Rulang Jiang, Ph.D.
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Contact
University of Rochester
School of Medicine and Dentistry
601 Elmwood Ave, Box 611
Rochester, New York 14642
Office: 585 273-1426
Fax: 585 276-0190

Craniofacial malformations, including cleft lip and palate, are common disfiguring birth defects in humans, occurring at a frequency of approximately 1 in 600 infants. The causes of such birth defects are complex, involving multiple genetic and environmental factors. To gain a better understanding of the molecular mechanisms underlying normal craniofacial development and the pathogenic processes leading to congenital craniofacial malformations, we are using a combination of genetic, biochemical, and embryological approaches to analyze craniofacial development in the model mammalian system, the laboratory mice. We are using both forward and reverse genetic approaches to investigate the molecular mechanisms of craniofacial birth defects. The forward genetic approach involves identification of causal genes and molecular pathways disrupted by uncharacterized mutations that cause craniofacial malformations including cleft lip and/or cleft palate (e.g., we recently positionally cloned the classic orofacial cleft mutation Dancer), whereas the reverse genetic approach involves generation and analyses of mice carrying null or conditional mutations using the Cre/loxP-mediated gene targeting techniques. Current gene targeting projects focus on investigating the roles of transcription factors and signaling molecules exhibiting tissue specific expression patterns during craniofacial development. In the last few years, we have analyzed more than five different mutant mouse strains with craniofacial developmental defects. Using these mutant mouse models, we are attempting to delineate the molecular pathways and to identify novel genes that interact with known critical regulators of craniofacial development using genetic modifier screening, genomic manipulations, microarray-based gene expression profiling, as well as protein-protein interaction studies. These studies are providing new insights into the molecular genetic mechanisms underlying human craniofacial development and birth defects.
Current Appointments
- Professor - Department of Biomedical Genetics, Center for Oral Biology (SMD)
- Professor - Department of Biology (RC)
- Professor - Department of Dentistry (SMD)
| Education | ||
|---|---|---|
| PhD Biology | Wesleyan University | 1995 |
| MS Genetics | Institute of Genetics, Chinese Academy of Sciences | 1987 |
| BS Biology | Nanjing Normal University | 1984 |
| Post-Doctoral Training & Residency | |
|---|---|
| Postdoc Associate, The Jackson Laboratory, Bar Harbor, ME | 1995 - 1998 |
| Postdoc Associate, Roche Institute of Molecular Biology, Nutley, NJ | 1994 - 1995 |
Lab Description
Molecular Genetic Basis of Craniofacial Development and Birth Defects
Lab Website
http://www.urmc.rochester.edu/biomedical-genetics/faculty/jiang-lab.cfm
| Recent Journal Articles |
|---|
| Showing the 5 most recent journal articles. (38 available) |
| Zhang Z; Lan Y; Chai Y; Jiang R. "Antagonistic actions of Msx1 and Osr2 pattern mammalian teeth into a single row." Science (New York, N.Y.). 2009; 323(5918):1232-4. |
| Lan Y; Jiang R. "Sonic hedgehog signaling regulates reciprocal epithelial-mesenchymal interactions controlling palatal outgrowth." Development (Cambridge, England). 2009; 136(8):1387-96. |
| Xiong W; He F; Morikawa Y; Yu X; Zhang Z; Lan Y; Jiang R; Cserjesi P; Chen Y. "Hand2 is required in the epithelium for palatogenesis in mice." Developmental biology. 2009; 330(1):131-41. Epub 2009 Mar 31. |
| Gao Y; Lan Y; Ovitt CE; Jiang R. "Functional equivalence of the zinc finger transcription factors Osr1 and Osr2 in mouse development." Developmental biology. 2009; 328(2):200-9. Epub 2009 Jan 14. |
| Richardson RJ; Dixon J; Jiang R; Dixon MJ. "Integration of IRF6 and Jagged2 signalling is essential for controlling palatal adhesion and fusion competence." Human molecular genetics. 2009; Epub 2009 May 13. |

