These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

107 related articles for article (PubMed ID: 9694584)

  • 1. 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; 274(2):159-66. PubMed ID: 9694584
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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. PubMed ID: 11733654
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 261(1):27-34. PubMed ID: 9187502
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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. PubMed ID: 9543549
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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. PubMed ID: 8554068
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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. PubMed ID: 1349196
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 235(1):41-57. PubMed ID: 7634491
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 240(2):372-5. PubMed ID: 9388484
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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. PubMed ID: 16788378
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Missense mutations of the butyrylcholinesterase gene in six Japanese patients with low cholinesterasemia: genetic analysis using sera stored in a freezer].
    Hidaka K; Watanabe Y; Ueda N; Tomita M; Higashi M; Abe K; Minatogawa Y; Iuchi I
    Rinsho Byori; 1999 Oct; 47(10):980-2. PubMed ID: 10590675
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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. PubMed ID: 11163024
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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. PubMed ID: 12417112
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel mutation in the BCHE gene and phenotype identified in a child with low butyrylcholinesterase activity: a case report.
    Yu R; Guo Y; Dan Y; Tan W; Mao Q; Deng G
    BMC Med Genet; 2018 Apr; 19(1):58. PubMed ID: 29631548
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Butyrylcholinesterase genes in individuals with abnormal inhibition numbers and with trace activity: one common mutation and two novel silent genes.
    Dey DC; Maekawa M; Sudo K; Kanno T
    Ann Clin Biochem; 1998 Mar; 35 ( Pt 2)():302-10. PubMed ID: 9547905
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Three different point mutations in the butyrylcholinesterase gene of three Japanese subjects with a silent phenotype: possible Japanese type alleles.
    Sudo K; Maekawa M; Kanno T; Akizuki S; Magara T
    Clin Biochem; 1996 Apr; 29(2):165-9. PubMed ID: 8601326
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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. PubMed ID: 18075469
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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. PubMed ID: 1415224
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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. PubMed ID: 2253336
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Three point mutations of human butyrylcholinesterase in a Japanese family and the alterations of three-dimensional structure.
    Asanuma K; Yagihashi A; Uehara N; Kida T; Watanabe N
    Clin Chim Acta; 1999 May; 283(1-2):33-42. PubMed ID: 10404729
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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. PubMed ID: 9191541
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.