about
Sox2 cooperates with Chd7 to regulate genes that are mutated in human syndromesThe detailed 3D multi-loop aggregate/rosette chromatin architecture and functional dynamic organization of the human and mouse genomes.The genome-wide dynamics of the binding of Ldb1 complexes during erythroid differentiation.Absence of common somatic alterations in genes on 1p and 19q in oligodendrogliomasMultiplexed chromosome conformation capture sequencing for rapid genome-scale high-resolution detection of long-range chromatin interactions.Targeted Next Generation Sequencing reveals previously unidentified TSC1 and TSC2 mutationsDynamic long-range chromatin interactions control Myb proto-oncogene transcription during erythroid developmentDeciphering the RNA landscape by RNAome sequencing.Control of developmentally primed erythroid genes by combinatorial co-repressor actionsDynamic regulation of the transcription initiation landscape at single nucleotide resolution during vertebrate embryogenesisNext generation sequencing of SNPs for non-invasive prenatal diagnosis: challenges and feasibility as illustrated by an application to β-thalassaemia.Genome-wide analysis shows that Ldb1 controls essential hematopoietic genes/pathways in mouse early development and reveals novel players in hematopoiesis.Comparison of Mycoplasma pneumoniae Genome Sequences from Strains Isolated from Symptomatic and Asymptomatic PatientsProteins that bind regulatory regions identified by histone modification chromatin immunoprecipitations and mass spectrometry.Genome-wide DNA methylation profiling of non-small cell lung carcinomas.An interaction network of mental disorder proteins in neural stem cellsNext-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects.Targeted Chromatin Capture (T2C): a novel high resolution high throughput method to detect genomic interactions and regulatory elements.Erratum: The genome-wide dynamics of the binding of Ldb1 complexes during erythroid differentiation.Clinical significance of immunohistochemistry for detection of BAP1 mutations in uveal melanoma.Genome-wide DNA methylation profiling using the methylation-dependent restriction enzyme LpnPI.Investigation of the spatial structure and interactions of the genome at sub-kilobase-pair resolution using T2C.UGT1A1 Genetic Variations and a Haplotype Associated with Neonatal Hyperbilirubinemia in Indonesian Population.Identification of microRNAs in Human Plasma
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P50
description
researcher ORCID ID = 0000-0002-8871-3659
@en
wetenschapper
@nl
name
Christel Kockx
@ast
Christel Kockx
@en
Christel Kockx
@es
Christel Kockx
@nl
type
label
Christel Kockx
@ast
Christel Kockx
@en
Christel Kockx
@es
Christel Kockx
@nl
prefLabel
Christel Kockx
@ast
Christel Kockx
@en
Christel Kockx
@es
Christel Kockx
@nl
P106
P108
P31
P496
0000-0002-8871-3659