X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (4630) 4630
Book Review (591) 591
Publication (545) 545
Newsletter (51) 51
Book Chapter (36) 36
Conference Proceeding (28) 28
Book / eBook (3) 3
Magazine Article (3) 3
Newspaper Article (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (4382) 4382
animals (3256) 3256
humans (2473) 2473
dystrophin (2203) 2203
mice (2140) 2140
dystrophin - metabolism (1577) 1577
dystrophin - genetics (1516) 1516
male (1324) 1324
duchenne muscular-dystrophy (1101) 1101
skeletal-muscle (1095) 1095
muscle, skeletal - metabolism (1070) 1070
biochemistry & molecular biology (989) 989
utrophin (959) 959
muscular dystrophy (922) 922
mice, inbred mdx (912) 912
neurosciences (901) 901
cell biology (870) 870
expression (851) 851
female (785) 785
duchenne muscular dystrophy (783) 783
mice, inbred c57bl (739) 739
immunohistochemistry (634) 634
muscular dystrophy, duchenne - genetics (614) 614
proteins (614) 614
genetics & heredity (612) 612
mutation (574) 574
muscle, skeletal - pathology (559) 559
muscular dystrophy, duchenne - metabolism (545) 545
disease models, animal (529) 529
molecular sequence data (505) 505
protein (496) 496
muscular dystrophies - metabolism (480) 480
gene (473) 473
gene expression (448) 448
clinical neurology (444) 444
medicine, research & experimental (441) 441
dystrophin - deficiency (439) 439
rats (433) 433
muscular dystrophies - genetics (431) 431
cells, cultured (427) 427
glycoprotein complex (425) 425
cytoskeletal proteins - metabolism (419) 419
muscles (415) 415
rodents (406) 406
research (397) 397
muscular-dystrophy (393) 393
analysis (392) 392
muscle (391) 391
adult (386) 386
skeletal muscle (386) 386
mdx mice (385) 385
musculoskeletal system (382) 382
musculoskeletal diseases (358) 358
child (354) 354
amino acid sequence (348) 348
membrane proteins - metabolism (347) 347
blotting, western (346) 346
mouse (344) 344
phenotype (343) 343
mdx mouse (342) 342
dystrophin-glycoprotein complex (334) 334
physiological aspects (324) 324
genetic aspects (320) 320
muscular dystrophy, duchenne - pathology (320) 320
muscular dystrophy, animal - metabolism (318) 318
muscles - metabolism (315) 315
article (313) 313
muscular dystrophy, duchenne - therapy (307) 307
base sequence (305) 305
muscle proteins - metabolism (301) 301
cells (298) 298
cell line (296) 296
protein binding (296) 296
mice, knockout (293) 293
pathology (291) 291
dystroglycans (290) 290
biotechnology & applied microbiology (288) 288
muscle fibers, skeletal - metabolism (284) 284
multidisciplinary sciences (280) 280
adolescent (276) 276
localization (275) 275
membrane glycoproteins - metabolism (273) 273
muscular dystrophy, animal - genetics (267) 267
sarcolemma (266) 266
dystrophin-associated proteins (261) 261
muscular dystrophy, duchenne - physiopathology (261) 261
dystroglycan (260) 260
genetics (259) 259
physiology (257) 257
exons (249) 249
regeneration (246) 246
extracellular-matrix (244) 244
dystrophin - analysis (241) 241
in-vivo (240) 240
muscular dystrophies - pathology (240) 240
cytoskeletal proteins - genetics (239) 239
mice, transgenic (239) 239
genes (237) 237
child, preschool (236) 236
duchenne's muscular dystrophy (236) 236
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (4579) 4579
Japanese (34) 34
Chinese (28) 28
Russian (18) 18
Spanish (11) 11
French (9) 9
German (5) 5
Dutch (3) 3
Polish (3) 3
Czech (2) 2
Hungarian (1) 1
Italian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal Article
Journal Article
Cell Death and Differentiation, ISSN 1350-9047, 2013, Volume 20, Issue 9, pp. 1194 - 1208
Journal Article
Nature, ISSN 0028-0836, 07/2017, Volume 547, Issue 7662, pp. 227 - 231
The regenerative capacity of the adult mammalian heart is limited, because of the reduced ability of cardiomyocytes to progress through mitosis(1). Endogenous... 
PRESSURE-OVERLOAD | GENE | ADULT HEART REGENERATION | MULTIDISCIPLINARY SCIENCES | IN-VIVO | MOUSE MODEL | MUSCLE | DUCHENNE MUSCULAR-DYSTROPHY | MICE | Protein-Serine-Threonine Kinases - deficiency | Phosphorylation | Cell Proliferation | Glycoproteins - metabolism | Dystroglycans - metabolism | Male | Phosphoproteins - metabolism | Heart Failure - prevention & control | Multiprotein Complexes - metabolism | Dystrophin - deficiency | Mice, Inbred mdx | Cardiomyopathies | Glycoproteins - deficiency | Multiprotein Complexes - deficiency | Dystrophin - metabolism | Protein-Serine-Threonine Kinases - metabolism | Myocytes, Cardiac - cytology | Mice, Inbred C57BL | Organ Size | Heart Failure - genetics | Pressure | Multiprotein Complexes - chemistry | Animals | Dystrophin - genetics | Myocytes, Cardiac - metabolism | Protein Binding | Mice | Muscular Dystrophy, Duchenne - metabolism | Muscular Dystrophy, Duchenne - genetics | Adaptor Proteins, Signal Transducing - metabolism | Heart | Genes | Homeostasis | Genomes | Kinases | Muscular dystrophy | Cell growth | Actin | Duchenne's muscular dystrophy | Cell cycle | Extracellular matrix | Heart diseases | Dystrophin | Deoxyribonucleic acid--DNA | Heart failure | Dystroglycan | Glycoprotein | Cardiomyocytes | Studies | Yes-associated protein | Regeneration | Point mutation | Cytoskeleton | Dystrophy | Mutation | Index Medicus
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
Journal Article
Developmental Biology, ISSN 0012-1606, 2008, Volume 318, Issue 1, pp. 92 - 101
Mechanical instability of skeletal muscle cells is the major cause of congenital muscular dystrophy. Here we show that the zebrafish mutant, that lacks a... 
MLP | loc | Integrin | Laminin | ILK | Zebrafish | Muscular dystrophy | β-parvin | Myotendinous junctions | CONGENITAL MUSCULAR-DYSTROPHY | PROTEIN-KINASE | beta-parvin | DEVELOPMENTAL BIOLOGY | DILATED CARDIOMYOPATHY | muscular dystrophy | CELL-SUBSTRATE INTERACTION | myotendinous junctions | MECHANICAL STRETCH SENSOR | laminin | MICE | zebrafish | integrin | EXPRESSION | EMBRYOS | Paxillin - metabolism | Paxillin - genetics | Zebrafish - anatomy & histology | Antigens, CD - classification | Humans | Oligonucleotides, Antisense - metabolism | Extracellular Matrix - metabolism | Integrin alpha Chains - classification | Muscle, Skeletal - metabolism | Phylogeny | Muscle, Skeletal - cytology | Zebrafish - embryology | Antigens, CD - genetics | Recombinant Fusion Proteins - metabolism | Antigens, CD - metabolism | Lim Kinases - metabolism | Extracellular Matrix - genetics | Actinin - genetics | Muscle, Skeletal - embryology | Protein-Serine-Threonine Kinases - metabolism | Actinin - metabolism | Zebrafish Proteins - metabolism | Protein-Serine-Threonine Kinases - genetics | Integrin alpha Chains - metabolism | Laminin - genetics | Two-Hybrid System Techniques | Phenotype | Animals | Oligonucleotides, Antisense - genetics | Cell Adhesion - physiology | Zebrafish - metabolism | Cytoskeleton - metabolism | Lim Kinases - genetics | Recombinant Fusion Proteins - genetics | Laminin - metabolism | Zebrafish Proteins - genetics | Integrin alpha Chains - genetics | Dystrophin | Utrophin | Integrins | Index Medicus
Journal Article
Nature Cell Biology, ISSN 1465-7392, 01/2018, Volume 20, Issue 1, pp. 46 - 57
Human pluripotent stem cells (hPSCs) can be directed to differentiate into skeletal muscle progenitor cells (SMPCs). However, the myogenicity of hPSC-SMPCs... 
PLURIPOTENT STEM-CELLS | DIRECTED DIFFERENTIATION | IN-VITRO | MYOGENIC DIFFERENTIATION | RNA-SEQ | FUNCTIONAL-ANALYSIS | DUCHENNE MUSCULAR-DYSTROPHY | SATELLITE CELLS | FETAL | LARGE GENE LISTS | CELL BIOLOGY | Receptor, ErbB-3 - metabolism | Humans | Middle Aged | PAX7 Transcription Factor - genetics | Male | PAX7 Transcription Factor - metabolism | Receptors, Nerve Growth Factor - metabolism | Muscle Fibers, Skeletal - metabolism | Myoblasts - metabolism | Gene Expression Regulation, Developmental | Myoblasts - cytology | Adult | Female | Myosins - metabolism | Cell Differentiation | Induced Pluripotent Stem Cells - cytology | Muscular Dystrophy, Duchenne - therapy | Dystrophin - metabolism | Induced Pluripotent Stem Cells - metabolism | Signal Transduction | Muscular Dystrophy, Duchenne - pathology | Receptor, ErbB-3 - genetics | Myosins - genetics | Nerve Tissue Proteins - genetics | Gene Editing | Receptors, Nerve Growth Factor - genetics | Nerve Tissue Proteins - metabolism | Transforming Growth Factor beta - genetics | Dystrophin - genetics | CRISPR-Cas Systems | Muscle Development - genetics | Muscle Fibers, Skeletal - cytology | Aged | Muscular Dystrophy, Duchenne - metabolism | Muscular Dystrophy, Duchenne - genetics | Transforming Growth Factor beta - metabolism | RNA sequencing | Usage | Growth | Stem cells | Muscle cells | Fetus | Research | Comparative analysis | Transforming growth factors | CRISPR | Satellite RNA | Fetuses | Muscles | Satellite cells | ErbB-3 protein | Ribonucleic acid--RNA | Cell surface | Muscular dystrophy | Myogenesis | Skeletal muscle | Gene sequencing | Musculoskeletal system | Signaling | Receptors | Nerve growth factor receptors | Duchenne's muscular dystrophy | Cells (biology) | Dystrophy | Differentiation | Dystrophin | Pluripotency | Index Medicus
Journal Article
Journal of Cell Biology, ISSN 0021-9525, 07/2017, Volume 216, Issue 7, pp. 2131 - 2150
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 06/2017, Volume 292, Issue 24, pp. 10180 - 10196
We have previously shown that dysbindin is a potent inducer of cardiomyocyte hypertrophy via activation of Rho-dependent serum-response factor (SRF) signaling.... 
COACTIVATOR HTIF1 | SCHIZOPHRENIA-RELATED PROTEIN | NUCLEAR RECEPTORS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CARDIAC-HYPERTROPHY | IN-VIVO | TRIPARTITE MOTIF | SERUM RESPONSE FACTOR | FAMILY PROTEINS | MUSCLE RING FINGER-1 | E3 UBIQUITIN LIGASE | Serum Response Factor - agonists | Serum Response Factor - genetics | Cardiomyopathy, Dilated - pathology | Rats, Wistar | Serum Response Factor - antagonists & inhibitors | Humans | Ubiquitin-Protein Ligases - antagonists & inhibitors | Recombinant Fusion Proteins - metabolism | Dystrophin-Associated Proteins - genetics | Dystrophin-Associated Proteins - metabolism | RNA Interference | Dystrophin-Associated Proteins - chemistry | Proteolysis | HEK293 Cells | Protein Stability | Peptide Fragments - genetics | Animals, Newborn | Recombinant Proteins - metabolism | Peptide Fragments - metabolism | Myocytes, Cardiac - cytology | Signal Transduction | Serum Response Factor - metabolism | Tripartite Motif Proteins - antagonists & inhibitors | Cardiomyopathy, Hypertrophic - metabolism | Carrier Proteins - antagonists & inhibitors | Cells, Cultured | Ubiquitin-Protein Ligases - metabolism | Rats | Recombinant Proteins - chemistry | Tripartite Motif Proteins - genetics | Transcription Factors - antagonists & inhibitors | Recombinant Fusion Proteins - chemistry | Transcription Factors - genetics | Cardiomyopathy, Dilated - metabolism | Transcription Factors - metabolism | Carrier Proteins - genetics | Myocytes, Cardiac - pathology | Peptide Fragments - chemistry | Animals | Carrier Proteins - metabolism | Myocytes, Cardiac - metabolism | Tripartite Motif Proteins - metabolism | Ubiquitin-Protein Ligases - genetics | Dysbindin | Apoptosis | Cardiomyopathy, Hypertrophic - pathology | Index Medicus | Molecular Bases of Disease | cardiac signaling | cardiomyocyte | TRIM24 | apoptosis | SRF-signaling | cardiac hypertrophy | cardiomyopathy | dysbindin | TRIM32 | X-linked inhibitor of apoptosis protein (XIAP)
Journal Article
NATURE, ISSN 0028-0836, 07/2017, Volume 547, Issue 7662, pp. 179 - 179
Journal Article