about
Screening of functional and positional candidate genes in families with common variable immunodeficiencyDeleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunityA hypomorphic recombination-activating gene 1 (RAG1) mutation resulting in a phenotype resembling common variable immunodeficiency.Extensive diversification of IgH subclass-encoding genes and IgM subclass switching in crocodilians.Physical mapping of the giant panda immunoglobulin heavy chain constant region genes.A regulatory role for NBS1 in strand-specific mutagenesis during somatic hypermutationCD27(-) B-cells produce class switched and somatically hyper-mutated antibodies during chronic HIV-1 infectionUnique DNA repair gene variations and potential associations with the primary antibody deficiency syndromes IgAD and CVIDDifferential role of nonhomologous end joining factors in the generation, DNA damage response, and myeloid differentiation of human induced pluripotent stem cells.High-density SNP mapping of the HLA region identifies multiple independent susceptibility loci associated with selective IgA deficiency.Novel mutation of the activation-induced cytidine deaminase gene in a Tajik family: special review on hyper-immunoglobulin M syndrome.Exome sequencing reveals novel mutation targets in diffuse large B-cell lymphomas derived from Chinese patients.Placental transfer of maternally-derived IgA precludes the use of guthrie card eluates as a screening tool for primary immunodeficiency diseases.Identification of IgF, a hinge-region-containing Ig class, and IgD in Xenopus tropicalisAberrant recombination and repair during immunoglobulin class switching in BRCA1-deficient human B cellsDCLRE1C (ARTEMIS) mutations causing phenotypes ranging from atypical severe combined immunodeficiency to mere antibody deficiency.Class switch recombination: a comparison between mouse and human.Antibody deficiency diseases.DNA repair genes are selectively mutated in diffuse large B cell lymphomasB-cell activating factor receptor deficiency is associated with an adult-onset antibody deficiency syndrome in humans.A regulatory role for the cohesin loader NIPBL in nonhomologous end joining during immunoglobulin class switch recombination.Non-homologous end joining in class switch recombination: the beginning of the endCo-expression of PD-L1 and p-AKT is associated with poor prognosis in diffuse large B-cell lymphoma via PD-1/PD-L1 axis activating intracellular AKT/mTOR pathway in tumor cellsCombined immunodeficiency and Epstein-Barr virus-induced B cell malignancy in humans with inherited CD70 deficiencyNew facets of antibody deficiencies.Genetic landscape and deregulated pathways in B-cell lymphoid malignancies.Genetic heterogeneity in primary and relapsed mantle cell lymphomas: Impact of recurrent CARD11 mutations.Distinct subtype distribution and somatic mutation spectrum of lymphomas in East Asia.Nurture your scientific curiosity early in your research career.Multiple IgH Isotypes Including IgD, Subclasses of IgM, and IgY Are Expressed in the Common Ancestors of Modern Birds.Genetic basis of PD-L1 overexpression in diffuse large B-cell lymphomas.Genetic Landscapes of Relapsed and Refractory Diffuse Large B-Cell Lymphomas.Disparate roles of ATR and ATM in immunoglobulin class switch recombination and somatic hypermutationXRCC4 deficiency in human subjects causes a marked neurological phenotype but no overt immunodeficiency.Impact of DNA ligase IV on nonhomologous end joining pathways during class switch recombination in human cells.The shared CTLA4-ICOS risk locus in celiac disease, IgA deficiency and common variable immunodeficiency.Artemis splice defects cause atypical SCID and can be restored in vitro by an antisense oligonucleotide.Severe congenital neutropenia or hyper-IgM syndrome? A novel mutation of CD40 ligand in a patient with severe neutropenia.Neonatal screening for severe primary immunodeficiency diseases using high-throughput triplex real-time PCR.Cytokine gene expression profiles in human lymphocytes induced by a formula of traditional Chinese medicine, vigconic VI-28.
P50
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P108
P106
P31
P496
0000-0003-1990-8804