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Journal of Medical Genetics, ISSN 0022-2593, 06/2016, Volume 53, Issue 6, pp. 403 - 418
Journal Article
International Journal of Molecular Sciences, ISSN 1661-6596, 12/2016, Volume 17, Issue 12, pp. 2004 - 2004
Journal Article
Molecular Therapy, ISSN 1525-0016, 02/2016, Volume 24, Issue 2, pp. 206 - 216
Journal Article
Osteoarthritis and Cartilage, ISSN 1063-4584, 2013, Volume 21, Issue 12, pp. 1813 - 1823
Summary Background Mucopolysaccharidoses (MPSs) are rare genetic diseases caused by a deficient activity of one of the lysosomal enzymes involved in the... 
Rheumatology | Osteoimmunology | Dysostosis multiplex | Mucopolysaccharidosis | Metabolic inflammation | anti-TNF | ISOFLAVONE EXTRACT | STORAGE DISEASE | GENISTEIN-MEDIATED INHIBITION | BONE-MARROW-TRANSPLANTATION | HURLER-DISEASE | JOINT DISEASE | RHEUMATOLOGY | GLYCOSAMINOGLYCAN SYNTHESIS | FELINE MODEL | GROWTH-PLATE | ORTHOPEDICS | ENZYME REPLACEMENT THERAPY | Synovitis - metabolism | Mucopolysaccharidosis VI - immunology | Mucopolysaccharidosis VII - metabolism | Mucopolysaccharidoses - metabolism | Humans | Mucopolysaccharidosis VI - complications | Bone Diseases - metabolism | Mucopolysaccharidoses - immunology | Bone Diseases - etiology | Mucopolysaccharidosis II - metabolism | Cartilage, Articular - metabolism | Dysostoses - metabolism | Synovitis - etiology | Synovitis - immunology | Mucopolysaccharidoses - complications | Joint Diseases - immunology | Mucopolysaccharidosis I - metabolism | Glycosaminoglycans - metabolism | Joint Diseases - metabolism | Glycosaminoglycans - immunology | Dysostoses - immunology | Bone Diseases - immunology | Mucopolysaccharidosis I - complications | Mucopolysaccharidosis II - complications | Mucopolysaccharidosis I - immunology | Joint Diseases - etiology | Mucopolysaccharidosis VI - metabolism | Mucopolysaccharidosis VII - immunology | Mucopolysaccharidosis II - immunology | Mucopolysaccharidosis VII - complications | Cartilage, Articular - immunology | Dysostoses - etiology | Enzymes | Medical colleges | Inflammation | Glycosaminoglycans | Medical genetics
Journal Article
Advanced Drug Delivery Reviews, ISSN 0169-409X, 2010, Volume 62, Issue 12, pp. 1167 - 1174
Journal Article
Prenatal Diagnosis, ISSN 0197-3851, 05/2017, Volume 37, Issue 5, pp. 435 - 439
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 11/2013, Volume 110, Issue 3, pp. 319 - 328
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 03/2012, Volume 7, Issue 3, p. e32419
The characteristic neurological feature of many neurogenetic diseases is intellectual disability. Although specific neuropathological features have been... 
BETA-GLUCURONIDASE DEFICIENCY | NEURODEGENERATIVE DISEASE | MOUSE-BRAIN | CHONDROITIN SULFATE | NERVOUS-SYSTEM | CELLS | INFLAMMATION | MULTIDISCIPLINARY SCIENCES | PATHOGENIC CASCADES | MUCOPOLYSACCHARIDOSIS TYPE-VII | UROTENSIN-II | Cell Cycle - genetics | Microglia - metabolism | Neurons - pathology | Mucopolysaccharidosis VII - metabolism | Transcriptome | Extracellular Matrix - metabolism | Male | Brain - metabolism | Gliosis - pathology | Microglia - pathology | Female | Neurons - metabolism | Mucopolysaccharidosis VII - genetics | Brain - cytology | Cell Adhesion - genetics | Gliosis - genetics | Myelin Sheath - physiology | Olfactory Bulb - pathology | Mucopolysaccharidosis VII - pathology | Gliosis - metabolism | Circadian Rhythm - genetics | Signal Transduction - genetics | Animals | Cell Nucleus - genetics | Ion Channels - metabolism | Mucopolysaccharidosis VII - immunology | Brain - pathology | Mice | Brain - immunology | Genetic research | Brain | Gene mutations | Gene expression | Genes | Analysis | Neurosciences | Animal models | Disease | Neuropathology | Intellectual disabilities | Gene regulation | Lysergic acid diethylamide | Cognitive ability | Nervous system | Mucopolysaccharidosis | Lysergide | Developmental stages | Neurodegeneration | Immune system | Inflammation | Substantia alba | Children & youth | Brain research | Hospitals | Point mutation | Stem cells | Chondroitin sulfate | Mutation | Aberration | Gene therapy | lysosomal storage diseases | Neurogenetics | Mental retardation | Molecular modelling | Oligodendrocytes | lysergide
Journal Article