Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM033160-03
Application #
4693667
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
3
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Roswell Park Cancer Institute Corp
Department
Type
DUNS #
City
Buffalo
State
NY
Country
United States
Zip Code
14263
Singh, U; Sun, T; Larsson, T et al. (2006) Expression and functional analysis of fibulin-1 (Fbln1) during normal and abnormal placental development of the mouse. Placenta 27:1014-21
Singh, Umashankar; Sun, Tong; Shi, Wei et al. (2005) Expression and functional analysis of genes deregulated in mouse placental overgrowth models: Car2 and Ncam1. Dev Dyn 234:1034-45
Elliott, Rosemary W; Poslinski, Diane; Tabaczynski, Debra et al. (2004) Loci affecting male fertility in hybrids between Mus macedonicus and C57BL/6. Mamm Genome 15:704-10
Elliott, R W; Miller, D R; Pearsall, R S et al. (2001) Genetic analysis of testis weight and fertility in an interspecies hybrid congenic strain for Chromosome X. Mamm Genome 12:45-51
Hemberger, M; Kurz, H; Orth, A et al. (2001) Genetic and developmental analysis of X-inactivation in interspecific hybrid mice suggests a role for the Y chromosome in placental dysplasia. Genetics 157:341-8
Hemberger, M C; Pearsall, R S; Zechner, U et al. (1999) Genetic dissection of X-linked interspecific hybrid placental dysplasia in congenic mouse strains. Genetics 153:383-90
Lueders, K K; Elliott, R W; Marenholz, I et al. (1999) Genomic organization and mapping of the human and mouse neuronal beta2-nicotinic acetylcholine receptor genes. Mamm Genome 10:900-5
LI, W; Elliott, R W; Novak, E K et al. (1999) cDNA sequence and mapping of the mouse Copb gene encoding the beta subunit of the COPI coatomer complex. Somat Cell Mol Genet 25:177-83
Zhao, X F; Colaizzo-Anas, T; Nowak, N J et al. (1998) The mammalian homologue of mago nashi encodes a serum-inducible protein. Genomics 47:319-22
Dal Zotto, L; Quaderi, N A; Elliott, R et al. (1998) The mouse Mid1 gene: implications for the pathogenesis of Opitz syndrome and the evolution of the mammalian pseudoautosomal region. Hum Mol Genet 7:489-99

Showing the most recent 10 out of 76 publications