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Literature DB >> 1769658

Refinement of the localization of human butyrylcholinesterase to chromosome 3q26.1-q26.2 using a PCR-derived probe.

G Gaughan¹, H Park, J Priddle, I Craig, S Craig.

Abstract

The gene for butyrylcholinesterase (EC 3.1.1.8) has been previously localized to three sites in the human genome, at 3q21, 3q26, and 16q21. In situ hybridization using a PCR-derived probe including the active site region gives a single hybridization signal and refines the localization to 3q26.1-q26.2.

Entities: Gene Species

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Year: 1991 PMID： 1769658 DOI： 10.1016/0888-7543(91)90155-8

Source DB: PubMed Journal: Genomics ISSN： 0888-7543 Impact factor: 5.736

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Cited

7 in total

1. Naturally occurring variations in the human cholinesterase genes: heritability and association with cardiovascular and metabolic traits.

Authors: Anne M Valle; Zoran Radic; Brinda K Rana; Vafa Mahboubi; Jennifer Wessel; Pei-an Betty Shih; Fangwen Rao; Daniel T O'Connor; Palmer Taylor
Journal: J Pharmacol Exp Ther Date: 2011-04-14 Impact factor: 4.030

2. Mapping a gene for adult-onset primary open-angle glaucoma to chromosome 3q.

Authors: M K Wirtz; J R Samples; P L Kramer; K Rust; J R Topinka; J Yount; R D Koler; T S Acott
Journal: Am J Hum Genet Date: 1997-02 Impact factor: 11.025

3. The human gene encoding acetylcholinesterase is located on the long arm of chromosome 7.

Authors: D K Getman; J H Eubanks; S Camp; G A Evans; P Taylor
Journal: Am J Hum Genet Date: 1992-07 Impact factor: 11.025

4. Identification of two different point mutations associated with the fluoride-resistant phenotype for human butyrylcholinesterase.

Authors: C P Nogueira; C F Bartels; M C McGuire; S Adkins; T Lubrano; H M Rubinstein; H Lightstone; A F Van der Spek; O Lockridge; B N La Du
Journal: Am J Hum Genet Date: 1992-10 Impact factor: 11.025

Refinement of the localization of human butyrylcholinesterase to chromosome 3q26.1-q26.2 using a PCR-derived probe.

1. Naturally occurring variations in the human cholinesterase genes: heritability and association with cardiovascular and metabolic traits.

2. Mapping a gene for adult-onset primary open-angle glaucoma to chromosome 3q.

3. The human gene encoding acetylcholinesterase is located on the long arm of chromosome 7.

4. Identification of two different point mutations associated with the fluoride-resistant phenotype for human butyrylcholinesterase.

5. Comparison of cognitive functions between people with silent and wild-type butyrylcholinesterase.

6. The C5 Variant of the Butyrylcholinesterase Tetramer Includes a Noncovalently Bound 60 kDa Lamellipodin Fragment.

7. Prolonged neuromuscular block associated with cholinesterase deficiency.