𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Point Mutations of the Mxil Gene are Rare in Prostate Cancers

✍ Scribed by Norihiko Kawamata; Dorothy Park; Sharon Wilczynski; Jun Yokota; H. Phillip Koeffler


Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
268 KB
Volume
29
Category
Article
ISSN
0270-4137

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Conserved region mutations of the p53 ge
✍ Petra Jernvall; Markus MΓ€kinen; Tuomo Karttunen; Jyrki MΓ€kelΓ€; Pirkko Vihko πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 French βš– 247 KB πŸ‘ 2 views

Distal colorectal cancers, especially those in the rectum, are more aggressive and more commonly recurrent than proximal cancers. We studied the possible relationship between p53-gene mutation type and location of the tumour, since mutations in the conserved areas of the p53 gene have been suggested

Mutation and expression analysis of thep
✍ Yokomizo, Akira; Mai, Ming; Bostwick, David G.; Tindall, Donald J.; Qian, Junqi; πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 365 KB πŸ‘ 1 views

BACKGROUND. p53 is the most highly mutated tumor suppressor gene in human cancers. Recently, p73, a first homologue of p53, was identified and considered to be an imprinted tumor suppressor gene. Thus, we analyzed the possible role of p73 in human prostate cancers. METHODS. We investigated the expre

Commonly occurring loss and mutation of
✍ Edward V. Prochownik; Linette Eagle Grove; Debra Deubler; Xiao Lin Zhu; Robert A πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 341 KB πŸ‘ 1 views

One of the most common chromosomal abnormalities in prostate cancer involves loss of 10q22-qter. Rarely, a smaller deletion, involving 10q24-q25, has been observed, suggesting the presence of a tumor suppressor gene at this site. We previously demonstrated that the MXI1 gene maps to 10q24-q25 and is

Expression and mutational analysis of th
✍ Latil, Alain; Pesche, Sandrine; ValοΏ½ri, Antoine; Fournier, Georges; Cussenot, Ol πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 229 KB πŸ‘ 2 views

BACKGROUND. Loss of heterozygosity (LOH) on chromosome arm 18q is common in sporadic prostate cancer and may be involved in cancer development through inactivation of tumor-suppressor genes (TSG). Recent identification, at 18q21.1, of MADR2/Smad2, a key component in transforming growth factor ␀ (TGF