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The New England Journal of Medicine|February 3, 2007
JAK2 exon 12 mutations in polycythemia vera and idiopathic erythrocytosisLinda M Scott, Wei Tong, Ross L Levine, et al.
The Journal of Allergy and Clinical Immunology|March 4, 2014
Mastocytosis associated with a rare germline KIT K509I mutation displays a well-differentiated mast cell phenotypeEunice Ching Chan, Yun Bai, Arnold S Kirshenbaum, et al.
The Journal of Allergy and Clinical Immunology|June 21, 2017
A distinct biomolecular profile identifies monoclonal mast cell disorders in patients with idiopathic anaphylaxisMelody C Carter, Avanti Desai, Hirsh D Komarow, et al.
Blood|May 22, 2010
JAK2 V617F impairs hematopoietic stem cell function in a conditional knock-in mouse model of JAK2 V617F-positive essential thrombocythemiaJuan Li, Dominik Spensberger, Jong Sook Ahn, et al.
The Journal of Biological Chemistry|September 14, 2017
ZNF143 protein is an important regulator of the myeloid transcription factor C/EBPαDavid Gonzalez, Annouck Luyten, Boris Bartholdy, et al.
Blood|July 29, 2006
Mutation of JAK2 in the myeloproliferative disorders: timing, clonality studies, cytogenetic associations, and role in leukemic transformationPeter J Campbell, E Joanna Baxter, Philip A Beer, et al.
Blood|March 23, 2010
The JAK2 46/1 haplotype predisposes to MPL-mutated myeloproliferative neoplasmsAmy V Jones, Peter J Campbell, Philip A Beer, et al.
Lancet (London, England)|December 6, 2005
Definition of subtypes of essential thrombocythaemia and relation to polycythaemia vera based on JAK2 V617F mutation status: a prospective studyPeter J Campbell, Linda M Scott, Georgina Buck, et al.
The New England Journal of Medicine|February 4, 2016
Vibratory Urticaria Associated with a Missense Variant in ADGRE2Steven E Boyden, Avanti Desai, Glenn Cruse, et al.
Lancet (London, England)|September 23, 2008
Mutations of JAK2 in acute lymphoblastic leukaemias associated with Down's syndromeDani Bercovich, Ithamar Ganmore, Linda M Scott, et al.
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