Search Results - "Grosveld, G."
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1
Forces driving the three‐dimensional folding of eukaryotic genomes
Published in Molecular systems biology (01-06-2018)“…The last decade has radically renewed our understanding of higher order chromatin folding in the eukaryotic nucleus. As a result, most current models are in…”
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2
Cohesin and CTCF differentially affect chromatin architecture and gene expression in human cells
Published in Proceedings of the National Academy of Sciences - PNAS (21-01-2014)“…Recent studies of genome-wide chromatin interactions have revealed that the human genome is partitioned into many self-associating topological domains. The…”
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3
Directed Migration of Cortical Interneurons Depends on the Cell-Autonomous Action of Sip1
Published in Neuron (Cambridge, Mass.) (09-01-2013)“…GABAergic interneurons mainly originate in the medial ganglionic eminence (MGE) of the embryonic ventral telencephalon (VT) and migrate tangentially to the…”
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r3Cseq: an R/Bioconductor package for the discovery of long-range genomic interactions from chromosome conformation capture and next-generation sequencing data
Published in Nucleic acids research (01-07-2013)“…The coupling of chromosome conformation capture (3C) with next-generation sequencing technologies enables the high-throughput detection of long-range genomic…”
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In vivo live imaging of RNA polymerase II transcription factories in primary cells
Published in Genes & development (01-04-2013)“…Transcription steps are marked by different modifications of the C-terminal domain of RNA polymerase II (RNAPII). Phosphorylation of Ser5 and Ser7 by…”
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6
Identification of multiple subsets of ventral interneurons and differential distribution along the rostrocaudal axis of the developing spinal cord
Published in PloS one (15-08-2013)“…The spinal cord contains neuronal circuits termed Central Pattern Generators (CPGs) that coordinate rhythmic motor activities. CPG circuits consist of motor…”
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Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin
Published in Nature genetics (01-09-2010)“…Hereditary persistence of fetal hemoglobin (HPFH) is characterized by persistent high levels of fetal hemoglobin (HbF) in adults. Several contributory factors,…”
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The 3D Structure of the Immunoglobulin Heavy-Chain Locus: Implications for Long-Range Genomic Interactions
Published in Cell (18-04-2008)“…The immunoglobulin heavy-chain ( Igh) locus is organized into distinct regions that contain multiple variable (V H), diversity (D H), joining (J H) and…”
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Gata-3 is an essential regulator of mammary-gland morphogenesis and luminal-cell differentiation
Published in Nature cell biology (01-02-2007)“…The transcription factor Gata-3 is a defining marker of the 'luminal' subtypes of breast cancer. To gain insight into the role of Gata-3 in breast epithelial…”
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10
The dynamic emergence of GATA1 complexes identified in in vitro embryonic stem cell differentiation and in vivo mouse fetal liver
Published in Haematologica (Roma) (01-07-2020)“…GATA1 is an essential transcriptional regulator of myeloid hematopoietic differentiation towards red blood cells. During erythroid differentiation, GATA1 forms…”
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11
Exploiting native forces to capture chromosome conformation in mammalian cell nuclei
Published in Molecular systems biology (01-12-2016)“…Mammalian interphase chromosomes fold into a multitude of loops to fit the confines of cell nuclei, and looping is tightly linked to regulated function…”
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12
Balancing of Histone H3K4 Methylation States by the Kdm5c/SMCX Histone Demethylase Modulates Promoter and Enhancer Function
Published in Cell reports (Cambridge) (25-04-2013)“…The functional organization of eukaryotic genomes correlates with specific patterns of histone methylations. Regulatory regions in genomes such as enhancers…”
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13
Compartmentalization of androgen receptors at endogenous genes in living cells
Published in Nucleic acids research (10-11-2023)“…Abstract A wide range of nuclear proteins are involved in the spatio-temporal organization of the genome through diverse biological processes such as gene…”
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14
The Gata3 transcription factor is required for the survival of embryonic and adult sympathetic neurons
Published in The Journal of neuroscience (11-08-2010)“…The transcription factor Gata3 is essential for the development of sympathetic neurons and adrenal chromaffin cells. As Gata3 expression is maintained up to…”
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15
RTTN Mutations Link Primary Cilia Function to Organization of the Human Cerebral Cortex
Published in American journal of human genetics (07-09-2012)“…Polymicrogyria is a malformation of the developing cerebral cortex caused by abnormal organization and characterized by many small gyri and fusion of the outer…”
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Sox2 regulates the emergence of lung basal cells by directly activating the transcription of Trp63
Published in American journal of respiratory cell and molecular biology (01-08-2014)“…Lung development is determined by the coordinated expression of several key genes. Previously, we and others have shown the importance of the sex determining…”
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17
Multiple interactions between regulatory regions are required to stabilize an active chromatin hub
Published in Genes & development (15-06-2004)“…The human beta-globin locus control region (LCR) is required for the maintenance of an open chromatin configuration of the locus. It interacts with the genes…”
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18
Enhancers and silencers: an integrated and simple model for their function
Published in Epigenetics & chromatin (09-01-2012)“…Regulatory DNA elements such as enhancers, silencers and insulators are embedded in metazoan genomes, and they control gene expression during development…”
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19
Exportin 4 mediates a novel nuclear import pathway for Sox family transcription factors
Published in The Journal of cell biology (06-04-2009)“…SRY and other Sox-type transcription factors are important developmental regulators with various implications in human disease. In this study, we identified…”
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MN1 overexpression is an important step in the development of inv(16) AML
Published in Leukemia (01-08-2007)“…The gene encoding the transcriptional co-activator MN1 is the target of the reciprocal chromosome translocation (12;22)(p13;q12) in some patients with acute…”
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