The Molecular and Technology TRANSFER Core will provide Center for Craniofacial Development and Disorders. Investigators with access to modern molecular genetics services including DNA synthesis, DNA sequencing, mutation detection, DNA isolation, cell culture, lymphocyte transformation, cryopreservation, physical mapping regents and specific YAC clones. This core will also assist investigators evaluate technologies developed in their studies for commercial licensing and patentability. The Molecular and Technology Transfer Core will provide reagents and services for the Clinical ore and Projects I, II, V, VI and VII. It will also advise Projects I and II involved in animal models; Projects III and VI concerned with therapeutics for craniosynostosis; Projects V, VI and VII developing DNA diagnostic testing; and Project VIII regarding behavioral and psychological services. This Core will monitor and enhance the ability of the Center to develop potentially marketable products and other effective interventions.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Comprehensive Center (P60)
Project #
5P60DE013078-05
Application #
6765349
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
5
Fiscal Year
2003
Total Cost
$254,104
Indirect Cost
Name
Johns Hopkins University
Department
Type
DUNS #
001910777
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Richtsmeier, Joan T (2018) A century of development. Am J Phys Anthropol 165:726-740
Taub, Margaret A; Schwender, Holger; Beaty, Terri H et al. (2012) Incorporating genotype uncertainties into the genotypic TDT for main effects and gene-environment interactions. Genet Epidemiol 36:225-34
Ludwig, Kerstin U; Mangold, Elisabeth; Herms, Stefan et al. (2012) Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci. Nat Genet 44:968-71
Hill, Cheryl A; Vaddi, S; Moffitt, Amanda et al. (2011) Intracranial volume and whole brain volume in infants with unicoronal craniosynostosis. Cleft Palate Craniofac J 48:394-8
Aldridge, Kristina (2011) Patterns of differences in brain morphology in humans as compared to extant apes. J Hum Evol 60:94-105
Richtsmeier, J T; Deleon, V B (2009) Morphological integration of the skull in craniofacial anomalies. Orthod Craniofac Res 12:149-58
Frazier, Brenda C; Mooney, Mark P; Losken, H Wolfgang et al. (2008) Comparison of craniofacial phenotype in craniosynostotic rabbits treated with anti-Tgf-beta2 at suturectomy site. Cleft Palate Craniofac J 45:571-82
Parsons, Trish; Ryan, Timothy M; Reeves, Roger H et al. (2007) Microstructure of trabecular bone in a mouse model for Down syndrome. Anat Rec (Hoboken) 290:414-21
Mooney, Mark P; Losken, H Wolfgang; Moursi, Amr M et al. (2007) Postoperative anti-Tgf-beta2 antibody therapy improves intracranial volume and craniofacial growth in craniosynostotic rabbits. J Craniofac Surg 18:336-46;discussion 347-9
Mooney, Mark P; Losken, H Wolfgang; Moursi, Amr M et al. (2007) Anti-TGF-beta2 antibody therapy inhibits postoperative resynostosis in craniosynostotic rabbits. Plast Reconstr Surg 119:1200-12;discussion 1213-5

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