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1)  tryptophan hydroxylase
色氨酸羟化酶
1.
Association study between schizophrenia and Tryptophan Hydroxylase 2 gene(rs1386494,G1463A) polymorphism in Yunnan Han and Jinuo population
云南汉族、基诺族色氨酸羟化酶2基因rs1386494、G1463A多态性与精神分裂症的关联研究
2.
Objective:To explore the relationship between the hepatic depression syndrome and hyperpyrexia of liver syndrome disorder and polymorphisms in the serotonin transporter (5 HTT) and tryptophan hydroxylase(TPH).
目的 :探讨肝气郁结证、肝火上炎证与五羟色胺转运体 (5 HTT)、色氨酸羟化酶 (TPH)基因三种多态性的相关性。
3.
To investigate the relationship between serotonin transporter(SERT or 5-HTT) gene-linked polymorphism (5-HTTLPR), 17bp varied number tandem repeats(VNTRs) polymorphism within intron 2 and A218C polymorphism within intron 7 of tryptophan hydroxylase-1(TPH-1)gene and irritable bowel syndrome (IBS), functional diarrhea(FDi) and functional constipation(FC).
探讨5-羟色胺转运体基因相关多态区(5-HTTLPR)、内含子2可变串联重复区(VNTRs)多态性和色氨酸羟化酶-1(TPH-1)基因内含子7 A218C多态性在肠易激综合征(IBS)、功能性腹泻(FDi)、功能性便秘(FC)中的意义。
2)  Tryptophan Hydroxylase 2
色氨酸羟化酶2
1.
Association Study between Schizophrenia and Tryptophan Hydroxylase 2 Gene (G1463A, rs1386494) Polymorphism in Yunnan Han and Jinuo Population;
云南汉族、基诺族色氨酸羟化酶2基因(TPH2)G1463A、rs1386494多态性及其单体型与精神分裂症关联研究
2.
Objective To explore the association between signal nucleotide polymorphisms(SNP)of the gene encoding tryptophan hydroxylase 2(TPH2)and attention deficit hyperactivity disorder(ADHD).
目的探讨色氨酸羟化酶2(TPH2)基因的单核苷酸多态性(SNP)位点rs11178997和rs4570625多态性与注意缺陷多动障碍(ADHD)之间的关系。
3)  Tryptophan hydroxylase-2,5-hydroxytryplamine
色氨酸羟化酶2,5-羟色胺
4)  tryptophan hydroxylase gene
色氨酸羟化酶基因
5)  tryptophanhydroxylase
色氨酸羟化酶基因(TPH)
6)  tryptophane hydroxylase inhibitors
色氨酸羟化酶抑制剂
补充资料:色氨酸羟化酶抑制剂
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性质:抑制色氨酸羟化酶(EC1.14.16.4)活性的物质。色氨酸羟化酶是动物组织中由色氨酸合成5-羟基色胺的关键酶。后者是一种强烈的血管收缩剂,如2,5-二氢-L-苯丙氨酸是研究5-羟基色胺作用的一个很好的工具,临床上可望用作降压药。

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