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Publication : Hypogonadotropic hypogonadism and peripheral neuropathy in Ebf2-null mice.

First Author  Corradi A Year  2003
Journal  Development Volume  130
Issue  2 Pages  401-10
PubMed ID  12466206 Mgi Jnum  J:80220
Mgi Id  MGI:2445333 Doi  10.1242/dev.00215
Citation  Corradi A, et al. (2003) Hypogonadotropic hypogonadism and peripheral neuropathy in Ebf2-null mice. Development 130(2):401-10
abstractText  Olf/Ebf transcription factors have been implicated in numerous developmental processes, ranging from B-cell development to neuronal differentiation. We describe mice that carry a targeted deletion within the Ebf2 (O/E3) gene. In Ebf2-null mutants, because of defective migration of gonadotropin releasing hormone-synthesizing neurons, formation of the neuroendocrine axis (which is essential for pubertal development) is impaired, leading to secondary hypogonadism. In addition, Ebf2(-/-) peripheral nerves feature defective axon sorting, hypomyelination, segmental dysmyelination and axonal damage, accompanied by a sharp decrease in motor nerve conduction velocity. Ebf2-null mice reveal a novel genetic cause of hypogonadotropic hypogonadism and peripheral neuropathy in the mouse, disclosing an important role for Ebf2 in neuronal migration and nerve development.
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