Functional analysis of a type IIB von Willebrand disease missense mutation: increased binding of large von Willebrand factor multimers to platelets.

Por Cooney, K A, Lyons, S E, Ginsburg, D
Publicado em 1992

Absence of truncating BRIP1 mutations in chromosome 17q-linked hereditary prostate cancer families

Por Ray, A M, Zuhlke, K A, Johnson, G R, Levin, A M, Douglas, J A, Lange, E M, Cooney, K A
Publicado em 2009

The molecular defect in type IIB von Willebrand disease. Identification of four potential missense mutations within the putative GpIb binding domain.

Por Cooney, K A, Nichols, W C, Bruck, M E, Bahou, W F, Shapiro, A D, Bowie, E J, Gralnick, H R, Ginsburg, D
Publicado em 1991

Hereditary prostate cancer in African American families: linkage analysis using markers that map to five candidate susceptibility loci

Por Brown, W M, Lange, E M, Chen, H, Zheng, S L, Chang, B, Wiley, K E, Isaacs, S D, Walsh, P C, Isaacs, W B, Xu, J, Cooney, K A
Publicado em 2004

Integrative molecular profiling of routine clinical prostate cancer specimens

Por Grasso, C. S., Cani, A. K., Hovelson, D. H., Quist, M. J., Douville, N. J., Yadati, V., Amin, A. M., Nelson, P. S., Betz, B. L., Liu, C-J., Knudsen, K. E., Cooney, K. A., Feng, F. Y., McDaniel, A. S., Tomlins, S. A.
Publicado no Ann Oncol (2015)