纯合型胱硫醚β-合酶缺乏症患者体内的血小板活化：一种普罗布考敏感现象。 - Suppr | 超能文献

In vivo platelet activation in homozygous cystathionine beta-synthase deficiency: a probucol-sensitive phenomenon.

作者信息

Di Minno G, Margaglione M, Cirillo F, Grandone E, Davì G, Ciabattoni G, Catalano I, Strisciuglio P, Andria G, Coppola A

机构信息

Clinica Medica, Istituto di Medicina Interna e Malattie Dismetaboliche, Nuovo Policlinico, Napoli, Italy.

出版信息

Trans Assoc Am Physicians. 1992;105:149-56.

Abstract

摘要

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

文档翻译

学术文献翻译模型，支持多种主流文档格式。

相似文献

1

In vivo platelet activation in homozygous cystathionine beta-synthase deficiency: a probucol-sensitive phenomenon.纯合型胱硫醚β-合酶缺乏症患者体内的血小板活化：一种普罗布考敏感现象。

Trans Assoc Am Physicians. 1992;105:149-56.

2

Abnormally high thromboxane biosynthesis in homozygous homocystinuria. Evidence for platelet involvement and probucol-sensitive mechanism.纯合子型同型胱氨酸尿症中血栓素生物合成异常增高。血小板参与及普罗布考敏感机制的证据。

J Clin Invest. 1993 Sep;92(3):1400-6. doi: 10.1172/JCI116715.

3

Platelet and monocyte variables in homocystinuria due to cystathionine-beta-synthase deficiency.由于胱硫醚-β-合酶缺乏导致的同型胱氨酸尿症中的血小板和单核细胞变量。

Haematologica. 1997 Mar-Apr;82(2):189-90.

4

Oxidative stress and platelet activation in homozygous homocystinuria.纯合子型同型胱氨酸尿症中的氧化应激与血小板活化

Circulation. 2001 Sep 4;104(10):1124-8. doi: 10.1161/hc3501.095287.

5

Defective cystathionine beta-synthase regulation by S-adenosylmethionine in a partially pyridoxine responsive homocystinuria patient.在一名对吡哆醇部分反应性的同型胱氨酸尿症患者中，S-腺苷甲硫氨酸对胱硫醚β-合酶的调节存在缺陷。

J Clin Invest. 1996 Jul 15;98(2):285-9. doi: 10.1172/JCI118791.

6

Homocystinuria due to a cystathionine beta-synthase deficiency: clinical manifestations and therapy.胱硫醚β-合酶缺乏所致同型胱氨酸尿症：临床表现与治疗

Johns Hopkins Med J. 1980 Mar;146(3):110-7.

7

The usefulness of pyridoxine in the treatment of homocystinuria: a review of postulated mechanisms of action and a new hypothesis.吡哆醇在同型胱氨酸尿症治疗中的作用：对假定作用机制的综述及新假说

Birth Defects Orig Artic Ser. 1976;12(3):347-57.

8

The molecular basis of cystathionine beta-synthase deficiency in Australian patients: genotype-phenotype correlations and response to treatment.澳大利亚患者中胱硫醚β-合酶缺乏症的分子基础：基因型-表型相关性及治疗反应

Hum Mutat. 2002 Aug;20(2):117-26. doi: 10.1002/humu.10104.

9

Platelet survival and morphology in homocystinuria due to cystathionine synthase deficiency.由于胱硫醚合成酶缺乏导致的同型胱氨酸尿症中的血小板存活和形态

N Engl J Med. 1976 Dec 2;295(23):1283-6. doi: 10.1056/NEJM197612022952303.

10

Mice deficient in cystathionine beta synthase display altered homocysteine remethylation pathway.缺乏胱硫醚β合酶的小鼠表现出同型半胱氨酸再甲基化途径的改变。

Mol Genet Metab. 2007 Aug;91(4):396-8. doi: 10.1016/j.ymgme.2007.05.002. Epub 2007 Jun 11.

引用本文的文献

1

Guidelines for the diagnosis and management of cystathionine beta-synthase deficiency.胱硫醚β-合酶缺乏症的诊断与管理指南。

J Inherit Metab Dis. 2017 Jan;40(1):49-74. doi: 10.1007/s10545-016-9979-0. Epub 2016 Oct 24.