Functional recovery after facial nerve crush is delayed in severe combined immunodeficient mice. (Q48426772)

11 February 2018

title

Functional recovery after facial nerve crush is delayed in severe combined immunodeficient mice. (English)

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11 February 2018

5

Kathryn J Jones

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11 February 2018

author name string

Craig J Serpe

1

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11 February 2018

Julie E Tetzlaff

2

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11 February 2018

Susanna Coers

3

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11 February 2018

Virginia M Sanders

4

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11 February 2018

publication date

1 December 2002

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11 February 2018

Brain, Behavior, and Immunity

published in

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11 February 2018

volume

16

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11 February 2018

issue

6

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11 February 2018

page(s)

808-812

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11 February 2018

A severe combined immunodeficiency mutation in the mouse

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Autoimmune T cells as potential neuroprotective therapy for spinal cord injury

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Neuronal survival after CNS insult is determined by a genetically encoded autoimmune response.

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Testosterone-induced acceleration of recovery from facial paralysis following crush axotomy of the facial nerve in male hamsters

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The axon reaction: a review of the principal features of perikaryal responses to axon injury.

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Cross talk between the immune system and the nervous system in response to injury: implications for regeneration.

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Immune surveillance in the injured nervous system: T-lymphocytes invade the axotomized mouse facial motor nucleus and aggregate around sites of neuronal degeneration.

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Exacerbation of facial motoneuron loss after facial nerve transection in severe combined immunodeficient (scid) mice

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RAG-2-deficient mice lack mature lymphocytes owing to inability to initiate V(D)J rearrangement

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Microglial-neuronal interactions

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Experiments on the Section of the Glossopharyngeal and Hypoglossal Nerves of the Frog, and Observations of the Alterations Produced Thereby in the Structure of Their Primitive Fibres

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Protective autoimmunity is a physiological response to CNS trauma.

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Development of antigenic heterogeneity in the splenic meshwork of severe combined immunodeficient (SCID) mice after reconstitution with T and B lymphocytes

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Identifiers

DOI

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11 February 2018

PubMed ID

12480509

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11 February 2018