Mucopolysaccharidosis in a Cat with Arylsulfatase B Deficiency: A Model of Maroteaux-Lamy Syndrome (Q39832785)

15 September 2017

Mucopolysaccharidosis in a Cat with Arylsulfatase B Deficiency: A Model of Maroteaux-Lamy Syndrome (English)

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https://api.crossref.org/works/10.1126/SCIENCE.144321

9 May 2022

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9 May 2022

author name string

P. F. Jezyk

1

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9 May 2022

M. E. Haskins

2

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9 May 2022

D. F. Patterson

3

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9 May 2022

W. J. Mellman

4

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9 May 2022

M. Greenstein

5

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9 May 2022

language of work or name

English

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publication date

1 November 1977

1 reference

15 September 2017

25 November 1977

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National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=144321

full work available at URL

9 May 2022

https://syndication.highwire.org/content/doi/10.1126/science.144321

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9 May 2022

1 reference

15 September 2017

198

1 reference

15 September 2017

834-836

1 reference

15 September 2017

4319

1 reference

GM 2 Ganglioside Lysosomal Storage Disease in Cats with α-Hexosaminidase Deficiency

15 September 2017

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.144321

Arylsulfatase B deficiency in Maroteaux-Lamy syndrome cultured fibroblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.144321

The defect in Hurler's and Hunter's syndromes: faulty degradation of mucopolysaccharide

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.144321

The fine structure of liver in children with Hurler's syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.144321

Inherited lysosomal storage diseases: an essay in comparative medicine

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.144321

Biochemical and ultrastructural studies in Hurler's syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.144321

Neuronal-visceral GM1 gangliosidosis in a dog with beta-galactosidase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.144321

Enzyme histochemical and ultrastructural alterations in the brains of Friesian calves with GM1 gangliosidosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.144321

Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome). I. Sulfatase B deficiency in tissues.

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.144321

Diagnosis of genetic mucopolysaccharidoses: Electrophoretic and enzymatic characterization of urinary glycosaminoglycans

21 January 2018

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.144321

21 January 2018

Archives of pathology

1

93

1

1972

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.144321

Arylsulfatase B deficiency in Maroteaux-Lamy syndrome: Cellular studies and carrier identification

9 May 2022

2

9

475

1975

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.144321

Infantile metachromatic leukodystrophy

9 May 2022

Federation Proceedings

0 references

13

282

1336

1970

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.144321

9 May 2022

Journal of Biochemistry

14

77

309

1975

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.144321

Simple measurement of urinary glycosaminoglycans and degradation products

9 May 2022

15

9

256

1974

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.144321

The mucopolysaccharidoses

9 May 2022

21

13

169

1976

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.144321

Helvetica paediatrica acta

9 May 2022

25

25

337

1970

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.144321

9 May 2022

Klinische Wochenschrift

28

19

1142

1966

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.144321

Analytical and preparative separation of acidic glycosaminoglycans by electrophoresis in barium acetate

9 May 2022

30

26

439

1968

1 reference

https://api.crossref.org/works/10.1126/SCIENCE.144321

9 May 2022

Identifiers

1 reference

15 September 2017

1 reference