X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1262) 1262
Book Review (334) 334
Publication (152) 152
Book Chapter (18) 18
Book / eBook (17) 17
Newspaper Article (10) 10
Conference Proceeding (2) 2
Newsletter (2) 2
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (1054) 1054
animals (540) 540
humans (500) 500
proteins (383) 383
biochemistry & molecular biology (342) 342
mice (293) 293
physiological aspects (258) 258
fatty acids (226) 226
metabolism (220) 220
gene expression (219) 219
enzymes (217) 217
lipids (210) 210
mutation (195) 195
male (194) 194
cell biology (193) 193
analysis (185) 185
research (182) 182
genes (160) 160
genetic aspects (160) 160
female (153) 153
neurosciences (145) 145
plant sciences (144) 144
biosynthesis (141) 141
research article (138) 138
genetics & heredity (137) 137
article (133) 133
neuronal ceroid-lipofuscinoses - genetics (133) 133
expression (132) 132
multidisciplinary sciences (127) 127
lipid metabolism (124) 124
protein (124) 124
signal transduction (113) 113
rodents (107) 107
neuronal ceroid-lipofuscinosis (106) 106
life sciences (104) 104
mice, knockout (104) 104
biochemistry (103) 103
molecular sequence data (103) 103
biology (102) 102
gene (102) 102
fatty acids - metabolism (99) 99
medicine (98) 98
biotechnology & applied microbiology (97) 97
gene expression profiling (93) 93
science (91) 91
gene-expression (88) 88
phenotype (88) 88
microbiology (86) 86
mice, inbred c57bl (85) 85
mitochondria (85) 85
neuronal ceroid lipofuscinosis (85) 85
neurons (84) 84
disease models, animal (82) 82
membrane proteins - genetics (82) 82
disease (79) 79
genetics (79) 79
proteomics (79) 79
batten-disease (78) 78
mutations (77) 77
amino acid sequence (76) 76
genetic research (76) 76
apoptosis (75) 75
neurodegeneration (75) 75
physiology (75) 75
oxidative stress (74) 74
thiolester hydrolases - genetics (74) 74
endocrinology & metabolism (73) 73
palmitoyl-protein thioesterase (73) 73
molecular biology (71) 71
amino acids (70) 70
biotechnology (70) 70
clinical neurology (70) 70
plants (70) 70
health aspects (69) 69
neuronal ceroid-lipofuscinoses - pathology (68) 68
thiolester hydrolases - metabolism (68) 68
liver (67) 67
biophysics (66) 66
cells (66) 66
genomics (65) 65
rats (62) 62
escherichia-coli (60) 60
identification (60) 60
mouse model (60) 60
saccharomyces-cerevisiae (59) 59
homeostasis (58) 58
metabolites (58) 58
gene expression regulation (57) 57
genomes (57) 57
kinases (57) 57
protein binding (57) 57
brain (56) 56
liver - metabolism (56) 56
review (56) 56
food and beverages (55) 55
arabidopsis-thaliana (54) 54
cells, cultured (54) 54
medicine, research & experimental (54) 54
neuronal ceroid-lipofuscinoses - metabolism (53) 53
batten disease (52) 52
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (7) 7
Collection Dvlpm't (Acquisitions) - Vendor file (3) 3
UofT at Mississauga - Stacks (3) 3
Chemistry (A D Allen) - Stacks (2) 2
Engineering & Comp. Sci. - Stacks (1) 1
Online Resources - Online (1) 1
St. Michael's College (John M. Kelly) - 2nd Floor (1) 1
UofT at Scarborough - Stacks (1) 1
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Experimental Cell Research, ISSN 0014-4827, 2006, Volume 312, Issue 9, pp. 1540 - 1553
Journal Article
Cell Stem Cell, ISSN 1934-5909, 2009, Volume 5, Issue 3, pp. 310 - 319
Journal Article
Journal of Child Neurology, ISSN 0883-0738, 9/2013, Volume 28, Issue 9, pp. 1106 - 1111
The neuronal ceroid lipofuscinoses are the most common autosomal recessive neurodegenerative disorders in children, with a worldwide incidence of 1 in 100 000... 
palmitoyl-protein thioesterase 1 | CLN1 | infantile neuronal ceroid lipofuscinosis | Batten disease | PROTEIN THIOESTERASE DEFICIENCY | TRANSLATION | CHILDHOOD | VARIANT | CLINICAL NEUROLOGY | PPT | NONSENSE-MEDIATED DECAY | DISEASE | PEDIATRICS | TERMINATION | Male | Neuronal Ceroid-Lipofuscinoses - genetics | Mutation | Membrane Proteins - genetics | Child | Humans | Index Medicus | Abundance
Journal Article
Journal Article
BBA - Molecular Basis of Disease, ISSN 0925-4439, 2006, Volume 1762, Issue 10, pp. 865 - 872
For the majority of families affected by one of the neuronal ceroid lipofuscinoses (NCLs), a biochemical and/or genetic diagnosis can be achieved. In an... 
Phenotype | NCL | Diagnosis | NICL | phenotype | PROTEIN THIOESTERASE DEFICIENCY | INFANTILE CLN1 | NEURORADIOLOGICAL FINDINGS | BIOCHEMISTRY & MOLECULAR BIOLOGY | POSTNATAL DIAGNOSIS | diagnosis | FOLLOW-UP | BIOPHYSICS | JANSKY-BIELSCHOWSKY DISEASE | JUVENILE | BATTEN-DISEASE | MUTATIONS | CATHEPSIN-D DEFICIENCY | Neurons | Children's hospitals
Journal Article
Journal Article
Journal Article
Journal of Inherited Metabolic Disease, ISSN 0141-8955, 10/2011, Volume 34, Issue 5, pp. 1083 - 1093
Journal Article
Journal of Developmental and Physical Disabilities, ISSN 1056-263X, 4/2012, Volume 24, Issue 2, pp. 155 - 165
The aim of this case study was to record and highlight the functional decline in a 23 year old man diagnosed with atypical juvenile neuronal ceroid... 
AJNCL, Batten Disease | Pediatrics | Child and School Psychology | Gait Analysis | Psychology | Physical Disabilities | Public Health/Gesundheitswesen | Rehabilitation | GAIT DEVIATION INDEX | PROTEIN THIOESTERASE DEFICIENCY | NCL | Gene mutations | Neurons | Genetic aspects | Mutation
Journal Article
Journal Article