Funding Agency

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
5R01DC005667-02
Application #
6693072
Study Section
Mammalian Genetics Study Section (MGN)
Program Officer
Shekim, Lana O
Project Start
2003-01-01
Project End
2007-12-31
Budget Start
2004-01-01
Budget End
2004-12-31
Support Year
2
Fiscal Year
2004
Total Cost
$344,663
Indirect Cost

  Institution

Name
University of California San Francisco
Department
Type
Schools of Medicine
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94143

  Publications

Jeong, Juhee; Cesario, Jeffry; Zhao, Yangu et al. (2012) Cleft palate defect of Dlx1/2-/- mutant mice is caused by lack of vertical outgrowth in the posterior palate. Dev Dyn 241:1757-69
Han, Jun; Mayo, Julie; Xu, Xun et al. (2009) Indirect modulation of Shh signaling by Dlx5 affects the oral-nasal patterning of palate and rescues cleft palate in Msx1-null mice. Development 136:4225-33
Jeong, Juhee; Li, Xue; McEvilly, Robert J et al. (2008) Dlx genes pattern mammalian jaw primordium by regulating both lower jaw-specific and upper jaw-specific genetic programs. Development 135:2905-16
Polley, Daniel G B; Cobos, Inma; Merzenich, Michael M et al. (2006) Severe hearing loss in Dlxl mutant mice. Hear Res 214:84-8
Depew, Michael J; Simpson, Carol A; Morasso, Maria et al. (2005) Reassessing the Dlx code: the genetic regulation of branchial arch skeletal pattern and development. J Anat 207:501-61