pubmed-article:16022592 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:16022592 | lifeskim:mentions | umls-concept:C0004461 | lld:lifeskim |
pubmed-article:16022592 | lifeskim:mentions | umls-concept:C0002351 | lld:lifeskim |
pubmed-article:16022592 | lifeskim:mentions | umls-concept:C0011164 | lld:lifeskim |
pubmed-article:16022592 | lifeskim:mentions | umls-concept:C0332523 | lld:lifeskim |
pubmed-article:16022592 | lifeskim:mentions | umls-concept:C1527148 | lld:lifeskim |
pubmed-article:16022592 | pubmed:dateCreated | 2005-7-18 | lld:pubmed |
pubmed-article:16022592 | pubmed:abstractText | The selective elimination of axons, dendrites, axon and dendrite branches, and synapses, without loss of the parent neurons, occurs during normal development of the nervous system as well as in response to injury or disease in the adult. The widespread developmental phenomena of exuberant axonal projections and synaptic connections require both small-scale and large-scale axon pruning to generate precise adult connectivity, and they provide a mechanism for neural plasticity in the developing and adult nervous system, as well as a mechanism to evolve differences between species in a projection system. Such pruning is also required to remove axonal connections damaged in the adult, to stabilize the affected neural circuits, and to initiate their repair. Pruning occurs through either retraction or degeneration. Here we review examples of these phenomena and consider potential cellular and molecular mechanisms that underlie axon retraction and degeneration and how they might relate to each other in development and disease. | lld:pubmed |
pubmed-article:16022592 | pubmed:language | eng | lld:pubmed |
pubmed-article:16022592 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16022592 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:16022592 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:16022592 | pubmed:issn | 0147-006X | lld:pubmed |
pubmed-article:16022592 | pubmed:author | pubmed-author:O'LearyDennis... | lld:pubmed |
pubmed-article:16022592 | pubmed:author | pubmed-author:LuoLiqunL | lld:pubmed |
pubmed-article:16022592 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:16022592 | pubmed:volume | 28 | lld:pubmed |
pubmed-article:16022592 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:16022592 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:16022592 | pubmed:pagination | 127-56 | lld:pubmed |
pubmed-article:16022592 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
pubmed-article:16022592 | pubmed:meshHeading | pubmed-meshheading:16022592... | lld:pubmed |
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pubmed-article:16022592 | pubmed:meshHeading | pubmed-meshheading:16022592... | lld:pubmed |
pubmed-article:16022592 | pubmed:year | 2005 | lld:pubmed |
pubmed-article:16022592 | pubmed:articleTitle | Axon retraction and degeneration in development and disease. | lld:pubmed |
pubmed-article:16022592 | pubmed:affiliation | Department of Biological Sciences, Neurosciences Program, Stanford University, Stanford, CA 94305, USA. lluo@stanford.edu | lld:pubmed |
pubmed-article:16022592 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:16022592 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
pubmed-article:16022592 | pubmed:publicationType | Review | lld:pubmed |
pubmed-article:16022592 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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