ExLibris header image
SFX Logo
Title: A comprehensive analysis of 22q11 gene expression in the developing and adult brain
Source:

Proceedings of the National Academy of Sciences of the United States of America [0027-8424] Maynard, T M yr:2003


Collapse list of basic services Basic
Full text
Full text available via PubMed Central
GO
Document delivery
Request document via Library/Bibliothek GO
Users interested in this article also expressed an interest in the following:
1. Paterlini, Marta, M. "Transcriptional and behavioral interaction between 22q11.2 orthologs modulates schizophrenia-related phenotypes in mice." Nature neuroscience 8.11 (2005): 1586-1594. Link to Full Text for this item Link to SFX for this item
2. Ahn, D. "T-box gene tbx5 is essential for formation of the pectoral limb bud." Nature 417.6890 (2002): 754-758. Link to Full Text for this item Link to SFX for this item
3. LaMantia, Anthony-Samuel W. "Loss of Gli3 and Shh function disrupts olfactory axon trajectories." Journal of comparative neurology 472.3 (2004): 292-307. Link to Full Text for this item Link to SFX for this item
4. Chakravarti, A.. "A Compelling Genetic Hypothesis for a Complex Disease: PRODH2/DGCR6 Variation Leads to Schizophrenia Susceptibility." Proceedings of the National Academy of Sciences of the United States of America 99.8 (2002): 4755-4756. Link to Full Text for this item Link to SFX for this item
5. Baldini, A. "Dissecting contiguous gene defects: TBX1." Current opinion in genetics & development 15.3 (2005): 279-284. Link to SFX for this item
6. Gogos, J. "The gene encoding proline dehydrogenase modulates sensorimotor gating in mice." Nature genetics 21.4 (1999): 434-439. Link to Full Text for this item Link to SFX for this item
7. Campion, D. "Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome." Human Molecular Genetics 16.1 (2006): 83-91. Link to SFX for this item
8. Reiss, Allan L L. "COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome." Nature neuroscience 8.11 (2005): 1500-2. Link to Full Text for this item Link to SFX for this item
9. Arguello, JA A. "Modeling madness in mice: One piece at a time." Neuron 52.1 (2006): 179-196. Link to SFX for this item
10. Gittes, G. "A role for sonic hedgehog signaling in the pathogenesis of human tracheoesophageal fistula." Journal of Pediatric Surgery 38.3 (2003): 465-8. Link to SFX for this item
11. Yamagishi, H. "Unraveling the genetic and developmental mysteries of 22q11 deletion syndrome." Trends in molecular medicine 9.9 (2003): 383-9. Link to SFX for this item
12. Reynolds, K. "Activity of the beta-retinoic acid receptor promoter in transgenic mice." Mechanisms of development 36.1-2 (1991): 15-29. Link to Full Text for this item Link to SFX for this item
13. "A genetic mechanism implicates chromosome 11 in schizophrenia and bipolar disease." Genetics 167.4 (2004): 1833-. Link to Full Text for this item Link to SFX for this item
14. Yang, Y. "LIM homeobox transcription factors integrate signaling events that control three-dimensional limb patterning and growth." Development 136.8 (2009): 15-15. Link to SFX for this item
15. Koshiba-Takeuchi, M. "Tbx5 and Tbx4 genes determine the wing/leg identity of limb buds." Nature 398.6730 (1999): 810-4. Link to Full Text for this item Link to SFX for this item
16. Ahlberg, P. "Ventastega curonica and the origin of tetrapod morphology." Nature 453.7199 (2008): 1199-1204. Link to Full Text for this item Link to SFX for this item
17. Wang, Qinghua H. "Control of synaptic strength, a novel function of Akt." Neuron 38.6 (2003): 915-928. Link to SFX for this item
18. Liao, J. "Full spectrum of malformations in velo-cardio-facial syndrome/DiGeorge syndrome mouse models by altering Tbx1 dosage." Human molecular genetics 13.15 (2004): 1577-85. Link to SFX for this item
19. Yagi, H. "Role of TBX1 in human del22q11.2 syndrome." The lancet 362.9393 (2003): 1366-73. Link to SFX for this item
20. Cloninger, C Robert R. "The Discovery of Susceptibility Genes for Mental Disorders." Proceedings of the National Academy of Sciences of the United States of America 99.21 (2002): 13365-13367. Link to Full Text for this item Link to SFX for this item
View More...
View Less...
Select All Clear All

Expand list of advanced services Advanced
A service provided by the Library of the Wissenschaftspark Albert Einstein, Potsdam, Germany.
© 2005 SFX by Ex Libris Inc.