Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features-Reference-Cited by-同舟云学术

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Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features

Published:2003-10-27 Issue:23 Volume:100 Page:13424-13429
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Roessler E.,Du Y.-Z.,Mullor J. L.,Casas E.,Allen W. P.,Gillessen-Kaesbach G.,Roeder E. R.,Ming J. E.,Altaba A. R. i.,Muenke M.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference43 articles.

1. Midline and laterality defects: Left and right meet in the middle

2. Proteolysis That Is Inhibited by Hedgehog Targets Cubitus interruptus Protein to the Nucleus and Converts It to a Repressor

3. Expression of the vertebrate Gli proteins in Drosophila reveals a distribution of activator and repressor activities

4. Combinatorial Gli gene function in floor plate and neuronal inductions by Sonic hedgehog

5. Gli proteins encode context-dependent positive and negative functions: implications for development and disease

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