The Administrative Core does the accounting, record keeping, purchasing, preparation of continuation reports and final drafts of manuscripts, seminar, meeting, and travel arrangements, and other reporting required for this Program and assists the PD in tracking oversight and compliance. Most of this activity is supported by the Institute of Neuroscience;the Program supports 15% of a Grant Administrator, 20% of an Office Specialist and 10% of the PD's salary.

Public Health Relevance

The aims of this Program Project Grant are to understand the developmental basis of phenotypic variation in three human diseases, Fraser syndrome. Usher syndrome and Hirschsprung disease. The four Core Units ~ Administration, Microimaging, Technical Support and Zebrafish Facility ~ provide the administrative and technical support required to accomplish the Aims of the Component Projects within this Program Project Grant.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Program Projects (P01)
Project #
5P01HD022486-27
Application #
8737028
Study Section
Special Emphasis Panel (ZHD1-DSR-Y)
Project Start
Project End
Budget Start
2014-07-01
Budget End
2015-06-30
Support Year
27
Fiscal Year
2014
Total Cost
$55,775
Indirect Cost
$17,310
Name
University of Oregon
Department
Type
DUNS #
948117312
City
Eugene
State
OR
Country
United States
Zip Code
97403
Blanco-Sánchez, Bernardo; Clément, Aurélie; Fierro Jr, Javier et al. (2014) Complexes of Usher proteins preassemble at the endoplasmic reticulum and are required for trafficking and ER homeostasis. Dis Model Mech 7:547-59
McMenamin, Sarah K; Bain, Emily J; McCann, Anna E et al. (2014) Thyroid hormone-dependent adult pigment cell lineage and pattern in zebrafish. Science 345:1358-61
Santos, M Emília; Braasch, Ingo; Boileau, Nicolas et al. (2014) The evolution of cichlid fish egg-spots is linked with a cis-regulatory change. Nat Commun 5:5149
Beahm, Brendan J; Dehnert, Karen W; Derr, Nicolas L et al. (2014) A visualizable chain-terminating inhibitor of glycosaminoglycan biosynthesis in developing zebrafish. Angew Chem Int Ed Engl 53:3347-52
DeLaurier, April; Huycke, Tyler R; Nichols, James T et al. (2014) Role of mef2ca in developmental buffering of the zebrafish larval hyoid dermal skeleton. Dev Biol 385:189-99
Kimmel, Charles B (2014) Skull developmental modularity: a view from a single bone - or two. J Appl Ichthyol 30:600-607
Beck, Bodo B; Phillips, Jennifer B; Bartram, Malte P et al. (2014) Mutation of POC1B in a severe syndromic retinal ciliopathy. Hum Mutat 35:1153-62
Sheehan-Rooney, Kelly; Swartz, Mary E; Zhao, Feng et al. (2013) Ahsa1 and Hsp90 activity confers more severe craniofacial phenotypes in a zebrafish model of hypoparathyroidism, sensorineural deafness and renal dysplasia (HDR). Dis Model Mech 6:1285-91
Paquette, Colleen E; Kent, Michael L; Buchner, Cari et al. (2013) A retrospective study of the prevalence and classification of intestinal neoplasia in zebrafish (Danio rerio). Zebrafish 10:228-36
Rodriguez-Mari, Adriana; Canestro, Cristian; BreMiller, Ruth A et al. (2013) Retinoic acid metabolic genes, meiosis, and gonadal sex differentiation in zebrafish. PLoS One 8:e73951

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