X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1586) 1586
Publication (257) 257
Newsletter (153) 153
Book / eBook (94) 94
Newspaper Article (71) 71
Book Review (36) 36
Book Chapter (32) 32
Dissertation (10) 10
Conference Proceeding (5) 5
Magazine Article (4) 4
Government Document (3) 3
Trade Publication Article (2) 2
Reference (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (1141) 1141
index medicus (915) 915
spinal muscular atrophy (751) 751
animals (472) 472
male (472) 472
female (453) 453
neurosciences (328) 328
clinical neurology (305) 305
spinal muscular-atrophy (291) 291
research (281) 281
muscular atrophy, spinal - genetics (266) 266
mice (250) 250
child (239) 239
adult (223) 223
proteins (218) 218
survival (200) 200
pediatrics (199) 199
neurology (188) 188
mutation (183) 183
analysis (180) 180
atrophy (179) 179
care and treatment (179) 179
mouse model (176) 176
disease (175) 175
disease models, animal (175) 175
neurons (175) 175
muscles (174) 174
child, preschool (173) 173
nervous system diseases (170) 170
amyotrophic-lateral-sclerosis (169) 169
health aspects (167) 167
adolescent (164) 164
article (162) 162
infant (159) 159
children (155) 155
genetics & heredity (155) 155
muscular dystrophy (153) 153
biochemistry & molecular biology (152) 152
genetic aspects (151) 151
medical research (143) 143
nervous system (143) 143
diagnosis (137) 137
middle aged (136) 136
phenotype (135) 135
survival of motor neuron 1 protein - genetics (132) 132
duchenne muscular-dystrophy (131) 131
smn protein (130) 130
neuromuscular diseases (129) 129
mortality (124) 124
cell biology (123) 123
medicine (123) 123
rodents (123) 123
amyotrophic lateral sclerosis (121) 121
aged (114) 114
muscular atrophy, spinal - pathology (113) 113
muscular atrophy, spinal - metabolism (111) 111
physiological aspects (110) 110
gene (108) 108
clinical trials (107) 107
skeletal-muscle (106) 106
medicine, experimental (105) 105
gene therapy (103) 103
musculoskeletal system (103) 103
medicine, research & experimental (102) 102
motor neurons (102) 102
diseases (101) 101
muscle, skeletal - pathology (101) 101
gene expression (100) 100
genetics (100) 100
infants (98) 98
patients (98) 98
sma (98) 98
muscular atrophy, spinal - therapy (97) 97
survival of motor neuron 2 protein - genetics (96) 96
genes (94) 94
risk factors (94) 94
messenger-rna (91) 91
single nucleotide (91) 91
research article (90) 90
cell survival (89) 89
muscular atrophy, spinal - physiopathology (88) 88
motor neurons - metabolism (87) 87
review (86) 86
infant, newborn (85) 85
respiratory system (85) 85
retrospective studies (85) 85
treatment outcome (85) 85
medicine & public health (83) 83
multidisciplinary sciences (83) 83
smn complex proteins (83) 83
identification (82) 82
muscular system (82) 82
protein (82) 82
muscle, skeletal - metabolism (81) 81
studies (81) 81
duchenne muscular dystrophy (80) 80
muscular diseases (80) 80
expression (77) 77
smn (77) 77
nerve tissue proteins - genetics (76) 76
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (79) 79
Holland Bloorview Kids Rehabilitation - Stacks (14) 14
Collection Dvlpm't (Acquisitions) - Closed Orders (3) 3
Providence Healthcare - Reference (3) 3
UofT at Scarborough - Stacks (3) 3
Humber River Regional Hospital - Church Stacks (2) 2
Lakeridge Health Sciences - Oshawa (2) 2
Providence Healthcare - Stacks (2) 2
St. Michael's Hospital - Stacks (2) 2
West Park Healthcare Centre - Stacks (2) 2
Collection Dvlpm't (Acquisitions) - Vendor file (1) 1
Credit Valley Hospital - Reference (1) 1
Dentistry (Harry R Abbott) - May be requested in 6-10 wks (1) 1
Gerstein Science - Reference (1) 1
Markham Stouffville Hospital - Stacks (1) 1
Mt Sinai Hospital - Pathology (1) 1
Online Resources - Online (1) 1
Robarts - Stacks (1) 1
Scarborough Hospital - General (1) 1
Sunnybrook Health Sciences Centre - Holland Reference (1) 1
Sunnybrook Health Sciences Centre - Holland Stacks (1) 1
Toronto East General Hospital - Stacks (1) 1
UTL at Downsview - May be requested (1) 1
UofT at Mississauga - Oversize (1) 1
UofT at Mississauga - Reference (1) 1
UofT at Mississauga - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1931) 1931
Spanish (4) 4
French (3) 3
Italian (2) 2
Japanese (2) 2
Portuguese (2) 2
Chinese (1) 1
German (1) 1
Russian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nature Chemical Biology, ISSN 1552-4450, 07/2015, Volume 11, Issue 7, pp. 511 - 517
Journal Article
Neuron, ISSN 0896-6273, 2009, Volume 63, Issue 3, pp. 316 - 328
Expansion of a polyglutamine tract in the androgen receptor (AR) causes spinal and bulbar muscular atrophy (SBMA). We previously showed that Akt-mediated... 
PROTEINS | HUMDISEASE | MOLNEURO | INSULIN | SURVIVAL | ANDROGEN RECEPTOR | SKELETAL-MUSCLE | HYPERTROPHY | KENNEDY-DISEASE | DEGRADATION | FOXO TRANSCRIPTION FACTORS | EXPRESSION | NEUROSCIENCES | GROWTH-FACTOR-I | Insulin-Like Growth Factor I - pharmacology | Humans | Receptors, Androgen - metabolism | Peptides - genetics | Ubiquitin - metabolism | Cercopithecus aethiops | Trinucleotide Repeat Expansion - physiology | Muscle, Skeletal - metabolism | Insulin-Like Growth Factor I - genetics | Phosphatidylinositol 3-Kinases - metabolism | Muscular Atrophy, Spinal - genetics | Phosphorylation - genetics | Muscular Atrophy - physiopathology | Peptides - metabolism | Transfection - methods | Time Factors | Muscle, Skeletal - drug effects | Muscle Proteins - metabolism | Behavior, Animal - drug effects | Phosphorylation - drug effects | Trinucleotide Repeat Expansion - drug effects | Oncogene Protein v-akt - metabolism | Disease Models, Animal | Muscular Atrophy, Spinal - mortality | Gene Expression Regulation - genetics | Mice, Inbred C57BL | Enzyme Inhibitors - pharmacology | Behavior, Animal - physiology | Mice, Transgenic | Mutation - genetics | Muscular Atrophy, Spinal - pathology | Serine - metabolism | Gene Expression Regulation - drug effects | Muscle Proteins - genetics | Animals | Receptors, Androgen - genetics | Muscular Atrophy, Spinal - therapy | Mice | Cell Line, Transformed | Insulin-Like Growth Factor I - metabolism | Medical colleges | Neurosciences | Peptide hormones | Neurons | Atrophy, Muscular | Growth factors | Cell culture | Phosphorylation | Statistical analysis | Disease | Insulin-like growth factors | Muscular system | Kinases | Molecular weight | Pathology | Musculoskeletal system | Rodents | Ligands | Index Medicus | Polyglutamine disease | spinal and bulbar muscular atrophy | androgen receptor | insulin-like growth factor 1 | skeletal muscle
Journal Article
Journal of Neuroscience, ISSN 0270-6474, 09/2010, Volume 30, Issue 36, pp. 12005 - 12019
Spinal muscular atrophy (SMA) is a common (similar to 1: 6400) autosomal recessive neuromuscular disorder caused by a paucity of the survival of motor neuron... 
LOCALIZATION | TERMINALS | PRODUCT | MOUSE MODEL | IN-VIVO | LEADS | RELEASE | IDENTIFICATION | NEUROSCIENCES | NEUROMUSCULAR-JUNCTIONS | SINGLE NUCLEOTIDE | Membrane Potentials - genetics | Age Factors | Synaptic Transmission - genetics | Humans | Gene Expression Regulation, Developmental - genetics | Nerve Degeneration - genetics | Synapses - pathology | Stem Cells - metabolism | Survival of Motor Neuron 2 Protein - metabolism | Choline O-Acetyltransferase - metabolism | Motor Neurons - pathology | Behavior, Animal | Muscular Atrophy, Spinal - genetics | Basic Helix-Loop-Helix Transcription Factors - metabolism | Survival of Motor Neuron 2 Protein - genetics | Isometric Contraction - physiology | Miniature Postsynaptic Potentials - genetics | Neuromuscular Junction - pathology | Disease Models, Animal | Animals, Newborn | Muscular Atrophy, Spinal - mortality | Muscular Atrophy, Spinal - metabolism | Receptors, Cholinergic - metabolism | Synapses - physiology | Kaplan-Meier Estimate | Mice, Transgenic | Oligodendrocyte Transcription Factor 2 | Mutation - genetics | Muscular Atrophy, Spinal - pathology | Motor Neurons - metabolism | Nerve Tissue Proteins - metabolism | Motor Activity - genetics | Patch-Clamp Techniques | Animals | Cell Count - methods | Analysis of Variance | Muscle, Skeletal - physiopathology | Luminescent Proteins - genetics | Mice | Muscle, Skeletal - pathology | Electromyography - methods
Journal Article
Journal Article
Journal Article
Molecular Therapy, ISSN 1525-0016, 02/2015, Volume 23, Issue 2, pp. 270 - 277
Journal Article