Lista de obras - Christel Kockx - Dominio Público Uruguay

Absence of common somatic alterations in genes on 1p and 19q in oligodendrogliomas

artículo científico publicado en 2011

An interaction network of mental disorder proteins in neural stem cells

artículo científico publicado en 2017

Clinical significance of immunohistochemistry for detection of BAP1 mutations in uveal melanoma.

artículo científico publicado en 2014

Comparison of Mycoplasma pneumoniae Genome Sequences from Strains Isolated from Symptomatic and Asymptomatic Patients

artículo científico publicado en 2016

Control of developmentally primed erythroid genes by combinatorial co-repressor actions

artículo científico publicado en 2015

Deciphering the RNA landscape by RNAome sequencing

artículo científico publicado en 2015

Dynamic long-range chromatin interactions control Myb proto-oncogene transcription during erythroid development

artículo científico publicado en 2011

Dynamic regulation of the transcription initiation landscape at single nucleotide resolution during vertebrate embryogenesis

artículo científico publicado en 2013

Erratum: The genome-wide dynamics of the binding of Ldb1 complexes during erythroid differentiation.

artículo científico publicado en 2010

Exome sequencing and functional analyses suggest that SIX6 is a gene involved in an altered proliferation-differentiation balance early in life and optic nerve degeneration at old age.

artículo científico publicado en 2013

Genome-wide DNA methylation profiling of non-small cell lung carcinomas

artículo científico publicado en 2012

Genome-wide DNA methylation profiling using the methylation-dependent restriction enzyme LpnPI.

artículo científico publicado en 2017

Genome-wide analysis shows that Ldb1 controls essential hematopoietic genes/pathways in mouse early development and reveals novel players in hematopoiesis

artículo científico publicado en 2013

Identification of microRNAs in Human Plasma

artículo científico publicado en 2015

Investigation of the spatial structure and interactions of the genome at sub-kilobase-pair resolution using T2C.

artículo científico publicado en 2018

Multiplexed chromosome conformation capture sequencing for rapid genome-scale high-resolution detection of long-range chromatin interactions

artículo científico publicado en 2013

Next generation sequencing of SNPs for non-invasive prenatal diagnosis: challenges and feasibility as illustrated by an application to β-thalassaemia.

scientific article published on 10 April 2013

Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects

artículo científico publicado en 2015

Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects.

artículo científico publicado en 2015

Proteins that bind regulatory regions identified by histone modification chromatin immunoprecipitations and mass spectrometry.

artículo científico publicado en 2015

Snail regulates MyoD binding-site occupancy to direct enhancer switching and differentiation-specific transcription in myogenesis

artículo científico publicado en 2012

Sox2 cooperates with Chd7 to regulate genes that are mutated in human syndromes

scientific journal article

Targeted Chromatin Capture (T2C): a novel high resolution high throughput method to detect genomic interactions and regulatory elements

artículo científico publicado en 2014

Targeted Next Generation Sequencing reveals previously unidentified TSC1 and TSC2 mutations

artículo científico publicado en 2015

The detailed 3D multi-loop aggregate/rosette chromatin architecture and functional dynamic organization of the human and mouse genomes.

artículo científico publicado en 2016

The genome-wide dynamics of the binding of Ldb1 complexes during erythroid differentiation

artículo científico publicado en 2010

Transcriptional dominance of Pax7 in adult myogenesis is due to high-affinity recognition of homeodomain motifs

artículo científico publicado en 2012

UGT1A1 Genetic Variations and a Haplotype Associated with Neonatal Hyperbilirubinemia in Indonesian Population.

artículo científico publicado en 2018

Lista de obras de Christel Kockx

Absence of common somatic alterations in genes on 1p and 19q in oligodendrogliomas

An interaction network of mental disorder proteins in neural stem cells

Clinical significance of immunohistochemistry for detection of BAP1 mutations in uveal melanoma.

Comparison of Mycoplasma pneumoniae Genome Sequences from Strains Isolated from Symptomatic and Asymptomatic Patients

Control of developmentally primed erythroid genes by combinatorial co-repressor actions

Deciphering the RNA landscape by RNAome sequencing

Dynamic long-range chromatin interactions control Myb proto-oncogene transcription during erythroid development

Dynamic regulation of the transcription initiation landscape at single nucleotide resolution during vertebrate embryogenesis

Erratum: The genome-wide dynamics of the binding of Ldb1 complexes during erythroid differentiation.

Exome sequencing and functional analyses suggest that SIX6 is a gene involved in an altered proliferation-differentiation balance early in life and optic nerve degeneration at old age.

Genome-wide DNA methylation profiling of non-small cell lung carcinomas

Genome-wide DNA methylation profiling using the methylation-dependent restriction enzyme LpnPI.

Genome-wide analysis shows that Ldb1 controls essential hematopoietic genes/pathways in mouse early development and reveals novel players in hematopoiesis

Identification of microRNAs in Human Plasma

Investigation of the spatial structure and interactions of the genome at sub-kilobase-pair resolution using T2C.

Multiplexed chromosome conformation capture sequencing for rapid genome-scale high-resolution detection of long-range chromatin interactions

Next generation sequencing of SNPs for non-invasive prenatal diagnosis: challenges and feasibility as illustrated by an application to β-thalassaemia.

Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects

Next-generation sequencing-based genome diagnostics across clinical genetics centers: implementation choices and their effects.

Proteins that bind regulatory regions identified by histone modification chromatin immunoprecipitations and mass spectrometry.

Snail regulates MyoD binding-site occupancy to direct enhancer switching and differentiation-specific transcription in myogenesis

Sox2 cooperates with Chd7 to regulate genes that are mutated in human syndromes

Targeted Chromatin Capture (T2C): a novel high resolution high throughput method to detect genomic interactions and regulatory elements

Targeted Next Generation Sequencing reveals previously unidentified TSC1 and TSC2 mutations

The 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

Transcriptional dominance of Pax7 in adult myogenesis is due to high-affinity recognition of homeodomain motifs

UGT1A1 Genetic Variations and a Haplotype Associated with Neonatal Hyperbilirubinemia in Indonesian Population.