Heparan sulfate proteoglycan-dependent induction of axon branching and axon misrouting by the Kallmann syndrome gene kal-1

Kallmann syndrome is a neurological disorder characterized by various behavioral and neuroanatomical defects. The X-linked form of this disease is caused by mutations in the KAL-1 gene, which codes for a secreted molecule that is expressed in restricted regions of the brain. Its molecular mechanism...

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Veröffentlicht in:	Proc Natl Acad Sci U S A
Hauptverfasser:	Bülow, Hannes E., Berry, Katherine L., Topper, Liat H., Peles, Elior, Hobert, Oliver
Format:	Artigo
Sprache:	Inglês
Veröffentlicht:	National Academy of Sciences 2002
Schlagworte:	Biological Sciences
Online-Zugang:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC122951/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11983919/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.092128099
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