Germline CARD11 Mutation in a Patient with Severe Congenital B Cell Lymphocytosis

GFI1B, EVI5, MYB—Additional genes that cooperate with the human BCL6 gene to promote the development of lymphomas

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Whole-exome sequencing links caspase recruitment domain 11 (CARD11) inactivation to severe combined immunodeficiency

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Deficiency of caspase recruitment domain family, member 11 (CARD11), causes profound combined immunodeficiency in human subjects

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Human lymphoma mutations reveal CARD11 as the switch between self-antigen–induced B cell death or proliferation and autoantibody production

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Congenital B cell lymphocytosis explained by novel germlineCARD11mutations

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A Quantitative Signaling Screen Identifies CARD11 Mutations in the CARD and LATCH Domains That Induce Bcl10 Ubiquitination and Human Lymphoma Cell Survival

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Frequent mutation of histone-modifying genes in non-Hodgkin lymphoma

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Epstein-Barr Virus Nuclear Antigen 3C Facilitates G1-S Transition by Stabilizing and Enhancing the Function of Cyclin D1

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Oncogenic CARD11 Mutations Induce Hyperactive Signaling by Disrupting Autoinhibition by the PKC-Responsive Inhibitory Domain

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Deficiency of Rap1-Binding Protein RAPL Causes Lymphoproliferative Disorders through Mislocalization of p27kip1

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Chronic active B-cell-receptor signalling in diffuse large B-cell lymphoma

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Oncogenic Activation of NF- B

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Clinicopathologic Features of CDK6 Translocation-associated B-cell Lymphoproliferative Disorders

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TNFAIP3/A20 functions as a novel tumor suppressor gene in several subtypes of non-Hodgkin lymphomas

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Mutations of multiple genes cause deregulation of NF-κB in diffuse large B-cell lymphoma

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Evidence for HIV-associated B cell exhaustion in a dysfunctional memory B cell compartment in HIV-infected viremic individuals

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Oncogenic CARD11 Mutations in Human Diffuse Large B Cell Lymphoma

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