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Items: 1 to 20 of 146

1.

Novel mutations in the BCHE gene in patients with no butyrylcholinesterase activity.

On-Kei Chan A, Lam CW, Tong SF, Man Tung C, Yung K, Chan YW, Au KM, Yuen YP, Hung CT, Ng KP, Shek CC.

Clin Chim Acta. 2005 Jan;351(1-2):155-9.

PMID:
15563885
2.

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.

3.

Two novel mutations in the BCHE gene in patients with prolonged duration of action of mivacurium or succinylcholine during anaesthesia.

Gätke MR, Bundgaard JR, Viby-Mogensen J.

Pharmacogenet Genomics. 2007 Nov;17(11):995-9.

PMID:
18075469
4.

Novel mutation and multiple mutations found in the human butyrylcholinesterase gene.

Liu W, Cheng J, Iwasaki A, Imanishi H, Hada T.

Clin Chim Acta. 2002 Dec;326(1-2):193-9.

PMID:
12417112
5.

Naturally occurring mutation Leu307Pro of human butyrylcholinesterase in the Vysya community of India.

Manoharan I, Wieseler S, Layer PG, Lockridge O, Boopathy R.

Pharmacogenet Genomics. 2006 Jul;16(7):461-8.

PMID:
16788378
6.

Two new mutations of the human BCHE gene (IVS3-14T>C and L574fsX576).

Parmo-Folloni F, Nunes K, Lepienski LM, Mikami LR, Souza RL, Tsuneto LT, Petzl-Erler ML, Chautard-Freire-Maia EA.

Chem Biol Interact. 2008 Sep 25;175(1-3):135-7. doi: 10.1016/j.cbi.2008.04.038. Epub 2008 May 4.

PMID:
18555211
7.

Genetic analysis of a Japanese patient with butyrylcholinesterase deficiency.

Hidaka K, Iuchi I, Tomita M, Watanabe Y, Minatogawa Y, Iwasaki K, Gotoh K, Shimizu C.

Ann Hum Genet. 1997 Nov;61(Pt 6):491-6.

8.

Five new naturally occurring mutations of the BCHE gene and frequencies of 12 butyrylcholinesterase alleles in a Brazilian population.

Mikami LR, Wieseler S, Souza RL, Schopfer LM, Nachon F, Lockridge O, Chautard-Freire-Maia EA.

Pharmacogenet Genomics. 2008 Mar;18(3):213-8. doi: 10.1097/FPC.0b013e3282f5107e.

PMID:
18300943
9.

Genetic mutations of butyrylcholine esterase identified from phenotypic abnormalities in Japan.

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

Clin Chem. 1997 Jun;43(6 Pt 1):924-9.

10.

Alport syndrome. Molecular genetic aspects.

Hertz JM.

Dan Med Bull. 2009 Aug;56(3):105-52.

PMID:
19728970
11.

Problem with detection of an insertion-type mutation in the BCHE gene in a patient with butyrylcholinesterase deficiency.

Maekawa M, Taniguchi T, Ishikawa J, Toyoda S, Takahata N.

Clin Chem. 2004 Dec;50(12):2410-1. No abstract available.

12.

Identification of missense mutation (G365R) of the butyrylcholinesterase (BCHE) gene in a Japanese patient with familial cholinesterasemia.

Sakamoto N, Maeda T, Hidaka K, Teranishi T, Toyoda M, Onishi Y, Kuroda S, Sakaguchi K, Fujisawa T, Maeda M, Watanabe Y, Iuchi I.

Kobe J Med Sci. 2001 Aug;47(4):153-60.

13.

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
14.

Nonsense mutation in exon 2 of the butyrylcholinesterase gene: a case of familial cholinesterasemia.

Hidaka K, Iuchi I, Yamasaki T, Ueda N, Hukano K.

Clin Chim Acta. 1997 May 6;261(1):27-34.

PMID:
9187502
15.

Production of the butyrylcholinesterase knockout mouse.

Li B, Duysen EG, Saunders TL, Lockridge O.

J Mol Neurosci. 2006;30(1-2):193-5.

PMID:
17192674
16.

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
17.

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
18.

Gene analysis of genomic DNA from stored serum by polymerase chain reaction: identification of three missense mutations in patients with cholinesterasemia and ABO genotyping.

Hidaka K, Watanabe Y, Tomita M, Ueda N, Higashi M, Minatogawa Y, Iuchi I.

Clin Chim Acta. 2001 Jan;303(1-2):61-7.

PMID:
11163024
19.

Molecular basis of succinylcholine sensitivity in a prairie Hutterite kindred and genetic characterization of the region containing the BCHE gene.

Zelinski T, Coghlan G, Mauthe J, Triggs-Raine B.

Mol Genet Metab. 2007 Feb;90(2):210-6. Epub 2006 Dec 12.

PMID:
17166756
20.

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