X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (2215) 2215
Newsletter (947) 947
Newspaper Article (689) 689
Publication (228) 228
Book / eBook (98) 98
Book Chapter (34) 34
Book Review (28) 28
Conference Proceeding (4) 4
Dissertation (2) 2
Streaming Video (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
muscular dystrophy (1685) 1685
humans (1398) 1398
index medicus (954) 954
research (954) 954
male (909) 909
female (718) 718
neuromuscular diseases (713) 713
duchenne muscular dystrophy (685) 685
neurosciences (653) 653
clinical neurology (599) 599
mutation (577) 577
animals (575) 575
genetic aspects (508) 508
adult (494) 494
muscle, skeletal - pathology (450) 450
muscles (398) 398
proteins (395) 395
middle aged (382) 382
reports (340) 340
medical research (326) 326
dystrophin (313) 313
physical fitness (313) 313
mice (310) 310
neurology (309) 309
disease (304) 304
analysis (287) 287
medicine, experimental (284) 284
genes (282) 282
child (280) 280
rodents (273) 273
utrophin (269) 269
muscle, skeletal - metabolism (261) 261
biopsy (257) 257
phenotype (256) 256
adolescent (254) 254
skeletal-muscle (252) 252
genetic research (251) 251
musculoskeletal system (234) 234
pathology (226) 226
genetic disorders (223) 223
care and treatment (214) 214
pedigree (206) 206
aged (200) 200
child, preschool (200) 200
gene expression (195) 195
genetics (194) 194
gene (190) 190
muscular diseases - genetics (187) 187
myopathy (181) 181
diagnosis (179) 179
genetics & heredity (177) 177
medicine (175) 175
atrophy (174) 174
muscular dystrophies - genetics (173) 173
cell biology (166) 166
expression (164) 164
gene therapy (162) 162
muscular atrophy - pathology (162) 162
muscular diseases - pathology (159) 159
pediatrics (159) 159
disease models, animal (158) 158
magnetic resonance imaging (157) 157
skeletal muscle (157) 157
infant (151) 151
article (143) 143
muscle (143) 143
muscle, skeletal - physiopathology (140) 140
muscular dystrophies - pathology (139) 139
muscular-dystrophy (138) 138
muscles - pathology (137) 137
immunohistochemistry (135) 135
biochemistry & molecular biology (133) 133
spinal muscular atrophy (129) 129
health aspects (127) 127
mutations (127) 127
electromyography (123) 123
mutation - genetics (118) 118
research article (118) 118
patients (117) 117
muscle proteins - genetics (116) 116
clinical trials (115) 115
physiology (115) 115
genomics (114) 114
physiological aspects (114) 114
dystrophy (110) 110
dna mutational analysis (109) 109
muscular disorders, atrophic - genetics (109) 109
muscle proteins - metabolism (106) 106
diseases (101) 101
protein (101) 101
stem cells (101) 101
cardiomyopathy (100) 100
muscular atrophy - genetics (100) 100
multidisciplinary sciences (99) 99
muscular atrophy - metabolism (97) 97
medicine, research & experimental (96) 96
muscular system (95) 95
young adult (95) 95
studies (94) 94
development and progression (92) 92
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (86) 86
Holland Bloorview Kids Rehabilitation - Stacks (9) 9
Providence Healthcare - Reference (3) 3
Providence Healthcare - Stacks (3) 3
Collection Dvlpm't (Acquisitions) - Vendor file (2) 2
Lakeridge Health Sciences - Oshawa (2) 2
Online Resources - Online (2) 2
St. Michael's Hospital - Stacks (2) 2
UTL at Downsview - May be requested (2) 2
Collection Dvlpm't (Acquisitions) - Closed Orders (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
Humber River Regional Hospital - Church Stacks (1) 1
Markham Stouffville Hospital - Stacks (1) 1
Mt Sinai Hospital - Pathology (1) 1
Scarborough Hospital - General (1) 1
Sunnybrook Health Sciences Centre - Holland Reference (1) 1
Sunnybrook Health Sciences Centre - Holland Stacks (1) 1
Sunnybrook Health Sciences Centre - Online (1) 1
Toronto East General Hospital - Stacks (1) 1
UofT at Mississauga - Oversize (1) 1
UofT at Mississauga - Reference (1) 1
UofT at Mississauga - Stacks (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


Neuron, ISSN 0896-6273, 04/2014, Volume 82, Issue 2, pp. 295 - 307
Journal Article
Nature, ISSN 0028-0836, 06/2007, Volume 447, Issue 7146, pp. 860 - 864
Journal Article
Journal of Experimental Medicine, ISSN 0022-1007, 06/2013, Volume 210, Issue 6, pp. 1137 - 1151
Journal Article
PLoS ONE, ISSN 1932-6203, 12/2012, Volume 7, Issue 12, p. e51238
Important insights concerning the molecular basis of skeletal muscle disuse-atrophy and aging related muscle loss have been obtained in cell culture and animal... 
PROLONGED BED REST | MESSENGER-RNA | MULTIDISCIPLINARY SCIENCES | IN-VIVO | GENE-EXPRESSION | HUMAN QUADRICEPS MUSCLE | LIMB IMMOBILIZATION | NF-KAPPA-B | PROTEIN-SYNTHESIS | DENERVATION ATROPHY | UBIQUITIN-PROTEASOME PATHWAY | Muscle Strength - genetics | Muscle Contraction - genetics | Humans | Middle Aged | Transcriptome | Apoptosis - genetics | Male | Muscle, Skeletal - metabolism | Muscular Disorders, Atrophic - physiopathology | NF-kappa B - metabolism | Muscle Fibers, Skeletal - metabolism | Tripartite Motif Proteins | Young Adult | Heat-Shock Proteins - genetics | Aging - genetics | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Adult | Muscular Disorders, Atrophic - pathology | Autophagy - genetics | Proto-Oncogene Proteins c-akt - metabolism | Muscular Disorders, Atrophic - metabolism | Cytokines - metabolism | Muscular Disorders, Atrophic - genetics | Organ Size | Signal Transduction - genetics | Transcription Factors - genetics | Forkhead Transcription Factors - genetics | Aging - pathology | Muscle Proteins - genetics | Aging - physiology | Muscle, Skeletal - physiopathology | Muscle Fibers, Skeletal - pathology | Aged | Muscle, Skeletal - pathology | Transcription, Genetic - genetics | Ubiquitin-Protein Ligases - genetics | Insulin-Like Growth Factor I - metabolism | Aging - metabolism | Muscles | Genetic transcription | RNA | Analysis | Cell culture | Health sciences | Phosphorylation | Animal models | Transcription factors | Transcription | Gene regulation | Immobilization | AKT protein | Insulin-like growth factors | Autophagy | Sports medicine | Proteins | Atrophy | Rodents | Aging | Tumor necrosis factor-TNF | Age | Inflammation | Gene expression | Skeletal muscle | Medicine | Studies | Biomechanics | Musculoskeletal system | Signaling | Exercise physiology | Microscopy | Protein synthesis | Phagocytosis | Apoptosis
Journal Article
JOURNAL OF CLINICAL INVESTIGATION, ISSN 0021-9738, 12/2007, Volume 117, Issue 12, pp. 3940 - 3951
Statins inhibit HMG-CoA reductase, a key enzyme in cholesterol synthesis, and are widely used to treat hyper-cholesterolemia. These drugs can lead to a number... 
MEDICINE, RESEARCH & EXPERIMENTAL | SKELETAL-MUSCLE | INDUCED RHABDOMYOLYSIS | IN-VITRO | IGF-I | PROTEASOME PATHWAY | FIBER TYPES | MITOCHONDRIAL-FUNCTION | GENE-EXPRESSION | ATROPHY INVOLVE | MYOPATHY | SKP Cullin F-Box Protein Ligases - genetics | Humans | Heat-Shock Proteins - genetics | Hydroxymethylglutaryl CoA Reductases - metabolism | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha | Muscle Proteins - metabolism | Trans-Activators - genetics | Muscular Disorders, Atrophic - enzymology | Muscular Disorders, Atrophic - pathology | Muscle, Skeletal - enzymology | Lovastatin - adverse effects | Zebrafish Proteins - metabolism | Heat-Shock Proteins - metabolism | Muscular Disorders, Atrophic - genetics | SKP Cullin F-Box Protein Ligases - metabolism | Transcription Factors - genetics | Cholesterol - metabolism | Zebrafish - genetics | Muscle Proteins - genetics | Transcription Factors - metabolism | Animals | Hydroxymethylglutaryl-CoA Reductase Inhibitors - adverse effects | Zebrafish - metabolism | Muscle Fibers, Skeletal - pathology | Trans-Activators - metabolism | Mice | Muscle, Skeletal - pathology | Zebrafish Proteins - genetics | Hydroxymethylglutaryl CoA Reductases - genetics | Muscle Fibers, Skeletal - enzymology | Muscular Disorders, Atrophic - chemically induced | Complications and side effects | Hypercholesterolemia | Dosage and administration | Research | Cholesterol metabolism | Risk factors | Statins
Journal Article
Neuron, ISSN 0896-6273, 2010, Volume 67, Issue 6, pp. 936 - 952
Spinobulbar muscular atrophy (SBMA) is a neurodegenerative disease caused by expansion of a polyglutamine tract in the androgen receptor (AR). This mutation... 
MEDIATED TRANSACTIVATION | MOTOR-NEURON DEGENERATION | POLYGLUTAMINE-INDUCED DISEASE | PROSTATE-CANCER CELLS | FAST AXONAL-TRANSPORT | TUMOR-SUPPRESSOR | HISTONE ACETYLTRANSFERASE ACTIVITY | TRANSGENIC MOUSE MODEL | NH2-TERMINAL DOMAIN | NEUROSCIENCES | ACTIVATION FUNCTION 2 | Eye - pathology | Salivary Glands - pathology | Locomotion - genetics | Humans | Receptors, Androgen - metabolism | Actins - metabolism | Blindness - pathology | Tubulin - metabolism | Transfection - methods | Furylfuramide - metabolism | Statistics, Nonparametric | Female | Receptors, Androgen - chemistry | Muscular Disorders, Atrophic - pathology | RNA Interference - physiology | Principal Component Analysis | Neuromuscular Junction - pathology | Disease Models, Animal | Eye - metabolism | Animals, Genetically Modified | Gene Expression Regulation - genetics | Oligonucleotide Array Sequence Analysis - methods | Drosophila | Muscular Disorders, Atrophic - genetics | Gene Expression Profiling - methods | Mutation - genetics | Blindness - genetics | Protein Transport - genetics | Trinucleotide Repeat Expansion | Motor Neurons - metabolism | Phenotype | Animals | Receptors, Androgen - genetics | Mutagenesis - physiology | Drosophila Proteins - genetics | Larva - physiology | Muscular Disorders, Atrophic - etiology | Salivary Glands - metabolism | Cell Line, Transformed | Neurosciences | Nervous system diseases | Analysis | Hormones | Universities and colleges | Atrophy, Muscular | Genetic screening | Studies | Proteins | Genotype & phenotype | Disease | Insects | Pathogenesis | Toxicity | Neurons | Rodents | Ligands | Mutation | Deoxyribonucleic acid--DNA | Androgen receptors
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 05/2016, Volume 25, Issue 10, pp. 1979 - 1989
Journal Article
Journal Article
FASEB Journal, ISSN 0892-6638, 06/2004, Volume 18, Issue 9, pp. 1025 - 1027
Skeletal muscle atrophy occurs as a consequence of injury, illness, surgery, and muscle disuse, impacting appreciably on health care costs and patient quality... 
proteasome | ACTIVATION | hypertrophy | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRANSCRIPTION | MUSCULAR-DYSTROPHY | CALPAIN SYSTEM | ubiquitin ligases | BURN INJURY | CELL BIOLOGY | calpain | BIOLOGY | CALCINEURIN | PROTEIN BREAKDOWN | KAPPA-B PATHWAY | proteolysis | UBIQUITIN-PROTEASOME PATHWAY | Insulin-Like Growth Factor I - pharmacology | Humans | Immobilization | RNA, Messenger - analysis | Male | Muscle, Skeletal - metabolism | Muscular Disorders, Atrophic - physiopathology | Gene Expression Profiling | Calpain - genetics | Proteasome Endopeptidase Complex | Muscular Atrophy - physiopathology | Time Factors | Adult | Isometric Contraction | Muscular Disorders, Atrophic - pathology | Muscular Atrophy - pathology | RNA, Messenger - genetics | Gene Expression Regulation | Protein-Serine-Threonine Kinases - genetics | Muscular Disorders, Atrophic - genetics | Organ Size | Muscular Atrophy - genetics | Multienzyme Complexes - genetics | Signal Transduction - genetics | Ubiquitin - genetics | Muscle, Skeletal - physiology | I-kappa B Kinase | Muscular Disorders, Atrophic - rehabilitation | Transforming Growth Factor beta - genetics | Signal Transduction - drug effects | Cysteine Endopeptidases - genetics | Adolescent | Muscular Atrophy - rehabilitation | Myostatin | Exercise - physiology | Muscle, Skeletal - pathology
Journal Article
Journal Article