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1. Full Text The growth cone cytoskeleton in Axon outgrowth and guidance
by Dent, Erik W and Gupton, Stephanie L and Gertler, Frank B
Cold Spring Harbor Perspectives in Biology, ISSN 1943-0264, 03/2011, Volume 3, Issue 3, pp. 1 - 39
Axon outgrowth and guidance to the proper target requires the coordination of filamentous (F)-actin and microtubules (MTs), the dynamic cytoskeletal polymers... 
CYCLASE-ASSOCIATED PROTEINS | CELL-ADHESION MOLECULE | ADENOMATOUS POLYPOSIS-COLI | ABELSON TYROSINE KINASE | PRIMARY CULTURED NEURONS | ABL-FAMILY KINASES | SERUM RESPONSE FACTOR | VERTEBRATE NERVOUS-SYSTEM | DOUBLECORTIN-LIKE-KINASE | VASODILATOR-STIMULATED PHOSPHOPROTEIN | CELL BIOLOGY | Growth Cones - physiology | Humans | Actins - metabolism | Cell Communication - physiology | Axons - physiology | Cytoskeleton - ultrastructure | Cell Movement - physiology | Animals | Growth Cones - ultrastructure | Models, Biological | Second Messenger Systems - physiology | Cytoskeleton - physiology | Cytoskeletal Proteins - physiology | 006
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2. Full Text Microtubule Stabilization Specifies Initial Neuronal Polarization
by Harald Witte and Dorothee Neukirchen and Frank Bradke
The Journal of Cell Biology, ISSN 0021-9525, 2/2008, Volume 180, Issue 3, pp. 619 - 632
Axon formation is the initial step in establishing neuronal polarity. We examine here the role of microtubule dynamics in neuronal polarization using... 
Axons | Growth cones | Neurites | Neuroscience | Neurons | Microtubules | Actins | Acetylation | Physiological regulation | T tests | PROTEIN | NEURITE OUTGROWTH | POLARITY | PHOSPHORYLATION | SYNTHASE KINASE 3-BETA | GROWTH | GSK-3-BETA | ESTABLISHMENT | HIPPOCAMPAL-NEURONS | BINDING | CELL BIOLOGY | Central Nervous System - ultrastructure | Central Nervous System - metabolism | Tubulin Modulators - pharmacology | Nocodazole - pharmacology | Glycogen Synthase Kinase 3 beta | Central Nervous System - embryology | Intercellular Signaling Peptides and Proteins - metabolism | Microtubules - metabolism | Neurons - ultrastructure | Microtubules - drug effects | Neurites - ultrastructure | Microtubules - ultrastructure | Hippocampus - ultrastructure | Cell Polarity - drug effects | Neurons - metabolism | Neurons - drug effects | Cell Differentiation - physiology | Neurites - drug effects | Protein-Serine-Threonine Kinases - metabolism | Hippocampus - embryology | Cells, Cultured | Paclitaxel - analogs & derivatives | Protein-Serine-Threonine Kinases - genetics | Rats | Neurites - metabolism | Glycogen Synthase Kinase 3 - metabolism | Mice, Knockout | Hippocampus - metabolism | Animals | Growth Cones - metabolism | Glycogen Synthase Kinase 3 - genetics | Growth Cones - ultrastructure | Cell Differentiation - drug effects | Cell Polarity - physiology | Mice | Growth Cones - drug effects | Evaluation | Cell physiology | Polarity (Biology) | Research | Properties
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3. Full Text Topography, Cell Response, and Nerve Regeneration
by Hoffman-Kim, D and Mitchel, JA and Bellamkonda, RV
2010, Annual Review of Biomedical Engineering, Volume 12, Issue 1, 29
In the body, cells encounter a complex milieu of signals, including topographical cues, in the form of the physical features of their surrounding environment.... 
contact guidance | ENGINEERING, BIOMEDICAL | neuron | cell tension | lithography | DEVELOPING CEREBRAL-CORTEX | SCHWANN-CELL | NANO-STRUCTURED SURFACES | NEURAL STEM-CELLS | GROWTH CONES | NEURITE OUTGROWTH | MULTIPLE GROOVED SUBSTRATA | SPINAL-CORD-INJURY | PERPENDICULAR CONTACT GUIDANCE | axon | FOCAL ADHESION KINASE | Growth Cones - physiology | Animals | Neurons - ultrastructure | Growth Cones - ultrastructure | Axons - ultrastructure | Neurons - physiology | Models, Animal | Axons - physiology | Coated Materials, Biocompatible | Nerve Regeneration | Regeneration | Analysis | Physiological aspects | Nervous system | Research | Cells | Biomedical engineering | Topographical drawing
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4. Full Text The bright side of the glial scar in CNS repair
by Rolls, Asya and Shechter, Ravid and Schwartz, Michal
Nature Reviews Neuroscience, ISSN 1471-003X, 03/2009, Volume 10, Issue 3, pp. 235 - 241
Following CNS injury, in an apparently counterintuitive response, scar tissue formation inhibits axonal growth, imposing a major barrier to regeneration.... 
Growth Cones - physiology | Neuroglia - ultrastructure | Cicatrix - prevention & control | Gliosis - therapy | Humans | Nerve Regeneration - physiology | Neuroglia - physiology | Gliosis - physiopathology | Brain Injuries - therapy | Brain Injuries - physiopathology | Animals | Growth Cones - ultrastructure | Neurogenesis - physiology | Cicatrix - physiopathology | Spinal Cord Injuries - physiopathology | Spinal Cord Injuries - therapy | Gliosis - prevention & control | Cicatrix - therapy | Extracellular Matrix Proteins - metabolism
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5. Full Text The emerging role of forces in axonal elongation
by Suter, Daniel M and Miller, Kyle E
Progress in Neurobiology, ISSN 0301-0082, 2011, Volume 94, Issue 2, pp. 91 - 101
â–º A common model proposes axons elongate through mass addition at the growth cone. â–º A new model suggests elongation occurs because growth cones generate... 
Axonal elongation | Force | Axon | Growth cone | Biophysics | Neuronal | Axonal growth | Neuron | Actin | Slow axonal transport | Microtubules | Myosin | Cytoskeleton | Mechanotransduction | Axonal transport | LIGHT-CHAIN KINASE | CYTOPLASMIC DYNEIN | NERVE REGENERATION | MICROTUBULE DYNAMICS | QUANTITATIVE-ANALYSIS | MYOSIN-II ACTIVITY | FLUORESCENT SPECKLE MICROSCOPY | FOCAL ADHESION KINASE | CYTOSKELETAL DYNAMICS | NEUROSCIENCES | GROWTH CONE MOTILITY | Growth Cones - physiology | Animals | Growth Cones - ultrastructure | Cell Shape | Humans | Axons - ultrastructure | Axons - physiology | Cytoskeleton - physiology | Cytoskeleton - ultrastructure | Synaptic Transmission | Neurological diseases | Axons | Movements | Dynamics | Polymerization | Genetics | Dynamical systems | Elongation
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6. Full Text Laminar Restriction of Retinal Ganglion Cell Dendrites and Axons: Subtype-Specific Developmental Patterns Revealed with Transgenic Markers
by Kim, In-Jung and Zhang, Yifeng and Meister, Markus and Sanes, Joshua R
Journal of Neuroscience, ISSN 0270-6474, 01/2010, Volume 30, Issue 4, pp. 1452 - 1462
Retinal ganglion cells (RGCs), which transfer information from the eye to the brain, are heterogeneous in structure and function, but developmental studies... 
SUPERIOR COLLICULUS | VISUAL EXPERIENCE | NICOTINIC ACETYLCHOLINE-RECEPTOR | POSTNATAL-DEVELOPMENT | MOUSE RETINA | MORPHOLOGICAL PROPERTIES | PROJECTIONS | MAMMALIAN RETINA | NEUROSCIENCES | MICE LACKING | LATERAL GENICULATE-NUCLEUS | Retina - growth & development | Visual Pathways - cytology | Superior Colliculi - ultrastructure | Dendrites - ultrastructure | Retina - embryology | Retinal Ganglion Cells - metabolism | Visual Pathways - embryology | Molecular Biology - methods | Retinal Ganglion Cells - cytology | Retina - cytology | Neurites - ultrastructure | Axons - ultrastructure | Cell Differentiation - physiology | Dendrites - metabolism | Superior Colliculi - metabolism | Visual Pathways - growth & development | Neuroanatomical Tract-Tracing Techniques - methods | Axons - metabolism | Mice, Transgenic | Neurites - metabolism | Luminescent Measurements - methods | Animals | Growth Cones - metabolism | Growth Cones - ultrastructure | Luminescent Proteins - genetics | Mice | Cell Shape - physiology
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7. Full Text Actin-binding proteins take the reins in growth cones
by Flynn, Kevin C and Bamburg, James R and Pak, Chi W
Nature Reviews Neuroscience, ISSN 1471-003X, 02/2008, Volume 9, Issue 2, pp. 136 - 147
Higher-order actin-based networks (actin superstructures) are important for growth-cone motility and guidance. Principles for generating, organizing and... 
F-ACTIN | MYOSIN-II ACTIVITY | LIM-KINASE | SLINGSHOT PHOSPHATASE | ARP2/3 COMPLEX | DEPOLYMERIZING FACTOR | MECHANICAL-PROPERTIES | NEUROSCIENCES | MYELIN-ASSOCIATED GLYCOPROTEIN | TROPOMYOSIN ISOFORMS | COFILIN PHOSPHORYLATION | Actin Cytoskeleton - metabolism | Central Nervous System - metabolism | Humans | Cell Membrane - ultrastructure | Central Nervous System - embryology | Cell Movement - physiology | Animals | Growth Cones - metabolism | Neuronal Plasticity - physiology | Central Nervous System - cytology | Growth Cones - ultrastructure | Neural Pathways - cytology | Neural Pathways - metabolism | Cell Membrane - metabolism | Microfilament Proteins - metabolism | Neural Pathways - embryology | Actin Cytoskeleton - ultrastructure | Cell Differentiation - physiology | Physiological aspects | Motility | Research | Actin | Neurons | Cells
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8. Full Text Disorganized Microtubules Underlie the Formation of Retraction Bulbs and the Failure of Axonal Regeneration
by Erturk, Ali and Hellal, Farida and Enes, Joana and Bradke, Frank
Journal of Neuroscience, ISSN 0270-6474, 08/2007, Volume 27, Issue 34, pp. 9169 - 9180
Axons in the CNS do not regrow after injury, whereas lesioned axons in the peripheral nervous system (PNS) regenerate. Lesioned CNS axons form characteristic... 
Regeneration | Growth cone | Microtubule | Retraction bulb | Dorsal root ganglia neurons (DRG neurons) | In vivo imaging | SENSORY AXONS | in vivo imaging | PERIPHERAL-NERVE REGENERATION | dorsal root ganglia neurons (DRG neurons) | regeneration | CHONDROITIN SULFATE PROTEOGLYCANS | GLIAL SCAR | NEUROSCIENCES | NEURONAL GROWTH CONES | DEGENERATION | growth cone | microtubule | NEURITE GROWTH | IN-VITRO | TRANSPORT | retraction bulb | SPINAL-CORD-INJURY | Paclitaxel - pharmacology | Microscopy, Electron, Transmission - methods | Tubulin Modulators - pharmacology | Nocodazole - pharmacology | Central Nervous System - pathology | Neurons - cytology | Axons - physiology | Ganglia, Spinal - cytology | Green Fluorescent Proteins - genetics | Sciatic Neuropathy - complications | Central Nervous System - injuries | Neurons - ultrastructure | Axons - ultrastructure | Neurons - metabolism | Growth Cones - physiology | Cells, Cultured | Microtubules - physiology | Axons - drug effects | Mice, Transgenic | Regeneration - physiology | Nerve Degeneration - pathology | Animals | Growth Cones - ultrastructure | Cerebellum - cytology | Luminescent Proteins - genetics | Mice | Growth Cones - drug effects | Nerve Degeneration - etiology
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9. Full Text Smn, the Spinal Muscular Atrophy-Determining Gene Product, Modulates Axon Growth and Localization of β-Actin mRNA in Growth Cones of Motoneurons
by Wilfried Rossoll and Sibylle Jablonka and Catia Andreassi and Ann-Kathrin Kröning and Kathrin Karle and Umrao R. Monani and Michael Sendtner
The Journal of Cell Biology, ISSN 0021-9525, 11/2003, Volume 163, Issue 4, pp. 801 - 812
Spinal muscular atrophy (SMA), a common autosomal recessive form of motoneuron disease in infants and young adults, is caused by mutations in the survival... 
Growth cones | Axons | Neurites | Messenger RNA | Neurons | Heterogeneous nuclear ribonucleoproteins | Cell lines | Actins | Antibodies | PC12 cells | β-actin | RNA transport | SMN | HnRNP R | SMA | SURVIVAL | GRY-RBP | hnRNP R | PROGRESSIVE-MOTOR-NEURONOPATHY | CYTOPLASMIC LOCALIZATION | beta-actin | BINDING PROTEIN | SNRNP BIOGENESIS | SINGLE NUCLEOTIDE | CELL-DEATH | CELL BIOLOGY | MOUSE MODEL | MISSENSE MUTATION | Spinal Cord - metabolism | Spinal Cord - growth & development | Nerve Tissue Proteins - deficiency | 3' Untranslated Regions - genetics | Cell Survival - genetics | Axons - physiology | RNA-Binding Proteins | RNA, Messenger - metabolism | PC12 Cells | Actins - genetics | Cell Differentiation - genetics | Motor Neurons - cytology | Spinal Cord - cytology | Cyclic AMP Response Element-Binding Protein | Disease Models, Animal | Nerve Tissue Proteins - physiology | Survival of Motor Neuron 1 Protein | Heterogeneous-Nuclear Ribonucleoproteins - metabolism | Rats | Mice, Transgenic | SMN Complex Proteins | Nerve Tissue Proteins - genetics | Heterogeneous-Nuclear Ribonucleoproteins - genetics | Motor Neurons - metabolism | Animals | Growth Cones - metabolism | Growth Cones - ultrastructure | Mice | SMN1 gene | spinal muscular atrophy | Smn protein | Heterogeneous-nuclear ribonucleoprotein R | SMA; SMN; RNA transport; β-actin; hnRNP R
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10. Full Text Peripheral regeneration
by Chen, Zu-Lin and Yu, Wei-Ming and Strickland, Sidney
Annual Review of Neuroscience, ISSN 0147-006X, 2007, Volume 30, Issue 1, pp. 209 - 233
Whereas the central nervous system (CNS) usually cannot regenerate, peripheral nerves regenerate spontaneously after injury because of a permissive environment... 
Conditioning lesion | Neurotrophic factors | Extracellular matrix proteins | Neurite outgrowth | Remyelination | Schwann cells | extracellular matrix proteins | NEUROTROPHIC FACTOR | AXON REGENERATION | LEUKEMIA INHIBITORY FACTOR | NEUROSCIENCES | SENSORY NEURONS | TISSUE-PLASMINOGEN-ACTIVATOR | INTERLEUKIN-6 MESSENGER-RNA | neurotrophic factors | SCIATIC-NERVE INJURY | SCHWANN-CELL DIFFERENTIATION | SPINAL-CORD-INJURY | neurite outgrowth | conditioning lesion | TRANSFORMING-GROWTH-FACTOR | remyelination | Humans | Nerve Regeneration - physiology | Axons - metabolism | Gene Expression Regulation - physiology | Nerve Growth Factors - metabolism | Hormones - genetics | Myelin Sheath - metabolism | Animals | Growth Cones - metabolism | Growth Cones - ultrastructure | Hormones - metabolism | Nerve Growth Factors - genetics | Peripheral Nerves - cytology | Axons - ultrastructure | Signal Transduction - physiology | Myelin Sheath - ultrastructure | Peripheral Nerves - metabolism | Nerves, Peripheral | Axons | Research
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