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IgA subclass switch recombination in human mucosal and systemic immune compartments

Mucosal immunology, 2014-05, Vol.7 (3), p.511-520

2014

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Immunity to SARS-CoV-2 up to 15 months after infection

iScience, 2022-02, Vol.25 (2), p.103743-103743, Article 103743

2022

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Limited cross-variant neutralization after primary Omicron infection: consideration for a variant-containing booster

Signal transduction and targeted therapy, 2022-08, Vol.7 (1), p.294-294, Article 294

2022

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Lactobacilli Expressing Variable Domain of Llama Heavy-Chain Antibody Fragments (Lactobodies) Confer Protection against Rotavirus-Induced Diarrhea

The Journal of infectious diseases, 2006-12, Vol.194 (11), p.1580-1588

2006

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Genetic basis of PD-L1 overexpression in diffuse large B-cell lymphomas

Blood, 2016-06, Vol.127 (24), p.3026-3034

2016

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Genetic landscape of hepatitis B virus–associated diffuse large B-cell lymphoma

Blood, 2018-06, Vol.131 (24), p.2670-2681

2018

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Genetic mechanisms of HLA-I loss and immune escape in diffuse large B cell lymphoma

Proceedings of the National Academy of Sciences - PNAS, 2021-06, Vol.118 (22), p.1

2021

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Neonatal screening for severe primary immunodeficiency diseases using high-throughput triplex real-time PCR

Blood, 2012-03, Vol.119 (11), p.2552-2555

2012

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A hypomorphic recombination-activating gene 1 ( RAG1 ) mutation resulting in a phenotype resembling common variable immunodeficiency

Journal of allergy and clinical immunology, 2014-12, Vol.134 (6), p.1375-1380

2014

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Exome sequencing reveals novel mutation targets in diffuse large B-cell lymphomas derived from Chinese patients

Blood, 2014-10, Vol.124 (16), p.2544-2553

2014

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The H2B deubiquitinase Usp22 promotes antibody class switch recombination by facilitating non-homologous end joining

Nature communications, 2018-03, Vol.9 (1), p.1006-12, Article 1006

2018

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Genome-wide CRISPR screens reveal synthetic lethal interaction between CREBBP and EP300 in diffuse large B-cell lymphoma

Cell death & disease, 2021-04, Vol.12 (5), p.419-419, Article 419

2021

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Genetic heterogeneity in primary and relapsed mantle cell lymphomas: Impact of recurrent CARD11 mutations

Oncotarget, 2016-06, Vol.7 (25), p.38180-38190

2016

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AID from bony fish catalyzes class switch recombination

The Journal of experimental medicine, 2005-09, Vol.202 (6), p.733-738

2005

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DCLRE1C (ARTEMIS) mutations causing phenotypes ranging from atypical severe combined immunodeficiency to mere antibody deficiency

Human molecular genetics, 2015-12, Vol.24 (25), p.7361-7372

2015

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DNA repair genes are selectively mutated in diffuse large B cell lymphomas

The Journal of experimental medicine, 2013-08, Vol.210 (9), p.1729-1742

2013

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Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases

Proceedings of the National Academy of Sciences - PNAS, 2009-11, Vol.106 (44), p.18680-18685

2009

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Selective IgA deficiency in early life: Association to infections and allergic diseases during childhood

Clinical immunology (Orlando, Fla.), 2009-10, Vol.133 (1), p.78-85

2009

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An Aged/Autoimmune B-cell Program Defines the Early Transformation of Extranodal Lymphomas

Cancer discovery, 2023-01, Vol.13 (1), p.216-243

2023

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Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency

Nature genetics, 2007-04, Vol.39 (4), p.429-430

2007

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DNA-PKcs Is Involved in Ig Class Switch Recombination in Human B Cells

The Journal of immunology (1950), 2015-12, Vol.195 (12), p.5608-5615

2015

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Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

Blood, 2009-02, Vol.113 (9), p.1967-1976

2009

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IgA subclass switch recombination in human mucosal and systemic immune compartments

Immunity to SARS-CoV-2 up to 15 months after infection

Genetic Landscapes of Relapsed and Refractory Diffuse Large B-Cell Lymphomas

Limited cross-variant neutralization after primary Omicron infection: consideration for a variant-containing booster

Lactobacilli Expressing Variable Domain of Llama Heavy-Chain Antibody Fragments (Lactobodies) Confer Protection against Rotavirus-Induced Diarrhea

Genetic basis of PD-L1 overexpression in diffuse large B-cell lymphomas

Genetic landscape of hepatitis B virus–associated diffuse large B-cell lymphoma

Genetic mechanisms of HLA-I loss and immune escape in diffuse large B cell lymphoma

Neonatal screening for severe primary immunodeficiency diseases using high-throughput triplex real-time PCR

A hypomorphic recombination-activating gene 1 ( RAG1 ) mutation resulting in a phenotype resembling common variable immunodeficiency

Human serum from SARS-CoV-2-vaccinated and COVID-19 patients shows reduced binding to the RBD of SARS-CoV-2 Omicron variant

Exome sequencing reveals novel mutation targets in diffuse large B-cell lymphomas derived from Chinese patients

The H2B deubiquitinase Usp22 promotes antibody class switch recombination by facilitating non-homologous end joining

Genome-wide CRISPR screens reveal synthetic lethal interaction between CREBBP and EP300 in diffuse large B-cell lymphoma

Genetic heterogeneity in primary and relapsed mantle cell lymphomas: Impact of recurrent CARD11 mutations

AID from bony fish catalyzes class switch recombination

DCLRE1C (ARTEMIS) mutations causing phenotypes ranging from atypical severe combined immunodeficiency to mere antibody deficiency

19n01, a broadly neutralizing antibody against omicron BA.1, BA.2, BA.4/5, and other SARS-CoV-2 variants of concern

DNA repair genes are selectively mutated in diffuse large B cell lymphomas

Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases

Selective IgA deficiency in early life: Association to infections and allergic diseases during childhood

An Aged/Autoimmune B-cell Program Defines the Early Transformation of Extranodal Lymphomas

Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency

DNA-PKcs Is Involved in Ig Class Switch Recombination in Human B Cells

Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes

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