Bone Marrow Microenvironment in an In Vitro Model of Gaucher Disease: Consequences of Glucocerebrosidase Deficiency-Reference-Cited by-同舟云学术

Bone Marrow Microenvironment in an In Vitro Model of Gaucher Disease: Consequences of Glucocerebrosidase Deficiency

Published:2012-01-20 Issue:2 Volume:21 Page:239-248
ISSN:1547-3287
Container-title:Stem Cells and Development
language:en
Short-container-title:Stem Cells and Development

Author:

Lecourt Séverine¹²³,Vanneaux Valérie¹²³,Cras Audrey¹²³,Freida Delphine¹²,Heraoui Djazia⁴,Herbi Linda¹²³,Caillaud Catherine⁵,Chomienne Christine³,Marolleau Jean-Pierre⁶,Belmatoug Nadia⁴,Larghero Jérôme¹²³

Affiliation:

1. Unité de Thérapie Cellulaire, Assistance Publique-Hôpitaux de Paris, Hôpital Saint Louis, Paris, France.

2. Univ Paris Diderot, Sorbonne Paris Cité, Paris, France.

3. INSERM UMRS940, Institut Universitaire d'Hématologie, Hôpital Saint-Louis, Paris, France.

4. Service de médecine interne, Assistance Publique-Hôpitaux de Paris, Hôpital Beaujon, Centre de réference pour les maladies lysosomales, Clichy, France.

5. Laboratoire de Génétique Métabolique, Assistance Publique-Hôpitaux de Paris, Hôpital Cochin, Paris, France.

6. Départment d'Hématologie Clinique, Hôpital d'Amiens, Amiens, France.

Publisher

Mary Ann Liebert Inc

Subject

Cell Biology,Developmental Biology,Hematology

Link

https://www.liebertpub.com/doi/pdf/10.1089/scd.2011.0365

Reference54 articles.

1. Phenotype, diagnosis, and treatment of Gaucher's disease

2. The Gaucher Registry

3. Pro-inflammatory cytokines and the pathogenesis of Gaucher's disease: increased release of interleukin-6 and interleukin-10

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