MYD88 somatic mutations in MALT lymphomas

Author:

Li Zhi-Ming,Rinaldi Andrea1,Cavalli Andrea2,Mensah Afua A.1,Ponzoni Maurilio3,Gascoyne Randy D.4,Bhagat Govind5,Zucca Emanuele6,Bertoni Francesco

Affiliation:

1. IOR-Institute of Oncology Research; Bellinzona; Switzerland

2. Department of Chemistry; University of Cambridge; Cambridge; UK

3. Unit of Lymphoid Malignancies; Department of Onco-Haematology; San Raffaele Scientific Institute; Milan; Italy

4. Department of Pathology; British Columbia Cancer Agency; Vancouver; BC; Canada

5. Herbert Irving Comprehensive Cancer Center; Department of Pathology and Cell Biology; Columbia University Medical Center and New York Presbyterian Hospital; New York; NY; USA

6. IOSI-Oncology Institute of Southern Switzerland; Bellinzona; Switzerland

Publisher

Wiley

Subject

Hematology

Reference10 articles.

1. MALT lymphomas: pathogenesis can drive treatment;Bertoni;Oncology (Williston Park),2011

2. Analysis of the chronic lymphocytic leukemia coding genome: role of NOTCH1 mutational activation;Fabbri;Journal of Experimental Medicine,2011

3. Interactive sites in the MyD88 Toll/Interleukin (IL) 1 receptor domain responsible for coupling to the IL1β signaling pathway;Li;Journal of Biological Chemistry,2005

4. Absence of NOTCH1 gene mutations in MALT lymphomas;Mensah;British Journal of Haematology,2012

5. Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma;Morin;Nature,2011

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