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Molecular Genetics and Metabolism, ISSN 1096-7192, 08/2008, Volume 94, Issue 4, pp. 391 - 396
Journal Article
Neurology, ISSN 0028-3878, 10/2014, Volume 83, Issue 17, pp. e166 - e168
Gangliosidoses are a group of rare lysosomal storage diseases (LySD) involving the accumulation of lipids in multiple organ systems, including the central and... 
CLINICAL NEUROLOGY | GM1-GANGLIOSIDOSIS | DISEASE | Gangliosidosis, GM1 - metabolism | Magnetic Resonance Imaging | Muscle Hypotonia - complications | Humans | Melanocytes - pathology | Pigmentation Disorders - complications | Female | Infant | 228 | Resident and Fellow Section | 156
Journal Article
MOLECULAR GENETICS AND METABOLISM, ISSN 1096-7192, 08/2008, Volume 94, Issue 4, pp. 391 - 396
Journal Article
Journal Article
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, ISSN 0006-291X, 03/2008, Volume 367, Issue 3, pp. 616 - 622
Journal Article
Reference
Journal Article
Journal Article
BBA - Molecular Basis of Disease, ISSN 0925-4439, 2011, Volume 1812, Issue 7, pp. 782 - 790
Journal Article
MOLECULAR THERAPY, ISSN 1525-0016, 03/2013, Volume 21, Issue 3, pp. 526 - 532
Lysosonnal beta-galactosidase (beta-Gal) deficiency causes a group of disorders that include neuronopathic GM(1) gangliosidosis and non-neuronopathic Morquio B... 
MEDICINE, RESEARCH & EXPERIMENTAL | HUMAN BETA-GALACTOSIDASE | MORQUIO B DISEASE | FLUOROUS IMINOALDITOLS | GAUCHER-DISEASE | LYSOSOMAL DISEASES | CHEMICAL CHAPERONE | ENZYME REPLACEMENT | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GM1 GANGLIOSIDOSIS | GENETICS & HEREDITY | BIOLOGICAL EVALUATION | MURINE G(M1)-GANGLIOSIDOSIS
Journal Article
BRAIN & DEVELOPMENT, ISSN 0387-7604, 06/2013, Volume 35, Issue 6, pp. 515 - 523
Journal Article
Journal Article
Journal Article
Indian pediatrics, 12/2016, Volume 53, Issue 12, p. 1133
Journal Article
Journal Article
The Journal of Pathology, ISSN 0022-3417, 09/2015, Volume 237, Issue 1, pp. 98 - 110
GM1 gangliosidosis ( GM1 ) is an inherited neurodegenerative disorder caused by mutations in the lysosomal β‐galactosidase (β‐gal) gene. Insufficient β‐gal... 
human disease model | induced pluripotent stem cells | GM1 gangliosidosis | neural progenitor cells | inflammasome | SOMATIC-CELLS | NEURAL ROSETTES | MOUSE | PATHOLOGY | PATHOGENESIS | UNFOLDED PROTEIN RESPONSE | G(M1)-GANGLIOSIDOSIS | ONCOLOGY | NLRP3 | DIFFERENTIATION | ACCUMULATION | BRAIN | Gangliosidosis, GM1 - metabolism | Inflammasomes - metabolism | Humans | Gangliosidosis, GM1 - immunology | Cellular Reprogramming | Neural Stem Cells - immunology | Lysosomes - metabolism | Inflammasomes - antagonists & inhibitors | Time Factors | Cell Shape | beta-Galactosidase - metabolism | Neural Stem Cells - transplantation | Interleukin 1 Receptor Antagonist Protein - pharmacology | Induced Pluripotent Stem Cells - metabolism | Biomarkers - metabolism | Induced Pluripotent Stem Cells - pathology | Cell Line | Induced Pluripotent Stem Cells - drug effects | Signal Transduction | Induced Pluripotent Stem Cells - transplantation | Mice, Inbred C57BL | Neural Stem Cells - drug effects | Gangliosidosis, GM1 - pathology | Genotype | Neural Stem Cells - pathology | Phenotype | Animals | Inflammasomes - immunology | Induced Pluripotent Stem Cells - immunology | Neural Stem Cells - metabolism | Immunologic Factors - pharmacology | Nervous system diseases | DNA microarrays | Analysis | Models | Cell differentiation | Embryonic stem cells | Intermediate filament proteins | Gangliosides
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