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1. Cell physiology
by Landowne, David
2006, Lange medical book, ISBN 0071104860, v, 154
Cell physiology
Book
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2. Full Text Myogenic satellite cells: physiology to molecular biology
by Thomas J. Hawke and Daniel J. Garry
Journal of Applied Physiology, ISSN 8750-7587, 08/2001, Volume 91, Issue 2, pp. 534 - 551
Adult skeletal muscle has a remarkable ability to regenerate following myotrauma. Because adult myofibers are terminally differentiated, the regeneration of... 
Transgenic models | Aging | Regeneration | Skeletal muscle | Stem cells | stem cells | DIGITORUM LONGUS MUSCLE | SPORT SCIENCES | PHYSIOLOGY | regeneration | FIBROBLAST-GROWTH-FACTOR | LEUKEMIA INHIBITORY FACTOR | MEDIATED GENE-THERAPY | IN-VITRO | LEVATOR ANI MUSCLE | HEMATOPOIETIC STEM-CELLS | DUCHENNE MUSCULAR-DYSTROPHY | aging | skeletal muscle | transgenic models | SKELETAL-MUSCLE REGENERATION | ADULT-RAT MUSCLE | Animals | Molecular Biology | Animals, Genetically Modified | Humans | Adult | Stem Cells - physiology | Cell Differentiation | Stem Cells - cytology | Muscle, Skeletal - physiology | Muscle, Skeletal - cytology | Embryonic and Fetal Development
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3. Human physiology
: from cells to systems
by Sherwood, Lauralee
2009, 7th ed., international ed., ISBN 9781408018705
Human phsiology
Book
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4. Full Text Type-2 pericytes participate in normal and tumoral angiogenesis
by Birbrair, Alexander and Zhang, Tan and Wang, Zhong-Min and Messi, Maria Laura and Olson, John D and Mintz, Akiva and Delbono, Osvaldo
American Journal of Physiology - Cell Physiology, ISSN 0363-6143, 07/2014, Volume 307, Issue 1, pp. C25 - C38
Tissue growth and function depend on vascularization, and vascular insufficiency or excess exacerbates many human diseases. Identification of the biological... 
Pericytes | Angiogenesis | Tumor | Stem cells | PROGENITOR CELLS | stem cells | PHYSIOLOGY | angiogenesis | pericytes | BONE-MARROW | NEURAL STEM | NG2 PROTEOGLYCAN | MESENCHYMAL STEM-CELLS | CELL BIOLOGY | tumor | CLINICAL-APPLICATIONS | ENDOTHELIAL-CELLS | SMOOTH-MUSCLE-CELLS | DIFFERENTIATION | PDGF-BB | Hindlimb | Human Umbilical Vein Endothelial Cells - metabolism | Coculture Techniques | Humans | Neovascularization, Pathologic | Male | Brain Neoplasms - blood supply | Green Fluorescent Proteins - genetics | Actins - genetics | Time Factors | Pericytes - pathology | Nestin - genetics | Ischemia - pathology | Disease Models, Animal | Muscle, Skeletal - blood supply | Biomarkers - metabolism | Green Fluorescent Proteins - metabolism | Promoter Regions, Genetic | Mice, Inbred C57BL | Pericytes - metabolism | Cells, Cultured | Ischemia - metabolism | Mice, Transgenic | Ischemia - physiopathology | Phenotype | Animals | Mice, Nude | Luminescent Proteins - genetics | Mice | Glioblastoma - blood supply | Neovascularization, Physiologic | Proteoglycans - genetics | Antigens - genetics | Luminescent Proteins - metabolism | Research | Neovascularization | Intermediate filament proteins | Analysis | Call for Papers
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5. Full Text Brain mesenchymal stem cells: physiology and pathological implications
by Pombero, Ana and Garcia‐Lopez, Raquel and Martinez, Salvador
Development, Growth & Differentiation, ISSN 0012-1592, 06/2016, Volume 58, Issue 5, pp. 469 - 480
Mesenchymal stem cells (MSCs) are defined as progenitor cells that give rise to a number of unique, differentiated mesenchymal cell types. This concept has... 
cancer | blood–brain barrier | pericyte | mesenchymal cells | neurovascular unit | blood-brain barrier | MULTIPOTENT PROGENITOR CELLS | BONE-MARROW | PERICYTE-COVERAGE | IMPROVE MOTOR FUNCTIONS | DEVELOPMENTAL BIOLOGY | CELL BIOLOGY | IN-VITRO | MARROW-DERIVED CELLS | SMOOTH-MUSCLE-CELLS | BLOOD-BRAIN | GROWTH-FACTOR | STROMAL CELLS | Neurons - pathology | Endothelial Cells - metabolism | Humans | Astrocytes - pathology | Mesenchymal Stromal Cells - metabolism | Neural Stem Cells - pathology | Blood-Brain Barrier - metabolism | Blood-Brain Barrier - pathology | Animals | Cell Differentiation | Neurons - metabolism | Mesenchymal Stromal Cells - pathology | Endothelial Cells - pathology | Neural Stem Cells - metabolism | Astrocytes - metabolism | Physiological aspects | Neurons | Stem cells | Skin & tissue grafts
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6. Full Text Carbon monoxide in lung cell physiology and disease
by Ryter, Stefan W and Ma, Kevin C and Choi, Augustine M. K
American Journal of Physiology - Cell Physiology, ISSN 0363-6143, 02/2018, Volume 314, Issue 2, pp. C211 - C227
Carbon monoxide (CO) is an endogenously produced gas that has gained recognition as a biological signal transduction effector with properties similar, but not... 
Lung disease | Mitochondria | Reactive oxygen species | Cell death | Sepsis | Inflammation | Carbon monoxide | Cell signaling | PROTEIN-KINASE PATHWAY | NRF2 ENHANCES SUSCEPTIBILITY | PHYSIOLOGY | cell death | mitochondria | carbon monoxide | lung disease | HEPATIC ISCHEMIA/REPERFUSION INJURY | CELL BIOLOGY | ISCHEMIA-REPERFUSION INJURY | CO-RELEASING MOLECULE | MICROSOMAL HEME OXYGENASE | inflammation | cell signaling | reactive oxygen species | UNCOUPLES MITOCHONDRIAL RESPIRATION | SMOOTH-MUSCLE-CELLS | IDIOPATHIC PULMONARY-FIBROSIS | NF-KAPPA-B | sepsis | Lung - pathology | Lung Diseases - metabolism | Carbon Monoxide - toxicity | Humans | Mitochondria - metabolism | Mitochondria - drug effects | Mitochondria - pathology | Carbon Monoxide - metabolism | Lung Diseases - drug therapy | Dose-Response Relationship, Drug | Animals | Carbon Monoxide - pharmacology | Signal Transduction - drug effects | Lung - drug effects | Lung - metabolism | Lung Diseases - pathology | Lungs | Health aspects | Theme
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7. Full Text BMP4 and BMP7 induce the white-to-brown transition of primary human adipose stem cells
by Elsen, Manuela and Raschke, Silja and Tennagels, Norbert and Schwahn, Uwe and Jelenik, Tomas and Roden, Michael and Romacho, Tania and Eckel, Jürgen
American Journal of Physiology - Cell Physiology, ISSN 0363-6143, 03/2014, Volume 306, Issue 5, pp. C431 - C440
While white adipose tissue (AT) is an energy storage depot, brown AT is specialized in energy dissipation. Uncoupling protein 1 (UCP1)-expressing adipocytes... 
Bone morphogenetic proteins | Brite adipocytes | Primary human preadipocytes | Adipogenesis | ADIPOCYTE LINEAGE | PHYSIOLOGY | MITOCHONDRIAL BIOGENESIS | TISSUE | ADULT HUMANS | primary human preadipocytes | CELL BIOLOGY | SKELETAL-MUSCLE | adipogenesis | brite adipocytes | MESSENGER-RNA | ENERGY HOMEOSTASIS | INSULIN-RESISTANCE | BONE MORPHOGENETIC PROTEIN-7 | FAT | bone morphogenetic proteins | Adipocytes, Brown - metabolism | Humans | Adipose Tissue, White - metabolism | Ion Channels - genetics | Mitochondrial Proteins - genetics | PPAR gamma - metabolism | RNA, Messenger - metabolism | Stem Cells - metabolism | Bone Morphogenetic Protein 4 - metabolism | Adipose Tissue, White - cytology | Time Factors | Mitochondrial Proteins - metabolism | Adult | Cell Transdifferentiation | Female | PPAR gamma - genetics | Recombinant Proteins - metabolism | Signal Transduction | Cells, Cultured | Gene Expression Regulation | Oxygen Consumption | Lipid Metabolism | Mitochondria - metabolism | Tumor Necrosis Factor Receptor Superfamily, Member 9 - metabolism | Adipose Tissue, Brown - cytology | Ion Channels - metabolism | Bone Morphogenetic Protein 7 - metabolism | Adipose Tissue, Brown - metabolism | Primary Cell Culture | Uncoupling Protein 1 | Adipocytes, White - metabolism | Adipose tissues | Physiological aspects | Stem cell research | Fat cells
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8. Full Text Caveolins and cavins in the trafficking, maturation, and degradation of caveolae: Implications for cell physiology
by Busija, Anna R and Patel, Hemal H and Insel, Paul A
American Journal of Physiology - Cell Physiology, ISSN 0363-6143, 04/2017, Volume 312, Issue 4, pp. C459 - C477
Caveolins (Cavs) are similar to 20 kDa scaffolding proteins that assemble as oligomeric complexes in lipid raft domains to form caveolae, flask-shaped plasma... 
Lipid raft | Cavin | Caveolae | Caveolin | PROTEIN-KINASE-A | PHYSIOLOGY | CHOLESTEROL-RICH DOMAINS | HETEROTRIMERIC G-PROTEINS | NITRIC-OXIDE SYNTHASE | GIRDLE MUSCULAR-DYSTROPHY | HUMAN BREAST-CANCER | PLASMA-MEMBRANE LOCALIZATION | CELL BIOLOGY | lipid raft | EPIDERMAL-GROWTH-FACTOR | SMOOTH-MUSCLE-CELLS | VASCULAR ENDOTHELIAL-CELLS | cavin | caveolae | caveolin | Animals | Models, Biological | Humans | Protein Transport - physiology | Caveolins - metabolism | Cell Physiological Phenomena - physiology | Membrane Proteins - metabolism | Caveolae - physiology | RNA-Binding Proteins - metabolism | Review
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9. Full Text Novel biochemical pathways of endoglin in vascular cell physiology
by Bernabeu, Carmelo and Conley, Barbara A and Vary, Calvin P.H
Journal of Cellular Biochemistry, ISSN 0730-2312, 12/2007, Volume 102, Issue 6, pp. 1375 - 1388
The broad role of the transforming growth factor beta (TGFβ) signaling pathway in vascular development, homeostasis, and repair is well appreciated. Endoglin... 
vascular endothelium | vascular pathology | vascular smooth muscle | endoglin | hereditary hemorrhagic telangiectasia | transforming growth factor‐beta receptors | Endoglin | Vascular endothelium | Hereditary hemorrhagic telangiectasia | Vascular smooth muscle | Transforming growth factor-beta receptors | Vascular pathology | STEM-CELLS | TGF-BETA | BIOCHEMISTRY & MOLECULAR BIOLOGY | BINDING PROTEIN ENDOGLIN | RGD-CONTAINING GLYCOPROTEIN | HUMAN ENDOTHELIAL-CELLS | CELL BIOLOGY | GROWTH-FACTOR-BETA | EXTRACELLULAR-MATRIX SYNTHESIS | transforming growth factor-beta receptors | RECEPTOR COMPLEX | SMOOTH-MUSCLE-CELLS | Telangiectasia, Hereditary Hemorrhagic - physiopathology | Receptors, Transforming Growth Factor beta - genetics | Muscle, Smooth, Vascular - metabolism | Signal Transduction | Humans | Models, Molecular | Receptors, Cell Surface - metabolism | Intracellular Signaling Peptides and Proteins - metabolism | Telangiectasia, Hereditary Hemorrhagic - genetics | Antigens, CD - metabolism | Endothelium, Vascular - physiology | Receptors, Cell Surface - ultrastructure | Animals | Receptors, Transforming Growth Factor beta - metabolism | Endothelium, Vascular - metabolism | Models, Biological | Antigens, CD - ultrastructure
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