Seq #146 Friday, 10 March 2006

2:00 PM-3:00 PM Dolphin Hotel Pacific Hall, Poster
Craniofacial Anomalies/ Genetics
 
1206  Brain Lateralization in Nonsyndromic Cleft Lip/Palate versus Control Groups
B.A. FRANKLIN1, S.M. WEINBERG2, C.A. BRANDON2, K.M. BARDI2, and M.L. MARAZITA2, 1University of Pittsburgh, School of Dental Medicine, PA, USA, 2University of Pittsburgh, PA, USA
1207  CBFA1 (RUNX2) Exon 1 Mutation Associated with CCD
R. SILBERSTEIN1, J. DONG2, S. CHARY-REDDY3, T. GU3, M. HERRERA3, and M. MACDOUGALL4, 1Private Practice, Higland Park, IL, USA, 2University of Alabama, Birmingham, USA, 3University of Texas - San Antonio / Health Science Ctr, USA, 4University of Alabama, School of Dentistry, Birmingham, USA
1208  Characterization of Pathways in the Spontaneous Cleft Lip Strain, A/WySn
B. NEWELL, University of Iowa College of Dentistry, Coralville, USA, S. BULLARD, College of Dentistry, Iowa City, IA, USA, H. MISHIMA, University of Iowa, Iowa City, USA, and A.C. LIDRAL, University of Iowa, USA
1209  Craniofacial and Intraoral Soft Tissue Findings in Hyper-IgE Syndrome Patients
D.L. DOMINGO1, N. TOMONA1, G.D. SINGH2, and T. HART1, 1National Institute of Dental and Craniofacial Research, Bethesda, MD, USA, 2University of Puerto Rico, San Juan, USA
1210  Deciphering Genetic Architecture of Facial Configuration using Congenic Mice
E.-K. PAE1, J. OH1, I. NISHIMURA1, C.-C.J. WANG1, M. POOLE1, and R. DAVIS2, 1UCLA School of Dentistry, Los Angeles, CA, USA, 2UCLA David Geffen School of Medicine, Los Angeles, CA, USA
1211  Runx2-Smad Molecular Interaction is Required for Integration of BMP Signal
A. JAVED1, J.-S. BAE2, F. AFZAL2, S. GUTIERREZ3, K. ZAIDI2, J. PRATAP2, A.J. VAN WIJNEN2, J.L. STEIN2, J.B. LIAN2, and G.S. STEIN2, 1University of Alabama, Institute of Oral Health Research, UAB School of Dentistry, Birmingham, USA, 2University of Massachusetts Medical School, Worcester, USA, 3Universidad de Concepcion, Chile
1212  Evaluating Non-coding Regions of PAX9 in Patients with Tooth Agenesis
C.M. CORBIN, W. SCRUGGS, E. BURNS, and S.A. FRAZIER-BOWERS, University of North Carolina, Chapel Hill, USA
1213  Evaluation of Candidate Genes at Chromosome 16q24.1 in NSCLP
B.T. CHIQUET1, A.M. CORTEZ2, S.H. BLANTON3, and J.T. HECHT2, 1UT Dental Branch, UT Graduate School of Biomedical Sciences, Houston, TX, USA, 2University of Texas - Houston/Health Science Center, UT Medical School, USA, 3University of Virginia, Charlottesville, VA, USA
1214  Fine Mapping Genetic Loci for Cleft Lip
A.C. LIDRAL1, L. MORENO1, M.L. MARAZITA2, M.E. COOPER2, B.S. MAHER2, T. MCHENRY2, C. VALENCIA-RAMIREZ3, A. HING4, T. BUSCH5, H. MISHIMA6, E. LAMMER7, M. JONES8, and M. ARCOS-BURGOS9, 1University of Iowa, USA, 2University of Pittsburgh, PA, USA, 3Universidad de Anioquia - Facultad de Odontologia, Medellín, Colombia, 4Children’s Hospital Medical Center, Craniofacial Center, Seattle, WA, 5University of Iowa, Dows Institute for Dental Research, Iowa City, USA, 6University of Iowa, Iowa City, USA, 7Childrens Hospital of Oakland Research Institute, CA, USA, 8Childrens Hospital of San Diego, Dysmorphology and Genetics, CA, USA, 9NHGRI/NIH, Medical Genetic Branch, Bethesda, DC, USA
1215  Molecular Characterization of a Novel PAX9 Mutation Crossing Tooth Agenesis
H. KAPADIA1, S.A. FRAZIER-BOWERS2, T. OGAWA1, and R. D'SOUZA3, 1University of Texas Health Science Center at Houston, Dental Branch, USA, 2University of North Carolina, Chapel Hill, USA, 3University of Texas - Houston/Health Science Center, USA
1216  Juvenile Hyaline Fibromatosis Due to Founder Mutation in Brazil
D. PALLOS1, P.S. HART2, M.D. RAMASWAMI2, A.C. ACEVEDO3, H. MESTRINHO3, C. SPECK4, and T. HART5, 1Universidade de Taubate, Brazil, 2National Insitutes of Health, Bethesda, MD, USA, 3Universidade De Brasilia, Brazil, 4Sarah Kubitschek Hospital, Brasilia, Brazil, 5National Institute of Dental and Craniofacial Research, Bethesda, MD, USA
1217  NFI-C Mutation Associated with Autosomal Recessive Radicular Dentin Dysplasia
M. MACDOUGALL1, J. DONG2, M. HERRERA3, M. GALINDO4, T. GU4, H.D. MESTRINHO5, L.M. PAULA6, and A.C. ACEVEDO5, 1University of Alabama, School of Dentistry, Birmingham, USA, 2University of Alabama, Birmingham, USA, 3University of Texas - San Antonio / Health Science Ctr, Dental School, USA, 4University of Texas - San Antonio / Health Science Ctr, USA, 5Universidade De Brasilia, Brasília, Brazil, 6Universidade De Brasilia, Brazil
1218  Oral Manifestations of Three Brazilian Patients with Kabuki make-up Syndrome
H.D. MESTRINHO, S.P. SOBRAL, M.G.F. MARCOS, I. FERRARI, H.P.N. SAFATLE, M.S. CÓRDOBA, B.R. VERSIANI, and A.C. ACEVEDO, Universidade De Brasilia, Brasília, Brazil
1219  Structure-Function Analysis of Human PAX9 Paired Domain Missense Mutations
H. KAPADIA, L. SHEVCHENKO, T. OGAWA, and R. D'SOUZA, University of Texas - Houston/Health Science Center, USA
1220  Systemic Osteoporosis with Inflammation in Mice Having a Cherubism Mutation
Y. UEKI1, C.-Y. LIN1, E. REICHENBERGER2, and B.R. OLSEN1, 1Harvard School of Dental Medicine, Boston, MA, USA, 2University of Connecticut, Farmington, USA
1221  WITHDRAWN
1222  Axenfeld-Rieger Syndrome: Involvement of PITX2A and LEF-1 Protein Interactions
L. TREVIÑO, University of Texas - Houston/Health Science Center, USA, and B.A. AMENDT, Texas A&M University System Health Science Center in Houston, USA

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