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Systemic mast cell activation disease: the role of molecular genetic alterations in pathogenesis, heritability and diagnostics

  1. Britta Haenisch,
  2. Markus M. Nöthen,
  3. Gerhard J. Molderings*

Article first published online: 2 OCT 2012

DOI: 10.1111/j.1365-2567.2012.03627.x

Issue

Immunology

Immunology

Volume 137, Issue 3, pages 197–205, November 2012

Additional Information

How to Cite

Haenisch, B., Nöthen, M. M. and Molderings, G. J. (2012), Systemic mast cell activation disease: the role of molecular genetic alterations in pathogenesis, heritability and diagnostics. Immunology, 137: 197–205. doi: 10.1111/j.1365-2567.2012.03627.x

Author Information

  1. Institute of Human Genetics, University Hospital of Bonn, Germany

* Correspondence: Gerhard J. Molderings, Institute of Human Genetics, University Hospital of Bonn, Sigmund-Freud-Strasse 25, D-53127 Bonn, Germany. Email: molderings@uni-bonn.de
Senior author: Gerhard J. Molderings

Publication History

  1. Issue published online: 2 OCT 2012
  2. Article first published online: 2 OCT 2012
  3. Accepted manuscript online: 7 SEP 2012 06:17AM EST
  4. Manuscript Accepted: 17 JUL 2012
  5. Manuscript Revised: 13 JUL 2012
  6. Manuscript Received: 13 JUN 2012

Funded by

  • B. Braun-Stiftung
  • Förderclub Mastzellforschung e.V.

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    B. Haenisch, S. Herms, G. J. Molderings, The transcriptome of the human mast cell leukemia cells HMC-1.2: an approach to identify specific changes in the gene expression profile in KitD816V systemic mastocytosis, Immunologic Research, 2013, 56, 1, 155

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