Meningeal cells and glia establish a permissive environment for axon regeneration after spinal cord injury in newts

Neural Development

Volumn 6, Issue 1, 2011, Pages

  Zukor, Katherine A ^a   Kent, David T ^a   Odelberg, Shannon J ^a  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BIOTIN; BIOTINYLATED DEXTRAN AMINE; DEXTRAN; DIAGNOSTIC AGENT; DRUG DERIVATIVE; NERVE PROTEIN; PROTEOCHONDROITIN SULFATE; SCLEROPROTEIN; VON WILLEBRAND ANTIGEN; VON WILLEBRAND FACTOR;

ANIMAL; ARTICLE; CONFOCAL MICROSCOPY; CONVALESCENCE; CYTOLOGY; DISEASE MODEL; ENDOTHELIUM CELL; GLIA; IMMUNOLOGY; MENINX; METABOLISM; METHODOLOGY; MYELINATED NERVE; NERVE FIBER; NERVE REGENERATION; PATHOPHYSIOLOGY; PHYSIOLOGY; SALAMANDER; SPINAL CORD INJURY; SWIMMING; TIME; TRANSMISSION ELECTRON MICROSCOPY; ULTRASTRUCTURE;

ANIMALS; AXONS; BIOTIN; CHONDROITIN SULFATE PROTEOGLYCANS; DEXTRANS; DISEASE MODELS, ANIMAL; ENDOTHELIAL CELLS; EXTRACELLULAR MATRIX PROTEINS; MENINGES; MICROSCOPY, CONFOCAL; MICROSCOPY, ELECTRON, TRANSMISSION; NERVE FIBERS, MYELINATED; NERVE REGENERATION; NERVE TISSUE PROTEINS; NEUROGLIA; RECOVERY OF FUNCTION; SALAMANDRIDAE; SPINAL CORD INJURIES; SWIMMING; TIME FACTORS; VON WILLEBRAND FACTOR;

EID: 78650772612     PISSN: None     EISSN: 17498104     Source Type: Journal    
DOI: 10.1186/1749-8104-6-1     Document Type: Article

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