about
Inhibition of anaplastic lymphoma kinase (ALK) activity provides a therapeutic approach for CLTC-ALK-positive human diffuse large B cell lymphomas.TNFAIP3 (A20) is a tumor suppressor gene in Hodgkin lymphoma and primary mediastinal B cell lymphoma.A comprehensive microarray-based DNA methylation study of 367 hematological neoplasmsLoss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance.Rare occurrence of biallelic CYLD gene mutations in classical Hodgkin lymphoma.Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome.DNA methylome analysis in Burkitt and follicular lymphomas identifies differentially methylated regions linked to somatic mutation and transcriptional control.Statistical inference of allelic imbalance from transcriptome data.Detection of genomic aberrations in molecularly defined Burkitt's lymphoma by array-based, high resolution, single nucleotide polymorphism analysis.Janus--a comprehensive tool investigating the two faces of transcription.Genetic characteristics of the human hepatic stellate cell line LX-2.A recurrent 11q aberration pattern characterizes a subset of MYC-negative high-grade B-cell lymphomas resembling Burkitt lymphoma.New insights into the genetics of X-linked dystonia-parkinsonism (XDP, DYT3).A summary of molecular genetic findings in fructose-1,6-bisphosphatase deficiency with a focus on a common long-range deletion and the role of MLPA analysis.Frequency and characterization of DNA methylation defects in children born SGA.Hunting for the 5th base: Techniques for analyzing DNA methylation.Immunoglobulin heavy chain locus chromosomal translocations in B-cell precursor acute lymphoblastic leukemia: rare clinical curios or potent genetic drivers?A de novo 1.1Mb microdeletion of chromosome 19p13.11 provides indirect evidence for EPS15L1 to be a strong candidate for split hand split foot malformation.Genetic lesions of the TRAF3 and MAP3K14 genes in classical Hodgkin lymphoma.Recurrent deletions of the TNFSF7 and TNFSF9 genes in 19p13.3 in diffuse large B-cell and Burkitt lymphomas.GeneChip analyses point to novel pathogenetic mechanisms in mantle cell lymphoma.
P50
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Inga Vater
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Inga Vater
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Inga Vater
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Inga Vater
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