X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (31) 31
animals (28) 28
mice (26) 26
life sciences (22) 22
male (16) 16
skeletal muscle (12) 12
skeletal-muscle (12) 12
humans (11) 11
disease models, animal (10) 10
genetics (10) 10
muscles (10) 10
musculoskeletal system (10) 10
genetics & heredity (9) 9
medicine, research & experimental (9) 9
mice, knockout (9) 9
mice, transgenic (9) 9
article (8) 8
biochemistry & molecular biology (8) 8
cellular biology (8) 8
muscle, skeletal - metabolism (8) 8
muscle, skeletal - pathology (8) 8
muscle, skeletal - physiopathology (8) 8
phenotype (8) 8
clinical neurology (7) 7
mice, inbred c57bl (7) 7
neurosciences (7) 7
expression (6) 6
female (6) 6
in-vivo (6) 6
muscle contraction (6) 6
muscle contraction - physiology (6) 6
muscular-dystrophy (6) 6
proteins (6) 6
gene (5) 5
molecular biology (5) 5
mouse model (5) 5
muscle, skeletal - physiology (5) 5
mutation (5) 5
rodents (5) 5
biochemistry, molecular biology (4) 4
cell biology (4) 4
cytology (4) 4
fatigue (4) 4
gene expression (4) 4
gene therapy (4) 4
genetic aspects (4) 4
genetic vectors (4) 4
hemophilia-b (4) 4
hypertrophy (4) 4
lipid phosphatase (4) 4
liver (4) 4
mdx mice (4) 4
mouse (4) 4
multidisciplinary sciences (4) 4
mutations (4) 4
myopathies, structural, congenital - genetics (4) 4
myotonic dystrophy (4) 4
myotonic dystrophy - genetics (4) 4
neurology (4) 4
original (4) 4
aav vector (3) 3
adenoassociated virus (3) 3
age (3) 3
age factors (3) 3
atrophy (3) 3
biology (3) 3
biotechnology & applied microbiology (3) 3
cancer (3) 3
cell line (3) 3
congenital, hereditary, and neonatal diseases and abnormalities (3) 3
ctg repeat (3) 3
dependovirus - genetics (3) 3
dystrophin - genetics (3) 3
dystrophin - metabolism (3) 3
electric stimulation (3) 3
energy metabolism (3) 3
exercise (3) 3
gene-expression (3) 3
glycogen (3) 3
health aspects (3) 3
immunology (3) 3
inactivation (3) 3
kinases (3) 3
medicine (3) 3
metabolism (3) 3
mice, 129 strain (3) 3
mice, inbred mdx (3) 3
muscle proteins - metabolism (3) 3
muscle weakness (3) 3
muscle weakness - genetics (3) 3
muscle weakness - physiopathology (3) 3
muscle, skeletal - drug effects (3) 3
musculoskeletal diseases (3) 3
myostatin (3) 3
myotubularin (3) 3
neurons and cognition (3) 3
physiological aspects (3) 3
physiology (3) 3
protein tyrosine phosphatases, non-receptor - genetics (3) 3
protein-serine-threonine kinases - genetics (3) 3
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nature Medicine, ISSN 1078-8956, 2011, Volume 17, Issue 6, pp. 720 - 725
Myotonic dystrophy is the most common muscular dystrophy in adults and the first recognized example of an RNA-mediated disease. Congenital myotonic dystrophy... 
MEDICINE, RESEARCH & EXPERIMENTAL | CTG REPEAT | CENTRONUCLEAR MYOPATHY | PROTEIN-KINASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | MYOTUBULAR MYOPATHY | CELL BIOLOGY | SKELETAL-MUSCLE | MESSENGER-RNA | GENE | CHLORIDE CHANNEL | AMPHIPHYSIN-2 BIN1 | MUTATIONS | Cell Line | RNA-Binding Proteins - physiology | Humans | Alternative Splicing - physiology | Exons - genetics | Muscle Weakness - genetics | Protein Isoforms - physiology | Tumor Suppressor Proteins - physiology | Adaptor Proteins, Signal Transducing - physiology | Myotonic Dystrophy - physiopathology | Animals | Tumor Suppressor Proteins - genetics | Adaptor Proteins, Signal Transducing - genetics | Myotonic Dystrophy - genetics | Mice | Nuclear Proteins - physiology | Muscle Weakness - physiopathology | Nuclear Proteins - genetics | Muscle Fibers, Skeletal - physiology | RNA-Binding Proteins - metabolism | Protein Isoforms - genetics | Muscle weakness | Myotonic dystrophy | RNA | Physiological aspects | Genetic aspects | Research | Risk factors | Musculoskeletal diseases | Musculoskeletal system | Biosynthesis | Protein synthesis | Muscular dystrophy | Index Medicus | Alternative Splicing | Exons | Myotonic Dystrophy | RNA-Binding Proteins | Nuclear Proteins | Life Sciences | Adaptor Proteins, Signal Transducing | Muscle Fibers, Skeletal | Protein Isoforms | Muscle Weakness | Tumor Suppressor Proteins | Cancer | Naturvetenskap | Natural Sciences
Journal Article
Journal of Neuropathology & Experimental Neurology, ISSN 0022-3069, 04/2018, Volume 77, Issue 4, pp. 282 - 295
Abstract X-linked myotubular myopathy (XLMTM) is a severe congenital disorder in male infants that leads to generalized skeletal muscle weakness and is... 
AAV vector | MTMR1 | MTMR2 | Myotubular myopathy | Mouse model | MTM1 | Myotubularin | MOUSE SKELETAL-MUSCLE | PROLONGS SURVIVAL | MARIE-TOOTH-DISEASE | CA2+ RELEASE | MUSCULAR-DYSTROPHY | PATHOLOGY | NEUROSCIENCES | MDX MICE | CLINICAL NEUROLOGY | GENE | LIPID PHOSPHATASE | CENTRONUCLEAR MYOPATHIES | PHOSPHATIDYLINOSITOL 3-PHOSPHATASES | Musculoskeletal system | Rodents | Index Medicus | Original
Journal Article
The Journal of Cell Biology, ISSN 0021-9525, 12/2009, Volume 187, Issue 6, pp. 859 - 874
Mammalian target of rapamycin (mTOR) is a key regulator of cell growth that associates with raptor and rictor to form the mTOR complex 1 (mTORC1) and mTORC2,... 
Birds of prey | Messenger RNA | Glycogen | Stem cells | Muscles | Mice | Gene expression regulation | Muscle fibers | Insulin | Skeletal muscle | MAMMALIAN TARGET | RAPAMYCIN | GLYCOGEN-SYNTHASE | CELLS | SIGNALING PATHWAYS | GLYCOPROTEIN COMPLEX | MUSCULAR-DYSTROPHY | ANIMAL-MODELS | DEFICIENT SKELETAL-MUSCLE | MDX MICE | CELL BIOLOGY | Muscular Dystrophy, Animal - genetics | Utrophin - metabolism | Age Factors | Muscular Dystrophy, Animal - physiopathology | Glycogen - metabolism | Muscle, Skeletal - drug effects | Female | Regulatory-Associated Protein of mTOR | Proto-Oncogene Proteins c-akt - metabolism | Dystrophin - metabolism | Rapamycin-Insensitive Companion of mTOR Protein | Severity of Illness Index | Muscle, Skeletal - enzymology | Mitochondria, Muscle - enzymology | Transduction, Genetic | Oxidation-Reduction | Mice, Inbred C57BL | Phosphotransferases (Alcohol Group Acceptor) - deficiency | Carrier Proteins - antagonists & inhibitors | Cells, Cultured | Rats | Electroporation | Phosphotransferases (Alcohol Group Acceptor) - genetics | Sirolimus - pharmacology | Mice, Knockout | Phosphotransferases (Alcohol Group Acceptor) - metabolism | Carrier Proteins - genetics | Phosphotransferases (Alcohol Group Acceptor) - antagonists & inhibitors | Adaptor Proteins, Signal Transducing | Animals | Carrier Proteins - metabolism | Muscle Contraction | Muscular Dystrophy, Animal - enzymology | Dystrophin - genetics | Energy Metabolism | Muscle, Skeletal - physiopathology | Glucose - metabolism | TOR Serine-Threonine Kinases | Enzyme Activation | Mutation | Glucose metabolism | Utrophin | Physiological aspects | Glucose | Dystrophin | Dextrose | Proteins | Pathology | Cell growth | Oxidation | Biochemistry | Metabolism | Kinases | Index Medicus | Life Sciences
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 12/2016, Volume 113, Issue 50, pp. 14432 - 14437
Journal Article
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 4098 - 13
Journal Article
Journal Article
American Journal of Physiology - Regulatory Integrative and Comparative Physiology, ISSN 0363-6119, 08/2014, Volume 307, Issue 4, pp. R444 - R454
Journal Article
PLoS Genetics, ISSN 1553-7390, 11/2012, Volume 8, Issue 11, pp. e1003043 - e1003043
Journal Article
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 8, pp. e23094 - e23094
Selenium is an essential trace element and selenoprotein N (SelN) was the first selenium-containing protein shown to be directly involved in human inherited... 
SKELETAL-MUSCLE | OXIDATIVE STRESS | ZEBRAFISH | ATROPHY | BIOLOGY | MUSCULAR-DYSTROPHY | PHENOTYPE | MICE | MUTATIONS | FORCED SWIMMING TEST | EXPRESSION | Protein Carbonylation | Selenoproteins - genetics | Muscle Contraction - genetics | Immunoblotting | Male | Mice, 129 Strain | Motor Activity | Stress, Psychological - psychology | Embryo, Mammalian - metabolism | Swimming - psychology | Gene Expression Regulation, Developmental | Muscular Diseases - physiopathology | Muscle Proteins - metabolism | Female | Selenoproteins - physiology | Muscle Proteins - physiology | Disease Models, Animal | Muscular Diseases - metabolism | Mice, Inbred C57BL | Mice, Transgenic | Reverse Transcriptase Polymerase Chain Reaction | Selenoproteins - metabolism | Mice, Knockout | Muscle Proteins - genetics | Phenotype | Animals | Embryo, Mammalian - embryology | Muscle, Skeletal - abnormalities | Muscle Contraction - physiology | Muscle, Skeletal - physiopathology | Mice | Muscle, Skeletal - pathology | Muscular Diseases - genetics | Stress, Psychological - physiopathology | Exercise | Animal behavior | Analysis | Genes | Muscles | Genetic aspects | Physical exercise | Oxidative stress | Calcium | Spine | Homeostasis | Muscle recovery | Amino acids | Rigidity | Inactivation | Proteins | Gene targeting | Rodents | Aging | Swimming | Selenium | Calcium homeostasis | Phenotypes | Deactivation | Contractility | Gene expression | Embryos | Muscle contraction | Skeletal muscle | Hereditary diseases | Musculoskeletal system | Life span | Trace elements | In vivo methods and tests | Mutation | Curvature | Myopathy | Index Medicus | Life Sciences | Molecular biology | Biochemistry, Molecular Biology
Journal Article
Molecular Therapy, ISSN 1525-0016, 03/2018, Volume 26, Issue 3, pp. 890 - 901
Glycogen storage disease type III (GSDIII) is an autosomal recessive disorder caused by a deficiency of glycogen-debranching enzyme (GDE), which results in... 
dual AAV vectors | acid-alpha-glucosidase | neuromuscular disease | gene therapy | glycogen storage disease type III | glycogenosis | Cori disease | adeno-associated vector | MEDICINE, RESEARCH & EXPERIMENTAL | EFFICACY | ADENOASSOCIATED VIRUS | TRANSDUCTION | GENOME | THERAPY | GLYCOGEN-STORAGE-DISEASE | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | AAV | MOUSE MODEL | IN-VIVO | GENETICS & HEREDITY | VECTORS | Dependovirus - genetics | Glycogen Storage Disease Type III - metabolism | Genetic Vectors - administration & dosage | Male | Muscle, Skeletal - metabolism | Hepatocytes - metabolism | Glycogen - metabolism | Glycogen Debranching Enzyme System - genetics | Disease Models, Animal | Gene Transfer Techniques | Gene Expression | Glycogen Storage Disease Type III - therapy | Glycogen Debranching Enzyme System - metabolism | Glycogen Storage Disease Type III - diagnosis | Liver - metabolism | Blood Glucose | Organ Specificity | Genetic Vectors - genetics | Glycogen Storage Disease Type III - genetics | Mice, Knockout | Phenotype | Animals | Biomarkers | Mice | Enzyme Activation | Genetic Therapy - methods | Enzymes | Phenotypes | Statistical analysis | Gene transfer | Glycogen | Cardiomyopathy | Liver | Glucose | Gene expression | Hypoglycemia | Metabolism | Vectors (Biology) | Hereditary diseases | Storage diseases | Consortia | Glucose metabolism | Musculoskeletal system | Biopsy | Gene therapy | Age | Index Medicus | Original
Journal Article