Accumulation of allelic losses on chromosome 10 in human gliomas at recurrence

Author:

Tokiyoshi K,Yoshimine T,Maruno M,Muhammad A K M G,Hayakawa T

Publisher

BMJ

Subject

Pathology and Forensic Medicine

Reference19 articles.

1. Molecular analysis of genetic abnormalities in human gliomas;Bello, M.J.; Campos, J.M.; Kusak, M.E.; Vaquero, J.; Sarasa, J.L.; Pestana, A.;Cancer Genet Cytogenet,1994

2. TP53 gene mutations and 17p deletions in human astrocytomas;Chung, R.; Whaley, J.; Kely, N.; Anderson, K.; Louis, D.; Menon, A.;Genes Chromosorn Cancer,1991

3. p53 mutations are associated with 17p allied loss in grade II and grade III astrocytoma;Deimiling, A.; Eibl, R.H.; Ohgaki, H.; Louis, D.N.; Ammon, K.; Peterson, I.;Cancer Res,1992

4. Subsets of glioblastoma multiforme defined by molecular genetic analysis;Deimling, A.; Ammon, K.; Schoenfeld, D.; Wiestler, O.D.; Seizinger, B.R.; Louis, D.N.;Brain Pathology,1993

5. Amplified and rearranged epidermal growth factor receptor genes in human gliomas reveal deletions of sequences encoding portions of;Ekstrand, A.J.; Sugawa, N.; James, C.D.; Collins, V.P.,1992

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