Genomic Aberrations in Multiple Myeloma
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Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-319-40320-5_3
Reference67 articles.
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2. Broderick P, Chubb D, Johnson DC et al (2012) Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. Nat Genet 44(1):58–61
3. Chubb D, Weinhold N, Broderick P et al (2013) Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. Nat Genet 45(10):1221–1225
4. Weinhold N, Johnson DC, Chubb D et al (2013) The CCND1 c.870G > A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. Nat Genet 45(5):522–525
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1. Aberrant non-canonical NF-κB signalling reprograms the epigenome landscape to drive oncogenic transcriptomes in multiple myeloma;Nature Communications;2024-03-21
2. Aberrant non-canonical NF-κB signalling reprograms the epigenome landscape to drive oncogenic transcriptomes in multiple myeloma;2024-01-09
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