X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (2691) 2691
Newsletter (423) 423
Publication (317) 317
Book Review (14) 14
Book Chapter (9) 9
Conference Proceeding (5) 5
Dissertation (5) 5
Magazine Article (3) 3
Newspaper Article (2) 2
Streaming Video (2) 2
Book / eBook (1) 1
Government Document (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (1858) 1858
mucopolysaccharidosis (1449) 1449
index medicus (956) 956
animals (881) 881
male (842) 842
genetics & heredity (834) 834
female (794) 794
enzymes (617) 617
medicine, research & experimental (582) 582
child (512) 512
mice (509) 509
enzyme replacement therapy (490) 490
glycosaminoglycans (440) 440
child, preschool (431) 431
glycosaminoglycans - metabolism (427) 427
research (398) 398
adolescent (370) 370
endocrinology & metabolism (363) 363
biochemistry & molecular biology (346) 346
disease (340) 340
adult (338) 338
disease models, animal (314) 314
analysis (302) 302
infant (289) 289
pediatrics (287) 287
care and treatment (286) 286
health aspects (254) 254
medical research (236) 236
mutation (229) 229
medicine, experimental (227) 227
cells, cultured (226) 226
gene therapy (225) 225
phenotype (225) 225
diagnosis (222) 222
lysosomal storage diseases (213) 213
transplantation (206) 206
lysosomal storage disease (201) 201
bone-marrow-transplantation (200) 200
genetics (188) 188
children (186) 186
glycosaminoglycans - urine (186) 186
mouse model (186) 186
mucopolysaccharidosis i - genetics (182) 182
article (180) 180
sulfates (179) 179
mucopolysaccharidosis i - metabolism (172) 172
medicine (170) 170
reports (167) 167
enzyme-replacement therapy (165) 165
biotechnology & applied microbiology (161) 161
expression (161) 161
hurler-syndrome (153) 153
metabolic diseases (153) 153
medicine & public health (152) 152
mice, inbred c57bl (152) 152
mucopolysaccharidosis type-vii (151) 151
fibroblasts - metabolism (149) 149
internal medicine (147) 147
genetic therapy (144) 144
treatment outcome (142) 142
mucopolysaccharidoses (141) 141
biochemistry, general (140) 140
brain - metabolism (139) 139
fibroblasts - enzymology (138) 138
lysosomes - enzymology (137) 137
mucopolysaccharidosis i - pathology (137) 137
mucopolysaccharidosis i - therapy (137) 137
hematopoietic stem cells (134) 134
lysosomes - metabolism (134) 134
mice, knockout (134) 134
fibroblasts (133) 133
genetic aspects (133) 133
mucopolysaccharidosis iii - genetics (132) 132
central-nervous-system (131) 131
physiological aspects (131) 131
brain (130) 130
brain - pathology (129) 129
mucopolysaccharidosis ii - genetics (127) 127
human genetics (126) 126
iduronidase - metabolism (125) 125
young adult (125) 125
lysosomal storage (123) 123
alpha-l-iduronidase (122) 122
glucuronidase - metabolism (122) 122
glucuronidase - genetics (118) 118
neurosciences (118) 118
genetic vectors (117) 117
lysosomal storage disorders (117) 117
biopharmaceutics (115) 115
identification (115) 115
iduronidase - genetics (115) 115
mucopolysaccharidosis i - diagnosis (115) 115
gene (114) 114
pathology (114) 114
infant, newborn (113) 113
gene expression (112) 112
cell line (110) 110
dogs (109) 109
beta-glucuronidase (107) 107
mucopolysaccharidosis i - enzymology (107) 107
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (3017) 3017
French (27) 27
Italian (25) 25
Polish (13) 13
Spanish (12) 12
German (9) 9
Russian (6) 6
Czech (5) 5
Portuguese (4) 4
Chinese (3) 3
Japanese (3) 3
Danish (2) 2
Hungarian (2) 2
Serbian (2) 2
Croatian (1) 1
Dutch (1) 1
Finnish (1) 1
Turkish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Blood, ISSN 0006-4971, 01/2011, Volume 117, Issue 3, pp. 839 - 847
Mucopolysaccharidosis type I (MPS IH; Hurler syndrome) is a congenital deficiency of alpha-L-iduronidase, leading to lysosomal storage of glycosaminoglycans... 
REPAIR | THERAPY | ABNORMALITIES | MICROGLIA | BONE-MARROW-TRANSPLANTATION | DISEASE | CENTRAL-NERVOUS-SYSTEM | HEPARAN-SULFATE | GENERATION | MICE | HEMATOLOGY | Homeodomain Proteins - metabolism | Humans | Child, Preschool | Infant | Male | Mesoderm - cytology | Promoter Regions, Genetic - genetics | SOXB1 Transcription Factors - metabolism | Octamer Transcription Factor-3 - genetics | DNA Methylation | Transfection | SOXB1 Transcription Factors - genetics | Kruppel-Like Transcription Factors - metabolism | HEK293 Cells | Cell Differentiation | Induced Pluripotent Stem Cells - cytology | Iduronidase - genetics | Induced Pluripotent Stem Cells - metabolism | Iduronidase - metabolism | Mucopolysaccharidosis I - metabolism | Nanog Homeobox Protein | Mucopolysaccharidosis I - pathology | Bone Marrow Cells - cytology | Stromal Cells - metabolism | Cells, Cultured | Keratinocytes - cytology | Proto-Oncogene Proteins c-myc - metabolism | Homeodomain Proteins - genetics | Hematopoietic System - cytology | Animals | Hematopoietic System - metabolism | Keratinocytes - metabolism | Octamer Transcription Factor-3 - metabolism | Mucopolysaccharidosis I - genetics | Mesoderm - metabolism | Mice | Proto-Oncogene Proteins c-myc - genetics | Kruppel-Like Transcription Factors - genetics | Bone Marrow Cells - metabolism | Stromal Cells - cytology | Hematopoiesis and Stem Cells
Journal Article
Journal Article
by Li, Y P
[Zhonghua yan ke za zhi] Chinese journal of ophthalmology, ISSN 0412-4081, 03/1991, Volume 27, Issue 2, p. 90
The ocular histopathology of type I mucopolysaccharidosis was studied with histochemical, ultrahistochemical, and ultrastructural techniques. The latter method... 
Eye - pathology | Mucopolysaccharidosis I - metabolism | Eye - ultrastructure | Mucopolysaccharidosis I - pathology | Humans | Adolescent | Histocytochemistry | Male | Microscopy, Electron
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
Journal Article
American Journal of Physiology - Cell Physiology, ISSN 0363-6143, 06/2008, Volume 294, Issue 6, pp. 1387 - 1397
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2012, Volume 7, Issue 4, p. e35787
Mucopolysaccharide diseases (MPS) are caused by deficiency of glycosaminoglycan (GAG) degrading enzymes, leading to GAG accumulation. Neurodegenerative MPS... 
TARGETED DISRUPTION | MICROGLIAL ACTIVATION | SANFILIPPO-SYNDROME | DISEASE | BIOLOGY | SYNDROME TYPE-B | MICE | HEPARAN-SULFATE PROTEOGLYCANS | LYSOSOMAL STORAGE DISORDERS | ALPHA-L-IDURONIDASE | BRAIN | Immunohistochemistry | Neurons - pathology | Mucopolysaccharidosis III - pathology | Male | Parietal Lobe - metabolism | Heparitin Sulfate - metabolism | Somatosensory Cortex - pathology | Lysosomes - metabolism | Homer Scaffolding Proteins | Mucopolysaccharidosis III - metabolism | Female | Lysosomes - pathology | Neurons - metabolism | G(M2) Ganglioside - biosynthesis | Disease Models, Animal | Glycosaminoglycans - biosynthesis | Mucopolysaccharidosis I - metabolism | Mucopolysaccharidosis I - pathology | Carrier Proteins - biosynthesis | Disease Progression | Parietal Lobe - pathology | Animals | Vesicle-Associated Membrane Protein 2 - biosynthesis | Mice | Cytokines - biosynthesis | Somatosensory Cortex - metabolism | Enzymes | Brain | Neurons | Analysis | Models | Gangliosides | Animal models | Gangliosidosis | Transplants & implants | Disease | Neuropathology | Genes | Cognitive ability | Ganglioside GM2 | Schizophrenia | Cortex (somatosensory) | Mucopolysaccharidosis | Cortex (motor) | Proteins | Blood-brain barrier | Neurodegeneration | Cortex (parietal) | Rodents | Fibroblasts | Bone marrow | Growth factors | Genotypes | Heparan sulfate | Synaptophysin | Inflammation | Electron microscopy | Sulfation | Membrane proteins | Pathology | Axons | Gliosis | Hospitals | Transmission electron microscopy | Acids | Life span | Cell number | Stem cells | Monocyte chemoattractant protein 1
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 02/2015, Volume 114, Issue 2, pp. 138 - 145
Journal Article
International Journal of Molecular Sciences, ISSN 1661-6596, 12/2016, Volume 17, Issue 12, pp. 2004 - 2004
Journal Article
Journal Article
Journal Article