Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY010321-03
Application #
2164116
Study Section
Visual Sciences A Study Section (VISA)
Project Start
1994-01-01
Project End
1997-12-31
Budget Start
1996-01-01
Budget End
1996-12-31
Support Year
3
Fiscal Year
1996
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Ophthalmology
Type
Schools of Medicine
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Favor, Jack; Bradley, Alan; Conte, Nathalie et al. (2009) Analysis of Pax6 contiguous gene deletions in the mouse, Mus musculus, identifies regions distinct from Pax6 responsible for extreme small-eye and belly-spotting phenotypes. Genetics 182:1077-88
Favor, Jack; Gloeckner, Christian Johannes; Neuhauser-Klaus, Angelika et al. (2008) Relationship of Pax6 activity levels to the extent of eye development in the mouse, Mus musculus. Genetics 179:1345-55
Favor, Jack; Gloeckner, Christian Johannes; Janik, Dirk et al. (2007) Type IV procollagen missense mutations associated with defects of the eye, vascular stability, the brain, kidney function and embryonic or postnatal viability in the mouse, Mus musculus: an extension of the Col4a1 allelic series and the identification of Genetics 175:725-36
Huang, Kristen M; Geunes-Boyer, Scarlett; Wu, Sufen et al. (2004) Organization and annotation of the Xcat critical region: elimination of seven positional candidate genes. Genomics 83:893-901
Yu, Jindan; Farjo, Rafal; MacNee, Sean P et al. (2003) Annotation and analysis of 10,000 expressed sequence tags from developing mouse eye and adult retina. Genome Biol 4:R65
Brooks, David G; Manova-Todorova, Katia; Farmer, Jennifer et al. (2002) Ferritin crystal cataracts in hereditary hyperferritinemia cataract syndrome. Invest Ophthalmol Vis Sci 43:1121-6
Favor, J; Peters, H; Hermann, T et al. (2001) Molecular characterization of Pax6(2Neu) through Pax6(10Neu): an extension of the Pax6 allelic series and the identification of two possible hypomorph alleles in the mouse Mus musculus. Genetics 159:1689-700
Sidjanin, D J; Parker-Wilson, D M; Neuhauser-Klaus, A et al. (2001) A 76-bp deletion in the Mip gene causes autosomal dominant cataract in Hfi mice. Genomics 74:313-9
Favor, J; Neuhauser-Klaus, A (2000) Saturation mutagenesis for dominant eye morphological defects in the mouse Mus musculus. Mamm Genome 11:520-5
Grimes, P A; Koeberlein, B; Favor, J et al. (1998) Abnormal eye development associated with Cat4a, a dominant mouse cataract mutation on chromosome 8. Invest Ophthalmol Vis Sci 39:1863-9

Showing the most recent 10 out of 15 publications