Articles

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (62014) 62014
Publication (7063) 7063
Book Review (940) 940
Newspaper Article (935) 935
Newsletter (506) 506
Book / eBook (488) 488
Book Chapter (353) 353
Conference Proceeding (94) 94
Magazine Article (72) 72
Dissertation (62) 62
Government Document (38) 38
Trade Publication Article (32) 32
Report (27) 27
Data Set (17) 17
Reference (17) 17
Transcript (14) 14
Web Resource (10) 10
Presentation (4) 4
Paper (2) 2
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
animals (39284) 39284
index medicus (28687) 28687
humans (24988) 24988
male (22060) 22060
rats (14360) 14360
female (12758) 12758
mice (11755) 11755
physiology (9849) 9849
research (8286) 8286
proteins (7039) 7039
cells, cultured (6980) 6980
muscles (6785) 6785
skeletal-muscle (6759) 6759
research article (6725) 6725
medicine (6724) 6724
rodents (6707) 6707
cell biology (6647) 6647
physiological aspects (6391) 6391
expression (6372) 6372
smooth muscle (6175) 6175
pharmacology & pharmacy (6136) 6136
multidisciplinary sciences (5659) 5659
gene expression (5494) 5494
smooth-muscle-cells (5126) 5126
biochemistry & molecular biology (4978) 4978
in vitro techniques (4916) 4916
health aspects (4880) 4880
science (4844) 4844
rats, sprague-dawley (4745) 4745
adult (4621) 4621
middle aged (4433) 4433
peripheral vascular disease (4366) 4366
signal transduction (4337) 4337
muscle, smooth, vascular - drug effects (4266) 4266
inflammation (4241) 4241
analysis (4194) 4194
oxidative stress (4157) 4157
dose-response relationship, drug (4121) 4121
muscle contraction - drug effects (4068) 4068
endocrinology & metabolism (4065) 4065
phosphorylation (3923) 3923
metabolism (3922) 3922
cardiac & cardiovascular systems (3915) 3915
cells (3897) 3897
kinases (3888) 3888
article (3861) 3861
muscle, skeletal - metabolism (3819) 3819
disease models, animal (3808) 3808
studies (3759) 3759
activation (3660) 3660
muscle (3640) 3640
muscle, skeletal - drug effects (3585) 3585
biology (3541) 3541
time factors (3536) 3536
apoptosis (3515) 3515
medicine, research & experimental (3415) 3415
atherosclerosis (3337) 3337
musculoskeletal system (3306) 3306
mice, inbred c57bl (3277) 3277
care and treatment (3263) 3263
neurosciences (3261) 3261
rats, wistar (3173) 3173
gene-expression (3159) 3159
aged (3123) 3123
hypertension (3058) 3058
muscle proteins (2972) 2972
diabetes (2885) 2885
calcium - metabolism (2865) 2865
cell line (2819) 2819
skeletal muscle (2764) 2764
smooth-muscle (2747) 2747
heart (2730) 2730
risk factors (2730) 2730
signal transduction - drug effects (2697) 2697
insulin (2657) 2657
inhibition (2631) 2631
biochemistry (2627) 2627
insulin resistance (2614) 2614
in-vitro (2585) 2585
cancer (2578) 2578
exercise (2576) 2576
disease (2564) 2564
nitric oxide (2510) 2510
genetic aspects (2483) 2483
muscle, smooth, vascular - metabolism (2458) 2458
in-vivo (2413) 2413
muscle contraction (2386) 2386
calcium (2325) 2325
proliferation (2322) 2322
rabbits (2291) 2291
respiratory system (2240) 2240
glucose (2190) 2190
endothelium (2177) 2177
review (2171) 2171
nitric-oxide (2134) 2134
obesity (2122) 2122
development and progression (2084) 2084
growth (2074) 2074
medical research (2067) 2067
muscle, smooth - drug effects (2061) 2061
more...
Library Location Library Location
Library Location Library Location
X
Sort by Item Count (A-Z)
Filter by Count
Gerstein Science - Stacks (381) 381
UTL at Downsview - May be requested (27) 27
UofT at Mississauga - Stacks (18) 18
Collection Dvlpm't (Acquisitions) - Closed Orders (17) 17
Collection Dvlpm't (Acquisitions) - Vendor file (16) 16
UofT at Scarborough - Stacks (11) 11
Holland Bloorview Kids Rehabilitation - Stacks (10) 10
Online Resources - Online (10) 10
Robarts - Stacks (8) 8
Dentistry (Harry R Abbott) - Withdrawn (5) 5
Sunnybrook Health Sciences Centre - Sunnybrook Stacks (5) 5
Dentistry (Harry R Abbott) - Stacks (4) 4
St. Michael's Hospital - Stacks (4) 4
Providence Healthcare - Stacks (3) 3
Scarborough Hospital - Birchmount (3) 3
Earth Sciences (Noranda) - Stacks (2) 2
Gerstein Science - Missing (2) 2
Humber River Regional Hospital - Church Stacks (2) 2
Physics - Stacks (2) 2
Providence Healthcare - Reference (2) 2
Royal Ontario Museum - Stacks (2) 2
Sunnybrook Health Sciences Centre - Holland Stacks (2) 2
West Park Healthcare Centre - Stacks (2) 2
Baycrest Hospital - Resident/Client Library (1) 1
Chemistry (A D Allen) - Stacks (1) 1
Credit Valley Hospital - Reserve desk (1) 1
Credit Valley Hospital - Stacks (1) 1
Dentistry (Harry R Abbott) - May be requested in 6-10 wks (1) 1
Earth Sciences (Noranda) - Missing (1) 1
Engineering & Comp. Sci. - Stacks (1) 1
Finch Reference (1) 1
Gerstein Science - Circulation Desk (1) 1
Gerstein Science - Not Returned (1) 1
Gerstein Science - Searching (1) 1
Humber River Regional Hospital - Online (1) 1
Indust. Rel's & Hum. Resources (Newman) - Library use only (1) 1
Lakeridge Health Sciences - Oshawa (1) 1
Markham Stouffville Hospital - Stacks (1) 1
Mt Sinai Hospital - Pathology (1) 1
OISE - Curriculum Resources (1) 1
OISE - May be requested in 6-10 wks (1) 1
Royal Ontario Museum - Periodical Stacks (1) 1
Scarborough Hospital - General (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 - Sunnybrook Reference (1) 1
Thomas Fisher Rare Book - Rare Book (1) 1
Toronto East General Hospital - Stacks (1) 1
Trillium Health Centre - Reserve desk (1) 1
UofT Schools - Stacks (1) 1
Victoria University E.J. Pratt - Stacks (1) 1
West Park Healthcare Centre - Hospital Department (1) 1
more...
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (63848) 63848
Russian (214) 214
German (112) 112
Japanese (74) 74
French (64) 64
Spanish (44) 44
Chinese (39) 39
Portuguese (20) 20
Ukrainian (19) 19
Polish (18) 18
Italian (11) 11
Korean (9) 9
Arabic (6) 6
Hungarian (5) 5
Slovak (5) 5
Turkish (4) 4
Bulgarian (3) 3
Dutch (3) 3
Danish (2) 2
Hebrew (2) 2
Swedish (2) 2
Croatian (1) 1
Czech (1) 1
Latin (1) 1
Lithuanian (1) 1
Norwegian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. Full Text Stem cell shape regulates a chondrogenic versus myogenic fate through rac1 and N-cadherin
by Gao, Lin and McBeath, Rowena and Chen, Christopher S
Stem Cells, ISSN 1066-5099, 03/2010, Volume 28, Issue 3, pp. 564 - 572
Human mesenchymal stem cells (hMSCs) are multipotent cells that can differentiate into many cell types. Chondrogenesis is induced in hMSCs cultured as a... 
Cell shape | Rac1 | Chondrogenesis | Smooth muscle cells | N-cadherin | Mesenchymal stem cells | MYOBLAST FUSION | CELL & TISSUE ENGINEERING | CELL BIOLOGY | ADHESION | ONCOLOGY | MESENCHYMAL PROGENITOR CELLS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENE-EXPRESSION | CYTOSKELETAL TENSION | DIFFERENTIATION | RHO-GTPASES | PROTEINS | HEMATOLOGY | MODULATION | MAMMARY EPITHELIAL-CELLS | Chondrocytes - cytology | Chondrogenesis - drug effects | Cadherins - metabolism | Humans | Extracellular Matrix - metabolism | Antigens, CD - genetics | Cell Lineage - drug effects | Transforming Growth Factor beta3 - metabolism | Antigens, CD - metabolism | Cell Differentiation - genetics | Chondrocytes - drug effects | Mesenchymal Stromal Cells - cytology | Cadherins - genetics | Myocytes, Smooth Muscle - drug effects | Myocytes, Smooth Muscle - cytology | Myocytes, Smooth Muscle - metabolism | Chondrocytes - metabolism | Transforming Growth Factor beta3 - pharmacology | Mesenchymal Stromal Cells - drug effects | Cell Adhesion - genetics | Muscle Development - physiology | Cells, Cultured | Gene Expression Regulation - physiology | Mesenchymal Stromal Cells - metabolism | Up-Regulation - genetics | Antigens, CD - drug effects | Cadherins - drug effects | Cell Adhesion - drug effects | Cell Lineage - physiology | Cell Shape - drug effects | Gene Expression Regulation - drug effects | Up-Regulation - drug effects | Chondrogenesis - physiology | Muscle Development - drug effects | rac1 GTP-Binding Protein - drug effects | Cell Differentiation - drug effects | Cell Shape - physiology | rac1 GTP-Binding Protein - metabolism | rac1 GTP-Binding Protein - genetics
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
2. Full Text Myogenic Progenitor Cells Control Extracellular Matrix Production by Fibroblasts during Skeletal Muscle Hypertrophy
by Fry, Christopher S and Kirby, Tyler J and Kosmac, Kate and McCarthy, John J and Peterson, Charlotte A
Cell Stem Cell, ISSN 1934-5909, 01/2017, Volume 20, Issue 1, pp. 56 - 69
Satellite cells, the predominant stem cell population in adult skeletal muscle, are activated in response to hypertrophic stimuli and give rise to myogenic... 
hypertrophy | Pax7 | exosomes | muscle | collagen | microRNA | fibrosis | muscle progenitor cells | extracellular matrix | satellite cells | FIBROSIS | REGENERATION | GENE-EXPRESSION | EXOSOMES | SELF-RENEWAL | DUCHENNE MUSCULAR-DYSTROPHY | MIRNAS | SATELLITE CELL | DIFFERENTIATION | CONNECTIVE-TISSUE | CELL & TISSUE ENGINEERING | CELL BIOLOGY | Exosomes - drug effects | Exosomes - metabolism | NIH 3T3 Cells | Cell Survival - genetics | Extracellular Matrix - metabolism | MicroRNAs - metabolism | PAX7 Transcription Factor - metabolism | Muscle Fibers, Skeletal - drug effects | Muscle Fibers, Skeletal - metabolism | Stem Cells - metabolism | Gene Knockdown Techniques | Cell Differentiation - genetics | Extracellular Matrix - genetics | Cell Nucleus - metabolism | Gene Deletion | Collagen - genetics | Fibroblasts - metabolism | Cell Survival - drug effects | Ribonuclease III - metabolism | Extracellular Matrix - drug effects | Satellite Cells, Skeletal Muscle - metabolism | Down-Regulation - drug effects | Fibroblasts - pathology | Down-Regulation - genetics | Collagen - metabolism | Satellite Cells, Skeletal Muscle - drug effects | Animals | Carrier Proteins - metabolism | Muscle Development - drug effects | Cell Differentiation - drug effects | Models, Biological | Fibroblasts - drug effects | Muscle Fibers, Skeletal - pathology | Tamoxifen - pharmacology | Muscle Development - genetics | Stem Cells - drug effects | Mice | MicroRNAs - genetics | Muscle, Skeletal - pathology | Cell Nucleus - drug effects | Hypertrophy | miRNA | Dicer | Muscle extracellular matrix
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. Full Text Fasudil improves survival and promotes skeletal muscle development in a mouse model of spinal muscular atrophy
by Bowerman, Melissa and Murray, Lyndsay M and Boyer, Justin G and Anderson, Carrie L and Kothary, Rashmi
BMC Medicine, ISSN 1741-7015, 03/2012, Volume 10, Issue 1, pp. 24 - 24
Background: Spinal muscular atrophy (SMA) is the leading genetic cause of infant death. It is caused by mutations/deletions of the survival motor neuron 1... 
Muscle | NMJ | Survival motor neuron protein | Fasudil | Spinal muscular atrophy | PROTEIN | fasudil | RHO-KINASE INHIBITOR | LIM-KINASE | SMN EXPRESSION | SINGLE NUCLEOTIDE | DEGENERATION | MEDICINE, GENERAL & INTERNAL | GENE | muscle | survival motor neuron protein | spinal muscular atrophy | ACTIN CYTOSKELETON | DIFFERENTIATION | NEUROMUSCULAR-JUNCTION | Anterior Horn Cells - drug effects | Spinal Cord - drug effects | Longevity - drug effects | 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine - analogs & derivatives | Muscle Fibers, Skeletal - drug effects | Survival of Motor Neuron 2 Protein - metabolism | Motor Neurons - pathology | Dose-Response Relationship, Drug | Motor Endplate - drug effects | Spinal Cord - pathology | Motor Endplate - pathology | Muscle, Skeletal - drug effects | Weight Gain - drug effects | Survival of Motor Neuron 2 Protein - deficiency | Muscular Atrophy, Spinal - physiopathology | Motor Neurons - drug effects | Disease Models, Animal | Muscle, Skeletal - growth & development | Mice, Inbred C57BL | Anterior Horn Cells - pathology | 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine - therapeutic use | 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine - administration & dosage | Muscular Atrophy, Spinal - pathology | Gait - drug effects | Phenotype | Animals | Muscle Development - drug effects | 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine - pharmacology | Muscle, Skeletal - physiopathology | Muscle Fibers, Skeletal - pathology | Survival Analysis | Muscular Atrophy, Spinal - drug therapy | Mice | Spinal Cord - physiopathology | Muscle, Skeletal - pathology | Myogenin - metabolism | Motor Endplate - physiopathology | Prevention | Complications and side effects | Prognosis | Vasodilators | Patient outcomes | Dosage and administration | Infants | Research | Drug therapy | Atrophy, Muscular | Risk factors | Medical research | Musculoskeletal system | Pathogenesis | Laboratories | Colleges & universities | Mutation | Muscular system | FDA approval | Kinases | Drug dosages
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. Full Text TWEAK, via its receptor Fn14, is a novel regulator of mesenchymal progenitor cells and skeletal muscle regeneration
by Weng, Shawn and Yagita, Hideo and Burkly, Linda C and Winkles, Jeffrey A and Browning, Beth and Zheng, Timothy S and Hsu, Yen-ming and Kostek, Christine A and Miller, Jeffrey Boone and Scott, Martin L and Brown, Sharron AN and Girgenrath, Mahasweta and Schneider, Pascal and Flavell, Richard A and Wang, Monica and Michaelson, Jennifer S and Allaire, Norm
The EMBO Journal, ISSN 0261-4189, 12/2006, Volume 25, Issue 24, pp. 5826 - 5839
Inflammation participates in tissue repair through multiple mechanisms including directly regulating the cell fate of resident progenitor cells critical for... 
Fn14 | TWEAK | inflammation | regeneration | muscle | Regeneration | Inflammation | Muscle | MACROPHAGES | MYOGENESIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | MOUSE | SATELLITE CELLS | PROLIFERATION | FAMILY | CELL BIOLOGY | TNF-ALPHA | DIFFERENTIATION | EXPRESSION | Tumor Necrosis Factors - genetics | Humans | Cobra Cardiotoxin Proteins - pharmacology | TWEAK Receptor | Muscle, Skeletal - cytology | RNA, Messenger - metabolism | Myoblasts - drug effects | Mesenchymal Stromal Cells - cytology | Muscle, Skeletal - drug effects | Myoblasts - cytology | Receptors, Tumor Necrosis Factor - deficiency | Receptors, Tumor Necrosis Factor - genetics | Receptors, Tumor Necrosis Factor - metabolism | Mesenchymal Stromal Cells - drug effects | RNA, Messenger - genetics | Cells, Cultured | Tumor Necrosis Factors - metabolism | Muscle, Skeletal - physiology | Gene Expression Regulation - drug effects | Cytokine TWEAK | Regeneration - drug effects | Animals | Muscle Development - drug effects | Cell Differentiation - drug effects | Models, Biological | Cell Proliferation - drug effects | Mice | Cell Cycle - drug effects | Cellular biology | Molecular biology | Rodents | Inflammatory diseases | Stem cells
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text Autocrine and Paracrine Angiopoietin 1/Tie-2 Signaling Promotes Muscle Satellite Cell Self-Renewal
by Abou-Khalil, Rana and Le Grand, Fabien and Pallafacchina, Giorgia and Valable, Samuel and Authier, François-Jérôme and Rudnicki, Michael A and Gherardi, Romain K and Germain, Stéphane and Chretien, Fabrice and Sotiropoulos, Athanassia and Lafuste, Peggy and Montarras, Didier and Chazaud, Bénédicte
Cell Stem Cell, ISSN 1934-5909, 2009, Volume 5, Issue 3, pp. 298 - 309
Mechanisms governing muscle satellite cell withdrawal from cell cycle to enter into quiescence remain poorly understood. We studied the role of angiopoietin 1... 
STEMCELL | RESERVE-CELLS | ANGIOGENESIS | TIE2 | INFLAMMATION | M-CADHERIN | QUIESCENCE | STEM-CELL | POTENTIAL MECHANISM | EXPRESSION | ADULT SKELETAL-MUSCLE | CELL & TISSUE ENGINEERING | CELL BIOLOGY | Gene Silencing - drug effects | Apoptosis - drug effects | Cell Count | Humans | Autocrine Communication - drug effects | PAX7 Transcription Factor - metabolism | Stem Cells - cytology | Angiopoietin-1 - metabolism | Stem Cells - metabolism | Protein Binding - drug effects | Receptor, TIE-2 - metabolism | Myocytes, Smooth Muscle - drug effects | Myocytes, Smooth Muscle - metabolism | Angiopoietin-1 - pharmacology | Fibroblasts - metabolism | Satellite Cells, Skeletal Muscle - cytology | Cells, Cultured | Satellite Cells, Skeletal Muscle - metabolism | Satellite Cells, Skeletal Muscle - drug effects | Satellite Cells, Skeletal Muscle - enzymology | Animals | Muscle Development - drug effects | Mitogen-Activated Protein Kinase 3 - metabolism | Signal Transduction - drug effects | Fibroblasts - drug effects | Paracrine Communication - drug effects | Stem Cells - drug effects | Cell Proliferation - drug effects | Mice | Mitogen-Activated Protein Kinase 1 - metabolism
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Mitophagy is required for mitochondrial biogenesis and myogenic differentiation of C2C12 myoblasts
by Sin, Jon and Andres, Allen M and Taylor, David J. R and Weston, Thomas and Hiraumi, Yoshimi and Stotland, Aleksandr and Kim, Brandon J and Huang, Chengqun and Doran, Kelly S and Gottlieb, Roberta A
Autophagy, ISSN 1554-8627, 02/2016, Volume 12, Issue 2, pp. 369 - 380
Myogenesis is a crucial process governing skeletal muscle development and homeostasis. Differentiation of primitive myoblasts into mature myotubes requires a... 
myoblasts | mitophagy | autophagy | differentiation | mitochondria | myotubes | myogenesis | Mitochondria | Myotubes | Differentiation | Mitophagy | Autophagy | Myogenesis | Myoblasts | ACTIVATION | MYOD | CELL BIOLOGY | SKELETAL-MUSCLE | BIOENERGETICS | STRESS | Cell Line | Mitochondria - metabolism | Mitochondria - drug effects | Muscle Fibers, Skeletal - drug effects | Muscle Fibers, Skeletal - metabolism | Mitochondria - ultrastructure | Oxidative Phosphorylation - drug effects | Organelle Biogenesis | Myoblasts - metabolism | Animals | Muscle Development - drug effects | Cell Differentiation - drug effects | Mitochondrial Degradation - drug effects | Models, Biological | Myoblasts - cytology | Macrolides - pharmacology | Myoblasts - ultrastructure | Muscle Fibers, Skeletal - cytology | Mice
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text Quercetin, a natural product supplement, impairs mitochondrial bioenergetics and locomotor behavior in larval zebrafish (Danio rerio)
by Zhang, Ji-Liang and Laurence Souders, Christopher and Denslow, Nancy D and Martyniuk, Christopher J
Toxicology and Applied Pharmacology, ISSN 0041-008X, 07/2017, Volume 327, pp. 30 - 38
Quercetin is a natural product that is sold as a supplement in health food stores. While there are reported benefits for this flavonoid as a dietary supplement... 
Mitochondrial respiration | Gene expression | Locomotor behavior | Quercetin | Myosin | APOPTOSIS | TRICLOSAN | CELLS | OXIDATIVE STRESS | FLAVONOIDS | TOXICITY | INDUCTION | PHARMACOLOGY & PHARMACY | TOXICOLOGY | DYSFUNCTION | EXPRESSION | EXPOSURE | Water Pollutants, Chemical | Transcription, Genetic - drug effects | MyoD Protein - biosynthesis | MyoD Protein - genetics | Male | Zebrafish | Dietary Supplements - toxicity | Mitochondria - metabolism | Mitochondria - drug effects | Abnormalities, Drug-Induced - pathology | Adenosine Triphosphate - biosynthesis | Animals | Muscle Development - drug effects | Quercetin - toxicity | Larva | Oxygen Consumption - drug effects | Muscle Development - genetics | Behavior, Animal - drug effects | Female | Swimming | Oxidative Stress - drug effects | Energy Metabolism - drug effects | Locomotion - drug effects | Flavonoids | Flavones | Bioflavonoids | Dietary supplements | Antioxidants | Grocery industry | Muscle proteins | Index Medicus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text Thyroid hormone and retinoic acid interact to regulate zebrafish craniofacial neural crest development
by Bohnsack, Brenda L and Kahana, Alon
Developmental Biology, ISSN 0012-1606, 01/2013, Volume 373, Issue 2, pp. 300 - 309
Craniofacial and ocular morphogenesis require proper regulation of cranial neural crest migration, proliferation, survival and differentiation. Although... 
Retinoid X receptor | Pharyngeal arch | Migration | Thyroid hormone | Craniofacial | Eye development | Neural crest | Pitx2 | Retinoic acid | Twist1 | CELLS | EMBRYONIC-DEVELOPMENT | MOUSE EMBRYOS | DEVELOPMENTAL BIOLOGY | SPECIFICATION | RECEPTOR-ALPHA | GENE-EXPRESSION | SAETHRE-CHOTZEN SYNDROME | CHICK-EMBRYO | Embryo, Nonmammalian - cytology | Thyroid Hormones - pharmacology | Apoptosis - drug effects | Embryo, Nonmammalian - metabolism | Zebrafish - embryology | Embryo, Nonmammalian - drug effects | Gene Knockdown Techniques | Neural Crest - metabolism | Eye - embryology | Eye - drug effects | Skull - drug effects | Tretinoin - pharmacology | Cell Survival - drug effects | Neural Crest - cytology | Zebrafish Proteins - metabolism | Gene Expression Regulation, Developmental - drug effects | Neural Crest - drug effects | Receptors, Thyroid Hormone - metabolism | Skull - embryology | Animals | Muscle Development - drug effects | Signal Transduction - drug effects | Models, Biological | Neural Crest - embryology | Cell Proliferation - drug effects | Face - embryology | Antithyroid Agents - pharmacology | Tretinoin | retinoid X receptor | Thyroid Hormone | retinoic acid | pharyngeal arch | eye development | twist1 | Neural Crest | pitx2
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
9. Full Text Cardiomyogenesis in the Adult Human Heart
by Kajstura, Jan and Urbanek, Konrad and Perl, Shira and Hosoda, Toru and Zheng, Hanqiao and Ogórek, Barbara and Ferreira-Martins, João and Goichberg, Polina and Rondon-Clavo, Carlos and Sanada, Fumihiro and DʼAmario, Domenico and Rota, Marcello and del Monte, Federica and Orlic, Donald and Tisdale, John and Leri, Annarosa and Anversa, Piero
Circulation Research, ISSN 0009-7330, 07/2010, Volume 107, Issue 2, pp. 305 - 315
RATIONALE:The ability of the human heart to regenerate large quantities of myocytes remains controversial, and the extent of myocyte renewal claimed by... 
myocyte regeneration | cell lifespan | DNA repair | cell fusion | ploidy | STEM-CELLS | ACTIVATION | CARDIAC & CARDIOVASCULAR SYSTEMS | MYOCYTES | ANGIOGENESIS | MULTIPOTENT | MOUSE | CARDIOMYOPATHY | INFARCTED MYOCARDIUM | CARDIAC PROGENITOR CELLS | DISEASE | PERIPHERAL VASCULAR DISEASE | HEMATOLOGY | Immunohistochemistry | Age Factors | Humans | Middle Aged | Rats, Inbred F344 | Male | Idoxuridine - therapeutic use | Radiation-Sensitizing Agents - therapeutic use | Young Adult | Cell Fusion | Flow Cytometry | Time Factors | Autopsy | Cell Nucleus - pathology | Cell Death | Adult | Female | Polyploidy | Rats | Myocardium - pathology | Fibroblasts - pathology | Neoplasms - drug therapy | Microscopy, Confocal | Myocytes, Cardiac - pathology | Regeneration | Phenotype | Animals | Muscle Development - drug effects | Myocytes, Cardiac - drug effects | DNA Repair | Fibroblasts - drug effects | Aged | Cell Proliferation - drug effects | Endothelial Cells - pathology | Neoplasms - pathology | Endothelial Cells - drug effects | Cell lifespan | Ploidy | Myocyte regeneration | Cell fusion
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
10. Full Text Highly efficient delivery of functional cargoes by the synergistic effect of GAG binding motifs and cell-penetrating peptides
by James E. Dixon and Gizem Osman and Gavin E. Morris and Hareklea Markides and Michael Rotherham and Zahia Bayoussef and Alicia J. El Haj and Chris Denning and Kevin M. Shakesheff
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 1/2016, Volume 113, Issue 3, pp. E291 - E299
Protein transduction domains (PTDs) are powerful nongenetic tools that allow intracellular delivery of conjugated cargoes to modify cell behavior. Their use in... 
Human embryonic stem cells | Transduction | Cell-penetrating peptides | Differentiation | Heparin-binding domain | differentiation | transduction | MULTIDISCIPLINARY SCIENCES | MECHANISMS | HEPARIN | MAMMALIAN-CELLS | IPS CELLS | PLURIPOTENT STEM-CELLS | cell-penetrating peptides | heparin-binding domain | MACROPINOCYTOSIS | GROWTH-FACTOR | PROTEINS | human embryonic stem cells | NIH 3T3 Cells | Homeodomain Proteins - metabolism | Human Embryonic Stem Cells - cytology | Humans | Mouse Embryonic Stem Cells - cytology | Mouse Embryonic Stem Cells - drug effects | Mouse Embryonic Stem Cells - metabolism | Drug Delivery Systems | Nanoparticles | Human Embryonic Stem Cells - drug effects | Integrases - metabolism | Cell Membrane - metabolism | Cell Membrane - drug effects | Cell-Penetrating Peptides - chemistry | Induced Pluripotent Stem Cells - metabolism | Protein Structure, Tertiary | Detergents - pharmacology | Human Embryonic Stem Cells - metabolism | Nanog Homeobox Protein | Induced Pluripotent Stem Cells - drug effects | Glycosaminoglycans - metabolism | Endocytosis - drug effects | Solubility | MyoD Protein - metabolism | Nucleic Acids - metabolism | Trypsin - metabolism | Amino Acid Motifs | Animals | Muscle Development - drug effects | Cell Differentiation - drug effects | Cell Proliferation - drug effects | Mice | Genome | Cell-Penetrating Peptides - metabolism | Physiological aspects | Physiological research | Cellular signal transduction | Glycosaminoglycans | Research | Proteins | Peptides | Cytoplasm | Binding sites | Stem cells | Biological Sciences | PNAS Plus
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights