Platelet dysfunction associated with wilms tumor and hyaluronic acid
β Scribed by Arthur W. Bracey; Alan H. B. Wu; Javier Aceves; Thomas Chow; Shirley Carlile; W. Keith Hoots
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 707 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0361-8609
No coin nor oath required. For personal study only.
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Wilms' tumor is a childhood nephroblastoma that is postulated to arise through the inactivation of a tumor suppressor gene by a two-hit mechanism. A candidate I I p I 3 Wilms' tumor gene, WTI. has been cloned and shown to encode a zinc finger protein. Patients with the WAGR syndrome (Wilms' tumor, a
## Abstract ## BACKGROUND Although metastatic disease is the primary cause of death from epithelial ovarian carcinoma, to the authors' knowledge the cellular mechanisms that regulate intraperitoneal metastasis are largely unknown. Metastasizing ovarian carcinoma cells encounter a collagenβrich mic