A Major Step on the Road to Understanding a Unique Posttranslational Modification and Its Role in a Genetic Disease
Author:
Publisher
Elsevier BV
Subject
General Biochemistry, Genetics and Molecular Biology
Reference7 articles.
1. Genetic complementation of steroid sulphatase after somatic cell hybridization of X-linked ichthyosis and multiple sulphatase deficiency
2. The Multiple Sulfatase Deficiency Gene Encodes an Essential and Limiting Factor for the Activity of Sulfatases
3. Multiple Sulfatase Deficiency Is Caused by Mutations in the Gene Encoding the Human Cα-Formylglycine Generating Enzyme
4. Multiple sulfatase deficiency and the nature of the sulfatase family;Hopwood,2001
5. The sulfatase gene family
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2. Optimisation of culture conditions for a producer clone coexpressing arylsulfatase B and a formylglycine-generating enzyme in order to increase the yield of arylsulfatase B;Biological Products. Prevention, Diagnosis, Treatment;2022-10-10
3. Post-translational modifications of proteins in antiphospholipid antibody syndrome;Critical Reviews in Clinical Laboratory Sciences;2019-08-26
4. Development of idursulfase therapy for mucopolysaccharidosis type II (Hunter syndrome): the past, the present and the future;Drug Design, Development and Therapy;2017-08
5. The Clinical Significance of Posttranslational Modification of Autoantigens;Clinical Reviews in Allergy & Immunology;2014-05-21
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