Plasma chitotriosidase and CCL18: early biochemical surrogate markers in type B Niemann-Pick disease (Q81384280)

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8 January 2020

title

Plasma chitotriosidase and CCL18: early biochemical surrogate markers in type B Niemann-Pick disease (English)

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8 January 2020

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8

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8 January 2020

Johannes Aerts

9

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8 January 2020

author name string

J Brinkman

1

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8 January 2020

F A Wijburg

2

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8 January 2020

C E Hollak

3

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8 January 2020

J E Groener

4

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8 January 2020

M Verhoek

5

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8 January 2020

S Scheij

6

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8 January 2020

J Aten

7

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8 January 2020

publication date

1 January 2005

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Journal of Inherited Metabolic Disease

8 January 2020

published in

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8 January 2020

volume

28

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8 January 2020

issue

1

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8 January 2020

page(s)

13-20

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Strong induction of members of the chitinase family of proteins in atherosclerosis: chitotriosidase and human cartilage gp-39 expressed in lesion macrophages.

8 January 2020

cites work

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12 December 2020

Hepatosplenomegalic lipidosis: what unless Gaucher? Adult cholesteryl ester storage disease (CESD) with anemia, mesenteric lipodystrophy, increased plasma chitotriosidase activity and a homozygous lysosomal acid lipase -1 exon 8 splice junction muta

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12 December 2020

Cloning of a cDNA encoding chitotriosidase, a human chitinase produced by macrophages

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12 December 2020

Marked elevation of plasma chitotriosidase activity. A novel hallmark of Gaucher disease

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12 December 2020

Replacement therapy for inherited enzyme deficiency--macrophage-targeted glucocerebrosidase for Gaucher's disease

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12 December 2020

Progressive liver failure in a patient with adult Niemann-Pick disease associated with generalized AL amyloidosis

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12 December 2020

The human chitotriosidase gene. Nature of inherited enzyme deficiency

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12 December 2020

Marked increase of methylumbelliferyl-tetra-N-acetylchitotetraoside hydrolase activity in plasma from Gaucher disease patients

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12 December 2020

Pathologic gene expression in Gaucher disease: up-regulation of cysteine proteinases including osteoclastic cathepsin K.

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12 December 2020

Clinically relevant therapeutic endpoints in type I Gaucher disease.

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12 December 2020

Infusion of recombinant human acid sphingomyelinase into niemann-pick disease mice leads to visceral, but not neurological, correction of the pathophysiology

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12 December 2020

Biochemical studies in Niemann-Pick disease. I. Major sphingolipids of liver and spleen

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12 December 2020

Biochemistry of glycosphingolipid storage disorders: implications for therapeutic intervention

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12 December 2020

Marked elevation of the chemokine CCL18/PARC in Gaucher disease: a novel surrogate marker for assessing therapeutic intervention

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12 December 2020

Elevated plasma chitotriosidase activity in various lysosomal storage disorders.

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12 December 2020

Transglycosidase activity of chitotriosidase: improved enzymatic assay for the human macrophage chitinase.

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12 December 2020

Isolation of cDNA clones encoding human acid sphingomyelinase: occurrence of alternatively processed transcripts

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12 December 2020

The demographics and distribution of type B Niemann-Pick disease: novel mutations lead to new genotype/phenotype correlations

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12 December 2020

Effect of 2-deoxyglucose on lysosomal enzymes in cultured human skin fibroblasts

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12 December 2020