c-kit activating mutation in a neonate with in-utero presentation of systemic mastocytosis associated with myeloproliferative disorder
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.1999.01683.x/fullpdf
Reference7 articles.
1. Neoplastic transformation of normal hematopoietic cells by constitutively activating mutations of c-kit receptor tyrosine kinase;Kitayama;Blood,1996
2. Somatic c-kit activating mutation in urticaria pigmentosa and aggressive mastocytosis: establishment of clonality in a human mast cell neoplasm;Longley;Nature Genetics,1996
3. c-kit mutation in a population of patients with mastocytosis;Nagata;International Archives of Allergy and Immunology,1997
4. Identification of a point mutation in the catalytic domain of the protooncogene c-kit in peripheral blood mononuclear cells of patients who have mastocytosis with an associated hematologic disorder;Nagata;Proceedings of the National Academy of Sciences of the United States of America,1995
5. A new c-kit mutation in a case of aggressive mast cell disease;Pignon;British Journal of Haematology,1997
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2. Paediatric mastocytosis: a systematic review of 1747 cases;British Journal of Dermatology;2015-02-08
3. Epidemiology, Prognosis, and Risk Factors in Mastocytosis;Immunology and Allergy Clinics of North America;2014-05
4. The novel HSP90 inhibitor STA-9090 exhibits activity against Kit-dependent and -independent malignant mast cell tumors;Experimental Hematology;2008-10
5. Systemic mastocytosis with diffuse cutaneous involvement and haematological disease presenting in utero treated unsuccessfully with vincristine;Clinical and Experimental Dermatology;2007-11-05
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