(Q33963579)

30 July 2017

1 reference

title

Alpha-L-iduronidase and enzyme replacement therapy for mucopolysaccharidosis I. (English)

1 reference

enzyme replacement therapy

30 July 2017

0 references

author name string

Doug A Brooks

series ordinal

1

1 reference

PubMed ID

12517274

30 July 2017

language of work or name

English

0 references

publication date

1 December 2002

1 reference

Expert Opinion on Biological Therapy

30 July 2017

1 reference

30 July 2017

2

1 reference

30 July 2017

8

1 reference

30 July 2017

967-976

1 reference

Gargoylism; a mucopolysaccharidosis.

30 July 2017

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

OCCURRENCE OF URINARY ACID MUCOPOLYSACCHARIDES IN THE HURLER SYNDROME.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

Hurler's syndrome: demonstration of an inherited disorder of connective tissue in cell culture

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

Scheie and Hurler syndromes: apparent identity of the biochemical defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

Inherited disorders of lysosomal metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

The defect in the Hurler and Scheie syndromes: deficiency of -L-iduronidase

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

Human kidney α-l-Iduronidase: Purification and characterization

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

Immunopurification and characterization of human alpha-L-iduronidase with the use of monoclonal antibodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

alpha-L-iduronidase in normal and mucopolysaccharidosis-type-I human skin fibroblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

A radioactive substrate and assay for α-l-iduronidase

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

Review: the immunochemical analysis of enzyme from mucopolysaccharidoses patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

Protein processing: a role in the pathophysiology of genetic disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

Mucopolysaccharidosis type I: identification of 13 novel mutations of the alpha-L-iduronidase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

Mutational analysis of 85 mucopolysaccharidosis type I families: frequency of known mutations, identification of 17 novel mutations and in vitro expression of missense mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

Molecular genetics of mucopolysaccharidosis type I: mutation analysis among the patients of the former Soviet Union

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

Hurler syndrome: A patient with abnormally high levels of α-l-iduronidase protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

Glycosidase active site mutations in human alpha-L-iduronidase.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

Molecular genetics of mucopolysaccharidosis type I: diagnostic, clinical, and biological implications.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

Active-site motifs of lysosomal acid hydrolases: invariant features of clan GH-A glycosyl hydrolases deduced from hydrophobic cluster analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

Catalytic mechanism of enzymic glycosyl transfer

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

Mechanisms of enzymatic glycoside hydrolysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

Structures and mechanisms of glycosyl hydrolases

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

Structural features of normal and mutant human lysosomal glycoside hydrolases deduced from bioinformatics analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

Prevalence of lysosomal storage disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

STEREOCHEMISTRY AND THE MECHANISM OF ENZYMATIC REACTIONS

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.2.8.967

21 January 2018

Identifiers

DOI

10.1517/14712598.2.8.967

1 reference

30 July 2017

1 reference

PubMed ID

12517274