Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Research Project (R01)
Project #
5R01HG000333-24
Application #
2208741
Study Section
Genome Study Section (GNM)
Program Officer
Feingold, Elise A
Project Start
1976-06-01
Project End
1998-05-31
Budget Start
1996-06-01
Budget End
1998-05-31
Support Year
24
Fiscal Year
1996
Total Cost
Indirect Cost
Name
Roswell Park Cancer Institute Corp
Department
Type
DUNS #
City
Buffalo
State
NY
Country
United States
Zip Code
14263
Penziner, Elizabeth; Williams, Janet K; Erwin, Cheryl et al. (2008) Perceptions of discrimination among persons who have undergone predictive testing for Huntington's disease. Am J Med Genet B Neuropsychiatr Genet 147:320-5
Zhang, J; Qin, S; Sait, S N et al. (2001) The pericentromeric region of human chromosome 11: evidence for a chromosome-specific duplication. Cytogenet Cell Genet 94:137-41
Scott, I C; Clark, T G; Takahara, K et al. (1999) Assignment of TLL1 and TLL2, which encode human BMP-1/Tolloid-related metalloproteases, to chromosomes 4q32-->q33 and 10q23-->q24 and assignment of murine Tll2 to chromosome 19. Cytogenet Cell Genet 86:64-5
Weber, T K; Conroy, J; Keitz, B et al. (1999) Genome-wide allelotyping indicates increased loss of heterozygosity on 9p and 14q in early age of onset colorectal cancer. Cytogenet Cell Genet 86:142-7
Stumpo, D J; Eddy Jr, R L; Haley, L L et al. (1998) Promoter sequence, expression, and fine chromosomal mapping of the human gene (MLP) encoding the MARCKS-like protein: identification of neighboring and linked polymorphic loci for MLP and MACS and use in the evaluation of human neural tube defects. Genomics 49:253-64
Higgins, M J; Day, C D; Smilinich, N J et al. (1998) Contig maps and genomic sequencing identify candidate genes in the usher 1C locus. Genome Res 8:57-68
Cooper, P R; Smilinich, N J; Day, C D et al. (1998) Divergently transcribed overlapping genes expressed in liver and kidney and located in the 11p15.5 imprinted domain. Genomics 49:38-51
Varon, R; Vissinga, C; Platzer, M et al. (1998) Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome. Cell 93:467-76
Watson Jr, B; Nowak, N J; Myracle, A D et al. (1997) The human angiotensinase C gene (HUMPCP) maps to 11q14 within 700 kb of D11S901: a candidate gene for essential hypertension. Genomics 44:365-7
Crider-Miller, S J; Reid, L H; Higgins, M J et al. (1997) Novel transcribed sequences within the BWS/WT2 region in 11p15.5: tissue-specific expression correlates with cancer type. Genomics 46:355-63

Showing the most recent 10 out of 51 publications