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Journal of Experimental Biology, ISSN 0022-0949, 09/2018, Volume 221, Issue 17, p. jeb184713
The hearts of smaller mammals tend to operate at higher mass-specific mechanical work rates than those of larger mammals. The ultrastructural characteristics... 
Mammal | Mitochondria | Predation | Capillarity | Cardiac | Myofibrils | BAR-HEADED GOOSE | MITOCHONDRIAL VOLUME | HIGH-ALTITUDE | LEFT-VENTRICLE | STEREOLOGICAL METHODS | LARGE PREDATORS | OXIDATIVE CAPACITY | MAMMALIAN RESPIRATORY SYSTEM | BIOLOGY | KANGAROO MACROPUS-FULIGINOSUS | SKELETAL-MUSCLES
Journal Article
Science, ISSN 0036-8075, 12/2015, Volume 350, Issue 6265, pp. aad0116 - aad0116
Journal Article
Nature Medicine, ISSN 1078-8956, 08/2006, Volume 12, Issue 8, pp. 908 - 916
Imatinib mesylate (Gleevec) is a small-molecule inhibitor of the fusion protein Bcr-Abl, the causal agent in chronic myelogenous leukemia. Here we report ten... 
CHRONIC MYELOGENOUS LEUKEMIA | ADJUVANT CHEMOTHERAPY | MEDICINE, RESEARCH & EXPERIMENTAL | C-ABL | ABL TYROSINE KINASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | N-TERMINAL KINASE | NEURONAL CELL-DEATH | ENDOPLASMIC-RETICULUM STRESS | HER2-POSITIVE BREAST-CANCER | CHRONIC MYELOID-LEUKEMIA | CELL BIOLOGY | UNFOLDED PROTEIN RESPONSE | Mitochondria, Heart - ultrastructure | Piperazines - administration & dosage | Calcium - metabolism | Mitochondria, Heart - pathology | Sarcoplasmic Reticulum - drug effects | Humans | Piperazines - toxicity | Antineoplastic Agents - administration & dosage | Mitochondria, Heart - drug effects | Ventricular Dysfunction, Left - chemically induced | Antineoplastic Agents - toxicity | Dose-Response Relationship, Drug | Mitochondrial Membranes - drug effects | Pyrimidines - toxicity | Time Factors | Adenosine Triphosphatases - analysis | Antineoplastic Agents - adverse effects | Sarcoplasmic Reticulum - ultrastructure | Antineoplastic Agents - pharmacology | Cell Death - drug effects | Membrane Potentials - drug effects | Severity of Illness Index | Cytochromes c - secretion | Echocardiography | Pyrimidines - administration & dosage | Mice, Inbred C57BL | Cells, Cultured | Injections, Intraperitoneal | Adenosine Triphosphatases - metabolism | Heart Failure - pathology | Pyrimidines - pharmacology | Imatinib Mesylate | Piperazines - adverse effects | Piperazines - pharmacology | Ventricular Dysfunction, Left - physiopathology | Myocytes, Cardiac - pathology | Animals | Myocytes, Cardiac - drug effects | Cell Membrane Permeability - drug effects | Pyrimidines - adverse effects | Sarcoplasmic Reticulum - pathology | Mice | Benzamides | Myocytes, Cardiac - ultrastructure | Heart Failure - chemically induced | Heart failure | Chemotherapy | Side effects | Inhibitor drugs | Toxicity | Cardiovascular disease | Cancer
Journal Article
Journal Article
Journal of Cellular and Molecular Medicine, ISSN 1582-1838, 11/2011, Volume 15, Issue 11, pp. 2539 - 2551
Induced pluripotent stem cells (iPSC) are generated from fully differentiated somatic cells that were reprogrammed into a pluripotent state. Human iPSC which... 
cardiomyocytes | action potentials | release units | induced pluripotent stem cells | human embryonic stem cells | sarcoplasmic reticulum | caveolae | Human embryonic stem cells | Action potentials | Caveolae | Induced pluripotent stem cells | Sarcoplasmic reticulum | Cardiomyocytes | MEDICINE, RESEARCH & EXPERIMENTAL | Ca2+-release units | FUNCTIONAL-PROPERTIES | CELL BIOLOGY | ORGANIZATION | SMOOTH-MUSCLE | ICLC | JUNCTIONS | DIFFERENTIATION | TELOCYTES | Mitochondria, Heart - ultrastructure | Myocardial Contraction | Embryonic Stem Cells - cytology | Excitation Contraction Coupling | Induced Pluripotent Stem Cells - physiology | Calcium - metabolism | Caveolae - ultrastructure | Humans | Cells, Cultured | Keratinocytes - cytology | Microscopy, Electron | Embryonic Stem Cells - physiology | Endoplasmic Reticulum - ultrastructure | Membrane Potentials | Hair Follicle - metabolism | Sarcoplasmic Reticulum - ultrastructure | Cell Differentiation | Fibroblasts - cytology | Induced Pluripotent Stem Cells - cytology | Myocytes, Cardiac - ultrastructure | Heart | Embryo cells | Ribosomes | Desmosomes | Lipids | Cell adhesion & migration | Mitochondria | Ultrastructure | Fibroblasts | Conflicts of interest | Autografts | Phenotypes | Calcium (intracellular) | Cardiac muscle | Glycogen | Data acquisition systems | Cloning | Keratinocytes | Electron microscopy | Cell differentiation | Mammals | Myofibrils | Transmission electron microscopy | Somatic cells | Stem cells | Plasma membranes | Disks | Software | Fascia | Endoplasmic reticulum | Pluripotency | Calcium ions | Original
Journal Article
Circulation Research, ISSN 0009-7330, 07/2015, Volume 117, Issue 4, pp. 346 - 351
Journal Article
Journal Article