血清胆碱酯酶（E2）连锁分析：定位于16号染色体的可能证据。 - Suppr

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超能文献

Serum cholinesterase (E2) linkage analysis: possible evidence for localization to chromosome 16.

作者信息

Lovrien E W, Magenis R E, Rivas M L, Lamvik N, Rowe S, Wood J, Hemmerling J

出版信息

Cytogenet Cell Genet. 1978;22(1-6):324-6. doi: 10.1159/000130964.

DOI:10.1159/000130964

PMID:752495

Abstract

摘要

相似文献

Serum cholinesterase (E2) linkage analysis: possible evidence for localization to chromosome 16.血清胆碱酯酶（E2）连锁分析：定位于16号染色体的可能证据。

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引用本文的文献

Genetic mapping: chromosomes 6-22.基因定位：6号至22号染色体。

Am J Hum Genet. 1982 Sep;34(5):730-42.

The use of mRNA translation in vitro and in ovo followed by crossed immunoelectrophoretic autoradiography to study the biosynthesis of human cholinesterases.利用体外和卵内mRNA翻译，随后进行交叉免疫电泳放射自显影来研究人胆碱酯酶的生物合成。

Cell Mol Neurobiol. 1986 Sep;6(3):227-37. doi: 10.1007/BF00711110.

Human cholinesterase genes localized by hybridization to chromosomes 3 and 16.通过杂交定位到3号和16号染色体上的人类胆碱酯酶基因。

Hum Genet. 1987 Dec;77(4):325-8. doi: 10.1007/BF00291419.

Molecular biological search for human genes encoding cholinesterases.对编码胆碱酯酶的人类基因进行分子生物学研究。

Mol Neurobiol. 1987 Spring-Summer;1(1-2):47-80. doi: 10.1007/BF02935264.

A linkage group with FRA16B (the fragile site at 16q22.1).一个与FRA16B（位于16q22.1的脆性位点）相关的连锁群。

Hum Genet. 1989 May;82(2):131-3. doi: 10.1007/BF00284044.

Comparison of butyrylcholinesterase and acetylcholinesterase.丁酰胆碱酯酶与乙酰胆碱酯酶的比较。

Biochem J. 1989 Jun 15;260(3):625-34. doi: 10.1042/bj2600625.

Human acetylcholinesterase and butyrylcholinesterase are encoded by two distinct genes.人类乙酰胆碱酯酶和丁酰胆碱酯酶由两个不同的基因编码。

Cell Mol Neurobiol. 1991 Feb;11(1):91-104. doi: 10.1007/BF00712802.

Proposed nomenclature for human butyrylcholinesterase genetic variants identified by DNA sequencing.通过DNA测序鉴定的人类丁酰胆碱酯酶基因变异的拟用命名法。

Cell Mol Neurobiol. 1991 Feb;11(1):79-89. doi: 10.1007/BF00712801.

Structural and functional investigations of cholinesterases by means of affinity electrophoresis.通过亲和电泳对胆碱酯酶进行结构和功能研究。

Cell Mol Neurobiol. 1991 Feb;11(1):173-89. doi: 10.1007/BF00712808.

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