Literature DB >> 23912

Synthetic substrate beta-glucosidase activity in leukocytes: a reproducible method for the identification of patients and carriers of Gaucher's disease.

D A Wenger, C Clark, M Sattler, C Wharton.   

Abstract

A method is described for the identification of patients and carriers of Gaucher's disease, using leukocytes from a small volume of blood. The fluorogenic substrate, 4-methylumbelliferyl-beta-D-glucopyranoside, was assayed in the presence of pure sodium taurocholate (2.5 mg/ml) and Triton X-100 (2.0 mg/ml). Some commercial brands of pure sodium taurocholate were satisfactory for this purpose. The pH optimum for controls, Gaucher disease carriers and Gaucher disease patients was 5.4 using citrate-phosphate buffer. Although leukocytes prepared from only a small amount of blood (2-8 ml) are required, there is sufficient quantity for measuring other lysosomal enzymes as controls. Using this method, 12 patients with all types of Gaucher's disease and 12 obligate heterozygotes were identified. Carrier status was predicted in six other family members and ruled out in six others. Eight unaffected people married to Gaucher carriers or Gaucher patients were predicted to be non-carriers of Gaucher's disease, thereby ruling out children affected with Gaucher's disease in that mating.

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Year:  1978        PMID: 23912     DOI: 10.1111/j.1399-0004.1978.tb04242.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  22 in total

1.  Glucosidase acid beta gene mutations in Egyptian children with Gaucher disease and relation to disease phenotypes.

Authors:  Zakarya El-Morsy; Mohamed T Khashaba; Othman El-Sayed Soliman; Sohier Yahia; Dina Abd El-Hady
Journal:  World J Pediatr       Date:  2011-06-01       Impact factor: 2.764

2.  Activator protein deficient Gaucher's disease. A second patient with the newly identified lipid storage disorder.

Authors:  H Christomanou; A Chabás; T Pámpols; A Guardiola
Journal:  Klin Wochenschr       Date:  1989-10-02

3.  Role of chitotriosidase (chitinase 1) under normal and disease conditions.

Authors:  Manasa Kanneganti; Alan Kamba; Emiko Mizoguchi
Journal:  J Epithel Biol Pharmacol       Date:  2012

4.  Intestinal neuronal degeneration in a patient with chronic idiopathic intestinal pseudoobstruction.

Authors:  R Schuster; P Ferenci; M Schmidbauer; G Lassmann; A Kiss; S Frotz; A Gangl
Journal:  Dig Dis Sci       Date:  1989-01       Impact factor: 3.199

5.  Genetic heterogeneity of membrane-bound beta-glucosidase in Gaucher's disease.

Authors:  M Carroll
Journal:  J Inherit Metab Dis       Date:  1981       Impact factor: 4.982

6.  β-Glucosidase 2 (GBA2) activity and imino sugar pharmacology.

Authors:  Christina M Ridley; Karen E Thur; Jessica Shanahan; Nagendra Babu Thillaiappan; Ann Shen; Karly Uhl; Charlotte M Walden; Ahad A Rahim; Simon N Waddington; Frances M Platt; Aarnoud C van der Spoel
Journal:  J Biol Chem       Date:  2013-07-23       Impact factor: 5.157

7.  Increased glucocerebrosidase (GBA) 2 activity in GBA1 deficient mice brains and in Gaucher leucocytes.

Authors:  Derek G Burke; Ahad A Rahim; Simon N Waddington; Stefan Karlsson; Ida Enquist; Kailash Bhatia; Atul Mehta; Ashok Vellodi; Simon Heales
Journal:  J Inherit Metab Dis       Date:  2012-11-15       Impact factor: 4.982

8.  The biochemical diagnosis of lysosomal storage diseases--a review of five years experience.

Authors:  I J Wallace; C A McCusker; D McCormick
Journal:  Ir J Med Sci       Date:  1990-07       Impact factor: 1.568

9.  Genetic heterogeneity in Gaucher disease.

Authors:  J Zlotogora; R Zaizov; C Klibansky; Y Matoth; G Bach; T Cohen
Journal:  J Med Genet       Date:  1986-08       Impact factor: 6.318

Review 10.  Gaucher disease: new developments in treatment and etiology.

Authors:  Ozgur Harmanci; Yusuf Bayraktar
Journal:  World J Gastroenterol       Date:  2008-07-07       Impact factor: 5.742

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