X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (3560) 3560
Publication (235) 235
Book Chapter (75) 75
Book Review (27) 27
Dissertation (16) 16
Conference Proceeding (13) 13
Government Document (2) 2
Paper (1) 1
Reference (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (1406) 1406
animals (1338) 1338
neurosciences (968) 968
gm1 ganglioside (864) 864
index medicus (825) 825
male (778) 778
gm1 (728) 728
biochemistry & molecular biology (727) 727
gangliosides (714) 714
ganglioside gm1 (620) 620
female (614) 614
mice (560) 560
clinical neurology (522) 522
rats (462) 462
ganglioside (358) 358
anti-gm1 antibodies (329) 329
adult (319) 319
g ganglioside - immunology (294) 294
middle aged (290) 290
immunology (283) 283
guillain-barre-syndrome (268) 268
g ganglioside - metabolism (259) 259
cell biology (248) 248
lipids (236) 236
biophysics (235) 235
guillain-barre syndrome (222) 222
brain (221) 221
g ganglioside - pharmacology (219) 219
cells, cultured (218) 218
antibodies (197) 197
gangliosides - immunology (196) 196
neuropathy (195) 195
gm1 gangliosidosis (194) 194
aged (192) 192
lipid rafts (187) 187
molecular sequence data (186) 186
cholesterol (183) 183
cholera toxin (176) 176
multifocal motor neuropathy (176) 176
proteins (175) 175
neurology (173) 173
cholera-toxin (168) 168
gangliosides - metabolism (168) 168
cells (167) 167
disease (167) 167
analysis (166) 166
conduction block (162) 162
binding (159) 159
neurons (159) 159
pharmacology & pharmacy (157) 157
enzyme-linked immunosorbent assay (152) 152
glycosphingolipids (151) 151
alzheimers-disease (150) 150
membranes (150) 150
gangliosidosis, gm1 - genetics (142) 142
expression (139) 139
mice, inbred c57bl (136) 136
alzheimer's disease (133) 133
protein (133) 133
beta-galactosidase - genetics (128) 128
mutation (128) 128
nerve growth-factor (128) 128
rats, sprague-dawley (128) 128
g ganglioside - chemistry (125) 125
disease models, animal (124) 124
guillain-barré syndrome (123) 123
infant (122) 122
carbohydrate sequence (120) 120
adolescent (117) 117
child (117) 117
polyneuropathy (116) 116
protein binding (115) 115
receptor (114) 114
cell membrane - metabolism (111) 111
biochemistry, general (109) 109
asialo gm1 (108) 108
guillain-barre syndrome - immunology (108) 108
immunohistochemistry (108) 108
article (107) 107
glycolipids (106) 106
time factors (106) 106
neurons - metabolism (105) 105
research (105) 105
autoantibodies - blood (104) 104
medicine, research & experimental (103) 103
plasma-membrane (103) 103
physiological aspects (101) 101
pathology (100) 100
activation (99) 99
cell line (99) 99
gangliosides - chemistry (99) 99
cholera toxin - metabolism (97) 97
nervous-system (94) 94
neurons - drug effects (94) 94
amyotrophic-lateral-sclerosis (93) 93
multidisciplinary sciences (90) 90
apoptosis (89) 89
brain - metabolism (89) 89
chromatography, thin layer (89) 89
polyradiculoneuropathy - immunology (89) 89
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (3474) 3474
Japanese (44) 44
French (40) 40
German (19) 19
Spanish (17) 17
Chinese (15) 15
Italian (6) 6
Portuguese (5) 5
Russian (5) 5
Polish (4) 4
Catalan (1) 1
Czech (1) 1
Hungarian (1) 1
Korean (1) 1
Serbian (1) 1
Swedish (1) 1
Turkish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 08/2008, Volume 94, Issue 4, pp. 391 - 396
Journal Article
Cellular and Molecular Life Sciences, ISSN 1420-682X, 6/2014, Volume 71, Issue 11, pp. 2017 - 2032
The ubiquitous distribution of lysosomes and their heterogeneous protein composition reflects the versatility of these organelles in maintaining cell... 
Life Sciences | Biochemistry, general | Protective protein/cathepsin A (PPCA) | Sialic acid | Elastin-binding protein (EBP) | Life Sciences, general | Neuraminidase 1 (NEU1) | Lysosomal exocytosis | β-Galactosidase (β-GAL) | Biomedicine general | Cell Biology | CATHEPSIN-A | CHAPERONE-MEDIATED AUTOPHAGY | BIOCHEMISTRY & MOLECULAR BIOLOGY | PLASMA-MEMBRANE | CELL BIOLOGY | beta-Galactosidase (beta-GAL) | HUMAN PROTECTIVE PROTEIN | ACID BETA-GALACTOSIDASE | GM1 GANGLIOSIDOSIS | MOUSE MODEL | ENDOPLASMIC-RETICULUM | ENZYME REPLACEMENT THERAPY | MEMBRANE-ASSOCIATED SIALIDASE | Lysosomal Storage Diseases - enzymology | Humans | Lysosomes - genetics | Lysosomes - enzymology | Multienzyme Complexes - metabolism | Neuraminidase - genetics | Gangliosidosis, GM1 - genetics | Cathepsin A - genetics | beta-Galactosidase - metabolism | Cathepsin A - metabolism | Lysosomes - pathology | Gangliosidosis, GM1 - enzymology | Disease Models, Animal | Mucolipidoses - enzymology | Signal Transduction | Gene Expression Regulation | Lysosomal Storage Diseases - genetics | Neuraminidase - metabolism | Gangliosidosis, GM1 - pathology | Mucolipidoses - genetics | Multienzyme Complexes - genetics | Lysosomal Storage Diseases - pathology | Mice, Knockout | Mucolipidoses - pathology | Animals | Mice | beta-Galactosidase - genetics | Enzymes | Hydrolases | Gangliosides | Elastin | Organic acids | Protein binding | Cellular biology | Metabolic disorders | Protective Protein | lysosomal exocytosis | Cathepsin A (PPCA) | sialic acid | elastin binding protein (EBP)
Journal Article
Molecular Genetics and Metabolism, ISSN 1096-7192, 06/2008, Volume 94, Issue 2, pp. 204 - 211
GM1 gangliosidosis is an inherited neurodegenerative disorder caused by lysosomal β-galactosidase deficiency, resulting in the storage of GM1 and GA1,... 
N-Butyldeoxynojirimycin | Glycosphingolipid | Imino sugar | GA1 | N-Butyldeoxygalactonojirimycin | GM1 | Lysosomal storage disease | Miglustat | GM1 gangliosidosis | Substrate reduction therapy | STORAGE | MEDICINE, RESEARCH & EXPERIMENTAL | GLYCOLIPID BIOSYNTHESIS | imino sugar | lysosomal storage disease | GLUCOSYLCERAMIDE SYNTHASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | PREVENTION | glycosphingolipid | SANDHOFF-DISEASE MICE | N-butyldeoxynojirimycin | GENETICS & HEREDITY | BETA-GALACTOSIDASE | substrate reduction therapy | N-butyldeoxygalactonojirimycin | miglustat | ACCUMULATION | INHIBITOR | BUTYLDEOXYGALACTONOJIRIMYCIN | Gangliosidosis, GM1 - metabolism | Gangliosidosis, GM1 - physiopathology | Humans | Motor Activity - drug effects | Protein Transport - drug effects | Gangliosidosis, GM1 - immunology | Brain - metabolism | Enzyme Inhibitors - administration & dosage | 1-Deoxynojirimycin - therapeutic use | Glucosyltransferases - metabolism | beta-Galactosidase - metabolism | 1-Deoxynojirimycin - administration & dosage | 1-Deoxynojirimycin - analogs & derivatives | Disease Models, Animal | Glucosyltransferases - antagonists & inhibitors | beta-Galactosidase - antagonists & inhibitors | Enzyme Inhibitors - therapeutic use | Gangliosidosis, GM1 - drug therapy | Mice, Knockout | Brain - drug effects | Animals | Feces - chemistry | Glycosphingolipids - antagonists & inhibitors | Glycosphingolipids - metabolism | Mice | beta-Galactosidase - genetics | Macrophage Activation - drug effects | Brain - immunology | Gangliosides | Analysis
Journal Article
BBA - Molecular Basis of Disease, ISSN 0925-4439, 2011, Volume 1812, Issue 7, pp. 782 - 790
Journal Article
Chemical Communications, ISSN 1359-7345, 4/2016, Volume 52, Issue 32, pp. 5497 - 5515
Lysosomal storage disorders (LSDs) are often caused by mutations that destabilize native folding and impair the trafficking of enzymes, leading to premature... 
Gangliosidosis, GM1 - metabolism | Molecular Mimicry | Carbohydrates - chemistry | Gaucher Disease - metabolism | Fabry Disease - metabolism | Humans | Molecular Chaperones - therapeutic use | Fabry Disease - drug therapy | Gangliosidosis, GM1 - drug therapy | Gaucher Disease - drug therapy
Journal Article
MOLECULAR NEUROBIOLOGY, ISSN 0893-7648, 10/2019, Volume 56, Issue 10, pp. 6673 - 6702
Recently, we demonstrated that the GM1 oligosaccharide, II(3)Neu5Ac-Gg(4) (OligoGM1), administered to cultured murine Neuro2a neuroblastoma cells interacts... 
Neuroprotection | Shotgun label-free proteomic | PROTECTION | MEMBRANE | KINASE INHIBITORS | INDUCTION | NEUROSCIENCES | NERVE GROWTH-FACTOR | GM1 ganglioside | Plasma membrane signaling | METABOLISM | HUMAN-BRAIN | TRK RECEPTORS | GM1 oligosaccharide chain | TrkA neurotrophin receptor | PARKINSONS-DISEASE | GANGLIOSIDE GM1
Journal Article