Search Results - "Gronemeyer, Hinrich"
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Dual role of DR5 in death and survival signaling leads to TRAIL resistance in cancer cells
Published in Cell death & disease (31-08-2017)“…Besides its tumor-selective apoptotic activity, tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) promotes pro-survival, proliferative or…”
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Functions, Therapeutic Applications, and Synthesis of Retinoids and Carotenoids
Published in Chemical reviews (08-01-2014)“…Alvarez et al investigated the functions, synthesis and uses of retinoids and carotenoids and detail how the knowledge gleaned from this research is being used…”
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3
Modulation of RXR function through ligand design
Published in Biochimica et biophysica acta (01-01-2012)“…As the promiscuous partner of heterodimeric associations, retinoid X receptors (RXRs) play a key role within the Nuclear Receptor (NR) superfamily. Some of the…”
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RAR and RXR modulation in cancer and metabolic disease
Published in Nature reviews. Drug discovery (01-10-2007)“…Retinoic acid receptors (RARs) are ligand-controlled transcription factors that function as heterodimers with retinoid X receptors (RXRs) to regulate cell…”
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The promise of retinoids to fight against cancer
Published in Nature reviews. Cancer (01-12-2001)“…Retinoids have a reputation for being both detrimental and beneficial: they are teratogens, but they also have tumour-suppressive capacity. Cell biology and…”
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Design of selective nuclear receptor modulators: RAR and RXR as a case study
Published in Nature reviews. Drug discovery (01-10-2007)“…Retinoic acid receptors (RARs) and retinoid X receptors (RXRs) are members of the nuclear receptor superfamily whose effects on cell growth and survival can be…”
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The inactive X chromosome is epigenetically unstable and transcriptionally labile in breast cancer
Published in Genome research (01-04-2015)“…Disappearance of the Barr body is considered a hallmark of cancer, although whether this corresponds to genetic loss or to epigenetic instability and…”
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International Union of Pharmacology. LXIII. Retinoid X Receptors
Published in Pharmacological reviews (01-12-2006)“…The physiological effects of retinoic acids (RAs) are mediated by members of two families of nuclear receptors, the retinoic acid receptors (RARs) and the…”
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The KDM5 family is required for activation of pro-proliferative cell cycle genes during adipocyte differentiation
Published in Nucleic acids research (28-02-2017)“…The KDM5 family of histone demethylases removes the H3K4 tri-methylation (H3K4me3) mark frequently found at promoter regions of actively transcribed genes and…”
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International Union of Pharmacology. LX. Retinoic Acid Receptors
Published in Pharmacological reviews (01-12-2006)“…Retinoid is a term for compounds that bind to and activate retinoic acid receptors (RARα, RARβ, and RARγ), members of the nuclear hormone receptor…”
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Dissecting the retinoid‐induced differentiation of F9 embryonal stem cells by integrative genomics
Published in Molecular systems biology (11-10-2011)“…Retinoic acid (RA) triggers physiological processes by activating heterodimeric transcription factors (TFs) comprising retinoic acid receptor (RARα, β, γ) and…”
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Single-tube linear DNA amplification (LinDA) for robust ChIP-seq
Published in Nature methods (01-07-2011)“…A linear, one-tube amplification procedure generates sufficient amounts of material from chromatin immunoprecipitation (ChIP) and reChIP experiments to allow…”
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13
The nuclear receptor ligand-binding domain: structure and function
Published in Current opinion in cell biology (01-06-1998)“…In the past few years our understanding of nuclear receptor action has dramatically improved as a result of the elucidation of the crystal structures of the…”
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Development of biotin-retinoid conjugates as chemical probes for analysis of retinoid function
Published in Bioorganic & medicinal chemistry letters (01-08-2018)“…[Display omitted] •Conjugate molecules of retinoid (Am580) and biotin were designed and synthesized.•One of the synthesized conjugates retained biological…”
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Nuclear receptor ligand-binding domains: three-dimensional structures, molecular interactions and pharmacological implications
Published in Trends in Pharmacological Sciences (01-10-2000)“…Nuclear receptors are members of a large family of ligand-inducible transcription factors that regulate gene programs underlying a plethora of…”
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Tumor-selective action of HDAC inhibitors involves TRAIL induction in acute myeloid leukemia cells
Published in Nature Medicine (01-01-2005)“…Chromatin is a dynamic macromolecular structure epigenetically modified to regulate specific gene expression. Altered chromatin function can lead to aberrant…”
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Selective class II HDAC inhibitors impair myogenesis by modulating the stability and activity of HDAC-MEF2 complexes
Published in EMBO reports (01-07-2009)“…Histone deacetylase (HDAC) inhibitors are promising new epi‐drugs, but the presence of both class I and class II enzymes in HDAC complexes precludes a detailed…”
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A quality control system for profiles obtained by ChIP sequencing
Published in Nucleic acids research (01-11-2013)“…The absence of a quality control (QC) system is a major weakness for the comparative analysis of genome-wide profiles generated by next-generation sequencing…”
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Multivalent DR5 Peptides Activate the TRAIL Death Pathway and Exert Tumoricidal Activity
Published in Cancer research (Chicago, Ill.) (01-02-2010)“…Ongoing clinical trials are exploring anticancer approaches based on signaling by TRAIL, a ligand for the cell death receptors DR4 and DR5. In this study, we…”
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Reconstructed cell fate-regulatory programs in stem cells reveal hierarchies and key factors of neurogenesis
Published in Genome research (01-11-2016)“…Cell lineages, which shape the body architecture and specify cell functions, derive from the integration of a plethora of cell intrinsic and extrinsic signals…”
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