Biochemical characterization of chitotriosidase enzyme: comparison between normal individuals and patients with Gaucher and with Niemann

Biochemical characterization of chitotriosidase enzyme: comparison between normal individuals and patients with Gaucher and with Niemann–Pick diseases

Published:2004-10 Issue:10 Volume:37 Page:893-897
ISSN:0009-9120
Container-title:Clinical Biochemistry
language:en
Short-container-title:Clinical Biochemistry

Author:

Wajner Alessandro,Michelin Kristiane,Burin Maira G.,Pires Ricardo F.,Pereira Maria Luiza S.,Giugliani Roberto,Coelho Janice C.

Publisher

Elsevier BV

Subject

Clinical Biochemistry,General Medicine

Reference19 articles.

1. Marked elevation of plasma chitotriosidase activity: a novel hallmark of Gaucher disease;Hollak;J. Clin. Invest.,1994

2. Synthesis, sorting and processing into distinct isoforms of human macrophage chitotriosidase;Renkema;Eur. J. Biochem.,1997

3. Purification and characterization of human chitotriosidase, a novel member of the chitinase family of proteins;Renkema;J. Biol. Chem.,1995

4. The human chitotriosidase gene. Nature of inherited enzyme deficiency;Boot;J. Biol. Chem.,1998

5. Chitotriosidase deficiency in survivors of Candida sepsis;Masoud;Blood Cells, Mol. Dis.,2002

Cited by 52 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Acid sphingomyelinase deficiency and Gaucher disease in adults: Similarities and differences in two macrophage storage disorders;JIMD Reports;2024-07-04

2. Chitinases production and their application;Fungal Secondary Metabolites;2024

3. The role of serum and bronchoalveolar lavage fluid chitotriosidase activity on diagnosis, disease characteristics and prognosis of sarcoidosis;Tuberk Toraks;2023-12-26

4. Upregulation of Cytotoxic T-cells in pediatric patients with Gaucher disease;Scientific Reports;2022-03-23

5. Patient-Specific iPSC-Derived Neural Differentiated and Hepatocyte-like Cells, Carrying the Compound Heterozygous Mutation p.V1023Sfs*15/p.G992R, Present the “Variant” Biochemical Phenotype of Niemann-Pick Type C1 Disease;International Journal of Molecular Sciences;2021-11-10