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Results: 1 to 20 of 109

Related Citations for PubMed (Select 2253336)

1.

Phenotypic and molecular biological analysis of human butyrylcholinesterase variants.

La Du BN, Bartels CF, Nogueira CP, Hajra A, Lightstone H, Van der Spek A, Lockridge O.

Clin Biochem. 1990 Oct;23(5):423-31.

PMID:
2253336
2.

DNA mutation associated with the human butyrylcholinesterase K-variant and its linkage to the atypical variant mutation and other polymorphic sites.

Bartels CF, Jensen FS, Lockridge O, van der Spek AF, Rubinstein HM, Lubrano T, La Du BN.

Am J Hum Genet. 1992 May;50(5):1086-103.

3.

DNA mutations associated with the human butyrylcholinesterase J-variant.

Bartels CF, James K, La Du BN.

Am J Hum Genet. 1992 May;50(5):1104-14.

4.

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

Nogueira CP, Bartels CF, McGuire MC, Adkins S, Lubrano T, Rubinstein HM, Lightstone H, Van der Spek AF, Lockridge O, La Du BN.

Am J Hum Genet. 1992 Oct;51(4):821-8.

5.

Structural basis of the butyrylcholinesterase H-variant segregating in two Danish families.

Jensen FS, Bartels CF, La Du BN.

Pharmacogenetics. 1992 Oct;2(5):234-40.

PMID:
1306123
6.

Genetic basis of the silent phenotype of serum butyrylcholinesterase in three compound heterozygotes.

Maekawa M, Sudo K, Kanno T, Kotani K, Dey DC, Ishikawa J, Izumi M, Etoh K.

Clin Chim Acta. 1995 Feb 28;235(1):41-57.

PMID:
7634491
7.

Frequency of butyrylcholinesterase gene mutations in individuals with abnormal inhibition numbers: an Italian-population study.

Lando G, Mosca A, Bonora R, Azzario F, Penco S, Marocchi A, Panteghini M, Patrosso MC.

Pharmacogenetics. 2003 May;13(5):265-70.

PMID:
12724618
8.

Identification of a frameshift mutation responsible for the silent phenotype of human serum cholinesterase, Gly 117 (GGT----GGAG).

Nogueira CP, McGuire MC, Graeser C, Bartels CF, Arpagaus M, Van der Spek AF, Lightstone H, Lockridge O, La Du BN.

Am J Hum Genet. 1990 May;46(5):934-42.

9.

Characterization of 12 silent alleles of the human butyrylcholinesterase (BCHE) gene.

Primo-Parmo SL, Bartels CF, Wiersema B, van der Spek AF, Innis JW, La Du BN.

Am J Hum Genet. 1996 Jan;58(1):52-64.

10.

Identification of the structural mutation responsible for the dibucaine-resistant (atypical) variant form of human serum cholinesterase.

McGuire MC, Nogueira CP, Bartels CF, Lightstone H, Hajra A, Van der Spek AF, Lockridge O, La Du BN.

Proc Natl Acad Sci U S A. 1989 Feb;86(3):953-7.

11.

Human butyrylcholinesterase L330I mutation belongs to a fluoride-resistant gene, by expression in human fetal kidney cells.

Sudo K, Maekawa M, Akizuki S, Magara T, Ogasawara H, Tanaka T.

Biochem Biophys Res Commun. 1997 Nov 17;240(2):372-5.

PMID:
9388484
12.
13.

Characterization of an unstable variant (BChE115D) of human butyrylcholinesterase.

Primo-Parmo SL, Lightstone H, La Du BN.

Pharmacogenetics. 1997 Feb;7(1):27-34.

PMID:
9110359
14.

[Gene analysis of human cholinesterase variants].

Muratani K, Hada T, Higashino K.

Nihon Rinsho. 1993 Feb;51(2):495-500. Review. Japanese.

PMID:
8464162
15.

Response to mivacurium in a patient compound heterozygous for a novel and a known silent mutation in the butyrylcholinesterase gene: genotyping by sequencing.

G├Ątke MR, Ostergaard D, Bundgaard JR, Varin F, Viby-Mogensen J.

Anesthesiology. 2001 Sep;95(3):600-6.

PMID:
11575530
16.

Identification of a point mutation associated with a silent phenotype of human serum butyrylcholinesterase--a case of familial cholinesterasemia.

Sakamoto N, Hidaka K, Fujisawa T, Maeda M, Iuchi I.

Clin Chim Acta. 1998 Jun 22;274(2):159-66.

PMID:
9694584
17.

Butyrylcholinesterase (BCHE) genotyping for post-succinylcholine apnea in an Australian population.

Yen T, Nightingale BN, Burns JC, Sullivan DR, Stewart PM.

Clin Chem. 2003 Aug;49(8):1297-308.

18.

Genotyping the butyrylcholinesterase in patients with prolonged neuromuscular block after succinylcholine.

Levano S, Ginz H, Siegemund M, Filipovic M, Voronkov E, Urwyler A, Girard T.

Anesthesiology. 2005 Mar;102(3):531-5.

PMID:
15731589
19.

Proposed nomenclature for human butyrylcholinesterase genetic variants identified by DNA sequencing.

La Du BN, Bartels CF, Nogueira CP, Arpagaus M, Lockridge O.

Cell Mol Neurobiol. 1991 Feb;11(1):79-89.

PMID:
2013061
20.
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