ELAC2/HPC2 involvement in hereditary and sporadic prostate cancer.
暂无分享,去创建一个
J. Schleutker | T. Tammela | O. Kallioniemi | A. Rökman | T. Ikonen | N. Mononen | V. Autio | M. Matikainen | P. Koivisto | Nina Mononen | Olli-P. Kallioniemi
[1] Peter Beighton,et al. de la Chapelle, A. , 1997 .
[2] L. Peltonen. Molecular background of the Finnish disease heritage. , 1997, Annals of medicine.
[3] F. Wright,et al. Linkage disequilibrium mapping in isolated populations: the example of Finland revisited. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[4] A. Syvänen. Solid-phase minisequencing as a tool to detect DNA polymorphism. , 1998, Methods in molecular biology.
[5] J. Carpten,et al. A genetic epidemiological study of hereditary prostate cancer (HPC) in Finland: frequent HPCX linkage in families with late-onset disease. , 2000, Clinical cancer research : an official journal of the American Association for Cancer Research.
[6] J. Schleutker,et al. Two percent of Finnish prostate cancer patients have a germ-line mutation in the hormone-binding domain of the androgen receptor gene. , 2000, Cancer research.
[7] J. Stanford,et al. Genetics of prostate cancer: too many loci, too few genes. , 2000, American journal of human genetics.
[8] T. Rebbeck,et al. Association of HPC2/ELAC2 genotypes and prostate cancer. , 2000, American journal of human genetics.
[9] Siavash Ghaffari,et al. A candidate prostate cancer susceptibility gene at chromosome 17p , 2001, Nature Genetics.
[10] J. Trachtenberg,et al. HPC2 variants and screen-detected prostate cancer. , 2001, American journal of human genetics.
[11] J. Carpten,et al. Evaluation of linkage and association of HPC2/ELAC2 in patients with familial or sporadic prostate cancer. , 2001, American journal of human genetics.