Glycosylation and functionality of recombinant β-glucocerebrosidase from various production systems

The uptake of recombinant glucocerebrosidases by blood monocytes from type 1 Gaucher disease patients is variable

(2012) Juliette Berger et al.   BRITISH JOURNAL OF HAEMATOLOGY

Elevated plasma glucosylsphingosine in Gaucher disease: relation to phenotype, storage cell markers, and therapeutic response

(2011) N. Dekker et al.   BLOOD

Pivotal trial with plant cell-expressed recombinant glucocerebrosidase, taliglucerase alfa, a novel enzyme replacement therapy for Gaucher disease

(2011) A. Zimran et al.   BLOOD

How I treat Gaucher disease

(2011) A. Zimran   BLOOD

Phase 1/2 and extension study of velaglucerase alfa replacement therapy in adults with type 1 Gaucher disease: 48-month experience

(2010) A. Zimran et al.   BLOOD

Development of Monocytes, Macrophages, and Dendritic Cells

(2010) F. Geissmann et al.   SCIENCE

Characterization of gene-activated human acid- -glucosidase: Crystal structure, glycan composition, and internalization into macrophages

(2009) B. Brumshtein et al.   GLYCOBIOLOGY

Optimization and Validation of Two Miniaturized Glucocerebrosidase Enzyme Assays for High Throughput Screening

(2008) Daniel Urban et al.   COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING

Macrophage differentiation and function in health and disease

(2008) Makoto Naito   PATHOLOGY INTERNATIONAL