descriptionPublicationkeyboard_double_arrow_right Article 19 Mar 2009 English Publisher:American Society of HematologyJournal:Blood, volume 113, pages 2,615-2,616 (issn: 0006-4971, eissn: 1528-0020,

Authors: Megan S. Lim;

doi: 10.1182/blood-2008-11-187161

pmid: 19299651

Unraveling ALK signaling through phosphoproteomics

- Summary
- Related research
  (1)
- Metrics

Abstract

In this issue of Blood , Boccalatte and colleagues report on innovative mass spectrometry–driven proteomic studies designed to determine the effect of the NPM-ALK oncogenic tyrosine kinase on the phosphoproteomic-signaling pathway of ALCL.[1][1] The t(2;5)(p23;q35) chromosomal aberration

Related Organizations

University of Michigan–Flint
United States
University of Michigan–Ann Arbor
United States

1 Research products, page 1 of 1

The enzymatic activity of 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase is enhanced by NPM-ALK: new insights in ALK-mediated pathogenesis and the treatment of ALCL
2009IsAmongTopNSimilarDocuments

Impact byBIP!

	citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).	2
	popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.	Average
	influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).	Average
	impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.	Average