Subtype-specific and co-occurring genetic alterations in B-cell non-Hodgkin lymphoma

Subtype-specific and co-occurring genetic alterations in B-cell non-Hodgkin lymphoma

B cell non-Hodgkin lymphoma (B-NHL) encompasses multiple clinically and phenotypically distinct subtypes of malignancy with unique molecular etiologies. Common subtypes of B-NHL, such as diffuse large B-cell lymphoma, have been comprehensively interrogated at the genomic level, but rarer subtypes, s...

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Main Authors: Akhter, A. (Author), Bhalla, K. (Author), Bouska, A. (Author), Buckley, S. (Author), Carey, C. (Author), Chen, B.J (Author), Davidson, M. (Author), Davis, R.E (Author), Deng, Q. (Author), Fowler, N.H (Author), Gandhi, M. (Author), Ghosh, S. (Author), Green, M.R (Author), Greiner, T. (Author), Hartert, K. (Author), Heavican, T. (Author), Iqbal, J. (Author), Jain, N. (Author), Lunning, M.A (Author), Ma, M.C.J (Author), Mansoor, A. (Author), Moore, D. (Author), Nastoupil, L.J (Author), Neelapu, S. (Author), Parekh, S. (Author), Perumal, D. (Author), Rodig, S.J (Author), Showell, J. (Author), Sohani, A.R (Author), Stewart, D. (Author), Street, L. (Author), Tadros, S. (Author), Tobin, J. (Author), Vose, J.M (Author), Westin, J.R (Author), Yang, H. (Author)
Format: Article
Language:English
Published: Ferrata Storti Foundation 2022
Subjects:
acute myeloid leukemia
Article
B lymphocyte
beta catenin
chromosome analysis
copy number variation
DNA methylation
DNA methyltransferase 3A
flow cytometry
gene duplication
gene expression
gene mutation
gene rearrangement
genetic analysis
hematologic disease
human
interferon consensus sequence binding protein
interferon regulatory factor 4
mutation
nonhodgkin lymphoma
overall survival
polymerase chain reaction
protein expression
protein p53
single nucleotide polymorphism
ubiquitination
upregulation
whole exome sequencing
whole genome sequencing
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