Published in J Immunol on April 15, 2002
Inhibition of the catalytic function of activation-induced cytidine deaminase promotes apoptosis of germinal center B cells in BXD2 mice. Arthritis Rheum (2011) 2.33
BAFF regulates B cell survival by downregulating the BH3-only family member Bim via the ERK pathway. J Exp Med (2005) 1.67
The latent membrane protein 1 (LMP1) oncogene of Epstein-Barr virus can simultaneously induce and inhibit apoptosis in B cells. J Virol (2012) 1.04
NSP 5a3a: a potential novel cancer target in head and neck carcinoma. Oncotarget (2010) 0.97
Characterisation of a novel A1-specific monoclonal antibody. Cell Death Dis (2014) 0.84
BCR-signaling-induced cell death demonstrates dependency on multiple BH3-only proteins in a murine model of B-cell lymphoma. Cell Death Differ (2015) 0.79
Green tea polyphenols induce cell death in breast cancer MCF-7 cells through induction of cell cycle arrest and mitochondrial-mediated apoptosis. J Zhejiang Univ Sci B (2017) 0.75
Activation of the MAP kinase pathway induces apoptosis in the Merkel cell carcinoma cell line UISO. J Invest Dermatol (2007) 3.26
Somatic mutation profiles of MSI and MSS colorectal cancer identified by whole exome next generation sequencing and bioinformatics analysis. PLoS One (2010) 2.10
Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene. Am J Hum Genet (2010) 1.86
Mutation frequencies of X-linked mental retardation genes in families from the EuroMRX consortium. Hum Mutat (2007) 1.68
Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci. Hum Genet (2006) 1.66
RelB forms transcriptionally inactive complexes with RelA/p65. J Biol Chem (2003) 1.63
Identification of mutations in TRAPPC9, which encodes the NIK- and IKK-beta-binding protein, in nonsyndromic autosomal-recessive mental retardation. Am J Hum Genet (2009) 1.58
TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy. Nat Genet (2008) 1.45
Mutations in the alpha 1,2-mannosidase gene, MAN1B1, cause autosomal-recessive intellectual disability. Am J Hum Genet (2011) 1.35
Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3. Eur J Hum Genet (2010) 1.29
SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly. Hum Genet (2005) 1.25
Mutations in NSUN2 cause autosomal-recessive intellectual disability. Am J Hum Genet (2012) 1.24
The stability and anti-apoptotic function of A1 are controlled by its C terminus. J Biol Chem (2006) 1.16
Mutation of the conserved polyadenosine RNA binding protein, ZC3H14/dNab2, impairs neural function in Drosophila and humans. Proc Natl Acad Sci U S A (2011) 1.11
Follicular regulatory T cells control humoral autoimmunity via NFAT2-regulated CXCR5 expression. J Exp Med (2014) 1.08
IL-2 and autoimmune disease. Cytokine Growth Factor Rev (2002) 1.07
Chromosome deletions in 13q33-34: report of four patients and review of the literature. Am J Med Genet A (2008) 1.05
Establishment of a mouse model with misregulated chromosome condensation due to defective Mcph1 function. PLoS One (2010) 1.04
ST3GAL3 mutations impair the development of higher cognitive functions. Am J Hum Genet (2011) 1.01
The Bcl-2 family member Bfl-1/A1 is strongly repressed in normal and malignant plasma cells but is a potent anti-apoptotic factor for myeloma cells. Br J Haematol (2004) 0.96
The complementarity determining region 2 of BV8S2 (V beta 8.2) contributes to antigen recognition by rat invariant NKT cell TCR. J Immunol (2006) 0.96
SUMOylation interferes with CCAAT/enhancer-binding protein beta-mediated c-myc repression, but not IL-4 activation in T cells. J Immunol (2006) 0.95
CCDC22 deficiency in humans blunts activation of proinflammatory NF-κB signaling. J Clin Invest (2013) 0.91
A distinctive gene expression fingerprint in mentally retarded male patients reflects disease-causing defects in the histone demethylase KDM5C. Pathogenetics (2010) 0.91
West syndrome caused by ST3Gal-III deficiency. Epilepsia (2012) 0.87
Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1. Eur J Hum Genet (2011) 0.87
A novel nonsense mutation in KDM5C/JARID1C gene causing intellectual disability, short stature and speech delay. Neurosci Lett (2011) 0.87
Cleavage of E-cadherin and β-catenin by calpain affects Wnt signaling and spheroid formation in suspension cultures of human pluripotent stem cells. Mol Cell Proteomics (2014) 0.84
Distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7. BMC Genomics (2014) 0.84
Pax-5 is a key regulator of the B cell-restricted expression of the CD23a isoform. Eur J Immunol (2003) 0.83
Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation. Eur J Hum Genet (2006) 0.83
Blimp-1Deltaexon7: a naturally occurring Blimp-1 deletion mutant with auto-regulatory potential. Exp Cell Res (2008) 0.82
A novel ALDH5A1 mutation is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability in an Iranian family. Am J Med Genet A (2013) 0.78
OLA-DRB1 microsatellite variants are associated with ovine growth and reproduction traits. Genet Sel Evol (2006) 0.76
Transcriptome Alterations In X-Irradiated Human Gingiva Fibroblasts. Health Phys (2016) 0.75
Submicroscopic genomic rearrangements change gene expression in T-cell large granular lymphocyte leukemia. Eur J Haematol (2014) 0.75