Characterization of 12 silent alleles of the human butyrylcholinesterase (BCHE) gene
about
Supporting precision medicine by data mining across multi-disciplines: an integrative approach for generating comprehensive linkages between single nucleotide variants (SNVs) and drug-binding sites.Characterization of a novel BCHE "silent" allele: point mutation (p.Val204Asp) causes loss of activity and prolonged apnea with suxamethonium.Butyrylcholinesterase and acetylcholinesterase activity and quantal transmitter release at normal and acetylcholinesterase knockout mouse neuromuscular junctions.Acetylcholinesterase deficiency contributes to neuromuscular junction dysfunction in type 1 diabetic neuropathy.Naturally Occurring Genetic Variants of Human Acetylcholinesterase and Butyrylcholinesterase and Their Potential Impact on the Risk of Toxicity from Cholinesterase Inhibitors.Prolonged neuromuscular blockade following succinylcholine administration to a patient with a reduced butyrylcholinesterase activity.
P2860
Characterization of 12 silent alleles of the human butyrylcholinesterase (BCHE) gene
description
1996 nî lūn-bûn
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1996年の論文
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1996年論文
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1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
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1996年论文
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name
Characterization of 12 silent alleles of the human butyrylcholinesterase (BCHE) gene
@ast
Characterization of 12 silent alleles of the human butyrylcholinesterase (BCHE) gene
@en
type
label
Characterization of 12 silent alleles of the human butyrylcholinesterase (BCHE) gene
@ast
Characterization of 12 silent alleles of the human butyrylcholinesterase (BCHE) gene
@en
prefLabel
Characterization of 12 silent alleles of the human butyrylcholinesterase (BCHE) gene
@ast
Characterization of 12 silent alleles of the human butyrylcholinesterase (BCHE) gene
@en
P2093
P2860
P1476
Characterization of 12 silent alleles of the human butyrylcholinesterase (BCHE) gene
@en
P2093
A F van der Spek
B Wiersema
C F Bartels
S L Primo-Parmo
P2860
P407
P577
1996-01-01T00:00:00Z