Zobrazeno 1 - 10
of 35
pro vyhledávání: '"E. A. Ostrander"'
Autor:
R. E. Griffiths, K. U. Ratnatunga, S. Casertano, M. Im, L. W. Neuschaefer, R. S. Ellis, G. F. Gilmore, R. A. W. Elson, K. Glazebrook, B. Santiago, R. A. Windhorst, S. P. Driver, E. J. Ostrander, S. B. Mutz, D. C. Koo, G. D. Illingworth, D. A. Forbes, A. C. Phillips, R. F. Green, J. P. Huchra, A. J. Tyson
Publikováno v:
Symposium - International Astronomical Union. 168:219-227
With HST and WFPC2, galaxies in the Medium Deep Survey can be reliably classified to magnitudesI814≲ 22.0 in the F814W band, at a mean redshift. The main result is the relatively high proportion (~40%) of objects which are in some way irregular or
Publikováno v:
Molecular ecology. 14(2)
Single nucleotide polymorphisms (SNPs) have the potential to become the genetic marker of choice in studies of the ecology and conservation of natural populations because of their capacity to access variability across the genome. In this study, we pr
Autor:
G M, Acland, E A, Ostrander
Publikováno v:
Heredity. 90(3)
Autor:
D J, Sidjanin, B, Zangerl, J L, Johnson, F, Xue, C, Mellersh, E A, Ostrander, G, Acland, G D, Aguirre
Publikováno v:
Animal genetics. 33(2)
Autor:
Q, Zhang, G M, Acland, B, Zangerl, J L, Johnson, Z, Mao, C J, Zeiss, E A, Ostrander, G D, Aguirre
Publikováno v:
Investigative ophthalmologyvisual science. 42(11)
Canine X-linked progressive retinal atrophy (XLPRA) is a hereditary, progressive retinal degeneration that has been mapped previously to the canine X chromosome in a region flanked by the dystrophin (DMD) and tissue inhibitor of metalloproteinase 1 (
Autor:
E L, Goode, J L, Stanford, M A, Peters, M, Janer, M, Gibbs, S, Kolb, M D, Badzioch, L, Hood, E A, Ostrander, G P, Jarvik
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 7(9)
Hereditary prostate cancer is an etiologically heterogeneous disease with six susceptibility loci mapped to date. We aimed to describe a collection of high-risk prostate cancer families and assess linkage to multiple markers at four loci: HPC1 (1q24-
Publikováno v:
Cancer. 92(3)
An increased incidence of breast carcinoma has been reported among relatives of individuals who are affected with the rare recessive disorder, ataxia-telangiectasia (A-T), and who are heterozygous for mutations in the ataxia-telangiectasia mutated (A
Autor:
E L, Goode, J L, Stanford, L, Chakrabarti, M, Gibbs, S, Kolb, R A, McIndoe, V A, Buckley, E F, Schuster, C L, Neal, E L, Miller, S, Brandzel, L, Hood, E A, Ostrander, G P, Jarvik
Publikováno v:
Genetic epidemiology. 18(3)
Confirmation of linkage and estimation of the proportion of families who are linked in large independent datasets is essential to understanding the significance of cancer susceptibility genes. We report here on an analysis of 150 high-risk prostate c