Dermatol. 1979 Dec;73(6):530-2. doi: 10.1111/1523-1747.ep12541401.

引用本文的文献

Action of the phosphonic analogue of tyrosine and of other tyrosine derivatives on rat liver tyrosine aminotransferase.磷酸酪氨酸类似物及其他酪氨酸衍生物对大鼠肝酪氨酸转氨酶的作用。

Amino Acids. 1993 Feb;5(1):33-7. doi: 10.1007/BF00806190.

The human tyrosine aminotransferase gene: characterization of restriction fragment length polymorphisms and haplotype analysis in a family with tyrosinemia type II.

Hum Genet. 1988 Jul;79(3):260-4. doi: 10.1007/BF00366248.

Point mutations in the tyrosine aminotransferase gene in tyrosinemia type II.II型酪氨酸血症中酪氨酸转氨酶基因的点突变。

Proc Natl Acad Sci U S A. 1992 Oct 1;89(19):9297-301. doi: 10.1073/pnas.89.19.9297.

本文引用的文献

The assay of aromatic amino acid transaminations and keto acid oxidation by the enol borate-tautomerase method.用烯醇硼酸互变异构酶法测定芳香族氨基酸转氨作用和酮酸氧化作用

J Biol Chem. 1958 Sep;233(3):668-73.

An exceptional case of tyrosinosis.酪氨酸血症的一个特殊病例。

J Ment Defic Res. 1968 Dec;12(4):269-81. doi: 10.1111/j.1365-2788.1968.tb00267.x.

Soluble and mitochondrial forms of tyrosine aminotransferase. Relationship to human tyrosinemia.酪氨酸转氨酶的可溶性和线粒体形式。与人类酪氨酸血症的关系。

Biochemistry. 1969 Feb;8(2):615-22. doi: 10.1021/bi00830a023.

Metabolic studies on two patients with nonhepatic tyrosinemia using deuterated tyrosine loads.对两名非肝性酪氨酸血症患者使用氘代酪氨酸负荷进行的代谢研究。

Pediatr Res. 1977 May;11(5):631-7. doi: 10.1203/00006450-197705000-00002.

Hepatic enzymes of tyrosine metabolism in tyrosinemia II.酪氨酸血症II型中酪氨酸代谢的肝脏酶

J Invest Dermatol. 1979 Dec;73(6):530-2. doi: 10.1111/1523-1747.ep12541401.

Tyrosine aminotransferase isoenzyme deficiency.酪氨酸转氨酶同工酶缺乏症。

J Pediatr. 1979 Jun;94(6):931-2. doi: 10.1016/s0022-3476(79)80222-x.

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