X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (12833) 12833
Book Review (2952) 2952
Newspaper Article (2392) 2392
Publication (1938) 1938
Newsletter (325) 325
Book Chapter (166) 166
Book / eBook (138) 138
Conference Proceeding (84) 84
Magazine Article (59) 59
Trade Publication Article (30) 30
Dissertation (25) 25
Web Resource (13) 13
Government Document (6) 6
Reference (3) 3
Transcript (3) 3
Data Set (1) 1
Streaming Video (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (11352) 11352
animals (9666) 9666
humans (6595) 6595
mice (5969) 5969
muscular dystrophy (5879) 5879
male (2878) 2878
rodents (2829) 2829
cell biology (2560) 2560
skeletal-muscle (2465) 2465
biochemistry & molecular biology (2298) 2298
duchenne muscular-dystrophy (2262) 2262
mutation (2232) 2232
studies (2204) 2204
proteins (2111) 2111
muscle, skeletal - metabolism (2026) 2026
female (1932) 1932
expression (1891) 1891
muscular-dystrophy (1864) 1864
muscles (1858) 1858
research (1801) 1801
disease models, animal (1786) 1786
genetics & heredity (1767) 1767
neurosciences (1767) 1767
dystrophin (1751) 1751
duchenne muscular dystrophy (1680) 1680
mice, inbred c57bl (1663) 1663
mice, inbred mdx (1555) 1555
gene expression (1487) 1487
muscle, skeletal - pathology (1476) 1476
dystrophin - genetics (1465) 1465
musculoskeletal system (1396) 1396
gene therapy (1380) 1380
skeletal muscle (1358) 1358
genetic aspects (1321) 1321
analysis (1261) 1261
medicine, research & experimental (1221) 1221
multidisciplinary sciences (1217) 1217
article (1148) 1148
genetics (1148) 1148
muscular dystrophies - genetics (1144) 1144
physiological aspects (1049) 1049
research article (1045) 1045
gene (1039) 1039
clinical neurology (1035) 1035
genes (1016) 1016
phenotype (1005) 1005
medicine (997) 997
muscular dystrophy, animal - genetics (977) 977
cells, cultured (974) 974
mice, knockout (961) 961
muscular dystrophy, duchenne - genetics (952) 952
utrophin (941) 941
muscle (940) 940
regeneration (916) 916
disease (859) 859
dystrophy (859) 859
physiology (853) 853
muscular system (843) 843
mouse (838) 838
molecular sequence data (834) 834
pathology (825) 825
cells (823) 823
dystrophin - metabolism (807) 807
biotechnology & applied microbiology (798) 798
mdx mice (790) 790
cell line (777) 777
biology (763) 763
mice, transgenic (755) 755
neurology (749) 749
science (749) 749
health aspects (741) 741
in-vivo (741) 741
protein (734) 734
stem cells (725) 725
musculoskeletal diseases (704) 704
life sciences (674) 674
rats (669) 669
adult (667) 667
muscular dystrophy, animal - pathology (657) 657
medical research (640) 640
muscular dystrophy, duchenne - metabolism (638) 638
gene-expression (637) 637
mouse model (636) 636
mdx mouse (623) 623
muscular dystrophy, animal - metabolism (623) 623
muscle, skeletal - physiopathology (618) 618
muscular dystrophies - metabolism (618) 618
molecular biology (617) 617
muscle proteins - genetics (610) 610
signal transduction (605) 605
hospitals (601) 601
muscle, skeletal - physiology (601) 601
amino acid sequence (595) 595
muscular dystrophy, duchenne - therapy (594) 594
immunohistochemistry (591) 591
child (587) 587
gene expression regulation (581) 581
mutations (581) 581
muscle, skeletal - cytology (575) 575
muscle proteins - metabolism (569) 569
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (106) 106
Holland Bloorview Kids Rehabilitation - Stacks (12) 12
Collection Dvlpm't (Acquisitions) - Closed Orders (4) 4
Online Resources - Online (4) 4
Providence Healthcare - Stacks (4) 4
Providence Healthcare - Reference (3) 3
Collection Dvlpm't (Acquisitions) - Vendor file (2) 2
Humber River Regional Hospital - Church Stacks (2) 2
Lakeridge Health Sciences - Oshawa (2) 2
Scarborough Hospital - General (2) 2
St. Michael's Hospital - Stacks (2) 2
Sunnybrook Health Sciences Centre - Holland Stacks (2) 2
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (2) 2
Toronto East General Hospital - Stacks (2) 2
UofT at Scarborough - Stacks (2) 2
Credit Valley Hospital - Reference (1) 1
Dentistry (Harry R Abbott) - May be requested in 6-10 wks (1) 1
Dentistry (Harry R Abbott) - Stacks (1) 1
Gerstein Science - Reference (1) 1
Markham Stouffville Hospital - Stacks (1) 1
Mt Sinai Hospital - Pathology (1) 1
St. Michael's College (John M. Kelly) - 2nd Floor (1) 1
Sunnybrook Health Sciences Centre - Holland Reference (1) 1
Sunnybrook Health Sciences Centre - Online (1) 1
UTL at Downsview - May be requested (1) 1
UofT Schools - Stacks (1) 1
UofT at Mississauga - Oversize (1) 1
UofT at Mississauga - Reference (1) 1
UofT at Mississauga - Stacks (1) 1
West Park Healthcare Centre - Hospital Department (1) 1
West Park Healthcare Centre - Stacks (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (15669) 15669
Japanese (78) 78
Russian (31) 31
French (30) 30
Portuguese (19) 19
Chinese (17) 17
Spanish (11) 11
German (9) 9
Polish (5) 5
Finnish (2) 2
Hebrew (1) 1
Korean (1) 1
Slovak (1) 1
Swedish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nature Communications, ISSN 2041-1723, 07/2017, Volume 8, Issue 1, pp. 16105 - 16105
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 06/2014, Volume 124, Issue 6, pp. 2651 - 2667
Duchenne muscular dystrophy (DMD) is caused by mutations in the gene encoding dystrophin, which results in dysfunctional signaling pathways within muscle.... 
MEDICINE, RESEARCH & EXPERIMENTAL | SKELETAL-MUSCLE | MDX MOUSE | MESSENGER-RNAS | CENTRONUCLEAR MYOPATHY | GLYCOPROTEIN COMPLEX | C2C12 MYOBLAST | TUMOR-SUPPRESSOR | CELL-PROLIFERATION | MYOBLAST FUSION | PROTEIN-KINASE B | Muscular Dystrophy, Animal - genetics | Up-Regulation | Humans | Male | MicroRNAs - metabolism | Muscle, Skeletal - metabolism | Muscle Fibers, Skeletal - metabolism | Muscular Dystrophy, Animal - pathology | Guanine Nucleotide Exchange Factors - metabolism | Base Sequence | Mice, Inbred mdx | Muscular Dystrophy, Animal - metabolism | Proto-Oncogene Proteins c-akt - metabolism | Cell Line | Guanine Nucleotide Exchange Factors - genetics | Signal Transduction | Mice, Inbred C57BL | PTEN Phosphohydrolase - metabolism | Mice, Transgenic | Muscular Dystrophy, Duchenne - pathology | Nerve Tissue Proteins - genetics | Sequence Homology, Nucleic Acid | Nerve Tissue Proteins - metabolism | Carrier Proteins - genetics | Animals | Carrier Proteins - metabolism | Muscle Fibers, Skeletal - pathology | Mice | MicroRNAs - genetics | Muscular Dystrophy, Duchenne - metabolism | Muscle, Skeletal - pathology | Muscular Dystrophy, Duchenne - genetics | MicroRNA | Cellular signal transduction | Genetic aspects | Diagnosis | Properties | Genetic regulation | Muscular dystrophy | Muscular system | Mutation | Rodents | Index Medicus | Abridged Index Medicus
Journal Article
Science, ISSN 0036-8075, 12/2004, Volume 306, Issue 5702, pp. 1796 - 1799
Most mutations in the dystrophin gene create a frameshift or a stop in the mRNA and are associated with severe Duchenne muscular dystrophy. Exon skipping that... 
Proteins | Legs | Messenger RNA | Reverse transcriptase polymerase chain reaction | Exons | Duchenne muscular dystrophy | Muscles | Small nuclear RNA | Reports | Muscle fibers | Genetic mutation | SKELETAL-MUSCLE | HEMOPHILIA-B | MULTIDISCIPLINARY SCIENCES | MDX MOUSE MUSCLE | MUTATION | DUCHENNE MUSCULAR-DYSTROPHY | GENE-TRANSFER | EXPRESSION | PRE-MESSENGER-RNA | DELIVERY | VECTOR | Dependovirus - genetics | Genetic Therapy | Muscular Dystrophy, Animal - genetics | Muscular Dystrophy, Animal - physiopathology | Muscle, Skeletal - metabolism | RNA, Messenger - metabolism | Muscular Dystrophy, Animal - pathology | RNA Splicing | Transfection | Muscular Dystrophy, Duchenne - physiopathology | RNA, Small Nuclear - genetics | Mice, Inbred mdx | Muscular Dystrophy, Animal - therapy | Muscular Dystrophy, Duchenne - therapy | Dystrophin - metabolism | Oligonucleotides, Antisense - pharmacology | Introns | RNA, Messenger - genetics | Muscular Dystrophy, Duchenne - pathology | Muscle, Skeletal - physiology | Muscle Fibers, Skeletal - immunology | Animals | Muscle Contraction | Dystrophin - genetics | Muscle Fibers, Skeletal - pathology | Mice | Muscle, Skeletal - pathology | Muscular Dystrophy, Duchenne - genetics | Mutation | RNA, Small Nuclear - metabolism | Genetic Vectors | Usage | Care and treatment | Genetic aspects | Gene therapy | Exon (Molecular genetics) | Ribonucleic acid--RNA | Genes | Rodents | Muscular dystrophy | Index Medicus
Journal Article
Journal Article
Cell, ISSN 0092-8674, 11/2015, Volume 163, Issue 5, pp. 1204 - 1213
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 04/2017, Volume 114, Issue 16, pp. 4213 - 4218
Duchenne muscular dystrophy (DMD) is a lethal genetic disorder caused by an absence of the dystrophin protein in bodywide muscles, including the heart.... 
Cardiac Purkinje fibers | Dystrophic dog model | Peptide-conjugated morpholinos | Duchenne muscular dystrophy | Exon skipping | MUSCLE PATHOLOGY | MULTIDISCIPLINARY SCIENCES | DMD GENE | CARDIOMYOPATHY | BODYWIDE | dystrophic dog model | peptide-conjugated morpholinos | MDX52 MICE | OLIGONUCLEOTIDES | RESCUE | exon skipping | LABORATORY-ANIMALS | cardiac Purkinje fibers | EXPRESSION | EXONS 45-55 | Genetic Therapy | Muscular Dystrophy, Animal - genetics | Exons | Male | Muscle, Skeletal - metabolism | Muscular Dystrophy, Animal - complications | Muscular Dystrophy, Duchenne - complications | Cardiomyopathies - etiology | Cardiomyopathies - therapy | Cell-Penetrating Peptides - pharmacology | Animals | Dogs | Morpholinos - pharmacology | Female | Muscular Dystrophy, Animal - therapy | Muscle, Skeletal - pathology | Muscular Dystrophy, Duchenne - genetics | Muscular Dystrophy, Duchenne - therapy | Dystrophin - metabolism | Disease Models, Animal | Heart | Physiological aspects | Health aspects | Conduction | Intravenous administration | Peptides | Toxicity | Cardiomyopathy | Effects | Muscular dystrophy | Fibers | Oligomers | Nerve conduction | Arginine | Duchenne's muscular dystrophy | Degeneration | Polymers | Heart diseases | Dystrophin | EKG | Cardiac muscle | Abnormalities | Muscles | Skeletal muscle | Purkinje fibers | Myocardium | Dystrophy | Index Medicus | Biological Sciences
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2012, Volume 109, Issue 50, pp. 20614 - 20619
Duchenne muscular dystrophy (DMD) is a devastating genetic muscular disorder of childhood marked by progressive debilitating muscle weakness and wasting, and... 
Artificial satellites | Plasmids | Duchenne muscular dystrophy | Stem cells | Muscles | Electroporation | Muscle fibers | Skeletal muscle | Hypertrophy | Myoblasts | Noncanonical Wnt signaling | REGENERATION | MULTIDISCIPLINARY SCIENCES | MOUSE | SUSCEPTIBILITY | INJURY | SATELLITE STEM-CELLS | MDX MICE | DAMAGE | noncanonical Wnt signaling | SKELETAL-MUSCLE | CONTRACTION | PATHWAY | skeletal muscle | Genetic Therapy | Muscular Dystrophy, Animal - genetics | Muscular Dystrophy, Animal - drug therapy | Muscular Dystrophy, Animal - physiopathology | Humans | Male | RNA, Messenger - metabolism | Muscular Dystrophy, Animal - pathology | Gene Knockdown Techniques | Wnt Proteins - genetics | Mice, Inbred mdx | Plasmids - genetics | Electrochemotherapy | MEF2 Transcription Factors | Myogenic Regulatory Factors - genetics | Signal Transduction | Mice, Inbred C57BL | RNA, Messenger - genetics | Myogenic Regulatory Factors - metabolism | Wnt Proteins - therapeutic use | Regeneration - physiology | Animals | Muscle Contraction - physiology | Muscle, Skeletal - physiopathology | Mice | Wnt Proteins - physiology | Muscle, Skeletal - pathology | Plasmids - administration & dosage | Physiological aspects | Care and treatment | Rapamycin | Health aspects | Muscular dystrophy | Signal transduction | Genetic disorders | Rodents | Cells | Index Medicus | Biological Sciences
Journal Article
Journal Article