Search Results - "Stickens, Dominique"
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Altered endochondral bone development in matrix metalloproteinase 13-deficient mice
Published in Development (Cambridge) (01-12-2004)“…The assembly and degradation of extracellular matrix (ECM) molecules are crucial processes during bone development. In this study, we show that ECM remodeling…”
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Mice deficient in Ext2 lack heparan sulfate and develop exostoses
Published in Development (Cambridge) (01-11-2005)“…Hereditary multiple exostoses (HME) is a genetically heterogeneous human disease characterized by the development of bony outgrowths near the ends of long…”
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How Proteases Regulate Bone Morphogenesis
Published in Annals of the New York Academy of Sciences (01-05-2003)“…: Matrix metalloproteinases (MMPs) degrade most components of the extracellular matrix (ECM), as well as many non‐ECM molecules. MMPs participate in (1)…”
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EXT genes are differentially expressed in bone and cartilage during mouse embryogenesis
Published in Developmental dynamics (2000)Get full text
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PPARδ modulation rescues mitochondrial fatty acid oxidation defects in the mdx model of muscular dystrophy
Published in Mitochondrion (01-05-2019)“…Duchenne muscular dystrophy (DMD) is a recessive, fatal X-linked disease that is characterized by progressive skeletal muscle wasting due to the absence of…”
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Discovery of N‑[Bis(4-methoxyphenyl)methyl]-4-hydroxy-2-(pyridazin-3-yl)pyrimidine-5-carboxamide (MK-8617), an Orally Active Pan-Inhibitor of Hypoxia-Inducible Factor Prolyl Hydroxylase 1–3 (HIF PHD1–3) for the Treatment of Anemia
Published in Journal of medicinal chemistry (22-12-2016)“…The discovery of novel 4-hydroxy-2-(heterocyclic)pyrimidine-5-carboxamide inhibitors of hypoxia-inducible factor (HIF) prolyl hydroxylases (PHD) is described…”
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Discovery of Orally Bioavailable and Liver-Targeted Hypoxia-Inducible Factor Prolyl Hydroxylase (HIF-PHD) Inhibitors for the Treatment of Anemia
Published in ACS medicinal chemistry letters (13-12-2018)“…We report herein the design and synthesis of a series of orally active, liver-targeted hypoxia-inducible factor prolyl hydroxylase (HIF-PHD) inhibitors for the…”
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Epidermal Development and Wound Healing in Matrix Metalloproteinase 13-Deficient Mice
Published in Journal of investigative dermatology (01-02-2006)“…Degradation of the extracellular matrix, which is an indispensable step in tissue remodelling processes such as embryonic development and wound healing of the…”
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A single dose of EGLN1 siRNA yields increased erythropoiesis in nonhuman primates
Published in Nucleic acid therapeutics (01-12-2014)“…Decreased production of erythropoietin (EPO) causes anemia in patients with chronic kidney disease, and recombinant human EPO is used to treat renal failure…”
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Metalloproteases and Adipogenesis: A Weighty Subject
Published in The American journal of pathology (01-05-2002)Get full text
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The EXT2 multiple exostoses gene defines a family of putative tumour suppressor genes
Published in Nature genetics (01-09-1996)“…Hereditary multiple exostoses (EXT) is an autosomal dominant condition characterized by short stature and the development of bony protuberances at the ends of…”
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Commentary: Metalloproteases and adipogenesis: A weighty subject
Published in The American journal of pathology (01-05-2002)Get full text
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EXT genes are differentially expressed in bone and cartilage during mouse embryogenesis
Published in Developmental dynamics (01-07-2000)“…Hereditary multiple exostoses (HME) is a genetically heterogeneous disease characterized by the development of bony protuberances at the ends of all long…”
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14
A sugar fix for bone tumours?
Published in Nature genetics (01-06-1998)“…The success of modern molecular biology has been radically enhanced by the ability to identify disease-related genes through positional cloning, helped by…”
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Isolation and Characterization of the Murine Homolog of the Human EXT2 Multiple Exostoses Gene
Published in Biochemical and molecular medicine (01-06-1997)“…Multiple exostoses is a polygenic disease of bone formation and development characterized by the presence of cartilage-capped osseous projections emanating…”
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Gene for multiple exostoses (EXT2) maps to 11(p11.2p12) and is deleted in patients with a contiguous gene syndrome
Published in American journal of medical genetics (17-02-1998)Get full text
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