CCL18: a urinary marker of Gaucher cell burden in Gaucher patients (Q83878822)

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28 January 2020

title

CCL18: a urinary marker of Gaucher cell burden in Gaucher patients (English)

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1

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Mirjam Langeveld

3

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28 January 2020

Herma Renkema

4

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28 January 2020

Johannes Aerts

9

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8

Johanna E Groener

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28 January 2020

5

Carla E M Hollak

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2

Marri Verhoek

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28 January 2020

Wilma E Donker-Koopman

7

object named as

Wilma E Donker-Koopman

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28 January 2020

author name string

Jan J Weening

6

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publication date

30 May 2006

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Journal of Inherited Metabolic Disease

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published in

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volume

29

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issue

4

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page(s)

564-571

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Novel oral treatment of Gaucher's disease with N-butyldeoxynojirimycin (OGT 918) to decrease substrate biosynthesis.

28 January 2020

cites work

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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

Clinical evaluation of chemokine and enzymatic biomarkers of Gaucher disease

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12 December 2020

Identification of a novel acidic mammalian chitinase distinct from chitotriosidase

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12 December 2020

Paediatric non-neuronopathic Gaucher disease: recommendations for treatment and monitoring

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12 December 2020

Comparison of the properties of a soluble form of glucocerebrosidase from human urine with those of the membrane-associated tissue enzyme

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12 December 2020

The human chitotriosidase gene. Nature of inherited enzyme deficiency

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12 December 2020

Plasma Creatinine Determination A New and Specific Jaffe Reaction Method

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12 December 2020

Inhibition of substrate synthesis as a strategy for glycolipid lysosomal storage disease therapy

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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

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

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

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12 December 2020

Future perspectives for glycolipid research in medicine

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12 December 2020

The role of the iminosugar N-butyldeoxynojirimycin (miglustat) in the management of type I (non-neuronopathic) Gaucher disease: a position statement

1 reference

12 December 2020

Gaucher cells demonstrate a distinct macrophage phenotype and resemble alternatively activated macrophages

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12 December 2020