𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Evidence of a hereditary p53 syndrome in cancer-prone families

Publisher
John Wiley and Sons
Year
1996
Tongue
French
Weight
425 KB
Volume
65
Category
Article
ISSN
0020-7136

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Multifocal accumulation of p53 protein i
Multifocal accumulation of p53 protein in esophageal carcinoma: Evidence for field cancerization
✍ Defa Tian; Zumei Feng; Nancy M. Hanley; R. Woodrow Setzer; Judy L. Mumford; Davi πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 French βš– 429 KB πŸ‘ 2 views

A systematic characterization of the cancerization field of esophageal carcinoma based on p53 protein accumulation has not been reported previously. The present report presents such a study based on 50 specimens of esophageal squamouscell carcinoma from northern China. To gain insight into the etiol

No evidence for a role ofBRCA1 orBRCA2 m
No evidence for a role ofBRCA1 orBRCA2 mutations in Ashkenazi Jewish families with hereditary prostate cancer
✍ Wilkens, Eric P.; Freije, Diha; Xu, Jianfeng; Nusskern, Deborah R.; Suzuki, Hiro πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 167 KB πŸ‘ 2 views

## BACKGROUND. Two genes responsible for hereditary breast cancer (BRCA1 and BRCA2) have been identified, and predisposing mutations identified. Several studies have provided evidence that germline mutations in BRCA1 and BRCA2 confer an increased risk of prostate cancer. Based on these findings, o

Features of gastric cancer in hereditary
Features of gastric cancer in hereditary non-polyposis colorectal cancer syndrome
✍ Markku Aarnio; Reijo Salovaara; Lauri A. Aaltonen; Jukka-Pekka Mecklin; Heikki J πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 French βš– 77 KB πŸ‘ 2 views

To identify characteristics of gastric cancer associated with hereditary non-polyposis colorectal cancer (HNPCC), we gathered clinical data and tumor samples relating to patients recorded in the Finnish HNPCC registry. Our series included 51 families with a characterized mutation and/or that met the