about
A physical map of the human genomeBreakpoint cloning and haplotype analysis indicate a single origin of the common Inv(10)(p11.2q21.2) mutation among northern EuropeansMicrobial exposure during early life has persistent effects on natural killer T cell functionMolecular cytogenetic analyses of immunoglobulin loci in nodular lymphocyte predominant Hodgkin's lymphoma reveal a recurrent IGH-BCL6 juxtapositionInhibition of anaplastic lymphoma kinase (ALK) activity provides a therapeutic approach for CLTC-ALK-positive human diffuse large B cell lymphomas.Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsyThe novel EPTP repeat defines a superfamily of proteins implicated in epileptic disordersEpigenome data release: a participant-centered approach to privacy protectionST18 is a breast cancer tumor suppressor gene at human chromosome 8q11.2.Epigenetic signatures associated with different levels of differentiation potential in human stem cellsGlial papillary tumour of the spinal cord with SMARCB1/INI1-loss and favourable long-term outcome.New insights into the biology and origin of mature aggressive B-cell lymphomas by combined epigenomic, genomic, and transcriptional profiling.TNFAIP3 (A20) is a tumor suppressor gene in Hodgkin lymphoma and primary mediastinal B cell lymphoma.Disorders of sex development expose transcriptional autonomy of genetic sex and androgen-programmed hormonal sex in human blood leukocytesA comprehensive microarray-based DNA methylation study of 367 hematological neoplasmsArray-based DNA methylation profiling of primary lymphomas of the central nervous system.The human retinoblastoma gene is imprinted.Alterations of microRNA and microRNA-regulated messenger RNA expression in germinal center B-cell lymphomas determined by integrative sequencing analysis.Changes in the pattern of DNA methylation associate with twin discordance in systemic lupus erythematosusRare occurrence of biallelic CYLD gene mutations in classical Hodgkin lymphoma.Pediatric follicular lymphoma--a clinico-pathological study of a population-based series of patients treated within the Non-Hodgkin's Lymphoma--Berlin-Frankfurt-Munster (NHL-BFM) multicenter trials.Lymphoma stem cells: enough evidence to support their existence?Germline nonsense mutation and somatic inactivation of SMARCA4/BRG1 in a family with rhabdoid tumor predisposition syndrome.DNA methylation profiles and their relationship with cytogenetic status in adult acute myeloid leukemia.Abstracts of the 52nd Workshop for Pediatric Research : Frankfurt, Germany. 27-28 October 2016.Epigenetic regulation of CD44 in Hodgkin and non-Hodgkin lymphoma.Whole-genome fingerprint of the DNA methylome during human B cell differentiation.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.Technology-specific error signatures in the 1000 Genomes Project data.Pipeline for large-scale microdroplet bisulfite PCR-based sequencing allows the tracking of hepitype evolution in tumors.Molecular remission is an independent predictor of clinical outcome in patients with mantle cell lymphoma after combined immunochemotherapy: a European MCL intergroup studyB-SOLANA: an approach for the analysis of two-base encoding bisulfite sequencing dataRecurrent involvement of the REL and BCL11A loci in classical Hodgkin lymphoma.Molecular characterization of a novel chromosomal translocation t(12;14)(q23;q11.2) in T-lymphoblastic lymphoma between the T-cell receptor delta-deleting elements (TRDREC and TRAJ61) and the hypothetical gene C12orf42.Conflicting results of prenatal FISH with different probes for Down's Syndrome critical regions associated with mosaicism for a de novo del(21)(q22) characterised by molecular karyotyping: Case reportFrequent occurrence of BCL6 rearrangements in nodular lymphocyte predominance Hodgkin lymphoma but not in classical Hodgkin lymphoma.A DNA methylation fingerprint of 1628 human samples.DNA-methylation profiling of fetal tissues reveals marked epigenetic differences between chorionic and amniotic samples.Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein.
P50
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P50
name
Reiner Siebert
@en
Reiner Siebert
@nl
Reiner Siebert
@pl
type
label
Reiner Siebert
@en
Reiner Siebert
@nl
Reiner Siebert
@pl
prefLabel
Reiner Siebert
@en
Reiner Siebert
@nl
Reiner Siebert
@pl