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 *

90 related articles for article (PubMed ID: 31307170)

  • 1. A Case Report of Primary Neonatal Hypocholinesterase Caused by Homozygous Frameshift Mutation of the utyrylcholinesterase (BCHE) Gene and Review of Literature.
    Lv HY; Yang LH; Bu LN; Wang QL; Gu XL; Wang ZY; Ren PS; Li LX
    Clin Lab; 2019 Jul; 65(7):. PubMed ID: 31307170
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. [Rapid detection of BCHE atypical variant (p.Asp70Gly) by high resolution melting curve analysis].
    Mabboux I; Dos Santos M; Courcelle S; Hary B; Ceppa F; Delacour H
    Ann Biol Clin (Paris); 2014; 72(5):543-8. PubMed ID: 25336127
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prolonged toxic effects after cocaine challenge in butyrylcholinesterase/plasma carboxylesterase double knockout mice: a model for butyrylcholinesterase-deficient humans.
    Duysen EG; Lockridge O
    Drug Metab Dispos; 2011 Aug; 39(8):1321-3. PubMed ID: 21540357
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Prolonged neuromuscular block in a patient with butyrylcholinesterase deficiency].
    Mabboux I; Hary B; Courcelle S; Ceppa F; Delacour H
    Arch Pediatr; 2016 May; 23(5):497-500. PubMed ID: 27017361
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An Indian butyrylcholinesterase variant L307P is not structurally stable: a molecular dynamics simulation study.
    David SM; Venkatesan SK; Boopathy R
    Chem Biol Interact; 2013 Mar; 203(1):30-5. PubMed ID: 23123771
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Family of a patient with serum cholinesterase deficiency.
    Ohara M; Hirohata M; Toshimori T; Miyatani H; Okamoto R; Hirasaki S; Kumashiro H; Moritani H; Tominaga Y; Imai M
    Intern Med; 1992 Mar; 31(3):397-9. PubMed ID: 1611195
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prolonged neuromuscular block associated with cholinesterase deficiency.
    Zhang C; Cao H; Wan ZG; Wang J
    Medicine (Baltimore); 2018 Dec; 97(52):e13714. PubMed ID: 30593143
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A mutation causing DHPR deficiency results in a frameshift and a secondary splicing defect.
    Smooker PM; Christodoulou J; McInnes RR; Cotton RG
    J Med Genet; 1995 Mar; 32(3):220-3. PubMed ID: 7783174
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. A novel homozygous frameshift mutation in the
    Saleh-Gohari N; Saeidi K; Zeighaminejad R
    J Clin Pathol; 2018 Sep; 71(9):821-824. PubMed ID: 29588375
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A family with hereditary serum cholinesterase deficiency.
    Hirasaki S; Koide N; Ujike K; Yamamoto H; Fujita Y; Tanigawa T
    Intern Med; 1995 Jul; 34(7):632-5. PubMed ID: 7496072
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Butyrylcholinesterase deficiency.
    Delacour H; Dedome E; Courcelle S; Hary B; Ceppa F
    Ann Biol Clin (Paris); 2016 Jun; 74(3):279-85. PubMed ID: 27237801
    [TBL] [Abstract][Full Text] [Related]  

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

  • 17. Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyl transferase 1A1 gene, and neonatal hyperbilirubinemia.
    Huang CS; Chang PF; Huang MJ; Chen ES; Chen WC
    Gastroenterology; 2002 Jul; 123(1):127-33. PubMed ID: 12105841
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A new compound heterozygous frameshift mutation in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene causes salt-wasting 3 beta-HSD deficiency congenital adrenal hyperplasia.
    Zhang L; Sakkal-Alkaddour H; Chang YT; Yang X; Pang S
    J Clin Endocrinol Metab; 1996 Jan; 81(1):291-5. PubMed ID: 8550766
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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. PubMed ID: 15563885
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Screening patients with prolonged neuromuscular blockade after succinylcholine and mivacurium.
    Cerf C; Mesguish M; Gabriel I; Amselem S; Duvaldestin P
    Anesth Analg; 2002 Feb; 94(2):461-6, table of contents. PubMed ID: 11812719
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.