Mice lacking asparaginyl endopeptidase develop disorders resembling hemophagocytic syndrome-Reference-Cited by-同舟云学术

Mice lacking asparaginyl endopeptidase develop disorders resembling hemophagocytic syndrome

Published:2008-12-23 Issue:2 Volume:106 Page:468-473
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Chan C.-B.,Abe M.,Hashimoto N.,Hao C.,Williams I. R.,Liu X.,Nakao S.,Yamamoto A.,Zheng C.,Henter J.-I.,Meeths M.,Nordenskjold M.,Li S.-Y.,Hara-Nishimura I.,Asano M.,Ye K.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference24 articles.

1. Familial and acquired hemophagocytic lymphohistiocytosis

2. Hemophagocytic syndromes

3. Perforin Gene Defects in Familial Hemophagocytic Lymphohistiocytosis

4. Munc13-4 Is Essential for Cytolytic Granules Fusion and Is Mutated in a Form of Familial Hemophagocytic Lymphohistiocytosis (FHL3)

5. Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome

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