Holoprosencephaly: A paradigm for the complex genetics of brain development-Reference-Cited by-同舟云学术

Holoprosencephaly: A paradigm for the complex genetics of brain development

Published:1998-08 Issue:5 Volume:21 Page:481-497
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Roessler E.¹,Muenke M.¹²

Affiliation:

1. ; Medical Genetics Branch; National Human Genome Research Institute, National Institutes of Health; 10 Center Drive, 10 C 101 Bethesda MD 20892-1852 USA

2. ; The Children's Hospital of Philadelphia; University of Pennsylvania School of Medicine, Departments of Pediatrics, Genetics, and Neurology; Philadelphia Pennsylvania USA

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1005406719292/fullpdf

Reference129 articles.

1. Hedgehog and its patched-smoothened receptor complex: a novel signalling mechanism at the cell surface;Alcedo;Biol Chem,1997

2. The Drosophila smoothened gene encodes a seven-pass membrane protein, a putative receptor for the Hedgehog signal;Alcedo;Cell,1996

3. Transcriptional activation of hedgehog target genes in Drosophila is mediated directly by the Cubitus interruptus protein, a member of the GLI family of zinc finger DNA-binding proteins;Alexander;Genes Dev,1996

4. Catching a Gli-mpse of hedgehog;Altaba;Cell,1997

5. The mouse Zic gene family;Aruga;J Biol Chem,1996

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