NcoI RFLP in the pseudogene (CYP2D8P) of the human debrisoquine 4-hydroxylase locus.
作者信息
Mura C, Broyart J P, Jacqz E, Elion J, Krishnamoorthy R
机构信息
INSERM U120, Hôpital Robert Debré, Paris, France.
出版信息
Nucleic Acids Res. 1991 Mar 11;19(5):1162. doi: 10.1093/nar/19.5.1162.
Abstract
摘要
相似文献
1
NcoI RFLP in the pseudogene (CYP2D8P) of the human debrisoquine 4-hydroxylase locus.人异喹胍4-羟化酶基因座假基因（CYP2D8P）中的NcoI限制性片段长度多态性
Nucleic Acids Res. 1991 Mar 11;19(5):1162. doi: 10.1093/nar/19.5.1162.
2
The human debrisoquine 4-hydroxylase (CYP2D) locus: sequence and identification of the polymorphic CYP2D6 gene, a related gene, and a pseudogene.
Am J Hum Genet. 1989 Dec;45(6):889-904.
3
A BamHI polymorphism in the human cytochrome P450 gene, CYP2D6.人类细胞色素P450基因CYP2D6中的BamHI多态性。
Clin Genet. 1995 Feb;47(2):103-4. doi: 10.1111/j.1399-0004.1995.tb03934.x.
4
Genetic polymorphism of debrisoquine oxidation: restriction fragment analysis and allele-specific amplification of mutant alleles of CYP2D6.异喹胍氧化的基因多态性：CYP2D6突变等位基因的限制性片段分析和等位基因特异性扩增
Methods Enzymol. 1991;206:173-83. doi: 10.1016/0076-6879(91)06088-k.
5
Dinucleotide repeat polymorphism at the human debrisoquine 4-hydroxylase (CYP2D) locus.人异喹胍4-羟化酶（CYP2D）基因座的二核苷酸重复多态性。
Nucleic Acids Res. 1991 Apr 25;19(8):1961.
6
Dinucleotide repeat polymorphism at the debrisoquine 4-hydroxylase (CYP2D) locus.去甲丙咪嗪4-羟化酶（CYP2D）基因座的二核苷酸重复多态性。
Nucleic Acids Res. 1991 May 25;19(10):2802. doi: 10.1093/nar/19.10.2802-a.
7
Identification of the primary gene defect at the cytochrome P450 CYP2D locus.细胞色素P450 CYP2D基因座上主要基因缺陷的鉴定。
Nature. 1990 Oct 25;347(6295):773-6. doi: 10.1038/347773a0.
8
Detection of debrisoquine hydroxylation phenotypes.去甲丙咪嗪羟化表型的检测。
Lancet. 1990 Dec 8;336(8728):1452-3. doi: 10.1016/0140-6736(90)93163-j.
9
Human debrisoquine 4-hydroxylase (P450IID1): cDNA and deduced amino acid sequence and assignment of the CYP2D locus to chromosome 22.
Genomics. 1988 Feb;2(2):174-9. doi: 10.1016/0888-7543(88)90100-0.
10
Detection of the poor metabolizer-associated CYP2D6(D) gene deletion allele by long-PCR technology.采用长链聚合酶链反应技术检测与代谢不良者相关的CYP2D6(D)基因缺失等位基因。
Pharmacogenetics. 1995 Aug;5(4):215-23. doi: 10.1097/00008571-199508000-00005.
引用本文的文献
1
Functional characterization of a first avian cytochrome P450 of the CYP2D subfamily (CYP2D49).鉴定首个禽类 CYP2D 亚家族细胞色素 P450（CYP2D49）的功能。
PLoS One. 2012;7(6):e38395. doi: 10.1371/journal.pone.0038395. Epub 2012 Jun 4.
2
An unequal cross-over event within the CYP2D gene cluster generates a chimeric CYP2D7/CYP2D6 gene which is associated with the poor metabolizer phenotype.CYP2D基因簇内的不等交换事件产生了一个嵌合的CYP2D7/CYP2D6基因，该基因与代谢不良表型相关。
Br J Clin Pharmacol. 1995 Oct;40(4):361-7. doi: 10.1111/j.1365-2125.1995.tb04558.x.
3
DNA haplotype dependency of debrisoquine 4-hydroxylase (CYP2D6) expression among extensive metabolisers.
Hum Genet. 1993 Oct;92(4):367-72. doi: 10.1007/BF01247337.
本文引用的文献
1
Human debrisoquine 4-hydroxylase (P450IID1): cDNA and deduced amino acid sequence and assignment of the CYP2D locus to chromosome 22.
Genomics. 1988 Feb;2(2):174-9. doi: 10.1016/0888-7543(88)90100-0.
2
The human debrisoquine 4-hydroxylase (CYP2D) locus: sequence and identification of the polymorphic CYP2D6 gene, a related gene, and a pseudogene.
Am J Hum Genet. 1989 Dec;45(6):889-904.
Zotero 插件