First characterization of platelet secretion defect in patients with familial hemophagocytic lymphohistiocytosis type 3 (FHL-3)-Reference-Cited by-同舟云学术

First characterization of platelet secretion defect in patients with familial hemophagocytic lymphohistiocytosis type 3 (FHL-3)

Published:2015-01-08 Issue:2 Volume:125 Page:412-414
ISSN:0006-4971
Container-title:Blood
language:en
Short-container-title:

Author:

Nakamura Lea¹,Bertling Anne²,Brodde Martin F.²,zur Stadt Udo³,Schulz Ansgar S.⁴,Ammann Sandra⁵,Sandrock-Lang Kirstin¹,Beutel Karin⁶,Zieger Barbara¹,Kehrel Beate E.²

Affiliation:

1. Department of Pediatrics and Adolescent Medicine, University Hospital Freiburg, Freiburg, Germany

2. Department of Anesthesiology, Intensive Care and Pain Medicine, Experimental and Clinical Hemostasis, University of Muenster, Muenster, Germany

3. Center for Diagnostic, University Medical Center Hamburg Eppendorf, Hamburg, Germany

4. Department of Pediatrics and Adolescent Medicine, University Hospital Ulm, Ulm, Germany

5. Center for Chronic Immunodeficiency, University of Freiburg, Freiburg, Germany

6. Department of Pediatric Hematology and Oncology, University Hospital Muenster, Muenster, Germany

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Link

http://ashpublications.org/blood/article-pdf/125/2/412/1385520/412.pdf

Reference10 articles.

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2. Munc13-4 regulates granule secretion in human neutrophils.;Pivot-Pajot;J Immunol,2008

3. Munc13-4 is a GTP-Rab27-binding protein regulating dense core granule secretion in platelets.;Shirakawa;J Biol Chem,2004

4. Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3).;Feldmann;Cell,2003

5. Munc13-4 is a limiting factor in the pathway required for platelet granule release and hemostasis.;Ren;Blood,2010

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